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GTGCCCACTCTGCCAGCATCATGAA[A/G]CCAATCAACGCACCAGGGATGTGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605044 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MED27 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
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
|
MED27 - mediator complex subunit 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001253881.1 | Intron | NP_001240810.1 | ||||
NM_001253882.1 | Intron | NP_001240811.1 | ||||
NM_004269.3 | Intron | NP_004260.2 | ||||
XM_005272236.3 | Intron | XP_005272293.1 | ||||
XM_017015329.1 | Intron | XP_016870818.1 | ||||
XM_017015330.1 | Intron | XP_016870819.1 |