Product Details
- SNP ID
-
rs143350900
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:46769869 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGCGCATCCGCGAACTCCCTGGACA[A/C]TAACACGCCGAAGTCAGCGTCCTCG
- Phenotype
-
MIM: 165330
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
WNT3
PubMed Links
Gene Details
- Gene
- WNT3
- Gene Name
- Wnt family member 3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_030753.4 |
665 |
Missense Mutation |
GTG,TTG |
V168L |
NP_110380.1 |
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