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 9:133352446 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981888

Most severe consequence
Clinical significance

Synonyms

LSDB 5516

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

9:g.133352446G>A
ENST00000371974.4:c.751C>T
ENSP00000361042.3:p.Gln251Ter
ENST00000437995.1:n.661C>T
ENST00000615505.1:c.424C>T
ENSP00000482067.1:p.Gln142Ter
ENST00000495952.2:n.741C>T

Variation displays