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- SNP ID:
- rs144655586
- Gene
-
C1orf216CLSPN - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 35725381 - 35725381 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
AAGCCAAATCCAAGGTCCCAAGGCT[C/T]TTGATCATCCAGTGCCCACAACAGA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
|
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Phenotype: |
MIM: 605434
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Literature Links: |
C1orf216 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
|
| C1orf216 - chromosome 1 open reading frame 216 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| CLSPN - claspin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001190481.1 | Intron | NP_001177410.1 | ||||
| NM_022111.3 | Intron | NP_071394.2 | ||||
| XM_011541938.2 | Intron | XP_011540240.1 | ||||
| XM_011541939.2 | Intron | XP_011540241.1 | ||||
| XM_011541940.2 | Intron | XP_011540242.1 | ||||
| XM_011541941.2 | Intron | XP_011540243.1 | ||||
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