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CCCGCTACTTCCAGAGCCGGGGCCC[A/G]CGGCAGGAGGCTGCCCTCAAGACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613198 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COX6B2 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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COX6B2 - cytochrome c oxidase subunit 6B2 | ||||||
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There are no transcripts associated with this gene. |
KMT5C - lysine methyltransferase 5C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032701.3 | 497 | Silent Mutation | CCA,CCG | P,P 83 | NP_116090.2 | |
XM_005259338.3 | 497 | Intron | XP_005259395.1 | |||
XM_006723442.3 | 497 | Intron | XP_006723505.1 | |||
XM_011527415.2 | 497 | Silent Mutation | CCA,CCG | P,P 83 | XP_011525717.1 | |
XM_017027388.1 | 497 | UTR 5 | XP_016882877.1 |
TMEM150B - transmembrane protein 150B | ||||||
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There are no transcripts associated with this gene. |