Variant #0000809948 (NC_000023.10:g.13734186A>G, OFD1(NM_003611.2):c.-19005A>G)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13734186A>G
DNA change (hg38) -
Published as TRAPPC2(NM_001011658.3):c.261T>C (p.H87=)
ISCN -
DB-ID OFD1_000130
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) 4.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC2 NM_001011658.3 -/. - c.261T>C r.(?) p.(His87=)
OFD1 NM_003611.2 -/. - c.-19005A>G r.(?) p.(=)