SFT2D1 SFT2 domain containing 1

Information
Symbol
SFT2D1
Type
protein-coding
Description
SFT2 domain containing 1
Entrez Gene ID
113402
Genome
hg19
Position
chr6:166,733,216-166,756,033
Genome
hg38
Position
chr6:166,319,728-166,342,545
HGNC
HGNC:21102 HGNC
Ensembl
ENSG00000198818 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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 :
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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 C6orf83
SYNONYM pRGR1
HGNC HGNC:21102 HGNC
Ensembl ENSG00000198818 Ensembl
AllianceGenome HGNC:21102
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361731.4 hg38 chr6 166,319,728 166,342,545 22,818
ENST00000361731.4 hg19 chr6 166,733,216 166,756,033 22,818
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