Variant #0000300972 (NC_000010.10:g.96039710T>C, PLCE1(NM_016341.3):c.4795+42T>C)

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.96039710T>C
DNA change (hg38) g.94279953T>C
Published as PLCE1(NM_016341.3):c.4795+42T>C
ISCN -
DB-ID PLCE1_000019
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01561 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCE1 NM_016341.3 -/. - c.4795+42T>C r.(=) p.(=)
PLCE1-AS1 NR_033969.1 -/. - n.745A>G r.(?) -