Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 10:80274639 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950788

Most severe consequence
Clinical significance

Synonyms

LSDB 16768

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

10:g.80274639A>C
ENST00000480845.1:n.198T>G
ENST00000372213.5:c.966T>G
ENSP00000361287.3:p.Ile322Met
ENST00000485270.3:n.478T>G

Variation displays