Variant #0000863734 (NC_000014.8:g.95597901T>G, NM_177438.2:c.383A>C (DICER1))

Chromosome 14
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.95597901T>G
DNA change (hg38) -
Published as DICER1(NM_001195573.1):c.383A>C (p.(Glu128Ala)), DICER1(NM_030621.4):c.383A>C (p.E128A)
ISCN -
DB-ID DICER1_000148 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DICER1 NM_177438.2 ?/. - c.383A>C r.(?) p.(Glu128Ala)


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