Variant #0001027444 (NC_000023.10:g.13732567T>A, NM_003611.2:c.-20624T>A (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.13732567T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID OFD1_000173
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC2 NM_001011658.3 +/. - c.382A>T r.(?) p.(Arg128*)
OFD1 NM_003611.2 +/. - c.-20624T>A r.(?) p.(=)
RAB9A NM_004251.4 +/. - c.*5096T>A r.(=) p.(=)


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