Variant #0000723443 (NC_000011.9:g.3845245C>T, NM_001256240.1:c.298C>T (PGAP2))

Chromosome 11
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.3845245C>T
DNA change (hg38) -
Published as PGAP2(NM_001346401.1):c.308C>T (p.P103L)
ISCN -
DB-ID NUP98_000009
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) 0.00037 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGAP2 NM_001256240.1 ?/. - c.298C>T r.(?) p.(Leu100Phe)
RHOG NM_001665.3 ?/. - c.*3548G>A r.(=) p.(=)
NUP98 NM_016320.4 ?/. - c.-26644G>A r.(?) p.(=)


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