Variant #0000867089 (NC_000023.10:g.13791089G>C, OFD1(NM_003611.2):c.*3862G>C)

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.13791089G>C
DNA change (hg38) -
Published as GPM6B(NM_001001995.3):c.898C>G (p.Q300E)
ISCN -
DB-ID OFD1_000163
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) 3.0E-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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPM6B NM_001001995.1 -?/. - c.898C>G r.(?) p.(Gln300Glu)
TRAPPC2 NM_001011658.3 -?/. - c.-38607C>G r.(?) p.(=)
OFD1 NM_003611.2 -?/. - c.*3862G>C r.(=) p.(=)