dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs1489849541
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr9:8460527 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- C>A / C>G / C>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
G=0.000012 (3/250720, GnomAD_exome)T=0.000007 (1/140168, GnomAD)T=0.00000 (0/10680, ALFA)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- PTPRD : Missense Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
Population | Group | Sample Size | Ref Allele | Alt Allele | Ref HMOZ | Alt HMOZ | HTRZ | HWEP |
---|---|---|---|---|---|---|---|---|
Total | Global | 10680 | C=1.00000 | T=0.00000 | 1.0 | 0.0 | 0.0 | N/A |
European | Sub | 6962 | C=1.0000 | T=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
African | Sub | 2294 | C=1.0000 | T=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
African Others | Sub | 84 | C=1.00 | T=0.00 | 1.0 | 0.0 | 0.0 | N/A |
African American | Sub | 2210 | C=1.0000 | T=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
Asian | Sub | 108 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
East Asian | Sub | 84 | C=1.00 | T=0.00 | 1.0 | 0.0 | 0.0 | N/A |
Other Asian | Sub | 24 | C=1.00 | T=0.00 | 1.0 | 0.0 | 0.0 | N/A |
Latin American 1 | Sub | 146 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
Latin American 2 | Sub | 610 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
South Asian | Sub | 94 | C=1.00 | T=0.00 | 1.0 | 0.0 | 0.0 | N/A |
Other | Sub | 466 | C=1.000 | T=0.000 | 1.0 | 0.0 | 0.0 | N/A |
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
DownloadStudy | Population | Group | Sample Size | Ref Allele | Alt Allele |
---|---|---|---|---|---|
gnomAD - Exomes | Global | Study-wide | 250720 | C=0.999988 | G=0.000012 |
gnomAD - Exomes | European | Sub | 134862 | C=0.999978 | G=0.000022 |
gnomAD - Exomes | Asian | Sub | 48996 | C=1.00000 | G=0.00000 |
gnomAD - Exomes | American | Sub | 34462 | C=1.00000 | G=0.00000 |
gnomAD - Exomes | African | Sub | 16228 | C=1.00000 | G=0.00000 |
gnomAD - Exomes | Ashkenazi Jewish | Sub | 10060 | C=1.00000 | G=0.00000 |
gnomAD - Exomes | Other | Sub | 6112 | C=1.0000 | G=0.0000 |
gnomAD - Genomes | Global | Study-wide | 140168 | C=0.999993 | T=0.000007 |
gnomAD - Genomes | European | Sub | 75912 | C=0.99999 | T=0.00001 |
gnomAD - Genomes | African | Sub | 42040 | C=1.00000 | T=0.00000 |
gnomAD - Genomes | American | Sub | 13634 | C=1.00000 | T=0.00000 |
gnomAD - Genomes | Ashkenazi Jewish | Sub | 3320 | C=1.0000 | T=0.0000 |
gnomAD - Genomes | East Asian | Sub | 3112 | C=1.0000 | T=0.0000 |
gnomAD - Genomes | Other | Sub | 2150 | C=1.0000 | T=0.0000 |
Allele Frequency Aggregator | Total | Global | 10680 | C=1.00000 | T=0.00000 |
Allele Frequency Aggregator | European | Sub | 6962 | C=1.0000 | T=0.0000 |
Allele Frequency Aggregator | African | Sub | 2294 | C=1.0000 | T=0.0000 |
Allele Frequency Aggregator | Latin American 2 | Sub | 610 | C=1.000 | T=0.000 |
Allele Frequency Aggregator | Other | Sub | 466 | C=1.000 | T=0.000 |
Allele Frequency Aggregator | Latin American 1 | Sub | 146 | C=1.000 | T=0.000 |
Allele Frequency Aggregator | Asian | Sub | 108 | C=1.000 | T=0.000 |
Allele Frequency Aggregator | South Asian | Sub | 94 | C=1.00 | T=0.00 |
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Sequence name | Change |
---|---|
GRCh38.p14 chr 9 | NC_000009.12:g.8460527C>A |
GRCh38.p14 chr 9 | NC_000009.12:g.8460527C>G |
GRCh38.p14 chr 9 | NC_000009.12:g.8460527C>T |
GRCh37.p13 chr 9 | NC_000009.11:g.8460527C>A |
GRCh37.p13 chr 9 | NC_000009.11:g.8460527C>G |
GRCh37.p13 chr 9 | NC_000009.11:g.8460527C>T |
PTPRD RefSeqGene | NG_033963.1:g.2157197G>T |
PTPRD RefSeqGene | NG_033963.1:g.2157197G>C |
PTPRD RefSeqGene | NG_033963.1:g.2157197G>A |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
PTPRD transcript variant 5 | NM_001040712.2:c.2517G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 5 precursor | NP_001035802.1:p.Met839Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 5 | NM_001040712.2:c.2517G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 5 precursor | NP_001035802.1:p.Met839Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 5 | NM_001040712.2:c.2517G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 5 precursor | NP_001035802.1:p.Met839Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 3 | NM_130392.3:c.2526G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 3 precursor | NP_569076.2:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 3 | NM_130392.3:c.2526G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 3 precursor | NP_569076.2:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 3 | NM_130392.3:c.2526G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 3 precursor | NP_569076.2:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 4 | NM_130393.3:c.2511G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 4 precursor | NP_569077.2:p.Met837Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 4 | NM_130393.3:c.2511G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 4 precursor | NP_569077.2:p.Met837Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 4 | NM_130393.3:c.2511G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 4 precursor | NP_569077.2:p.Met837Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 1 | NM_002839.4:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 1 precursor | NP_002830.1:p.Met1253Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 1 | NM_002839.4:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 1 precursor | NP_002830.1:p.Met1253Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 1 | NM_002839.4:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 1 precursor | NP_002830.1:p.Met1253Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 2 | NM_130391.4:c.2526G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 2 precursor | NP_569075.2:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 2 | NM_130391.4:c.2526G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 2 precursor | NP_569075.2:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 2 | NM_130391.4:c.2526G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 2 precursor | NP_569075.2:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 6 | NM_001171025.2:c.2496G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 6 precursor | NP_001164496.1:p.Met832Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 6 | NM_001171025.2:c.2496G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 6 precursor | NP_001164496.1:p.Met832Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 6 | NM_001171025.2:c.2496G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 6 precursor | NP_001164496.1:p.Met832Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 9 | NM_001377958.1:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 9 precursor |
NP_001364887.1:p.Met1254I… NP_001364887.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 9 | NM_001377958.1:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 9 precursor |
NP_001364887.1:p.Met1254I… NP_001364887.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 9 | NM_001377958.1:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 9 precursor |
