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ATTCCAGGCTGCCTTCTGTATACCA[A/G]GACTGGCTCCGCCCCACACCTCACC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC191 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 - 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 |
CCDC191 - coiled-coil domain containing 191 | ||||||
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There are no transcripts associated with this gene. |
QTRT2 - queuine tRNA-ribosyltransferase accessory subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256835.1 | 235 | Missense Mutation | AAG,AGG | K,R 50 | NP_001243764.1 | |
NM_001256836.1 | 235 | Intron | NP_001243765.1 | |||
NM_001256837.1 | 235 | Intron | NP_001243766.1 | |||
NM_024638.3 | 235 | Missense Mutation | AAG,AGG | K,R 38 | NP_078914.1 | |
XM_005247769.3 | 235 | Intron | XP_005247826.1 | |||
XM_005247770.3 | 235 | UTR 5 | XP_005247827.1 | |||
XM_006713744.3 | 235 | Intron | XP_006713807.1 | |||
XM_011513137.2 | 235 | Missense Mutation | AAG,AGG | K,R 50 | XP_011511439.1 | |
XM_017007182.1 | 235 | UTR 5 | XP_016862671.1 | |||
XM_017007183.1 | 235 | Intron | XP_016862672.1 | |||
XM_017007184.1 | 235 | UTR 5 | XP_016862673.1 |