Variant #0000252527 (NC_000023.10:g.13764954del, NM_003611.2:c.710del (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.13764954del
DNA change (hg38) g.13746835del
Published as OFD1(NM_003611.3):c.710delA (p.K237Sfs*6)
ISCN -
DB-ID OFD1_000015
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC2 NM_001011658.3 +/. - c.-12464del r.(?) p.(=)
OFD1 NM_003611.2 +/. - c.710del r.(?) p.(Lys237SerfsTer6)


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