Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCCTCCAGGCCCAGAACGGAGCC[G/T]CCTTGGCCTCGGGGTCTCCCTACAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607183 | ||||||||||||||||||||
Literature Links: |
SEC24A 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 |
SEC24A - SEC24 homolog A, COPII coat complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252231.1 | 359 | Missense Mutation | GCC,TCC | A,S 23 | NP_001239160.1 | |
NM_021982.2 | 359 | Missense Mutation | GCC,TCC | A,S 23 | NP_068817.1 | |
XM_006714523.2 | 359 | Missense Mutation | GCC,TCC | A,S 23 | XP_006714586.1 | |
XM_017008961.1 | 359 | Intron | XP_016864450.1 | |||
XM_017008962.1 | 359 | Intron | XP_016864451.1 | |||
XM_017008963.1 | 359 | Missense Mutation | GCC,TCC | A,S 23 | XP_016864452.1 |