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GGAAGGCCCGGTGGAGCAGCACAGC[C/T]GCGTGCTCTGTGGGGGAAACGGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611345 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INTS1 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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INTS1 - integrator complex subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080453.2 | 6719 | Silent Mutation | GCA,GCG | A,A 2155 | NP_001073922.2 | |
XM_011515260.1 | 6719 | Silent Mutation | GCA,GCG | A,A 2165 | XP_011513562.1 | |
XM_011515262.2 | 6719 | Intron | XP_011513564.1 | |||
XM_017011959.1 | 6719 | Silent Mutation | GCA,GCG | A,A 2216 | XP_016867448.1 | |
XM_017011960.1 | 6719 | Silent Mutation | GCA,GCG | A,A 2206 | XP_016867449.1 |