ClinVar Miner

List of variants in gene MYH14 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 195
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280 0.00303
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met) rs112716976 0.00107
NM_001145809.2(MYH14):c.4033G>A (p.Ala1345Thr) rs148054042 0.00104
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394 0.00062
NM_001145809.2(MYH14):c.1919G>A (p.Arg640Gln) rs199696801 0.00052
NM_001145809.2(MYH14):c.1419C>T (p.Arg473=) rs371946306 0.00038
NM_001145809.2(MYH14):c.4705G>T (p.Ala1569Ser) rs145522874 0.00038
NM_001145809.2(MYH14):c.3850C>T (p.Arg1284Trp) rs201515738 0.00037
NM_001145809.2(MYH14):c.1427G>A (p.Arg476His) rs375694189 0.00033
NM_001145809.2(MYH14):c.1026G>A (p.Pro342=) rs368124508 0.00029
NM_001145809.2(MYH14):c.5452C>T (p.Arg1818Cys) rs377096949 0.00029
NM_001145809.2(MYH14):c.5599C>T (p.Arg1867Cys) rs187789045 0.00029
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400 0.00027
NM_001145809.2(MYH14):c.4943G>A (p.Arg1648Lys) rs727503228 0.00023
NM_001145809.2(MYH14):c.1155C>T (p.Asn385=) rs558991834 0.00022
NM_001145809.2(MYH14):c.2645C>T (p.Ala882Val) rs202065396 0.00021
NM_001145809.2(MYH14):c.3404G>A (p.Arg1135Gln) rs369620344 0.00020
NM_001145809.2(MYH14):c.3149A>G (p.Asp1050Gly) rs550238145 0.00018
NM_001145809.2(MYH14):c.3514C>A (p.Arg1172=) rs373919106 0.00016
NM_001145809.2(MYH14):c.4564G>A (p.Val1522Ile) rs375563286 0.00016
NM_001145809.2(MYH14):c.1210+12G>A rs367560074 0.00015
NM_001145809.2(MYH14):c.1244G>A (p.Gly415Glu) rs368472938 0.00014
NM_001145809.2(MYH14):c.4827G>A (p.Leu1609=) rs201418071 0.00014
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307 0.00014
NM_001145809.2(MYH14):c.4740C>T (p.Asp1580=) rs751909208 0.00013
NM_001145809.2(MYH14):c.1301A>G (p.Tyr434Cys) rs556541366 0.00012
NM_001145809.2(MYH14):c.3819C>T (p.Ala1273=) rs750779364 0.00012
NM_001145809.2(MYH14):c.4445G>A (p.Arg1482Gln) rs746594902 0.00012
NM_001145809.2(MYH14):c.1133C>T (p.Ser378Leu) rs150806988 0.00011
NM_001145809.2(MYH14):c.1329+7G>A rs374953263 0.00011
NM_001145809.2(MYH14):c.3304C>T (p.Arg1102Trp) rs397516629 0.00011
NM_001145809.2(MYH14):c.5961-10C>T rs776693090 0.00011
NM_001145809.2(MYH14):c.1120C>T (p.Leu374=) rs374603776 0.00010
NM_001145809.2(MYH14):c.1918C>T (p.Arg640Trp) rs376267080 0.00010
NM_001145809.2(MYH14):c.1833C>T (p.Val611=) rs775077510 0.00009
NM_001145809.2(MYH14):c.2544C>T (p.Ile848=) rs761170226 0.00009
NM_001145809.2(MYH14):c.3295+11G>A rs377046198 0.00009
NM_001145809.2(MYH14):c.693+12C>T rs370673291 0.00009
NM_001145809.2(MYH14):c.2921G>A (p.Arg974His) rs113993956 0.00008
