Variant #0000286167 (NC_000019.9:g.7590053G>A, NC_000019.9(NM_020533.2):c.237+1G>A (MCOLN1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7590053G>A
DNA change (hg38) g.7525167G>A
Published as MCOLN1(NM_020533.3):c.237+1G>A
ISCN -
DB-ID MCOLN1_000005
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF358 NM_018083.4 +/. - c.*4218G>A r.(=) p.(=)
MCOLN1 NM_020533.2 +/. - c.237+1G>A r.spl? p.?


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