RNASEH2C ribonuclease H2 subunit C

Information
Symbol
RNASEH2C
Type
protein-coding
Description
ribonuclease H2 subunit C
Entrez Gene ID
84153
Genome
hg19
Position
chr11:65,485,144-65,488,269
Genome
hg38
Position
chr11:65,717,673-65,720,798
MIM
610330 OMIM
HGNC
HGNC:24116 HGNC
Ensembl
ENSG00000172922 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 10
Benign 0 30
Likely benign 0 332
Conflicting classifications of pathogenicity 0 14
Uncertain significance 0 348
Ranking
ClinVar
0
0
64
640
8
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
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 AGS3
SYNONYM AYP1
MIM 610330 OMIM
HGNC HGNC:24116 HGNC
Ensembl ENSG00000172922 Ensembl
AllianceGenome HGNC:24116
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000527610.1 hg38 chr11 65,719,721 65,720,801 1,081
ENST00000308418.10 hg38 chr11 65,717,673 65,720,798 3,126
ENST00000308418.10 hg19 chr11 65,485,144 65,488,269 3,126
ENST00000527610.1 hg19 chr11 65,487,192 65,488,272 1,081
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