Variant ID | 25148 |
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Entrez Gene ID | 205428 |
Gene | C3orf58 (GeneCards) |
Location | hg19 3:143912759-143912759
hg38 3:144193917-144193917 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000003.11:g.143912759 T>C (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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0.00003237 |
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SNP ID (dbSNP ID version 137) | rs115990818 |
EIGEN score | -0.2134 |
CADD Raw score (version 1.3) | 0.462353 (Deleterious) |
FATHMM raw prediction score | 0.15926 (Tolerated) |
Deleterious probability by DeFine | 0.0822 (Neutral) |
Entrez Gene ID | 205428 (NCBI Gene) |
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Official Gene Symbol | C3orf58 (GeneCards) |
Number of variants in C3orf58 in this database | 27 (view all the variants) |
Full name | chromosome 3 open reading frame 58 |
Band | 3q24 |
Other IDs | Vega: OTTHUMG00000159380 OMIM: 612200 HGNC: HGNC:28490 Ensembl: ENSG00000181744 |
Other names | DIA1, HASF, GoPro49 |
Summary | None |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |