Product Details

SNP ID

rs145448730

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:29269088 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAAATGCTTCTTGGTGGGGTAGAC[A/C]CCTAAGCGCCGCAGAAAGTCCCAGG

Phenotype

MIM: 608243

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

FAM189A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs61749506] 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

FAM189A1

Gene Name

family with sequence similarity 189 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015307.1	729	Intron			NP_056122.1
XM_011521407.2	729	Intron			XP_011519709.1

Gene

NSMCE3

Gene Name

NSE3 homolog, SMC5-SMC6 complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138704.3	729	Silent Mutation	GGG,GGT	G206G	NP_619649.1

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