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.
rs1486370368
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr4:153632760 (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
- G>A
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
- A=0.000004 (1/251448, GnomAD_exome)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- TMEM131L : Missense 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").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| gnomAD - Exomes | Global | Study-wide | 251448 | G=0.999996 | A=0.000004 |
| gnomAD - Exomes | European | Sub | 135378 | G=0.999993 | A=0.000007 |
| gnomAD - Exomes | Asian | Sub | 49010 | G=1.00000 | A=0.00000 |
| gnomAD - Exomes | American | Sub | 34590 | G=1.00000 | A=0.00000 |
| gnomAD - Exomes | African | Sub | 16254 | G=1.00000 | A=0.00000 |
| gnomAD - Exomes | Ashkenazi Jewish | Sub | 10076 | G=1.00000 | A=0.00000 |
| gnomAD - Exomes | Other | Sub | 6140 | G=1.0000 | A=0.0000 |
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 4 | NC_000004.12:g.153632760G>A |
| GRCh37.p13 chr 4 | NC_000004.11:g.154553912G>A |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| TMEM131L transcript variant 1 | NM_001131007.2:c.4250G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform 1 precursor |
NP_001124479.1:p.Cys1417T… NP_001124479.1:p.Cys1417Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant 2 | NM_015196.4:c.4247G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform 2 precursor | NP_056011.3:p.Cys1416Tyr | C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X38 |
XM_047449929.1:c.4295-143… XM_047449929.1:c.4295-1432G>A |
N/A | Intron Variant |
| TMEM131L transcript variant X39 | XM_047449930.1:c. | N/A | Genic Downstream Transcript Variant |
| TMEM131L transcript variant X1 | XM_047449899.1:c.4394G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X1 |
XP_047305855.1:p.Cys1465T… XP_047305855.1:p.Cys1465Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X2 | XM_047449900.1:c.4391G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X2 |
XP_047305856.1:p.Cys1464T… XP_047305856.1:p.Cys1464Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X3 | XM_047449901.1:c.4391G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X3 |
XP_047305857.1:p.Cys1464T… XP_047305857.1:p.Cys1464Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X4 | XM_011531780.2:c.4337G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X4 |
XP_011530082.1:p.Cys1446T… XP_011530082.1:p.Cys1446Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X5 | XM_011531781.2:c.4334G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X5 |
XP_011530083.1:p.Cys1445T… XP_011530083.1:p.Cys1445Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X6 | XM_047449902.1:c.4334G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X6 |
XP_047305858.1:p.Cys1445T… XP_047305858.1:p.Cys1445Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X7 | XM_047449903.1:c.4331G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X7 |
XP_047305859.1:p.Cys1444T… XP_047305859.1:p.Cys1444Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X8 | XM_047449904.1:c.4316G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X8 |
XP_047305860.1:p.Cys1439T… XP_047305860.1:p.Cys1439Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X9 | XM_047449905.1:c.4313G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X9 |
XP_047305861.1:p.Cys1438T… XP_047305861.1:p.Cys1438Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X10 | XM_024453956.2:c.4307G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X10 |
