Variant #0000949653 (NC_000011.9:g.3849236C>T, NM_001256240.1:c.*2548C>T (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.3849236C>T
DNA change (hg38) -
Published as RHOG(NM_001665.4):c.133G>A (p.A45T)
ISCN -
DB-ID NUP98_000018
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) 0.00117 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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.*2548C>T r.(=) p.(=)
RHOG NM_001665.3 -?/. - c.133G>A r.(?) p.(Ala45Thr)
NUP98 NM_016320.4 -?/. - c.-30635G>A r.(?) p.(=)


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