Variant #0000539585 (NC_000010.10:g.14950588dup, NM_001033855.1:c.1903dup (DCLRE1C))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.14950588dup
DNA change (hg38) g.14908589dup
Published as DCLRE1C(NM_001289079.1):c.1543dupA (p.S515Kfs*6)
ISCN -
DB-ID DCLRE1C_000012 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +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.1903dup r.(?) p.(Ser635LysfsTer6)
SUV39H2 NM_024670.3 +/. - c.*6077dup r.(?) p.(=)


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