NM_001145809.2(MYH14):c.4950G>A (p.Arg1650=) rs763245691 0.00008
NM_001145809.2(MYH14):c.1593C>T (p.Ile531=) rs780603261 0.00007
NM_001145809.2(MYH14):c.3680+10G>A rs773742154 0.00007
NM_001145809.2(MYH14):c.3777C>T (p.His1259=) rs371116668 0.00007
NM_001145809.2(MYH14):c.4467C>T (p.Asp1489=) rs746379075 0.00007
NM_001145809.2(MYH14):c.4922G>A (p.Arg1641His) rs373651452 0.00007
NM_001145809.2(MYH14):c.5244G>A (p.Leu1748=) rs201101562 0.00006
NM_001145809.2(MYH14):c.5469+13del rs760445854 0.00006
NM_001145809.2(MYH14):c.1182C>T (p.Thr394=) rs749828438 0.00005
NM_001145809.2(MYH14):c.1608C>T (p.Leu536=) rs769161197 0.00005
NM_001145809.2(MYH14):c.4377C>T (p.Ala1459=) rs779641478 0.00005
NM_001145809.2(MYH14):c.4799A>G (p.Asn1600Ser) rs769482601 0.00005
NM_001145809.2(MYH14):c.1665C>T (p.Pro555=) rs202104229 0.00004
NM_001145809.2(MYH14):c.2892C>T (p.Ala964=) rs765237528 0.00004
NM_001145809.2(MYH14):c.3295+10C>T rs375601953 0.00004
NM_001145809.2(MYH14):c.3585G>A (p.Ala1195=) rs368190437 0.00004
NM_001145809.2(MYH14):c.3756G>A (p.Val1252=) rs368640289 0.00004
NM_001145809.2(MYH14):c.3876C>T (p.Ser1292=) rs368466364 0.00004
NM_001145809.2(MYH14):c.5127+12C>T rs373755483 0.00004
NM_001145809.2(MYH14):c.5168G>A (p.Arg1723His) rs200923933 0.00004
NM_001145809.2(MYH14):c.975C>T (p.Ala325=) rs553878240 0.00004
NM_001145809.2(MYH14):c.1800C>T (p.Ala600=) rs745625855 0.00003
NM_001145809.2(MYH14):c.3467+9T>G rs1378826651 0.00003
NM_001145809.2(MYH14):c.3705G>A (p.Thr1235=) rs775178805 0.00003
NM_001145809.2(MYH14):c.3884G>A (p.Arg1295Gln) rs377014092 0.00003
NM_001145809.2(MYH14):c.4539+10C>T rs561531825 0.00003
NM_001145809.2(MYH14):c.4903G>A (p.Glu1635Lys) rs140157424 0.00003
NM_001145809.2(MYH14):c.5463C>T (p.Leu1821=) rs370616094 0.00003
NM_001145809.2(MYH14):c.1482+19A>C rs1415565574 0.00002
NM_001145809.2(MYH14):c.327C>T (p.Asp109=) rs780322540 0.00002
NM_001145809.2(MYH14):c.3477C>T (p.Asp1159=) rs541345064 0.00002
NM_001145809.2(MYH14):c.3680+20C>T rs759192060 0.00002
NM_001145809.2(MYH14):c.4773C>T (p.Ala1591=) rs746906367 0.00002
NM_001145809.2(MYH14):c.5207G>A (p.Ser1736Asn) rs776401666 0.00002
NM_001145809.2(MYH14):c.5566C>T (p.Arg1856Trp) rs539875477 0.00002
NM_001145809.2(MYH14):c.6030C>T (p.Ser2010=) rs555872040 0.00002
NM_001145809.2(MYH14):c.1038C>T (p.Pro346=) rs555327826 0.00001
NM_001145809.2(MYH14):c.1821C>T (p.Tyr607=) rs775552897 0.00001
NM_001145809.2(MYH14):c.1897T>C (p.Leu633=) rs1162570765 0.00001
NM_001145809.2(MYH14):c.2460C>T (p.Arg820=) rs374603035 0.00001
NM_001145809.2(MYH14):c.2547C>T (p.Val849=) rs1159355381 0.00001
