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TCTTCACCCAGTTCTTACCCGCCAG[C/T]TGTGAATAAGGGCAGGAAGGTAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602184 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NDUFV3 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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NDUFV3 - NADH:ubiquinone oxidoreductase subunit V3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001503.1 | 332 | Intron | NP_001001503.1 | |||
NM_021075.3 | 332 | Missense Mutation | GCT,GTT | A,V 89 | NP_066553.3 | |
XM_011529586.2 | 332 | Missense Mutation | GCT,GTT | A,V 89 | XP_011527888.1 | |
XM_017028359.1 | 332 | Intron | XP_016883848.1 |