Variant #0000326688 (NC_000019.9:g.49472804G>A, NM_001161587.1:c.1763C>T (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.49472804G>A
DNA change (hg38) g.48969547G>A
Published as GYS1(NM_001161587.1):c.1763C>T (p.(Ser588Phe))
ISCN -
DB-ID GYS1_000001
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 2018-01-15 20:58:59 +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.*2812G>A r.(=) p.(=)
GYS1 NM_001161587.1 ?/. - c.1763C>T r.(?) p.(Ser588Phe)
GYS1 NM_002103.4 ?/. - c.1955C>T r.(?) p.(Ser652Phe)


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