Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCTGCGGGGCCGGCGACATGGAT[A/C]CCCTGTTCCAGCAAACGCACAAGTG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604027 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GOSR2 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)
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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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GOSR2 - golgi SNAP receptor complex member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012511.2 | 92 | Missense Mutation | ACC,CCC | T,P 3 | NP_001012529.1 | |
NM_001321133.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | NP_001308062.1 | |
NM_001321134.1 | 92 | UTR 5 | NP_001308063.1 | |||
NM_004287.4 | 92 | Missense Mutation | ACC,CCC | T,P 3 | NP_004278.2 | |
NM_054022.3 | 92 | Missense Mutation | ACC,CCC | T,P 3 | NP_473363.1 | |
XM_005257844.3 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_005257901.1 | |
XM_006722190.3 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_006722253.1 | |
XM_011525501.2 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_011523803.1 | |
XM_011525502.2 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_011523804.1 | |
XM_017025378.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880867.1 | |
XM_017025379.1 | 92 | UTR 5 | XP_016880868.1 | |||
XM_017025380.1 | 92 | UTR 5 | XP_016880869.1 | |||
XM_017025381.1 | 92 | UTR 5 | XP_016880870.1 | |||
XM_017025382.1 | 92 | UTR 5 | XP_016880871.1 | |||
XM_017025383.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880872.1 | |
XM_017025384.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880873.1 | |
XM_017025385.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880874.1 | |
XM_017025386.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880875.1 | |
XM_017025387.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880876.1 | |
XM_017025388.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880877.1 | |
XM_017025389.1 | 92 | UTR 5 | XP_016880878.1 | |||
XM_017025390.1 | 92 | UTR 5 | XP_016880879.1 | |||
XM_017025391.1 | 92 | UTR 5 | XP_016880880.1 | |||
XM_017025392.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880881.1 | |
XM_017025393.1 | 92 | Missense Mutation | ACC,CCC | T,P 3 | XP_016880882.1 | |
XM_017025394.1 | 92 | UTR 5 | XP_016880883.1 | |||
XM_017025395.1 | 92 | UTR 5 | XP_016880884.1 |
Set Membership: |
HapMap |