Variant #0001055383 (NC_000016.9:g.2287231C>G, NM_004424.3:c.*1658C>G (E4F1))

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.2287231C>G
DNA change (hg38) -
Published as DNASE1L2(NM_001374.3):c.246C>G (p.(His82Gln))
ISCN -
DB-ID DNASE1L2_000011
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) 0.00038 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECI1 NM_001178029.1 ?/. - c.*2749G>C r.(=) p.(=)
DNASE1L2 NM_001374.2 ?/. - c.246C>G r.(?) p.(His82Gln)
E4F1 NM_004424.3 ?/. - c.*1658C>G r.(=) p.(=)


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