RFTN2 raftlin family member 2

Information
Symbol
RFTN2
Type
protein-coding
Description
raftlin family member 2
Entrez Gene ID
130132
Genome
hg19
Position
chr2:198,432,948-198,540,311
Genome
hg38
Position
chr2:197,568,224-197,675,587
MIM
618215 OMIM
HGNC
HGNC:26402 HGNC
Ensembl
ENSG00000162944 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
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 :
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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 C2orf11
SYNONYM Raftlin-2
MIM 618215 OMIM
HGNC HGNC:26402 HGNC
Ensembl ENSG00000162944 Ensembl
AllianceGenome HGNC:26402
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000295049.9 hg38 chr2 197,568,224 197,675,587 107,364
ENST00000295049.9 hg19 chr2 198,432,948 198,540,311 107,364
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