Product Details

SNP ID

rs3820622

Assay Type

Functionally tested

NCBI dbSNP Submissions

38

Location

Chr.1:227919580 on Build GRCh38

Set Membership

JSNP

Context Sequence [VIC/FAM]

CAACCCGCCCAGAACCCAGCCCACA[A/G]CCATCAGGACACCCACAAGACGGAG

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	3607	Intron			NP_003386.1
XM_011544271.2	3607	UTR 3			XP_011542573.1

View Full Product Details