Product Details

SNP ID
rs78596202
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:32447867 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGAGCAGCCACCCTGCCTGGCAT[C/T]TGGGAGGTGTACCTTCCTTGGCACT
Phenotype
MIM: 612990
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ASXL1 PubMed Links

Gene Details

Gene
ASXL1
Gene Name
additional sex combs like 1, transcriptional regulator
There are no transcripts associated with this gene.

Gene
NOL4L
Gene Name
nucleolar protein 4 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256798.1 Intron NP_001243727.1
NM_080616.4 Intron NP_542183.2
XM_005260282.4 Intron XP_005260339.1
XM_005260283.4 Intron XP_005260340.1
XM_005260284.4 Intron XP_005260341.1
XM_005260285.4 Intron XP_005260342.2
XM_005260286.4 Intron XP_005260343.1
XM_005260288.2 Intron XP_005260345.1
XM_005260289.4 Intron XP_005260346.1
XM_006723702.3 Intron XP_006723765.1
XM_006723703.3 Intron XP_006723766.1
XM_011528562.2 Intron XP_011526864.1
XM_011528563.1 Intron XP_011526865.1
XM_017027669.1 Intron XP_016883158.1
XM_017027670.1 Intron XP_016883159.1

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