Variant ID | 3062 |
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Entrez Gene ID | 53353 |
Gene | LRP1B (GeneCards) |
Location | hg19 2:142228513-142228513
hg38 2:141470944-141470944 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000002.11:g.142228513 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 | 243199373 |
MAF in gnomAD genome (version 2.0.1) | 0.0000323 |
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SNP ID (dbSNP ID version 137) | rs149083610 |
EIGEN score | -0.0144 |
CADD Raw score (version 1.3) | -0.032407 (Deleterious) |
FATHMM raw prediction score | 0.12023 (Tolerated) |
Deleterious probability by DeFine | 0.4525 (Neutral) |
Entrez Gene ID | 53353 (NCBI Gene) |
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Official Gene Symbol | LRP1B (GeneCards) |
Number of variants in LRP1B in this database | 23 (view all the variants) |
Full name | LDL receptor related protein 1B |
Band | 2q22.1-q22.2 |
Other IDs | Vega: OTTHUMG00000131799 OMIM: 608766 HGNC: HGNC:6693 Ensembl: ENSG00000168702 |
Other names | LRP-1B, LRPDIT, LRP-DIT |
Summary | This gene encodes a member of the low density lipoprotein (LDL) receptor family. These receptors play a wide variety of roles in normal cell function and development due to their interactions with multiple ligands. Disruption of this gene has been reported in several types of cancer. [provided by RefSeq, Jun 2016] |
Individual ID | 29217584.05 (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; |