Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.08 (T)
Location

Chromosome 6:111913262 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_047349

This variation has 11 HGVS names - click the plus to show

6:g.111913262C>T
ENST00000532353.1:n.112-5779C>T
ENST00000392556.4:c.-1209G>A
ENST00000368761.5:c.28G>A
ENSP00000357750.5:p.Asp10Asn
ENST00000359831.4:c.28G>A
ENSP00000352889.4:p.Asp10Asn
ENST00000528599.1:n.223G>A
ENST00000532708.1:n.254G>A
ENST00000340026.6:c.55G>A
ENSP00000345984.6:p.Asp19Asn

This variation has assays on 4 chips - click the plus to show

Variation displays