ClinVar Miner

List of variants in gene SLC9A6 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln) rs146263125 0.00166
NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=) rs151178361 0.00022
NM_001379110.1(SLC9A6):c.15C>G (p.Ile5Met) rs782296172 0.00004
NM_001379110.1(SLC9A6):c.1081-8C>T rs1060504684 0.00001
NM_001379110.1(SLC9A6):c.1385C>T (p.Thr462Met) rs1229345478 0.00001
NM_001379110.1(SLC9A6):c.256A>G (p.Ser86Gly) rs587784401 0.00001
NM_001379110.1(SLC9A6):c.744-7T>C rs1556618483 0.00001
GRCh37/hg19 Xq26.3(chrX:135092601-135092742)x4
NM_001379110.1(SLC9A6):c.*1G>C rs2521487076
NM_001379110.1(SLC9A6):c.*4T>C rs2521487124
NM_001379110.1(SLC9A6):c.1164C>T (p.Val388=) rs1556619315
NM_001379110.1(SLC9A6):c.1342C>T (p.Arg448Ter) rs122461162
NM_001379110.1(SLC9A6):c.1389T>C (p.Leu463=) rs1556620345
NM_001379110.1(SLC9A6):c.1503T>C (p.His501=) rs2071271908
NM_001379110.1(SLC9A6):c.1661+1G>A rs796053283
NM_001379110.1(SLC9A6):c.170-6T>A
NM_001379110.1(SLC9A6):c.178G>A (p.Val60Met) rs906567942
NM_001379110.1(SLC9A6):c.1812T>C (p.Asn604=)
NM_001379110.1(SLC9A6):c.1869A>T (p.Thr623=) rs2071565905
NM_001379110.1(SLC9A6):c.321T>C (p.Ile107=)
NM_001379110.1(SLC9A6):c.442_444delinsC (p.Lys148fs) rs2148149936
NM_001379110.1(SLC9A6):c.529A>G (p.Ile177Val) rs587784402
NM_001379110.1(SLC9A6):c.743+2dup rs1603201598
NM_001379110.1(SLC9A6):c.743+3_743+6del rs2148156632
NM_001379110.1(SLC9A6):c.837C>T (p.Phe279=) rs2521290502
NM_001379110.1(SLC9A6):c.991G>C (p.Gly331Arg) rs2148174022

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.