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AGGAAGGGATTGACACACTGCACTT[C/T]GCAGAGCTGCTTATGACATCAGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603731 | ||||||||||||||||||||
Literature Links: |
CNOT8 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 |
CNOT8 - CCR4-NOT transcription complex subunit 8 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301073.1 | 255 | Silent Mutation | TTC,TTT | F,F 136 | NP_001288002.1 | |
NM_001301074.1 | 255 | Intron | NP_001288003.1 | |||
NM_001301075.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | NP_001288004.1 | |
NM_001301077.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | NP_001288006.1 | |
NM_001301080.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | NP_001288009.1 | |
NM_001301082.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | NP_001288011.1 | |
NM_001301083.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | NP_001288012.1 | |
NM_001301086.1 | 255 | Intron | NP_001288015.1 | |||
NM_004779.5 | 255 | Silent Mutation | TTC,TTT | F,F 136 | NP_004770.4 | |
XM_005268527.2 | 255 | Intron | XP_005268584.1 | |||
XM_011537706.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | XP_011536008.1 | |
XM_011537708.2 | 255 | Silent Mutation | TTC,TTT | F,F 30 | XP_011536010.1 | |
XM_017010048.1 | 255 | Silent Mutation | TTC,TTT | F,F 136 | XP_016865537.1 | |
XM_017010049.1 | 255 | Silent Mutation | TTC,TTT | F,F 136 | XP_016865538.1 | |
XM_017010050.1 | 255 | Silent Mutation | TTC,TTT | F,F 136 | XP_016865539.1 | |
XM_017010051.1 | 255 | Silent Mutation | TTC,TTT | F,F 136 | XP_016865540.1 | |
XM_017010052.1 | 255 | Intron | XP_016865541.1 | |||
XM_017010053.1 | 255 | Intron | XP_016865542.1 | |||
XM_017010054.1 | 255 | Intron | XP_016865543.1 | |||
XM_017010055.1 | 255 | Intron | XP_016865544.1 | |||
XM_017010056.1 | 255 | Intron | XP_016865545.1 | |||
XM_017010057.1 | 255 | Silent Mutation | TTC,TTT | F,F 30 | XP_016865546.1 | |
XM_017010058.1 | 255 | Intron | XP_016865547.1 |