Variant #0000983781 (NC_000020.10:g.33872191A>G, NM_002212.3:c.100T>C (EIF6))

Chromosome 20
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.33872191A>G
DNA change (hg38) -
Published as EIF6(NM_002212.4):c.100T>C (p.(Phe34Leu))
ISCN -
DB-ID EIF6_000002
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) 0.00021 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 2024-04-19 20:27:30 +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     
EIF6 NM_002212.3 -?/. - c.100T>C r.(?) p.(Phe34Leu)
FAM83C NM_178468.5 -?/. - c.*2147T>C r.(=) p.(=)


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