Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCGGTGGTGGTTGCCCTTGCGAC[C/T]GTGCTCATTCTGGATGTAGGTGACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 103000 MIM: 610135 | ||||||||||||||||||||
Literature Links: |
AK1 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 |
AK1 - adenylate kinase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000476.2 | 1152 | Intron | NP_000467.1 | |||
NM_001318121.1 | 1152 | Intron | NP_001305050.1 | |||
NM_001318122.1 | 1152 | Intron | NP_001305051.1 | |||
XM_017014427.1 | 1152 | UTR 5 | XP_016869916.1 | |||
XM_017014428.1 | 1152 | Intron | XP_016869917.1 |
ST6GALNAC6 - ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286999.1 | 1152 | Silent Mutation | ACA,ACG | T,T 299 | NP_001273928.1 | |
NM_001287000.1 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | NP_001273929.1 | |
NM_001287001.1 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | NP_001273930.1 | |
NM_001287002.1 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | NP_001273931.1 | |
NM_001287003.1 | 1152 | UTR 3 | NP_001273932.1 | |||
NM_013443.4 | 1152 | Missense Mutation | AGT,GGT | S,G 301 | NP_038471.2 | |
XM_011518610.2 | 1152 | Missense Mutation | AGT,GGT | S,G 301 | XP_011516912.1 | |
XM_011518611.2 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | XP_011516913.1 | |
XM_017014658.1 | 1152 | Silent Mutation | ACA,ACG | T,T 324 | XP_016870147.1 | |
XM_017014659.1 | 1152 | Silent Mutation | ACA,ACG | T,T 299 | XP_016870148.1 | |
XM_017014660.1 | 1152 | Missense Mutation | AGT,GGT | S,G 326 | XP_016870149.1 | |
XM_017014661.1 | 1152 | Silent Mutation | ACA,ACG | T,T 265 | XP_016870150.1 | |
XM_017014662.1 | 1152 | Silent Mutation | ACA,ACG | T,T 265 | XP_016870151.1 | |
XM_017014663.1 | 1152 | Silent Mutation | ACA,ACG | T,T 265 | XP_016870152.1 | |
XM_017014664.1 | 1152 | Silent Mutation | ACA,ACG | T,T 265 | XP_016870153.1 | |
XM_017014665.1 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | XP_016870154.1 | |
XM_017014666.1 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | XP_016870155.1 | |
XM_017014667.1 | 1152 | Missense Mutation | AGT,GGT | S,G 267 | XP_016870156.1 |