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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:
F10
& Disease:
FA7D
, 3 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
311266
F10
c.-40C>T
--
NM_000504.4
M
SNV
LB
2
+
0
F10
c.-40C>T
--
NM_001312674.2
SNV
LB
2
+
0
F10
c.-40C>T
--
NM_001312675.2
SNV
LB
2
+
0
3 Results, 20 per Page
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