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 4:54727444 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1252, COSM1253, COSM1255 ; HGMD-PUBLIC CM013551

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 9 synonyms - Show

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 4 phenotypes.

Variant displays