- databases for immunodeficiency-causing variations
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FASLGbase
Variation registry for Autoimmune lymphoproliferative syndrome, type 1B (ALPS1B)
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ADAbase
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RASGRP2base
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SERPING1base
SH2D1Abase
SLC35C1base
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STX11base
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TAZbase
TCN2base
TLR3base
TMC6base
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TNFRSF13Bbase
TYK2base
UNC13Dbase
UNC93B1base
UNGbase
WASbase
ZAP70base
FASLGbase mutation types
FASLGbase mutation types
The number of analyzed patients
Missense
1
Deletion inframe
1
Total
2
The number of unrelated patients
Missense
1
Deletion inframe
1
Total
2
This site is updated by
Gerard Schaafsma
© Protein Structure and Bioinformatics, Lund University, 2017
Last modified 17.04.2024
