Variant #0001040438 (NC_000015.9:g.51868398_51868400dup, NC_000015.9(NM_015263.3):c.88-5_88-3dup (DMXL2))

Chromosome 15
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.51868398_51868400dup
DNA change (hg38) -
Published as DMXL2(NM_001174116.1):c.88-5_88-3dupTTT, DMXL2(NM_001174116.3):c.88-5_88-3dupTTT
ISCN -
DB-ID DMXL2_000019 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMXL2 NM_015263.3 -/. - c.88-5_88-3dup r.spl? p.?


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