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AAAATATTGTGAAATAGTGCCTTTC[C/T]GCCCTTCAGGTTCACTTCGCGAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602776 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
REV3L 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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REV3L - REV3 like, DNA directed polymerase zeta catalytic subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286431.1 | 9716 | Missense Mutation | CAG,CGG | Q,R 2951 | NP_001273360.1 | |
NM_001286432.1 | 9716 | Missense Mutation | CAG,CGG | Q,R 2951 | NP_001273361.1 | |
NM_002912.4 | 9716 | Missense Mutation | CAG,CGG | Q,R 3029 | NP_002903.3 | |
XM_011536028.1 | 9716 | Missense Mutation | CAG,CGG | Q,R 3056 | XP_011534330.1 | |
XM_011536029.2 | 9716 | Missense Mutation | CAG,CGG | Q,R 3055 | XP_011534331.1 | |
XM_011536030.2 | 9716 | Missense Mutation | CAG,CGG | Q,R 3030 | XP_011534332.1 | |
XM_011536031.2 | 9716 | Missense Mutation | CAG,CGG | Q,R 2978 | XP_011534333.1 | |
XM_011536032.2 | 9716 | Missense Mutation | CAG,CGG | Q,R 2978 | XP_011534334.1 | |
XM_011536036.2 | 9716 | Intron | XP_011534338.1 | |||
XM_017011152.1 | 9716 | Missense Mutation | CAG,CGG | Q,R 2977 | XP_016866641.1 | |
XM_017011153.1 | 9716 | Missense Mutation | CAG,CGG | Q,R 2977 | XP_016866642.1 | |
XM_017011154.1 | 9716 | Missense Mutation | CAG,CGG | Q,R 2977 | XP_016866643.1 | |
XM_017011155.1 | 9716 | Intron | XP_016866644.1 |