Variant #0000236324 (NC_000004.11:g.147028554_qterdelins[NC_000023.10:pter_32567260inv])

Individual ID 00122471
Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.147028554_qterdelins[NC_000023.10:pter_32567260inv]
DNA change (hg38) -
Published as -
ISCN 46,X,t(X;4)(p21.2;q31.22)
DB-ID chr4_000578
Variant remarks translocation, der4, includes deletion 147028556_147028561
Reference PubMed: Giacalone 1992
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-12-10 13:27:04 +01:00 (CET)
Date last edited 2020-05-12 19:21:26 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000122939 DNA Southern;SEQ - - DMD 2 Johan den Dunnen


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