Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.37 (G)
Location

Chromosome 14:23392602 (forward strand) | View in location tab

Co-located

with COSMIC COSM3753908 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

14:g.23392602A>G
ENST00000405093.6:c.3302T>C
ENSP00000386041.3:p.Val1101Ala
ENST00000356287.3:c.3302T>C
ENSP00000348634.3:p.Val1101Ala
LRG_389:g.20676T>C
LRG_389t1:c.3302T>C
LRG_389p1:p.Val1101Ala

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 4075 individual genotypes, is associated with 2 phenotypes and is mentioned in 9 citations.

Variation displays