Variant #0000658628 (NC_000019.9:g.49468837C>T, NM_001161587.1:c.*3708G>A (GYS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49468837C>T
DNA change (hg38) g.48965580C>T
Published as FTL(NM_000146.3):c.73C>T (p.L25=)
ISCN -
DB-ID BAX_000011
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) 0.00041 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTL NM_000146.3 -?/. - c.73C>T r.(?) p.(Leu25=)
GYS1 NM_001161587.1 -?/. - c.*3708G>A r.(=) p.(=)
GYS1 NM_002103.4 -?/. - c.*3708G>A r.(=) p.(=)
BAX NM_138763.3 -?/. - c.*3944C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.