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ACAAAGCACTTGTCCAATAACTGCC[A/G]GTGTATAACTCTGGTAAAGCTGGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610061 MIM: 608733 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAH7 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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DNAH7 - dynein axonemal heavy chain 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018897.2 | Intron | NP_061720.2 | ||||
XM_011511487.2 | Intron | XP_011509789.1 | ||||
XM_011511488.2 | Intron | XP_011509790.1 | ||||
XM_011511489.2 | Intron | XP_011509791.1 | ||||
XM_011511490.2 | Intron | XP_011509792.1 | ||||
XM_011511491.2 | Intron | XP_011509793.1 | ||||
XM_011511492.2 | Intron | XP_011509794.1 | ||||
XM_011511493.2 | Intron | XP_011509795.1 | ||||
XM_011511494.2 | Intron | XP_011509796.1 | ||||
XM_011511495.2 | Intron | XP_011509797.1 | ||||
XM_011511497.2 | Intron | XP_011509799.1 | ||||
XM_017004504.1 | Intron | XP_016859993.1 |
SLC39A10 - solute carrier family 39 member 10 | ||||||
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There are no transcripts associated with this gene. |