Variant #0000618311 (NC_000020.10:g.8689379G>A, NM_015192.3:c.1230G>A (PLCB1))

Chromosome 20
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.8689379G>A
DNA change (hg38) g.8708732G>A
Published as PLCB1(NM_015192.4):c.1230G>A (p.S410=), PLCB1(NM_182734.2):c.1230G>A (p.S410=), PLCB1(NM_182734.3):c.1230G>A (p.S410=)
ISCN -
DB-ID PLCB1_000014 See all 3 reported entries
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) 0.00073 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCB1 NM_015192.3 -?/. - c.1230G>A r.(?) p.(Ser410=)


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