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: < 0.01 (T)
Location

Chromosome 11:64757826 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930630

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

11:g.64757826C>T
ENST00000164139.3:c.613G>A
ENSP00000164139.3:p.Gly205Ser
ENST00000377432.5:c.349G>A
ENSP00000366650.3:p.Gly117Ser

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays