Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 124089 MIM: 609358 MIM: 613232 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
COX6B1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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COX6B1 - cytochrome c oxidase subunit 6B1 | ||||||
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There are no transcripts associated with this gene. |
ETV2 - ETS variant 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300974.1 | 1196 | UTR 5 | NP_001287903.1 | |||
NM_001304549.1 | 1196 | Intron | NP_001291478.1 | |||
NM_014209.3 | 1196 | Missense Mutation | AAC,GAC | N,D 90 | NP_055024.2 | |
XM_005258652.2 | 1196 | Missense Mutation | AAC,GAC | N,D 118 | XP_005258709.1 | |
XM_011526624.2 | 1196 | UTR 5 | XP_011524926.1 | |||
XM_017026472.1 | 1196 | Missense Mutation | AAC,GAC | N,D 91 | XP_016881961.1 |
RBM42 - RNA binding motif protein 42 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |