Variant #0001004273 (NC_000019.9:g.10225103G>A, NM_003755.3:c.*687C>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.10225103G>A
DNA change (hg38) -
Published as P2RY11(NM_002566.4):c.814G>A (p.(Val272Met))
ISCN -
DB-ID EIF3G_000008
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) 0.00199 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 2024-08-28 13:16:32 +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     
PPAN-P2RY11 NM_001040664.2 -?/. - c.2074G>A r.(?) p.(Val692Met)
P2RY11 NM_002566.4 -?/. - c.814G>A r.(?) p.(Val272Met)
EIF3G NM_003755.3 -?/. - c.*687C>T r.(=) p.(=)
PPAN NM_020230.5 -?/. - c.*3262G>A r.(=) p.(=)


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