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GGAAAGGACATGCTTTTGTTTCCCA[C/T]CGACTGTTTAATTTTTTTGGCTGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 605960 MIM: 182891 | ||||||||||||||||||||
Literature Links: |
EXOSC10 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 |
EXOSC10 - exosome component 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001998.2 | 2663 | Missense Mutation | ATG,GTG | M,V 862 | NP_001001998.1 | |
NM_002685.3 | 2663 | Missense Mutation | ATG,GTG | M,V 837 | NP_002676.1 | |
XM_005263475.2 | 2663 | Missense Mutation | ATG,GTG | M,V 867 | XP_005263532.2 | |
XM_017001494.1 | 2663 | Missense Mutation | ATG,GTG | M,V 451 | XP_016856983.1 | |
XM_017001495.1 | 2663 | Missense Mutation | ATG,GTG | M,V 446 | XP_016856984.1 | |
XM_017001496.1 | 2663 | Missense Mutation | ATG,GTG | M,V 435 | XP_016856985.1 | |
XM_017001497.1 | 2663 | Missense Mutation | ATG,GTG | M,V 430 | XP_016856986.1 |
SRM - spermidine synthase | ||||||
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There are no transcripts associated with this gene. |