Product Details

SNP ID

rs77625174

Assay Type

Functionally tested

NCBI dbSNP Submissions

23

Location

Chr.1:227921008 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGACGTGCTAGAAAAGCCTCTCA[G/T]TCCTTGCAGGTGTAGACCCCTCATA

Phenotype

MIM: 602863

Polymorphism

G/T, Transversion 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	2179	Intron			NP_003386.1
XM_011544271.2	2179	UTR 3			XP_011542573.1

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