UNC93B1 (NM_030930.4) sequence variants
(IIAE1, UNC93, UNC93B, Unc-93B1)

Editor(s): Marie-louise FRÉMOND   Clémence DAVID   

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Total current number of sequence variants for UNC93B1 : 32

*Name as first published or submitted to Infevers. May be different from the HGVS edited protein and sequence names.

** If you have new data: please send us a re-evaluation proposal here

HGVS sequence name
HGVS protein name
Usual name*
Classification**
Status**
Simple variant
Complex alleles
exon 2
c.145_147dup
p.(Glu49dup)
E49dup
PathogenicTo be validated
 2025-08-11 
exon 2
c.148C>A
p.(Arg50Ser)
R50S
Likely benignTo be validated
 2025-08-11 
exon 2
c.193C>G
p.(Leu65Val)
L65V
Likely benignTo be validated
 2025-08-11 
exon 3
c.275A>G
p.(Glu92Gly)
E92G
PathogenicTo be validated
 2025-08-11 
exon 3
c.278C>T
p.(Thr93Ile)
T93I
PathogenicTo be validated
 2025-08-11 
exon 3
c.349G>T
p.(Val117Leu)
V117L
PathogenicTo be validated
 2025-08-11 
exon 3
c.385C>A
p.(Leu129Ile)
L129I
Likely benignTo be validated
 2025-08-11 
exon 4
c.470G>A
p.(Arg157His) 
R157H
Likely benignTo be validated
 2025-08-11 
exon 4
c.491C>T
p.(Ser164Leu)
S164L
Likely benignTo be validated
 2025-08-11 
exon 5
c.626C>T
p.(Pro209Leu)
P209L
Likely benignTo be validated
 2025-08-11 
exon 7
c.891C>G
p.(Phe297Leu)
F297L
Likely benignTo be validated
 2025-08-11 
exon 7
c.895G>T
p.(Ala299Ser)
A299S
Likely benignTo be validated
 2025-08-11 
exon 8
c.940A>G
p.(Thr314Ala)
T314A
PathogenicTo be validated
 2025-08-11 
exon 8
c.951C>G
p.Ile317Met
I317M
PathogenicTo be validated
 2025-08-01 
exon 8
c.973G>T
p.Gly325Cys
G325C
PathogenicTo be validated
 2025-08-01 
exon 8
c.989T>G
p.Leu330Arg
L330R
PathogenicTo be validated
 2025-08-01 
exon 8
c.1006C>T
p.(Arg336Cys)
R336C
PathogenicTo be validated
 2025-08-11 
exon 8
c.1007G>T
p.(Arg336Leu)
R336L
PathogenicTo be validated
 2025-08-11 
exon 9
c.1138G>A
p.(Val380Met)
V380M
Likely benignTo be validated
 2025-08-11 
exon 9
c.1163C>T
p.(Ala388Val)
A388V
Likely benignTo be validated
 2025-08-11 
exon 9
c.1210C>T
p.(Pro404Ser)
P404S
Likely benignTo be validated
 2025-08-11 
exon 10
c.1398A>C
p.Arg466Ser
R466S
PathogenicTo be validated
 2025-08-01 
exon 10
c.1453G>A
p.(Val485Met)
V485M
Likely benignTo be validated
 2025-08-11 
exon 11
c.1574_1575delinsCT
p.Arg525Pro
R525P
PathogenicTo be validated
 2025-08-01 
exon 11
c.1594C>A
p.(Pro532Thr)
P532T
Likely benignTo be validated
 2025-08-11 
exon 11
c.1661G>A
p.(Gly554Asp)
G554D
Likely benignTo be validated
 2025-08-11 
exon 11
c.1720G>C
p.(Glu574Gln) 
E574Q
Likely benignTo be validated
 2025-08-11 
exon 11
c.1724C>A
p.(Pro575His)
P575H
Likely benignTo be validated
 2025-08-11 
exon 11
c.1768G>A
p.(Gly590Arg)
G590R
Likely benignTo be validated
 2025-08-11 
exon 11
c.1768G>T
p.(Gly590Trp)
G590W
Likely benignTo be validated
 2025-08-11 
exon 11
c.1772G>A
p.(Gly591Glu)
G591E
Likely benignTo be validated
 2025-08-11 
exon 11
c.1777G>A
p.(Gly593Arg)
G593R
Likely benignTo be validated
 2025-08-11