NP_001364887.1:p.Met1254I… NP_001364887.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 7 | NM_001377946.1:c.2508G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 7 precursor | NP_001364875.1:p.Met836Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 7 | NM_001377946.1:c.2508G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 7 precursor | NP_001364875.1:p.Met836Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 7 | NM_001377946.1:c.2508G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 7 precursor | NP_001364875.1:p.Met836Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 8 | NM_001377947.1:c.2520G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 8 precursor | NP_001364876.1:p.Met840Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 8 | NM_001377947.1:c.2520G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 8 precursor | NP_001364876.1:p.Met840Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 8 | NM_001377947.1:c.2520G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 8 precursor | NP_001364876.1:p.Met840Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 10 | NM_001378058.1:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 10 precursor |
NP_001364987.1:p.Met1253I… NP_001364987.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 10 | NM_001378058.1:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 10 precursor |
NP_001364987.1:p.Met1253I… NP_001364987.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant 10 | NM_001378058.1:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform 10 precursor |
NP_001364987.1:p.Met1253I… NP_001364987.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X1 | XM_017014958.3:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_016870447.1:p.Met1254I… XP_016870447.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X1 | XM_017014958.3:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_016870447.1:p.Met1254I… XP_016870447.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X1 | XM_017014958.3:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_016870447.1:p.Met1254I… XP_016870447.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X2 | XM_017014961.3:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_016870450.1:p.Met1254I… XP_016870450.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X2 | XM_017014961.3:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_016870450.1:p.Met1254I… XP_016870450.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X2 | XM_017014961.3:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_016870450.1:p.Met1254I… XP_016870450.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X3 | XM_047423641.1:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_047279597.1:p.Met1254I… XP_047279597.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X3 | XM_047423641.1:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_047279597.1:p.Met1254I… XP_047279597.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X3 | XM_047423641.1:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X1 |
XP_047279597.1:p.Met1254I… XP_047279597.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X4 | XM_017014964.3:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X2 |
XP_016870453.1:p.Met1253I… XP_016870453.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X4 | XM_017014964.3:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X2 |
XP_016870453.1:p.Met1253I… XP_016870453.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X4 | XM_017014964.3:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X2 |
XP_016870453.1:p.Met1253I… XP_016870453.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X5 | XM_017014963.3:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X3 |
XP_016870452.1:p.Met1254I… XP_016870452.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X5 | XM_017014963.3:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X3 |
XP_016870452.1:p.Met1254I… XP_016870452.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X5 | XM_017014963.3:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X3 |
XP_016870452.1:p.Met1254I… XP_016870452.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X6 | XM_017014965.3:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X4 |
XP_016870454.1:p.Met1253I… XP_016870454.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X6 | XM_017014965.3:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X4 |
XP_016870454.1:p.Met1253I… XP_016870454.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X6 | XM_017014965.3:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X4 |
XP_016870454.1:p.Met1253I… XP_016870454.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X7 | XM_006716817.5:c.3756G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X5 |
XP_006716880.1:p.Met1252I… XP_006716880.1:p.Met1252Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X7 | XM_006716817.5:c.3756G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X5 |
XP_006716880.1:p.Met1252I… XP_006716880.1:p.Met1252Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X7 | XM_006716817.5:c.3756G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X5 |
XP_006716880.1:p.Met1252I… XP_006716880.1:p.Met1252Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X8 | XM_017014966.3:c.3753G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X6 |
XP_016870455.1:p.Met1251I… XP_016870455.1:p.Met1251Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X8 | XM_017014966.3:c.3753G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X6 |
XP_016870455.1:p.Met1251I… XP_016870455.1:p.Met1251Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X8 | XM_017014966.3:c.3753G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X6 |
XP_016870455.1:p.Met1251I… XP_016870455.1:p.Met1251Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X9 | XM_017014967.3:c.3750G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X7 |
XP_016870456.1:p.Met1250I… XP_016870456.1:p.Met1250Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X9 | XM_017014967.3:c.3750G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X7 |
XP_016870456.1:p.Met1250I… XP_016870456.1:p.Met1250Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X9 | XM_017014967.3:c.3750G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X7 |
XP_016870456.1:p.Met1250I… XP_016870456.1:p.Met1250Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X10 | XM_017014968.3:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X8 |
XP_016870457.1:p.Met1254I… XP_016870457.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X10 | XM_017014968.3:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X8 |
XP_016870457.1:p.Met1254I… XP_016870457.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X10 | XM_017014968.3:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X8 |
XP_016870457.1:p.Met1254I… XP_016870457.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X11 | XM_047423642.1:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X9 |
XP_047279598.1:p.Met1253I… XP_047279598.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X11 | XM_047423642.1:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X9 |
XP_047279598.1:p.Met1253I… XP_047279598.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X11 | XM_047423642.1:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X9 |
XP_047279598.1:p.Met1253I… XP_047279598.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X12 | XM_017014970.3:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X10 |
XP_016870459.1:p.Met1253I… XP_016870459.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X12 | XM_017014970.3:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X10 |
XP_016870459.1:p.Met1253I… XP_016870459.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X12 | XM_017014970.3:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X10 |
