Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 10:73499529 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS010092

Most severe consequence
Clinical significance

Synonyms

LSDB 13243

This variation has 4 HGVS names - click the plus to show

10:g.73499529G>C
ENST00000224721.6:c.4503G>C
ENSP00000224721.6:p.Gln1501His
ENST00000398792.3:n.1177G>C

Variation displays