Genomic variant #0000046827

Individual ID 00024258
Chromosome 12
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.6219651C>A
DNA change (hg38) g.6110485C>A
Published as -
ISCN -
DB-ID VWF_000025
Variant remarks Functional analysis: rVWF expression in COS-7 cells
Reference PubMed: Baronciani et al., 2003; PubMed: Baronciani et al., 2008
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.421G>T r.(?) EAHAD-CFDB: +? p.(Asp141Tyr) - - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024252 DNA PCR;SEQ;SSCA - - VWF 2 Daniel J Hampshire