Search Thermo Fisher Scientific
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CTTTTAAGTTGAAGTTTATACTGTG[C/T]TTGTCCAAGCCATGTGAATGATCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614136 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRAPPC8 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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TRAPPC8 - trafficking protein particle complex 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014939.3 | 4428 | Missense Mutation | NP_055754.2 | |||
XM_005258233.2 | 4428 | Missense Mutation | XP_005258290.1 | |||
XM_005258234.2 | 4428 | Missense Mutation | XP_005258291.1 | |||
XM_005258235.3 | 4428 | Missense Mutation | XP_005258292.1 | |||
XM_006722420.3 | 4428 | Intron | XP_006722483.1 | |||
XM_011525884.2 | 4428 | UTR 3 | XP_011524186.1 | |||
XM_017025615.1 | 4428 | Missense Mutation | XP_016881104.1 | |||
XM_017025616.1 | 4428 | Missense Mutation | XP_016881105.1 | |||
XM_017025617.1 | 4428 | UTR 3 | XP_016881106.1 |