Variant #0000867083 (NC_000023.10:g.13769452G>A, OFD1(NM_003611.2):c.1020G>A)

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.13769452G>A
DNA change (hg38) -
Published as OFD1(NM_001330210.2):c.600G>A (p.E200=), OFD1(NM_003611.3):c.1020G>A (p.E340=)
ISCN -
DB-ID OFD1_000151 See all 2 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) 0.00163 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC2 NM_001011658.3 -?/. - c.-16970C>T r.(?) p.(=)
OFD1 NM_003611.2 -?/. - c.1020G>A r.(?) p.(Glu340=)