RFWD3 ring finger and WD repeat domain 3

Information
Symbol
RFWD3
Type
protein-coding
Description
ring finger and WD repeat domain 3
Entrez Gene ID
55159
Genome
hg19
Position
chr16:74,655,297-74,700,775
Genome
hg38
Position
chr16:74,621,399-74,666,877
MIM
614151 OMIM
HGNC
HGNC:25539 HGNC
Ensembl
ENSG00000168411 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 0 42
Likely benign 0 334
Conflicting classifications of pathogenicity 0 14
Uncertain significance 0 544
Ranking
ClinVar
0
0
78
840
4
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 :
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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 FANCW
SYNONYM RNF201
MIM 614151 OMIM
HGNC HGNC:25539 HGNC
Ensembl ENSG00000168411 Ensembl
AllianceGenome HGNC:25539
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361070.9 hg38 chr16 74,621,399 74,666,877 45,479
ENST00000571750.5 hg38 chr16 74,623,429 74,666,870 43,442
ENST00000361070.9 hg19 chr16 74,655,297 74,700,775 45,479
ENST00000571750.5 hg19 chr16 74,657,327 74,700,768 43,442
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