Original source

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

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

Chromosome 1:109610108 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021611

Most severe consequence
Clinical significance

Synonyms

LSDB 2414

This variation has 6 HGVS names - click the plus to show

1:g.109610108G>A
ENST00000369851.5:c.*17786G>A
ENST00000351050.4:c.235C>T
ENSP00000251337.3:p.Gln79Ter
ENST00000622865.1:c.235C>T
ENSP00000482596.1:p.Gln79Ter

Variation displays