Variant #0000608962 (NC_000004.11:g.106395191_106395199dup, NM_176869.2:c.18_26dup (PPA2))

Chromosome 4
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.106395191_106395199dup
DNA change (hg38) g.105474034_105474042dup
Published as PPA2(NM_176869.2):c.18_26dupGCTGCTGCG (p.L7_R9dup), PPA2(NM_176869.3):c.18_26dupGCTGCTGCG (p.L7_R9dup)
ISCN -
DB-ID PPA2_000034 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPA2 NM_176869.2 ?/. - c.18_26dup r.(?) p.(Leu7_Arg9dup)


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