ClinVar Miner

List of variants in gene LZTR1 reported as likely pathogenic by Invitae

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.1397G>A (p.Arg466Gln) rs587777180 0.00006
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.2326-2A>G rs1475060729 0.00002
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.1785+1G>A rs145594158 0.00001
NM_006767.4(LZTR1):c.200+2T>G rs573971763 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.510-2A>G rs1458682620 0.00001
NM_006767.4(LZTR1):c.651+1G>T rs1450044732 0.00001
NM_006767.4(LZTR1):c.993+1G>A rs770368435 0.00001
NM_006767.4(LZTR1):c.1150-1G>C
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.1260+1G>C
NM_006767.4(LZTR1):c.1260+2T>A
NM_006767.4(LZTR1):c.1260+2T>C
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.1449+1G>A
NM_006767.4(LZTR1):c.1450-1G>A
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.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.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.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.2326-1G>A
NM_006767.4(LZTR1):c.2348_2351del (p.Thr783fs) rs587777179
NM_006767.4(LZTR1):c.2417T>G (p.Leu806Trp) rs2147970908
NM_006767.4(LZTR1):c.264-1G>A
NM_006767.4(LZTR1):c.264-2A>C
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.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.509+1G>A
NM_006767.4(LZTR1):c.594-1G>C
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.652-1G>T
NM_006767.4(LZTR1):c.652-2A>C
NM_006767.4(LZTR1):c.652-2A>G
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.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

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