Variant #0000856379 (NC_000023.10:g.13785278G>A, OFD1(NM_003611.2):c.2632G>A)

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.13785278G>A
DNA change (hg38) -
Published as OFD1(NM_003611.3):c.2632G>A (p.E878K)
ISCN -
DB-ID OFD1_000159
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPM6B NM_001001995.1 -/. - c.*5722C>T r.(=) p.(=)
TRAPPC2 NM_001011658.3 -/. - c.-32796C>T r.(?) p.(=)
OFD1 NM_003611.2 -/. - c.2632G>A r.(?) p.(Glu878Lys)