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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:
FGFR3
& Disease:
KERSEB
, 10 results
Search
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
16332
FGFR3
c.742C>T
p.Arg248Cys (p.R248C)
NM_000142.5
M
SNV
P
28
+
26
FGFR3
c.742C>T
p.Arg248Cys (p.R248C)
NM_001163213.2
SNV
P
28
+
26
FGFR3
c.742C>T
p.Arg248Cys (p.R248C)
NM_001354809.2
SNV
P
28
+
26
FGFR3
c.742C>T
p.Arg248Cys (p.R248C)
NM_001354810.2
SNV
P
28
+
26
FGFR3
c.742C>T
p.Arg248Cys (p.R248C)
NM_022965.4
SNV
P
28
+
26
16339
FGFR3
c.746C>G
p.Ser249Cys (p.S249C)
NM_000142.5
M
SNV
P
22
+
13
FGFR3
c.746C>G
p.Ser249Cys (p.S249C)
NM_001163213.2
SNV
P
22
+
13
FGFR3
c.746C>G
p.Ser249Cys (p.S249C)
NM_001354809.2
SNV
P
22
+
13
FGFR3
c.746C>G
p.Ser249Cys (p.S249C)
NM_001354810.2
SNV
P
22
+
13
FGFR3
c.746C>G
p.Ser249Cys (p.S249C)
NM_022965.4
SNV
P
22
+
13
10 Results, 20 per Page
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