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
Location

Chromosome 17:39725125 (forward strand) | View in location tab

Co-located

with COSMIC COSM686 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

17:g.39725125A>G
ENST00000583038.3:n.3704A>G
ENST00000580074.1:c.676A>G
ENSP00000463002.1:p.Asn226Ser
ENST00000584450.3:c.2570A>G
ENSP00000463714.1:p.Asn857Ser
ENST00000541774.3:c.2525A>G
ENSP00000446466.1:p.Asn842Ser
ENST00000445658.4:c.1742A>G
ENSP00000404047.2:p.Asn581Ser
ENST00000269571.7:c.2570A>G
ENSP00000269571.4:p.Asn857Ser
ENST00000406381.4:c.2480A>G
ENSP00000385185.2:p.Asn827Ser
ENST00000578373.3:c.*2360A>G
ENST00000584601.3:c.2480A>G
ENSP00000462438.1:p.Asn827Ser

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays