Variant #0000951489 (NC_000020.10:g.9438055T>C, NC_000020.10(NM_000933.3):c.2961-6T>C (PLCB4))

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.9438055T>C
DNA change (hg38) -
Published as PLCB4(NM_000933.3):c.2961-6T>C (p.(=)), PLCB4(NM_001172646.1):c.2997-6T>C
ISCN -
DB-ID PLCB4_000017 See all 2 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) 0.00125 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCB4 NM_000933.3 -?/. - c.2961-6T>C r.(=) p.(=)


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