Variant #0000678810 (NC_000010.10:g.14950436_14950439del, NM_001033855.1:c.2050_2053del (DCLRE1C))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.14950436_14950439del
DNA change (hg38) -
Published as DCLRE1C(NM_001289079.1):c.1690_1693delAAAA (p.K564Efs*6)
ISCN -
DB-ID DCLRE1C_000020
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCLRE1C NM_001033855.1 +?/. - c.2050_2053del r.(?) p.(Lys684GlufsTer6)
SUV39H2 NM_024670.3 +?/. - c.*5925_*5928del r.(=) p.(=)


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