Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCCGCCGACCCGGAAGGTCCCGAG[G/T]GGGGCTGCAGCCTGGCCTGGCGCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
INTS3 - integrator complex subunit 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324475.1 | 393 | Intron | NP_001311404.1 | |||
NM_023015.4 | 393 | Intron | NP_075391.3 | |||
XM_005245459.2 | 393 | Intron | XP_005245516.1 | |||
XM_005245461.2 | 393 | Intron | XP_005245518.1 | |||
XM_006711490.3 | 393 | Intron | XP_006711553.1 | |||
XM_011509906.2 | 393 | Intron | XP_011508208.1 | |||
XM_017002132.1 | 393 | Intron | XP_016857621.1 |
SLC27A3 - solute carrier family 27 member 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317929.1 | 393 | Missense Mutation | GGG,TGG | G,W 110 | NP_001304858.1 | |
NM_024330.1 | 393 | Missense Mutation | GGG,TGG | G,W 110 | NP_077306.1 |