{{Rsnum
|rsid=137854556
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NF1
|position=31235729
|Gene_s=NF1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=613113
|variant=0022
|rsnum=137854556
}}{{ClinVar
|rsid=137854556
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=29562747
|CHROM=17
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=NF1:4763
|GENE_NAME=NF1
|GENE_ID=4763
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.29562747G>A; NC_000017.10:g.29562747G>C
|CLNSRC=UniProtKB (variants); OMIM Allelic Variant
|CLNSRCID=VAR_017555; 613113.0022
|CLNSIG=5
|CLNCUI=C0027831
|CLNDBN=not provided; Neurofibromatosis, type 1
|Disease=not provided; Neurofibromatosis
|CLNACC=RCV000059193.1; RCV000000381.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1109:C0027831:162200:636:92824003
}}{{PMID Auto
|PMID=10712197
|Title=Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain.
|OA=1
}}

{{PMID Auto
|PMID=15060124
|Title=Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain.
|OA=1
}}