Product Details
- SNP ID
-
rs10064232
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:40910263 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AAAGATAAGACCAAAGATAGAAATC[A/G]CTATCATAGACTAAATCTCTGGAAT
- Phenotype
-
MIM: 217070
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C7
PubMed Links
Gene Details
- Gene
- C7
- Gene Name
- complement component 7
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_000587.2 |
|
Intron |
|
|
NP_000578.2 |
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