List of variants in gene MYL2 reported as likely benign by Invitae

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: 106

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.342G>A (p.Leu114=)	rs199572927	0.00032
NM_000432.4(MYL2):c.275-14G>C	rs375703502	0.00025
NM_000432.4(MYL2):c.274+8C>T	rs397516400	0.00014
NM_000432.4(MYL2):c.274+9G>A	rs371405579	0.00010
NM_000432.4(MYL2):c.387G>A (p.Arg129=)	rs774686046	0.00006
NM_000432.4(MYL2):c.169+18G>C	rs375152116	0.00004
NM_000432.4(MYL2):c.353+16G>A	rs572363699	0.00004
NM_000432.4(MYL2):c.354-18G>A	rs752927354	0.00003
NM_000432.4(MYL2):c.375G>A (p.Thr125=)	rs190020833	0.00003
NM_000432.4(MYL2):c.216G>A (p.Glu72=)	rs376506450	0.00002
NM_000432.4(MYL2):c.222G>A (p.Pro74=)	rs372644111	0.00002
NM_000432.4(MYL2):c.274+7T>C	rs771812779	0.00002
NM_000432.4(MYL2):c.354-8C>A	rs767657562	0.00002
NM_000432.4(MYL2):c.468G>A (p.Val156=)	rs137984206	0.00002
NM_000432.4(MYL2):c.474C>T (p.Ile158=)	rs1423130699	0.00002
NM_000432.4(MYL2):c.120G>A (p.Arg40=)	rs571489007	0.00001
NM_000432.4(MYL2):c.138G>A (p.Lys46=)	rs1267967428	0.00001
NM_000432.4(MYL2):c.147G>A (p.Leu49=)	rs749936467	0.00001
NM_000432.4(MYL2):c.156C>A (p.Thr52=)	rs761358011	0.00001
NM_000432.4(MYL2):c.169+13C>T	rs367740411	0.00001
NM_000432.4(MYL2):c.169+7C>T	rs371784522	0.00001
NM_000432.4(MYL2):c.170-14G>C	rs371431719	0.00001
NM_000432.4(MYL2):c.264G>A (p.Glu88=)	rs1187321974	0.00001
NM_000432.4(MYL2):c.275-12G>A	rs750937792	0.00001
NM_000432.4(MYL2):c.275-8C>T	rs765328765	0.00001
NM_000432.4(MYL2):c.303C>T (p.Asn101=)	rs1317472220	0.00001
NM_000432.4(MYL2):c.315G>C (p.Val105=)	rs768415509	0.00001
NM_000432.4(MYL2):c.353+7G>A	rs764227154	0.00001
NM_000432.4(MYL2):c.354-20C>G	rs376261948	0.00001
NM_000432.4(MYL2):c.403-11G>A	rs1212140808	0.00001
NM_000432.4(MYL2):c.403-20G>A	rs759088974	0.00001
NM_000432.4(MYL2):c.403-8C>T	rs1440682502	0.00001
NM_000432.4(MYL2):c.408C>T (p.Asp136=)	rs1356499130	0.00001
NM_000432.4(MYL2):c.447C>T (p.Asn149=)	rs397516405	0.00001
NM_000432.4(MYL2):c.483C>T (p.His161=)	rs886039108	0.00001
NM_000432.4(MYL2):c.94-16C>G	rs745969429	0.00001
NM_000432.4(MYL2):c.94-9C>T	rs1476443487	0.00001
NM_000432.4(MYL2):c.123T>C (p.Asp41=)
NM_000432.4(MYL2):c.135C>T (p.Asp45=)	rs199474807
NM_000432.4(MYL2):c.141C>T (p.Asn47=)	rs199474808
NM_000432.4(MYL2):c.170-17T>C	rs1453191107
NM_000432.4(MYL2):c.170-20G>A
NM_000432.4(MYL2):c.170-20GT[3]	rs764824483
NM_000432.4(MYL2):c.172C>A (p.Arg58=)	rs756671869
NM_000432.4(MYL2):c.174A>G (p.Arg58=)	rs777225996
NM_000432.4(MYL2):c.183G>A (p.Val61=)	rs933908830
NM_000432.4(MYL2):c.222G>T (p.Pro74=)
NM_000432.4(MYL2):c.249C>T (p.Leu83=)	rs1240275237
NM_000432.4(MYL2):c.274+11_274+12insGC
NM_000432.4(MYL2):c.274+13G>A
NM_000432.4(MYL2):c.274+18T>A
NM_000432.4(MYL2):c.274+20T>C
NM_000432.4(MYL2):c.274+9G>C
NM_000432.4(MYL2):c.274+9GT[4]
NM_000432.4(MYL2):c.275-15T>C
NM_000432.4(MYL2):c.275-16C>G	rs1377138024
NM_000432.4(MYL2):c.275-18C>T
NM_000432.4(MYL2):c.275-19G>A
NM_000432.4(MYL2):c.285T>G (p.Pro95=)	rs1592799785
NM_000432.4(MYL2):c.298C>G (p.Leu100Val)	rs573898913
NM_000432.4(MYL2):c.300C>T (p.Leu100=)	rs1253123682
NM_000432.4(MYL2):c.308T>G (p.Phe103Cys)	rs547860537
NM_000432.4(MYL2):c.330C>A (p.Gly110=)
NM_000432.4(MYL2):c.351T>C (p.Asp117=)
NM_000432.4(MYL2):c.353+12C>T
NM_000432.4(MYL2):c.353+16G>T	rs572363699
NM_000432.4(MYL2):c.353+19G>A
NM_000432.4(MYL2):c.353+21A>C	rs2136770699
NM_000432.4(MYL2):c.353+9G>A	rs2136770734
NM_000432.4(MYL2):c.354-17C>G	rs2136770510
NM_000432.4(MYL2):c.354-4G>A
NM_000432.4(MYL2):c.354-6C>G	rs977023771
NM_000432.4(MYL2):c.354-6C>T	rs977023771
NM_000432.4(MYL2):c.354-8C>G	rs767657562
NM_000432.4(MYL2):c.354-8C>T
NM_000432.4(MYL2):c.367C>T (p.Leu123=)	rs2136770433
NM_000432.4(MYL2):c.369G>A (p.Leu123=)	rs2136770430
NM_000432.4(MYL2):c.375G>C (p.Thr125=)	rs190020833
NM_000432.4(MYL2):c.402+10T>A	rs2136770333
NM_000432.4(MYL2):c.402+17A>G	rs1555257745
NM_000432.4(MYL2):c.402+20A>C
NM_000432.4(MYL2):c.402+7G>C
NM_000432.4(MYL2):c.402+8G>T	rs886048959
NM_000432.4(MYL2):c.402+9G>A
NM_000432.4(MYL2):c.403-15G>C	rs202105636
NM_000432.4(MYL2):c.403-16T>C
NM_000432.4(MYL2):c.403-18G>A
NM_000432.4(MYL2):c.403-4G>C	rs200888544
NM_000432.4(MYL2):c.403-7A>C	rs2071650175
NM_000432.4(MYL2):c.403-9T>C
NM_000432.4(MYL2):c.417C>T (p.Phe139=)	rs781107246
NM_000432.4(MYL2):c.420C>A (p.Ala140=)
NM_000432.4(MYL2):c.420C>T (p.Ala140=)	rs369489428
NM_000432.4(MYL2):c.429C>G (p.Pro143=)	rs374328118
NM_000432.4(MYL2):c.435C>T (p.Asp145=)	rs766907447
NM_000432.4(MYL2):c.444C>T (p.Gly148=)	rs1555257596
NM_000432.4(MYL2):c.465G>C (p.Leu155=)	rs1256208287
NM_000432.4(MYL2):c.480C>T (p.Thr160=)	rs727505065
NM_000432.4(MYL2):c.486A>C (p.Gly162=)	rs1177510197
NM_000432.4(MYL2):c.486A>T (p.Gly162=)
NM_000432.4(MYL2):c.501G>A (p.Ter167=)	rs2136767524
NM_000432.4(MYL2):c.94-10C>T	rs2071684471
NM_000432.4(MYL2):c.94-15A>C	rs1202280683
NM_000432.4(MYL2):c.94-17T>C
NM_000432.4(MYL2):c.94-19A>G	rs921973455
NM_000432.4(MYL2):c.99C>T (p.Phe33=)	rs2136774131

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