Product Details

SNP ID

hCV25958535

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:38110701 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCCCTTGGTAGTAGAGATGTAGT[A/T]CTACAGATAACTGTTTCTTCCTTTT

Phenotype

MIM: 604782

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

ASH2L PubMed Links

Additional Information

For this assay, SNP(s) [rs376065614] 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

ASH2L

Gene Name

ASH2 like histone lysine methyltransferase complex subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105214.2		Intron			NP_001098684.1
NM_001261832.1		Intron			NP_001248761.1
NM_001282272.1		Intron			NP_001269201.1
NM_004674.4		Intron			NP_004665.2

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