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AGCCCGCGATGAGCTGCCGCACGGC[A/G]CTGATCTCCGTGGGGCTGAGCTGAG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 2416 | Silent Mutation | AGC,AGT | S,S 649 | NP_001243727.1 | |
NM_080616.4 | 2416 | Silent Mutation | AGC,AGT | S,S 405 | NP_542183.2 | |
XM_005260282.4 | 2416 | Silent Mutation | AGC,AGT | S,S 514 | XP_005260339.1 | |
XM_005260283.4 | 2416 | Silent Mutation | AGC,AGT | S,S 514 | XP_005260340.1 | |
XM_005260284.4 | 2416 | Silent Mutation | AGC,AGT | S,S 514 | XP_005260341.1 | |
XM_005260285.4 | 2416 | Silent Mutation | AGC,AGT | S,S 571 | XP_005260342.2 | |
XM_005260286.4 | 2416 | Silent Mutation | AGC,AGT | S,S 514 | XP_005260343.1 | |
XM_005260288.2 | 2416 | Silent Mutation | AGC,AGT | S,S 405 | XP_005260345.1 | |
XM_005260289.4 | 2416 | Silent Mutation | AGC,AGT | S,S 405 | XP_005260346.1 | |
XM_006723702.3 | 2416 | Silent Mutation | AGC,AGT | S,S 514 | XP_006723765.1 | |
XM_006723703.3 | 2416 | Silent Mutation | AGC,AGT | S,S 514 | XP_006723766.1 | |
XM_011528562.2 | 2416 | Intron | XP_011526864.1 | |||
XM_011528563.1 | 2416 | Intron | XP_011526865.1 | |||
XM_017027669.1 | 2416 | Silent Mutation | AGC,AGT | S,S 405 | XP_016883158.1 | |
XM_017027670.1 | 2416 | Intron | XP_016883159.1 |