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TGAACATGGACATGAGCATGGACAT[C/T]ATAAAATGGAACTTCCAGATTATAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603839 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM126B 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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FAM126B - family with sequence similarity 126 member B | ||||||
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There are no transcripts associated with this gene. |
NDUFB3 - NADH:ubiquinone oxidoreductase subunit B3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257102.1 | 357 | Missense Mutation | CAT,TAT | H,Y 12 | NP_001244031.1 | |
NM_002491.2 | 357 | Missense Mutation | CAT,TAT | H,Y 12 | NP_002482.1 | |
XM_011511230.2 | 357 | Intron | XP_011509532.1 | |||
XM_017004186.1 | 357 | Missense Mutation | CAT,TAT | H,Y 12 | XP_016859675.1 |