Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 10:82034395 (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.82034395A>C
ENST00000480845.1:n.198T>G
ENST00000485270.1:n.478T>G
ENST00000372213.3:c.966T>G
ENSP00000361287.3:p.Ile322Met

Variation displays