Variant #0000184167 (NC_000023.10:g.(148568630_148571844)_(148586884_?)inv, IDS(NM_000202.5):c.(?_-217)_(1006+1_1007-1)inv)

Individual ID 00114411
Chromosome X
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(148568630_148571844)_(148586884_?)inv
DNA change (hg38) -
Published as -
ISCN -
DB-ID IDS_000082 See all 11 reported entries
Variant remarks -
Reference PubMed: Isogai 1998
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDS NM_000202.5 +/. 1_7i c.(?_-217)_(1006+1_1007-1)inv r.? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000114868 DNA Southern - - IDS 1 Johan den Dunnen