Variant #0000624049 (NC_000019.9:g.49468765A>G, NM_001161587.1:c.*3780T>C (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.49468765A>G
DNA change (hg38) g.48965508A>G
Published as FTL(NM_000146.3):c.1A>G (p.M1?, p.(Met1?))
ISCN -
DB-ID BAX_000008 See all 2 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) 1.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTL NM_000146.3 +/. - c.1A>G r.(?) p.(Met1?)
GYS1 NM_001161587.1 +/. - c.*3780T>C r.(=) p.(=)
GYS1 NM_002103.4 +/. - c.*3780T>C r.(=) p.(=)
BAX NM_138763.3 +/. - c.*3872A>G r.(=) p.(=)


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