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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:
CCNH
& Disease:
Basal Cell Carcinoma, Multiple
, 8 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
411714
CCNH
c.934-18626_934-18622del
--
NM_001364075.2
Del
P
3
+
3
411713
CCNH
c.933+5522G>A
--
NM_001364075.2
SNV
P
3
+
2
565648
CCNH
c.933+18103G>A
--
NM_001364075.2
SNV
P
3
+
1
213660
CCNH
c.933+18532G>A
--
NM_001364075.2
SNV
P
3
+
1
464870
CCNH
c.934-18669G>C
--
NM_001364075.2
SNV
P
3
+
1
1078218
CCNH
c.934-36525T>C
--
NM_001364075.2
SNV
LB
3
+
0
931156
CCNH
c.933+8140C>T
--
NM_001364075.2
SNV
LP
2
+
0
1691334
CCNH
c.933+16531A>T
--
NM_001364075.2
SNV
VUS
3
+
0
8 Results, 20 per Page
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