ClinVar Miner

List of variants in gene LZTR1 reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 156
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.264-13G>A rs587777176 0.00017
NM_006767.4(LZTR1):c.2428C>T (p.Arg810Trp) rs776893978 0.00009
NM_006767.4(LZTR1):c.1084C>T (p.Arg362Ter) rs189150283 0.00007
NM_006767.4(LZTR1):c.1397G>A (p.Arg466Gln) rs587777180 0.00006
NM_006767.4(LZTR1):c.1018C>T (p.Arg340Ter) rs149850248 0.00005
NM_006767.4(LZTR1):c.2387T>C (p.Ile796Thr) rs141672122 0.00005
NM_006767.4(LZTR1):c.1943-1G>A rs1189015572 0.00004
NM_006767.4(LZTR1):c.842C>T (p.Pro281Leu) rs1390048261 0.00003
NM_006767.4(LZTR1):c.1794C>A (p.Cys598Ter) rs982944299 0.00002
NM_006767.4(LZTR1):c.2326-2A>G rs1475060729 0.00002
NM_006767.4(LZTR1):c.2463dup (p.Asp822fs) rs781251567 0.00002
NM_006767.4(LZTR1):c.-38T>A rs1459786357 0.00001
NM_006767.4(LZTR1):c.1251C>G (p.Tyr417Ter) rs1924657431 0.00001
NM_006767.4(LZTR1):c.1260+1G>A rs143868364 0.00001
NM_006767.4(LZTR1):c.1261-2A>G rs759240190 0.00001
NM_006767.4(LZTR1):c.1729C>T (p.Gln577Ter) rs1390034681 0.00001
NM_006767.4(LZTR1):c.1733_1734del (p.Asn578fs) rs1460026299 0.00001
NM_006767.4(LZTR1):c.1785+1G>A rs145594158 0.00001
NM_006767.4(LZTR1):c.200+2T>G rs573971763 0.00001
NM_006767.4(LZTR1):c.2407-2A>G rs1158550690 0.00001
NM_006767.4(LZTR1):c.365C>T (p.Ser122Leu) rs587777177 0.00001
NM_006767.4(LZTR1):c.401-2A>G rs1222197005 0.00001
NM_006767.4(LZTR1):c.401-2_401-1del rs769200796 0.00001
NM_006767.4(LZTR1):c.509G>A (p.Arg170Gln) rs781431741 0.00001
NM_006767.4(LZTR1):c.510-2A>G rs1458682620 0.00001
NM_006767.4(LZTR1):c.651+1G>T rs1450044732 0.00001
NM_006767.4(LZTR1):c.671dup (p.Ser227fs) rs1351226319 0.00001
NM_006767.4(LZTR1):c.848G>A (p.Arg283Gln) rs1223430276 0.00001
NM_006767.4(LZTR1):c.955C>T (p.Gln319Ter) rs1924617179 0.00001
NM_006767.4(LZTR1):c.993+1G>A rs770368435 0.00001
NM_006767.4(LZTR1):c.1005_1012del (p.Glu336fs) rs753474547
NM_006767.4(LZTR1):c.1033G>T (p.Glu345Ter) rs761956867
NM_006767.4(LZTR1):c.1149+1G>A rs767191322
NM_006767.4(LZTR1):c.1150-1G>C
NM_006767.4(LZTR1):c.1199T>C (p.Met400Thr)
NM_006767.4(LZTR1):c.1210G>C (p.Gly404Arg)
NM_006767.4(LZTR1):c.1214G>C (p.Gly405Ala)
NM_006767.4(LZTR1):c.1235G>A (p.Arg412His) rs935736801
NM_006767.4(LZTR1):c.1243G>T (p.Glu415Ter)
NM_006767.4(LZTR1):c.1250A>C (p.Tyr417Ser) rs1057524046
NM_006767.4(LZTR1):c.1260+1G>C
NM_006767.4(LZTR1):c.1260+2T>A
