Product Details

SNP ID
rs200703770
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:39462418 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCACAAACATCGTCACCACCAGC[A/G]CAGGCGTTCCCGGGACTTACTAAAA
Phenotype
MIM: 615514
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CDK12 PubMed Links

Gene Details

Gene
CDK12
Gene Name
cyclin dependent kinase 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015083.2 908 Missense Mutation CAC,CGC H116R NP_055898.1
NM_016507.3 908 Missense Mutation CAC,CGC H116R NP_057591.2
XM_005257456.3 908 Missense Mutation CAC,CGC H116R XP_005257513.1
XM_005257458.4 908 Missense Mutation CAC,CGC H116R XP_005257515.1
XM_011524892.2 908 Missense Mutation CAC,CGC H116R XP_011523194.1
XM_011524893.2 908 Missense Mutation CAC,CGC H116R XP_011523195.1
XM_011524894.2 908 Missense Mutation CAC,CGC H116R XP_011523196.1
XM_011524895.2 908 Missense Mutation CAC,CGC H116R XP_011523197.1
XM_011524896.2 908 Missense Mutation CAC,CGC H116R XP_011523198.1
XM_011524897.2 908 Missense Mutation CAC,CGC H116R XP_011523199.1
XM_011524898.2 908 Missense Mutation CAC,CGC H116R XP_011523200.1
XM_011524899.2 908 Missense Mutation CAC,CGC H116R XP_011523201.1
XM_011524900.2 908 Missense Mutation CAC,CGC H116R XP_011523202.1
XM_011524901.2 908 Missense Mutation CAC,CGC H116R XP_011523203.1
XM_011524902.2 908 Missense Mutation CAC,CGC H116R XP_011523204.1
XM_011524903.2 908 Missense Mutation CAC,CGC H116R XP_011523205.1
XM_011524905.2 908 Missense Mutation CAC,CGC H116R XP_011523207.1
XM_011524906.2 908 Missense Mutation CAC,CGC H116R XP_011523208.1
XM_011524907.2 908 Missense Mutation CAC,CGC H116R XP_011523209.1
XM_017024744.1 908 Missense Mutation CAC,CGC H116R XP_016880233.1
XM_017024745.1 908 Missense Mutation CAC,CGC H116R XP_016880234.1
XM_017024746.1 908 Missense Mutation CAC,CGC H116R XP_016880235.1
XM_017024747.1 908 Missense Mutation CAC,CGC H116R XP_016880236.1
XM_017024748.1 908 Missense Mutation CAC,CGC H116R XP_016880237.1
XM_017024749.1 908 Missense Mutation CAC,CGC H116R XP_016880238.1
XM_017024750.1 908 Missense Mutation CAC,CGC H116R XP_016880239.1
XM_017024751.1 908 Missense Mutation CAC,CGC H116R XP_016880240.1
XM_017024752.1 908 Missense Mutation CAC,CGC H116R XP_016880241.1
XM_017024753.1 908 Missense Mutation CAC,CGC H116R XP_016880242.1

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