Variant ID | 29374 |
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Entrez Gene ID | 113146 |
Gene | AHNAK2 (GeneCards) |
Location | hg19 14:105413930-105413930
hg38 14:104947593-104947593 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
Method | MiSeq |
Mutation(HGVS format) | NC_000014.8:g.105413930 C>T (Genome Assembly: hg19) |
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 | 107349540 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.7439 |
CADD Raw score (version 1.3) | 3.026088 (Deleterious) |
FATHMM raw prediction score | 0.05088 (Tolerated) |
SIFT score | 0.239 (Tolerated) |
MutationTaster score | 1 (Tolerated) |
MutatioinAssessor score | 2.08 (Deleterious) |
PROVEAN score | -1.9 (Tolerated) |
MetaSVM score | -0.946 (Tolerated) |
MetaLR score | 0.004 (Tolerated) |
MCAP score | 0.016 (Tolerated) |
FitCons score | 0.707 (Highly Significant p < 0.003 ) |
Genomic Evolutionary Rate Profiling (GERP) score | 0.858 |
PhyloP score based on multiple alignment of 100 vertebrates | 0.432 |
PhastCons score based on multiple alignment of 100 vertebrates | 0 |
SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 4.402 |
Deleterious probability by iFish2 | 0.0254 (Neutral) |
Deleterious probability by DeFine | 0.7031 (Deleterious) |
Entrez Gene ID | 113146 (NCBI Gene) |
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Official Gene Symbol | AHNAK2 (GeneCards) |
Number of variants in AHNAK2 in this database | 3 (view all the variants) |
Full name | AHNAK nucleoprotein 2 |
Band | 14q32.33 |
Other IDs | Vega: OTTHUMG00000170765 OMIM: 608570 HGNC: HGNC:20125 Ensembl: ENSG00000185567 |
Other names | C14orf78 |
Summary | This gene encodes a large nucleoprotein. The encoded protein has a tripartite domain structure with a relatively short N-terminus and a long C-terminus, separated by a large body of repeats. The N-terminal PSD-95/Discs-large/ZO-1 (PDZ)-like domain is thought to function in the formation of stable homodimers. The encoded protein may play a role in calcium signaling by associating with calcium channel proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017] |
Individual ID | 28714951.50 (view all the variants in this individual) |
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Pubmed ID | 28714951 |
Whose mosaic mutation | Patient |
Phenotype | 3 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
OMIM ID | 209850 |
Pubmed ID | 28714951 |
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Title | Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder |
Journal | Nat Neurosci |
Publication date | 2017.07 |
Disease | Autism Spectrum Disorders |
Incidence | 0.01 |
Number of cases | cases of unknown sex: 376; |