Product Details

SNP ID

rs142010266

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:227921640 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCCGGCTCTGTGTGTTATGGCCGC[A/G]GCCACAGCAGATGCTCTCGCAGTTC

Phenotype

MIM: 602863

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WNT9A PubMed Links

Gene Details

Gene

WNT9A

Gene Name

Wnt family member 9A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003395.2	1547	Missense Mutation	CGC,TGC	R326C	NP_003386.1
XM_011544271.2	1547	Missense Mutation	CGC,TGC	R256C	XP_011542573.1

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