This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
T/A/C/G|Ancestral: T|Ambiguity code: N
Location

Chromosome 4:54727437 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1216, COSM1219, COSM1221 ; HGMD-PUBLIC CM005329

Most severe consequence
 
Missense variant
Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 12 transcripts.

Variant displays