XP_016870459.1:p.Met1253I… XP_016870459.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X13 | XM_017014969.3:c.3744G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X11 |
XP_016870458.1:p.Met1248I… XP_016870458.1:p.Met1248Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X13 | XM_017014969.3:c.3744G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X11 |
XP_016870458.1:p.Met1248I… XP_016870458.1:p.Met1248Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X13 | XM_017014969.3:c.3744G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X11 |
XP_016870458.1:p.Met1248I… XP_016870458.1:p.Met1248Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X14 | XM_024447625.2:c.3741G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X12 |
XP_024303393.1:p.Met1247I… XP_024303393.1:p.Met1247Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X14 | XM_024447625.2:c.3741G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X12 |
XP_024303393.1:p.Met1247I… XP_024303393.1:p.Met1247Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X14 | XM_024447625.2:c.3741G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X12 |
XP_024303393.1:p.Met1247I… XP_024303393.1:p.Met1247Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X15 | XM_017014971.3:c.3735G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X13 |
XP_016870460.1:p.Met1245I… XP_016870460.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X15 | XM_017014971.3:c.3735G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X13 |
XP_016870460.1:p.Met1245I… XP_016870460.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X15 | XM_017014971.3:c.3735G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X13 |
XP_016870460.1:p.Met1245I… XP_016870460.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X16 | XM_017014972.3:c.3735G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X14 |
XP_016870461.1:p.Met1245I… XP_016870461.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X16 | XM_017014972.3:c.3735G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X14 |
XP_016870461.1:p.Met1245I… XP_016870461.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X16 | XM_017014972.3:c.3735G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X14 |
XP_016870461.1:p.Met1245I… XP_016870461.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X17 | XM_017014974.3:c.3732G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X15 |
XP_016870463.1:p.Met1244I… XP_016870463.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X17 | XM_017014974.3:c.3732G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X15 |
XP_016870463.1:p.Met1244I… XP_016870463.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X17 | XM_017014974.3:c.3732G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X15 |
XP_016870463.1:p.Met1244I… XP_016870463.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X18 | XM_047423643.1:c.3723G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X16 |
XP_047279599.1:p.Met1241I… XP_047279599.1:p.Met1241Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X18 | XM_047423643.1:c.3723G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X16 |
XP_047279599.1:p.Met1241I… XP_047279599.1:p.Met1241Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X18 | XM_047423643.1:c.3723G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X16 |
XP_047279599.1:p.Met1241I… XP_047279599.1:p.Met1241Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X19 | XM_017014977.3:c.3735G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X17 |
XP_016870466.1:p.Met1245I… XP_016870466.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X19 | XM_017014977.3:c.3735G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X17 |
XP_016870466.1:p.Met1245I… XP_016870466.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X19 | XM_017014977.3:c.3735G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X17 |
XP_016870466.1:p.Met1245I… XP_016870466.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X20 | XM_017014976.3:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X18 |
XP_016870465.1:p.Met1254I… XP_016870465.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X20 | XM_017014976.3:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X18 |
XP_016870465.1:p.Met1254I… XP_016870465.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X20 | XM_017014976.3:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X18 |
XP_016870465.1:p.Met1254I… XP_016870465.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X21 | XM_047423644.1:c.3732G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X19 |
XP_047279600.1:p.Met1244I… XP_047279600.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X21 | XM_047423644.1:c.3732G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X19 |
XP_047279600.1:p.Met1244I… XP_047279600.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X21 | XM_047423644.1:c.3732G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X19 |
XP_047279600.1:p.Met1244I… XP_047279600.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X22 | XM_017014978.3:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X20 |
XP_016870467.1:p.Met1254I… XP_016870467.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X22 | XM_017014978.3:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X20 |
XP_016870467.1:p.Met1254I… XP_016870467.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X22 | XM_017014978.3:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X20 |
XP_016870467.1:p.Met1254I… XP_016870467.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X23 | XM_017014979.3:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X21 |
XP_016870468.1:p.Met1253I… XP_016870468.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X23 | XM_017014979.3:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X21 |
XP_016870468.1:p.Met1253I… XP_016870468.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X23 | XM_017014979.3:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X21 |
XP_016870468.1:p.Met1253I… XP_016870468.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X24 | XM_006716823.4:c.3762G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X22 |
XP_006716886.1:p.Met1254I… XP_006716886.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X24 | XM_006716823.4:c.3762G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X22 |
XP_006716886.1:p.Met1254I… XP_006716886.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X24 | XM_006716823.4:c.3762G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X22 |
XP_006716886.1:p.Met1254I… XP_006716886.1:p.Met1254Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X25 | XM_047423645.1:c.3720G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X23 |
XP_047279601.1:p.Met1240I… XP_047279601.1:p.Met1240Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X25 | XM_047423645.1:c.3720G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X23 |
XP_047279601.1:p.Met1240I… XP_047279601.1:p.Met1240Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X25 | XM_047423645.1:c.3720G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X23 |
XP_047279601.1:p.Met1240I… XP_047279601.1:p.Met1240Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X26 | XM_047423646.1:c.3717G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X24 |
XP_047279602.1:p.Met1239I… XP_047279602.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X26 | XM_047423646.1:c.3717G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X24 |
