Variant #0000980424 (NC_000012.11:g.65152856A>C, NC_000012.11(NM_002076.3):c.192+9T>G (GNS))

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.65152856A>C
DNA change (hg38) -
Published as GNS(NM_002076.4):c.192+9T>G
ISCN -
DB-ID GNS_000039
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNS NM_002076.3 -?/. - c.192+9T>G r.(=) p.(=)
TBC1D30 NM_015279.1 -?/. - c.-65804A>C r.(?) p.(=)


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