Variant #0000169155 (NC_000011.9:g.2021134_2021176|gom)

Individual ID 00103960
Chromosome 11
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.2021134_2021176|gom
DNA change (hg38) g.1999904_1999946|gom
Published as -
ISCN -
DB-ID chr11_000773 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP -
Methylation 0.83
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jack Brzezinski
Database submission license No license selected
Created by Jack Brzezinski
Date created 2017-04-26 15:42:25 +02:00 (CEST)
Date last edited 2019-07-31 12:46:16 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000104427 DNA SEQp nephroblastoma - H19, KCNQ1OT1 2 Jack Brzezinski


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