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TGCGATGGGCACGCGTGCAGCGTGG[C/T]CGTCCACCAAGGTACGGGGGTGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600328 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105371763 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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LOC105371763 - uncharacterized LOC105371763 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017025495.1 | 111 | Intron | XP_016880984.1 |
MIR4734 - microRNA 4734 | ||||||
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There are no transcripts associated with this gene. |
MLLT6 - MLLT6, PHD finger domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005937.3 | 111 | Missense Mutation | GCC,GTC | A,V 33 | NP_005928.2 | |
XM_006721911.2 | 111 | Missense Mutation | GCC,GTC | A,V 33 | XP_006721974.1 | |
XM_017024648.1 | 111 | Intron | XP_016880137.1 | |||
XM_017024649.1 | 111 | Missense Mutation | GCC,GTC | A,V 33 | XP_016880138.1 | |
XM_017024650.1 | 111 | Missense Mutation | GCC,GTC | A,V 33 | XP_016880139.1 |