Variant #0000855582 (NC_000019.9:g.39421241C>T, NM_017827.3:c.136G>A (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.39421241C>T
DNA change (hg38) -
Published as SARS2(NM_001145901.1):c.136G>A (p.E46K)
ISCN -
DB-ID MRPS12_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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
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.136G>A r.(?) p.(Glu46Lys)
SARS2 NM_017827.3 ?/. - c.136G>A r.(?) p.(Glu46Lys)
MRPS12 NM_021107.1 ?/. - c.-694C>T r.(?) p.(=)


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