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TGCTGCAGGAGGAGCTCTTCCTCTA[C/T]GGGCTCCTCAGCCTCTGGCCCACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611987 MIM: 609511 | ||||||||||||||||||||
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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There are no transcripts associated with this gene. |
RBSN - rabenosyn, RAB effector | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001302378.1 | 2659 | Missense Mutation | ATA,GTA | I,V 734 | NP_001289307.1 | |
NM_022340.3 | 2659 | Missense Mutation | ATA,GTA | I,V 734 | NP_071735.2 | |
XM_005265384.4 | 2659 | Missense Mutation | ATA,GTA | I,V 734 | XP_005265441.1 | |
XM_005265385.4 | 2659 | Missense Mutation | ATA,GTA | I,V 734 | XP_005265442.1 | |
XM_011534001.2 | 2659 | Missense Mutation | ATA,GTA | I,V 646 | XP_011532303.1 | |
XM_017007023.1 | 2659 | Missense Mutation | ATA,GTA | I,V 734 | XP_016862512.1 | |
XM_017007024.1 | 2659 | Missense Mutation | ATA,GTA | I,V 645 | XP_016862513.1 | |
XM_017007025.1 | 2659 | Missense Mutation | ATA,GTA | I,V 645 | XP_016862514.1 | |
XM_017007026.1 | 2659 | Missense Mutation | ATA,GTA | I,V 549 | XP_016862515.1 | |
XM_017007027.1 | 2659 | Missense Mutation | ATA,GTA | I,V 495 | XP_016862516.1 | |
XM_017007028.1 | 2659 | Missense Mutation | ATA,GTA | I,V 495 | XP_016862517.1 |