FAM185A family with sequence similarity 185 member A
Information
- Symbol
- FAM185A
- Type
- protein-coding
- Description
- family with sequence similarity 185 member A
- Entrez Gene ID
- 222234
- Genome
- hg19
- Position
- chr7:102,389,446-102,449,672
- Genome
- hg38
- Position
- chr7:102,748,999-102,809,225
- HGNC
- HGNC:22412 HGNC
- Ensembl
- ENSG00000222011 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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38 |
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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
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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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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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ENST00000409231.7 | hg38 | chr7 | 102,749,028 | 102,808,840 | 59,813 |
ENST00000413034.3 | hg38 | chr7 | 102,748,999 | 102,809,225 | 60,227 |
ENST00000413034.3 | hg19 | chr7 | 102,389,446 | 102,449,672 | 60,227 |
ENST00000409231.7 | hg19 | chr7 | 102,389,475 | 102,449,287 | 59,813 |
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