Product Details

SNP ID

rs28694577

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.4:153347356 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

GATTTCTCTGATTTGTCTCTTCAAG[C/T]CAGGCAATACATGATGTCACTGAAT

Phenotype

MIM: 611422 MIM: 614141

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MND1 PubMed Links

Additional Information

For this assay, SNP(s) [rs74875228] 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

MND1

Gene Name

meiotic nuclear divisions 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001253861.1		Intron			NP_001240790.1
NM_032117.3		Intron			NP_115493.1
XM_005263275.2		Intron			XP_005263332.1
XM_017008688.1		Intron			XP_016864177.1

Gene

TRIM2

Gene Name

tripartite motif containing 2

There are no transcripts associated with this gene.

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