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TGGGGCAGGCCTGACCGGCTGGGCA[C/T]GTTCTGAGGGGTTGTCTGAACGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603952 MIM: 607445 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DRG1 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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DRG1 - developmentally regulated GTP binding protein 1 | ||||||
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There are no transcripts associated with this gene. |
EIF4ENIF1 - eukaryotic translation initiation factor 4E nuclear import factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164501.1 | 3284 | Missense Mutation | ATG,GTG | M,V 928 | NP_001157973.1 | |
NM_001164502.1 | 3284 | Missense Mutation | ATG,GTG | M,V 754 | NP_001157974.1 | |
NM_019843.3 | 3284 | Missense Mutation | ATG,GTG | M,V 928 | NP_062817.2 | |
XM_005261686.2 | 3284 | Missense Mutation | ATG,GTG | M,V 929 | XP_005261743.1 | |
XM_005261687.2 | 3284 | Missense Mutation | ATG,GTG | M,V 929 | XP_005261744.1 | |
XM_005261688.2 | 3284 | Missense Mutation | ATG,GTG | M,V 929 | XP_005261745.1 | |
XM_006724281.3 | 3284 | Missense Mutation | ATG,GTG | M,V 970 | XP_006724344.3 | |
XM_011530280.1 | 3284 | Missense Mutation | ATG,GTG | M,V 928 | XP_011528582.1 | |
XM_011530281.2 | 3284 | Missense Mutation | ATG,GTG | M,V 929 | XP_011528583.1 | |
XM_017028863.1 | 3284 | Missense Mutation | ATG,GTG | M,V 969 | XP_016884352.1 | |
XM_017028864.1 | 3284 | Missense Mutation | ATG,GTG | M,V 928 | XP_016884353.1 |