ClinVar Miner

List of variants in gene MYO3A reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_017433.5(MYO3A):c.1559C>T (p.Ala520Val) rs72787346 0.00218
NM_017433.5(MYO3A):c.1275G>A (p.Gln425=) rs77562287 0.00150
NM_017433.5(MYO3A):c.424C>T (p.His142Tyr) rs140301218 0.00121
NM_017433.5(MYO3A):c.585+4A>T rs202189844 0.00095
NM_017433.5(MYO3A):c.177C>T (p.Asp59=) rs139958275 0.00085
NM_017433.5(MYO3A):c.546G>T (p.Arg182=) rs148349532 0.00072
NM_017433.5(MYO3A):c.3729G>A (p.Arg1243=) rs146832858 0.00069
NM_017433.5(MYO3A):c.409-18A>G rs191938902 0.00049
NM_017433.5(MYO3A):c.3255C>T (p.Ser1085=) rs35541310 0.00044
NM_017433.5(MYO3A):c.3000-11T>C rs375346333 0.00036
NM_017433.5(MYO3A):c.1248A>G (p.Gln416=) rs143749728 0.00035
NM_017433.5(MYO3A):c.3932C>G (p.Thr1311Ser) rs146693681 0.00033
NM_017433.5(MYO3A):c.426T>G (p.His142Gln) rs189595832 0.00029
NM_017433.5(MYO3A):c.1562+13C>T rs371977805 0.00024
NM_017433.5(MYO3A):c.303+13G>C rs370111724 0.00024
NM_017433.5(MYO3A):c.1941A>G (p.Gln647=) rs778345128 0.00023
NM_017433.5(MYO3A):c.1668A>G (p.Leu556=) rs112809849 0.00018
NM_017433.5(MYO3A):c.906G>A (p.Thr302=) rs139818474 0.00014
NM_017433.5(MYO3A):c.4407T>C (p.Asn1469=) rs199843655 0.00010
NM_017433.5(MYO3A):c.610G>A (p.Asp204Asn) rs3737274 0.00009
NM_017433.5(MYO3A):c.4242G>A (p.Ser1414=) rs370029963 0.00008
NM_017433.5(MYO3A):c.1777-4T>G rs41279910 0.00007
NM_017433.5(MYO3A):c.3027C>T (p.Ser1009=) rs141341808 0.00007
NM_017433.5(MYO3A):c.4272T>A (p.Gly1424=) rs780271562 0.00006
NM_017433.5(MYO3A):c.1725C>G (p.Ser575=) rs201882363 0.00004
NM_017433.5(MYO3A):c.1893C>T (p.Ala631=) rs576387395 0.00004
NM_017433.5(MYO3A):c.2376A>G (p.Glu792=) rs758480848 0.00004
NM_017433.5(MYO3A):c.2703C>A (p.Ile901=) rs201429267 0.00003
NM_017433.5(MYO3A):c.472T>C (p.Leu158=) rs1412624643 0.00003
NM_017433.5(MYO3A):c.732-19T>C rs757402790 0.00003
NM_017433.5(MYO3A):c.953+17T>G rs377301180 0.00003
NM_017433.5(MYO3A):c.1904-13G>A rs911249864 0.00001
NM_017433.5(MYO3A):c.2331T>C (p.Asp777=) rs775141112 0.00001
NM_017433.5(MYO3A):c.2505+12A>G rs1222923903 0.00001
NM_017433.5(MYO3A):c.2754A>G (p.Thr918=) rs780196851 0.00001
NM_017433.5(MYO3A):c.4371A>T (p.Ser1457=) rs1021696700 0.00001
NM_017433.5(MYO3A):c.4662T>C (p.His1554=) rs768565288 0.00001
NM_017433.5(MYO3A):c.798-6G>A rs770441498 0.00001
NM_017433.5(MYO3A):c.1038A>G (p.Leu346=) rs727505229
NM_017433.5(MYO3A):c.1104_1105delinsTA (p.Val369Ile) rs386742102
NM_017433.5(MYO3A):c.115T>C (p.Leu39=)
