Variant #0000786105 (NC_000003.11:g.?, NC_000003.11(NM_000187.3):c.283-9199_434+1688del (HGD))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) -
Published as ex5,6 del
ISCN -
DB-ID HGD_000197
Variant remarks -
Reference Ascher (2019) - data and classification copied from HGD mutations database
ClinVar ID -
dbSNP ID -
Origin Germline
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 2021-05-21 10:09:09 +02:00 (CEST)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGD NM_000187.3 +/+ 4i_6i c.283-9199_434+1688del r.(?) p.(Leu95Metfs*33)


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