NM_006767.4(LZTR1):c.1260+2T>C
NM_006767.4(LZTR1):c.1284dup (p.Leu429fs) rs2147966682
NM_006767.4(LZTR1):c.1317_1323dup (p.Phe442fs) rs1131691862
NM_006767.4(LZTR1):c.1339T>G (p.Phe447Val) rs1312334046
NM_006767.4(LZTR1):c.1353+1G>A
NM_006767.4(LZTR1):c.1353+1G>T
NM_006767.4(LZTR1):c.1353+2T>C
NM_006767.4(LZTR1):c.1353+2T>G
NM_006767.4(LZTR1):c.1354-2A>G
NM_006767.4(LZTR1):c.1447C>T (p.Gln483Ter) rs752547717
NM_006767.4(LZTR1):c.1449+1G>A
NM_006767.4(LZTR1):c.1450-1G>A
NM_006767.4(LZTR1):c.1472del (p.Pro491fs)
NM_006767.4(LZTR1):c.150_151del (p.Val51fs) rs1194536394
NM_006767.4(LZTR1):c.1605C>A (p.Tyr535Ter) rs753347937
NM_006767.4(LZTR1):c.1615+1G>C rs1381717741
NM_006767.4(LZTR1):c.1615+2T>A rs1180748005
NM_006767.4(LZTR1):c.1616-1G>A
NM_006767.4(LZTR1):c.1616-1G>C
NM_006767.4(LZTR1):c.1616-2A>G rs1328046881
NM_006767.4(LZTR1):c.1687G>C (p.Glu563Gln) rs1374240053
NM_006767.4(LZTR1):c.1702C>T (p.Gln568Ter)
NM_006767.4(LZTR1):c.1785+2T>A
NM_006767.4(LZTR1):c.1786-2A>C
NM_006767.4(LZTR1):c.1786-2A>G rs2147968271
NM_006767.4(LZTR1):c.1866_1867dup (p.Pro623fs) rs1601722136
NM_006767.4(LZTR1):c.1887_1888insAG (p.Arg630fs) rs1924776706
NM_006767.4(LZTR1):c.1942+1G>A
NM_006767.4(LZTR1):c.1942+2T>C
NM_006767.4(LZTR1):c.1943-2A>C
NM_006767.4(LZTR1):c.1943-2A>G rs768770438
NM_006767.4(LZTR1):c.200+1G>C
NM_006767.4(LZTR1):c.200+1G>T
NM_006767.4(LZTR1):c.200+2T>C
NM_006767.4(LZTR1):c.2069+1G>A
NM_006767.4(LZTR1):c.2069+1G>C rs200472467
NM_006767.4(LZTR1):c.2069+2T>C
NM_006767.4(LZTR1):c.2070-1G>A
NM_006767.4(LZTR1):c.2070-2A>G rs774954465
NM_006767.4(LZTR1):c.2090G>A (p.Arg697Gln) rs370638947
NM_006767.4(LZTR1):c.2113C>T (p.Gln705Ter) rs778396468
NM_006767.4(LZTR1):c.2134G>T (p.Glu712Ter) rs1409419929
NM_006767.4(LZTR1):c.2219+1G>A
NM_006767.4(LZTR1):c.2219+1G>C
NM_006767.4(LZTR1):c.2219+1G>T rs1342909456
NM_006767.4(LZTR1):c.2219+2C>A
NM_006767.4(LZTR1):c.2220-1G>C rs1924863354
NM_006767.4(LZTR1):c.2220-2A>C
NM_006767.4(LZTR1):c.2264G>T (p.Arg755Leu) rs762834512
NM_006767.4(LZTR1):c.2303dup (p.Thr769fs) rs1231204217
NM_006767.4(LZTR1):c.2326-1G>A
NM_006767.4(LZTR1):c.2347dup (p.Thr783fs)
NM_006767.4(LZTR1):c.2348_2351del (p.Thr783fs) rs587777179
NM_006767.4(LZTR1):c.2404_2405delinsTTGG (p.Lys802fs) rs1601723893
NM_006767.4(LZTR1):c.2406+1G>T rs770322736
NM_006767.4(LZTR1):c.2407-2A>C rs1158550690
NM_006767.4(LZTR1):c.2412dup (p.Lys805fs) rs1924895839
NM_006767.4(LZTR1):c.2417T>G (p.Leu806Trp) rs2147970908
NM_006767.4(LZTR1):c.2443C>T (p.Gln815Ter)
NM_006767.4(LZTR1):c.264-1G>A
NM_006767.4(LZTR1):c.264-2A>C
NM_006767.4(LZTR1):c.272T>C (p.Met91Thr) rs1555927321
NM_006767.4(LZTR1):c.320+1G>A rs943939913
NM_006767.4(LZTR1):c.320+1G>C rs943939913
NM_006767.4(LZTR1):c.320+2T>A
NM_006767.4(LZTR1):c.320+2T>G
NM_006767.4(LZTR1):c.321-1G>A
NM_006767.4(LZTR1):c.321-2A>G
NM_006767.4(LZTR1):c.321-2del
NM_006767.4(LZTR1):c.347C>T (p.Ala116Val)
NM_006767.4(LZTR1):c.348_349insT (p.Pro117fs) rs1555927544
NM_006767.4(LZTR1):c.352dup (p.Arg118fs) rs1486960809
NM_006767.4(LZTR1):c.370GTC[1] (p.Val125del) rs755783378
NM_006767.4(LZTR1):c.400+1G>A
NM_006767.4(LZTR1):c.400+1G>C rs1555927561
NM_006767.4(LZTR1):c.401-1G>C rs747225246
NM_006767.4(LZTR1):c.431C>A (p.Ser144Tyr) rs771885420
NM_006767.4(LZTR1):c.436T>A (p.Leu146Met) rs1555927611
NM_006767.4(LZTR1):c.438del (p.Lys147fs) rs1555927613
NM_006767.4(LZTR1):c.509+1G>A
NM_006767.4(LZTR1):c.509+1G>T rs886041542
NM_006767.4(LZTR1):c.542dup (p.Val182fs) rs1601717797
NM_006767.4(LZTR1):c.594-1G>C
NM_006767.4(LZTR1):c.597G>C (p.Leu199Phe) rs1555927827
NM_006767.4(LZTR1):c.604_605del (p.Met202fs)
NM_006767.4(LZTR1):c.609G>A (p.Trp203Ter) rs778525532
NM_006767.4(LZTR1):c.628dup (p.Arg210fs) rs1457594219
NM_006767.4(LZTR1):c.649G>T (p.Glu217Ter) rs1302923931
NM_006767.4(LZTR1):c.651+1G>A
NM_006767.4(LZTR1):c.651+2T>A
NM_006767.4(LZTR1):c.651+2T>C
NM_006767.4(LZTR1):c.651+5G>A rs766055427
NM_006767.4(LZTR1):c.652-1G>T
NM_006767.4(LZTR1):c.652-2A>C
NM_006767.4(LZTR1):c.652-2A>G
NM_006767.4(LZTR1):c.677del (p.Pro226fs)
NM_006767.4(LZTR1):c.677dup (p.Ser227fs) rs777054968
NM_006767.4(LZTR1):c.685T>G (p.Cys229Gly) rs886041925
NM_006767.4(LZTR1):c.730T>C (p.Ser244Pro) rs1601718760
NM_006767.4(LZTR1):c.737A>C (p.Gln246Pro) rs1057518336
NM_006767.4(LZTR1):c.774del (p.Phe258fs) rs780267761
NM_006767.4(LZTR1):c.791+1G>A rs148031742
NM_006767.4(LZTR1):c.792-1G>A
NM_006767.4(LZTR1):c.792-1G>C
NM_006767.4(LZTR1):c.792-1G>T
NM_006767.4(LZTR1):c.794G>A (p.Trp265Ter)
NM_006767.4(LZTR1):c.842del (p.Pro281fs) rs1419091884
NM_006767.4(LZTR1):c.955del (p.Gln319fs) rs1386054181
NM_006767.4(LZTR1):c.967_980del (p.Val323fs)
NM_006767.4(LZTR1):c.993+1G>T rs770368435
NM_006767.4(LZTR1):c.993+2T>G
NM_006767.4(LZTR1):c.994-1G>A
NM_006767.4(LZTR1):c.994-1G>T rs758238174
NM_006767.4(LZTR1):c.994-2A>T

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.