Variant #0001004798 (NC_000019.9:g.41937777T>C, NM_198540.2:c.-3596A>G (B3GNT8))

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.41937777T>C
DNA change (hg38) -
Published as ATP5SL(NM_018035.2):c.*359A>G (p.?)
ISCN -
DB-ID ATP5SL_000003
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5SL NM_018035.2 ?/. - c.*359A>G r.(=) p.(=)
B3GNT8 NM_198540.2 ?/. - c.-3596A>G r.(?) p.(=)


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