Product Details

SNP ID

rs201624630

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:13877385 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAATGCTGGAGCCGGTGTCAGCCC[C/T]GGAGCCGATGCCAGCGCCGGAGTCG

Phenotype

MIM: 612746 MIM: 608229

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C19orf57 PubMed Links

Additional Information

For this assay, SNP(s) [rs567049270] 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

C19orf57

Gene Name

chromosome 19 open reading frame 57

There are no transcripts associated with this gene.

Gene

MIR181C

Gene Name

microRNA 181c

There are no transcripts associated with this gene.

Gene

MIR181D

Gene Name

microRNA 181d

There are no transcripts associated with this gene.

Gene

NANOS3

Gene Name

nanos C2HC-type zinc finger 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098622.2	1003	Missense Mutation	CCG,CTG	P46L	NP_001092092.1
XM_011527964.2	1003	Missense Mutation	CCG,CTG	P46L	XP_011526266.1

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