FAM230I family with sequence similarity 230 member I
Information
- Symbol
- FAM230I
- Type
- ncRNA
- Description
- family with sequence similarity 230 member I
- Entrez Gene ID
- 388882
- Genome
- hg19
- Position
- chr22:23,804,273-23,829,167
- Genome
- hg38
- Position
- chr22:23,462,086-23,486,980
- HGNC
- HGNC:52446 HGNC
- Ensembl
- ENSG00000178248 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 5 | 0 |
Ranking
ClinVar | |
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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
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 |
Search Word
Target data | : |
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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Search word | : | |
Filtering | : |
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 |
Type | ID |
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SYNONYM | LINC01658 |
HGNC | HGNC:52446 HGNC |
Ensembl | ENSG00000178248 Ensembl |
AllianceGenome | HGNC:52446 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000320372.9 | hg38 | chr22 | 23,462,086 | 23,486,980 | 24,895 |
ENST00000320372.9 | hg19 | chr22 | 23,804,273 | 23,829,167 | 24,895 |
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