Variant #0000568797 (NC_000019.9:g.7584555G>C, NM_020533.2:c.-3082G>C (MCOLN1))

Chromosome 19
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.7584555G>C
DNA change (hg38) g.7519669G>C
Published as ZNF358(NM_018083.4):c.427G>C (p.(Ala143Pro))
ISCN -
DB-ID MCOLN1_000013
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.427G>C r.(?) p.(Ala143Pro)
MCOLN1 NM_020533.2 -?/. - c.-3082G>C r.(?) p.(=)


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