Original source

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

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

Chromosome 1:26126722 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022835 ; PhenCode SEPN1:c.1A>G (A/G)

Most severe consequence
Clinical significance

Synonyms

LSDB 13656

This variation has 7 HGVS names - click the plus to show

1:g.26126722A>G
ENST00000361547.2:c.1A>G
ENSP00000355141.2:p.Met1?
ENST00000354177.4:c.1A>G
ENSP00000346109.4:p.Met1?
ENST00000374315.1:c.1A>G
ENSP00000363434.1:p.Met1?

Variation displays