ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000009.12:g.137200984C>A rs66708191 0.28431
NM_001128228.3(TPRN):c.559G>T (p.Ala187Ser) rs9411313 0.27092
NM_001128228.3(TPRN):c.1725+151C>T rs72763294 0.22381
NM_001128228.3(TPRN):c.1073T>C (p.Leu358Pro) rs60910563 0.01648
NM_001128228.3(TPRN):c.1725+10G>C rs79139547 0.01622
NM_001128228.3(TPRN):c.1138G>T (p.Ala380Ser) rs190167940 0.01244
NM_001128228.3(TPRN):c.858C>T (p.Cys286=) rs375619082 0.01068
NM_001128228.3(TPRN):c.891C>G (p.Phe297Leu) rs147404722 0.00686
NM_001128228.3(TPRN):c.1929G>A (p.Val643=) rs115446132 0.00430
NM_001128228.3(TPRN):c.533C>T (p.Ala178Val) rs971592946 0.00396
NM_001128228.3(TPRN):c.609C>T (p.Asn203=) rs546101231 0.00320
NM_001128228.3(TPRN):c.969C>T (p.Leu323=) rs145558759 0.00289
NM_001128228.3(TPRN):c.1748A>G (p.Lys583Arg) rs139459217 0.00238
NM_001128228.3(TPRN):c.1256C>T (p.Pro419Leu) rs149753507 0.00148
NM_001128228.3(TPRN):c.1967-26G>A rs375685083 0.00064
NM_001128228.3(TPRN):c.1094A>G (p.Gln365Arg) rs780953179 0.00028
NM_001128228.3(TPRN):c.2073+10G>C rs368771637 0.00027
NM_001128228.3(TPRN):c.1818GGA[10] (p.Glu621dup) rs376810326
NM_001128228.3(TPRN):c.1818GGA[7] (p.Glu620_Glu621del) rs376810326
NM_001128228.3(TPRN):c.1818GGA[8] (p.Glu621del) rs376810326
NM_001128228.3(TPRN):c.894G>A (p.Glu298=) rs539737661

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.