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- SNP ID:
- rs772880482
- Gene
-
CLPTM1L - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.5: 1335081 - 1335081 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CCGAACTGCTGCAGGGAGTACACGG[C/T]GTCCTGCATGTGGATCCAGAAGCGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612585
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Literature Links: |
CLPTM1L 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 |
| CLPTM1L - CLPTM1 like | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_030782.4 | 965 | Missense Mutation | ACC,GCC | T,A 258 | NP_110409.2 | |
| XM_011514144.2 | 965 | Missense Mutation | ACC,GCC | T,A 257 | XP_011512446.1 | |
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