Genomic variant #0000046821

Individual ID 00024255
Chromosome 12
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6219696_6219697delinsG
DNA change (hg38) g.6110530_6110531delinsG
Published as -
ISCN -
DB-ID VWF_000019 See all 7 reported entries
Variant remarks -
Reference PubMed: Corrales et al., 2009
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Daniel J Hampshire




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

ClassClinical     

Protein     

Predict/MutationTaster     

Predict/PolyPhen     

Predict/SIFT     
VWF NM_000552.3 +?/+? 5 c.375_376delinsC r.(?) EAHAD-CFDB: +? p.(Tyr126Thrfs*49) - - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024249 DNA PCR;SEQ - - VWF 3 Daniel J Hampshire