Variant #0000665705 (NC_000008.10:g.[NC_000019.9:(35762292_35940346)_qter]delins(119038109_119106577)_qter)

Individual ID 00133225
Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.[NC_000019.9:(35762292_35940346)_qter]delins(119038109_119106577)_qter
DNA change (hg38) -
Published as -
ISCN t(8;19)(q24.11;q13.13)
DB-ID chr8_000000 See all 5 reported entries
Variant remarks BAC clones RP11-89P19, RP11-260I14, and RP11-2D13 give split signal
Reference -
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Ivy Jennes
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-05-13 12:08:02 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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0000134060 DNA FISH - - EXT1 4 Ivy Jennes


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