Genomic variant #0000333223

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.14930369_14930371del
DNA change (hg38) -
Published as MOSPD2(NM_001177475.1):c.691-2_691del (p.?)
ISCN -
DB-ID MOSPD2_000006
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) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
MOSPD2 NM_152581.3 ?/. - c.880-2_880del VUS r.spl? p.?