ClinVar Miner

List of variants in gene MAST1 reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 167
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HGVS dbSNP gnomAD frequency
NM_014975.3(MAST1):c.1530C>T (p.His510=) rs35952311 0.00362
NM_014975.3(MAST1):c.3366T>C (p.Asp1122=) rs148457369 0.00250
NM_014975.3(MAST1):c.1009+11G>C
NM_014975.3(MAST1):c.1009+7del
NM_014975.3(MAST1):c.1065C>T (p.Asp355=)
NM_014975.3(MAST1):c.1077+16T>A
NM_014975.3(MAST1):c.1149T>C (p.Gly383=)
NM_014975.3(MAST1):c.1155C>T (p.Tyr385=)
NM_014975.3(MAST1):c.1157+9C>G
NM_014975.3(MAST1):c.1158-14C>G
NM_014975.3(MAST1):c.1158-17del
NM_014975.3(MAST1):c.1251G>A (p.Gln417=)
NM_014975.3(MAST1):c.1320C>T (p.Ser440=)
NM_014975.3(MAST1):c.1367-17C>A
NM_014975.3(MAST1):c.1367-20G>A
NM_014975.3(MAST1):c.1368C>T (p.Gly456=)
NM_014975.3(MAST1):c.1371C>T (p.Gly457=)
NM_014975.3(MAST1):c.1374C>T (p.Asp458=)
NM_014975.3(MAST1):c.1384C>T (p.Leu462=)
NM_014975.3(MAST1):c.1404G>A (p.Ala468=)
NM_014975.3(MAST1):c.1410C>G (p.Pro470=)
NM_014975.3(MAST1):c.1443G>A (p.Thr481=)
NM_014975.3(MAST1):c.1449A>T (p.Leu483=)
NM_014975.3(MAST1):c.1453C>T (p.Leu485=)
NM_014975.3(MAST1):c.1485C>T (p.His495=)
NM_014975.3(MAST1):c.1497G>A (p.Lys499=)
NM_014975.3(MAST1):c.1506-14A>G
NM_014975.3(MAST1):c.1506-17C>T
NM_014975.3(MAST1):c.1506-17_1506-15dup
NM_014975.3(MAST1):c.1506-8G>T
NM_014975.3(MAST1):c.1548C>T (p.Phe516=)
NM_014975.3(MAST1):c.1581C>T (p.Thr527=)
NM_014975.3(MAST1):c.1593T>C (p.Tyr531=)
NM_014975.3(MAST1):c.1605C>T (p.Ile535=)
NM_014975.3(MAST1):c.1639-5C>T
NM_014975.3(MAST1):c.1639-6C>T
NM_014975.3(MAST1):c.1641G>A (p.Val547=)
NM_014975.3(MAST1):c.1647G>A (p.Gly549=)
NM_014975.3(MAST1):c.173-13C>G
NM_014975.3(MAST1):c.173-9C>G
NM_014975.3(MAST1):c.1804+12G>A
NM_014975.3(MAST1):c.1804+14C>G
NM_014975.3(MAST1):c.1833G>A (p.Glu611=)
NM_014975.3(MAST1):c.1906+13T>A
NM_014975.3(MAST1):c.1907-5C>T
NM_014975.3(MAST1):c.1908C>T (p.Gly636=)
NM_014975.3(MAST1):c.201C>T (p.Asn67=)
NM_014975.3(MAST1):c.2029+18G>A
NM_014975.3(MAST1):c.2062T>C (p.Tyr688His)
NM_014975.3(MAST1):c.207C>A (p.Ser69=)
NM_014975.3(MAST1):c.2085G>A (p.Glu695=)
NM_014975.3(MAST1):c.2094C>T (p.Pro698=)
NM_014975.3(MAST1):c.2139+10G>A
NM_014975.3(MAST1):c.2139+12C>T