XP_047279602.1:p.Met1239I… XP_047279602.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X26 | XM_047423646.1:c.3717G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X24 |
XP_047279602.1:p.Met1239I… XP_047279602.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X27 | XM_006716825.5:c.3759G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X25 |
XP_006716888.1:p.Met1253I… XP_006716888.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X27 | XM_006716825.5:c.3759G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X25 |
XP_006716888.1:p.Met1253I… XP_006716888.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X27 | XM_006716825.5:c.3759G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X25 |
XP_006716888.1:p.Met1253I… XP_006716888.1:p.Met1253Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X28 | XM_047423647.1:c.3756G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X26 |
XP_047279603.1:p.Met1252I… XP_047279603.1:p.Met1252Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X28 | XM_047423647.1:c.3756G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X26 |
XP_047279603.1:p.Met1252I… XP_047279603.1:p.Met1252Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X28 | XM_047423647.1:c.3756G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X26 |
XP_047279603.1:p.Met1252I… XP_047279603.1:p.Met1252Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X29 | XM_047423648.1:c.3693G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X27 |
XP_047279604.1:p.Met1231I… XP_047279604.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X29 | XM_047423648.1:c.3693G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X27 |
XP_047279604.1:p.Met1231I… XP_047279604.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X29 | XM_047423648.1:c.3693G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X27 |
XP_047279604.1:p.Met1231I… XP_047279604.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X30 | XM_047423649.1:c.3690G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X28 |
XP_047279605.1:p.Met1230I… XP_047279605.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X30 | XM_047423649.1:c.3690G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X28 |
XP_047279605.1:p.Met1230I… XP_047279605.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X30 | XM_047423649.1:c.3690G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X28 |
XP_047279605.1:p.Met1230I… XP_047279605.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X31 | XM_047423650.1:c.3735G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X29 |
XP_047279606.1:p.Met1245I… XP_047279606.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X31 | XM_047423650.1:c.3735G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X29 |
XP_047279606.1:p.Met1245I… XP_047279606.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X31 | XM_047423650.1:c.3735G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X29 |
XP_047279606.1:p.Met1245I… XP_047279606.1:p.Met1245Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X32 | XM_047423651.1:c.3693G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X30 |
XP_047279607.1:p.Met1231I… XP_047279607.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X32 | XM_047423651.1:c.3693G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X30 |
XP_047279607.1:p.Met1231I… XP_047279607.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X32 | XM_047423651.1:c.3693G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X30 |
XP_047279607.1:p.Met1231I… XP_047279607.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X33 | XM_017014980.3:c.3732G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X31 |
XP_016870469.1:p.Met1244I… XP_016870469.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X33 | XM_017014980.3:c.3732G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X31 |
XP_016870469.1:p.Met1244I… XP_016870469.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X33 | XM_017014980.3:c.3732G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X31 |
XP_016870469.1:p.Met1244I… XP_016870469.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X34 | XM_047423652.1:c.3732G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X32 |
XP_047279608.1:p.Met1244I… XP_047279608.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X34 | XM_047423652.1:c.3732G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X32 |
XP_047279608.1:p.Met1244I… XP_047279608.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X34 | XM_047423652.1:c.3732G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X32 |
XP_047279608.1:p.Met1244I… XP_047279608.1:p.Met1244Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X35 | XM_047423653.1:c.3717G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X33 |
XP_047279609.1:p.Met1239I… XP_047279609.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X35 | XM_047423653.1:c.3717G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X33 |
XP_047279609.1:p.Met1239I… XP_047279609.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X35 | XM_047423653.1:c.3717G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X33 |
XP_047279609.1:p.Met1239I… XP_047279609.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X36 | XM_047423654.1:c.3729G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X34 |
XP_047279610.1:p.Met1243I… XP_047279610.1:p.Met1243Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X36 | XM_047423654.1:c.3729G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X34 |
XP_047279610.1:p.Met1243I… XP_047279610.1:p.Met1243Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X36 | XM_047423654.1:c.3729G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X34 |
XP_047279610.1:p.Met1243I… XP_047279610.1:p.Met1243Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X37 | XM_047423655.1:c.3723G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X35 |
XP_047279611.1:p.Met1241I… XP_047279611.1:p.Met1241Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X37 | XM_047423655.1:c.3723G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X35 |
XP_047279611.1:p.Met1241I… XP_047279611.1:p.Met1241Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X37 | XM_047423655.1:c.3723G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X35 |
XP_047279611.1:p.Met1241I… XP_047279611.1:p.Met1241Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X38 | XM_047423656.1:c.3720G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X36 |
XP_047279612.1:p.Met1240I… XP_047279612.1:p.Met1240Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X38 | XM_047423656.1:c.3720G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X36 |
XP_047279612.1:p.Met1240I… XP_047279612.1:p.Met1240Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X38 | XM_047423656.1:c.3720G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X36 |
XP_047279612.1:p.Met1240I… XP_047279612.1:p.Met1240Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X39 | XM_047423657.1:c.3717G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X37 |
XP_047279613.1:p.Met1239I… XP_047279613.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X39 | XM_047423657.1:c.3717G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X37 |
XP_047279613.1:p.Met1239I… XP_047279613.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X39 | XM_047423657.1:c.3717G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X37 |
XP_047279613.1:p.Met1239I… XP_047279613.1:p.Met1239Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X40 | XM_006716827.5:c.3690G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X38 |
