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GCAGGTGGAAGAGGGGGTAGGAGGC[A/C]GTGCGCCTCCAGCATCCTCGCCCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609667 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TAGAP 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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TAGAP - T-cell activation RhoGTPase activating protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278733.1 | 2226 | Missense Mutation | GGC,TGC | G,C 569 | NP_001265662.1 | |
NM_054114.4 | 2226 | Missense Mutation | GGC,TGC | G,C 632 | NP_473455.2 | |
NM_138810.3 | 2226 | Intron | NP_620165.1 | |||
NM_152133.2 | 2226 | Missense Mutation | GGC,TGC | G,C 454 | NP_687034.1 |