Original source

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

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

Chromosome 10:82034355 (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.82034355C>T
ENST00000480845.1:n.238G>A
ENST00000372213.3:c.1006G>A
ENSP00000361287.3:p.Gly336Arg
ENST00000485270.1:n.518G>A

Variation displays