Variant #0000324824 (NC_000016.9:g.67226272C>T, NM_001040715.1:c.-9164G>A (KIAA0895L))

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.67226272C>T
DNA change (hg38) g.67192369C>T
Published as E2F4(NM_001950.3):c.135+7C>T (p.(=))
ISCN -
DB-ID E2F4_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) 0.0008 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     
KIAA0895L NM_001040715.1 ?/. - c.-9164G>A r.(?) p.(=)
E2F4 NM_001950.3 ?/. - c.135+7C>T r.(=) p.(=)
EXOC3L1 NM_178516.3 ?/. - c.-2406G>A r.(?) p.(=)


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