Original source

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

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

Chromosome 6:162443371 (forward strand) | View in location tab

Co-located

with COSMIC COSM3622686 (G/A), COSM3622685 (G/A) ; HGMD-PUBLIC CM025200

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_019735

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays