Variant #0000324828 (NC_000016.9:g.67237622G>A, NM_001950.3:c.*5596G>A (E2F4))

Chromosome 16
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.67237622G>A
DNA change (hg38) g.67203719G>A
Published as ELMO3(NM_024712.3):c.2164G>A (p.(Glu722Lys))
ISCN -
DB-ID ELMO3_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) 0.00046 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 2018-01-15 20:58:59 +01:00 (CET)
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     
E2F4 NM_001950.3 ?/. - c.*5596G>A r.(=) p.(=)
LRRC29 NM_012163.2 ?/. - c.*3792C>T r.(=) p.(=)
ELMO3 NM_024712.3 ?/. - c.2164G>A r.(?) p.(Glu722Lys)


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