Variant #0000914238 (NC_000014.8:g.88452945G>A, NM_000153.3:c.330C>T (GALC))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88452945G>A
DNA change (hg38) -
Published as GALC(NM_000153.3):c.330C>T (p.D110=), GALC(NM_000153.4):c.330C>T (p.D110=, p.(Asp110=)), GALC(NM_001201402.2):c.252C>T (p.D84=)
ISCN -
DB-ID GALC_000039 See all 7 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) 0.0332 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.330C>T r.(?) p.(Asp110=)


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