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 5:132659419 (forward strand)|View in location tab

Co-located variant

COSMIC COSM109445

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000005.8:g.132023010C>T

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is mentioned in 1 citation.

Somatic mutation displays