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 1:173903902 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920113

Most severe consequence
Clinical significance

Synonyms

LSDB 367

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

1:g.173903902G>A
ENST00000367698.3:c.1382C>T
ENSP00000356671.3:p.Pro461Leu
ENST00000617423.1:c.767C>T
ENSP00000478688.1:p.Pro256Leu

Variation displays