Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 12:90964302 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.10:g.89882210C>T

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and is mentioned in 1 citation.

Somatic mutation displays