NM_014975.3(MAST1):c.255C>T (p.Asp85=)
NM_014975.3(MAST1):c.2566+14C>G
NM_014975.3(MAST1):c.2567-15T>C
NM_014975.3(MAST1):c.2595C>T (p.Cys865=)
NM_014975.3(MAST1):c.2612G>T (p.Gly871Val)
NM_014975.3(MAST1):c.2631G>A (p.Arg877=)
NM_014975.3(MAST1):c.2715T>G (p.Thr905=)
NM_014975.3(MAST1):c.2730C>A (p.Ile910=)
NM_014975.3(MAST1):c.2757T>C (p.Ser919=)
NM_014975.3(MAST1):c.2773+18C>A
NM_014975.3(MAST1):c.2773+7C>T
NM_014975.3(MAST1):c.2774-12G>T
NM_014975.3(MAST1):c.2774-17T>C
NM_014975.3(MAST1):c.279G>A (p.Ser93=)
NM_014975.3(MAST1):c.2894G>A (p.Arg965His)
NM_014975.3(MAST1):c.2898C>T (p.Ser966=)
NM_014975.3(MAST1):c.2919G>A (p.Ser973=)
NM_014975.3(MAST1):c.2958C>T (p.Val986=)
NM_014975.3(MAST1):c.2976T>C (p.Asp992=)
NM_014975.3(MAST1):c.2988C>T (p.Val996=)
NM_014975.3(MAST1):c.3003+12T>C
NM_014975.3(MAST1):c.3024A>G (p.Pro1008=)
NM_014975.3(MAST1):c.3027C>A (p.Ala1009=)
NM_014975.3(MAST1):c.3127-15G>C
NM_014975.3(MAST1):c.3127-16C>T
NM_014975.3(MAST1):c.3127-16dup
NM_014975.3(MAST1):c.3142G>T (p.Ala1048Ser)
NM_014975.3(MAST1):c.3156G>A (p.Thr1052=)
NM_014975.3(MAST1):c.3162C>T (p.Phe1054=)
NM_014975.3(MAST1):c.321C>T (p.Thr107=)
NM_014975.3(MAST1):c.3223C>A (p.Arg1075=)
NM_014975.3(MAST1):c.322G>A (p.Val108Ile)
NM_014975.3(MAST1):c.3252G>A (p.Glu1084=)
NM_014975.3(MAST1):c.3263+8C>T
NM_014975.3(MAST1):c.3264-12C>T
NM_014975.3(MAST1):c.3264-13C>T
NM_014975.3(MAST1):c.3271C>T (p.Arg1091Cys)
NM_014975.3(MAST1):c.328-5C>T
NM_014975.3(MAST1):c.3291G>A (p.Lys1097=)
NM_014975.3(MAST1):c.3306G>C (p.Ser1102=)
NM_014975.3(MAST1):c.3360C>T (p.Ser1120=)
NM_014975.3(MAST1):c.3372C>T (p.Leu1124=)
NM_014975.3(MAST1):c.3402G>C (p.Ala1134=)
NM_014975.3(MAST1):c.3452-17C>T
NM_014975.3(MAST1):c.3474C>T (p.Ser1158=)
NM_014975.3(MAST1):c.3492C>G (p.Pro1164=)
NM_014975.3(MAST1):c.3507G>A (p.Ser1169=)
NM_014975.3(MAST1):c.3534C>T (p.Ser1178=)
NM_014975.3(MAST1):c.3570G>A (p.Gln1190=)
NM_014975.3(MAST1):c.3636C>T (p.Ser1212=)
NM_014975.3(MAST1):c.3639C>G (p.Pro1213=)
NM_014975.3(MAST1):c.3708G>C (p.Pro1236=)
NM_014975.3(MAST1):c.3715C>T (p.Leu1239=)
NM_014975.3(MAST1):c.3732C>T (p.Pro1244=)
NM_014975.3(MAST1):c.3774G>C (p.Ser1258=)
NM_014975.3(MAST1):c.3801C>G (p.Ala1267=)
NM_014975.3(MAST1):c.3808C>T (p.Leu1270=)
