Variant Details for FAM150B


Gene Symbol: | FAM150B ( PRO1097,RGPG542 ) |
---|---|
Gene Full Name: | family with sequence similarity 150, member B |
Band: | 2p25.3 |
Quick Links | Entrez ID:285016; OMIM: NA; Uniprot ID:F150B_HUMAN; ENSEMBL ID: ENSG00000189292; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |


Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. Chromosome coordinates: hg19
Genetic Category | CNVs/SVs | de novo Mutations | Mosaics SNVs | NGS Other Mutations | Low-Scale Gene Mutations | Linkage Regions | Total |
---|---|---|---|---|---|---|---|
Number | 2 | 0 | 0 | 0 | 0 | 2 | 4 |


CNV ID | Chr | Band | Start | End | Size | Gain/Loss | UCSC Browser | Reference |
---|---|---|---|---|---|---|---|---|
AutCNV0000200 | 2 | 2p25.3 | 54074 | 1198910 | 1144836 | loss | external link | Christian, 2008 |
AutCNV0003469 | 2 | 2p25.3 | 29443 | 1157068 | 1127625 | loss | external link | Gai, 2011 |


iFish (integrated Functional inference of SNVs in human) is based on gene/gene family customized models to classify missense mutations.
Chr | Pos | Ref | Alt | Coding | AA | Validated Method | iFish Prediction | iFish Probability | Reference |
---|---|---|---|---|---|---|---|---|---|
No related data! |


Chr | Position | Ref | Alt | Genotype | Validated Method | Reference |
---|---|---|---|---|---|---|
No related data! |


Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
---|---|---|---|---|---|---|---|---|---|
No related data! |


Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
---|---|---|---|---|---|---|---|---|---|
No related data! |


Linkage Name | Band | Chr | Marker | LOD | NPL | P Value | Reference |
---|---|---|---|---|---|---|---|
AutLD0000070 | 2p25.3 | 2 | D2S319 | 1.2 | - | - | Buxbaum, 2001 |
AutLD0000151 | 2p25.3-p24.1 | 2 | rs792065 | 1.87 | - | - | Allen-Brady, 2010 |