Variant #0000561248 (NC_000017.10:g.37830315_37830316insTACTCTG, PGAP3(NM_033419.3):c.496-9_496-8insCAGAGTA)

Chromosome 17
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.37830315_37830316insTACTCTG
DNA change (hg38) g.39674062_39674063insTACTCTG
Published as -
ISCN -
DB-ID PGAP3_000027
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) Variant not found in online data sets
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGAP3 NM_033419.3 ?/. - c.496-9_496-8insCAGAGTA r.(=) p.(=)