Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGAGGCTCCCAAGTACCCGCAGGA[A/G]CAGCCCTGTGTCCTGGAAACGGAAG
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 |
---|---|---|
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 |
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 | 975 | Missense Mutation | CTC,TTC | L,F 125 | NP_001268386.1 | |
NM_001281458.1 | 975 | Missense Mutation | CTC,TTC | L,F 268 | NP_001268387.1 | |
NM_001281459.1 | 975 | Missense Mutation | CTC,TTC | L,F 104 | NP_001268388.1 | |
NM_001281460.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | NP_001268389.1 | |
NM_015945.11 | 975 | Missense Mutation | CTC,TTC | L,F 239 | NP_057029.8 | |
NM_173073.3 | 975 | Missense Mutation | CTC,TTC | L,F 218 | NP_775096.1 | |
NM_173179.3 | 975 | Missense Mutation | CTC,TTC | L,F 239 | NP_775271.1 | |
XM_011528831.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_011527133.1 | |
XM_011528832.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_011527134.1 | |
XM_011528833.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_011527135.1 | |
XM_011528834.1 | 975 | Missense Mutation | CTC,TTC | L,F 238 | XP_011527136.1 | |
XM_011528835.1 | 975 | Missense Mutation | CTC,TTC | L,F 201 | XP_011527137.1 | |
XM_011528836.1 | 975 | Missense Mutation | CTC,TTC | L,F 125 | XP_011527138.1 | |
XM_011528837.1 | 975 | Missense Mutation | CTC,TTC | L,F 125 | XP_011527139.1 | |
XM_011528838.1 | 975 | Missense Mutation | CTC,TTC | L,F 87 | XP_011527140.1 | |
XM_017027856.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_016883345.1 | |
XM_017027857.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_016883346.1 | |
XM_017027858.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_016883347.1 | |
XM_017027859.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_016883348.1 | |
XM_017027860.1 | 975 | Missense Mutation | CTC,TTC | L,F 239 | XP_016883349.1 | |
XM_017027861.1 | 975 | Missense Mutation | CTC,TTC | L,F 218 | XP_016883350.1 | |
XM_017027862.1 | 975 | Silent Mutation | TGC,TGT | C,C 251 | XP_016883351.1 |