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- SNP ID:
- rs796151455
- Gene
-
BCL2L14 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 12072471 - 12072471 on Build GRCh38
- Polymorphism:
- T/G, Transversion substitution
- Context Sequence [VIC/FAM]:
GACCAAGAAAAGAACCTCTGTAGCC[T/G]TGCTTCTGAGAGTGCAGGTTTGTTA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606126
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Literature Links: |
BCL2L14 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 |
| BCL2L14 - BCL2 like 14 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_030766.1 | 610 | Intron | NP_110393.1 | |||
| NM_138722.1 | 610 | Intron | NP_620048.1 | |||
| NM_138723.1 | 610 | Intron | NP_620049.1 | |||
| XM_006719151.3 | 610 | UTR 5 | XP_006719214.1 | |||
| XM_011520848.1 | 610 | UTR 5 | XP_011519150.1 | |||
| XM_011520849.1 | 610 | Intron | XP_011519151.1 | |||
| XM_017019963.1 | 610 | Intron | XP_016875452.1 | |||
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