Variant #0000542649 (NC_000011.9:g.119056215C>T, NM_170722.1:c.*1526C>T (NLRX1))

Chromosome 11
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.119056215C>T
DNA change (hg38) g.119185506C>T
Published as PDZD3(NM_001168468.2):c.12C>T (p.A4=)
ISCN -
DB-ID PDZD3_000006
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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC153 NM_001145018.1 -?/. - c.*4794G>A r.(=) p.(=)
NLRX1 NM_170722.1 -?/. - c.*1526C>T r.(=) p.(=)


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