XP_024309724.1:p.Cys1436T… XP_024309724.1:p.Cys1436Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X11 | XM_047449906.1:c.4304G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X11 |
XP_047305862.1:p.Cys1435T… XP_047305862.1:p.Cys1435Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X12 | XM_024453957.2:c.4304G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X12 |
XP_024309725.1:p.Cys1435T… XP_024309725.1:p.Cys1435Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X13 | XM_047449907.1:c.4301G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X13 |
XP_047305863.1:p.Cys1434T… XP_047305863.1:p.Cys1434Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X14 | XM_047449908.1:c.4259G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X14 |
XP_047305864.1:p.Cys1420T… XP_047305864.1:p.Cys1420Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X15 | XM_047449909.1:c.4256G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X15 |
XP_047305865.1:p.Cys1419T… XP_047305865.1:p.Cys1419Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X16 | XM_047449910.1:c.4253G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X16 |
XP_047305866.1:p.Cys1418T… XP_047305866.1:p.Cys1418Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X17 | XM_017007925.2:c.4247G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X17 |
XP_016863414.1:p.Cys1416T… XP_016863414.1:p.Cys1416Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X18 | XM_017007926.2:c.4244G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X18 |
XP_016863415.1:p.Cys1415T… XP_016863415.1:p.Cys1415Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X19 | XM_047449911.1:c.4229G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X19 |
XP_047305867.1:p.Cys1410T… XP_047305867.1:p.Cys1410Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X20 | XM_047449912.1:c.4226G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X20 |
XP_047305868.1:p.Cys1409T… XP_047305868.1:p.Cys1409Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X21 | XM_047449913.1:c.4172G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X21 |
XP_047305869.1:p.Cys1391T… XP_047305869.1:p.Cys1391Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X22 | XM_047449914.1:c.4169G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X22 |
XP_047305870.1:p.Cys1390T… XP_047305870.1:p.Cys1390Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X23 | XM_047449915.1:c.4169G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X23 |
XP_047305871.1:p.Cys1390T… XP_047305871.1:p.Cys1390Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X24 | XM_047449916.1:c.4166G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X24 |
XP_047305872.1:p.Cys1389T… XP_047305872.1:p.Cys1389Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X25 | XM_047449917.1:c.4142G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X25 |
XP_047305873.1:p.Cys1381T… XP_047305873.1:p.Cys1381Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X26 | XM_047449918.1:c.4139G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X26 |
XP_047305874.1:p.Cys1380T… XP_047305874.1:p.Cys1380Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X27 | XM_047449919.1:c.4136G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X27 |
XP_047305875.1:p.Cys1379T… XP_047305875.1:p.Cys1379Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X28 | XM_011531783.2:c.4085G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X28 |
XP_011530085.1:p.Cys1362T… XP_011530085.1:p.Cys1362Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X29 | XM_047449920.1:c.4082G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X29 |
