Variant #0001004978 (NC_000019.9:g.49469172A>G, NM_001161587.1:c.*3373T>C (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.49469172A>G
DNA change (hg38) -
Published as FTL(NM_000146.3):c.248A>G (p.K83R, p.(Lys83Arg))
ISCN -
DB-ID FTL_000032 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) 0 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.248A>G r.(?) p.(Lys83Arg)
GYS1 NM_001161587.1 -?/. - c.*3373T>C r.(=) p.(=)
GYS1 NM_002103.4 -?/. - c.*3373T>C r.(=) p.(=)
BAX NM_138763.3 -?/. - c.*4279A>G r.(=) p.(=)


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