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CCTCCAGCTCCTTGAGAGAGCCAGA[A/G]TTGAGAAGAAAATGAGCCTGAAGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611352 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INTS9 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
|
INTS9 - integrator complex subunit 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145159.2 | 2265 | UTR 3 | NP_001138631.1 | |||
NM_001172562.1 | 2265 | UTR 3 | NP_001166033.1 | |||
NM_018250.3 | 2265 | UTR 3 | NP_060720.2 | |||
XM_006716356.2 | 2265 | UTR 3 | XP_006716419.1 | |||
XM_006716357.3 | 2265 | Intron | XP_006716420.1 | |||
XM_011544573.1 | 2265 | UTR 3 | XP_011542875.1 | |||
XM_011544574.1 | 2265 | UTR 3 | XP_011542876.1 | |||
XM_011544575.2 | 2265 | UTR 3 | XP_011542877.1 | |||
XM_011544576.1 | 2265 | UTR 3 | XP_011542878.1 |