Product Details

SNP ID

rs141597087

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:22120287 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCACAGAAGTCGGGGCTAGGCTC[C/T]AAGTACACCAGGTCCTCATCTGTGT

Phenotype

MIM: 603490

Polymorphism

C/T, 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	992	Silent Mutation	TTA,TTG	L273L	NP_110388.2
XM_011541597.2	992	Silent Mutation	TTA,TTG	L295L	XP_011539899.1
XM_011541598.2	992	Silent Mutation	TTA,TTG	L218L	XP_011539900.1
XM_011541599.1	992	Intron			XP_011539901.1

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