Product Details

SNP ID

rs79297344

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:38304914 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCAAGAAGCCCAAAGTGAAGAAG[A/G]AGGAGAAGGGCAAGAAGGAGAAGGG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C19orf33 PubMed Links

Additional Information

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

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	431	UTR 3			NP_001304730.1
NM_033520.2	431	Missense Mutation	AAG,GAG	K91E	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	431	UTR 3			NP_001034760.1
NM_001039672.2	431	UTR 3			NP_001034761.1
NM_001039673.2	431	UTR 3			NP_001034762.1
NM_001145461.1	431	UTR 3			NP_001138933.1
NM_001145462.1	431	UTR 3			NP_001138934.1
NM_001145463.1	431	UTR 3			NP_001138935.1
XM_005259385.3	431	Intron			XP_005259442.1
XM_017027449.1	431	Intron			XP_016882938.1
XM_017027450.1	431	Intron			XP_016882939.1
XM_017027451.1	431	Intron			XP_016882940.1

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