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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:
PEX10
& Disease:
SPAX
, 6 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
1027530
PEX10
c.496del
p.Val166fs (p.V166fs)
NM_002617.4
M
Del
P
2
+
3
PEX10
c.496delG
--
NM_153818.2
Del
P
2
+
3
PEX10
c.496del
p.Val166fs (p.V166fs)
NM_001374425.1
Del
P
2
+
3
PEX10
c.64del
p.Val22fs (p.V22fs)
NM_001374426.1
Del
P
2
+
3
PEX10
c.64del
p.Val22fs (p.V22fs)
NM_001374427.1
Del
P
2
+
3
PEX10
c.496del
p.Val166fs (p.V166fs)
NM_153818.2
Del
P
2
+
3
6 Results, 20 per Page
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