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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:
MYH10
& Disease:
Hypertelorism
, 4 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
625873
MYH10
c.4505G>C
p.Arg1502Pro (p.R1502P)
NM_001256012.3
M
SNV
P
4
+
0
MYH10
c.4439G>C
p.Arg1480Pro (p.R1480P)
NM_001256095.2
SNV
P
4
+
0
MYH10
c.4442G>C
p.Arg1481Pro (p.R1481P)
NM_001375266.1
SNV
P
4
+
0
MYH10
c.4412G>C
p.Arg1471Pro (p.R1471P)
NM_005964.5
SNV
P
4
+
0
4 Results, 20 per Page
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