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AGTTTGCTAGATGATGCTAAGGCCC[A/G]CTTAAGAAAGTATGATATTGGAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609231 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NUDT7 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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NUDT7 - nudix hydrolase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105663.2 | 156 | Missense Mutation | CAC,CGC | H,R 22 | NP_001099133.1 | |
NM_001243657.1 | 156 | Missense Mutation | CAC,CGC | H,R 22 | NP_001230586.1 | |
NM_001243660.1 | 156 | Missense Mutation | CAC,CGC | H,R 22 | NP_001230589.1 | |
NM_001243661.1 | 156 | Missense Mutation | CAC,CGC | H,R 22 | NP_001230590.1 | |
XM_011523032.2 | 156 | Missense Mutation | CAC,CGC | H,R 22 | XP_011521334.1 | |
XM_011523033.2 | 156 | Missense Mutation | CAC,CGC | H,R 22 | XP_011521335.1 | |
XM_017023170.1 | 156 | Missense Mutation | CAC,CGC | H,R 22 | XP_016878659.1 |