Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCATCAGGGGATTTTCTTGGGCAG[C/G]GGATTAATGATCCCACTCTCGATGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615365 | ||||||||||||||||||||
Literature Links: |
AK8 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 |
AK8 - adenylate kinase 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317958.1 | 1355 | Silent Mutation | CCC,CCG | P,P 269 | NP_001304887.1 | |
NM_001317959.1 | 1355 | Silent Mutation | CCC,CCG | P,P 301 | NP_001304888.1 | |
NM_152572.2 | 1355 | Silent Mutation | CCC,CCG | P,P 473 | NP_689785.1 | |
XM_005272169.2 | 1355 | Silent Mutation | CCC,CCG | P,P 485 | XP_005272226.1 | |
XM_006716965.2 | 1355 | Silent Mutation | CCC,CCG | P,P 401 | XP_006717028.1 | |
XM_011518277.2 | 1355 | Intron | XP_011516579.1 | |||
XM_011518278.2 | 1355 | Silent Mutation | CCC,CCG | P,P 399 | XP_011516580.1 | |
XM_017014308.1 | 1355 | Silent Mutation | CCC,CCG | P,P 301 | XP_016869797.1 |