ClinVar Miner

List of variants in gene TCTN2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024809.5(TCTN2):c.*493T>A rs569489612 0.00338
NM_024809.5(TCTN2):c.720C>G (p.Pro240=) rs149430216 0.00236
NM_024809.5(TCTN2):c.-2G>A rs141768405 0.00224
NM_024809.5(TCTN2):c.615C>T (p.Gly205=) rs147485641 0.00143
NM_024809.5(TCTN2):c.668C>T (p.Thr223Met) rs145374149 0.00124
NM_024809.5(TCTN2):c.776A>G (p.Gln259Arg) rs151318349 0.00070
NM_024809.5(TCTN2):c.571T>G (p.Ser191Ala) rs146698907 0.00036
NM_024809.5(TCTN2):c.1756G>A (p.Gly586Ser) rs199543783 0.00020
NM_024809.5(TCTN2):c.631G>A (p.Val211Ile) rs544183268 0.00010
NM_024809.5(TCTN2):c.564+3A>C rs761089886 0.00007
NM_024809.5(TCTN2):c.*146C>T rs1046414186 0.00004
NM_024809.5(TCTN2):c.1055T>A (p.Ile352Asn) rs762326056 0.00004
NM_024809.5(TCTN2):c.1474G>T (p.Val492Phe) rs1449279317 0.00004
NM_024809.5(TCTN2):c.1544C>T (p.Ala515Val) rs748105865 0.00004
NM_024809.5(TCTN2):c.577A>C (p.Asn193His) rs370944870 0.00004
NM_024809.5(TCTN2):c.271G>T (p.Val91Leu) rs371662397 0.00003
NM_024809.5(TCTN2):c.1612C>T (p.Arg538Cys) rs561214391 0.00002
NM_024809.5(TCTN2):c.1813G>A (p.Glu605Lys) rs768079186 0.00002
NM_024809.5(TCTN2):c.1967G>C (p.Trp656Ser) rs200159224 0.00002
NM_024809.5(TCTN2):c.1235-3T>C rs1156410703 0.00001
NM_024809.5(TCTN2):c.1849G>A (p.Val617Ile) rs376095561 0.00001
NM_024809.5(TCTN2):c.2005G>A (p.Val669Ile) rs768699111 0.00001
NM_024809.5(TCTN2):c.267+4A>C rs199924687 0.00001
NM_024809.5(TCTN2):c.429T>C (p.Ile143=) rs188417716 0.00001
NM_024809.5(TCTN2):c.89T>C (p.Ile30Thr) rs760245764 0.00001
NM_024809.5(TCTN2):c.1100-10G>A rs794727008
NM_024809.5(TCTN2):c.1123A>G (p.Thr375Ala) rs1256664879
NM_024809.5(TCTN2):c.1234+3A>T
NM_024809.5(TCTN2):c.1319A>C (p.Gln440Pro) rs1956109718
NM_024809.5(TCTN2):c.1386G>T (p.Trp462Cys) rs727504176
NM_024809.5(TCTN2):c.1394-10_1394-5del rs754718630
NM_024809.5(TCTN2):c.1531T>G (p.Ser511Ala) rs2135852888
NM_024809.5(TCTN2):c.1556C>G (p.Ala519Gly) rs1221017555
NM_024809.5(TCTN2):c.1748A>T (p.Glu583Val)
NM_024809.5(TCTN2):c.1896-5T>C rs2135862725
NM_024809.5(TCTN2):c.191-10_191-8del rs1955759155
NM_024809.5(TCTN2):c.1972C>T (p.Gln658Ter)
NM_024809.5(TCTN2):c.671C>T (p.Thr224Met) rs376996387
NM_024809.5(TCTN2):c.758G>T (p.Gly253Val) rs1955979058
NM_024809.5(TCTN2):c.810C>A (p.Asp270Glu) rs144567556

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.