Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome 8:99820031 (forward strand) | View in location tab

Co-located

with COSMIC COSM3698730 (A/G), COSM3698729 (A/G) ; HGMD-PUBLIC CM041280

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

8:g.99820031A>G
ENST00000358544.4:c.8978A>G
ENSP00000351346.2:p.Asn2993Ser
ENST00000357162.4:c.8903A>G
ENSP00000349685.2:p.Asn2968Ser

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays