ClinVar Miner

List of variants in gene ASXL1 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_015338.6(ASXL1):c.2444= (p.Pro815=) rs6058694 0.99998
NM_015338.6(ASXL1):c.3759T>C (p.Ser1253=) rs4911231 0.34448
NM_015338.6(ASXL1):c.3973C>T (p.Leu1325Phe) rs6057581 0.02807
NM_015338.6(ASXL1):c.582C>T (p.His194=) rs116633791 0.02660
NM_015338.6(ASXL1):c.2985C>T (p.His995=) rs62206933 0.02455
NM_015338.6(ASXL1):c.2251G>A (p.Val751Ile) rs6058693 0.02141
NM_015338.6(ASXL1):c.2250C>T (p.Pro750=) rs35712951 0.01615
NM_015338.6(ASXL1):c.374-9C>T rs6087903 0.01488
NM_015338.6(ASXL1):c.2513A>G (p.Lys838Arg) rs35632616 0.01055
NM_015338.6(ASXL1):c.3306G>T (p.Glu1102Asp) rs139115934 0.00916
NM_015338.6(ASXL1):c.1954G>A (p.Gly652Ser) rs3746609 0.00875
NM_015338.6(ASXL1):c.3692C>T (p.Ser1231Phe) rs74638057 0.00841
NM_015338.6(ASXL1):c.3519G>A (p.Leu1173=) rs117901891 0.00839
NM_015338.6(ASXL1):c.3498C>G (p.Ser1166Arg) rs75887545 0.00728
NM_015338.6(ASXL1):c.2395G>T (p.Asp799Tyr) rs143594454 0.00568
NM_015338.6(ASXL1):c.3513G>A (p.Arg1171=) rs150391716 0.00538
NM_015338.6(ASXL1):c.1965C>T (p.Thr655=) rs79865730 0.00535
NM_015338.6(ASXL1):c.540C>T (p.Asn180=) rs74346706 0.00341
NM_015338.6(ASXL1):c.3745A>G (p.Met1249Val) rs146141075 0.00205
NM_015338.6(ASXL1):c.3384C>T (p.Asp1128=) rs149359320 0.00156
NM_015338.6(ASXL1):c.373+16T>G rs2145009 0.00148
NM_015338.6(ASXL1):c.1429G>C (p.Glu477Gln) rs141346625 0.00131
NM_015338.6(ASXL1):c.252+11T>C rs143337375 0.00128
NM_015338.6(ASXL1):c.2222A>T (p.Asp741Val) rs149971443 0.00117
NM_015338.6(ASXL1):c.4189G>A (p.Gly1397Ser) rs146464648 0.00113
NM_015338.6(ASXL1):c.4098C>T (p.Ser1366=) rs143041800 0.00078
NM_015338.6(ASXL1):c.1923C>T (p.Ile641=) rs551524526 0.00042
NM_015338.6(ASXL1):c.2337T>G (p.Pro779=) rs143613684 0.00031
NM_015338.6(ASXL1):c.2336C>T (p.Pro779Leu) rs41289850 0.00024
NM_015338.6(ASXL1):c.1474G>C (p.Ala492Pro) rs145913172 0.00020
NM_015338.6(ASXL1):c.3148A>G (p.Met1050Val) rs370804022 0.00019
NM_015338.6(ASXL1):c.2423C>A (p.Pro808His) rs141610022 0.00018
NM_015338.6(ASXL1):c.1557C>T (p.Pro519=) rs142869492 0.00017
NM_015338.6(ASXL1):c.2127C>T (p.Ala709=) rs140458480 0.00016
NM_015338.6(ASXL1):c.2593G>A (p.Glu865Lys) rs147895689 0.00016
NM_015338.6(ASXL1):c.2419G>A (p.Val807Ile) rs138624526 0.00015
NM_015338.6(ASXL1):c.3379G>A (p.Asp1127Asn) rs201009558 0.00015
NM_015338.6(ASXL1):c.3675A>T (p.Lys1225Asn) rs753682901 0.00015
NM_015338.6(ASXL1):c.252+11del rs758156686 0.00014
NM_015338.6(ASXL1):c.4139C>G (p.Ala1380Gly) rs139319958 0.00013
NM_015338.6(ASXL1):c.1831G>A (p.Ala611Thr) rs372418554 0.00011
NM_015338.6(ASXL1):c.605C>T (p.Pro202Leu) rs750262296 0.00010
NM_015338.6(ASXL1):c.3959C>T (p.Ala1320Val) rs760162421 0.00009
