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SNP ID

rs144907447

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:48979535 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCAAGAGTCTGCAACTGGTACTC[C/G]AGCCCAGTCTGCAGCTGTTGAGCCG

Phenotype

MIM: 164820 MIM: 601906

Polymorphism

C/G, Transversion 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	370	Missense Mutation	CAG,GAG	Q58E	NP_005421.1

Gene

WNT10B

Gene Name

Wnt family member 10B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003394.3	370	Intron			NP_003385.2

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