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SNP ID

rs200151492

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:48981281 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGATGTGCTGCGCGACCGCTTCGAC[C/G]GCGCCTCGCGCGTCCTGTACGGCAA

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	952	Missense Mutation	CGC,GGC	R252G	NP_005421.1

Gene

WNT10B

Gene Name

Wnt family member 10B

There are no transcripts associated with this gene.

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