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TCTTCTGATAGTGTTTCCCAGATTG[A/G]CTCCTTGATGTGTTCTGGTAACTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611976 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MRPS10 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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MRPS10 - mitochondrial ribosomal protein S10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018141.3 | 606 | Missense Mutation | CCA,TCA | P,S 187 | NP_060611.2 | |
XM_005249206.2 | 606 | Missense Mutation | CCA,TCA | P,S 186 | XP_005249263.1 | |
XM_011514724.2 | 606 | Missense Mutation | CCA,TCA | P,S 197 | XP_011513026.1 | |
XM_011514725.2 | 606 | Missense Mutation | CCA,TCA | P,S 196 | XP_011513027.1 | |
XM_017010996.1 | 606 | Missense Mutation | CCA,TCA | P,S 146 | XP_016866485.1 |