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Search Thermo Fisher Scientific
GCTGTTTGATGACTTCAAGAAGATG[C/T]GCGAGCAGATGTGAGTGCCCCCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610197 | ||||||||||||||||||||
Literature Links: |
MED25 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 |
MED25 - mediator complex subunit 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030973.3 | 457 | Missense Mutation | CGC,TGC | R,C 132 | NP_112235.2 | |
XM_011527353.1 | 457 | Missense Mutation | CGC,TGC | R,C 132 | XP_011525655.1 |
MIR6800 - microRNA 6800 | ||||||
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There are no transcripts associated with this gene. |