Product Details
- SNP ID
-
rs111903589
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:35057142 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTAGCCATACAGGTCATCATCATTG[C/T]CTTCTGTGTATACACTGCCACCTGT
- Phenotype
-
MIM: 601023
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
VCP
PubMed Links
Gene Details
- Gene
- VCP
- Gene Name
- valosin containing protein
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_007126.3 |
2785 |
Missense Mutation |
GAC,GGC |
D799G |
NP_009057.1 |
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