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- SNP ID:
- rs142609038
- Gene
-
TBX3 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 114671868 - 114671868 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
ACGGGGACGCGCTGCGGGACCTGTC[A/C]GGCTTGGCTTCCAAGCCGCTAACCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601621
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Literature Links: |
TBX3 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
|
| TBX3 - T-box 3 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_005996.3 | 3109 | Silent Mutation | CCG,CCT | P,P 715 | NP_005987.3 | |
| NM_016569.3 | 3109 | Silent Mutation | CCG,CCT | P,P 735 | NP_057653.3 | |
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