CRYGC crystallin gamma C

Information
Symbol
CRYGC
Type
protein-coding
Description
crystallin gamma C
Entrez Gene ID
1420
Genome
hg19
Position
chr2:208,992,861-208,994,552
Genome
hg38
Position
chr2:208,128,137-208,129,828
MIM
123680 OMIM
HGNC
HGNC:2410 HGNC
Ensembl
ENSG00000163254 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 1 28
Likely pathogenic 0 10
Benign 10 24
Likely benign 0 26
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 66
Ranking
ClinVar
0
0
22
118
10
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 CCL
SYNONYM CRYG3
SYNONYM CTRCT2
MIM 123680 OMIM
HGNC HGNC:2410 HGNC
Ensembl ENSG00000163254 Ensembl
AllianceGenome HGNC:2410
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000282141.4 hg38 chr2 208,128,137 208,129,828 1,692
ENST00000282141.4 hg19 chr2 208,992,861 208,994,552 1,692
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