ClinVar Miner

List of variants in gene MYH7 reported as likely benign by Color

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Total variants: 48
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HGVS dbSNP
NM_000257.4(MYH7):c.1065C>T (p.Ala355=) rs778136999
NM_000257.4(MYH7):c.1139-14C>T rs397516091
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met) rs121913653
NM_000257.4(MYH7):c.1671G>A (p.Leu557=) rs149386750
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.2301C>T (p.Ala767=) rs768380939
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.2923-6C>T rs587781082
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.300G>A (p.Ala100=) rs757141502
NM_000257.4(MYH7):c.3100-15C>T rs534114622
NM_000257.4(MYH7):c.3372C>T (p.Ala1124=) rs1372163543
NM_000257.4(MYH7):c.3387G>A (p.Arg1129=) rs1566528000
NM_000257.4(MYH7):c.3402G>A (p.Lys1134=) rs587781083
NM_000257.4(MYH7):c.3414C>T (p.Asp1138=) rs1566527962
NM_000257.4(MYH7):c.3432G>A (p.Glu1144=) rs552605072
NM_000257.4(MYH7):c.3474C>T (p.Ser1158=) rs587780395
NM_000257.4(MYH7):c.354G>A (p.Ser118=) rs368925624
NM_000257.4(MYH7):c.3555C>T (p.His1185=) rs1387218063
NM_000257.4(MYH7):c.3567C>T (p.Ala1189=) rs1165812799
NM_000257.4(MYH7):c.3603C>G (p.Ala1201=) rs201576345
NM_000257.4(MYH7):c.3609G>T (p.Leu1203=) rs1555337108
NM_000257.4(MYH7):c.3621C>T (p.Ile1207=) rs529700838
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739
NM_000257.4(MYH7):c.372C>T (p.Thr124=) rs755855267
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser) rs574005462
NM_000257.4(MYH7):c.3861G>C (p.Leu1287=) rs150292548
NM_000257.4(MYH7):c.3960G>A (p.Glu1320=) rs147797612
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.3993C>T (p.His1331=) rs200288088
NM_000257.4(MYH7):c.4041C>T (p.Tyr1347=) rs1199930760
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=) rs776282574
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=) rs777053791
NM_000257.4(MYH7):c.5400C>T (p.Ala1800=) rs556490774
NM_000257.4(MYH7):c.5421C>T (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5451G>A (p.Ala1817=) rs138682220
NM_000257.4(MYH7):c.5484C>T (p.Ala1828=) rs202175645
NM_000257.4(MYH7):c.5560-14C>A rs375621171
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722
NM_000257.4(MYH7):c.5656-4G>A rs397516250
NM_000257.4(MYH7):c.633G>A (p.Pro211=) rs587781087
NM_000257.4(MYH7):c.705C>T (p.Thr235=) rs552415639
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342

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