XP_047305876.1:p.Cys1361T… XP_047305876.1:p.Cys1361Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X30 | XM_047449921.1:c.4055G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X30 |
XP_047305877.1:p.Cys1352T… XP_047305877.1:p.Cys1352Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X31 | XM_047449922.1:c.4052G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X31 |
XP_047305878.1:p.Cys1351T… XP_047305878.1:p.Cys1351Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X32 | XM_047449923.1:c.3998G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X32 |
XP_047305879.1:p.Cys1333T… XP_047305879.1:p.Cys1333Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X33 | XM_047449924.1:c.3995G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X33 |
XP_047305880.1:p.Cys1332T… XP_047305880.1:p.Cys1332Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X34 | XM_047449925.1:c.3995G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X34 |
XP_047305881.1:p.Cys1332T… XP_047305881.1:p.Cys1332Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X35 | XM_047449926.1:c.3992G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X35 |
XP_047305882.1:p.Cys1331T… XP_047305882.1:p.Cys1331Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X36 | XM_047449927.1:c.3977G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X36 |
XP_047305883.1:p.Cys1326T… XP_047305883.1:p.Cys1326Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X37 | XM_047449928.1:c.3974G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X37 |
XP_047305884.1:p.Cys1325T… XP_047305884.1:p.Cys1325Tyr |
C (Cys) > Y (Tyr) | Missense Variant |
| TMEM131L transcript variant X40 | XM_024453958.2:c.2372G>A | C [TGT] > Y [TAT] | Coding Sequence Variant |
| transmembrane protein 131-like isoform X40 | XP_024309726.1:p.Cys791Tyr | C (Cys) > Y (Tyr) | 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 | G= | A |
|---|---|---|
| GRCh38.p14 chr 4 | NC_000004.12:g.153632760= | NC_000004.12:g.153632760G>A |
| GRCh37.p13 chr 4 | NC_000004.11:g.154553912= | NC_000004.11:g.154553912G>A |
| TMEM131L transcript variant 2 | NM_015196.4:c.4247= | NM_015196.4:c.4247G>A |
| TMEM131L transcript variant 2 | NM_015196.3:c.4247= | NM_015196.3:c.4247G>A |
| TMEM131L transcript variant X4 | XM_011531780.2:c.4337= | XM_011531780.2:c.4337G>A |
| TMEM131L transcript variant X1 | XM_011531780.1:c.4337= | XM_011531780.1:c.4337G>A |
| TMEM131L transcript variant X5 | XM_011531781.2:c.4334= | XM_011531781.2:c.4334G>A |
| TMEM131L transcript variant X2 | XM_011531781.1:c.4334= | XM_011531781.1:c.4334G>A |
| TMEM131L transcript variant X28 | XM_011531783.2:c.4085= | XM_011531783.2:c.4085G>A |
| TMEM131L transcript variant X7 | XM_011531783.1:c.4085= | XM_011531783.1:c.4085G>A |
| TMEM131L transcript variant X10 | XM_024453956.2:c.4307= | XM_024453956.2:c.4307G>A |
| TMEM131L transcript variant X3 | XM_024453956.1:c.4307= | XM_024453956.1:c.4307G>A |
| TMEM131L transcript variant X12 | XM_024453957.2:c.4304= | XM_024453957.2:c.4304G>A |
| TMEM131L transcript variant X4 | XM_024453957.1:c.4304= | XM_024453957.1:c.4304G>A |
| TMEM131L transcript variant 1 | NM_001131007.2:c.4250= | NM_001131007.2:c.4250G>A |
| TMEM131L transcript variant 1 | NM_001131007.1:c.4250= | NM_001131007.1:c.4250G>A |
| TMEM131L transcript variant X17 | XM_017007925.2:c.4247= | XM_017007925.2:c.4247G>A |
| TMEM131L transcript variant X5 | XM_017007925.1:c.4247= | XM_017007925.1:c.4247G>A |
| TMEM131L transcript variant X18 | XM_017007926.2:c.4244= | XM_017007926.2:c.4244G>A |
| TMEM131L transcript variant X6 | XM_017007926.1:c.4244= | XM_017007926.1:c.4244G>A |
| TMEM131L transcript variant X40 | XM_024453958.2:c.2372= | XM_024453958.2:c.2372G>A |