XP_006716890.1:p.Met1230I… XP_006716890.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X40 | XM_006716827.5:c.3690G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X38 |
XP_006716890.1:p.Met1230I… XP_006716890.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X40 | XM_006716827.5:c.3690G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X38 |
XP_006716890.1:p.Met1230I… XP_006716890.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X41 | XM_047423658.1:c.3696G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X39 |
XP_047279614.1:p.Met1232I… XP_047279614.1:p.Met1232Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X41 | XM_047423658.1:c.3696G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X39 |
XP_047279614.1:p.Met1232I… XP_047279614.1:p.Met1232Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X41 | XM_047423658.1:c.3696G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X39 |
XP_047279614.1:p.Met1232I… XP_047279614.1:p.Met1232Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X42 | XM_047423659.1:c.3693G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X40 |
XP_047279615.1:p.Met1231I… XP_047279615.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X42 | XM_047423659.1:c.3693G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X40 |
XP_047279615.1:p.Met1231I… XP_047279615.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X42 | XM_047423659.1:c.3693G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X40 |
XP_047279615.1:p.Met1231I… XP_047279615.1:p.Met1231Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X43 | XM_047423660.1:c.3690G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X41 |
XP_047279616.1:p.Met1230I… XP_047279616.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X43 | XM_047423660.1:c.3690G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X41 |
XP_047279616.1:p.Met1230I… XP_047279616.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X43 | XM_047423660.1:c.3690G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X41 |
XP_047279616.1:p.Met1230I… XP_047279616.1:p.Met1230Ile |
M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X44 | XM_017014982.3:c.2529G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X42 | XP_016870471.1:p.Met843Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X44 | XM_017014982.3:c.2529G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X42 | XP_016870471.1:p.Met843Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X44 | XM_017014982.3:c.2529G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X42 | XP_016870471.1:p.Met843Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X45 | XM_017014983.3:c.2526G>T | M [ATG] > I [ATT] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X43 | XP_016870472.1:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X45 | XM_017014983.3:c.2526G>C | M [ATG] > I [ATC] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X43 | XP_016870472.1:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
PTPRD transcript variant X45 | XM_017014983.3:c.2526G>A | M [ATG] > I [ATA] | Coding Sequence Variant |
receptor-type tyrosine-protein phosphatase delta isoform X43 | XP_016870472.1:p.Met842Ile | M (Met) > I (Ile) | Missense Variant |
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
Placement | C= | A | G | T |
---|---|---|---|---|
GRCh38.p14 chr 9 | NC_000009.12:g.8460527= | NC_000009.12:g.8460527C>A | NC_000009.12:g.8460527C>G | NC_000009.12:g.8460527C>T |
GRCh37.p13 chr 9 | NC_000009.11:g.8460527= | NC_000009.11:g.8460527C>A | NC_000009.11:g.8460527C>G | NC_000009.11:g.8460527C>T |
PTPRD RefSeqGene | NG_033963.1:g.2157197= | NG_033963.1:g.2157197G>T | NG_033963.1:g.2157197G>C | NG_033963.1:g.2157197G>A |
PTPRD transcript variant 1 | NM_002839.4:c.3759= | NM_002839.4:c.3759G>T | NM_002839.4:c.3759G>C | NM_002839.4:c.3759G>A |
PTPRD transcript variant 1 | NM_002839.3:c.3759= | NM_002839.3:c.3759G>T | NM_002839.3:c.3759G>C | NM_002839.3:c.3759G>A |
PTPRD transcript variant 2 | NM_130391.4:c.2526= | NM_130391.4:c.2526G>T | NM_130391.4:c.2526G>C | NM_130391.4:c.2526G>A |
PTPRD transcript variant 2 | NM_130391.3:c.2526= | NM_130391.3:c.2526G>T | NM_130391.3:c.2526G>C | NM_130391.3:c.2526G>A |
PTPRD transcript variant 3 | NM_130392.3:c.2526= | NM_130392.3:c.2526G>T | NM_130392.3:c.2526G>C | NM_130392.3:c.2526G>A |
PTPRD transcript variant 4 | NM_130393.3:c.2511= | NM_130393.3:c.2511G>T | NM_130393.3:c.2511G>C | NM_130393.3:c.2511G>A |
PTPRD transcript variant 6 | NM_001171025.2:c.2496= | NM_001171025.2:c.2496G>T | NM_001171025.2:c.2496G>C | NM_001171025.2:c.2496G>A |
PTPRD transcript variant 6 | NM_001171025.1:c.2496= | NM_001171025.1:c.2496G>T | NM_001171025.1:c.2496G>C | NM_001171025.1:c.2496G>A |
PTPRD transcript variant 5 | NM_001040712.2:c.2517= | NM_001040712.2:c.2517G>T | NM_001040712.2:c.2517G>C | NM_001040712.2:c.2517G>A |
PTPRD transcript variant 9 | NM_001377958.1:c.3762= | NM_001377958.1:c.3762G>T | NM_001377958.1:c.3762G>C | NM_001377958.1:c.3762G>A |
PTPRD transcript variant 10 | NM_001378058.1:c.3759= | NM_001378058.1:c.3759G>T | NM_001378058.1:c.3759G>C | NM_001378058.1:c.3759G>A |
PTPRD transcript variant 8 | NM_001377947.1:c.2520= | NM_001377947.1:c.2520G>T | NM_001377947.1:c.2520G>C | NM_001377947.1:c.2520G>A |
PTPRD transcript variant 7 | NM_001377946.1:c.2508= | NM_001377946.1:c.2508G>T | NM_001377946.1:c.2508G>C | NM_001377946.1:c.2508G>A |
PTPRD transcript variant X7 | XM_006716817.5:c.3756= | XM_006716817.5:c.3756G>T | XM_006716817.5:c.3756G>C | XM_006716817.5:c.3756G>A |
PTPRD transcript variant X10 | XM_006716817.4:c.3756= | XM_006716817.4:c.3756G>T | XM_006716817.4:c.3756G>C | XM_006716817.4:c.3756G>A |
PTPRD transcript variant X10 | XM_006716817.3:c.3756= | XM_006716817.3:c.3756G>T | XM_006716817.3:c.3756G>C | XM_006716817.3:c.3756G>A |
PTPRD transcript variant X5 | XM_006716817.2:c.3756= | XM_006716817.2:c.3756G>T | XM_006716817.2:c.3756G>C | XM_006716817.2:c.3756G>A |
PTPRD transcript variant X5 | XM_006716817.1:c.3756= | XM_006716817.1:c.3756G>T | XM_006716817.1:c.3756G>C | XM_006716817.1:c.3756G>A |
PTPRD transcript variant X27 | XM_006716825.5:c.3759= | XM_006716825.5:c.3759G>T | XM_006716825.5:c.3759G>C | XM_006716825.5:c.3759G>A |
PTPRD transcript variant X27 | XM_006716825.4:c.3759= | XM_006716825.4:c.3759G>T | XM_006716825.4:c.3759G>C | XM_006716825.4:c.3759G>A |
PTPRD transcript variant X26 | XM_006716825.3:c.3759= | XM_006716825.3:c.3759G>T | XM_006716825.3:c.3759G>C | XM_006716825.3:c.3759G>A |
PTPRD transcript variant X17 | XM_006716825.2:c.3759= | XM_006716825.2:c.3759G>T | XM_006716825.2:c.3759G>C | XM_006716825.2:c.3759G>A |
PTPRD transcript variant X13 | XM_006716825.1:c.3759= | XM_006716825.1:c.3759G>T | XM_006716825.1:c.3759G>C | XM_006716825.1:c.3759G>A |
PTPRD transcript variant X40 | XM_006716827.5:c.3690= | XM_006716827.5:c.3690G>T | XM_006716827.5:c.3690G>C | XM_006716827.5:c.3690G>A |
PTPRD transcript variant X29 | XM_006716827.4:c.3690= | XM_006716827.4:c.3690G>T | XM_006716827.4:c.3690G>C | XM_006716827.4:c.3690G>A |
PTPRD transcript variant X28 | XM_006716827.3:c.3690= | XM_006716827.3:c.3690G>T | XM_006716827.3:c.3690G>C | XM_006716827.3:c.3690G>A |
PTPRD transcript variant X19 | XM_006716827.2:c.3690= | XM_006716827.2:c.3690G>T | XM_006716827.2:c.3690G>C | XM_006716827.2:c.3690G>A |
PTPRD transcript variant X15 | XM_006716827.1:c.3690= | XM_006716827.1:c.3690G>T | XM_006716827.1:c.3690G>C | XM_006716827.1:c.3690G>A |
PTPRD transcript variant X24 | XM_006716823.4:c.3762= | XM_006716823.4:c.3762G>T | XM_006716823.4:c.3762G>C | XM_006716823.4:c.3762G>A |
