Product Details

SNP ID
rs200673028
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:138596502 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAGACAGATGAGAAGAGACACAGG[A/G]CCCCCAGTATTGATGCACTCATAAG
Phenotype
MIM: 611700
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SVOPL PubMed Links

Gene Details

Gene
SVOPL
Gene Name
SVOP like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001139456.1 1073 Missense Mutation GCC,GTC A461V NP_001132928.1
NM_174959.3 1073 Missense Mutation GCC,GTC A309V NP_777619.1
XM_005250143.3 1073 Missense Mutation GCC,GTC A461V XP_005250200.1
XM_011515797.2 1073 Missense Mutation GCC,GTC A309V XP_011514099.1
XM_017011746.1 1073 Missense Mutation GCC,GTC A370V XP_016867235.1
XM_017011747.1 1073 Missense Mutation GCC,GTC A309V XP_016867236.1
XM_017011748.1 1073 Missense Mutation GCC,GTC A309V XP_016867237.1

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