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CCCCACACAGAACCAGAGGGCATAG[C/T]GTGGTGAGCGTCCGCTTCCTTCCGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610837 MIM: 603734 | ||||||||||||||||||||
Literature Links: |
BCL2L12 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 |
BCL2L12 - BCL2 like 12 | ||||||
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There are no transcripts associated with this gene. |
IRF3 - interferon regulatory factor 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197122.1 | 1333 | Silent Mutation | ACA,ACG | T,T 346 | NP_001184051.1 | |
NM_001197123.1 | 1333 | Missense Mutation | CAC,CGC | H,R 306 | NP_001184052.1 | |
NM_001197124.1 | 1333 | Missense Mutation | CAC,CGC | H,R 214 | NP_001184053.1 | |
NM_001197125.1 | 1333 | Missense Mutation | CAC,CGC | H,R 195 | NP_001184054.1 | |
NM_001197126.1 | 1333 | Missense Mutation | CAC,CGC | H,R 195 | NP_001184055.1 | |
NM_001197127.1 | 1333 | Missense Mutation | CAC,CGC | H,R 68 | NP_001184056.1 | |
NM_001197128.1 | 1333 | Missense Mutation | CAC,CGC | H,R 68 | NP_001184057.1 | |
NM_001571.5 | 1333 | Missense Mutation | CAC,CGC | H,R 341 | NP_001562.1 | |
XM_006723197.1 | 1333 | Silent Mutation | ACA,ACG | T,T 346 | XP_006723260.1 | |
XM_006723198.1 | 1333 | Silent Mutation | ACA,ACG | T,T 346 | XP_006723261.1 | |
XM_006723200.1 | 1333 | Silent Mutation | ACA,ACG | T,T 311 | XP_006723263.1 | |
XM_006723201.1 | 1333 | Silent Mutation | ACA,ACG | T,T 200 | XP_006723264.1 | |
XM_006723202.2 | 1333 | Silent Mutation | ACA,ACG | T,T 200 | XP_006723265.1 | |
XM_017026766.1 | 1333 | Missense Mutation | CAC,CGC | H,R 341 | XP_016882255.1 | |
XM_017026767.1 | 1333 | Missense Mutation | CAC,CGC | H,R 341 | XP_016882256.1 |
SCAF1 - SR-related CTD associated factor 1 | ||||||
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There are no transcripts associated with this gene. |