Genomic variant #0000573699

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135115680del
DNA change (hg38) g.136033521del
Published as SLC9A6(NM_001042537.1):c.1727+28delA
ISCN -
DB-ID SLC9A6_000054
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_Utrecht
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A6 NM_001042537.1 -/. - c.1727+28del r.(=) p.(=)
SLC9A6 NM_006359.2 -/. - c.1631+28del r.(=) p.(=)