Variant #0000558298 (NC_000016.9:g.4945402_4945404del, NM_002705.4:c.1102_1104del (PPL))

Chromosome 16
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.4945402_4945404del
DNA change (hg38) g.4895401_4895403del
Published as PPL(NM_002705.4):c.1102_1104del (p.(Glu368del)), PPL(NM_002705.5):c.1102_1104delGAG (p.E368del)
ISCN -
DB-ID PPL_000008 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) 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPL NM_002705.4 -?/. - c.1102_1104del r.(?) p.(Glu368del)


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