ClinVar Miner

List of variants in gene SLC39A4 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_130849.4(SLC39A4):c.751= (p.Arg251=) rs2977838 0.96739
NM_130849.4(SLC39A4):c.1150-42= rs4992316 0.95529
NM_130849.4(SLC39A4):c.172G>A (p.Ala58Thr) rs2280838 0.51612
NM_130849.4(SLC39A4):c.193-89A>C rs2280839 0.49986
NM_130849.4(SLC39A4):c.1287+22C>G rs736676 0.44902
NM_130849.4(SLC39A4):c.340G>A (p.Ala114Thr) rs17855765 0.43910
NM_130849.4(SLC39A4):c.1069A>G (p.Thr357Ala) rs2272662 0.43646
NM_130849.4(SLC39A4):c.1114= (p.Val372=) rs1871534 0.24978
NM_130849.4(SLC39A4):c.1419+28= rs2928381 0.14052
NM_130849.4(SLC39A4):c.193-113T>C rs115637224 0.05521
NM_130849.4(SLC39A4):c.1475-38G>T rs116260554 0.05236
NM_130849.4(SLC39A4):c.1141A>G (p.Thr381Ala) rs75920625 0.04681
NM_130849.4(SLC39A4):c.63G>C (p.Thr21=) rs13251676 0.04058
NM_130849.4(SLC39A4):c.751C>T (p.Arg251Trp) rs2977838 0.03261
NM_130849.4(SLC39A4):c.850G>A (p.Glu284Lys) rs7823979 0.02971
NM_130849.4(SLC39A4):c.251C>T (p.Pro84Leu) rs117535951 0.02765
NM_130849.4(SLC39A4):c.276C>T (p.Tyr92=) rs4355816 0.02200
NM_130849.4(SLC39A4):c.-21T>G rs77422016 0.01680
NM_130849.4(SLC39A4):c.473= (p.Met158=) rs1871533 0.00808
NM_130849.4(SLC39A4):c.948C>T (p.Pro316=) rs60615103 0.00469
NM_130849.4(SLC39A4):c.532A>T (p.Ser178Cys) rs113717209 0.00402
NM_130849.4(SLC39A4):c.1495A>G (p.Met499Val) rs145832695 0.00335
NM_130849.4(SLC39A4):c.10C>T (p.Leu4=) rs144946747 0.00288
NM_130849.4(SLC39A4):c.504G>A (p.Glu168=) rs138825974 0.00178
NM_130849.4(SLC39A4):c.1659G>C (p.Leu553=) rs143778004 0.00170
NM_130849.4(SLC39A4):c.1704G>A (p.Thr568=) rs115808560 0.00165
NM_130849.4(SLC39A4):c.1150-15G>A rs200673705 0.00148
NM_130849.4(SLC39A4):c.1743C>T (p.Val581=) rs144252108 0.00130
NM_130849.4(SLC39A4):c.1851C>T (p.Pro617=) rs61729885 0.00116
NM_130849.4(SLC39A4):c.66G>A (p.Ala22=) rs142910470 0.00116
NM_130849.4(SLC39A4):c.257C>T (p.Pro86Leu) rs187080747 0.00098
NM_130849.4(SLC39A4):c.976+15C>T rs183614749 0.00058
NM_130849.4(SLC39A4):c.390C>T (p.Leu130=) rs782454483 0.00039
NM_130849.4(SLC39A4):c.321C>T (p.Pro107=) rs148918238 0.00031
NM_130849.4(SLC39A4):c.615C>T (p.Phe205=) rs201681875 0.00023
NM_130849.4(SLC39A4):c.1629G>A (p.Gly543=) rs548092140 0.00022
NM_130849.4(SLC39A4):c.1149+9C>T rs139192292 0.00009
NM_130849.4(SLC39A4):c.804+9C>T rs200693339 0.00009
NM_130849.4(SLC39A4):c.1149+10C>T rs782654111 0.00007
NM_130849.4(SLC39A4):c.213C>T (p.Ala71=) rs577104686 0.00006
NM_130849.4(SLC39A4):c.150G>A (p.Thr50=) rs541710271 0.00004
NM_130849.4(SLC39A4):c.225C>T (p.Gly75=) rs376105192 0.00003
NM_130849.4(SLC39A4):c.1149+10del rs1255181865
NM_130849.4(SLC39A4):c.1149+10dup
NM_130849.4(SLC39A4):c.1149+8C>T rs376765006
NM_130849.4(SLC39A4):c.1150-11del
NM_130849.4(SLC39A4):c.1474+14dup
NM_130849.4(SLC39A4):c.1627+16G>A
NM_130849.4(SLC39A4):c.192+5C>A rs73374077
NM_130849.4(SLC39A4):c.258G>A (p.Pro86=) rs369791792
NM_130849.4(SLC39A4):c.475-3dup
NM_130849.4(SLC39A4):c.804+18del
NM_130849.4(SLC39A4):c.805-12G>A
NM_130849.4(SLC39A4):c.805-12G>T rs139609894
NM_130849.4(SLC39A4):c.805-3del
NM_130849.4(SLC39A4):c.805-3dup rs2130799323
NM_130849.4(SLC39A4):c.977-3del
NM_130849.4(SLC39A4):c.977-3dup

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.