Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 10:82034291 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950789

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16770

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

10:g.82034291G>A
ENST00000480845.1:n.302C>T
ENST00000485270.1:n.582C>T
ENST00000372213.3:c.1070C>T
ENSP00000361287.3:p.Pro357Leu

Variation displays