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- SNP ID:
- rs78922224
- Gene
-
BCL2L14 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 12088758 - 12088758 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
AAGAACAAGGTGAAGGTTCTCCCTC[C/G]AAAGGTATCCGTGTCTCCCAACCCC
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
|
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
|
| BCL2L14 - BCL2 like 14 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_030766.1 | Intron | NP_110393.1 | ||||
| NM_138722.1 | Intron | NP_620048.1 | ||||
| NM_138723.1 | Intron | NP_620049.1 | ||||
| XM_006719151.3 | Intron | XP_006719214.1 | ||||
| XM_011520848.1 | Intron | XP_011519150.1 | ||||
| XM_011520849.1 | Intron | XP_011519151.1 | ||||
| XM_017019963.1 | Intron | XP_016875452.1 | ||||
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