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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:
DSD
, 4 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
929443
MYRF
c.2572+1G>A
--
NM_001127392.3
M
SNV
P
2
+
1
MYRF
c.2467+1G>A
--
NM_013279.4
SNV
P
2
+
1
1202589
MYRF
c.313A>G
p.Asn105Asp (p.N105D)
NM_001127392.3
M
SNV
LP
1
+
0
MYRF
c.286A>G
p.Asn96Asp (p.N96D)
NM_013279.4
SNV
LP
1
+
0
4 Results, 20 per Page
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