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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Mutation Direct
Effortless mutation search and display tool
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Search criteria:
Gene:
CARD10
& Disease:
POAG
, 5 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
224912
CARD10
c.635G>A
p.Arg212His (p.R212H)
NM_014550.4
M
SNV
VUS
1
+
1
224913
CARD10
c.983C>T
p.Ala328Val (p.A328V)
NM_014550.4
M
SNV
VUS
1
+
1
224914
CARD10
c.1024G>A
p.Val342Met (p.V342M)
NM_014550.4
M
SNV
VUS
1
+
1
224915
CARD10
c.1210C>T
p.Arg404Trp (p.R404W)
NM_014550.4
M
SNV
VUS
1
+
1
224916
CARD10
c.2485C>T
p.Arg829Trp (p.R829W)
NM_014550.4
M
SNV
VUS
1
+
1
5 Results, 20 per Page
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