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GTGAACACCAGGCCGTGCTGCAAAG[C/T]CTGTCCCAGACCATTGAGTGTCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609577 MIM: 611822 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CUL7 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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CUL7 - cullin 7 | ||||||
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There are no transcripts associated with this gene. |
KLC4 - kinesin light chain 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289034.1 | 255 | Silent Mutation | AGC,AGT | S,S 46 | NP_001275963.1 | |
NM_001289035.1 | 255 | Silent Mutation | AGC,AGT | S,S 46 | NP_001275964.1 | |
NM_138343.3 | 255 | Silent Mutation | AGC,AGT | S,S 46 | NP_612352.1 | |
NM_201521.2 | 255 | Silent Mutation | AGC,AGT | S,S 46 | NP_958929.1 | |
NM_201522.2 | 255 | Silent Mutation | AGC,AGT | S,S 46 | NP_958930.1 | |
NM_201523.2 | 255 | Silent Mutation | AGC,AGT | S,S 64 | NP_958931.1 | |
XM_011514989.1 | 255 | Silent Mutation | AGC,AGT | S,S 64 | XP_011513291.1 | |
XM_017011457.1 | 255 | Silent Mutation | AGC,AGT | S,S 46 | XP_016866946.1 |
MRPL2 - mitochondrial ribosomal protein L2 | ||||||
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There are no transcripts associated with this gene. |