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GCCGCTGCGCCCTGCGCTTCTCCTT[A/G]CGCTTCAGGGCCTCCTGCAGCAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 185641 MIM: 185642 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MED22 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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MED22 - mediator complex subunit 22 | ||||||
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There are no transcripts associated with this gene. |
SURF6 - surfeit 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278942.1 | 963 | UTR 3 | NP_001265871.1 | |||
NM_006753.5 | 963 | Silent Mutation | CGC,CGT | R,R 295 | NP_006744.2 |