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 17:21416455 (forward strand)|View in location tab

Co-located variant

COSMIC COSM4600498

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000017.9:g.21260360C>G

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 10 sample genotypes.

Variant displays