Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTGGTCTTTAGAATGAGGTGCTCA[C/T]CTGGAATAGGTTTCTTGGTAATTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610257 | ||||||||||||||||||||
Literature Links: |
SEC31A 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 |
SEC31A - SEC31 homolog A, COPII coat complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077206.3 | 3421 | Missense Mutation | GAT,GGT | D,G 1000 | NP_001070674.1 | |
NM_001077207.3 | 3421 | Missense Mutation | GAT,GGT | D,G 1114 | NP_001070675.1 | |
NM_001077208.3 | 3421 | Missense Mutation | GAT,GGT | D,G 1099 | NP_001070676.1 | |
NM_001191049.2 | 3421 | Missense Mutation | GAT,GGT | D,G 1094 | NP_001177978.1 | |
NM_001300744.2 | 3421 | Missense Mutation | GAT,GGT | D,G 961 | NP_001287673.1 | |
NM_001300745.2 | 3421 | Missense Mutation | GAT,GGT | D,G 1060 | NP_001287674.1 | |
NM_001318119.1 | 3421 | Missense Mutation | GAT,GGT | D,G 1099 | NP_001305048.1 | |
NM_001318120.1 | 3421 | Missense Mutation | GAT,GGT | D,G 1114 | NP_001305049.1 | |
NM_016211.4 | 3421 | Missense Mutation | GAT,GGT | D,G 1075 | NP_057295.2 |