Variant #0000806758 (NC_000015.9:g.51773257C>T, NM_015263.3:c.6046G>A (DMXL2))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.51773257C>T
DNA change (hg38) -
Published as DMXL2(NM_001174116.1):c.6046G>A (p.D2016N), DMXL2(NM_001174116.3):c.6046G>A (p.D2016N)
ISCN -
DB-ID DMXL2_000022 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) 0.00177 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 2021-09-17 14:40:49 +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.6046G>A r.(?) p.(Asp2016Asn)


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