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CTTTTGGAAAGAATCTAAGGTGTGT[A/G]ATCTAATAGGCTGGATCTACCAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604613 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBX18 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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TBX18 - T-box 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080508.2 | Intron | NP_001073977.1 | ||||
XM_006715602.3 | Intron | XP_006715665.2 | ||||
XM_011536247.2 | Intron | XP_011534549.2 | ||||
XM_011536248.2 | Intron | XP_011534550.2 | ||||
XM_011536249.2 | Intron | XP_011534551.2 | ||||
XM_017011472.1 | Intron | XP_016866961.1 | ||||
XM_017011473.1 | Intron | XP_016866962.1 |