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GCCGAGATAGACTTGCTGAGCAGCA[C/T]GCTGGCCGAGCTGAATGGGGGTCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616861 MIM: 614469 MIM: 602933 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR6875 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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MIR6875 - microRNA 6875 | ||||||
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There are no transcripts associated with this gene. |
SLC12A9 - solute carrier family 12 member 9 | ||||||
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There are no transcripts associated with this gene. |
SRRT - serrate, RNA effector molecule | ||||||
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There are no transcripts associated with this gene. |
TRIP6 - thyroid hormone receptor interactor 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003302.2 | 478 | Missense Mutation | ACG,ATG | T,M 103 | NP_003293.2 |