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TCATTGCATTTTGTAGGTGAGGAAA[C/T]GAAAGCCTAAAATTAGTCTGTCATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610222 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC107987276 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LOC107987276 - translation initiation factor IF-2-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017028183.1 | Intron | XP_016883672.1 |
RIN2 - Ras and Rab interactor 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242581.1 | Intron | NP_001229510.1 | ||||
NM_018993.3 | Intron | NP_061866.1 | ||||
XM_005260731.2 | Intron | XP_005260788.1 | ||||
XM_005260733.2 | Intron | XP_005260790.1 | ||||
XM_006723574.3 | Intron | XP_006723637.1 | ||||
XM_006723575.3 | Intron | XP_006723638.1 | ||||
XM_006723577.2 | Intron | XP_006723640.1 | ||||
XM_011529255.2 | Intron | XP_011527557.2 | ||||
XM_011529257.1 | Intron | XP_011527559.1 | ||||
XM_011529258.2 | Intron | XP_011527560.1 | ||||
XM_011529259.2 | Intron | XP_011527561.1 | ||||
XM_017027887.1 | Intron | XP_016883376.1 | ||||
XM_017027888.1 | Intron | XP_016883377.1 | ||||
XM_017027889.1 | Intron | XP_016883378.1 | ||||
XM_017027890.1 | Intron | XP_016883379.1 | ||||
XM_017027891.1 | Intron | XP_016883380.1 | ||||
XM_017027892.1 | Intron | XP_016883381.1 | ||||
XM_017027893.1 | Intron | XP_016883382.1 |