Variant #0000351256 (NC_000019.9:g.49468597G>A, NM_001161587.1:c.*3948C>T (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.49468597G>A
DNA change (hg38) g.48965340G>A
Published as FTL(NM_000146.3):c.-168G>A
ISCN -
DB-ID FTL_000003 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.-168G>A r.(?) p.(=)
GYS1 NM_001161587.1 +/. - c.*3948C>T r.(=) p.(=)
GYS1 NM_002103.4 +/. - c.*3948C>T r.(=) p.(=)
BAX NM_138763.3 +/. - c.*3704G>A r.(=) p.(=)


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