Genomic variant #0000333224

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.14932620C>A
DNA change (hg38) -
Published as MOSPD2(NM_001177475.1):c.804-5C>A (p.?)
ISCN -
DB-ID MOSPD2_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00587 View details
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
MOSPD2 NM_152581.3 -?/. - c.993-5C>A likely benign r.spl? p.?