Variant #0000653987 (NC_000001.10:g.245019454_245019455del, NM_031844.2:c.1919_1920del (HNRNPU))

Chromosome 1
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.245019454_245019455del
DNA change (hg38) g.244856152_244856153del
Published as HNRNPU(NM_031844.2):c.1919_1920delTT (p.F640Yfs*7)
ISCN -
DB-ID HNRNPU_000032
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPU NM_031844.2 ?/. - c.1919_1920del r.(?) p.(Phe640TyrfsTer7)


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