Product Details

SNP ID
rs148627056
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:155612511 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTCTTGTCTGCCCCTTGTCCTTG[C/G]GTGGGAGCCTGGGCCTGCGACCCGA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
MSTO1 PubMed Links

Gene Details

Gene
MSTO1
Gene Name
misato 1, mitochondrial distribution and morphology regulator
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256532.1 994 Missense Mutation CGT,GGT R303G NP_001243461.1
NM_001256533.1 994 Missense Mutation CGT,GGT R303G NP_001243462.1
NM_018116.3 994 Missense Mutation CGT,GGT R303G NP_060586.2
XM_006711421.1 994 Missense Mutation CGT,GGT R248G XP_006711484.1
XM_006711423.2 994 Missense Mutation CGT,GGT R125G XP_006711486.1
XM_011509695.1 994 Missense Mutation CGT,GGT R303G XP_011507997.1
XM_011509696.1 994 Missense Mutation CGT,GGT R303G XP_011507998.1
XM_011509697.1 994 Missense Mutation CGT,GGT R303G XP_011507999.1
XM_011509698.1 994 Missense Mutation CGT,GGT R303G XP_011508000.1
XM_011509699.1 994 Missense Mutation CGT,GGT R303G XP_011508001.1
XM_011509700.1 994 Missense Mutation CGT,GGT R303G XP_011508002.1
XM_011509701.1 994 Missense Mutation CGT,GGT R303G XP_011508003.1
XM_011509702.1 994 Intron XP_011508004.1
XM_011509703.1 994 Missense Mutation CGT,GGT R248G XP_011508005.1
XM_011509704.1 994 Missense Mutation CGT,GGT R248G XP_011508006.1
XM_011509705.1 994 Missense Mutation CGT,GGT R248G XP_011508007.1
XM_011509706.1 994 Missense Mutation CGT,GGT R126G XP_011508008.1
XM_011509707.1 994 Missense Mutation CGT,GGT R125G XP_011508009.1
XM_011509708.1 994 Missense Mutation CGT,GGT R125G XP_011508010.1
XM_011509709.2 994 Missense Mutation CGT,GGT R303G XP_011508011.1
XM_017001603.1 994 Missense Mutation CGT,GGT R126G XP_016857092.1
XM_017001604.1 994 Missense Mutation CGT,GGT R126G XP_016857093.1
XM_017001605.1 994 Missense Mutation CGT,GGT R126G XP_016857094.1
XM_017001606.1 994 Missense Mutation CGT,GGT R125G XP_016857095.1
XM_017001607.1 994 Missense Mutation CGT,GGT R125G XP_016857096.1
XM_017001608.1 994 Missense Mutation CGT,GGT R125G XP_016857097.1
XM_017001609.1 994 Missense Mutation CGT,GGT R125G XP_016857098.1
XM_017001610.1 994 Missense Mutation CGT,GGT R122G XP_016857099.1
XM_017001611.1 994 Missense Mutation CGT,GGT R122G XP_016857100.1
XM_017001612.1 994 Missense Mutation CGT,GGT R125G XP_016857101.1
XM_017001613.1 994 Missense Mutation CGT,GGT R122G XP_016857102.1
XM_017001614.1 994 Missense Mutation CGT,GGT R125G XP_016857103.1
XM_017001615.1 994 Missense Mutation CGT,GGT R122G XP_016857104.1
XM_017001616.1 994 Intron XP_016857105.1

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