Variant #0000322285 (NC_000011.9:g.64032784G>A, NM_000932.2:c.2845G>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.64032784G>A
DNA change (hg38) g.64265312G>A
Published as PLCB3(NM_000932.2):c.2845G>A (p.(Val949Met))
ISCN -
DB-ID PLCB3_000002
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) 0.0052 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +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.2845G>A r.(?) p.(Val949Met)
BAD NM_032989.2 -?/. - c.*4897C>T r.(=) p.(=)


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