Product Details

SNP ID

rs112452625

Assay Type

Functionally tested

NCBI dbSNP Submissions

8

Location

Chr.1:22120197 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACAGCACAGCAGCTCACAGCCGTC[A/G]ATGGCCTTGGACGTCTTGTTGCATG

Phenotype

MIM: 603490

Polymorphism

A/G, Transition 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	1082	Silent Mutation	ATC,ATT	I303I	NP_110388.2
XM_011541597.2	1082	Silent Mutation	ATC,ATT	I325I	XP_011539899.1
XM_011541598.2	1082	Silent Mutation	ATC,ATT	I248I	XP_011539900.1
XM_011541599.1	1082	Intron			XP_011539901.1

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