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 1:173904007 (forward strand) | View in location tab

Co-located

with COSMIC COSM76381 (G/A) ; HGMD-PUBLIC CM890019

Most severe consequence
Clinical significance

Synonyms

LSDB 343

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

1:g.173904007G>A
ENST00000367698.3:c.1277C>T
ENSP00000356671.3:p.Ser426Leu
ENST00000617423.1:c.662C>T
ENSP00000478688.1:p.Ser221Leu

Variation displays