Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 17:35577445 (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 9 HGVS names - click the plus to show

17:g.35577445T>A
ENST00000225873.6:c.273A>T
ENSP00000225873.3:p.Arg91Ser
ENST00000613219.2:c.273A>T
ENSP00000482609.1:p.Arg91Ser
ENST00000585380.1:c.273A>T
ENSP00000466280.1:p.Arg91Ser
ENST00000586663.1:c.273A>T
ENSP00000466894.1:p.Arg91Ser

Variation displays