Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTTTCGCTCTCACTACCATCTGCC[A/G]CTGCGGGGTCCAAAGACATCGAACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 602942 | ||||||||||||||||||||
Literature Links: |
EVI5 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 |
EVI5 - ecotropic viral integration site 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308248.1 | 2437 | Missense Mutation | GCG,GTG | A,V 783 | NP_001295177.1 | |
NM_005665.5 | 2437 | Missense Mutation | GCG,GTG | A,V 772 | NP_005656.4 | |
XM_017002269.1 | 2437 | Missense Mutation | GCG,GTG | A,V 892 | XP_016857758.1 | |
XM_017002270.1 | 2437 | Missense Mutation | GCG,GTG | A,V 889 | XP_016857759.1 | |
XM_017002271.1 | 2437 | Missense Mutation | GCG,GTG | A,V 865 | XP_016857760.1 | |
XM_017002272.1 | 2437 | Missense Mutation | GCG,GTG | A,V 859 | XP_016857761.1 | |
XM_017002273.1 | 2437 | Missense Mutation | GCG,GTG | A,V 848 | XP_016857762.1 | |
XM_017002274.1 | 2437 | Missense Mutation | GCG,GTG | A,V 848 | XP_016857763.1 | |
XM_017002275.1 | 2437 | Missense Mutation | GCG,GTG | A,V 848 | XP_016857764.1 | |
XM_017002276.1 | 2437 | Missense Mutation | GCG,GTG | A,V 821 | XP_016857765.1 | |
XM_017002277.1 | 2437 | Missense Mutation | GCG,GTG | A,V 816 | XP_016857766.1 | |
XM_017002278.1 | 2437 | Missense Mutation | GCG,GTG | A,V 810 | XP_016857767.1 | |
XM_017002279.1 | 2437 | Missense Mutation | GCG,GTG | A,V 803 | XP_016857768.1 | |
XM_017002280.1 | 2437 | Missense Mutation | GCG,GTG | A,V 788 | XP_016857769.1 | |
XM_017002281.1 | 2437 | Missense Mutation | GCG,GTG | A,V 780 | XP_016857770.1 | |
XM_017002282.1 | 2437 | UTR 3 | XP_016857771.1 | |||
XM_017002283.1 | 2437 | UTR 3 | XP_016857772.1 | |||
XM_017002284.1 | 2437 | Missense Mutation | GCG,GTG | A,V 739 | XP_016857773.1 | |
XM_017002285.1 | 2437 | UTR 3 | XP_016857774.1 | |||
XM_017002286.1 | 2437 | Missense Mutation | GCG,GTG | A,V 684 | XP_016857775.1 | |
XM_017002287.1 | 2437 | Missense Mutation | GCG,GTG | A,V 684 | XP_016857776.1 | |
XM_017002288.1 | 2437 | Missense Mutation | GCG,GTG | A,V 684 | XP_016857777.1 |