Variant #0001004979 (NC_000019.9:g.49469598G>T, NM_001161587.1:c.*2947C>A (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.49469598G>T
DNA change (hg38) -
Published as FTL(NM_000146.3):c.310G>T (p.(Glu104*))
ISCN -
DB-ID BAX_000019
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTL NM_000146.3 +/. - c.310G>T r.(?) p.(Glu104*)
GYS1 NM_001161587.1 +/. - c.*2947C>A r.(=) p.(=)
GYS1 NM_002103.4 +/. - c.*2947C>A r.(=) p.(=)
BAX NM_138763.3 +/. - c.*4705G>T r.(=) p.(=)


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