Product Details

SNP ID

hCV328440

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.1:22119056 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCACAGCCCTTTCCTCCCTCCCTCT[A/C]GCAGGTGTGTGTGTGTGTGTTTTCC

Phenotype

MIM: 603490

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

WNT4 PubMed Links

Gene Details

Gene

WNT4

Gene Name

Wnt family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030761.4	2154	UTR 3			NP_110388.2

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