SPATA31F1 SPATA31 subfamily F member 1

Information
Symbol
SPATA31F1
Type
protein-coding
Description
SPATA31 subfamily F member 1
Entrez Gene ID
259308
Genome
hg19
Position
chr9:34,723,050-34,729,485
Genome
hg38
Position
chr9:34,723,053-34,729,488
HGNC
HGNC:41911 HGNC
Ensembl
ENSG00000205108 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 26
Uncertain significance 0 164
Ranking
ClinVar
0
0
0
196
10
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 :
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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 :
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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 C9orf144B
SYNONYM FAM205A
HGNC HGNC:41911 HGNC
Ensembl ENSG00000205108 Ensembl
AllianceGenome HGNC:41911
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378788.4 hg38 chr9 34,723,053 34,729,488 6,436
ENST00000378788.4 hg19 chr9 34,723,050 34,729,485 6,436
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