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 17:33904199 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981517

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.33904199G>A
ENST00000225873.4:c.538C>T
ENSP00000225873.3:p.Arg180Ter
ENST00000585380.1:c.538C>T
ENSP00000466280.1:p.Arg180Ter
HG385_PATCH:g.33904199G>A
ENST00000586663.1:c.538C>T
ENSP00000466894.1:p.Arg180Ter

Variation displays