Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCGGCACGAGGGCAACCGACTGTAC[C/T]GCGAGCGCCAGGTGGAGGCGGCACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LONRF3 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 |
LONRF3 - LON peptidase N-terminal domain and ring finger 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031855.2 | 930 | Missense Mutation | CGC,TGC | R,C 255 | NP_001027026.1 | |
NM_001289109.1 | 930 | Intron | NP_001276038.1 | |||
NM_024778.5 | 930 | Missense Mutation | CGC,TGC | R,C 255 | NP_079054.3 | |
XM_005262476.2 | 930 | Missense Mutation | CGC,TGC | R,C 255 | XP_005262533.1 | |
XM_011531398.2 | 930 | Missense Mutation | CGC,TGC | R,C 255 | XP_011529700.1 | |
XM_017029845.1 | 930 | Missense Mutation | CGC,TGC | R,C 255 | XP_016885334.1 |