Variant ID | 15768 |
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Entrez Gene ID | 81846 |
Gene | SBF2 (GeneCards) |
Location | hg19 11:10122951-10122951
hg38 11:10101404-10101404 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000011.9:g.10122951 C>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 135006516 |
MAF in gnomAD genome (version 2.0.1) | 0.00003231 |
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EIGEN score | -0.2425 |
CADD Raw score (version 1.3) | 0.401817 (Deleterious) |
FATHMM raw prediction score | 0.14268 (Tolerated) |
Deleterious probability by DeFine | 0.1257 (Neutral) |
Entrez Gene ID | 81846 (NCBI Gene) |
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Official Gene Symbol | SBF2 (GeneCards) |
Number of variants in SBF2 in this database | 3 (view all the variants) |
Full name | SET binding factor 2 |
Band | 11p15.4 |
Other IDs | Vega: OTTHUMG00000165890 OMIM: 607697 HGNC: HGNC:2135 Ensembl: ENSG00000133812 |
Other names | CMT4B2, MTMR13, DENND7B |
Summary | This gene encodes a pseudophosphatase and member of the myotubularin-related protein family. This gene maps within the CMT4B2 candidate region of chromosome 11p15 and mutations in this gene have been associated with Charcot-Marie-Tooth Disease, type 4B2. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.15 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
Journal | Science |
Publication date | 2018.02 |
Disease | Cockayne syndrome Xeroderma Pigmentosum |
Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |