Variant #0000855657 (NC_000019.9:g.49469054G>C, NM_001161587.1:c.*3491C>G (GYS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49469054G>C
DNA change (hg38) -
Published as FTL(NM_000146.3):c.130G>C (p.A44P)
ISCN -
DB-ID BAX_000015
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 2022-05-09 15:47:41 +02:00 (CEST)
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.130G>C r.(?) p.(Ala44Pro)
GYS1 NM_001161587.1 ?/. - c.*3491C>G r.(=) p.(=)
GYS1 NM_002103.4 ?/. - c.*3491C>G r.(=) p.(=)
BAX NM_138763.3 ?/. - c.*4161G>C r.(=) p.(=)


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