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 11:17387491 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040763

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

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

11:g.17387491G>A
ENST00000526912.1:c.340C>T
ENSP00000432729.1:p.Arg114Cys
ENST00000528731.1:c.340C>T
ENSP00000434755.1:p.Arg114Cys
ENST00000339994.4:c.601C>T
ENSP00000345708.4:p.Arg201Cys

Variation displays