Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 1:115033456 (forward strand) | View in location tab

Co-located

with COSMIC COSM894304 (G/A) ; HGMD-PUBLIC CM900214

Most severe consequence
Clinical significance

Synonyms

LSDB 5593

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

1:g.115033456G>T
ENST00000256592.2:c.94G>T
ENSP00000256592.1:p.Glu32Ter
ENST00000369517.1:c.94G>T
ENSP00000358530.1:p.Glu32Ter

Variation displays