FAM197Y9 family with sequence similarity 197 Y-linked member 9

Information
Symbol
FAM197Y9
Type
ncRNA
Description
family with sequence similarity 197 Y-linked member 9
Entrez Gene ID
100132932
Genome
hg19
Position
chrY:6,124,308-6,131,994
Genome
hg38
Position
chrY:6,256,267-6,263,953
HGNC
HGNC:37477 HGNC
Ensembl
ENSG00000290448 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:37477 HGNC
Ensembl ENSG00000290448 Ensembl
AllianceGenome HGNC:37477
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000451062.1 hg38 chrY 6,256,267 6,263,953 7,687
ENST00000452103.5 hg38 chrY 6,258,333 6,263,935 5,603
ENST00000451062.1 hg19 chrY 6,124,308 6,131,994 7,687
ENST00000452103.5 hg19 chrY 6,126,374 6,131,976 5,603
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