Variant #0000036953 (NC_000023.10:g.135122262C>T, SLC9A6(NM_006359.2):c.1755C>T)

Individual ID 00016995
Chromosome X
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135122262C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC9A6_000004 See all 5 reported entries
Variant remarks Variant Error [EMISMATCH/EREF]: This transcript variant does not match the reference sequence. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID rs2307131
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.03612 View details
Owner Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A6 NM_001042537.1 ?/? - c.1755C>T r.(=) p.(=)
SLC9A6 NM_006359.2 -/? 15 c.1755C>T r.(?) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000016972 DNA SEQ - - SLC9A6 5 Johan den Dunnen