Variant #0000344216 (NC_000023.10:g.13786874A>T, OFD1(NM_003611.2):c.2966A>T)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.13786874A>T
DNA change (hg38) g.13768755A>T
Published as -
ISCN -
DB-ID OFD1_000055
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPM6B NM_001001995.1 ?/. - c.*4126T>A r.(=) p.(=)
TRAPPC2 NM_001011658.3 ?/. - c.-34392T>A r.(?) p.(=)
OFD1 NM_003611.2 ?/. - c.2966A>T r.(?) p.(Asp989Val)