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.
rs1466508125
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr13:111153937 (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>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
None
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
-
ARHGEF7 : Synonymous VariantLOC101060553 : 2KB Upstream Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
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").
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 13 | NC_000013.11:g.111153937C>T |
| GRCh37.p13 chr 13 | NC_000013.10:g.111806284C>T |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| ARHGEF7 transcript variant 4 |
NM_001113512.2:c.165+3824… NM_001113512.2:c.165+38246C>T |
N/A | Intron Variant |
| ARHGEF7 transcript variant 14 | NM_001354048.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 22 | NM_001354056.1:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 25 | NM_001354059.2:c.-337= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 23 | NM_001354057.2:c.-252= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 26 | NM_001354060.2:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 24 | NM_001354058.2:c.-286= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 18 | NM_001354052.2:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 16 | NM_001354050.2:c.-189= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 17 | NM_001354051.2:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 11 | NM_001330598.2:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 15 | NM_001354049.2:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 19 | NM_001354053.2:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 1 | NM_003899.5:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 10 | NM_001330597.2:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 6 | NM_001320851.2:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 20 | NM_001354054.2:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant 5 | NM_001113513.2:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant 8 | NM_001320853.2:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant 9 | NM_001320854.2:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant 21 | NM_001354055.2:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant 27 | NM_001354061.2:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant 7 | NM_001320852.1:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform e | NP_001307781.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant 2 | NM_145735.3:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform b | NP_663788.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant 3 | NM_001113511.2:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform c | NP_001106983.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant 13 | NM_001354047.1:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform j | NP_001340976.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant 12 | NM_001354046.2:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform i | NP_001340975.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X2 |
XM_047430723.1:c.165+3824… XM_047430723.1:c.165+38246C>T |
N/A | Intron Variant |
| ARHGEF7 transcript variant X3 |
XM_047430724.1:c.165+3824… XM_047430724.1:c.165+38246C>T |
N/A | Intron Variant |
| ARHGEF7 transcript variant X9 |
XM_047430729.1:c.165+3824… XM_047430729.1:c.165+38246C>T |
N/A | Intron Variant |
| ARHGEF7 transcript variant X13 | XM_047430733.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X15 | XM_047430735.1:c.-189= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X16 | XM_047430736.1:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X18 | XM_047430738.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X21 | XM_047430741.1:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X23 | XM_047430742.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X24 | XM_017020822.2:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X26 | XM_047430744.1:c.-189= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X27 | XM_047430745.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X30 | XM_047430747.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X31 | XM_047430748.1:c.-274= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X32 | XM_047430750.1:c.-189= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X33 | XM_047430751.1:c.-58= | N/A | 5 Prime UTR Variant |
| ARHGEF7 transcript variant X5 | XM_047430725.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X7 | XM_047430727.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X11 | XM_047430730.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X14 | XM_047430734.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X17 | XM_047430737.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X19 | XM_047430739.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X20 | XM_047430740.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X25 | XM_047430743.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X28 | XM_047430746.1:c. | N/A | Genic Upstream Transcript Variant |
