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TTGCAGCTCAATATGGTCATTATTC[C/T]ACAGCAGAAGTACTCCTTCGAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
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Literature Links: |
GABPB2 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 |
GABPB2 - GA binding protein transcription factor beta subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323906.1 | 487 | Silent Mutation | TCC,TCT | S,S 52 | NP_001310835.1 | |
NM_001323907.1 | 487 | Intron | NP_001310836.1 | |||
NM_001323908.1 | 487 | Silent Mutation | TCC,TCT | S,S 52 | NP_001310837.1 | |
NM_001323909.1 | 487 | Silent Mutation | TCC,TCT | S,S 52 | NP_001310838.1 | |
NM_001323910.1 | 487 | Silent Mutation | TCC,TCT | S,S 68 | NP_001310839.1 | |
NM_001323911.1 | 487 | Silent Mutation | TCC,TCT | S,S 52 | NP_001310840.1 | |
NM_001323912.1 | 487 | Intron | NP_001310841.1 | |||
NM_001323913.1 | 487 | Intron | NP_001310842.1 | |||
NM_144618.2 | 487 | Silent Mutation | TCC,TCT | S,S 52 | NP_653219.1 | |
XM_017000246.1 | 487 | Silent Mutation | TCC,TCT | S,S 68 | XP_016855735.1 | |
XM_017000247.1 | 487 | Silent Mutation | TCC,TCT | S,S 68 | XP_016855736.1 | |
XM_017000248.1 | 487 | Silent Mutation | TCC,TCT | S,S 64 | XP_016855737.1 | |
XM_017000249.1 | 487 | Silent Mutation | TCC,TCT | S,S 52 | XP_016855738.1 | |
XM_017000250.1 | 487 | Silent Mutation | TCC,TCT | S,S 68 | XP_016855739.1 | |
XM_017000251.1 | 487 | Silent Mutation | TCC,TCT | S,S 64 | XP_016855740.1 | |
XM_017000252.1 | 487 | Intron | XP_016855741.1 | |||
XM_017000253.1 | 487 | Silent Mutation | TCC,TCT | S,S 68 | XP_016855742.1 | |
XM_017000254.1 | 487 | Intron | XP_016855743.1 |