Variant #0000548998 (NC_000012.11:g.65153052C>G, NM_002076.3:c.5G>C (GNS))

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.65153052C>G
DNA change (hg38) g.64759272C>G
Published as GNS(NM_002076.4):c.5G>C (p.(Arg2Pro))
ISCN -
DB-ID GNS_000028
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) 0.00016 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNS NM_002076.3 ?/. - c.5G>C r.(?) p.(Arg2Pro)
TBC1D30 NM_015279.1 ?/. - c.-65608C>G r.(?) p.(=)


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