NM_015338.6(ASXL1):c.1162G>A (p.Val388Ile) rs145699348 0.00007
NM_015338.6(ASXL1):c.1907C>T (p.Ala636Val) rs370230857 0.00007
NM_015338.6(ASXL1):c.2618C>T (p.Pro873Leu) rs202098158 0.00006
NM_015338.6(ASXL1):c.2731C>T (p.Pro911Ser) rs371903529 0.00006
NM_015338.6(ASXL1):c.3460G>C (p.Gly1154Arg) rs199571804 0.00006
NM_015338.6(ASXL1):c.2387G>C (p.Trp796Ser) rs770674396 0.00005
NM_015338.6(ASXL1):c.2802T>C (p.Ala934=) rs571165637 0.00005
NM_015338.6(ASXL1):c.1200C>T (p.Ala400=) rs750058388 0.00004
NM_015338.6(ASXL1):c.2958C>T (p.Asn986=) rs200471411 0.00004
NM_015338.6(ASXL1):c.1956C>T (p.Gly652=) rs773591664 0.00003
NM_015338.6(ASXL1):c.2671G>A (p.Val891Ile) rs774520876 0.00003
NM_015338.6(ASXL1):c.3427A>C (p.Ser1143Arg) rs752770575 0.00003
NM_015338.6(ASXL1):c.4343A>G (p.Gln1448Arg) rs772452614 0.00003
NM_015338.6(ASXL1):c.1394A>G (p.His465Arg) rs749568474 0.00002
NM_015338.6(ASXL1):c.3152G>A (p.Arg1051His) rs771896604 0.00002
NM_015338.6(ASXL1):c.3273C>T (p.Ala1091=) rs377353179 0.00002
NM_015338.6(ASXL1):c.4244G>A (p.Arg1415Gln) rs143328954 0.00002
NM_015338.6(ASXL1):c.471+17G>A rs753933545 0.00002
NM_015338.6(ASXL1):c.1988G>A (p.Ser663Asn) rs763013543 0.00001
NM_015338.6(ASXL1):c.2495A>G (p.Asp832Gly) rs759926643 0.00001
NM_015338.6(ASXL1):c.2714A>T (p.Asp905Val) rs758140687 0.00001
NM_015338.6(ASXL1):c.2751A>G (p.Glu917=) rs768964987 0.00001
NM_015338.6(ASXL1):c.3398C>T (p.Ser1133Phe) rs1244161898 0.00001
NM_015338.6(ASXL1):c.3522G>C (p.Lys1174Asn) rs747485168 0.00001
NM_015338.6(ASXL1):c.3646G>C (p.Val1216Leu) rs200817247 0.00001
NM_015338.6(ASXL1):c.3662C>A (p.Thr1221Lys) rs545612479 0.00001
NM_015338.6(ASXL1):c.581A>G (p.His194Arg) rs771351026 0.00001
NM_015338.6(ASXL1):c.1929G>A (p.Gly643=) rs373998853
NM_015338.6(ASXL1):c.1929G>T (p.Gly643=) rs373998853
NM_015338.6(ASXL1):c.2152A>G (p.Arg718Gly) rs1158922559
NM_015338.6(ASXL1):c.2324T>C (p.Leu775Ser) rs752263134
NM_015338.6(ASXL1):c.2648A>G (p.Glu883Gly) rs2515568717
NM_015338.6(ASXL1):c.2711A>G (p.Asn904Ser) rs765155567
NM_015338.6(ASXL1):c.280C>T (p.Pro94Ser) rs2011386312
NM_015338.6(ASXL1):c.2894G>A (p.Arg965Gln) rs2011792041
NM_015338.6(ASXL1):c.2895AGG[1] (p.Gly967del) rs762939072
NM_015338.6(ASXL1):c.2939T>A (p.Ile980Asn) rs775628738
NM_015338.6(ASXL1):c.3271G>A (p.Ala1091Thr) rs2011830516
NM_015338.6(ASXL1):c.3443G>A (p.Arg1148His) rs555465153
NM_015338.6(ASXL1):c.3674A>G (p.Lys1225Arg) rs2145385499
NM_015338.6(ASXL1):c.3910C>G (p.Leu1304Val) rs747267907
NM_015338.6(ASXL1):c.4521G>A (p.Ala1507=) rs760605807
NM_015338.6(ASXL1):c.57+19G>A rs200198574
NM_015338.6(ASXL1):c.57+23dup rs757765039
NM_015338.6(ASXL1):c.993T>C (p.His331=)

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