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 10:73492049 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030204

Most severe consequence
Clinical significance

Synonyms

LSDB 13251

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

10:g.73492049G>A
ENST00000398786.2:c.-6+5436C>T
ENST00000224721.6:c.4036G>A
ENSP00000224721.6:p.Asp1346Asn
ENST00000398792.3:n.713G>A

Variation displays