Variant #0000553242 (NC_000014.8:g.88452941T>C, NM_000153.3:c.334A>G (GALC))

Chromosome 14
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.88452941T>C
DNA change (hg38) g.87986597T>C
Published as GALC(NM_000153.3):c.334A>G (p.T112A), GALC(NM_000153.4):c.334A>G (p.T112A, p.(Thr112Ala))
ISCN -
DB-ID GALC_000004 See all 9 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) 0.00252 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 2024-04-19 20:27:30 +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.334A>G r.(?) p.(Thr112Ala)


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