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TGGGTCCTCTTGCCACGGTGTGGTC[G/T]GTTCTGGGGGCCGCTTTCCCGCCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300403 MIM: 300080 | ||||||||||||||||||||
Literature Links: |
NDUFB11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NDUFB11 - NADH:ubiquinone oxidoreductase subunit B11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135998.2 | 683 | Missense Mutation | CAG,CCG | Q,P 51 | NP_001129470.1 | |
NM_019056.6 | 683 | Missense Mutation | CAG,CCG | Q,P 51 | NP_061929.2 |
RBM10 - RNA binding motif protein 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204466.1 | 683 | Intron | NP_001191395.1 | |||
NM_001204467.1 | 683 | Intron | NP_001191396.1 | |||
NM_001204468.1 | 683 | Intron | NP_001191397.1 | |||
NM_005676.4 | 683 | Intron | NP_005667.2 | |||
NM_152856.2 | 683 | Intron | NP_690595.1 | |||
XM_005272677.4 | 683 | Intron | XP_005272734.1 | |||
XM_005272678.4 | 683 | Intron | XP_005272735.1 | |||
XM_005272679.4 | 683 | Intron | XP_005272736.1 | |||
XM_006724563.1 | 683 | Intron | XP_006724626.1 | |||
XM_011543989.2 | 683 | Intron | XP_011542291.1 | |||
XM_017029884.1 | 683 | Intron | XP_016885373.1 | |||
XM_017029885.1 | 683 | Intron | XP_016885374.1 |