Product Details

SNP ID
rs201393187
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:82759374 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAATAGAAAGTGACATGTTTTGGCA[C/T]TGAAATGCCATTATGTACCTTTAGA
Phenotype
MIM: 612675
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FSD2 PubMed Links

Gene Details

Gene
FSD2
Gene Name
fibronectin type III and SPRY domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007122.3 2407 Missense Mutation ATG,GTG M742V NP_001007123.1
NM_001281805.1 2407 Missense Mutation ATG,GTG M697V NP_001268734.1
NM_001281806.1 2407 Missense Mutation ATG,GTG M697V NP_001268735.1
XM_005272425.4 2407 Missense Mutation ATG,GTG M742V XP_005272482.1
XM_011521235.2 2407 Missense Mutation ATG,GTG M665V XP_011519537.1
XM_017021924.1 2407 Intron XP_016877413.1
Gene
SCARNA15
Gene Name
small Cajal body-specific RNA 15
There are no transcripts associated with this gene.

Gene
SNHG21
Gene Name
small nucleolar RNA host gene 21
There are no transcripts associated with this gene.

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