FAM156A family with sequence similarity 156 member A
Information
- Symbol
- FAM156A
- Type
- protein-coding
- Description
- family with sequence similarity 156 member A
- Entrez Gene ID
- 29057
- Genome
- hg19
- Position
- chrX:52,976,462-52,987,715
- Genome
- hg38
- Position
- chrX:52,947,254-52,958,518
- HGNC
- HGNC:30114 HGNC
- Ensembl
- ENSG00000268350 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Filtering | : |
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 | PRO0659 |
SYNONYM | TMEM29 |
HGNC | HGNC:30114 HGNC |
Ensembl | ENSG00000268350 Ensembl |
AllianceGenome | HGNC:30114 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000623782.3 | hg38 | chrX | 52,947,258 | 52,995,472 | 48,215 |
ENST00000615092.4 | hg38 | chrX | 52,947,258 | 52,995,472 | 48,215 |
ENST00000611661.4 | hg38 | chrX | 52,947,254 | 52,995,464 | 48,211 |
ENST00000617970.4 | hg38 | chrX | 52,947,254 | 52,958,501 | 11,248 |
ENST00000612915.4 | hg38 | chrX | 52,947,258 | 52,995,472 | 48,215 |
ENST00000622447.5 | hg38 | chrX | 52,947,254 | 52,958,518 | 11,265 |
ENST00000596733.7 | hg38 | chrX | 52,947,258 | 52,958,414 | 11,157 |
ENST00000617970.4 | hg19 | chrX | 52,976,462 | 52,987,698 | 11,237 |
ENST00000596733.7 | hg19 | chrX | 52,976,466 | 52,987,611 | 11,146 |
ENST00000611661.4 | hg19 | chrX | 52,976,462 | 53,024,643 | 48,182 |
ENST00000615092.4 | hg19 | chrX | 52,976,466 | 53,024,651 | 48,186 |
ENST00000612915.4 | hg19 | chrX | 52,976,466 | 53,024,651 | 48,186 |
ENST00000622447.5 | hg19 | chrX | 52,976,462 | 52,987,715 | 11,254 |
ENST00000623782.3 | hg19 | chrX | 52,976,466 | 53,024,651 | 48,186 |
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