NM_017433.5(MYO3A):c.1251T>C (p.Ser417=)
NM_017433.5(MYO3A):c.1256T>C (p.Ile419Thr)
NM_017433.5(MYO3A):c.1272T>C (p.Asp424=) rs1232445975
NM_017433.5(MYO3A):c.1276-4A>G
NM_017433.5(MYO3A):c.1341G>A (p.Gln447=)
NM_017433.5(MYO3A):c.1344G>T (p.Leu448=)
NM_017433.5(MYO3A):c.1359+15T>C
NM_017433.5(MYO3A):c.1563-15T>C
NM_017433.5(MYO3A):c.1643C>A (p.Pro548His) rs143918373
NM_017433.5(MYO3A):c.1661+13G>T rs1464936109
NM_017433.5(MYO3A):c.168+8A>T
NM_017433.5(MYO3A):c.1692A>C (p.Val564=)
NM_017433.5(MYO3A):c.1695A>G (p.Gln565=)
NM_017433.5(MYO3A):c.1950C>T (p.Leu650=)
NM_017433.5(MYO3A):c.1995C>T (p.Pro665=)
NM_017433.5(MYO3A):c.2046A>G (p.Leu682=)
NM_017433.5(MYO3A):c.2092T>C (p.Leu698=)
NM_017433.5(MYO3A):c.2114+15A>G
NM_017433.5(MYO3A):c.2148T>C (p.Leu716=)
NM_017433.5(MYO3A):c.2196G>A (p.Leu732=)
NM_017433.5(MYO3A):c.2262+8T>C
NM_017433.5(MYO3A):c.2416+10C>G
NM_017433.5(MYO3A):c.2416+14C>G
NM_017433.5(MYO3A):c.258T>C (p.Phe86=)
NM_017433.5(MYO3A):c.2670A>T (p.Ile890=)
NM_017433.5(MYO3A):c.2697A>G (p.Lys899=) rs2131909222
NM_017433.5(MYO3A):c.2793+20T>C
NM_017433.5(MYO3A):c.3003C>T (p.Tyr1001=) rs2131990421
NM_017433.5(MYO3A):c.304-6G>C
NM_017433.5(MYO3A):c.3192T>A (p.Ala1064=) rs1397884738
NM_017433.5(MYO3A):c.3398+17T>C
NM_017433.5(MYO3A):c.3501C>G (p.Ser1167=)
NM_017433.5(MYO3A):c.3585G>T (p.Val1195=) rs372169216
NM_017433.5(MYO3A):c.3744G>A (p.Arg1248=) rs2132036817
NM_017433.5(MYO3A):c.3762A>G (p.Lys1254=)
NM_017433.5(MYO3A):c.3801A>G (p.Pro1267=)
NM_017433.5(MYO3A):c.4047A>G (p.Ala1349=)
NM_017433.5(MYO3A):c.409-6T>C
NM_017433.5(MYO3A):c.4200T>C (p.His1400=)
NM_017433.5(MYO3A):c.4293+19T>G
NM_017433.5(MYO3A):c.4293+22_4293+25del
NM_017433.5(MYO3A):c.4438+11G>A rs2132054803
NM_017433.5(MYO3A):c.4476C>G (p.Pro1492=)
NM_017433.5(MYO3A):c.4545+13C>G
NM_017433.5(MYO3A):c.4581A>G (p.Lys1527=)
NM_017433.5(MYO3A):c.4641T>C (p.Ser1547=)
NM_017433.5(MYO3A):c.4752C>G (p.Pro1584=) rs562384478
NM_017433.5(MYO3A):c.4770A>G (p.Arg1590=)
NM_017433.5(MYO3A):c.4806C>T (p.Leu1602=)
NM_017433.5(MYO3A):c.508+19G>A
NM_017433.5(MYO3A):c.508+19G>T
NM_017433.5(MYO3A):c.567G>A (p.Pro189=)
NM_017433.5(MYO3A):c.585+10A>T
NM_017433.5(MYO3A):c.594A>C (p.Ala198=)
NM_017433.5(MYO3A):c.594A>T (p.Ala198=)
NM_017433.5(MYO3A):c.615C>A (p.Thr205=) rs55634590
NM_017433.5(MYO3A):c.731+15A>T rs183347061
NM_017433.5(MYO3A):c.798-16T>C
NM_017433.5(MYO3A):c.798-17C>A
NM_017433.5(MYO3A):c.844T>C (p.Leu282=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.