Product Details

SNP ID

rs78761037

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:38105428 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTGGCCTTAAAGCGGTCGTGGAA[C/T]TATGCTTCCTCAGGCAGGCGGTGGA

Phenotype

MIM: 604782

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ASH2L PubMed Links

Additional Information

For this assay, SNP(s) [rs75541171] 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

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	464	Intron			NP_001098684.1
NM_001261832.1	464	Intron			NP_001248761.1
NM_001282272.1	464	Intron			NP_001269201.1
NM_004674.4	464	Intron			NP_004665.2
XM_005273682.1	464	UTR 5			XP_005273739.1
XM_005273683.1	464	Intron			XP_005273740.1
XM_006716412.1	464	UTR 5			XP_006716475.1
XM_006716413.2	464	Intron			XP_006716476.1

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