Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 5:132384281 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991136

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

5:g.132384281A>G
ENST00000245407.5:c.632A>G
ENSP00000245407.3:p.Tyr211Cys
ENST00000437841.4:c.394-1047A>G
ENST00000435065.4:c.704A>G
ENSP00000402760.2:p.Tyr235Cys
ENST00000461013.3:n.8054A>G
ENST00000415928.3:c.401A>G
ENSP00000388838.1:p.Tyr134Cys

Variation displays