| ARHGEF7 transcript variant X1 | XM_047430722.1:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X1 | XP_047286678.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X4 | XM_006719956.4:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X4 | XP_006720019.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X6 | XM_047430726.1:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X6 | XP_047286682.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X8 | XM_047430728.1:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X8 | XP_047286684.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X10 | XM_017020815.2:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X10 | XP_016876304.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X12 | XM_047430732.1:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X12 | XP_047286688.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X29 | XM_011521133.3:c.198C>T | C [TGC] > C [TGT] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 7 isoform X18 | XP_011519435.1:p.Cys66= | C (Cys) > C (Cys) | Synonymous Variant |
| ARHGEF7 transcript variant X22 | XR_007063704.1:n.1106C>T | N/A | Non Coding Transcript Variant |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| LOC101060553 transcript | NR_120398.1:n. | N/A | Upstream Transcript 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= | T |
|---|---|---|
| GRCh38.p14 chr 13 | NC_000013.11:g.111153937= | NC_000013.11:g.111153937C>T |
| GRCh37.p13 chr 13 | NC_000013.10:g.111806284= | NC_000013.10:g.111806284C>T |
| ARHGEF7 transcript variant 1 | NM_003899.5:c.-274= | NM_003899.5:c.-274C>T |
| ARHGEF7 transcript variant 1 | NM_003899.4:c.-274= | NM_003899.4:c.-274C>T |
| ARHGEF7 transcript variant 1 | NM_003899.3:c.-274= | NM_003899.3:c.-274C>T |
| ARHGEF7 transcript variant X4 | XM_006719956.4:c.198= | XM_006719956.4:c.198C>T |
| ARHGEF7 transcript variant X1 | XM_006719956.3:c.198= | XM_006719956.3:c.198C>T |
| ARHGEF7 transcript variant X5 | XM_006719956.2:c.198= | XM_006719956.2:c.198C>T |
| ARHGEF7 transcript variant X13 | XM_006719956.1:c.198= | XM_006719956.1:c.198C>T |
| ARHGEF7 transcript variant 2 | NM_145735.3:c.198= | NM_145735.3:c.198C>T |
| ARHGEF7 transcript variant 2 | NM_145735.2:c.198= | NM_145735.2:c.198C>T |
| ARHGEF7 transcript variant X29 | XM_011521133.3:c.198= | XM_011521133.3:c.198C>T |
| ARHGEF7 transcript variant X13 | XM_011521133.2:c.198= | XM_011521133.2:c.198C>T |
| ARHGEF7 transcript variant X19 | XM_011521133.1:c.198= | XM_011521133.1:c.198C>T |
| ARHGEF7 transcript variant 3 | NM_001113511.2:c.198= | NM_001113511.2:c.198C>T |
| ARHGEF7 transcript variant 3 | NM_001113511.1:c.198= | NM_001113511.1:c.198C>T |
| ARHGEF7 transcript variant X10 | XM_017020815.2:c.198= | XM_017020815.2:c.198C>T |
| ARHGEF7 transcript variant X3 | XM_017020815.1:c.198= | XM_017020815.1:c.198C>T |
| ARHGEF7 transcript variant 12 | NM_001354046.2:c.198= | NM_001354046.2:c.198C>T |
| ARHGEF7 transcript variant 12 | NM_001354046.1:c.198= | NM_001354046.1:c.198C>T |
| ARHGEF7 transcript variant 26 | NM_001354060.2:c.-274= | NM_001354060.2:c.-274C>T |
| ARHGEF7 transcript variant 26 | NM_001354060.1:c.-274= | NM_001354060.1:c.-274C>T |
| ARHGEF7 transcript variant 17 | NM_001354051.2:c.-274= | NM_001354051.2:c.-274C>T |
| ARHGEF7 transcript variant 17 | NM_001354051.1:c.-274= | NM_001354051.1:c.-274C>T |
| ARHGEF7 transcript variant 25 | NM_001354059.2:c.-337= | NM_001354059.2:c.-337C>T |
| ARHGEF7 transcript variant 25 | NM_001354059.1:c.-337= | NM_001354059.1:c.-337C>T |
| ARHGEF7 transcript variant 24 | NM_001354058.2:c.-286= | NM_001354058.2:c.-286C>T |
| ARHGEF7 transcript variant 24 | NM_001354058.1:c.-286= | NM_001354058.1:c.-286C>T |
| ARHGEF7 transcript variant 10 | NM_001330597.2:c.-274= | NM_001330597.2:c.-274C>T |
| ARHGEF7 transcript variant 10 | NM_001330597.1:c.-274= | NM_001330597.1:c.-274C>T |
| ARHGEF7 transcript variant 15 | NM_001354049.2:c.-274= | NM_001354049.2:c.-274C>T |
| ARHGEF7 transcript variant 15 | NM_001354049.1:c.-274= | NM_001354049.1:c.-274C>T |
| ARHGEF7 transcript variant 23 | NM_001354057.2:c.-252= | NM_001354057.2:c.-252C>T |
| ARHGEF7 transcript variant 23 | NM_001354057.1:c.-252= | NM_001354057.1:c.-252C>T |
| ARHGEF7 transcript variant 16 | NM_001354050.2:c.-189= | NM_001354050.2:c.-189C>T |
| ARHGEF7 transcript variant 16 | NM_001354050.1:c.-189= | NM_001354050.1:c.-189C>T |
| ARHGEF7 transcript variant 20 | NM_001354054.2:c.-274= | NM_001354054.2:c.-274C>T |
