Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 7:128846396 (forward strand)|View in location tab

Co-located variant

COSMIC COSM106745

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB NC_000007.12:g.128273686C>T

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is mentioned in 1 citation.

Somatic mutation displays