NM_014975.3(MAST1):c.3820T>C (p.Leu1274=)
NM_014975.3(MAST1):c.3865G>A (p.Val1289Met)
NM_014975.3(MAST1):c.3951C>G (p.Val1317=)
NM_014975.3(MAST1):c.3957C>T (p.Gly1319=)
NM_014975.3(MAST1):c.4035G>A (p.Leu1345=)
NM_014975.3(MAST1):c.4065G>T (p.Val1355=)
NM_014975.3(MAST1):c.4071C>T (p.Ser1357=)
NM_014975.3(MAST1):c.4094dup (p.Ala1366fs)
NM_014975.3(MAST1):c.4122G>A (p.Ala1374=)
NM_014975.3(MAST1):c.414G>C (p.Gly138=)
NM_014975.3(MAST1):c.4155C>T (p.Asp1385=)
NM_014975.3(MAST1):c.420C>T (p.Thr140=)
NM_014975.3(MAST1):c.4276T>C (p.Ser1426Pro)
NM_014975.3(MAST1):c.4344G>A (p.Val1448=)
NM_014975.3(MAST1):c.4347G>T (p.Val1449=)
NM_014975.3(MAST1):c.4356T>C (p.Pro1452=)
NM_014975.3(MAST1):c.435C>T (p.Asp145=)
NM_014975.3(MAST1):c.4413C>A (p.Pro1471=)
NM_014975.3(MAST1):c.4413C>T (p.Pro1471=)
NM_014975.3(MAST1):c.4444T>G (p.Leu1482Val)
NM_014975.3(MAST1):c.4476C>T (p.Ser1492=)
NM_014975.3(MAST1):c.4494C>T (p.Pro1498=)
NM_014975.3(MAST1):c.4517A>C (p.Glu1506Ala)
NM_014975.3(MAST1):c.453C>T (p.Arg151=)
NM_014975.3(MAST1):c.4569A>C (p.Ala1523=)
NM_014975.3(MAST1):c.4577C>T (p.Pro1526Leu)
NM_014975.3(MAST1):c.4581C>T (p.Val1527=)
NM_014975.3(MAST1):c.4593C>T (p.Ser1531=)
NM_014975.3(MAST1):c.4596C>A (p.Leu1532=)
NM_014975.3(MAST1):c.4596C>T (p.Leu1532=)
NM_014975.3(MAST1):c.4695C>T (p.Pro1565=)
NM_014975.3(MAST1):c.4704G>A (p.Pro1568=)
NM_014975.3(MAST1):c.488+20C>T
NM_014975.3(MAST1):c.780T>C (p.Tyr260=)
NM_014975.3(MAST1):c.786C>T (p.Arg262=)
NM_014975.3(MAST1):c.789T>C (p.Ser263=)
NM_014975.3(MAST1):c.83+12A>T
NM_014975.3(MAST1):c.84-19del
NM_014975.3(MAST1):c.84-4G>A
NM_014975.3(MAST1):c.84-5C>T
NM_014975.3(MAST1):c.84-8C>T
NM_014975.3(MAST1):c.849A>G (p.Ser283=)
NM_014975.3(MAST1):c.876+7G>A
NM_014975.3(MAST1):c.877-12G>A
NM_014975.3(MAST1):c.877-13T>C
NM_014975.3(MAST1):c.877-17C>G
NM_014975.3(MAST1):c.877-7G>A
NM_014975.3(MAST1):c.877-9del
NM_014975.3(MAST1):c.888C>T (p.Pro296=)
NM_014975.3(MAST1):c.954G>A (p.Thr318=)
NM_014975.3(MAST1):c.954G>C (p.Thr318=)
NM_014975.3(MAST1):c.960C>A (p.Ile320=)
NM_014975.3(MAST1):c.969C>T (p.Tyr323=)
NM_014975.3(MAST1):c.96T>C (p.Ser32=)
NM_014975.3(MAST1):c.97A>C (p.Asn33His)
NM_014975.3(MAST1):c.993C>T (p.Thr331=)

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