Variant #0000317011 (NC_000023.10:g.13752240C>T, NM_003611.2:c.-951C>T (OFD1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13752240C>T
DNA change (hg38) g.13734121C>T
Published as TRAPPC2(NM_001128835.2):c.12G>A (p.W4*), TRAPPC2(NM_001128835.3):c.12G>A (p.(Trp4Ter))
ISCN -
DB-ID OFD1_000009 See all 4 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) 0.0004 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.-97G>A r.(?) p.(=)
OFD1 NM_003611.2 -?/. - c.-951C>T r.(?) p.(=)


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