Variant #0000553256 (NC_000014.8:g.88459835C>A, NM_000153.3:c.-327G>T (GALC))

Chromosome 14
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.88459835C>A
DNA change (hg38) g.87993491C>A
Published as GALC(NM_001201402.1):c.9G>T (p.G3=), GALC(NM_001201402.2):c.9G>T (p.G3=, p.(Gly3=))
ISCN -
DB-ID GALC_000082 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) 0.00126 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALC NM_000153.3 -?/. - c.-327G>T r.(?) p.(=)


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