SPATA31G1 SPATA31 subfamily G member 1

Information
Symbol
SPATA31G1
Type
protein-coding
Description
SPATA31 subfamily G member 1
Entrez Gene ID
138724
Genome
hg19
Position
chr9:35,042,237-35,045,983
Genome
hg38
Position
chr9:35,042,240-35,045,986
HGNC
HGNC:31418 HGNC
Ensembl
ENSG00000174038 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
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 C9orf131
HGNC HGNC:31418 HGNC
Ensembl ENSG00000174038 Ensembl
AllianceGenome HGNC:31418
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000354479.5 hg38 chr9 35,041,095 35,045,982 4,888
ENST00000421362.6 hg38 chr9 35,041,095 35,045,982 4,888
ENST00000312292.6 hg38 chr9 35,042,240 35,045,986 3,747
ENST00000354479.5 hg19 chr9 35,041,092 35,045,979 4,888
ENST00000421362.6 hg19 chr9 35,041,092 35,045,979 4,888
ENST00000312292.6 hg19 chr9 35,042,237 35,045,983 3,747
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