Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGCGCACCTCCCAGTAGTGGTGCC[C/T]GGCCTGGAAGCTCTGGGCACATTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611844 | ||||||||||||||||||||
Literature Links: |
MRPL38 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 |
MRPL38 - mitochondrial ribosomal protein L38 | ||||||
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There are no transcripts associated with this gene. |
TRIM65 - tripartite motif containing 65 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256124.1 | 1181 | Missense Mutation | AGG,GGG | R,G 360 | NP_001243053.1 | |
NM_173547.3 | 1181 | Missense Mutation | AGG,GGG | R,G 382 | NP_775818.2 | |
XM_006721760.3 | 1181 | Missense Mutation | AGG,GGG | R,G 395 | XP_006721823.1 | |
XM_006721761.3 | 1181 | Missense Mutation | AGG,GGG | R,G 373 | XP_006721824.1 | |
XM_011524499.2 | 1181 | Intron | XP_011522801.1 | |||
XM_011524500.2 | 1181 | Intron | XP_011522802.1 | |||
XM_011524501.2 | 1181 | Intron | XP_011522803.1 | |||
XM_011524502.2 | 1181 | Intron | XP_011522804.1 | |||
XM_011524503.2 | 1181 | Intron | XP_011522805.1 | |||
XM_017024343.1 | 1181 | Intron | XP_016879832.1 | |||
XM_017024344.1 | 1181 | UTR 3 | XP_016879833.1 |