Product Details
- SNP ID
-
rs146567646
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:218423794 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCACTCACCATGACCAAGCTGAGC[A/G]CCCAAGTCAAAGGCTCTCTCAACAT
- Phenotype
-
MIM: 193040
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
VIL1
PubMed Links
Gene Details
- Gene
- VIL1
- Gene Name
- villin 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_007127.2 |
81 |
Missense Mutation |
ACC,GCC |
T6A |
NP_009058.2 |
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