Variant #0000565491 (NC_000019.9:g.10224669G>A, NM_003755.3:c.*1121C>T (EIF3G))

Chromosome 19
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.10224669G>A
DNA change (hg38) g.10113993G>A
Published as P2RY11(NM_002566.4):c.380G>A (p.R127H), PPAN-P2RY11(NM_001040664.2):c.1640G>A (p.R547H)
ISCN -
DB-ID EIF3G_000004
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) 3.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPAN-P2RY11 NM_001040664.2 ?/. - c.1640G>A r.(?) p.(Arg547His)
P2RY11 NM_002566.4 ?/. - c.380G>A r.(?) p.(Arg127His)
EIF3G NM_003755.3 ?/. - c.*1121C>T r.(=) p.(=)
PPAN NM_020230.5 ?/. - c.*2828G>A r.(=) p.(=)


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