Product Details

SNP ID
rs111567903
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:38107139 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGGGATTTGTACAAAATGGTTCA[C/T]GGCTGACACATTTGGCATAGATACC
Phenotype
MIM: 604782
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ASH2L PubMed Links

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_001105214.2 533 Missense Mutation ACG,ATG T31M NP_001098684.1
NM_001261832.1 533 Missense Mutation ACG,ATG T31M NP_001248761.1
NM_001282272.1 533 Intron NP_001269201.1
NM_004674.4 533 Missense Mutation ACG,ATG T125M NP_004665.2
XM_005273682.1 533 Missense Mutation ACG,ATG T125M XP_005273739.1
XM_005273683.1 533 Missense Mutation ACG,ATG T31M XP_005273740.1
XM_006716412.1 533 Missense Mutation ACG,ATG T125M XP_006716475.1
XM_006716413.2 533 Intron XP_006716476.1

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