Variant #0000895078 (NC_000019.9:g.49481243T>C, NM_001161587.1:c.1054A>G (GYS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49481243T>C
DNA change (hg38) -
Published as GYS1(NM_001161587.1):c.1054A>G (p.(Met352Val)), GYS1(NM_002103.5):c.1246A>G (p.M416V)
ISCN -
DB-ID GYS1_000004 See all 4 reported entries
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) 0.01895 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 2022-11-01 13:41:49 +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     
GYS1 NM_001161587.1 -/. - c.1054A>G r.(?) p.(Met352Val)
GYS1 NM_002103.4 -/. - c.1246A>G r.(?) p.(Met416Val)


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