Genomic variant #0000298368

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.135080635dup
DNA change (hg38) g.135998476dup
Published as SLC9A6(NM_001042537.1):c.604-6_604-5insT
ISCN -
DB-ID SLC9A6_000014 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A6 NM_001042537.1 -/. - c.604-6dup r.(=) p.(=)
SLC9A6 NM_006359.2 -/. - c.508-6dup r.(=) p.(=)