Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCCAAACCAAAGGCGAGAATCCC[A/G]CCAAGGAAGAGGCTCCCAAGTACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SLC35C2 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) - Not Available | |||
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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SLC35C2 - solute carrier family 35 member C2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281457.1 | 1007 | Silent Mutation | GGC,GGT | G,G 135 | NP_001268386.1 | |
NM_001281458.1 | 1007 | Silent Mutation | GGC,GGT | G,G 278 | NP_001268387.1 | |
NM_001281459.1 | 1007 | Silent Mutation | GGC,GGT | G,G 114 | NP_001268388.1 | |
NM_001281460.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | NP_001268389.1 | |
NM_015945.11 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | NP_057029.8 | |
NM_173073.3 | 1007 | Silent Mutation | GGC,GGT | G,G 228 | NP_775096.1 | |
NM_173179.3 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | NP_775271.1 | |
XM_011528831.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_011527133.1 | |
XM_011528832.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_011527134.1 | |
XM_011528833.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_011527135.1 | |
XM_011528834.1 | 1007 | Silent Mutation | GGC,GGT | G,G 248 | XP_011527136.1 | |
XM_011528835.1 | 1007 | Silent Mutation | GGC,GGT | G,G 211 | XP_011527137.1 | |
XM_011528836.1 | 1007 | Silent Mutation | GGC,GGT | G,G 135 | XP_011527138.1 | |
XM_011528837.1 | 1007 | Silent Mutation | GGC,GGT | G,G 135 | XP_011527139.1 | |
XM_011528838.1 | 1007 | Silent Mutation | GGC,GGT | G,G 97 | XP_011527140.1 | |
XM_017027856.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_016883345.1 | |
XM_017027857.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_016883346.1 | |
XM_017027858.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_016883347.1 | |
XM_017027859.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_016883348.1 | |
XM_017027860.1 | 1007 | Silent Mutation | GGC,GGT | G,G 249 | XP_016883349.1 | |
XM_017027861.1 | 1007 | Silent Mutation | GGC,GGT | G,G 228 | XP_016883350.1 | |
XM_017027862.1 | 1007 | Missense Mutation | GCG,GTG | A,V 262 | XP_016883351.1 |