Variant #0000003197 (NC_000016.10:g.28932042C>T, NM_001178098.2:c.42C>T (CD19))

Individual ID 00000832
Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.28932042C>T
Published as CD19
Reference Intan Juliana Abd Hamid et al. (2020)
DB-ID CD19_000003
dbSNP ID rs1031168890
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Noorzalifah Binti Mazuki
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Noorzalifah Binti Mazuki
Date created 2021-08-10 12:41:06 +08:00 (CST)
Date last edited 2022-01-25 09:34:50 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
CD19 NM_001178098.2 ?/. - c.42C>T CD19 r.(=) p.(=) ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000946 DNA ? CD19 1 Noorzalifah Binti Mazuki