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 5:13901585 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020270

Most severe consequence
Clinical significance

Synonyms

LSDB 11781

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

5:g.13901585G>A
ENST00000265104.4:c.1828C>T
ENSP00000265104.4:p.Gln610Ter

Variation displays