Variant #0000247120 (NC_000012.11:g.77419593A>G, NM_203394.2:c.2310T>C (E2F7))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77419593A>G
DNA change (hg38) g.77025813A>G
Published as E2F7(NM_203394.3):c.2310T>C (p.S770=)
ISCN -
DB-ID E2F7_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) 0.08308 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-02 17:04:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
E2F7 NM_203394.2 -/. - c.2310T>C r.(?) p.(Ser770=)


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