Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 17:37881378 (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 19 HGVS names - click the plus to show

17:g.37881378A>G
ENST00000583038.1:n.3704A>G
ENST00000580074.1:c.676A>G
ENSP00000463002.1:p.Asn226Ser
ENST00000584450.1:c.2570A>G
ENSP00000463714.1:p.Asn857Ser
ENST00000541774.1:c.2525A>G
ENSP00000446466.1:p.Asn842Ser
ENST00000445658.2:c.1742A>G
ENSP00000404047.2:p.Asn581Ser
ENST00000269571.5:c.2570A>G
ENSP00000269571.4:p.Asn857Ser
ENST00000406381.2:c.2480A>G
ENSP00000385185.2:p.Asn827Ser
ENST00000578373.1:c.*2360A>G
ENST00000540147.1:c.2480A>G
ENSP00000443562.1:p.Asn827Ser
ENST00000584601.1:c.2480A>G
ENSP00000462438.1:p.Asn827Ser

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5, Illumina_ImmunoChip

Variation displays