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TGTGACTGGCCACCTTCTTGGCCAG[C/G]AGCAGGGCCAGCACCAGCATGGTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601997 | ||||||||||||||||||||
Literature Links: |
BCL2L13 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 |
BCL2L13 - BCL2 like 13 | ||||||
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There are no transcripts associated with this gene. |
BID - BH3 interacting domain death agonist | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001196.3 | 565 | Silent Mutation | CTC,CTG | L,L 154 | NP_001187.1 | |
NM_001244567.1 | 565 | Silent Mutation | CTC,CTG | L,L 154 | NP_001231496.1 | |
NM_001244569.1 | 565 | Silent Mutation | CTC,CTG | L,L 58 | NP_001231498.1 | |
NM_001244570.1 | 565 | Silent Mutation | CTC,CTG | L,L 58 | NP_001231499.1 | |
NM_001244572.1 | 565 | Silent Mutation | CTC,CTG | L,L 58 | NP_001231501.1 | |
NM_197966.2 | 565 | Silent Mutation | CTC,CTG | L,L 200 | NP_932070.1 | |
NM_197967.2 | 565 | Silent Mutation | CTC,CTG | L,L 58 | NP_932071.1 | |
XM_017028906.1 | 565 | Silent Mutation | CTC,CTG | L,L 154 | XP_016884395.1 |