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AGGCCCCGGCCGCGGCCGCATACGC[C/T]GTGCTGCCCGTCGGGGTGGACACGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 611616 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NADK 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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NADK - NAD kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198993.1 | 901 | Silent Mutation | ACA,ACG | T,T 325 | NP_001185922.1 | |
NM_001198994.1 | 901 | Silent Mutation | ACA,ACG | T,T 470 | NP_001185923.1 | |
NM_001198995.1 | 901 | Silent Mutation | ACA,ACG | T,T 293 | NP_001185924.1 | |
NM_023018.4 | 901 | Silent Mutation | ACA,ACG | T,T 325 | NP_075394.3 | |
XM_005244778.2 | 901 | Silent Mutation | ACA,ACG | T,T 325 | XP_005244835.1 | |
XM_006710837.2 | 901 | Silent Mutation | ACA,ACG | T,T 325 | XP_006710900.1 | |
XM_006710838.2 | 901 | Silent Mutation | ACA,ACG | T,T 238 | XP_006710901.1 | |
XM_006710839.1 | 901 | Silent Mutation | ACA,ACG | T,T 429 | XP_006710902.1 | |
XM_011542006.1 | 901 | Silent Mutation | ACA,ACG | T,T 222 | XP_011540308.1 | |
XM_011542007.1 | 901 | Silent Mutation | ACA,ACG | T,T 222 | XP_011540309.1 | |
XM_011542008.1 | 901 | Silent Mutation | ACA,ACG | T,T 222 | XP_011540310.1 | |
XM_011542009.2 | 901 | Silent Mutation | ACA,ACG | T,T 222 | XP_011540311.1 | |
XM_017002143.1 | 901 | Silent Mutation | ACA,ACG | T,T 325 | XP_016857632.1 | |
XM_017002144.1 | 901 | Silent Mutation | ACA,ACG | T,T 213 | XP_016857633.1 | |
XM_017002145.1 | 901 | Silent Mutation | ACA,ACG | T,T 203 | XP_016857634.1 | |
XM_017002146.1 | 901 | Silent Mutation | ACA,ACG | T,T 203 | XP_016857635.1 |
SLC35E2 - solute carrier family 35 member E2 | ||||||
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There are no transcripts associated with this gene. |