Product Details

SNP ID

rs200926173

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:93728244 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTAAGAAAGGATCAACAAGCAGAA[C/G]ATGATGAGGATGACGAGTTAGATGT

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FAM92A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs147392141] are located under a primer 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

FAM92A1

Gene Name

family with sequence similarity 92 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001283034.1	8327	Intron			NP_001269963.1
NM_145269.4	8327	Intron			NP_660312.2
XM_005250787.2	8327	Missense Mutation	CAT,GAT	H203D	XP_005250844.1

Gene

RBM12B

Gene Name

RNA binding motif protein 12B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203390.2	8327	Intron			NP_976324.2
XM_005250915.4	8327	UTR 3			XP_005250972.1
XM_011517027.2	8327	UTR 3			XP_011515329.1
XM_011517028.2	8327	UTR 3			XP_011515330.1
XM_011517029.2	8327	UTR 3			XP_011515331.1
XM_017013406.1	8327	UTR 3			XP_016868895.1
XM_017013407.1	8327	UTR 3			XP_016868896.1
XM_017013408.1	8327	UTR 3			XP_016868897.1

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