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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:
DCX
& Disease:
BH
, 10 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
1699053
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_001195553.2
M
Dup
P
2
+
3
DCX
c.722_725dup
p.Leu243fs (p.L243fs)
NM_000555.3
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_001369370.1
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_001369371.1
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_001369372.1
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_001369373.1
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_001369374.1
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_178151.3
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_178152.3
Dup
P
2
+
3
DCX
c.479_482dup
p.Leu162fs (p.L162fs)
NM_178153.3
Dup
P
2
+
3
10 Results, 20 per Page
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