Product Details

SNP ID
rs201870201
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:127886783 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAGGGCATGCGCTGGAGGCGGGGC[C/T]GCTGGCTGGGACAGAGCAGACGGGC
Phenotype
MIM: 103000 MIM: 610135
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
AK1 PubMed Links

Gene Details

Gene
AK1
Gene Name
adenylate kinase 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000476.2 1069 Intron NP_000467.1
NM_001318121.1 1069 Intron NP_001305050.1
NM_001318122.1 1069 Intron NP_001305051.1
XM_017014427.1 1069 Intron XP_016869916.1
XM_017014428.1 1069 Intron XP_016869917.1
Gene
ST6GALNAC6
Gene Name
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286999.1 1069 Missense Mutation NP_001273928.1
NM_001287000.1 1069 Missense Mutation NP_001273929.1
NM_001287001.1 1069 Missense Mutation NP_001273930.1
NM_001287002.1 1069 Missense Mutation NP_001273931.1
NM_001287003.1 1069 UTR 3 NP_001273932.1
NM_013443.4 1069 Missense Mutation NP_038471.2
XM_011518610.2 1069 Missense Mutation XP_011516912.1
XM_011518611.2 1069 Missense Mutation XP_011516913.1
XM_017014658.1 1069 Missense Mutation XP_016870147.1
XM_017014659.1 1069 Missense Mutation XP_016870148.1
XM_017014660.1 1069 Missense Mutation XP_016870149.1
XM_017014661.1 1069 Missense Mutation XP_016870150.1
XM_017014662.1 1069 Missense Mutation XP_016870151.1
XM_017014663.1 1069 Missense Mutation XP_016870152.1
XM_017014664.1 1069 Missense Mutation XP_016870153.1
XM_017014665.1 1069 Missense Mutation XP_016870154.1
XM_017014666.1 1069 Missense Mutation XP_016870155.1
XM_017014667.1 1069 Missense Mutation XP_016870156.1

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