Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTGAGTGAGCACCACAAAGTGGAC[A/G]GGAAGGCAGGAAGTACGGTCCTGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608771 | ||||||||||||||||||||
Literature Links: |
MED13L 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 |
MED13L - mediator complex subunit 13 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015335.4 | 6634 | Silent Mutation | CCC,CCT | P,P 2193 | NP_056150.1 | |
XM_011538080.2 | 6634 | Silent Mutation | CCC,CCT | P,P 2205 | XP_011536382.1 | |
XM_011538081.2 | 6634 | Silent Mutation | CCC,CCT | P,P 2204 | XP_011536383.1 | |
XM_011538082.2 | 6634 | Silent Mutation | CCC,CCT | P,P 2195 | XP_011536384.1 | |
XM_017019090.1 | 6634 | Silent Mutation | CCC,CCT | P,P 2192 | XP_016874579.1 |