Product Details
- SNP ID
-
rs147980923
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:132683264 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCATACAACCTCCCAAACAGAGTT[A/G]CTGTTAAGACAGGTCCGGATGTTGG
- Phenotype
-
MIM: 603570
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
VNN1
PubMed Links
Gene Details
- Gene
- VNN1
- Gene Name
- vanin 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004666.2 |
1438 |
Missense Mutation |
GCA,GTA |
A473V |
NP_004657.2 |
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