Variant #0000516590 (NC_000002.11:g.68408109_68408111del, NM_020143.2:c.*6175_*6177del (PNO1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.68408109_68408111del
DNA change (hg38) g.68180977_68180979del
Published as PPP3R1(NM_000945.4):c.501_503delGGT (p.V168del)
ISCN -
DB-ID PNO1_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP3R1 NM_000945.3 ?/. - c.501_503del r.(?) p.(Val168del)
PNO1 NM_020143.2 ?/. - c.*6175_*6177del r.(=) p.(=)


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