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AGGGAGCAGCCACCCTGCCTGGCAT[C/T]TGGGAGGTGTACCTTCCTTGGCACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612990 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASXL1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ASXL1 - additional sex combs like 1, transcriptional regulator | ||||||
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There are no transcripts associated with this gene. |
NOL4L - nucleolar protein 4 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |