Variant #0000096341 (NC_000019.9:g.39406677C>T, NM_017827.3:c.1347G>A (SARS2))

Chromosome 19
Allele Both (homozygous)
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.39406677C>T
DNA change (hg38) g.38916037C>T
Published as -
ISCN -
DB-ID SARS2_000001 See all 2 reported entries
Variant remarks affects splicing
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Henna Tyynismaa
Database submission license No license selected
Created by Henna Tyynismaa
Date created 2016-05-06 12:58:36 +02:00 (CEST)
Date last edited 2020-07-15 18:05:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SARS2 NM_001145901.1 +/. 15 c.1353G>A r.spl p.(Thr451=)
SARS2 NM_017827.3 +/. 14 c.1347G>A r.spl p.(Thr449=)



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