Product Details

SNP ID
rs9807787
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:33580364 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATTGTTTGCTCGGCCATTAATTCAG[A/G]ATTGTGTGGGGATGTGCAAGGCTTC
Phenotype
MIM: 615115
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ASXL3 PubMed Links

Gene Details

Gene
ASXL3
Gene Name
additional sex combs like 3, transcriptional regulator
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030632.2 Intron NP_085135.1
XM_005258356.1 Intron XP_005258413.1
XM_011526205.2 Intron XP_011524507.1
XM_011526206.2 Intron XP_011524508.1
XM_011526209.1 Intron XP_011524511.1
XM_011526210.1 Intron XP_011524512.1
XM_011526212.1 Intron XP_011524514.1
XM_011526213.1 Intron XP_011524515.1
XM_017026012.1 Intron XP_016881501.1
XM_017026013.1 Intron XP_016881502.1
XM_017026014.1 Intron XP_016881503.1

View Full Product Details