Variant ID | 22585 |
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Entrez Gene ID | 80745 |
Gene | THUMPD2 (GeneCards) |
Location | hg19 2:40088847-40088847
hg38 2:39861707-39861707 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000002.11:g.40088847 C>A (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 | 243199373 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3402 |
CADD Raw score (version 1.3) | -0.024484 (Deleterious) |
FATHMM raw prediction score | 0.07541 (Tolerated) |
Deleterious probability by DeFine | 0.0702 (Neutral) |
Entrez Gene ID | 80745 (NCBI Gene) |
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Official Gene Symbol | THUMPD2 (GeneCards) |
Number of variants in THUMPD2 in this database | 4 (view all the variants) |
Full name | THUMP domain containing 2 |
Band | 2p22.1 |
Other IDs | Vega: OTTHUMG00000102149 OMIM: 611751 HGNC: HGNC:14890 Ensembl: ENSG00000138050 |
Other names | C2orf8 |
Summary | None |
Individual ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
Journal | Science |
Publication date | 2018.02 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 3; |