Variant #0000539588 (NC_000010.10:g.14977469C>T, NM_001033855.1:c.457G>A (DCLRE1C))

Chromosome 10
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.14977469C>T
DNA change (hg38) g.14935470C>T
Published as DCLRE1C(NM_001033858.3):c.97G>A (p.G33R), DCLRE1C(NM_001289079.2):c.97G>A (p.G33R)
ISCN -
DB-ID DCLRE1C_000008 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) 0.01043 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +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.457G>A r.(?) p.(Gly153Arg)


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