ClinVar Miner

List of variants in gene TENM4 reported as likely benign for not provided

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Gene type:
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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_001098816.3(TENM4):c.6234C>T (p.Asn2078=) rs139879711 0.00753
NM_001098816.3(TENM4):c.8010C>T (p.Tyr2670=) rs34562198 0.00484
NM_001098816.3(TENM4):c.1869C>T (p.Cys623=) rs34791547 0.00428
NM_001098816.3(TENM4):c.8000A>G (p.Gln2667Arg) rs78572681 0.00393
NM_001098816.3(TENM4):c.2804C>G (p.Pro935Arg) rs141706152 0.00347
NM_001098816.3(TENM4):c.1453C>T (p.Pro485Ser) rs191549326 0.00292
NM_001098816.3(TENM4):c.3663C>T (p.Asn1221=) rs181990145 0.00133
NM_001098816.3(TENM4):c.7312C>T (p.His2438Tyr) rs199909021 0.00130
NM_001098816.3(TENM4):c.1553G>A (p.Arg518Gln) rs201191369 0.00098
NM_001098816.3(TENM4):c.5612C>G (p.Pro1871Arg) rs199973967 0.00090
NM_001098816.3(TENM4):c.6354G>A (p.Glu2118=) rs201663167 0.00068
NM_001098816.3(TENM4):c.2709C>A (p.Gly903=) rs201248880 0.00067
NM_001098816.3(TENM4):c.4895G>A (p.Arg1632His) rs199687168 0.00066
NM_001098816.3(TENM4):c.5287G>A (p.Gly1763Arg) rs201995608 0.00041
NM_001098816.3(TENM4):c.6966G>A (p.Lys2322=) rs376842336 0.00031
NM_001098816.3(TENM4):c.8198G>A (p.Arg2733Gln) rs185503085 0.00025
NM_001098816.3(TENM4):c.5545A>G (p.Thr1849Ala) rs772977333 0.00014
NM_001098816.3(TENM4):c.4413C>T (p.Thr1471=) rs759332892 0.00004
NM_001098816.3(TENM4):c.5733C>T (p.Gly1911=) rs373347923 0.00004
NM_001098816.3(TENM4):c.3861C>A (p.Pro1287=) rs939901922 0.00002
NM_001098816.3(TENM4):c.5115T>C (p.Asn1705=) rs932804067 0.00001
NM_001098816.3(TENM4):c.2003C>T (p.Ser668Leu)
NM_001098816.3(TENM4):c.2046G>A (p.Val682=)
NM_001098816.3(TENM4):c.2179+16_2179+17insGGGGAGGAAGGGTGGGTGGAGGAGGAGTGGGGGTGGGGAAGAATGAGGGGTGGGGTGTGGAGGGT
NM_001098816.3(TENM4):c.2238C>T (p.Cys746=)
NM_001098816.3(TENM4):c.2271G>A (p.Gln757=)
NM_001098816.3(TENM4):c.2313C>T (p.Arg771=)
NM_001098816.3(TENM4):c.2458G>A (p.Val820Ile)
NM_001098816.3(TENM4):c.2481A>C (p.Gly827=)
NM_001098816.3(TENM4):c.2721G>A (p.Thr907=)
NM_001098816.3(TENM4):c.277G>A (p.Gly93Arg)
NM_001098816.3(TENM4):c.318C>T (p.Gly106=)
NM_001098816.3(TENM4):c.3720C>T (p.Asp1240=)
NM_001098816.3(TENM4):c.3818A>G (p.His1273Arg)
NM_001098816.3(TENM4):c.4316G>A (p.Arg1439His) rs201076845
NM_001098816.3(TENM4):c.4497T>C (p.Thr1499=)
NM_001098816.3(TENM4):c.4653C>T (p.Tyr1551=)
NM_001098816.3(TENM4):c.4845C>T (p.Asp1615=)
NM_001098816.3(TENM4):c.5270G>A (p.Arg1757Gln)
NM_001098816.3(TENM4):c.5395A>C (p.Asn1799His)
NM_001098816.3(TENM4):c.5543G>A (p.Arg1848His)
NM_001098816.3(TENM4):c.5604G>A (p.Ala1868=)
NM_001098816.3(TENM4):c.6111G>A (p.Thr2037=) rs376416432
NM_001098816.3(TENM4):c.648G>C (p.Thr216=)
NM_001098816.3(TENM4):c.678C>T (p.Ala226=)
NM_001098816.3(TENM4):c.696T>C (p.Pro232=) rs1591115573
NM_001098816.3(TENM4):c.7146C>T (p.Tyr2382=)
NM_001098816.3(TENM4):c.7353G>A (p.Met2451Ile)
NM_001098816.3(TENM4):c.7503C>T (p.Tyr2501=)
NM_001098816.3(TENM4):c.7579C>A (p.Gln2527Lys)
NM_001098816.3(TENM4):c.7686C>T (p.Ser2562=)
NM_001098816.3(TENM4):c.8115C>T (p.Arg2705=)

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