Genomic variant #0000132573

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.83764184G>A
DNA change (hg38) g.84134868G>A
Published as 197C>T
ISCN -
DB-ID SEMA3A_000007 See all 4 reported entries
Variant remarks cDNA expression cloning in COS7 cells showed impaired SEMA3A secretion and in GN11 cells (embryonic) reducd SEMA3A signaling activity
Reference PubMed: Hanchate 2012, Journal: Hanchate 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00031 View details
Owner Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
SEMA3A NM_006080.2 +/. 2 c.196C>T - - p.Arg66Trp