Variant #0000852896 (NC_000011.9:g.3848892G>A, NM_001256240.1:c.*2204G>A (PGAP2))

Chromosome 11
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.3848892G>A
DNA change (hg38) -
Published as RHOG(NM_001665.4):c.477C>T (p.A159=)
ISCN -
DB-ID NUP98_000013
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 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 2022-05-09 15:40:45 +02:00 (CEST)
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.*2204G>A r.(=) p.(=)
RHOG NM_001665.3 -?/. - c.477C>T r.(?) p.(Ala159=)
NUP98 NM_016320.4 -?/. - c.-30291C>T r.(?) p.(=)


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