SFT2D2 SFT2 domain containing 2

Information
Symbol
SFT2D2
Type
protein-coding
Description
SFT2 domain containing 2
Entrez Gene ID
375035
Genome
hg19
Position
chr1:168,195,242-168,222,259
Genome
hg38
Position
chr1:168,226,004-168,253,021
HGNC
HGNC:25140 HGNC
Ensembl
ENSG00000213064 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
24
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
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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 UNQ512
SYNONYM dJ747L4.C1.2
HGNC HGNC:25140 HGNC
Ensembl ENSG00000213064 Ensembl
AllianceGenome HGNC:25140
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000367829.5 hg38 chr1 168,225,950 168,239,160 13,211
ENST00000271375.7 hg38 chr1 168,226,004 168,253,021 27,018
ENST00000630869.1 hg38 chr1 168,226,008 168,243,140 17,133
ENST00000367829.5 hg19 chr1 168,195,188 168,208,398 13,211
ENST00000271375.7 hg19 chr1 168,195,242 168,222,259 27,018
ENST00000630869.1 hg19 chr1 168,195,246 168,212,378 17,133
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