RWDD2B RWD domain containing 2B

Information
Symbol
RWDD2B
Type
protein-coding
Description
RWD domain containing 2B
Entrez Gene ID
10069
Genome
hg19
Position
chr21:30,376,705-30,391,670
Genome
hg38
Position
chr21:29,004,384-29,019,349
MIM
617843 OMIM
HGNC
HGNC:1302 HGNC
Ensembl
ENSG00000156253 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
38
0
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 C21orf6
SYNONYM GL011
MIM 617843 OMIM
HGNC HGNC:1302 HGNC
Ensembl ENSG00000156253 Ensembl
AllianceGenome HGNC:1302
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000493196.2 hg38 chr21 29,004,384 29,019,349 14,966
ENST00000493196.2 hg19 chr21 30,376,705 30,391,670 14,966
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