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GAAACCATCGATCTTGGCGGAGATG[A/T]GTTTGGATCCGAAGAGAACGAGACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614139 MIM: 608998 | ||||||||||||||||||||
Literature Links: |
TRAPPC12 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 |
TRAPPC12 - trafficking protein particle complex 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321102.1 | 761 | Missense Mutation | GAG,GTG | E,V 42 | NP_001308031.1 | |
NM_016030.5 | 761 | Missense Mutation | GAG,GTG | E,V 42 | NP_057114.5 | |
XM_011510350.2 | 761 | Missense Mutation | GAG,GTG | E,V 42 | XP_011508652.1 | |
XM_011510352.2 | 761 | Missense Mutation | GAG,GTG | E,V 42 | XP_011508654.1 | |
XM_011510353.2 | 761 | Missense Mutation | GAG,GTG | E,V 42 | XP_011508655.1 | |
XM_011510354.2 | 761 | Missense Mutation | GAG,GTG | E,V 42 | XP_011508656.1 | |
XM_011510355.2 | 761 | Intron | XP_011508657.1 | |||
XM_011510356.1 | 761 | Intron | XP_011508658.1 | |||
XM_017004257.1 | 761 | Missense Mutation | GAG,GTG | E,V 42 | XP_016859746.1 |
TSSC1 - tumor suppressing subtransferable candidate 1 | ||||||
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There are no transcripts associated with this gene. |