PTPRD transcript variant X25 | XM_006716823.3:c.3762= | XM_006716823.3:c.3762G>T | XM_006716823.3:c.3762G>C | XM_006716823.3:c.3762G>A |
PTPRD transcript variant X24 | XM_006716823.2:c.3762= | XM_006716823.2:c.3762G>T | XM_006716823.2:c.3762G>C | XM_006716823.2:c.3762G>A |
PTPRD transcript variant X15 | XM_006716823.1:c.3762= | XM_006716823.1:c.3762G>T | XM_006716823.1:c.3762G>C | XM_006716823.1:c.3762G>A |
PTPRD transcript variant X1 | XM_017014958.3:c.3762= | XM_017014958.3:c.3762G>T | XM_017014958.3:c.3762G>C | XM_017014958.3:c.3762G>A |
PTPRD transcript variant X1 | XM_017014958.2:c.3762= | XM_017014958.2:c.3762G>T | XM_017014958.2:c.3762G>C | XM_017014958.2:c.3762G>A |
PTPRD transcript variant X1 | XM_017014958.1:c.3762= | XM_017014958.1:c.3762G>T | XM_017014958.1:c.3762G>C | XM_017014958.1:c.3762G>A |
PTPRD transcript variant X6 | XM_017014965.3:c.3759= | XM_017014965.3:c.3759G>T | XM_017014965.3:c.3759G>C | XM_017014965.3:c.3759G>A |
PTPRD transcript variant X8 | XM_017014965.2:c.3759= | XM_017014965.2:c.3759G>T | XM_017014965.2:c.3759G>C | XM_017014965.2:c.3759G>A |
PTPRD transcript variant X8 | XM_017014965.1:c.3759= | XM_017014965.1:c.3759G>T | XM_017014965.1:c.3759G>C | XM_017014965.1:c.3759G>A |
PTPRD transcript variant X4 | XM_017014964.3:c.3759= | XM_017014964.3:c.3759G>T | XM_017014964.3:c.3759G>C | XM_017014964.3:c.3759G>A |
PTPRD transcript variant X7 | XM_017014964.2:c.3759= | XM_017014964.2:c.3759G>T | XM_017014964.2:c.3759G>C | XM_017014964.2:c.3759G>A |
PTPRD transcript variant X7 | XM_017014964.1:c.3759= | XM_017014964.1:c.3759G>T | XM_017014964.1:c.3759G>C | XM_017014964.1:c.3759G>A |
PTPRD transcript variant X5 | XM_017014963.3:c.3762= | XM_017014963.3:c.3762G>T | XM_017014963.3:c.3762G>C | XM_017014963.3:c.3762G>A |
PTPRD transcript variant X6 | XM_017014963.2:c.3762= | XM_017014963.2:c.3762G>T | XM_017014963.2:c.3762G>C | XM_017014963.2:c.3762G>A |
PTPRD transcript variant X6 | XM_017014963.1:c.3762= | XM_017014963.1:c.3762G>T | XM_017014963.1:c.3762G>C | XM_017014963.1:c.3762G>A |
PTPRD transcript variant X8 | XM_017014966.3:c.3753= | XM_017014966.3:c.3753G>T | XM_017014966.3:c.3753G>C | XM_017014966.3:c.3753G>A |
PTPRD transcript variant X9 | XM_017014966.2:c.3753= | XM_017014966.2:c.3753G>T | XM_017014966.2:c.3753G>C | XM_017014966.2:c.3753G>A |
PTPRD transcript variant X9 | XM_017014966.1:c.3753= | XM_017014966.1:c.3753G>T | XM_017014966.1:c.3753G>C | XM_017014966.1:c.3753G>A |
PTPRD transcript variant X9 | XM_017014967.3:c.3750= | XM_017014967.3:c.3750G>T | XM_017014967.3:c.3750G>C | XM_017014967.3:c.3750G>A |
PTPRD transcript variant X11 | XM_017014967.2:c.3750= | XM_017014967.2:c.3750G>T | XM_017014967.2:c.3750G>C | XM_017014967.2:c.3750G>A |
PTPRD transcript variant X11 | XM_017014967.1:c.3750= | XM_017014967.1:c.3750G>T | XM_017014967.1:c.3750G>C | XM_017014967.1:c.3750G>A |
PTPRD transcript variant X10 | XM_017014968.3:c.3762= | XM_017014968.3:c.3762G>T | XM_017014968.3:c.3762G>C | XM_017014968.3:c.3762G>A |
PTPRD transcript variant X12 | XM_017014968.2:c.3762= | XM_017014968.2:c.3762G>T | XM_017014968.2:c.3762G>C | XM_017014968.2:c.3762G>A |
PTPRD transcript variant X12 | XM_017014968.1:c.3762= | XM_017014968.1:c.3762G>T | XM_017014968.1:c.3762G>C | XM_017014968.1:c.3762G>A |
PTPRD transcript variant X12 | XM_017014970.3:c.3759= | XM_017014970.3:c.3759G>T | XM_017014970.3:c.3759G>C | XM_017014970.3:c.3759G>A |
PTPRD transcript variant X14 | XM_017014970.2:c.3759= | XM_017014970.2:c.3759G>T | XM_017014970.2:c.3759G>C | XM_017014970.2:c.3759G>A |
PTPRD transcript variant X14 | XM_017014970.1:c.3759= | XM_017014970.1:c.3759G>T | XM_017014970.1:c.3759G>C | XM_017014970.1:c.3759G>A |
PTPRD transcript variant X13 | XM_017014969.3:c.3744= | XM_017014969.3:c.3744G>T | XM_017014969.3:c.3744G>C | XM_017014969.3:c.3744G>A |
PTPRD transcript variant X13 | XM_017014969.2:c.3744= | XM_017014969.2:c.3744G>T | XM_017014969.2:c.3744G>C | XM_017014969.2:c.3744G>A |
PTPRD transcript variant X13 | XM_017014969.1:c.3744= | XM_017014969.1:c.3744G>T | XM_017014969.1:c.3744G>C | XM_017014969.1:c.3744G>A |
PTPRD transcript variant X16 | XM_017014972.3:c.3735= | XM_017014972.3:c.3735G>T | XM_017014972.3:c.3735G>C | XM_017014972.3:c.3735G>A |
PTPRD transcript variant X17 | XM_017014972.2:c.3735= | XM_017014972.2:c.3735G>T | XM_017014972.2:c.3735G>C | XM_017014972.2:c.3735G>A |
PTPRD transcript variant X16 | XM_017014972.1:c.3735= | XM_017014972.1:c.3735G>T | XM_017014972.1:c.3735G>C | XM_017014972.1:c.3735G>A |
PTPRD transcript variant X15 | XM_017014971.3:c.3735= | XM_017014971.3:c.3735G>T | XM_017014971.3:c.3735G>C | XM_017014971.3:c.3735G>A |
PTPRD transcript variant X16 | XM_017014971.2:c.3735= | XM_017014971.2:c.3735G>T | XM_017014971.2:c.3735G>C | XM_017014971.2:c.3735G>A |
PTPRD transcript variant X15 | XM_017014971.1:c.3735= | XM_017014971.1:c.3735G>T | XM_017014971.1:c.3735G>C | XM_017014971.1:c.3735G>A |
PTPRD transcript variant X17 | XM_017014974.3:c.3732= | XM_017014974.3:c.3732G>T | XM_017014974.3:c.3732G>C | XM_017014974.3:c.3732G>A |
PTPRD transcript variant X19 | XM_017014974.2:c.3732= | XM_017014974.2:c.3732G>T | XM_017014974.2:c.3732G>C | XM_017014974.2:c.3732G>A |
PTPRD transcript variant X18 | XM_017014974.1:c.3732= | XM_017014974.1:c.3732G>T | XM_017014974.1:c.3732G>C | XM_017014974.1:c.3732G>A |
PTPRD transcript variant X19 | XM_017014977.3:c.3735= | XM_017014977.3:c.3735G>T | XM_017014977.3:c.3735G>C | XM_017014977.3:c.3735G>A |
PTPRD transcript variant X22 | XM_017014977.2:c.3735= | XM_017014977.2:c.3735G>T | XM_017014977.2:c.3735G>C | XM_017014977.2:c.3735G>A |
PTPRD transcript variant X21 | XM_017014977.1:c.3735= | XM_017014977.1:c.3735G>T | XM_017014977.1:c.3735G>C | XM_017014977.1:c.3735G>A |
PTPRD transcript variant X20 | XM_017014976.3:c.3762= | XM_017014976.3:c.3762G>T | XM_017014976.3:c.3762G>C | XM_017014976.3:c.3762G>A |
PTPRD transcript variant X21 | XM_017014976.2:c.3762= | XM_017014976.2:c.3762G>T | XM_017014976.2:c.3762G>C | XM_017014976.2:c.3762G>A |
PTPRD transcript variant X20 | XM_017014976.1:c.3762= | XM_017014976.1:c.3762G>T | XM_017014976.1:c.3762G>C | XM_017014976.1:c.3762G>A |
PTPRD transcript variant X22 | XM_017014978.3:c.3762= | XM_017014978.3:c.3762G>T | XM_017014978.3:c.3762G>C | XM_017014978.3:c.3762G>A |
PTPRD transcript variant X23 | XM_017014978.2:c.3762= | XM_017014978.2:c.3762G>T | XM_017014978.2:c.3762G>C | XM_017014978.2:c.3762G>A |
PTPRD transcript variant X22 | XM_017014978.1:c.3762= | XM_017014978.1:c.3762G>T | XM_017014978.1:c.3762G>C | XM_017014978.1:c.3762G>A |
PTPRD transcript variant X23 | XM_017014979.3:c.3759= | XM_017014979.3:c.3759G>T | XM_017014979.3:c.3759G>C | XM_017014979.3:c.3759G>A |
PTPRD transcript variant X24 | XM_017014979.2:c.3759= | XM_017014979.2:c.3759G>T | XM_017014979.2:c.3759G>C | XM_017014979.2:c.3759G>A |
PTPRD transcript variant X23 | XM_017014979.1:c.3759= | XM_017014979.1:c.3759G>T | XM_017014979.1:c.3759G>C | XM_017014979.1:c.3759G>A |
PTPRD transcript variant X2 | XM_017014961.3:c.3762= | XM_017014961.3:c.3762G>T | XM_017014961.3:c.3762G>C | XM_017014961.3:c.3762G>A |
PTPRD transcript variant X4 | XM_017014961.2:c.3762= | XM_017014961.2:c.3762G>T | XM_017014961.2:c.3762G>C | XM_017014961.2:c.3762G>A |
PTPRD transcript variant X4 | XM_017014961.1:c.3762= | XM_017014961.1:c.3762G>T | XM_017014961.1:c.3762G>C | XM_017014961.1:c.3762G>A |
PTPRD transcript variant X33 | XM_017014980.3:c.3732= | XM_017014980.3:c.3732G>T | XM_017014980.3:c.3732G>C | XM_017014980.3:c.3732G>A |
