Product Details
- SNP ID
-
rs11559137
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:45207470 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GGACAAAAAGGCAAGCAACAAACTG[A/G]ATCCAAAGGCAGTTTTTCTATTCAA
- Phenotype
-
MIM: 182140
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SEMG1
PubMed Links
Gene Details
- Gene
- SEMG1
- Gene Name
- semenogelin I
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_003007.4 |
263 |
Missense Mutation |
GAA,GGA |
E58G |
NP_002998.1 |
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