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 | MAF: 0.04 (A)
Location

Chromosome 6:111591867 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

6:g.111591867G>A
ENST00000392556.5:c.247C>T
ENSP00000376339.5:p.Arg83Trp
ENST00000532353.1:n.112-5971G>A
ENST00000368761.6:c.220C>T
ENSP00000357750.5:p.Arg74Trp
ENST00000359831.5:c.220C>T
ENSP00000352889.4:p.Arg74Trp
ENST00000528599.1:n.415C>T
ENST00000532708.2:n.446C>T
ENST00000340026.7:c.247C>T
ENSP00000345984.6:p.Arg83Trp

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

Variation displays