NM_001145809.2(MYH14):c.2694+15G>A rs373564756 0.00001
NM_001145809.2(MYH14):c.2900C>T (p.Thr967Met) rs142134135 0.00001
NM_001145809.2(MYH14):c.3347G>A (p.Arg1116Gln) rs767489401 0.00001
NM_001145809.2(MYH14):c.3427C>T (p.Leu1143=) rs770366755 0.00001
NM_001145809.2(MYH14):c.351C>T (p.Asn117=) rs755596399 0.00001
NM_001145809.2(MYH14):c.393C>T (p.Ser131=) rs778036519 0.00001
NM_001145809.2(MYH14):c.4033-7C>T rs751864175 0.00001
NM_001145809.2(MYH14):c.4290+7A>C rs1212558607 0.00001
NM_001145809.2(MYH14):c.4413G>A (p.Glu1471=) rs771604158 0.00001
NM_001145809.2(MYH14):c.4669C>T (p.Arg1557Cys) rs780299880 0.00001
NM_001145809.2(MYH14):c.4755G>A (p.Val1585=) rs746095774 0.00001
NM_001145809.2(MYH14):c.4824A>G (p.Glu1608=) rs375214134 0.00001
NM_001145809.2(MYH14):c.5121G>A (p.Lys1707=) rs1054806111 0.00001
NM_001145809.2(MYH14):c.5202G>A (p.Arg1734=) rs768918317 0.00001
NM_001145809.2(MYH14):c.651C>T (p.His217=) rs779573887 0.00001
NM_001145809.2(MYH14):c.1074G>A (p.Glu358=)
NM_001145809.2(MYH14):c.1101C>T (p.His367=)
NM_001145809.2(MYH14):c.1115-9C>T
NM_001145809.2(MYH14):c.1210+11C>T
NM_001145809.2(MYH14):c.1329+9G>A
NM_001145809.2(MYH14):c.1365C>T (p.Thr455=) rs763440469
NM_001145809.2(MYH14):c.1377C>T (p.Leu459=)
NM_001145809.2(MYH14):c.1464G>T (p.Ala488=)
NM_001145809.2(MYH14):c.1483-20C>T
NM_001145809.2(MYH14):c.1557C>T (p.Phe519=)
NM_001145809.2(MYH14):c.1638C>T (p.Ile546=) rs2123306669
NM_001145809.2(MYH14):c.1656+13C>A
NM_001145809.2(MYH14):c.1707G>C (p.Pro569=)
NM_001145809.2(MYH14):c.1749G>A (p.Glu583=)
NM_001145809.2(MYH14):c.1830+16G>A
NM_001145809.2(MYH14):c.1887C>T (p.Asn629=)
NM_001145809.2(MYH14):c.1945+19C>A
NM_001145809.2(MYH14):c.2045-6T>C rs2034625736
NM_001145809.2(MYH14):c.2055C>T (p.Ile685=)
NM_001145809.2(MYH14):c.2088C>T (p.Asp696=)
NM_001145809.2(MYH14):c.2100T>C (p.Gly700=)
NM_001145809.2(MYH14):c.2286C>T (p.Val762=)
NM_001145809.2(MYH14):c.234G>A (p.Ala78=)
NM_001145809.2(MYH14):c.2354+16G>A
NM_001145809.2(MYH14):c.2425-17del
NM_001145809.2(MYH14):c.2523C>T (p.Asp841=)
NM_001145809.2(MYH14):c.2535C>G (p.Thr845=)
NM_001145809.2(MYH14):c.2580T>A (p.Ala860=)
NM_001145809.2(MYH14):c.2585+13G>A
NM_001145809.2(MYH14):c.2589C>T (p.Ala863=)
NM_001145809.2(MYH14):c.2646G>A (p.Ala882=)
NM_001145809.2(MYH14):c.2695-19C>T
NM_001145809.2(MYH14):c.276G>A (p.Pro92=) rs913915720
NM_001145809.2(MYH14):c.2826+10C>G rs1236916887
NM_001145809.2(MYH14):c.2970C>T (p.Gly990=)
NM_001145809.2(MYH14):c.3069G>A (p.Ala1023=)
NM_001145809.2(MYH14):c.3138G>C (p.Leu1046=)
NM_001145809.2(MYH14):c.321C>A (p.Ala107=) rs2032142561
NM_001145809.2(MYH14):c.3296-11C>T
