Genomic variant #0000018847

Individual ID 00001517
Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.2056861_2056862ins
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr9_000300 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Gijs Santen
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Variants found     

Owner     
0000001288 DNA SEQ - - ARID1A, ARID1B, SMARCA2, SMARCA4, SMARCB1, SMARCE1 10 Gijs Santen