Variant #0000851614 (NC_000007.13:g.42088222T>C, NM_000168.5:c.547A>G (GLI3))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42088222T>C
DNA change (hg38) -
Published as GLI3(NM_000168.5):c.547A>G (p.T183A), GLI3(NM_000168.6):c.547A>G (p.T183A)
ISCN -
DB-ID GLI3_000001 See all 5 reported entries
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) 0.54387 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +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.547A>G r.(?) p.(Thr183Ala)


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