Variant #0000722752 (NC_000010.10:g.14950941T>C, NM_001033855.1:c.1545A>G (DCLRE1C))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.14950941T>C
DNA change (hg38) -
Published as DCLRE1C(NM_001289079.1):c.1185A>G (p.G395=)
ISCN -
DB-ID DCLRE1C_000022
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) 0.00135 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.1545A>G r.(?) p.(Gly515=)
SUV39H2 NM_024670.3 -?/. - c.*6430T>C r.(=) p.(=)


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