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AAAATCTGCCTTACCCTTTTAACAA[A/G]GGTCAAGAGTAAATTTTTCCTTAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606126 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BCL2L14 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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BCL2L14 - BCL2 like 14 | ||||||
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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 |