Variant #0001030880 (NC_000023.10:g.13764930_13764933del, NM_003611.2:c.686_689del (OFD1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13764930_13764933del
DNA change (hg38) -
Published as -
ISCN -
DB-ID OFD1_000175
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-04-22 03:50:10 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OFD1 NM_003611.2 +/. - c.686_689del r.(?) p.(Lys229IlefsTer13)


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