Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 8:97156888 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

8:g.97156888T>C
ENST00000287020.5:c.1271A>G
ENSP00000287020.4:p.Lys424Arg

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays