Variant #0000568802 (NC_000019.9:g.7584923C>G, NM_020533.2:c.-2714C>G (MCOLN1))

Chromosome 19
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.7584923C>G
DNA change (hg38) g.7520037C>G
Published as ZNF358(NM_018083.4):c.795C>G (p.(Cys265Trp))
ISCN -
DB-ID MCOLN1_000018
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF358 NM_018083.4 ?/. - c.795C>G r.(?) p.(Cys265Trp)
MCOLN1 NM_020533.2 ?/. - c.-2714C>G r.(?) p.(=)


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