Overview

Variant ID 11309
Entrez Gene ID 223117
Gene SEMA3D (GeneCards)
Location hg19 7:86230381-86230381
hg38 7:86601065-86601065
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000007.13:g.86230381 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
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 159138663

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1375
CADD Raw score (version 1.3) 0.429621 (Deleterious)
FATHMM raw prediction score 0.16394 (Tolerated)
Deleterious probability by DeFine 0.1134 (Neutral)
Entrez Gene ID 223117 (NCBI Gene)
Official Gene Symbol SEMA3D (GeneCards)
Number of variants in SEMA3D in this database 17 (view all the variants)
Full name semaphorin 3D
Band 7q21.11
Other IDs Vega: OTTHUMG00000154569
OMIM: 609907
HGNC: HGNC:10726
Ensembl: ENSG00000153993
Other names coll-2, Sema-Z2
Summary This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin like domain and a C-terminal basic domain. The protein encoded by this gene binds neuropilin and plays an important role in cardiovascular development. [provided by RefSeq, Aug 2016]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
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;