CNGA3 cyclic nucleotide gated channel subunit alpha 3

Information
Symbol
CNGA3
Type
protein-coding
Description
cyclic nucleotide gated channel subunit alpha 3
Entrez Gene ID
1261
Genome
hg19
Position
chr2:98,962,919-99,015,064
Genome
hg38
Position
chr2:98,346,456-98,398,601
MIM
600053 OMIM
HGNC
HGNC:2150 HGNC
Ensembl
ENSG00000144191 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 4 226
Likely pathogenic 0 176
Benign 0 46
Likely benign 0 336
Conflicting classifications of pathogenicity 0 118
not provided 1 0
Uncertain significance 0 518
Ranking
ClinVar
0
0
174
1,004
84
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CCNCa
SYNONYM ACHM2
SYNONYM CCNC1
SYNONYM CCNCalpha
SYNONYM CNCG3
SYNONYM CNG3
MIM 600053 OMIM
HGNC HGNC:2150 HGNC
Ensembl ENSG00000144191 Ensembl
AllianceGenome HGNC:2150
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000272602.7 hg38 chr2 98,346,456 98,398,601 52,146
ENST00000436404.6 hg38 chr2 98,346,188 98,397,344 51,157
ENST00000436404.6 hg19 chr2 98,962,651 99,013,807 51,157
ENST00000272602.7 hg19 chr2 98,962,919 99,015,064 52,146
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