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SNP ID

rs148154047

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:48981534 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTGCTGCGGCAGGGGCCACCGCA[C/T]GCGCACGCAGCGCGTCACCGAGCGC

Phenotype

MIM: 164820 MIM: 601906

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WNT1 PubMed Links

Gene Details

Gene

WNT1

Gene Name

Wnt family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005430.3	1205	Missense Mutation	ACG,ATG	T336M	NP_005421.1

Gene

WNT10B

Gene Name

Wnt family member 10B

There are no transcripts associated with this gene.

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