Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGAGGGGGCTTCCCTCTCTTGCTC[C/G]CGAATAAGGAGCCCAGGAGGGAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610166 | ||||||||||||||||||||
Literature Links: |
IQSEC1 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 |
IQSEC1 - IQ motif and Sec7 domain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134382.2 | 3362 | Missense Mutation | GCG,GGG | A,G 974 | NP_001127854.1 | |
NM_014869.6 | 3362 | Intron | NP_055684.3 | |||
XM_011534304.2 | 3362 | Missense Mutation | GCG,GGG | A,G 1082 | XP_011532606.1 | |
XM_011534305.2 | 3362 | Missense Mutation | GCG,GGG | A,G 992 | XP_011532607.1 | |
XM_011534306.2 | 3362 | Missense Mutation | GCG,GGG | A,G 989 | XP_011532608.1 | |
XM_011534307.2 | 3362 | Missense Mutation | GCG,GGG | A,G 989 | XP_011532609.1 | |
XM_011534308.2 | 3362 | Missense Mutation | GCG,GGG | A,G 988 | XP_011532610.1 | |
XM_011534310.2 | 3362 | UTR 3 | XP_011532612.1 | |||
XM_011534311.2 | 3362 | Missense Mutation | GCG,GGG | A,G 866 | XP_011532613.1 | |
XM_011534312.2 | 3362 | Missense Mutation | GCG,GGG | A,G 866 | XP_011532614.1 | |
XM_011534313.2 | 3362 | Missense Mutation | GCG,GGG | A,G 866 | XP_011532615.1 | |
XM_011534314.2 | 3362 | Missense Mutation | GCG,GGG | A,G 866 | XP_011532616.1 | |
XM_011534315.2 | 3362 | UTR 3 | XP_011532617.1 | |||
XM_017007581.1 | 3362 | Missense Mutation | GCG,GGG | A,G 1072 | XP_016863070.1 | |
XM_017007582.1 | 3362 | Missense Mutation | GCG,GGG | A,G 1067 | XP_016863071.1 |