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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:
HRAS
& Disease:
Spermatocytoma
, 4 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
12601
HRAS
c.181C>A
p.Gln61Lys (p.Q61K)
NM_005343.4
M
SNV
P
5
+
3
HRAS
c.181C>A
p.Gln61Lys (p.Q61K)
NM_001130442.3
SNV
P
5
+
3
HRAS
c.-139C>A
--
NM_001318054.2
SNV
P
5
+
3
HRAS
c.181C>A
p.Gln61Lys (p.Q61K)
NM_176795.5
SNV
P
5
+
3
4 Results, 20 per Page
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