Product Details

SNP ID

rs10421208

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:10853947 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGGAGGGACTGCTGGCATGTGTCA[A/G]TAGGCTGAGGCAGGTGGATCACTTA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C19orf38 PubMed Links

Additional Information

For this assay, SNP(s) [rs545079431] 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

C19orf38

Gene Name

chromosome 19 open reading frame 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136482.1		Intron			NP_001129954.1
XM_005259846.4		Intron			XP_005259903.1
XM_005259847.4		Intron			XP_005259904.1

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