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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:
MYRF
& Disease:
NNO1
, 2 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
635185
MYRF
c.3361del
p.Arg1121fs (p.R1121fs)
NM_001127392.3
M
Del
P
1
+
1
MYRF
c.3241del
p.Arg1081fs (p.R1081fs)
NM_013279.4
Del
P
1
+
1
2 Results, 20 per Page
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