Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.36 (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
ENST00000405093.5: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

Variation displays