Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 6:112061120 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

6:g.112061120C>T
ENST00000361714.3:c.178C>T
ENSP00000354734.2:p.Arg60Cys
ENST00000620524.1:c.178C>T
ENSP00000478049.1:p.Arg60Cys
ENST00000409166.3:c.-507-159C>T
ENST00000368663.3:c.112C>T
ENSP00000357652.3:p.Arg38Cys
ENST00000454589.3:c.178C>T
ENSP00000395928.1:p.Arg60Cys
ENST00000368664.5:c.232C>T
ENSP00000357653.3:p.Arg78Cys
ENST00000230529.7:c.178C>T
ENSP00000230529.5:p.Arg60Cys
ENST00000368666.4:c.232C>T
ENSP00000357655.3:p.Arg78Cys
ENST00000604763.3:c.178C>T
ENSP00000473777.1:p.Arg60Cys

This variation has assays on 7 chips - click the plus to show

Variation displays