Genomic variant #0000000912

Chromosome 22
Allele Unknown
Affects function (reported) Affects function
Affects function (concluded) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.30070880C>T
Published as -
GERP 4.500
Segregation -
DB-ID NF2_000008
dbSNP ID rs74315504
Frequency -
Sources ; clinvar;
Reference 7913580
Variant remarks -
Genetic origin -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

Protein     

GVS function     

Position     

Exon     

PolyPhen     

RNA change     

SIFT     
NF2 NM_000268.3 +/+ c.1396C>T p.(Arg466*) stop_gained - 13/16 - r.(?) -


ClinVar @ MSeqDR

404358
MedGen:C0027832,OMIM:101000,Orphanet:ORPHA637,SNOMED CT:92503002
Neurofibromatosis, type 2
HGVS variant names NC 000022.10:g.30070880C>G
criteria provided, single submitter
Clinical Significance
single nucleotide variant
SO:0001483
Gene symbol:Gene id. NF2:4771
SO:0001583|missense variant,SO:0001627|intron variant
1
dbSNP ID 74315504
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

18334
MedGen:C0027832,OMIM:101000,Orphanet:ORPHA637,SNOMED CT:92503002
Neurofibromatosis, type 2
HGVS variant names NC 000022.10:g.30070880C>T
criteria provided, single submitter
Clinical Significance
single nucleotide variant
SO:0001483
OMIM Allelic Variant:607379.0014
Gene symbol:Gene id. NF2:4771
SO:0001587|nonsense,SO:0001627|intron variant
1
dbSNP ID 74315504
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

variation_namechromseq_region_startseq_region_endallele_stringminor_alleleminor_allele_freqvariation_setPhenotype_description
rs74315504223007088030070880C/TOMIM phenotype variantsNEUROFIBROMATOSIS, TYPE II
rs74315504223007088030070880C/TOMIM phenotype variantsNeurofibromatosis, type 2
CM941106223007088030070880HGMD_MUTATIONHGMD-PUBLIC variantsAnnotated by HGMD but no phenotype description is publicly available