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TTGGGCTTCCTGTCCTTTTAGTACA[A/C]CTGACTCACTCTTCTTTACTTGGGA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C6orf10 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)
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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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C6orf10 - chromosome 6 open reading frame 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286474.1 | 1642 | Missense Mutation | GAT,GCT | D,A 477 | NP_001273403.1 | |
NM_001286475.1 | 1642 | Missense Mutation | GAT,GCT | D,A 463 | NP_001273404.1 | |
NM_006781.4 | 1642 | Missense Mutation | GAT,GCT | D,A 479 | NP_006772.3 | |
XM_017010182.1 | 1642 | Missense Mutation | XP_016865671.1 | |||
XM_017010183.1 | 1642 | Intron | XP_016865672.1 | |||
XM_017010184.1 | 1642 | Intron | XP_016865673.1 | |||
XM_017010185.1 | 1642 | Missense Mutation | XP_016865674.1 |
LOC101929163 - uncharacterized LOC101929163 | ||||||
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There are no transcripts associated with this gene. |