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- SNP ID:
- rs184050237
- Gene
-
CDK10SPATA2L - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.16: 89691490 - 89691490 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GGAGATCACGCTGCTGCTCCGCCTG[C/T]GTCATCCGAACATCGTGGAGCTGAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603464
|
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Literature Links: |
CDK10 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| CDK10 - cyclin dependent kinase 10 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001098533.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | NP_001092003.2 | |
| NM_001160367.1 | 254 | Missense Mutation | CGT,TGT | R,C 23 | NP_001153839.1 | |
| NM_052987.3 | 254 | Missense Mutation | CGT,TGT | R,C 23 | NP_443713.2 | |
| NM_052988.4 | 254 | Missense Mutation | CGT,TGT | R,C 94 | NP_443714.3 | |
| XM_006721308.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_006721371.1 | |
| XM_006721310.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_006721373.1 | |
| XM_011523405.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_011521707.1 | |
| XM_011523406.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_011521708.1 | |
| XM_011523407.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_011521709.1 | |
| XM_011523408.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_011521710.1 | |
| XM_011523410.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521712.1 | |
| XM_011523411.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521713.1 | |
| XM_011523412.1 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521714.1 | |
| XM_011523413.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521715.1 | |
| XM_011523414.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521716.1 | |
| XM_011523415.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521717.1 | |
| XM_011523416.2 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_011521718.1 | |
| XM_011523417.2 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_011521719.1 | |
| XM_017023806.1 | 254 | Missense Mutation | CGT,TGT | R,C 57 | XP_016879295.1 | |
| XM_017023807.1 | 254 | Missense Mutation | CGT,TGT | R,C 94 | XP_016879296.1 | |
| XM_017023808.1 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_016879297.1 | |
| XM_017023809.1 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_016879298.1 | |
| XM_017023810.1 | 254 | Missense Mutation | CGT,TGT | R,C 23 | XP_016879299.1 | |
| SPATA2L - spermatogenesis associated 2 like | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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