Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 10:71793532 (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 5 HGVS names - click the plus to show

10:g.71793532G>A
ENST00000622827.2:c.6604G>A
ENSP00000483211.1:p.Asp2202Asn
ENST00000224721.8:c.6754G>A
ENSP00000224721.7:p.Asp2252Asn

Variation displays