ClinVar Miner

List of variants in gene combination TBCEL-TECTA, TECTA reported by PreventionGenetics, part of Exact Sciences

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_005422.4(TECTA):c.5171G>A (p.Ser1724Asn) rs526433 0.99235
NM_005422.4(TECTA):c.1485A>G (p.Ala495=) rs536069 0.76077
NM_005422.4(TECTA):c.1111A>G (p.Arg371Gly) rs612969 0.48670
NM_005422.4(TECTA):c.4098G>A (p.Thr1366=) rs12275038 0.28426
NM_005422.4(TECTA):c.4105+13C>T rs7130952 0.26144
NM_005422.4(TECTA):c.2256C>T (p.Ile752=) rs10502247 0.25910
NM_005422.4(TECTA):c.5634C>T (p.Ser1878=) rs2155369 0.10906
NM_005422.4(TECTA):c.56A>G (p.Gln19Arg) rs35507522 0.03926
NM_005422.4(TECTA):c.624+11C>G rs73599492 0.03810
NM_005422.4(TECTA):c.4422C>T (p.Asn1474=) rs33981325 0.02261
NM_005422.4(TECTA):c.5012C>T (p.Ser1671Leu) rs142948530 0.00672
NM_005422.4(TECTA):c.5384-19G>A rs7111480 0.00609
NM_005422.4(TECTA):c.790+12C>T rs138644808 0.00563
NM_005422.4(TECTA):c.-1-12T>C rs145916279 0.00352
NM_005422.4(TECTA):c.3304G>A (p.Val1102Ile) rs34658230 0.00253
NM_005422.4(TECTA):c.1436C>T (p.Pro479Leu) rs35107075 0.00186
NM_005422.4(TECTA):c.701A>G (p.Gln234Arg) rs144682235 0.00179
NM_005422.4(TECTA):c.2061C>G (p.Asn687Lys) rs139165033 0.00171
NM_005422.4(TECTA):c.5160C>T (p.Asp1720=) rs142657158 0.00154
NM_005422.4(TECTA):c.3097C>T (p.Arg1033Trp) rs142486386 0.00149
NM_005422.4(TECTA):c.3492C>T (p.Thr1164=) rs144012985 0.00138
NM_005422.4(TECTA):c.4720A>G (p.Ile1574Val) rs147354818 0.00123
NM_005422.4(TECTA):c.1085G>T (p.Ser362Ile) rs149001418 0.00104
NM_005422.4(TECTA):c.1509C>T (p.Cys503=) rs61733565 0.00050
NM_005422.4(TECTA):c.2299C>A (p.Arg767=) rs140534420 0.00041
NM_005422.4(TECTA):c.199-4G>A rs373736415 0.00034
NM_005422.4(TECTA):c.5836T>C (p.Tyr1946His) rs144343770 0.00032
NM_005422.4(TECTA):c.1651G>A (p.Val551Met) rs200857366 0.00026
NM_005422.4(TECTA):c.327C>T (p.Gly109=) rs727504830 0.00026
NM_005422.4(TECTA):c.4315C>A (p.Leu1439Ile) rs202199158 0.00026
NM_005422.4(TECTA):c.33C>A (p.Val11=) rs140393508 0.00015
NM_005422.4(TECTA):c.4813G>A (p.Val1605Ile) rs201952240 0.00014
NM_005422.4(TECTA):c.3064G>A (p.Gly1022Ser) rs767265599 0.00012
NM_005422.4(TECTA):c.4824C>T (p.Ile1608=) rs747713348 0.00011
NM_005422.4(TECTA):c.1621G>A (p.Val541Met) rs370652301 0.00006
NM_005422.4(TECTA):c.5142C>T (p.Tyr1714=) rs151087951 0.00004
NM_005422.4(TECTA):c.5211C>T (p.Tyr1737=) rs753147946 0.00004
NM_005422.4(TECTA):c.1522A>C (p.Thr508Pro) rs772553666 0.00003
NM_005422.4(TECTA):c.487-7C>G rs368627411 0.00002
NM_005422.4(TECTA):c.4812C>T (p.Asn1604=) rs746681819 0.00001
NM_005422.4(TECTA):c.1204-10T>A
NM_005422.4(TECTA):c.1948T>A (p.Cys650Ser)
NM_005422.4(TECTA):c.199-3T>C
NM_005422.4(TECTA):c.249G>A (p.Thr83=)
NM_005422.4(TECTA):c.25del (p.Ile9fs)
NM_005422.4(TECTA):c.3221C>G (p.Thr1074Ser)
NM_005422.4(TECTA):c.3569C>A (p.Pro1190His)
NM_005422.4(TECTA):c.3842G>T (p.Cys1281Phe)
NM_005422.4(TECTA):c.3945C>T (p.His1315=)
NM_005422.4(TECTA):c.4274G>A (p.Cys1425Tyr)
NM_005422.4(TECTA):c.4375T>C (p.Cys1459Arg)
NM_005422.4(TECTA):c.4497C>A (p.Asp1499Glu)
NM_005422.4(TECTA):c.4690-4A>G
NM_005422.4(TECTA):c.5243G>A (p.Ser1748Asn)
NM_005422.4(TECTA):c.5383+1G>A
NM_005422.4(TECTA):c.5583G>A (p.Val1861=)
NM_005422.4(TECTA):c.5591A>G (p.Asn1864Ser) rs1003951217
NM_005422.4(TECTA):c.6205G>C (p.Glu2069Gln)
NM_005422.4(TECTA):c.790+7del

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