ISTH mutations

Back to Master table   Advanced search

Search for:     Any field VWD Classification Exon No Nucleotide Change Amino Acid Substitution Alleles Functional Studies Country Laboratory Comments Reference Ref.   Contains Equals Starts with ... More than ... Less than ... Equal or more than ... Equal or less than ... Empty

Details found: 3 Page 1 of 1

Records Per Page: 10 20 30 50 100 500

Exon No	Alleles	VWD Classification	Nucleotide Change	Amino Acid Substitution	Functional Studies	Country	Laboratory	Comments	Ref.
26	110	Type 1	3467C>T	T1156M	No	Spain	Casana		Casaņa et al, 2001
26	20	Type 1	3467C>T	T1156M	No	Sweden	Holmberg
26	200	Type 3	3467C>T	T1156M	No	Spain	Vidal	Compound heterozygous mutation found in trans with mutation c.7730-1G>C. VWF:Ag More ...