Variant #0000275889 (NC_000020.10:g.32264747C>T, NM_001024675.1:c.*8706C>T (ACTL10))

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.32264747C>T
DNA change (hg38) g.33676941C>T
Published as E2F1(NM_005225.2):c.1105G>A (p.V369M)
ISCN -
DB-ID E2F1_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
ACTL10 NM_001024675.1 -?/. - c.*8706C>T r.(=) p.(=)
E2F1 NM_005225.2 -?/. - c.1105G>A r.(?) p.(Val369Met)
NECAB3 NM_031231.3 -?/. - c.-2589G>A r.(?) p.(=)
C20orf144 NM_080825.3 -?/. - c.*13074C>T r.(=) p.(=)


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