Variant #0000567942 (NC_000019.9:g.49490629C>T, NC_000019.9(NM_001161587.1):c.301-1337G>A (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.49490629C>T
DNA change (hg38) g.48987372C>T
Published as GYS1(NM_002103.4):c.314G>A (p.R105H)
ISCN -
DB-ID GYS1_000010
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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
GYS1 NM_001161587.1 ?/. - c.301-1337G>A r.(=) p.(=)
GYS1 NM_002103.4 ?/. - c.314G>A r.(?) p.(Arg105His)


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