List of variants in gene MYL3 reported as likely benign for Hypertrophic cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 91

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HGVS	dbSNP	gnomAD frequency
NM_000258.3(MYL3):c.69C>T (p.Pro23=)	rs2233264	0.02058
NM_000258.3(MYL3):c.559+6C>T	rs199474709	0.00077
NM_000258.3(MYL3):c.482-14C>A	rs201780962	0.00048
NM_000258.3(MYL3):c.307+15C>T	rs184025552	0.00036
NM_000258.3(MYL3):c.482-17C>T	rs201289145	0.00030
NM_000258.3(MYL3):c.307+16G>A	rs759754750	0.00029
NM_000258.3(MYL3):c.516G>A (p.Leu172=)	rs367761724	0.00008
NM_000258.3(MYL3):c.420C>T (p.Phe140=)	rs201138698	0.00006
NM_000258.3(MYL3):c.552C>T (p.Asn184=)	rs140829951	0.00006
NM_000258.3(MYL3):c.399C>T (p.Phe133=)	rs112992334	0.00005
NM_000258.3(MYL3):c.158-10C>T	rs765419653	0.00004
NM_000258.3(MYL3):c.246G>A (p.Ala82=)	rs368364468	0.00004
NM_000258.3(MYL3):c.307+17A>G	rs1302011738	0.00004
NM_000258.3(MYL3):c.130-10C>T	rs374988162	0.00003
NM_000258.3(MYL3):c.477G>A (p.Thr159=)	rs148365503	0.00003
NM_000258.3(MYL3):c.92G>A (p.Arg31His)	rs199639940	0.00003
NM_000258.3(MYL3):c.105C>T (p.Val35=)	rs771114109	0.00002
NM_000258.3(MYL3):c.158-8C>G	rs937857201	0.00002
NM_000258.3(MYL3):c.219C>T (p.Tyr73=)	rs780500137	0.00002
NM_000258.3(MYL3):c.360C>T (p.His120=)	rs1314822874	0.00002
NM_000258.3(MYL3):c.532G>A (p.Asp178Asn)	rs145520567	0.00002
NM_000258.3(MYL3):c.183C>T (p.Phe61=)	rs368118534	0.00001
NM_000258.3(MYL3):c.198G>A (p.Lys66=)	rs781357657	0.00001
NM_000258.3(MYL3):c.222G>A (p.Gly74=)	rs144543453	0.00001
NM_000258.3(MYL3):c.247C>T (p.Leu83=)	rs1246506798	0.00001
NM_000258.3(MYL3):c.258C>T (p.Asn86=)	rs759363076	0.00001
NM_000258.3(MYL3):c.27G>A (p.Lys9=)	rs994017710	0.00001
NM_000258.3(MYL3):c.381A>C (p.Thr127=)	rs758267230	0.00001
NM_000258.3(MYL3):c.426G>A (p.Lys142=)	rs1435096286	0.00001
NM_000258.3(MYL3):c.429G>A (p.Glu143=)	rs746210438	0.00001
NM_000258.3(MYL3):c.435T>C (p.Asn145=)	rs774762882	0.00001
NM_000258.3(MYL3):c.465C>T (p.His155=)	rs147125759	0.00001
NM_000258.3(MYL3):c.482-20C>T	rs199811108	0.00001
NM_000258.3(MYL3):c.483T>G (p.Gly161=)	rs1345959283	0.00001
NM_000258.3(MYL3):c.501C>T (p.Asp167=)	rs552824036	0.00001
NM_000258.3(MYL3):c.504A>G (p.Glu168=)	rs1575497436	0.00001
NM_000258.3(MYL3):c.507G>A (p.Val169=)	rs1166390418	0.00001
