Product Details

SNP ID

rs139591787

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:38304952 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAGGAGAAGGGCAAGAAGAAGGA[C/G]GCTCCCCACTGAAGGGCCCTGGACA

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

C19orf33 PubMed Links

Additional Information

For this assay, SNP(s) [rs139805446,rs147127327] 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

C19orf33

Gene Name

chromosome 19 open reading frame 33

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317801.1	469	UTR 3			NP_001304730.1
NM_033520.2	469	Missense Mutation	GAC,GAG	D103E	NP_277055.1

Gene

YIF1B

Gene Name

Yip1 interacting factor homolog B, membrane trafficking protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039671.2	469	UTR 3			NP_001034760.1
NM_001039672.2	469	UTR 3			NP_001034761.1
NM_001039673.2	469	UTR 3			NP_001034762.1
NM_001145461.1	469	UTR 3			NP_001138933.1
NM_001145462.1	469	UTR 3			NP_001138934.1
NM_001145463.1	469	UTR 3			NP_001138935.1
XM_005259385.3	469	Intron			XP_005259442.1
XM_017027449.1	469	Intron			XP_016882938.1
XM_017027450.1	469	Intron			XP_016882939.1
XM_017027451.1	469	Intron			XP_016882940.1

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