Variant #0000623998 (NC_000019.9:g.39401286C>T, NM_017827.3:c.*4960G>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.39401286C>T
DNA change (hg38) g.38910646C>T
Published as CCER2(NM_001243212.1):c.628G>A (p.E210K)
ISCN -
DB-ID NFKBIB_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
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     
SARS2 NM_001145901.1 ?/. - c.*4960G>A r.(=) p.(=)
NFKBIB NM_002503.4 ?/. - c.*1814C>T r.(=) p.(=)
SIRT2 NM_012237.3 ?/. - c.-11125G>A r.(?) p.(=)
SARS2 NM_017827.3 ?/. - c.*4960G>A r.(=) p.(=)


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