Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611987 MIM: 601426 | ||||||||||||||||||||
Literature Links: |
MRPS25 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 |
MRPS25 - mitochondrial ribosomal protein S25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022497.4 | 2143 | Intron | NP_071942.1 |
NR2C2 - nuclear receptor subfamily 2 group C member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291694.1 | 2143 | Missense Mutation | GCC,GTC | A,V 594 | NP_001278623.1 | |
NM_003298.4 | 2143 | Missense Mutation | GCC,GTC | A,V 613 | NP_003289.2 | |
XM_011534058.2 | 2143 | Missense Mutation | GCC,GTC | A,V 646 | XP_011532360.1 | |
XM_011534059.2 | 2143 | Missense Mutation | GCC,GTC | A,V 646 | XP_011532361.1 | |
XM_011534061.2 | 2143 | Missense Mutation | GCC,GTC | A,V 646 | XP_011532363.1 | |
XM_011534063.2 | 2143 | Missense Mutation | GCC,GTC | A,V 627 | XP_011532365.1 | |
XM_011534064.2 | 2143 | Missense Mutation | GCC,GTC | A,V 613 | XP_011532366.1 | |
XM_011534065.2 | 2143 | Missense Mutation | GCC,GTC | A,V 613 | XP_011532367.1 | |
XM_011534066.2 | 2143 | Missense Mutation | GCC,GTC | A,V 613 | XP_011532368.1 | |
XM_017007118.1 | 2143 | Missense Mutation | GCC,GTC | A,V 646 | XP_016862607.1 | |
XM_017007119.1 | 2143 | Missense Mutation | GCC,GTC | A,V 646 | XP_016862608.1 | |
XM_017007120.1 | 2143 | Missense Mutation | GCC,GTC | A,V 594 | XP_016862609.1 |