Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGTGGTGGATAATACTCCTCTCC[A/G]CTCACTTGTCTTATACAATGGAGCA
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 | 6444 | Missense Mutation | CGG,TGG | R,W 3983 | NP_061720.2 | |
XM_011511487.2 | 6444 | Missense Mutation | CGG,TGG | R,W 3983 | XP_011509789.1 | |
XM_011511488.2 | 6444 | Missense Mutation | CGG,TGG | R,W 3943 | XP_011509790.1 | |
XM_011511489.2 | 6444 | Missense Mutation | CGG,TGG | R,W 3937 | XP_011509791.1 | |
XM_011511490.2 | 6444 | Missense Mutation | CGG,TGG | R,W 3908 | XP_011509792.1 | |
XM_011511491.2 | 6444 | Intron | XP_011509793.1 | |||
XM_011511492.2 | 6444 | Intron | XP_011509794.1 | |||
XM_011511493.2 | 6444 | Intron | XP_011509795.1 | |||
XM_011511494.2 | 6444 | Intron | XP_011509796.1 | |||
XM_011511495.2 | 6444 | Intron | XP_011509797.1 | |||
XM_011511497.2 | 6444 | Missense Mutation | CGG,TGG | R,W 2107 | XP_011509799.1 | |
XM_017004504.1 | 6444 | Missense Mutation | CGG,TGG | R,W 3892 | XP_016859993.1 |
SLC39A10 - solute carrier family 39 member 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127257.1 | 6444 | Intron | NP_001120729.1 | |||
NM_020342.2 | 6444 | Intron | NP_065075.1 | |||
XM_005246689.4 | 6444 | Intron | XP_005246746.2 | |||
XM_011511504.2 | 6444 | Intron | XP_011509806.1 | |||
XM_011511505.2 | 6444 | Intron | XP_011509807.1 | |||
XM_011511506.2 | 6444 | Intron | XP_011509808.1 | |||
XM_011511507.2 | 6444 | Intron | XP_011509809.1 | |||
XM_017004522.1 | 6444 | Intron | XP_016860011.1 | |||
XM_017004523.1 | 6444 | Intron | XP_016860012.1 |