Product Details

SNP ID

rs141220509

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:113817691 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTCTTTAAACTGTGTAAGTCTGTG[C/G]AATGACCTAGAGGTGCTGACCCAGG

Phenotype

MIM: 616444

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

RBM19 PubMed Links

Additional Information

For this assay, SNP(s) [rs56766711] 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

RBM19

Gene Name

RNA binding motif protein 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146698.1	3466	Intron			NP_001140170.1
NM_001146699.1	3466	UTR 3			NP_001140171.1
NM_016196.3	3466	Intron			NP_057280.2
XM_017020280.1	3466	UTR 3			XP_016875769.1
XM_017020281.1	3466	Intron			XP_016875770.1

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