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CAAGATCGACTCCCTGGACGCCCTC[A/G]TCAAGCTGCAGGTGTTGTCGCTGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DRC3 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 |
DRC3 - dynein regulatory complex subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130090.1 | 780 | Missense Mutation | ATC,GTC | I,V 131 | NP_001123562.1 | |
NM_001130091.1 | 780 | Missense Mutation | ATC,GTC | I,V 131 | NP_001123563.1 | |
NM_001130092.1 | 780 | Missense Mutation | ATC,GTC | I,V 131 | NP_001123564.1 | |
NM_031294.3 | 780 | Missense Mutation | ATC,GTC | I,V 131 | NP_112584.3 | |
XM_006721583.3 | 780 | Missense Mutation | ATC,GTC | I,V 131 | XP_006721646.1 | |
XM_011524018.2 | 780 | Missense Mutation | ATC,GTC | I,V 151 | XP_011522320.1 | |
XM_011524019.2 | 780 | Missense Mutation | ATC,GTC | I,V 151 | XP_011522321.1 | |
XM_011524020.2 | 780 | Missense Mutation | ATC,GTC | I,V 151 | XP_011522322.1 | |
XM_011524021.2 | 780 | Missense Mutation | ATC,GTC | I,V 151 | XP_011522323.1 | |
XM_011524022.2 | 780 | Missense Mutation | ATC,GTC | I,V 151 | XP_011522324.1 | |
XM_011524023.2 | 780 | Missense Mutation | ATC,GTC | I,V 151 | XP_011522325.1 | |
XM_011524025.2 | 780 | Intron | XP_011522327.1 | |||
XM_011524026.2 | 780 | Intron | XP_011522328.1 |