Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A/G | Ancestral: T | Ambiguity code: D
Location

Chromosome 4:54727447 (forward strand) | View in location tab

Co-located

with COSMIC COSM1257 (T/A), COSM36302 (T/C), COSM1260 (T/G) ; HGMD-PUBLIC CM077194, CD982724

Most severe consequence
 
Missense variant

This variant has 3 synonyms - click the plus to show

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts.

Variant displays