Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGCCCATGGACGCCTCTGAGGAGC[C/T]GCTGCCGCCGGTGATCTACACCATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602103 | ||||||||||||||||||||
Literature Links: |
TRAPPC10 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 |
TRAPPC10 - trafficking protein particle complex 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003274.4 | 182 | Missense Mutation | CCG,CTG | P,L 7 | NP_003265.3 | |
XM_005261168.4 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_005261225.1 | |
XM_011529714.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528016.1 | |
XM_011529715.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528017.1 | |
XM_011529716.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528018.1 | |
XM_011529717.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528019.1 | |
XM_011529718.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528020.1 | |
XM_011529719.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528021.1 | |
XM_011529720.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528022.1 | |
XM_011529721.2 | 182 | Intron | XP_011528023.1 | |||
XM_011529722.2 | 182 | Intron | XP_011528024.1 | |||
XM_011529723.2 | 182 | Intron | XP_011528025.1 | |||
XM_011529725.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528027.1 | |
XM_011529726.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528028.1 | |
XM_011529727.2 | 182 | Intron | XP_011528029.1 | |||
XM_011529728.2 | 182 | Intron | XP_011528030.1 | |||
XM_011529729.2 | 182 | Intron | XP_011528031.1 | |||
XM_011529730.2 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_011528032.1 | |
XM_017028454.1 | 182 | Missense Mutation | CCG,CTG | P,L 7 | XP_016883943.1 | |
XM_017028455.1 | 182 | Intron | XP_016883944.1 |