Variant #0000565490 (NC_000019.9:g.10224430C>A, NM_003755.3:c.*1360G>T (EIF3G))

Chromosome 19
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.10224430C>A
DNA change (hg38) g.10113754C>A
Published as P2RY11(NM_002566.4):c.141C>A (p.(=))
ISCN -
DB-ID EIF3G_000003
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) 0.00076 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 11:32:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPAN-P2RY11 NM_001040664.2 -?/. - c.1401C>A r.(?) p.(Gly467=)
P2RY11 NM_002566.4 -?/. - c.141C>A r.(?) p.(Gly47=)
EIF3G NM_003755.3 -?/. - c.*1360G>T r.(=) p.(=)
PPAN NM_020230.5 -?/. - c.*2589C>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.