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- SNP ID:
- rs76953457
- Gene
-
CLASRP - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 45057756 - 45057756 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
ACCAGCTCCCCTTTCTCAGGCTGGC[A/G]GAGAAGAAGGCTTCCATCGGTTATA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
CLASRP 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
|
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AMR
|
| CLASRP - CLK4 associating serine/arginine rich protein | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001278439.1 | 569 | Silent Mutation | GCA,GCG | A,A 95 | NP_001265368.1 | |
| NM_007056.2 | 569 | Silent Mutation | GCA,GCG | A,A 157 | NP_008987.2 | |
| XM_011526396.2 | 569 | Silent Mutation | GCA,GCG | A,A 157 | XP_011524698.1 | |
| XM_011526397.2 | 569 | UTR 5 | XP_011524699.1 | |||
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