Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 10:73553289 (forward strand) | View in location tab

Co-located

with COSMIC COSM1238472 (G/A) ; HGMD-PUBLIC CM010183

Most severe consequence
Clinical significance

Synonyms

LSDB 13248

This variation has 3 HGVS names - click the plus to show

10:g.73553289G>A
ENST00000224721.6:c.6619G>A
ENSP00000224721.6:p.Asp2207Asn

Variation displays