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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:
MYD88
& Disease:
CLL
, 8 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
37055
MYD88
c.755T>C
p.Leu252Pro (p.L252P)
NM_002468.5
M
SNV
P
8
+
5
MYD88
c.439T>C
p.Ter147Arg (p.X147R)
NM_001172566.2
SNV
P
8
+
5
MYD88
c.779T>C
p.Leu260Pro (p.L260P)
NM_001172567.2
SNV
P
8
+
5
MYD88
c.620T>C
p.Leu207Pro (p.L207P)
NM_001172568.2
SNV
P
8
+
5
MYD88
c.574T>C
p.Ter192Arg (p.X192R)
NM_001172569.3
SNV
P
8
+
5
MYD88
c.736T>C
p.Ter246Arg (p.X246R)
NM_001365876.1
SNV
P
8
+
5
MYD88
c.601T>C
p.Ter201Arg (p.X201R)
NM_001365877.1
SNV
P
8
+
5
MYD88
c.712T>C
p.Ter238Arg (p.X238R)
NM_001374787.1
SNV
P
8
+
5
8 Results, 20 per Page
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