Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
19 submissions
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Phenotype: |
MIM: 609375 MIM: 609852 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LIN9 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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LIN9 - lin-9 DREAM MuvB core complex component | ||||||
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There are no transcripts associated with this gene. |
MIXL1 - Mix paired-like homeobox | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282402.1 | 637 | Silent Mutation | TGC,TGT | C,C 191 | NP_001269331.1 | |
NM_031944.2 | 637 | Silent Mutation | TGC,TGT | C,C 183 | NP_114150.1 |
Set Membership: |
JSNP |