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 10:80275178 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001219

Most severe consequence
Clinical significance

Synonyms

LSDB 16776

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

10:g.80275178G>A
ENST00000480845.1:n.22C>T
ENST00000372213.5:c.790C>T
ENSP00000361287.3:p.Arg264Cys
ENST00000485270.3:n.302C>T

Variation displays