Variant #0000565493 (NC_000019.9:g.10225253A>C, NM_003755.3:c.*537T>G (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.10225253A>C
DNA change (hg38) g.10114577A>C
Published as P2RY11(NM_002566.4):c.964A>C (p.M322L), PPAN-P2RY11(NM_001040664.2):c.2224A>C (p.M742L)
ISCN -
DB-ID EIF3G_000006
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) 0.00025 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.2224A>C r.(?) p.(Met742Leu)
P2RY11 NM_002566.4 ?/. - c.964A>C r.(?) p.(Met322Leu)
EIF3G NM_003755.3 ?/. - c.*537T>G r.(=) p.(=)
PPAN NM_020230.5 ?/. - c.*3412A>C r.(=) p.(=)


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