Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 1:183194854 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941036

Most severe consequence
Clinical significance

Synonyms

LSDB 3776

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

1:g.183194854C>G
ENST00000493293.1:c.1065C>G
ENSP00000432063.1:p.Tyr355Ter
ENST00000264144.4:c.1065C>G
ENSP00000264144.4:p.Tyr355Ter

Variation displays