Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611518 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DOCK10 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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DOCK10 - dedicator of cytokinesis 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290263.1 | 6994 | Intron | NP_001277192.1 | |||
NM_014689.2 | 6994 | Intron | NP_055504.2 | |||
XM_005246673.4 | 6994 | Intron | XP_005246730.1 | |||
XM_006712617.3 | 6994 | Intron | XP_006712680.1 | |||
XM_017004441.1 | 6994 | Missense Mutation | AAT,CAT | N,H 2240 | XP_016859930.1 | |
XM_017004442.1 | 6994 | Missense Mutation | AAT,CAT | N,H 2231 | XP_016859931.1 | |
XM_017004443.1 | 6994 | Missense Mutation | AAT,CAT | N,H 2227 | XP_016859932.1 | |
XM_017004444.1 | 6994 | Missense Mutation | AAT,CAT | N,H 2225 | XP_016859933.1 | |
XM_017004445.1 | 6994 | Missense Mutation | AAT,CAT | N,H 2221 | XP_016859934.1 | |
XM_017004446.1 | 6994 | Missense Mutation | AAT,CAT | N,H 2191 | XP_016859935.1 | |
XM_017004447.1 | 6994 | Intron | XP_016859936.1 |
Set Membership: |
HapMap Validated |