Overview

Variant ID 29724
Entrez Gene ID 53353
Gene LRP1B (GeneCards)
Location hg19 2:141291600-141291600
hg38 2:140534031-140534031
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method NextSeq500
Mutation(HGVS format) NC_000002.11:g.141291600 T>C (Genome Assembly: hg19)

Other information

Exon or Intron Exon
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

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.5859
CADD Raw score (version 1.3) 0.51234 (Deleterious)
FATHMM raw prediction score 0.1816 (Tolerated)
Deleterious probability by DeFine 0.6694 (Deleterious)
Entrez Gene ID 53353 (NCBI Gene)
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 #1

Individual ID 28867142.25 (view all the variants in this individual)
Pubmed ID 28867142
Whose mosaic mutation Male Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28867142

Pubmed ID 28867142
Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Journal American Journal of Human Genetics
Publication date 2017.08
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 247;