Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTATAGAGGCCTCGGTCATCAACC[A/G]CATTATTATCTCCTTTGGTCAAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SEC11A 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 |
SEC11A - SEC11 homolog A, signal peptidase complex subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271918.1 | 877 | Missense Mutation | GCG,GTG | A,V 93 | NP_001258847.1 | |
NM_001271919.1 | 877 | Intron | NP_001258848.1 | |||
NM_001271920.1 | 877 | Missense Mutation | GCG,GTG | A,V 119 | NP_001258849.1 | |
NM_001271921.1 | 877 | Missense Mutation | GCG,GTG | A,V 69 | NP_001258850.1 | |
NM_001271922.1 | 877 | Missense Mutation | GCG,GTG | A,V 119 | NP_001258851.1 | |
NM_014300.3 | 877 | Missense Mutation | GCG,GTG | A,V 119 | NP_055115.1 |