Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTGACCTTGAGGAACGAGGTCTGG[A/G]TGGGGTCCAGTTTTGAGTTACATTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605272 MIM: 616956 | ||||||||||||||||||||
Literature Links: |
MIR6717 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 |
MIR6717 - microRNA 6717 | ||||||
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There are no transcripts associated with this gene. |
NDRG2 - NDRG family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282211.1 | 851 | Missense Mutation | ACC,ATC | T,I 277 | NP_001269140.1 | |
NM_001282212.1 | 851 | Intron | NP_001269141.1 | |||
NM_001282213.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | NP_001269142.1 | |
NM_001282214.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | NP_001269143.1 | |
NM_001282215.1 | 851 | Missense Mutation | ACC,ATC | T,I 270 | NP_001269144.1 | |
NM_001282216.1 | 851 | Missense Mutation | ACC,ATC | T,I 221 | NP_001269145.1 | |
NM_001320329.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | NP_001307258.1 | |
NM_016250.2 | 851 | Missense Mutation | ACC,ATC | T,I 267 | NP_057334.1 | |
NM_201535.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | NP_963293.1 | |
NM_201536.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | NP_963294.1 | |
NM_201537.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | NP_963831.1 | |
NM_201538.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | NP_963832.1 | |
NM_201539.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | NP_963833.1 | |
NM_201540.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | NP_963834.1 | |
NM_201541.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | NP_963835.1 | |
XM_011536996.2 | 851 | Missense Mutation | ACC,ATC | T,I 281 | XP_011535298.1 | |
XM_011536997.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | XP_011535299.1 | |
XM_011536998.1 | 851 | Missense Mutation | ACC,ATC | T,I 281 | XP_011535300.1 | |
XM_011536999.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | XP_011535301.1 | |
XM_011537001.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | XP_011535303.1 | |
XM_011537002.1 | 851 | Missense Mutation | ACC,ATC | T,I 267 | XP_011535304.1 | |
XM_017021480.1 | 851 | Intron | XP_016876969.1 | |||
XM_017021481.1 | 851 | Intron | XP_016876970.1 | |||
XM_017021482.1 | 851 | Intron | XP_016876971.1 | |||
XM_017021483.1 | 851 | Intron | XP_016876972.1 | |||
XM_017021484.1 | 851 | Intron | XP_016876973.1 | |||
XM_017021485.1 | 851 | Intron | XP_016876974.1 | |||
XM_017021486.1 | 851 | Intron | XP_016876975.1 | |||
XM_017021487.1 | 851 | Intron | XP_016876976.1 | |||
XM_017021488.1 | 851 | Intron | XP_016876977.1 | |||
XM_017021489.1 | 851 | Intron | XP_016876978.1 | |||
XM_017021490.1 | 851 | Intron | XP_016876979.1 | |||
XM_017021491.1 | 851 | Intron | XP_016876980.1 | |||
XM_017021492.1 | 851 | Intron | XP_016876981.1 | |||
XM_017021493.1 | 851 | Intron | XP_016876982.1 | |||
XM_017021494.1 | 851 | Missense Mutation | ACC,ATC | T,I 299 | XP_016876983.1 | |
XM_017021495.1 | 851 | Missense Mutation | ACC,ATC | T,I 299 | XP_016876984.1 | |
XM_017021496.1 | 851 | Missense Mutation | ACC,ATC | T,I 285 | XP_016876985.1 | |
XM_017021497.1 | 851 | Intron | XP_016876986.1 |
TPPP2 - tubulin polymerization promoting protein family member 2 | ||||||
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There are no transcripts associated with this gene. |