Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 14:23424842 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4050071 ; HGMD-PUBLIC HM971868

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_042810

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, has 2504 sample genotypes and is associated with 3 phenotypes.

Variant displays