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ACCTTTCTCATTCACGGCTCGCGGC[A/G]CTTTAGCTACTCAGAGGCGGAGCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 611347 MIM: 604193 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INTS3 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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INTS3 - integrator complex subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324475.1 | 475 | Intron | NP_001311404.1 | |||
NM_023015.4 | 475 | Intron | NP_075391.3 | |||
XM_005245459.2 | 475 | Intron | XP_005245516.1 | |||
XM_005245461.2 | 475 | Intron | XP_005245518.1 | |||
XM_006711490.3 | 475 | Intron | XP_006711553.1 | |||
XM_011509906.2 | 475 | Intron | XP_011508208.1 | |||
XM_017002132.1 | 475 | Intron | XP_016857621.1 |
SLC27A3 - solute carrier family 27 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317929.1 | 475 | Missense Mutation | CAC,CGC | H,R 137 | NP_001304858.1 | |
NM_024330.1 | 475 | Missense Mutation | CAC,CGC | H,R 137 | NP_077306.1 |