| TMEM131L transcript variant X8 | XM_024453958.1:c.2372= | XM_024453958.1:c.2372G>A |
| TMEM131L transcript variant X1 | XM_047449899.1:c.4394= | XM_047449899.1:c.4394G>A |
| TMEM131L transcript variant X3 | XM_047449901.1:c.4391= | XM_047449901.1:c.4391G>A |
| TMEM131L transcript variant X2 | XM_047449900.1:c.4391= | XM_047449900.1:c.4391G>A |
| TMEM131L transcript variant X6 | XM_047449902.1:c.4334= | XM_047449902.1:c.4334G>A |
| TMEM131L transcript variant X7 | XM_047449903.1:c.4331= | XM_047449903.1:c.4331G>A |
| TMEM131L transcript variant X8 | XM_047449904.1:c.4316= | XM_047449904.1:c.4316G>A |
| TMEM131L transcript variant X9 | XM_047449905.1:c.4313= | XM_047449905.1:c.4313G>A |
| TMEM131L transcript variant X14 | XM_047449908.1:c.4259= | XM_047449908.1:c.4259G>A |
| TMEM131L transcript variant X15 | XM_047449909.1:c.4256= | XM_047449909.1:c.4256G>A |
| TMEM131L transcript variant X16 | XM_047449910.1:c.4253= | XM_047449910.1:c.4253G>A |
| TMEM131L transcript variant X25 | XM_047449917.1:c.4142= | XM_047449917.1:c.4142G>A |
| TMEM131L transcript variant X26 | XM_047449918.1:c.4139= | XM_047449918.1:c.4139G>A |
| TMEM131L transcript variant X27 | XM_047449919.1:c.4136= | XM_047449919.1:c.4136G>A |
| TMEM131L transcript variant X29 | XM_047449920.1:c.4082= | XM_047449920.1:c.4082G>A |
| TMEM131L transcript variant X11 | XM_047449906.1:c.4304= | XM_047449906.1:c.4304G>A |
| TMEM131L transcript variant X13 | XM_047449907.1:c.4301= | XM_047449907.1:c.4301G>A |
| TMEM131L transcript variant X19 | XM_047449911.1:c.4229= | XM_047449911.1:c.4229G>A |
| TMEM131L transcript variant X20 | XM_047449912.1:c.4226= | XM_047449912.1:c.4226G>A |
| TMEM131L transcript variant X21 | XM_047449913.1:c.4172= | XM_047449913.1:c.4172G>A |
| TMEM131L transcript variant X23 | XM_047449915.1:c.4169= | XM_047449915.1:c.4169G>A |
| TMEM131L transcript variant X22 | XM_047449914.1:c.4169= | XM_047449914.1:c.4169G>A |
| TMEM131L transcript variant X24 | XM_047449916.1:c.4166= | XM_047449916.1:c.4166G>A |
| TMEM131L transcript variant X30 | XM_047449921.1:c.4055= | XM_047449921.1:c.4055G>A |
| TMEM131L transcript variant X31 | XM_047449922.1:c.4052= | XM_047449922.1:c.4052G>A |
| TMEM131L transcript variant X32 | XM_047449923.1:c.3998= | XM_047449923.1:c.3998G>A |
| TMEM131L transcript variant X34 | XM_047449925.1:c.3995= | XM_047449925.1:c.3995G>A |
| TMEM131L transcript variant X33 | XM_047449924.1:c.3995= | XM_047449924.1:c.3995G>A |
| TMEM131L transcript variant X35 | XM_047449926.1:c.3992= | XM_047449926.1:c.3992G>A |
| TMEM131L transcript variant X36 | XM_047449927.1:c.3977= | XM_047449927.1:c.3977G>A |
| TMEM131L transcript variant X37 | XM_047449928.1:c.3974= | XM_047449928.1:c.3974G>A |
| transmembrane protein 131-like isoform 2 precursor | NP_056011.3:p.Cys1416= | NP_056011.3:p.Cys1416Tyr |
| transmembrane protein 131-like isoform X4 | XP_011530082.1:p.Cys1446= | XP_011530082.1:p.Cys1446Tyr |
| transmembrane protein 131-like isoform X5 | XP_011530083.1:p.Cys1445= | XP_011530083.1:p.Cys1445Tyr |
| transmembrane protein 131-like isoform X28 | XP_011530085.1:p.Cys1362= | XP_011530085.1:p.Cys1362Tyr |
| transmembrane protein 131-like isoform X10 | XP_024309724.1:p.Cys1436= | XP_024309724.1:p.Cys1436Tyr |
| transmembrane protein 131-like isoform X12 | XP_024309725.1:p.Cys1435= | XP_024309725.1:p.Cys1435Tyr |
| transmembrane protein 131-like isoform 1 precursor | NP_001124479.1:p.Cys1417= | NP_001124479.1:p.Cys1417Tyr |
| transmembrane protein 131-like isoform X17 | XP_016863414.1:p.Cys1416= | XP_016863414.1:p.Cys1416Tyr |
| transmembrane protein 131-like isoform X18 | XP_016863415.1:p.Cys1415= | XP_016863415.1:p.Cys1415Tyr |
