ClinVar Miner

List of variants in gene TTC21B reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NC_000002.12:g.165953863A>G rs1347041 0.99997
NM_024753.5(TTC21B):c.430-42C>T rs10930190 0.99611
NC_000002.12:g.165953924del rs5836068 0.99606
NM_024753.5(TTC21B):c.2138+330A>G rs10198692 0.99193
NM_024753.5(TTC21B):c.2323-288A>G rs7557256 0.99186
NM_024753.5(TTC21B):c.826A>G (p.Thr276Ala) rs7592429 0.95088
NM_024753.5(TTC21B):c.895-99T>G rs1560597 0.95076
NM_024753.5(TTC21B):c.552+133A>G rs13000534 0.95023
NM_024753.5(TTC21B):c.601G>A (p.Val201Met) rs1432273 0.61903
NM_024753.5(TTC21B):c.710+87G>T rs7592392 0.61894
NM_024753.5(TTC21B):c.429+110G>C rs6432853 0.61115
NM_024753.5(TTC21B):c.2951-287T>C rs13404648 0.43749
NM_024753.5(TTC21B):c.2462-304A>G rs11897687 0.43136
NM_024753.5(TTC21B):c.2138+48G>A rs7590559 0.40515
NM_024753.5(TTC21B):c.2323-203T>A rs199843227 0.35201
NM_024753.5(TTC21B):c.1695C>T (p.Tyr565=) rs6750044 0.34586
NM_024753.5(TTC21B):c.2175T>C (p.Phe725=) rs10176588 0.33260
NC_000002.12:g.165954060C>A rs6432854 0.30411
NM_024753.5(TTC21B):c.2323-201T>A rs62177811 0.29286
NM_024753.5(TTC21B):c.429+152A>C rs12329293 0.29162
NM_024753.5(TTC21B):c.3264-230A>G rs1529648 0.25366
NM_024753.5(TTC21B):c.1675-110A>G rs3749030 0.15566
NM_024753.5(TTC21B):c.1088-94G>A rs1560596 0.14538
NM_024753.5(TTC21B):c.1516+148T>C rs2163648 0.13306
NM_024753.5(TTC21B):c.3460-50G>A rs34701755 0.11735
NM_024753.5(TTC21B):c.710+93A>T rs12623658 0.11694
NM_024753.5(TTC21B):c.2323-205A>T rs7557161 0.11260
NM_024753.4(TTC21B):c.-145G>A rs111867313 0.09068
NM_024753.5(TTC21B):c.2951-219A>G rs13392714 0.04686
NM_024753.5(TTC21B):c.3806-96C>A rs75988164 0.04600
NM_024753.5(TTC21B):c.2323-117A>G rs7557045 0.04088
NM_024753.5(TTC21B):c.2211+13A>G rs73969727 0.04080
NM_024753.5(TTC21B):c.2758-173G>C rs57257954 0.04076
NM_024753.4(TTC21B):c.-409A>G rs79930369 0.03539
NM_024753.5(TTC21B):c.1185+23C>G rs62177816 0.03486
NM_024753.5(TTC21B):c.3685-72A>G rs16851206 0.03257
NM_024753.5(TTC21B):c.21+177C>T rs116502006 0.02943
NM_024753.5(TTC21B):c.3806-131C>T rs113973637 0.02839
NM_024753.5(TTC21B):c.2951-273G>A rs78871784 0.02028
NM_024753.5(TTC21B):c.2323-201del rs368877172 0.01791
NM_024753.5(TTC21B):c.1417C>T (p.Leu473Phe) rs2163649 0.01776
NM_024753.5(TTC21B):c.795+44T>C rs1432272 0.01775
NM_024753.5(TTC21B):c.1899+312G>A rs145951763 0.01616
NM_024753.5(TTC21B):c.2334C>T (p.Tyr778=) rs79656636 0.01606
NM_024753.5(TTC21B):c.263-222A>T rs115411054 0.01593
NM_024753.5(TTC21B):c.894+108G>A rs115224320 0.01588
NM_024753.5(TTC21B):c.1387C>T (p.Pro463Ser) rs16851307 0.01408
NM_024753.5(TTC21B):c.2385G>C (p.Leu795=) rs80225158 0.01377
NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu) rs80026831 0.01296
NM_024753.5(TTC21B):c.838A>G (p.Met280Val) rs112868646 0.01295
NM_024753.5(TTC21B):c.2742C>T (p.Cys914=) rs73018799 0.01072
NM_024753.5(TTC21B):c.2462-19A>C rs146509360 0.00946
NM_024753.5(TTC21B):c.1965G>A (p.Arg655=) rs16822802 0.00798
NM_024753.5(TTC21B):c.1870A>G (p.Ile624Val) rs77106136 0.00617
NM_024753.5(TTC21B):c.2322+3A>G rs79037278 0.00575
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val) rs146496725 0.00537
NM_024753.5(TTC21B):c.2950+16T>C rs142565795 0.00455
NM_024753.5(TTC21B):c.724G>A (p.Asp242Asn) rs74447004 0.00356
NM_024753.5(TTC21B):c.1846C>T (p.Arg616Cys) rs139441507 0.00235
NM_024753.5(TTC21B):c.1087+151_1087+152insTAAAAA rs79188732
NM_024753.5(TTC21B):c.114C>G (p.Val38=) rs34486024
NM_024753.5(TTC21B):c.1387-277del rs57171027
NM_024753.5(TTC21B):c.1387-58dup rs58208220
NM_024753.5(TTC21B):c.21+142G>A rs6716946
NM_024753.5(TTC21B):c.21+2TGAGCGGG[5] rs59477041
NM_024753.5(TTC21B):c.21+2TGAGCGGG[6] rs59477041
NM_024753.5(TTC21B):c.21+2TGAGCGGG[7] rs59477041
NM_024753.5(TTC21B):c.21+33_21+34insGCGGGTGAGCGG rs569432248
NM_024753.5(TTC21B):c.2323-205_2323-204insT rs200422083
NM_024753.5(TTC21B):c.2323-207A>T rs545838216
NM_024753.5(TTC21B):c.2462-160del rs58336772
NM_024753.5(TTC21B):c.2569-10dup rs144600502
NM_024753.5(TTC21B):c.2569-28del rs79777167
NM_024753.5(TTC21B):c.263-110_263-107del rs5836067
NM_024753.5(TTC21B):c.2758-144dup rs200057550
NM_024753.5(TTC21B):c.2758-196dup rs56346146
NM_024753.5(TTC21B):c.3519T>C (p.Thr1173=) rs115504901
NM_024753.5(TTC21B):c.3873+148C>A rs3764998
NM_024753.5(TTC21B):c.3874-236_3874-235insTA rs10688149
NM_024753.5(TTC21B):c.553-295_553-294insTCC rs68036135

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