Variant #0001040433 (NC_000015.9:g.51772229C>G, NM_015263.3:c.6672G>C (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.51772229C>G
DNA change (hg38) -
Published as DMXL2(NM_001174116.1):c.6672G>C (p.L2224F), DMXL2(NM_001378457.1):c.6672G>C (p.(Leu2224Phe))
ISCN -
DB-ID DMXL2_000032 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) 7.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMXL2 NM_015263.3 ?/. - c.6672G>C r.(?) p.(Leu2224Phe)


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