Data Export Options:


UNIQUE (Without Patient Data) :
MULTIPLE (With Patient Data) :



  Search Results: 1 unique variant retrieved.



p.Tyr128Cys (Legacy AA No. 68)
Variant Type:
Point
Domain:
EGF1
Sequence Context:
TAT > TGT
Variant Effect:
Missense
Location:
Exon (5)
No of bases:
1
No. of patients reported:
7
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click here to see if there is the available information.

Patient Information : Show


Factor VII Variant Database