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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:
ASTN2
& Disease:
H-CK
, 3 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
291311
ASTN2
c.2806+26663TA[4]
--
NM_001365068.1
M
MS
P
2
+
0
ASTN2
c.2653+26663TA[4]
--
NM_014010.5
MS
P
2
+
0
ASTN2
c.2794+26663TA[4]
--
NM_001365069.1
MS
P
2
+
0
3 Results, 20 per Page
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