Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCGTGCCAGCTGTGTGTCCCGGT[C/T]GCTAAGGATAGGGCAAAAGGGCACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DCAKD 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 |
DCAKD - dephospho-CoA kinase domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128631.2 | 762 | Missense Mutation | NP_001122103.1 | |||
NM_001288654.2 | 762 | Missense Mutation | NP_001275583.1 | |||
NM_001288655.1 | 762 | Missense Mutation | NP_001275584.1 | |||
NM_001321326.1 | 762 | Missense Mutation | NP_001308255.1 | |||
NM_024819.6 | 762 | Missense Mutation | NP_079095.3 | |||
XM_005257688.2 | 762 | Intron | XP_005257745.1 | |||
XM_011525262.2 | 762 | Missense Mutation | XP_011523564.1 | |||
XM_017025102.1 | 762 | Intron | XP_016880591.1 | |||
XM_017025103.1 | 762 | Intron | XP_016880592.1 | |||
XM_017025104.1 | 762 | Intron | XP_016880593.1 | |||
XM_017025105.1 | 762 | Missense Mutation | XP_016880594.1 | |||
XM_017025106.1 | 762 | Missense Mutation | XP_016880595.1 |