Variant #0000002905 (NC_000016.10:g.6137C>G, NM_001178098.2:c.520C>G (CD19))

Individual ID 00000714
Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.6137C>G
Published as -
Reference Adiratna Mat Ripen et al.(2020)
DB-ID CD19_000001 See all 2 reported entries
dbSNP ID rs2904880
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-06-27 11:43:31 +08:00 (CST)
Date last edited 2021-08-01 13:12:08 +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 -/. 3 c.520C>G - r.(?) p.(Leu174Val) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000787 DNA PCR;SEQ CD19 1 Nur Aisyah Athirah