Product Details

SNP ID
rs75379074
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:83460154 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTATCTTGATTAGGTTCATCATATA[C/T]AAATGCCACTTTTTTTTTTTTTTGA
Phenotype
MIM: 611143 MIM: 606769 MIM: 611983
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM175A PubMed Links
Additional Information
For this assay, SNP(s) [rs36014997] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
FAM175A
Gene Name
family with sequence similarity 175 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_139076.2 3516 Intron NP_620775.2
XM_005263280.4 3516 UTR 3 XP_005263337.1
XM_017008694.1 3516 UTR 3 XP_016864183.1
Gene
HELQ
Gene Name
helicase, POLQ-like
There are no transcripts associated with this gene.

Gene
MRPS18C
Gene Name
mitochondrial ribosomal protein S18C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297767.1 3516 Intron NP_001284696.1
NM_001297769.1 3516 Intron NP_001284698.1
NM_001297770.1 3516 Intron NP_001284699.1
NM_016067.3 3516 Intron NP_057151.1

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