Variant #0001054380 (NC_000012.11:g.57859658C>T, NM_005269.2:c.712C>T (GLI1))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57859658C>T
DNA change (hg38) -
Published as GLI1(NM_005269.3):c.712C>T (p.(Arg238Cys))
ISCN -
DB-ID ARHGAP9_000017
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLI1 NM_005269.2 ?/. - c.712C>T r.(?) p.(Arg238Cys)
ARHGAP9 NM_032496.2 ?/. - c.*6642G>A r.(=) p.(=)


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