Genomic variant #0000531302

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.150715141G>C
DNA change (hg38) -
Published as ATG9B(NM_173681.5):c.1873-4C>G (p.?)
ISCN -
DB-ID ATG9B_000010
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0.00098 View details
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
NOS3 NM_000603.4 -?/. - c.*3884G>C likely benign r.(=) p.(=)
ATG9B NM_173681.5 -?/. - c.1873-4C>G likely benign r.spl? p.?