Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGAGCCACTCTTCTTTTGGAATTCT[G/T]CAGCAATTTCCTCAAAAGACTTTCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 138160 | |||||||||||||||||||||||
Literature Links: |
SLC2A2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
SLC2A2 - solute carrier family 2 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000340.1 | 1799 | Missense Mutation | NP_000331.1 | |||
NM_001278658.1 | 1799 | Missense Mutation | NP_001265587.1 | |||
NM_001278659.1 | 1799 | Missense Mutation | NP_001265588.1 | |||
XM_011513087.2 | 1799 | Missense Mutation | XP_011511389.1 | |||
XM_011513089.2 | 1799 | Missense Mutation | XP_011511391.1 |