Genomic variant #0000132564

Individual ID 00081739
Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.83634712C>T
DNA change (hg38) g.84005396C>T
Published as -
ISCN -
DB-ID SEMA3A_000006 See all 7 reported entries
Variant remarks -
Reference PubMed: Hanchate 2012, Journal: Hanchate 2012, OMIM:var0002
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 13/1542 control chromosomes
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.01046 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 +/. 11 c.1303G>A - r.(?) p.(Val435Ile)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000081868 DNA SEQ - - SEMA3A 1 Johan den Dunnen