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TCCCCAACATGGCGGCTCCCCAAGA[C/T]GTCCACGTCCGGATCTGTAACCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603291 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BNIP1 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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BNIP1 - BCL2 interacting protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001205.2 | 122 | Silent Mutation | GAC,GAT | D,D 6 | NP_001196.2 | |
NM_013978.2 | 122 | Silent Mutation | GAC,GAT | D,D 6 | NP_053581.2 | |
NM_013979.2 | 122 | Silent Mutation | GAC,GAT | D,D 6 | NP_053582.2 | |
NM_013980.2 | 122 | Silent Mutation | GAC,GAT | D,D 6 | NP_053583.2 | |
XM_011534638.1 | 122 | Missense Mutation | GAC,GAT | D,D 6 | XP_011532940.1 | |
XM_011534639.1 | 122 | Missense Mutation | GAC,GAT | D,D 6 | XP_011532941.1 |
CREBRF - CREB3 regulatory factor | ||||||
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There are no transcripts associated with this gene. |