ClinVar Miner

List of variants in gene TTC21B reported as likely benign for not provided

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Gene type:
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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_024753.5(TTC21B):c.2462-258A>G rs7595385 0.02712
NM_024753.5(TTC21B):c.1088-122A>G rs1864811 0.01776
NM_024753.5(TTC21B):c.1417C>T (p.Leu473Phe) rs2163649 0.01776
NM_024753.5(TTC21B):c.796-245A>G rs75769101 0.01776
NM_024753.5(TTC21B):c.3874-266T>G rs6710866 0.01749
NM_024753.5(TTC21B):c.3459+154T>G rs16851239 0.01740
NM_024753.5(TTC21B):c.3460-135T>C rs16851211 0.01740
NM_024753.5(TTC21B):c.2758-142T>G rs74473855 0.01472
NM_024753.5(TTC21B):c.1387-266A>G rs111499060 0.01442
NM_024753.5(TTC21B):c.895-253G>A rs116825599 0.01411
NM_024753.5(TTC21B):c.553-66C>G rs60855239 0.01409
NM_024753.5(TTC21B):c.2461+267C>T rs114942914 0.01406
NM_024753.5(TTC21B):c.2569-56C>T rs111971431 0.01389
NM_024753.5(TTC21B):c.2569-166T>C rs112730235 0.01378
NM_024753.5(TTC21B):c.552+139G>A rs114579734 0.01369
NM_024753.5(TTC21B):c.1516+201G>T rs111404978 0.01298
NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu) rs80026831 0.01296
NM_024753.5(TTC21B):c.2868+60A>G rs112316994 0.01295
NM_024753.5(TTC21B):c.838A>G (p.Met280Val) rs112868646 0.01295
NM_024753.5(TTC21B):c.2757+37C>G rs112913515 0.01292
NM_024753.5(TTC21B):c.2139-162G>A rs112559852 0.01291
NM_024753.5(TTC21B):c.2323-143A>G rs113645302 0.01291
NM_024753.5(TTC21B):c.1674+282G>A rs113126126 0.01289
NM_024753.5(TTC21B):c.429+252C>G rs139365675 0.01206
NM_024753.5(TTC21B):c.430-52A>G rs188695480 0.01203
NM_024753.5(TTC21B):c.2323-206A>T rs868052575 0.01127
NM_024753.5(TTC21B):c.2742C>T (p.Cys914=) rs73018799 0.01072
NM_024753.5(TTC21B):c.1900-125A>G rs111802423 0.01037
NM_024753.5(TTC21B):c.3874-205C>T rs148034638 0.01008
NM_024753.5(TTC21B):c.21+165C>T rs116031802 0.00997
NM_024753.5(TTC21B):c.263-91_263-90del rs112877551 0.00934
NM_024753.5(TTC21B):c.2323-203del rs199591458 0.00729
NM_024753.5(TTC21B):c.3684+202T>C rs80121423 0.00707
NM_024753.5(TTC21B):c.553-262C>G rs138046258 0.00627
NM_024753.5(TTC21B):c.1870A>G (p.Ile624Val) rs77106136 0.00617
NM_024753.5(TTC21B):c.1516+165C>G rs113588383 0.00591
NM_024753.5(TTC21B):c.2322+216C>T rs79430999 0.00576
NM_024753.5(TTC21B):c.2322+3A>G rs79037278 0.00575
NM_024753.5(TTC21B):c.3874-301T>C rs12620082 0.00573
NM_024753.5(TTC21B):c.2212-306A>G rs78702415 0.00554
NM_024753.5(TTC21B):c.1087+42A>G rs78518087 0.00548
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val) rs146496725 0.00537
NM_024753.5(TTC21B):c.3684+223G>A rs60697420 0.00463
NM_024753.5(TTC21B):c.895-194T>C rs183590740 0.00432
NM_024753.5(TTC21B):c.3806-287T>G rs59508470 0.00426
NM_024753.5(TTC21B):c.724G>A (p.Asp242Asn) rs74447004 0.00356
