Genomic variant #0000036947

Individual ID 00016995
Chromosome X
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.135104682G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC9A6_000008 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs6654309
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
SLC9A6 NM_001042537.1 ?/? - c.1351-63G>A - r.(=) p.(=)
SLC9A6 NM_006359.2 -/? 10i c.1351-63G>A - r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000016972 DNA SEQ - - SLC9A6 5 Johan den Dunnen