Variant #0000617741 (NC_000019.9:g.49468847C>G, NM_001161587.1:c.*3698G>C (GYS1))

Chromosome 19
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.49468847C>G
DNA change (hg38) g.48965590C>G
Published as -
ISCN -
DB-ID BAX_000009
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTL NM_000146.3 ?/. - c.83C>G r.(?) p.(Ser28Cys)
GYS1 NM_001161587.1 ?/. - c.*3698G>C r.(=) p.(=)
GYS1 NM_002103.4 ?/. - c.*3698G>C r.(=) p.(=)
BAX NM_138763.3 ?/. - c.*3954C>G r.(=) p.(=)


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