Variant #0000567937 (NC_000019.9:g.49469986C>T, NM_001161587.1:c.*2559G>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.49469986C>T
DNA change (hg38) g.48966729C>T
Published as FTL(NM_000146.3):c.522C>T (p.H174=), FTL(NM_000146.4):c.522C>T (p.H174=)
ISCN -
DB-ID FTL_000033 See all 3 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) 0.00223 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 2019-07-18 18:22:55 +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.522C>T r.(?) p.(His174=)
GYS1 NM_001161587.1 -?/. - c.*2559G>A r.(=) p.(=)
GYS1 NM_002103.4 -?/. - c.*2559G>A r.(=) p.(=)
BAX NM_138763.3 -?/. - c.*5093C>T r.(=) p.(=)


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