Variant #0000853927 (NC_000014.8:g.95574727C>T, NM_177438.2:c.2370G>A (DICER1))

Chromosome 14
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.95574727C>T
DNA change (hg38) -
Published as DICER1(NM_030621.4):c.2370G>A (p.R790=), DICER1(NM_177438.2):c.2370G>A (p.R790=), DICER1(NM_177438.3):c.2370G>A (p.R790=)
ISCN -
DB-ID DICER1_000141 See all 3 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) 0.00177 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DICER1 NM_177438.2 -/. - c.2370G>A r.(?) p.(Arg790=)


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