Variant #0000621885 (NC_000007.13:g.42187851C>T, NM_000168.5:c.341G>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.42187851C>T
DNA change (hg38) g.42148252C>T
Published as GLI3(NM_000168.5):c.341G>A (p.R114K, p.(Arg114Lys)), GLI3(NM_000168.6):c.341G>A (p.R114K)
ISCN -
DB-ID GLI3_000139 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) 0.00243 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.341G>A r.(?) p.(Arg114Lys)


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