Overview

Variant ID 1114
Entrez Gene ID 1755
Gene DMBT1 (GeneCards)
Location hg19 10:124351937-124351937
hg38 10:122592421-122592421
Disease Human Skin Fibroblasts (view all the variants in this disease)
Method HiSeq 2500
Mutation(HGVS format) NC_000010.10:g.124351937 T>C (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 776
Amino acid changes in protein C > R
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.639
CADD Raw score (version 1.3) 2.796922 (Deleterious)
FATHMM raw prediction score 0.97317 (Tolerated)
SIFT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.045 (Deleterious)
PROVEAN score -5.85 (Deleterious)
MetaSVM score -0.28 (Tolerated)
MetaLR score 0.292 (Tolerated)
MCAP score 0.046 (Deleterious)
FitCons score 0.549 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 3.86
PhyloP score based on multiple alignment of 100 vertebrates 7.504
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 13.012
Deleterious probability by iFish2 0.967 (Deleterious)
Deleterious probability by DeFine 0.9657 (Deleterious)
Entrez Gene ID 1755 (NCBI Gene)
Official Gene Symbol DMBT1 (GeneCards)
Number of variants in DMBT1 in this database 3 (view all the variants)
Full name deleted in malignant brain tumors 1
Band 10q26.13
Other IDs Vega: OTTHUMG00000019185
OMIM: 601969
HGNC: HGNC:2926
Ensembl: ENSG00000187908
Other names SAG, GP340, SALSA, mclin
Summary Loss of sequences from human chromosome 10q has been associated with the progression of human cancers. This gene was originally isolated based on its deletion in a medulloblastoma cell line. This gene is expressed with transcripts of 6.0, 7.5, and 8.0 kb in fetal lung and with one transcript of 8.0 kb in adult lung, although the 7.5 kb transcript has not been characterized. The encoded protein precursor is a glycoprotein containing multiple scavenger receptor cysteine-rich (SRCR) domains separated by SRCR-interspersed domains (SID). Transcript variant 2 (8.0 kb) has been shown to bind surfactant protein D independently of carbohydrate recognition. This indicates that DMBT1 may not be a classical tumor suppressor gene, but rather play a role in the interaction of tumor cells and the immune system. [provided by RefSeq, Mar 2016]

Individual #1

Individual ID 27788131.02 (view all the variants in this individual)
Pubmed ID 27788131
Whose mosaic mutation Normal  
Phenotype 1  
Disease Human Skin Fibroblasts (view all the variants in this disease)
OMIM ID 120353

Publication #1: 27788131

Pubmed ID 27788131
Title The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin Fibroblasts.
Journal PLoS Genetics
Publication date 2016.10
Disease Human Skin Fibroblasts
Population Caucasian
Number of cases Male cases: 2;