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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:
GNB1
& Disease:
Hypothyroidism
, 3 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
208722
GNB1
c.239T>C
p.Ile80Thr (p.I80T)
NM_002074.5
M
SNV
P
8
+
7
GNB1
c.-62T>C
--
NM_001282538.2
SNV
P
8
+
7
GNB1
c.239T>C
p.Ile80Thr (p.I80T)
NM_001282539.2
SNV
P
8
+
7
3 Results, 20 per Page
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