Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 10:80274599 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001220

Most severe consequence
Clinical significance

Synonyms

LSDB 16777

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

10:g.80274599C>T
ENST00000480845.1:n.238G>A
ENST00000485270.3:n.518G>A
ENST00000372213.5:c.1006G>A
ENSP00000361287.3:p.Gly336Arg

Variation displays