Variant #0000249577 (NC_000019.9:g.49469013A>G, NM_001161587.1:c.*3532T>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.49469013A>G
DNA change (hg38) g.48965756A>G
Published as FTL(NM_000146.4):c.103-14A>G
ISCN -
DB-ID FTL_000029
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.103-14A>G r.(=) p.(=)
GYS1 NM_001161587.1 -?/. - c.*3532T>C r.(=) p.(=)
GYS1 NM_002103.4 -?/. - c.*3532T>C r.(=) p.(=)
BAX NM_138763.3 -?/. - c.*4120A>G r.(=) p.(=)


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