Variant #0000544836 (NC_000011.9:g.64037784G>A, NM_000932.2:c.*2756G>A (PLCB3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64037784G>A
DNA change (hg38) g.64270312G>A
Published as BAD(NM_004322.3):c.404C>T (p.(Ala135Val))
ISCN -
DB-ID BAD_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
PLCB3 NM_000932.2 -?/. - c.*2756G>A r.(=) p.(=)
BAD NM_032989.2 -?/. - c.404C>T r.(?) p.(Ala135Val)


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