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TGGACATGGAGGCCATGCTGGACAC[C/T]GTGCAGGCCTGGCTGAGCAGCCCGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608705 | ||||||||||||||||||||
Literature Links: |
NMRK2 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 |
NMRK2 - nicotinamide riboside kinase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289117.1 | 509 | Silent Mutation | ACC,ACT | T,T 73 | NP_001276046.1 | |
NM_170678.2 | 509 | Silent Mutation | ACC,ACT | T,T 68 | NP_733778.1 | |
XM_006722725.3 | 509 | Silent Mutation | ACC,ACT | T,T 73 | XP_006722788.1 | |
XM_006722726.3 | 509 | Silent Mutation | ACC,ACT | T,T 73 | XP_006722789.1 | |
XM_017026597.1 | 509 | Silent Mutation | ACC,ACT | T,T 68 | XP_016882086.1 |