Variant #0000515047 (NC_000002.11:g.232952256C>T, NM_152383.4:c.426C>T (DIS3L2))

Chromosome 2
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.232952256C>T
DNA change (hg38) g.232087546C>T
Published as DIS3L2(NM_001257281.1):c.426C>T (p.(Pro142=)), DIS3L2(NM_152383.5):c.426C>T (p.P142=)
ISCN -
DB-ID DIS3L2_000010 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) 0.01145 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIS3L2 NM_152383.4 -/. - c.426C>T r.(?) p.(Pro142=)


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