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AGGGACGGAAGTAGGCGGGCTCAGG[C/T]CTGCGCCTCCAGGGCACACACGTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611966 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRAPPC9 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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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TRAPPC9 - trafficking protein particle complex 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160372.3 | 3724 | Missense Mutation | ACC,GCC | T,A 1148 | NP_001153844.1 | |
NM_001321646.1 | 3724 | Missense Mutation | ACC,GCC | T,A 1139 | NP_001308575.1 | |
NM_031466.7 | 3724 | Missense Mutation | ACC,GCC | T,A 1246 | NP_113654.4 | |
XM_011517326.2 | 3724 | Missense Mutation | ACC,GCC | T,A 1237 | XP_011515628.1 | |
XM_011517328.2 | 3724 | Intron | XP_011515630.1 | |||
XM_011517330.2 | 3724 | Missense Mutation | ACC,GCC | T,A 631 | XP_011515632.1 | |
XM_017013893.1 | 3724 | Intron | XP_016869382.1 | |||
XM_017013894.1 | 3724 | Missense Mutation | ACC,GCC | T,A 688 | XP_016869383.1 |