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CTGTTTTTTTTTCACCCTCACTGAC[A/G]TTAGCAGTGGCCCCTTCCCGTTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 607999 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASH1L 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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ASH1L - ASH1 like histone lysine methyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018489.2 | 3636 | Silent Mutation | NP_060959.2 | |||
XM_005245337.4 | 3636 | Intron | XP_005245394.1 | |||
XM_006711450.3 | 3636 | Silent Mutation | XP_006711513.1 | |||
XM_006711451.3 | 3636 | Silent Mutation | XP_006711514.1 | |||
XM_006711452.3 | 3636 | Silent Mutation | XP_006711515.1 | |||
XM_011509769.2 | 3636 | Intron | XP_011508071.1 | |||
XM_011509770.2 | 3636 | Silent Mutation | XP_011508072.1 | |||
XM_017001784.1 | 3636 | Silent Mutation | XP_016857273.1 | |||
XM_017001785.1 | 3636 | Silent Mutation | XP_016857274.1 | |||
XM_017001786.1 | 3636 | Intron | XP_016857275.1 | |||
XM_017001787.1 | 3636 | Intron | XP_016857276.1 | |||
XM_017001788.1 | 3636 | Silent Mutation | XP_016857277.1 |
MIR555 - microRNA 555 | ||||||
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There are no transcripts associated with this gene. |
RUSC1 - RUN and SH3 domain containing 1 | ||||||
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There are no transcripts associated with this gene. |