| ARHGEF7 transcript variant 20 | NM_001354054.1:c.-274= | NM_001354054.1:c.-274C>T |
| ARHGEF7 transcript variant 18 | NM_001354052.2:c.-274= | NM_001354052.2:c.-274C>T |
| ARHGEF7 transcript variant 18 | NM_001354052.1:c.-274= | NM_001354052.1:c.-274C>T |
| ARHGEF7 transcript variant 11 | NM_001330598.2:c.-58= | NM_001330598.2:c.-58C>T |
| ARHGEF7 transcript variant 11 | NM_001330598.1:c.-58= | NM_001330598.1:c.-58C>T |
| ARHGEF7 transcript variant X24 | XM_017020822.2:c.-58= | XM_017020822.2:c.-58C>T |
| ARHGEF7 transcript variant X9 | XM_017020822.1:c.-58= | XM_017020822.1:c.-58C>T |
| ARHGEF7 transcript variant 19 | NM_001354053.2:c.-58= | NM_001354053.2:c.-58C>T |
| ARHGEF7 transcript variant 19 | NM_001354053.1:c.-58= | NM_001354053.1:c.-58C>T |
| ARHGEF7 transcript variant 6 | NM_001320851.2:c.-58= | NM_001320851.2:c.-58C>T |
| ARHGEF7 transcript variant 6 | NM_001320851.1:c.-58= | NM_001320851.1:c.-58C>T |
| ARHGEF7 transcript variant X1 | XM_047430722.1:c.198= | XM_047430722.1:c.198C>T |
| ARHGEF7 transcript variant 7 | NM_001320852.1:c.198= | NM_001320852.1:c.198C>T |
| ARHGEF7 transcript variant X6 | XM_047430726.1:c.198= | XM_047430726.1:c.198C>T |
| ARHGEF7 transcript variant 13 | NM_001354047.1:c.198= | NM_001354047.1:c.198C>T |
| ARHGEF7 transcript variant X8 | XM_047430728.1:c.198= | XM_047430728.1:c.198C>T |
| ARHGEF7 transcript variant X12 | XM_047430732.1:c.198= | XM_047430732.1:c.198C>T |
| ARHGEF7 transcript variant 14 | NM_001354048.1:c.-274= | NM_001354048.1:c.-274C>T |
| ARHGEF7 transcript variant 22 | NM_001354056.1:c.-58= | NM_001354056.1:c.-58C>T |
| ARHGEF7 transcript variant X18 | XM_047430738.1:c.-274= | XM_047430738.1:c.-274C>T |
| ARHGEF7 transcript variant X13 | XM_047430733.1:c.-274= | XM_047430733.1:c.-274C>T |
| ARHGEF7 transcript variant X15 | XM_047430735.1:c.-189= | XM_047430735.1:c.-189C>T |
| ARHGEF7 transcript variant X23 | XM_047430742.1:c.-274= | XM_047430742.1:c.-274C>T |
| ARHGEF7 transcript variant X27 | XM_047430745.1:c.-274= | XM_047430745.1:c.-274C>T |
| ARHGEF7 transcript variant X16 | XM_047430736.1:c.-58= | XM_047430736.1:c.-58C>T |
| ARHGEF7 transcript variant X21 | XM_047430741.1:c.-58= | XM_047430741.1:c.-58C>T |
| ARHGEF7 transcript variant X26 | XM_047430744.1:c.-189= | XM_047430744.1:c.-189C>T |
| ARHGEF7 transcript variant X22 | XR_007063704.1:n.1106= | XR_007063704.1:n.1106C>T |
| ARHGEF7 transcript variant X30 | XM_047430747.1:c.-274= | XM_047430747.1:c.-274C>T |
| ARHGEF7 transcript variant X31 | XM_047430748.1:c.-274= | XM_047430748.1:c.-274C>T |
| ARHGEF7 transcript variant X32 | XM_047430750.1:c.-189= | XM_047430750.1:c.-189C>T |
| ARHGEF7 transcript variant X33 | XM_047430751.1:c.-58= | XM_047430751.1:c.-58C>T |
| rho guanine nucleotide exchange factor 7 isoform X4 | XP_006720019.1:p.Cys66= | XP_006720019.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform b | NP_663788.1:p.Cys66= | NP_663788.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform X18 | XP_011519435.1:p.Cys66= | XP_011519435.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform c | NP_001106983.1:p.Cys66= | NP_001106983.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform X10 | XP_016876304.1:p.Cys66= | XP_016876304.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform i | NP_001340975.1:p.Cys66= | NP_001340975.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform X1 | XP_047286678.1:p.Cys66= | XP_047286678.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform e | NP_001307781.1:p.Cys66= | NP_001307781.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform X6 | XP_047286682.1:p.Cys66= | XP_047286682.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform j | NP_001340976.1:p.Cys66= | NP_001340976.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform X8 | XP_047286684.1:p.Cys66= | XP_047286684.1:p.Cys66= |
| rho guanine nucleotide exchange factor 7 isoform X12 | XP_047286688.1:p.Cys66= | XP_047286688.1:p.Cys66= |
| ARHGEF7 transcript variant 4 | NM_001113512.1:c.165+38246= | NM_001113512.1:c.165+38246C>T |
| ARHGEF7 transcript variant 4 | NM_001113512.2:c.165+38246= | NM_001113512.2:c.165+38246C>T |
| ARHGEF7 transcript variant X2 | XM_047430723.1:c.165+38246= | XM_047430723.1:c.165+38246C>T |
| ARHGEF7 transcript variant X3 | XM_047430724.1:c.165+38246= | XM_047430724.1:c.165+38246C>T |
| ARHGEF7 transcript variant X9 | XM_047430729.1:c.165+38246= | XM_047430729.1:c.165+38246C>T |
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 | ss2740518451 | Nov 08, 2017 (151) |
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).
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1466508125
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genomic regions, transcripts, and products
Top▲
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.