NM_001145809.2(MYH14):c.3330G>A (p.Glu1110=)
NM_001145809.2(MYH14):c.333C>T (p.Ala111=)
NM_001145809.2(MYH14):c.3360G>C (p.Gly1120=)
NM_001145809.2(MYH14):c.3441G>A (p.Glu1147=)
NM_001145809.2(MYH14):c.3468-5C>T
NM_001145809.2(MYH14):c.3603C>T (p.Asp1201=) rs757735473
NM_001145809.2(MYH14):c.3609C>T (p.Gly1203=)
NM_001145809.2(MYH14):c.3657C>T (p.Ser1219=)
NM_001145809.2(MYH14):c.3660C>T (p.Thr1220=) rs1311243819
NM_001145809.2(MYH14):c.3690G>A (p.Arg1230=)
NM_001145809.2(MYH14):c.3744C>T (p.His1248=)
NM_001145809.2(MYH14):c.3798G>A (p.Leu1266=) rs1601005216
NM_001145809.2(MYH14):c.3825+14G>A
NM_001145809.2(MYH14):c.3825+14G>C
NM_001145809.2(MYH14):c.3825+7T>G rs1353379371
NM_001145809.2(MYH14):c.3826-6C>T
NM_001145809.2(MYH14):c.3997C>G (p.Arg1333Gly)
NM_001145809.2(MYH14):c.4032+13G>A
NM_001145809.2(MYH14):c.405+18G>C
NM_001145809.2(MYH14):c.406-18C>T
NM_001145809.2(MYH14):c.4137+16del rs2123419147
NM_001145809.2(MYH14):c.4137+19C>T
NM_001145809.2(MYH14):c.4260G>A (p.Ala1420=)
NM_001145809.2(MYH14):c.4291-9T>C
NM_001145809.2(MYH14):c.4306C>T (p.Arg1436Trp) rs762144894
NM_001145809.2(MYH14):c.441G>A (p.Pro147=)
NM_001145809.2(MYH14):c.4539+14G>A rs779431768
NM_001145809.2(MYH14):c.4752+12C>T
NM_001145809.2(MYH14):c.4753-7C>T
NM_001145809.2(MYH14):c.4890C>T (p.Leu1630=)
NM_001145809.2(MYH14):c.5037G>A (p.Lys1679=)
NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys) rs556548077
NM_001145809.2(MYH14):c.504C>T (p.His168=)
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.5157G>A (p.Val1719=)
NM_001145809.2(MYH14):c.519C>T (p.His173=)
NM_001145809.2(MYH14):c.5214G>A (p.Lys1738=)
NM_001145809.2(MYH14):c.5256+11G>C
NM_001145809.2(MYH14):c.5257-11C>T
NM_001145809.2(MYH14):c.5257-7A>C
NM_001145809.2(MYH14):c.525C>T (p.Tyr175=)
NM_001145809.2(MYH14):c.5265C>T (p.Ala1755=)
NM_001145809.2(MYH14):c.5345+16G>A
NM_001145809.2(MYH14):c.5469+18C>T
NM_001145809.2(MYH14):c.5679-8C>T rs1019880621
NM_001145809.2(MYH14):c.5754G>C (p.Glu1918Asp)
NM_001145809.2(MYH14):c.5760G>A (p.Arg1920=)
NM_001145809.2(MYH14):c.5838G>A (p.Glu1946=)
NM_001145809.2(MYH14):c.5841C>T (p.Ala1947=)
NM_001145809.2(MYH14):c.594A>T (p.Gly198=) rs1195002362
NM_001145809.2(MYH14):c.5960+16G>A
NM_001145809.2(MYH14):c.5961-15C>T
NM_001145809.2(MYH14):c.645C>T (p.Leu215=)
NM_001145809.2(MYH14):c.660G>A (p.Ser220=) rs201835322
NM_001145809.2(MYH14):c.693+13G>A
NM_001145809.2(MYH14):c.69G>A (p.Ala23=)
NM_001145809.2(MYH14):c.718-4G>A
NM_001145809.2(MYH14):c.810+14G>T
NM_001145809.2(MYH14):c.96C>T (p.Arg32=)
NM_001145809.2(MYH14):c.974-7C>T

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