Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 11:17409129 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050282

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.17409129C>G
ENST00000526912.1:c.249G>C
ENSP00000432729.1:p.Lys83Asn
ENST00000528731.1:c.249G>C
ENSP00000434755.1:p.Lys83Asn
ENST00000339994.4:c.510G>C
ENSP00000345708.4:p.Lys170Asn

Variation displays