Genomic variant #0000036955

Individual ID 00017022
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.135067656_135067991del
DNA change (hg38) g.135985497_135985832del
Published as -
ISCN -
DB-ID SLC9A6_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Andreas Tzschach




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
SLC9A6 NM_006359.2 +/? 1_1i c.-6_325+5del - r.0? p.0?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000016999 DNA SEQ-NG-I - - SLC9A6 1 Andreas Tzschach