PTPRD transcript variant X28 | XM_017014980.2:c.3732= | XM_017014980.2:c.3732G>T | XM_017014980.2:c.3732G>C | XM_017014980.2:c.3732G>A |
PTPRD transcript variant X27 | XM_017014980.1:c.3732= | XM_017014980.1:c.3732G>T | XM_017014980.1:c.3732G>C | XM_017014980.1:c.3732G>A |
PTPRD transcript variant X44 | XM_017014982.3:c.2529= | XM_017014982.3:c.2529G>T | XM_017014982.3:c.2529G>C | XM_017014982.3:c.2529G>A |
PTPRD transcript variant X31 | XM_017014982.2:c.2529= | XM_017014982.2:c.2529G>T | XM_017014982.2:c.2529G>C | XM_017014982.2:c.2529G>A |
PTPRD transcript variant X30 | XM_017014982.1:c.2529= | XM_017014982.1:c.2529G>T | XM_017014982.1:c.2529G>C | XM_017014982.1:c.2529G>A |
PTPRD transcript variant X45 | XM_017014983.3:c.2526= | XM_017014983.3:c.2526G>T | XM_017014983.3:c.2526G>C | XM_017014983.3:c.2526G>A |
PTPRD transcript variant X32 | XM_017014983.2:c.2526= | XM_017014983.2:c.2526G>T | XM_017014983.2:c.2526G>C | XM_017014983.2:c.2526G>A |
PTPRD transcript variant X31 | XM_017014983.1:c.2526= | XM_017014983.1:c.2526G>T | XM_017014983.1:c.2526G>C | XM_017014983.1:c.2526G>A |
PTPRD transcript variant X14 | XM_024447625.2:c.3741= | XM_024447625.2:c.3741G>T | XM_024447625.2:c.3741G>C | XM_024447625.2:c.3741G>A |
PTPRD transcript variant X15 | XM_024447625.1:c.3741= | XM_024447625.1:c.3741G>T | XM_024447625.1:c.3741G>C | XM_024447625.1:c.3741G>A |
PTPRD transcript variant X3 | XM_047423641.1:c.3762= | XM_047423641.1:c.3762G>T | XM_047423641.1:c.3762G>C | XM_047423641.1:c.3762G>A |
PTPRD transcript variant X11 | XM_047423642.1:c.3759= | XM_047423642.1:c.3759G>T | XM_047423642.1:c.3759G>C | XM_047423642.1:c.3759G>A |
PTPRD transcript variant X21 | XM_047423644.1:c.3732= | XM_047423644.1:c.3732G>T | XM_047423644.1:c.3732G>C | XM_047423644.1:c.3732G>A |
PTPRD transcript variant X25 | XM_047423645.1:c.3720= | XM_047423645.1:c.3720G>T | XM_047423645.1:c.3720G>C | XM_047423645.1:c.3720G>A |
PTPRD transcript variant X28 | XM_047423647.1:c.3756= | XM_047423647.1:c.3756G>T | XM_047423647.1:c.3756G>C | XM_047423647.1:c.3756G>A |
PTPRD transcript variant X30 | XM_047423649.1:c.3690= | XM_047423649.1:c.3690G>T | XM_047423649.1:c.3690G>C | XM_047423649.1:c.3690G>A |
PTPRD transcript variant X32 | XM_047423651.1:c.3693= | XM_047423651.1:c.3693G>T | XM_047423651.1:c.3693G>C | XM_047423651.1:c.3693G>A |
PTPRD transcript variant X31 | XM_047423650.1:c.3735= | XM_047423650.1:c.3735G>T | XM_047423650.1:c.3735G>C | XM_047423650.1:c.3735G>A |
PTPRD transcript variant X34 | XM_047423652.1:c.3732= | XM_047423652.1:c.3732G>T | XM_047423652.1:c.3732G>C | XM_047423652.1:c.3732G>A |
PTPRD transcript variant X36 | XM_047423654.1:c.3729= | XM_047423654.1:c.3729G>T | XM_047423654.1:c.3729G>C | XM_047423654.1:c.3729G>A |
PTPRD transcript variant X35 | XM_047423653.1:c.3717= | XM_047423653.1:c.3717G>T | XM_047423653.1:c.3717G>C | XM_047423653.1:c.3717G>A |
PTPRD transcript variant X39 | XM_047423657.1:c.3717= | XM_047423657.1:c.3717G>T | XM_047423657.1:c.3717G>C | XM_047423657.1:c.3717G>A |
PTPRD transcript variant X18 | XM_047423643.1:c.3723= | XM_047423643.1:c.3723G>T | XM_047423643.1:c.3723G>C | XM_047423643.1:c.3723G>A |
PTPRD transcript variant X26 | XM_047423646.1:c.3717= | XM_047423646.1:c.3717G>T | XM_047423646.1:c.3717G>C | XM_047423646.1:c.3717G>A |
PTPRD transcript variant X29 | XM_047423648.1:c.3693= | XM_047423648.1:c.3693G>T | XM_047423648.1:c.3693G>C | XM_047423648.1:c.3693G>A |
PTPRD transcript variant X37 | XM_047423655.1:c.3723= | XM_047423655.1:c.3723G>T | XM_047423655.1:c.3723G>C | XM_047423655.1:c.3723G>A |
PTPRD transcript variant X38 | XM_047423656.1:c.3720= | XM_047423656.1:c.3720G>T | XM_047423656.1:c.3720G>C | XM_047423656.1:c.3720G>A |
PTPRD transcript variant X41 | XM_047423658.1:c.3696= | XM_047423658.1:c.3696G>T | XM_047423658.1:c.3696G>C | XM_047423658.1:c.3696G>A |
PTPRD transcript variant X42 | XM_047423659.1:c.3693= | XM_047423659.1:c.3693G>T | XM_047423659.1:c.3693G>C | XM_047423659.1:c.3693G>A |
PTPRD transcript variant X43 | XM_047423660.1:c.3690= | XM_047423660.1:c.3690G>T | XM_047423660.1:c.3690G>C | XM_047423660.1:c.3690G>A |
receptor-type tyrosine-protein phosphatase delta isoform 1 precursor | NP_002830.1:p.Met1253= | NP_002830.1:p.Met1253Ile | NP_002830.1:p.Met1253Ile | NP_002830.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform 2 precursor | NP_569075.2:p.Met842= | NP_569075.2:p.Met842Ile | NP_569075.2:p.Met842Ile | NP_569075.2:p.Met842Ile |
receptor-type tyrosine-protein phosphatase delta isoform 3 precursor | NP_569076.2:p.Met842= | NP_569076.2:p.Met842Ile | NP_569076.2:p.Met842Ile | NP_569076.2:p.Met842Ile |
receptor-type tyrosine-protein phosphatase delta isoform 4 precursor | NP_569077.2:p.Met837= | NP_569077.2:p.Met837Ile | NP_569077.2:p.Met837Ile | NP_569077.2:p.Met837Ile |
receptor-type tyrosine-protein phosphatase delta isoform 6 precursor | NP_001164496.1:p.Met832= | NP_001164496.1:p.Met832Ile | NP_001164496.1:p.Met832Ile | NP_001164496.1:p.Met832Ile |
receptor-type tyrosine-protein phosphatase delta isoform 5 precursor | NP_001035802.1:p.Met839= | NP_001035802.1:p.Met839Ile | NP_001035802.1:p.Met839Ile | NP_001035802.1:p.Met839Ile |
receptor-type tyrosine-protein phosphatase delta isoform 9 precursor | NP_001364887.1:p.Met1254= | NP_001364887.1:p.Met1254Ile | NP_001364887.1:p.Met1254Ile | NP_001364887.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform 10 precursor | NP_001364987.1:p.Met1253= | NP_001364987.1:p.Met1253Ile | NP_001364987.1:p.Met1253Ile | NP_001364987.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform 8 precursor | NP_001364876.1:p.Met840= | NP_001364876.1:p.Met840Ile | NP_001364876.1:p.Met840Ile | NP_001364876.1:p.Met840Ile |
receptor-type tyrosine-protein phosphatase delta isoform 7 precursor | NP_001364875.1:p.Met836= | NP_001364875.1:p.Met836Ile | NP_001364875.1:p.Met836Ile | NP_001364875.1:p.Met836Ile |
receptor-type tyrosine-protein phosphatase delta isoform X5 | XP_006716880.1:p.Met1252= | XP_006716880.1:p.Met1252Ile | XP_006716880.1:p.Met1252Ile | XP_006716880.1:p.Met1252Ile |
receptor-type tyrosine-protein phosphatase delta isoform X25 | XP_006716888.1:p.Met1253= | XP_006716888.1:p.Met1253Ile | XP_006716888.1:p.Met1253Ile | XP_006716888.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform X38 | XP_006716890.1:p.Met1230= | XP_006716890.1:p.Met1230Ile | XP_006716890.1:p.Met1230Ile | XP_006716890.1:p.Met1230Ile |
receptor-type tyrosine-protein phosphatase delta isoform X22 | XP_006716886.1:p.Met1254= | XP_006716886.1:p.Met1254Ile | XP_006716886.1:p.Met1254Ile | XP_006716886.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X1 | XP_016870447.1:p.Met1254= | XP_016870447.1:p.Met1254Ile | XP_016870447.1:p.Met1254Ile | XP_016870447.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X4 | XP_016870454.1:p.Met1253= | XP_016870454.1:p.Met1253Ile | XP_016870454.1:p.Met1253Ile | XP_016870454.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform X2 | XP_016870453.1:p.Met1253= | XP_016870453.1:p.Met1253Ile | XP_016870453.1:p.Met1253Ile | XP_016870453.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform X3 | XP_016870452.1:p.Met1254= | XP_016870452.1:p.Met1254Ile | XP_016870452.1:p.Met1254Ile | XP_016870452.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X6 | XP_016870455.1:p.Met1251= | XP_016870455.1:p.Met1251Ile | XP_016870455.1:p.Met1251Ile | XP_016870455.1:p.Met1251Ile |
