ClinVar Miner

List of variants in gene TEAD1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 107
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HGVS dbSNP gnomAD frequency
NM_021961.6(TEAD1):c.698C>T (p.Ser233Leu) rs140310944 0.00045
NM_021961.6(TEAD1):c.1168-10A>G rs118071160 0.00026
NM_021961.6(TEAD1):c.465+8A>G rs199752430 0.00026
NM_021961.6(TEAD1):c.465+13C>T rs370856457 0.00024
NM_021961.6(TEAD1):c.575-13A>T rs377506698 0.00014
NM_021961.6(TEAD1):c.252G>A (p.Thr84=) rs144369913 0.00010
NM_021961.6(TEAD1):c.512+15G>C rs539557904 0.00006
NM_021961.6(TEAD1):c.111C>T (p.Pro37=) rs553921798 0.00004
NM_021961.6(TEAD1):c.650G>A (p.Arg217His) rs188077520 0.00004
NM_021961.6(TEAD1):c.1128T>C (p.Tyr376=) rs751604377 0.00003
NM_021961.6(TEAD1):c.615C>G (p.Ala205=) rs774352850 0.00003
NM_021961.6(TEAD1):c.699+7G>A rs368255240 0.00002
NM_021961.6(TEAD1):c.1023T>C (p.Tyr341=) rs769981588 0.00001
NM_021961.6(TEAD1):c.1035G>A (p.Glu345=) rs766852492 0.00001
NM_021961.6(TEAD1):c.117C>T (p.Ile39=) rs1208773012 0.00001
NM_021961.6(TEAD1):c.1242C>T (p.His414=) rs776934406 0.00001
NM_021961.6(TEAD1):c.268-6C>G rs367668145 0.00001
NM_021961.6(TEAD1):c.396G>A (p.Ser132=) rs745753913 0.00001
NM_021961.6(TEAD1):c.459G>A (p.Ala153=) rs755050202 0.00001
NM_021961.6(TEAD1):c.513-6T>C rs755570239 0.00001
NM_021961.6(TEAD1):c.574+14A>C rs752522355 0.00001
NM_021961.6(TEAD1):c.594C>T (p.Ala198=) rs376731523 0.00001
NM_021961.6(TEAD1):c.600T>C (p.Ala200=) rs370373018 0.00001
NM_021961.6(TEAD1):c.846A>G (p.Gln282=) rs754662369 0.00001
NM_021961.6(TEAD1):c.936C>T (p.Tyr312=) rs745858857 0.00001
NM_021961.6(TEAD1):c.1014+15G>T
NM_021961.6(TEAD1):c.1015-4A>C rs746485324
NM_021961.6(TEAD1):c.1029G>A (p.Arg343=)
NM_021961.6(TEAD1):c.1038T>C (p.Asn346=)
NM_021961.6(TEAD1):c.1050A>T (p.Val350=)
NM_021961.6(TEAD1):c.1053C>T (p.Tyr351=)
NM_021961.6(TEAD1):c.1065C>T (p.Arg355=)
NM_021961.6(TEAD1):c.1158A>C (p.Thr386=)
NM_021961.6(TEAD1):c.1167+18T>G
NM_021961.6(TEAD1):c.1167+18_1167+19del
NM_021961.6(TEAD1):c.1167+19T>C
NM_021961.6(TEAD1):c.1168-10del
NM_021961.6(TEAD1):c.1168-16T>C
NM_021961.6(TEAD1):c.1170G>A (p.Val390=)
NM_021961.6(TEAD1):c.1173A>G (p.Val391=) rs2134179528
NM_021961.6(TEAD1):c.1188A>C (p.Thr396=) rs1949116614
NM_021961.6(TEAD1):c.1197T>C (p.Thr399=)
NM_021961.6(TEAD1):c.1266G>A (p.Arg422=)
NM_021961.6(TEAD1):c.129T>C (p.Phe43=)
NM_021961.6(TEAD1):c.135G>A (p.Glu45=) rs2133925844
NM_021961.6(TEAD1):c.156A>T (p.Pro52=)