| transmembrane protein 131-like isoform X40 | XP_024309726.1:p.Cys791= | XP_024309726.1:p.Cys791Tyr |
| transmembrane protein 131-like isoform X1 | XP_047305855.1:p.Cys1465= | XP_047305855.1:p.Cys1465Tyr |
| transmembrane protein 131-like isoform X3 | XP_047305857.1:p.Cys1464= | XP_047305857.1:p.Cys1464Tyr |
| transmembrane protein 131-like isoform X2 | XP_047305856.1:p.Cys1464= | XP_047305856.1:p.Cys1464Tyr |
| transmembrane protein 131-like isoform X6 | XP_047305858.1:p.Cys1445= | XP_047305858.1:p.Cys1445Tyr |
| transmembrane protein 131-like isoform X7 | XP_047305859.1:p.Cys1444= | XP_047305859.1:p.Cys1444Tyr |
| transmembrane protein 131-like isoform X8 | XP_047305860.1:p.Cys1439= | XP_047305860.1:p.Cys1439Tyr |
| transmembrane protein 131-like isoform X9 | XP_047305861.1:p.Cys1438= | XP_047305861.1:p.Cys1438Tyr |
| transmembrane protein 131-like isoform X14 | XP_047305864.1:p.Cys1420= | XP_047305864.1:p.Cys1420Tyr |
| transmembrane protein 131-like isoform X15 | XP_047305865.1:p.Cys1419= | XP_047305865.1:p.Cys1419Tyr |
| transmembrane protein 131-like isoform X16 | XP_047305866.1:p.Cys1418= | XP_047305866.1:p.Cys1418Tyr |
| transmembrane protein 131-like isoform X25 | XP_047305873.1:p.Cys1381= | XP_047305873.1:p.Cys1381Tyr |
| transmembrane protein 131-like isoform X26 | XP_047305874.1:p.Cys1380= | XP_047305874.1:p.Cys1380Tyr |
| transmembrane protein 131-like isoform X27 | XP_047305875.1:p.Cys1379= | XP_047305875.1:p.Cys1379Tyr |
| transmembrane protein 131-like isoform X29 | XP_047305876.1:p.Cys1361= | XP_047305876.1:p.Cys1361Tyr |
| transmembrane protein 131-like isoform X11 | XP_047305862.1:p.Cys1435= | XP_047305862.1:p.Cys1435Tyr |
| transmembrane protein 131-like isoform X13 | XP_047305863.1:p.Cys1434= | XP_047305863.1:p.Cys1434Tyr |
| transmembrane protein 131-like isoform X19 | XP_047305867.1:p.Cys1410= | XP_047305867.1:p.Cys1410Tyr |
| transmembrane protein 131-like isoform X20 | XP_047305868.1:p.Cys1409= | XP_047305868.1:p.Cys1409Tyr |
| transmembrane protein 131-like isoform X21 | XP_047305869.1:p.Cys1391= | XP_047305869.1:p.Cys1391Tyr |
| transmembrane protein 131-like isoform X23 | XP_047305871.1:p.Cys1390= | XP_047305871.1:p.Cys1390Tyr |
| transmembrane protein 131-like isoform X22 | XP_047305870.1:p.Cys1390= | XP_047305870.1:p.Cys1390Tyr |
| transmembrane protein 131-like isoform X24 | XP_047305872.1:p.Cys1389= | XP_047305872.1:p.Cys1389Tyr |
| transmembrane protein 131-like isoform X30 | XP_047305877.1:p.Cys1352= | XP_047305877.1:p.Cys1352Tyr |
| transmembrane protein 131-like isoform X31 | XP_047305878.1:p.Cys1351= | XP_047305878.1:p.Cys1351Tyr |
| transmembrane protein 131-like isoform X32 | XP_047305879.1:p.Cys1333= | XP_047305879.1:p.Cys1333Tyr |
| transmembrane protein 131-like isoform X34 | XP_047305881.1:p.Cys1332= | XP_047305881.1:p.Cys1332Tyr |
| transmembrane protein 131-like isoform X33 | XP_047305880.1:p.Cys1332= | XP_047305880.1:p.Cys1332Tyr |
| transmembrane protein 131-like isoform X35 | XP_047305882.1:p.Cys1331= | XP_047305882.1:p.Cys1331Tyr |
| transmembrane protein 131-like isoform X36 | XP_047305883.1:p.Cys1326= | XP_047305883.1:p.Cys1326Tyr |
| transmembrane protein 131-like isoform X37 | XP_047305884.1:p.Cys1325= | XP_047305884.1:p.Cys1325Tyr |
| TMEM131L transcript variant X38 | XM_047449929.1:c.4295-1432= | XM_047449929.1:c.4295-1432G>A |
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 | ss2734782048 | Nov 08, 2017 (151) |
| 2 | gnomAD - Exomes | NC_000004.11 - 154553912 | Jul 13, 2019 (153) |
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 rs1486370368
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.