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CAAAGAATAGAAGATTCTGTGCTGA[A/T]TGGATGCTCTGAGCAGCAGGAAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609233 | ||||||||||||||||||||
Literature Links: |
NUDT13 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 |
NUDT13 - nudix hydrolase 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001283014.1 | 561 | Missense Mutation | AAT,ATT | N,I 96 | NP_001269943.1 | |
NM_001283015.1 | 561 | Missense Mutation | AAT,ATT | N,I 96 | NP_001269944.1 | |
NM_001283016.1 | 561 | UTR 5 | NP_001269945.1 | |||
NM_001283017.1 | 561 | UTR 5 | NP_001269946.1 | |||
NM_001283019.1 | 561 | UTR 5 | NP_001269948.1 | |||
NM_015901.5 | 561 | Missense Mutation | AAT,ATT | N,I 96 | NP_056985.3 | |
XM_017016033.1 | 561 | Missense Mutation | AAT,ATT | N,I 96 | XP_016871522.1 |