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- SNP ID:
- rs11965012
- Gene
-
TAB2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.6: 149219867 - 149219867 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
CAAGCAATTCTCAATTTTTTTCAAT[G/T]TCAGGACCTCTTTACGCTCTTAAAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605101
|
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Literature Links: |
TAB2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| TAB2 - TGF-beta activated kinase 1/MAP3K7 binding protein 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001292034.2 | Intron | NP_001278963.1 | ||||
| NM_001292035.2 | Intron | NP_001278964.1 | ||||
| NM_015093.5 | Intron | NP_055908.1 | ||||
| XM_011535633.2 | Intron | XP_011533935.1 | ||||
| XM_017010591.1 | Intron | XP_016866080.1 | ||||
| XM_017010592.1 | Intron | XP_016866081.1 | ||||
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