NM_000258.3(MYL3):c.560-10T>G	rs749105574	0.00001
NM_000258.3(MYL3):c.560-15T>G	rs1041055773	0.00001
NM_000258.3(MYL3):c.6C>A (p.Ala2=)	rs971197044	0.00001
NM_000258.3(MYL3):c.78C>T (p.Pro26=)	rs764784092	0.00001
NM_000258.3(MYL3):c.105C>G (p.Val35=)	rs771114109
NM_000258.3(MYL3):c.108G>A (p.Glu36=)	rs2106914319
NM_000258.3(MYL3):c.129+16G>A	rs2106914252
NM_000258.3(MYL3):c.129+17G>T	rs2106914248
NM_000258.3(MYL3):c.129+19T>C
NM_000258.3(MYL3):c.130-12G>T	rs2106910597
NM_000258.3(MYL3):c.130-14G>A
NM_000258.3(MYL3):c.132T>C (p.Ile44=)	rs2106910567
NM_000258.3(MYL3):c.147G>A (p.Glu49=)	rs1004231349
NM_000258.3(MYL3):c.157+10G>A	rs2106910419
NM_000258.3(MYL3):c.157+9G>C
NM_000258.3(MYL3):c.158-17C>T	rs2106910239
NM_000258.3(MYL3):c.162C>T (p.Phe54=)
NM_000258.3(MYL3):c.165G>A (p.Lys55=)	rs397516277
NM_000258.3(MYL3):c.170C>A (p.Ala57Asp)	rs139794067
NM_000258.3(MYL3):c.171C>G (p.Ala57=)
NM_000258.3(MYL3):c.171C>T (p.Ala57=)
NM_000258.3(MYL3):c.178C>T (p.Leu60=)	rs1367233580
NM_000258.3(MYL3):c.195C>G (p.Pro65=)	rs1553639934
NM_000258.3(MYL3):c.216C>T (p.Thr72=)
NM_000258.3(MYL3):c.252C>T (p.Gly84=)
NM_000258.3(MYL3):c.270A>G (p.Ala90=)
NM_000258.3(MYL3):c.307+16G>C
NM_000258.3(MYL3):c.307+16G>T
NM_000258.3(MYL3):c.308-16G>A
NM_000258.3(MYL3):c.308-17G>C	rs914051059
NM_000258.3(MYL3):c.308-9T>C	rs2106907897
NM_000258.3(MYL3):c.354C>G (p.Leu118=)
NM_000258.3(MYL3):c.36T>C (p.Asp12=)	rs138567316
NM_000258.3(MYL3):c.393G>A (p.Glu131=)
NM_000258.3(MYL3):c.405G>A (p.Glu135=)	rs1575497812
NM_000258.3(MYL3):c.411G>A (p.Leu137=)	rs2233265
NM_000258.3(MYL3):c.412C>A (p.Arg138=)	rs1471322504
NM_000258.3(MYL3):c.441T>C (p.Thr147=)
NM_000258.3(MYL3):c.450T>C (p.Gly150=)
NM_000258.3(MYL3):c.477G>T (p.Thr159=)	rs148365503
NM_000258.3(MYL3):c.481+10G>C	rs1575497732
NM_000258.3(MYL3):c.481+15C>T	rs1701966300
NM_000258.3(MYL3):c.481+17C>T
NM_000258.3(MYL3):c.514T>C (p.Leu172=)	rs1390485854
NM_000258.3(MYL3):c.51C>A (p.Pro17=)
NM_000258.3(MYL3):c.549C>T (p.Ile183=)	rs963631094
NM_000258.3(MYL3):c.559+16_559+31del
NM_000258.3(MYL3):c.559+20G>A
NM_000258.3(MYL3):c.560-15T>A
NM_000258.3(MYL3):c.560-7T>C
NM_000258.3(MYL3):c.60T>A (p.Ala20=)
NM_000258.3(MYL3):c.96T>A (p.Pro32=)	rs886058582
NM_000258.3(MYL3):c.96T>G (p.Pro32=)	rs886058582
NM_000258.3(MYL3):c.99G>A (p.Lys33=)

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