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Search Thermo Fisher Scientific
CACGATGGCTTCTCTGGGGTAGGCG[C/T]GAAGGCGGCAGAGCTGCTACAAGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
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Literature Links: |
MSTO1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MSTO1 - misato 1, mitochondrial distribution and morphology regulator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256532.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | NP_001243461.1 | |
NM_001256533.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | NP_001243462.1 | |
NM_018116.3 | 815 | Missense Mutation | GCG,GTG | A,V 243 | NP_060586.2 | |
XM_006711421.1 | 815 | Missense Mutation | GCG,GTG | A,V 188 | XP_006711484.1 | |
XM_006711423.2 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_006711486.1 | |
XM_011509695.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011507997.1 | |
XM_011509696.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011507998.1 | |
XM_011509697.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011507999.1 | |
XM_011509698.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011508000.1 | |
XM_011509699.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011508001.1 | |
XM_011509700.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011508002.1 | |
XM_011509701.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011508003.1 | |
XM_011509702.1 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011508004.1 | |
XM_011509703.1 | 815 | Missense Mutation | GCG,GTG | A,V 188 | XP_011508005.1 | |
XM_011509704.1 | 815 | Missense Mutation | GCG,GTG | A,V 188 | XP_011508006.1 | |
XM_011509705.1 | 815 | Missense Mutation | GCG,GTG | A,V 188 | XP_011508007.1 | |
XM_011509706.1 | 815 | Missense Mutation | GCG,GTG | A,V 66 | XP_011508008.1 | |
XM_011509707.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_011508009.1 | |
XM_011509708.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_011508010.1 | |
XM_011509709.2 | 815 | Missense Mutation | GCG,GTG | A,V 243 | XP_011508011.1 | |
XM_017001603.1 | 815 | Missense Mutation | GCG,GTG | A,V 66 | XP_016857092.1 | |
XM_017001604.1 | 815 | Missense Mutation | GCG,GTG | A,V 66 | XP_016857093.1 | |
XM_017001605.1 | 815 | Missense Mutation | GCG,GTG | A,V 66 | XP_016857094.1 | |
XM_017001606.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_016857095.1 | |
XM_017001607.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_016857096.1 | |
XM_017001608.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_016857097.1 | |
XM_017001609.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_016857098.1 | |
XM_017001610.1 | 815 | Missense Mutation | GCG,GTG | A,V 62 | XP_016857099.1 | |
XM_017001611.1 | 815 | Missense Mutation | GCG,GTG | A,V 62 | XP_016857100.1 | |
XM_017001612.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_016857101.1 | |
XM_017001613.1 | 815 | Missense Mutation | GCG,GTG | A,V 62 | XP_016857102.1 | |
XM_017001614.1 | 815 | Missense Mutation | GCG,GTG | A,V 65 | XP_016857103.1 | |
XM_017001615.1 | 815 | Missense Mutation | GCG,GTG | A,V 62 | XP_016857104.1 | |
XM_017001616.1 | 815 | Missense Mutation | GCG,GTG | A,V 66 | XP_016857105.1 |