Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 10:72360648 (forward strand) | View in location tab

Co-located

with PhenCode PRF1base_D0067:g.3284G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

10:g.72360648C>T
ENST00000373209.2:c.11G>A
ENSP00000362305.1:p.Arg4His
ENST00000441259.1:c.11G>A
ENSP00000398568.1:p.Arg4His
LRG_94:g.6884G>A
LRG_94t1.1:c.11G>A
LRG_94p1.1:p.Arg4His

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays