Original source

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

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

Chromosome 17:33902932 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM045955

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

17:g.33902932G>A
ENST00000225873.4:c.949C>T
ENSP00000225873.3:p.Leu317Phe
ENST00000586663.1:c.949C>T
ENSP00000466894.1:p.Leu317Phe
HG385_PATCH:g.33902932G>A

Variation displays