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 |
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Ranking
ClinVar | |
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0 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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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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