Product Details

SNP ID
rs7689667
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:83409201 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCATAAATCATTCCAAATGACTGTG[C/T]TGTCCAAGATATGCAGAGGCACAAG
Phenotype
MIM: 606769
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
HELQ PubMed Links

Gene Details

Gene
HELQ
Gene Name
helicase, POLQ-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297755.1 Intron NP_001284684.1
NM_001297756.1 Intron NP_001284685.1
NM_001297757.1 Intron NP_001284686.1
NM_001297758.1 Intron NP_001284687.1
NM_001297759.1 Intron NP_001284688.1
NM_133636.3 Intron NP_598375.2
XM_005262711.1 Intron XP_005262768.1
XM_005262713.2 Intron XP_005262770.1
XM_006714076.2 Intron XP_006714139.1
XM_011531580.2 Intron XP_011529882.1
XM_017007679.1 Intron XP_016863168.1
XM_017007680.1 Intron XP_016863169.1
XM_017007681.1 Intron XP_016863170.1
XM_017007682.1 Intron XP_016863171.1
XM_017007683.1 Intron XP_016863172.1

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