Variant #0001056655 (NC_000019.9:g.39406392G>A, NC_000019.9(NM_017827.3):c.1414-3C>T (SARS2))

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.39406392G>A
DNA change (hg38) -
Published as SARS2(NM_017827.4):c.1414-3C>T
ISCN -
DB-ID SARS2_000025
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SARS2 NM_001145901.1 ?/. - c.1420-3C>T r.spl? p.?
SARS2 NM_017827.3 ?/. - c.1414-3C>T r.spl? p.?


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