Variant #0000969836 (NC_000019.9:g.49488841_49488842del, NM_001161587.1:c.507_508del (GYS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49488841_49488842del
DNA change (hg38) -
Published as GYS1(NM_002103.5):c.699_700delAG (p.R236Afs*56)
ISCN -
DB-ID GYS1_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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +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     
GYS1 NM_001161587.1 +/. - c.507_508del r.(?) p.(Arg172Alafs*56)
GYS1 NM_002103.4 +/. - c.699_700del r.(?) p.(Arg236Alafs*56)


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