NM_021961.6(TEAD1):c.203-10T>C
NM_021961.6(TEAD1):c.21C>T (p.Ser7=) rs745585390
NM_021961.6(TEAD1):c.252G>T (p.Thr84=) rs144369913
NM_021961.6(TEAD1):c.258C>G (p.Thr86=) rs1947521822
NM_021961.6(TEAD1):c.268-11C>T
NM_021961.6(TEAD1):c.268-14C>T
NM_021961.6(TEAD1):c.268-16_268-13del rs775869852
NM_021961.6(TEAD1):c.268-4G>C
NM_021961.6(TEAD1):c.268-5T>G
NM_021961.6(TEAD1):c.369G>A (p.Ala123=)
NM_021961.6(TEAD1):c.390C>T (p.Ile130=)
NM_021961.6(TEAD1):c.399C>T (p.Ala133=) rs2134094602
NM_021961.6(TEAD1):c.423G>T (p.Gly141=)
NM_021961.6(TEAD1):c.444G>A (p.Pro148=)
NM_021961.6(TEAD1):c.462G>A (p.Pro154=) rs752862372
NM_021961.6(TEAD1):c.465+17G>T
NM_021961.6(TEAD1):c.474G>A (p.Pro158=)
NM_021961.6(TEAD1):c.496C>G (p.Pro166Ala)
NM_021961.6(TEAD1):c.507A>C (p.Ser169=) rs565795088
NM_021961.6(TEAD1):c.510A>G (p.Gln170=)
NM_021961.6(TEAD1):c.512+10A>G rs2134096465
NM_021961.6(TEAD1):c.512+14G>A
NM_021961.6(TEAD1):c.512+19G>T
NM_021961.6(TEAD1):c.512+9G>C
NM_021961.6(TEAD1):c.513-12C>G
NM_021961.6(TEAD1):c.513-15TC[2]
NM_021961.6(TEAD1):c.513-17C>T
NM_021961.6(TEAD1):c.525T>C (p.Phe175=)
NM_021961.6(TEAD1):c.540C>T (p.Tyr180=)
NM_021961.6(TEAD1):c.575-14G>A
NM_021961.6(TEAD1):c.575-15C>T
NM_021961.6(TEAD1):c.575-7C>G
NM_021961.6(TEAD1):c.591G>A (p.Ser197=)
NM_021961.6(TEAD1):c.624T>C (p.Gly208=)
NM_021961.6(TEAD1):c.627C>T (p.Arg209=)
NM_021961.6(TEAD1):c.651C>T (p.Arg217=)
NM_021961.6(TEAD1):c.675C>G (p.Leu225=) rs148823826
NM_021961.6(TEAD1):c.699+18G>A
NM_021961.6(TEAD1):c.699+7G>T rs368255240
NM_021961.6(TEAD1):c.699+9G>T
NM_021961.6(TEAD1):c.700-15G>T
NM_021961.6(TEAD1):c.708A>G (p.Lys236=) rs1948433409
NM_021961.6(TEAD1):c.717C>T (p.Phe239=)
NM_021961.6(TEAD1):c.723C>T (p.His241=)
NM_021961.6(TEAD1):c.732T>C (p.His244=)
NM_021961.6(TEAD1):c.738C>T (p.Asn246=) rs374784841
NM_021961.6(TEAD1):c.795A>G (p.Lys265=)
NM_021961.6(TEAD1):c.81T>A (p.Ile27=)
NM_021961.6(TEAD1):c.858C>T (p.Phe286=)
NM_021961.6(TEAD1):c.861C>T (p.Leu287=) rs201373762
NM_021961.6(TEAD1):c.873+14T>C
NM_021961.6(TEAD1):c.873+16C>A
NM_021961.6(TEAD1):c.873+9G>A rs1948434849
NM_021961.6(TEAD1):c.874-11C>T
NM_021961.6(TEAD1):c.874-19T>A
NM_021961.6(TEAD1):c.874-20C>T
NM_021961.6(TEAD1):c.897A>G (p.Gln299=)
NM_021961.6(TEAD1):c.909G>C (p.Gly303=) rs2134163021
NM_021961.6(TEAD1):c.951T>C (p.Asn317=)
NM_021961.6(TEAD1):c.99G>A (p.Gly33=)
NM_021961.6(TEAD1):c.99G>C (p.Gly33=) rs771743451

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