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GTCATTCACAAAGGCCTCCACGATG[A/G]CGGGGGTGATCTCCTCCACGTCCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612600 MIM: 612895 | ||||||||||||||||||||
Literature Links: |
MRM3 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 |
MRM3 - mitochondrial rRNA methyltransferase 3 | ||||||
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There are no transcripts associated with this gene. |
NXN - nucleoredoxin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001205319.1 | 1153 | Missense Mutation | GCC,GTC | A,V 308 | NP_001192248.1 | |
NM_022463.4 | 1153 | Missense Mutation | GCC,GTC | A,V 416 | NP_071908.2 | |
XM_005256756.4 | 1153 | Missense Mutation | GCC,GTC | A,V 356 | XP_005256813.1 | |
XM_005256758.3 | 1153 | Missense Mutation | GCC,GTC | A,V 303 | XP_005256815.1 | |
XM_017024949.1 | 1153 | Intron | XP_016880438.1 |