Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 17:33904464 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040240

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

17:g.33904464T>A
ENST00000225873.4:c.273A>T
ENSP00000225873.3:p.Arg91Ser
ENST00000585380.1:c.273A>T
ENSP00000466280.1:p.Arg91Ser
HG385_PATCH:g.33904464T>A
ENST00000586663.1:c.273A>T
ENSP00000466894.1:p.Arg91Ser

Variation displays