ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_012210.4(TRIM32):c.521C>T (p.Ser174Phe) rs138699534 0.00019
NM_012210.4(TRIM32):c.578G>A (p.Arg193His) rs373853273 0.00019
NM_012210.4(TRIM32):c.863C>A (p.Pro288His) rs367574371 0.00012
NM_012210.4(TRIM32):c.1012G>A (p.Ala338Thr) rs141806013 0.00008
NM_012210.4(TRIM32):c.265G>A (p.Ala89Thr) rs539376933 0.00005
NM_012210.4(TRIM32):c.1544G>A (p.Arg515Gln) rs781359060 0.00004
NM_012210.4(TRIM32):c.496C>T (p.Arg166Trp) rs752016708 0.00004
NM_012210.4(TRIM32):c.133C>T (p.Arg45Cys) rs753738560 0.00003
NM_012210.4(TRIM32):c.1361T>C (p.Val454Ala) rs781475334 0.00003
NM_012210.4(TRIM32):c.1384G>A (p.Val462Met) rs772922696 0.00003
NM_012210.4(TRIM32):c.1648T>C (p.Phe550Leu) rs752860146 0.00003
NM_012210.4(TRIM32):c.1930A>G (p.Ser644Gly) rs1462453134 0.00003
NM_012210.4(TRIM32):c.206G>A (p.Arg69His) rs11556350 0.00003
NM_012210.4(TRIM32):c.410C>T (p.Pro137Leu) rs897930061 0.00002
NM_012210.4(TRIM32):c.1004G>A (p.Ser335Asn) rs778321975 0.00001
NM_012210.4(TRIM32):c.1081A>T (p.Met361Leu) rs1262205918 0.00001
NM_012210.4(TRIM32):c.1306A>G (p.Met436Val) rs746383181 0.00001
NM_012210.4(TRIM32):c.136C>G (p.Gln46Glu) rs1193048642 0.00001
NM_012210.4(TRIM32):c.1523G>A (p.Ser508Asn) rs1291429914 0.00001
NM_012210.4(TRIM32):c.1618C>T (p.Arg540Trp) rs147803099 0.00001
NM_012210.4(TRIM32):c.1709C>T (p.Ser570Leu) rs746590049 0.00001
NM_012210.4(TRIM32):c.326G>A (p.Arg109Gln) rs748324526 0.00001
NM_012210.4(TRIM32):c.32T>C (p.Leu11Pro) rs767818381 0.00001
NM_012210.4(TRIM32):c.809C>G (p.Pro270Arg) rs1861004120 0.00001
NM_012210.4(TRIM32):c.97C>T (p.Arg33Cys) rs778141507 0.00001
NM_012210.4(TRIM32):c.1222C>G (p.Arg408Gly) rs3747835
NM_012210.4(TRIM32):c.138G>C (p.Gln46His) rs1860949227
NM_012210.4(TRIM32):c.1423A>G (p.Ile475Val)
NM_012210.4(TRIM32):c.1526G>C (p.Cys509Ser)
NM_012210.4(TRIM32):c.1685G>A (p.Gly562Asp) rs1221648426
NM_012210.4(TRIM32):c.1757G>C (p.Arg586Pro) rs866695848
NM_012210.4(TRIM32):c.1787G>A (p.Arg596His) rs750300057
NM_012210.4(TRIM32):c.1864A>G (p.Ile622Val) rs1366193406
NM_012210.4(TRIM32):c.280G>A (p.Ala94Thr) rs1231169096
NM_012210.4(TRIM32):c.286G>A (p.Gly96Arg) rs752329242
NM_012210.4(TRIM32):c.323C>T (p.Pro108Leu) rs2491058537
NM_012210.4(TRIM32):c.330A>T (p.Gln110His) rs770015462
NM_012210.4(TRIM32):c.457T>A (p.Leu153Ile) rs2491059792
NM_012210.4(TRIM32):c.479T>C (p.Met160Thr) rs199699832
NM_012210.4(TRIM32):c.590A>G (p.Asp197Gly) rs1860988255
NM_012210.4(TRIM32):c.602G>A (p.Arg201His)
NM_012210.4(TRIM32):c.653G>T (p.Ser218Ile)
NM_012210.4(TRIM32):c.658G>A (p.Val220Met)
NM_012210.4(TRIM32):c.713G>A (p.Arg238His) rs564290779
NM_012210.4(TRIM32):c.722A>C (p.Tyr241Ser)
NM_012210.4(TRIM32):c.811C>G (p.Arg271Gly) rs372298402
NM_012210.4(TRIM32):c.811C>T (p.Arg271Trp) rs372298402
NM_012210.4(TRIM32):c.872T>C (p.Ile291Thr)
NM_012210.4(TRIM32):c.917C>G (p.Ser306Cys) rs756710806

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.