Product Details

SNP ID
rs1659831
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:138597161 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATTCAGATACTCCATCTCATACTT[C/T]AGTTTCTCTTGGTCTGTGTTCTTGA
Phenotype
MIM: 611700
Polymorphism
C/T, 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 Intron NP_001132928.1
NM_174959.3 Intron NP_777619.1
XM_005250143.3 Intron XP_005250200.1
XM_011515797.2 Intron XP_011514099.1
XM_017011746.1 Intron XP_016867235.1
XM_017011747.1 Intron XP_016867236.1
XM_017011748.1 Intron XP_016867237.1

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