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TCTGTGCCCACCGCCTCTCGTCATC[A/G]TATGCAGCCCTCTCCGTTACCCTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605245 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GARNL3 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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GARNL3 - GTPase activating Rap/RanGAP domain like 3 | ||||||
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There are no transcripts associated with this gene. |
SLC2A8 - solute carrier family 2 member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271711.1 | Intron | NP_001258640.1 | ||||
NM_001271712.1 | Intron | NP_001258641.1 | ||||
NM_014580.4 | Intron | NP_055395.2 | ||||
XM_006717084.3 | Intron | XP_006717147.1 | ||||
XM_011518602.2 | Intron | XP_011516904.1 | ||||
XM_011518603.2 | Intron | XP_011516905.1 | ||||
XM_011518604.2 | Intron | XP_011516906.1 | ||||
XM_017014653.1 | Intron | XP_016870142.1 |