Variant ID | 23721 |
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Entrez Gene ID | 729420 |
Gene | LMO7DN (GeneCards) |
Location | hg19 13:76465054-76465054
hg38 13:75890918-75890918 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000013.10:g.76465054 G>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 | 115169878 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.0026 |
CADD Raw score (version 1.3) | -0.137488 (Deleterious) |
FATHMM raw prediction score | 0.07398 (Tolerated) |
Deleterious probability by DeFine | 0.4129 (Neutral) |
Entrez Gene ID | 729420 (NCBI Gene) |
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Official Gene Symbol | LMO7DN (GeneCards) |
Number of variants in LMO7DN in this database | 22 (view all the variants) |
Full name | LMO7 downstream neighbor |
Band | 13q22.2 |
Other IDs | Vega: OTTHUMG00000187426 HGNC: HGNC:44370 Ensembl: ENSG00000178734 |
Other names | C13orf45 |
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; |