Original source

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

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

Chromosome 4:73740676 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3781187

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs4986969

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2506 sample genotypes and is mentioned in 1 citation.

Variant displays