Variant #0000532010 (NC_000007.13:g.42079774_42079775dup, NM_000168.5:c.891_892dup (GLI3))

Chromosome 7
Allele Unknown
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.42079774_42079775dup
DNA change (hg38) g.42040175_42040176dup
Published as GLI3(NM_000168.5):c.891_892dupAC (p.P298Hfs*13)
ISCN -
DB-ID GLI3_000179
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-22 15:45:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLI3 NM_000168.5 +/. - c.891_892dup r.(?) p.(Pro298HisfsTer13)


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