Genomic variant #0000001892

Individual ID 00000208
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.47342008_47342009insCGCG
DNA change (hg38) g.47482609_47482610insCGCG
Published as -
ISCN -
DB-ID ZNF41_000010
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Yu Sun




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
ZNF41 NM_007130.2 ?/. - c.-431_-430insCGCG - - p.(=)
CXorf24 XR_110617.1 ?/. - n.151_152insCGCG - - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000000209 DNA SEQ-NG-I - - - 6369 Yu Sun