NM_024753.5(TTC21B):c.1571C>G (p.Ser524Cys) rs145436538 0.00355
NM_024753.5(TTC21B):c.2568+45A>T rs73969724 0.00307
NM_024753.5(TTC21B):c.3416T>C (p.Val1139Ala) rs149454830 0.00267
NM_024753.5(TTC21B):c.1676T>G (p.Val559Gly) rs149325238 0.00190
NM_024753.5(TTC21B):c.2951-42G>A rs75714816 0.00190
NM_024753.5(TTC21B):c.2600G>A (p.Arg867His) rs76726265 0.00161
NM_024753.5(TTC21B):c.1867T>C (p.Leu623=) rs140107312 0.00129
NM_024753.5(TTC21B):c.2161A>C (p.Asn721His) rs146637219 0.00124
NM_024753.5(TTC21B):c.588T>G (p.Gly196=) rs144458105 0.00111
NM_024753.5(TTC21B):c.2472G>A (p.Leu824=) rs114725374 0.00107
NM_024753.5(TTC21B):c.3874-14T>C rs200347449 0.00096
NM_024753.5(TTC21B):c.691A>T (p.Thr231Ser) rs149925563 0.00071
NM_024753.5(TTC21B):c.3797C>T (p.Pro1266Leu) rs140384742 0.00054
NM_024753.5(TTC21B):c.553-5A>C rs544620018 0.00051
NM_024753.5(TTC21B):c.1650A>G (p.Glu550=) rs145926679 0.00050
NM_024753.5(TTC21B):c.468A>G (p.Gly156=) rs139457042 0.00020
NM_024753.5(TTC21B):c.2227G>A (p.Val743Ile) rs183367929 0.00019
NM_024753.5(TTC21B):c.549T>C (p.Gly183=) rs141664029 0.00014
NM_024753.5(TTC21B):c.783G>T (p.Gly261=) rs200255917 0.00009
NM_024753.5(TTC21B):c.3552G>A (p.Ala1184=) rs148113339 0.00008
NM_024753.5(TTC21B):c.1551C>T (p.His517=) rs753874300 0.00002
NM_024753.5(TTC21B):c.1386+15G>A rs201281283 0.00001
NM_024753.5(TTC21B):c.1851A>G (p.Leu617=) rs1267179534 0.00001
NM_024753.5(TTC21B):c.2258C>T (p.Pro753Leu) rs539769126 0.00001
NM_024753.5(TTC21B):c.2928G>A (p.Gln976=) rs774490142 0.00001
NM_024753.5(TTC21B):c.2967A>G (p.Leu989=) rs749030495 0.00001
NM_024753.5(TTC21B):c.3936G>A (p.Ala1312=) rs201470854 0.00001
NM_024753.5(TTC21B):c.843A>G (p.Glu281=) rs201311475 0.00001
NM_024753.5(TTC21B):c.1387-121_1387-117del rs142391567
NM_024753.5(TTC21B):c.1956A>G (p.Glu652=) rs1686129480
NM_024753.5(TTC21B):c.2049A>G (p.Glu683=) rs1574099991
NM_024753.5(TTC21B):c.21+2TGAGCGGG[8] rs59477041
NM_024753.5(TTC21B):c.21+32_21+33insTGAGCGGA rs1471663226
NM_024753.5(TTC21B):c.21+82G>A rs113984110
NM_024753.5(TTC21B):c.2211+135T>G rs141635439
NM_024753.5(TTC21B):c.2323-215dup rs1167955966
NM_024753.5(TTC21B):c.2461+123G>A rs74734002
NM_024753.5(TTC21B):c.2461+320_2461+322del rs142633603
NM_024753.5(TTC21B):c.2550G>T (p.Ala850=) rs144151561
NM_024753.5(TTC21B):c.2569-39dup rs79777167
NM_024753.5(TTC21B):c.263-10C>T rs1574143267
NM_024753.5(TTC21B):c.263-146dup rs201993628
NM_024753.5(TTC21B):c.2652T>A (p.Ala884=) rs1574082673
NM_024753.5(TTC21B):c.2758-144_2758-143dup rs200057550
NM_024753.5(TTC21B):c.3519T>C (p.Thr1173=) rs115504901
NM_024753.5(TTC21B):c.3519T>G (p.Thr1173=) rs115504901
NM_024753.5(TTC21B):c.3828C>T (p.Tyr1276=) rs751390551
NM_024753.5(TTC21B):c.429+258_429+261del rs138083821
NM_024753.5(TTC21B):c.966G>A (p.Gln322=) rs1574121127

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