FAM163A family with sequence similarity 163 member A
Information
- Symbol
- FAM163A
- Type
- protein-coding
- Description
- family with sequence similarity 163 member A
- Entrez Gene ID
- 148753
- Genome
- hg19
- Position
- chr1:179,712,426-179,785,333
- Genome
- hg38
- Position
- chr1:179,743,291-179,816,198
- MIM
- 611727 OMIM
- HGNC
- HGNC:28274 HGNC
- Ensembl
- ENSG00000143340 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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28 |
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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
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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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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 |
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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 |
Type | ID |
---|---|
SYNONYM | C1orf76 |
SYNONYM | NDSP |
MIM | 611727 OMIM |
HGNC | HGNC:28274 HGNC |
Ensembl | ENSG00000143340 Ensembl |
AllianceGenome | HGNC:28274 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000341785.5 | hg38 | chr1 | 179,743,291 | 179,816,198 | 72,908 |
ENST00000341785.5 | hg19 | chr1 | 179,712,426 | 179,785,333 | 72,908 |
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