Variant #0001080006 (NC_000007.13:g.42079691C>T, NM_000168.5:c.974G>A (GLI3))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42079691C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr7_007604
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs781356257
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-07-10 16:54:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLI3 NM_000168.5 -?/. - c.974G>A r.(?) p.(Arg325His)


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