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- SNP ID:
- rs868311537
- Gene
-
RPRD1A - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.18: 36006670 - 36006670 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
CAGCATCACCTGATAAAAAGGGAGT[C/G]CCCCATCCCCCAGCCCAATTATGAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610347
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Literature Links: |
RPRD1A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| RPRD1A - regulation of nuclear pre-mRNA domain containing 1A | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001303411.1 | Intron | NP_001290340.1 | ||||
| NM_001303412.1 | Intron | NP_001290341.1 | ||||
| NM_001303413.1 | Intron | NP_001290342.1 | ||||
| NM_018170.4 | Intron | NP_060640.2 | ||||
| XM_011526048.1 | Intron | XP_011524350.1 | ||||
| XM_011526049.1 | Intron | XP_011524351.1 | ||||
| XM_011526050.1 | Intron | XP_011524352.1 | ||||
| XM_017025808.1 | Intron | XP_016881297.1 | ||||
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