Genomic variant #0000619961

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.92928129_92928131dup
DNA change (hg38) -
Published as NAP1L3(NM_004538.5):c.177_178insGGC (p.(Gly59dup))
ISCN -
DB-ID NAP1L3_000010
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
NAP1L3 NM_004538.5 -?/. - c.175_177dup likely benign r.(?) p.(Gly59dup)
FAM133A NM_173698.2 -?/. - c.-1389_-1387dup likely benign r.(?) p.(=)