receptor-type tyrosine-protein phosphatase delta isoform X7 | XP_016870456.1:p.Met1250= | XP_016870456.1:p.Met1250Ile | XP_016870456.1:p.Met1250Ile | XP_016870456.1:p.Met1250Ile |
receptor-type tyrosine-protein phosphatase delta isoform X8 | XP_016870457.1:p.Met1254= | XP_016870457.1:p.Met1254Ile | XP_016870457.1:p.Met1254Ile | XP_016870457.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X10 | XP_016870459.1:p.Met1253= | XP_016870459.1:p.Met1253Ile | XP_016870459.1:p.Met1253Ile | XP_016870459.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform X11 | XP_016870458.1:p.Met1248= | XP_016870458.1:p.Met1248Ile | XP_016870458.1:p.Met1248Ile | XP_016870458.1:p.Met1248Ile |
receptor-type tyrosine-protein phosphatase delta isoform X14 | XP_016870461.1:p.Met1245= | XP_016870461.1:p.Met1245Ile | XP_016870461.1:p.Met1245Ile | XP_016870461.1:p.Met1245Ile |
receptor-type tyrosine-protein phosphatase delta isoform X13 | XP_016870460.1:p.Met1245= | XP_016870460.1:p.Met1245Ile | XP_016870460.1:p.Met1245Ile | XP_016870460.1:p.Met1245Ile |
receptor-type tyrosine-protein phosphatase delta isoform X15 | XP_016870463.1:p.Met1244= | XP_016870463.1:p.Met1244Ile | XP_016870463.1:p.Met1244Ile | XP_016870463.1:p.Met1244Ile |
receptor-type tyrosine-protein phosphatase delta isoform X17 | XP_016870466.1:p.Met1245= | XP_016870466.1:p.Met1245Ile | XP_016870466.1:p.Met1245Ile | XP_016870466.1:p.Met1245Ile |
receptor-type tyrosine-protein phosphatase delta isoform X18 | XP_016870465.1:p.Met1254= | XP_016870465.1:p.Met1254Ile | XP_016870465.1:p.Met1254Ile | XP_016870465.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X20 | XP_016870467.1:p.Met1254= | XP_016870467.1:p.Met1254Ile | XP_016870467.1:p.Met1254Ile | XP_016870467.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X21 | XP_016870468.1:p.Met1253= | XP_016870468.1:p.Met1253Ile | XP_016870468.1:p.Met1253Ile | XP_016870468.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform X1 | XP_016870450.1:p.Met1254= | XP_016870450.1:p.Met1254Ile | XP_016870450.1:p.Met1254Ile | XP_016870450.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X31 | XP_016870469.1:p.Met1244= | XP_016870469.1:p.Met1244Ile | XP_016870469.1:p.Met1244Ile | XP_016870469.1:p.Met1244Ile |
receptor-type tyrosine-protein phosphatase delta isoform X42 | XP_016870471.1:p.Met843= | XP_016870471.1:p.Met843Ile | XP_016870471.1:p.Met843Ile | XP_016870471.1:p.Met843Ile |
receptor-type tyrosine-protein phosphatase delta isoform X43 | XP_016870472.1:p.Met842= | XP_016870472.1:p.Met842Ile | XP_016870472.1:p.Met842Ile | XP_016870472.1:p.Met842Ile |
receptor-type tyrosine-protein phosphatase delta isoform X12 | XP_024303393.1:p.Met1247= | XP_024303393.1:p.Met1247Ile | XP_024303393.1:p.Met1247Ile | XP_024303393.1:p.Met1247Ile |
receptor-type tyrosine-protein phosphatase delta isoform X1 | XP_047279597.1:p.Met1254= | XP_047279597.1:p.Met1254Ile | XP_047279597.1:p.Met1254Ile | XP_047279597.1:p.Met1254Ile |
receptor-type tyrosine-protein phosphatase delta isoform X9 | XP_047279598.1:p.Met1253= | XP_047279598.1:p.Met1253Ile | XP_047279598.1:p.Met1253Ile | XP_047279598.1:p.Met1253Ile |
receptor-type tyrosine-protein phosphatase delta isoform X19 | XP_047279600.1:p.Met1244= | XP_047279600.1:p.Met1244Ile | XP_047279600.1:p.Met1244Ile | XP_047279600.1:p.Met1244Ile |
receptor-type tyrosine-protein phosphatase delta isoform X23 | XP_047279601.1:p.Met1240= | XP_047279601.1:p.Met1240Ile | XP_047279601.1:p.Met1240Ile | XP_047279601.1:p.Met1240Ile |
receptor-type tyrosine-protein phosphatase delta isoform X26 | XP_047279603.1:p.Met1252= | XP_047279603.1:p.Met1252Ile | XP_047279603.1:p.Met1252Ile | XP_047279603.1:p.Met1252Ile |
receptor-type tyrosine-protein phosphatase delta isoform X28 | XP_047279605.1:p.Met1230= | XP_047279605.1:p.Met1230Ile | XP_047279605.1:p.Met1230Ile | XP_047279605.1:p.Met1230Ile |
receptor-type tyrosine-protein phosphatase delta isoform X30 | XP_047279607.1:p.Met1231= | XP_047279607.1:p.Met1231Ile | XP_047279607.1:p.Met1231Ile | XP_047279607.1:p.Met1231Ile |
receptor-type tyrosine-protein phosphatase delta isoform X29 | XP_047279606.1:p.Met1245= | XP_047279606.1:p.Met1245Ile | XP_047279606.1:p.Met1245Ile | XP_047279606.1:p.Met1245Ile |
receptor-type tyrosine-protein phosphatase delta isoform X32 | XP_047279608.1:p.Met1244= | XP_047279608.1:p.Met1244Ile | XP_047279608.1:p.Met1244Ile | XP_047279608.1:p.Met1244Ile |
receptor-type tyrosine-protein phosphatase delta isoform X34 | XP_047279610.1:p.Met1243= | XP_047279610.1:p.Met1243Ile | XP_047279610.1:p.Met1243Ile | XP_047279610.1:p.Met1243Ile |
receptor-type tyrosine-protein phosphatase delta isoform X33 | XP_047279609.1:p.Met1239= | XP_047279609.1:p.Met1239Ile | XP_047279609.1:p.Met1239Ile | XP_047279609.1:p.Met1239Ile |
receptor-type tyrosine-protein phosphatase delta isoform X37 | XP_047279613.1:p.Met1239= | XP_047279613.1:p.Met1239Ile | XP_047279613.1:p.Met1239Ile | XP_047279613.1:p.Met1239Ile |
receptor-type tyrosine-protein phosphatase delta isoform X16 | XP_047279599.1:p.Met1241= | XP_047279599.1:p.Met1241Ile | XP_047279599.1:p.Met1241Ile | XP_047279599.1:p.Met1241Ile |
receptor-type tyrosine-protein phosphatase delta isoform X24 | XP_047279602.1:p.Met1239= | XP_047279602.1:p.Met1239Ile | XP_047279602.1:p.Met1239Ile | XP_047279602.1:p.Met1239Ile |
receptor-type tyrosine-protein phosphatase delta isoform X27 | XP_047279604.1:p.Met1231= | XP_047279604.1:p.Met1231Ile | XP_047279604.1:p.Met1231Ile | XP_047279604.1:p.Met1231Ile |
receptor-type tyrosine-protein phosphatase delta isoform X35 | XP_047279611.1:p.Met1241= | XP_047279611.1:p.Met1241Ile | XP_047279611.1:p.Met1241Ile | XP_047279611.1:p.Met1241Ile |
receptor-type tyrosine-protein phosphatase delta isoform X36 | XP_047279612.1:p.Met1240= | XP_047279612.1:p.Met1240Ile | XP_047279612.1:p.Met1240Ile | XP_047279612.1:p.Met1240Ile |
receptor-type tyrosine-protein phosphatase delta isoform X39 | XP_047279614.1:p.Met1232= | XP_047279614.1:p.Met1232Ile | XP_047279614.1:p.Met1232Ile | XP_047279614.1:p.Met1232Ile |
receptor-type tyrosine-protein phosphatase delta isoform X40 | XP_047279615.1:p.Met1231= | XP_047279615.1:p.Met1231Ile | XP_047279615.1:p.Met1231Ile | XP_047279615.1:p.Met1231Ile |
receptor-type tyrosine-protein phosphatase delta isoform X41 | XP_047279616.1:p.Met1230= | XP_047279616.1:p.Met1230Ile | XP_047279616.1:p.Met1230Ile | XP_047279616.1:p.Met1230Ile |
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
No | Submitter | Submission ID | Date (Build) |
---|---|---|---|
1 | GNOMAD | ss2737501558 | Nov 08, 2017 (151) |
2 | GNOMAD | ss2748153974 | Nov 08, 2017 (151) |
3 | GNOMAD | ss2875148649 | Nov 08, 2017 (151) |
4 | EVA | ss5935974179 | Oct 16, 2022 (156) |
5 | gnomAD - Genomes | NC_000009.12 - 8460527 | Apr 27, 2021 (155) |
6 | gnomAD - Exomes | NC_000009.11 - 8460527 | Jul 13, 2019 (153) |
7 | ALFA | NC_000009.12 - 8460527 | Apr 27, 2021 (155) |
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
---|---|---|---|
ss5935974179 | NC_000009.11:8460526:C:A | NC_000009.12:8460526:C:A | |
6680221, ss2737501558, ss5935974179 | NC_000009.11:8460526:C:G | NC_000009.12:8460526:C:G | (self) |
ss2748153974, ss2875148649, ss5935974179 | NC_000009.11:8460526:C:T | NC_000009.12:8460526:C:T | (self) |
317384359, 12013346496 | NC_000009.12:8460526:C:T | NC_000009.12:8460526:C:T | (self) |
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1489849541
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genomic regions, transcripts, and products
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Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.