Variant #0000537759 (NC_000009.11:g.2039795_2039796insCGC, SMARCA2(NM_003070.3):c.685_686insCGC)

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2039795_2039796insCGC
DNA change (hg38) g.2039795_2039796insCGC
Published as SMARCA2(NM_003070.4):c.685_686insCGC (p.Q228_Q229insP)
ISCN -
DB-ID SMARCA2_000119 See all 2 reported entries
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA2 NM_003070.3 -/. - c.685_686insCGC r.(?) p.(Gln228_Gln229insPro)