Variant #0000950005 (NC_000012.11:g.57863433C>T, NM_004990.3:c.-18441C>T (MARS))

Chromosome 12
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.57863433C>T
DNA change (hg38) -
Published as GLI1(NM_001160045.1):c.1144C>T (p.(Arg382Trp))
ISCN -
DB-ID ARHGAP9_000014
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) 0.0027 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 2023-11-27 17:35:39 +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     
MARS NM_004990.3 -?/. - c.-18441C>T r.(?) p.(=)
GLI1 NM_005269.2 -?/. - c.1528C>T r.(?) p.(Arg510Trp)
ARHGAP9 NM_032496.2 -?/. - c.*2867G>A r.(=) p.(=)


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