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 10:71793370 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021546

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11604444, 13250

This variation has 5 HGVS names - click the plus to show

10:g.71793370G>A
ENST00000622827.1:c.6442G>A
ENSP00000483211.1:p.Asp2148Asn
ENST00000224721.7:c.6592G>A
ENSP00000224721.7:p.Asp2198Asn

Variation displays