Variant #0000885017 (NC_000002.11:g.232995439T>G, NC_000002.11(NM_152383.4):c.702+10T>G (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.232995439T>G
DNA change (hg38) -
Published as DIS3L2(NM_001257282.1):c.712T>G (p.Y238D, p.(Tyr238Asp)), DIS3L2(NM_152383.4):c.702+10T>G, DIS3L2(NM_152383.5):c.702+10T>G
ISCN -
DB-ID DIS3L2_000013 See all 4 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) 0.00424 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +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.702+10T>G r.(=) p.(=)


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