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TGTGTTGCAGTATGAGATGTACACC[A/G]TCGAGCGGAATGCAGAGCGGACCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611353 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INTS10 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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INTS10 - integrator complex subunit 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018142.2 | 99 | Missense Mutation | ATC,GTC | I,V 49 | NP_060612.2 | |
XM_005273555.3 | 99 | Missense Mutation | ATC,GTC | I,V 49 | XP_005273612.1 | |
XM_005273556.3 | 99 | Missense Mutation | ATC,GTC | I,V 49 | XP_005273613.1 | |
XM_005273557.3 | 99 | Missense Mutation | ATC,GTC | I,V 49 | XP_005273614.1 | |
XM_006716355.2 | 99 | UTR 5 | XP_006716418.1 | |||
XM_017013606.1 | 99 | Missense Mutation | ATC,GTC | I,V 49 | XP_016869095.1 | |
XM_017013607.1 | 99 | Missense Mutation | ATC,GTC | I,V 49 | XP_016869096.1 | |
XM_017013608.1 | 99 | UTR 5 | XP_016869097.1 | |||
XM_017013609.1 | 99 | UTR 5 | XP_016869098.1 |