Product Details

SNP ID
rs79455213
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:29672507 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGTCAGAAAGGCCATTTATTTA[C/T]GTTTCAAGATGCTCACTGCCTCCTT
Phenotype
MIM: 159465 MIM: 612192
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MOG PubMed Links

Gene Details

Gene
MOG
Gene Name
myelin oligodendrocyte glycoprotein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008228.2 1570 Intron NP_001008229.1
NM_001008229.2 1570 Intron NP_001008230.1
NM_001170418.1 1570 Intron NP_001163889.1
NM_002433.4 1570 Intron NP_002424.3
NM_206809.3 1570 Intron NP_996532.2
NM_206810.3 1570 Intron NP_996533.2
NM_206811.3 1570 Intron NP_996534.2
NM_206812.3 1570 Intron NP_996535.2
NM_206814.5 1570 Intron NP_996537.3
XM_005249131.3 1570 Intron XP_005249188.1
Gene
ZFP57
Gene Name
ZFP57 zinc finger protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001109809.2 1570 Missense Mutation CAT,CGT H535R NP_001103279.2
XM_006715087.3 1570 Missense Mutation CAT,CGT H463R XP_006715150.1
XM_011514570.2 1570 Missense Mutation CAT,CGT H535R XP_011512872.1

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