Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCAACCTAAAATACGTTTCCCTGG[C/G]AATTTTGGTCTTTCAGACTACCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 605632 | ||||||||||||||||||||
Literature Links: |
SLC35A3 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 |
SLC35A3 - solute carrier family 35 member A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271684.1 | 846 | Missense Mutation | GCA,GGA | A,G 11 | NP_001258613.1 | |
NM_001271685.1 | 846 | Missense Mutation | GCA,GGA | A,G 53 | NP_001258614.1 | |
NM_012243.2 | 846 | Missense Mutation | GCA,GGA | A,G 11 | NP_036375.1 | |
XM_005270691.4 | 846 | Missense Mutation | GCA,GGA | A,G 11 | XP_005270748.1 | |
XM_011541135.2 | 846 | Missense Mutation | GCA,GGA | A,G 53 | XP_011539437.1 | |
XM_011541136.2 | 846 | Missense Mutation | GCA,GGA | A,G 11 | XP_011539438.1 | |
XM_011541137.2 | 846 | Missense Mutation | GCA,GGA | A,G 53 | XP_011539439.1 | |
XM_011541138.2 | 846 | Missense Mutation | GCA,GGA | A,G 53 | XP_011539440.1 | |
XM_017000869.1 | 846 | Missense Mutation | GCA,GGA | A,G 11 | XP_016856358.1 | |
XM_017000870.1 | 846 | Missense Mutation | GCA,GGA | A,G 11 | XP_016856359.1 | |
XM_017000871.1 | 846 | Missense Mutation | GCA,GGA | A,G 11 | XP_016856360.1 | |
XM_017000872.1 | 846 | UTR 5 | XP_016856361.1 |