Product Details

SNP ID
rs199949744
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:40392166 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGGAGTGGCTGCGTTTGGCCTTG[A/C]CCTCCAACGGCAAGGGGAGCAGGCT
Phenotype
MIM: 612808
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
LRFN2 PubMed Links

Gene Details

Gene
LRFN2
Gene Name
leucine rich repeat and fibronectin type III domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020737.2 3558 Missense Mutation NP_065788.1
XM_011514761.2 3558 Missense Mutation XP_011513063.1
XM_011514762.2 3558 Missense Mutation XP_011513064.1
XM_017011110.1 3558 Missense Mutation XP_016866599.1
XM_017011111.1 3558 Intron XP_016866600.1

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