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GGAGGAGATAAACTACTCACTGTCA[A/G]TGTCCTCGATGAGGCTGGCGGTGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603884 MIM: 607281 | ||||||||||||||||||||
Literature Links: |
BAG4 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 |
BAG4 - BCL2 associated athanogene 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204878.1 | 451 | Intron | NP_001191807.1 | |||
NM_004874.3 | 451 | Intron | NP_004865.1 |
LSM1 - LSM1 homolog, mRNA degradation associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014462.2 | 451 | Missense Mutation | ACT,ATT | T,I 14 | NP_055277.1 |