Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAATCTTTACCTTGTTGTTTTATGC[C/T]GAAGATCAACTATGACATCTACATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 614136 | ||||||||||||||||||||
Literature Links: |
TRAPPC8 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
TRAPPC8 - trafficking protein particle complex 8 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014939.3 | 4366 | Missense Mutation | CAG,CGG | Q,R 1353 | NP_055754.2 | |
XM_005258233.2 | 4366 | Missense Mutation | CAG,CGG | Q,R 1354 | XP_005258290.1 | |
XM_005258234.2 | 4366 | Intron | XP_005258291.1 | |||
XM_005258235.3 | 4366 | Missense Mutation | CAG,CGG | Q,R 1079 | XP_005258292.1 | |
XM_006722420.3 | 4366 | Intron | XP_006722483.1 | |||
XM_011525884.2 | 4366 | UTR 3 | XP_011524186.1 | |||
XM_017025615.1 | 4366 | Missense Mutation | CAG,CGG | Q,R 1328 | XP_016881104.1 | |
XM_017025616.1 | 4366 | Intron | XP_016881105.1 | |||
XM_017025617.1 | 4366 | UTR 3 | XP_016881106.1 |