List of variants in gene MYL2 reported as uncertain significance for not specified

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.141C>A (p.Asn47Lys)	rs199474808	0.00038
NM_000432.4(MYL2):c.401A>C (p.Glu134Ala)	rs143139258	0.00029
NM_000432.4(MYL2):c.275-14G>C	rs375703502	0.00025
NM_000432.4(MYL2):c.359G>A (p.Arg120Gln)	rs192057022	0.00009
NM_000432.4(MYL2):c.374C>T (p.Thr125Met)	rs375667565	0.00009
NM_000432.4(MYL2):c.433G>A (p.Asp145Asn)	rs199567559	0.00005
NM_000432.4(MYL2):c.459G>C (p.Lys153Asn)	rs149078011	0.00004
NM_000432.4(MYL2):c.163G>T (p.Ala55Ser)	rs727504425	0.00002
NM_000432.4(MYL2):c.184A>T (p.Lys62Ter)	rs201728041	0.00002
NM_000432.4(MYL2):c.101C>T (p.Thr34Ile)	rs876657894	0.00001
NM_000432.4(MYL2):c.170G>A (p.Gly57Glu)	rs199474809	0.00001
NM_000432.4(MYL2):c.257T>C (p.Phe86Ser)	rs730880950	0.00001
NM_000432.4(MYL2):c.278C>A (p.Ala93Glu)	rs774193307	0.00001
NM_000432.4(MYL2):c.428C>T (p.Pro143Leu)	rs727504341	0.00001
NM_000432.4(MYL2):c.119G>A (p.Arg40Lys)	rs727503299
NM_000432.4(MYL2):c.119G>T (p.Arg40Met)	rs727503299
NM_000432.4(MYL2):c.142G>T (p.Asp48Tyr)	rs727504405
NM_000432.4(MYL2):c.169+20C>T
NM_000432.4(MYL2):c.181G>C (p.Val61Leu)	rs730880949
NM_000432.4(MYL2):c.188del (p.Asn63fs)	rs1177936172
NM_000432.4(MYL2):c.275G>T (p.Gly92Val)	rs727503297
NM_000432.4(MYL2):c.313G>A (p.Val105Met)	rs397516401
NM_000432.4(MYL2):c.358C>T (p.Arg120Trp)	rs397516404
NM_000432.4(MYL2):c.359G>C (p.Arg120Pro)
NM_000432.4(MYL2):c.389T>G (p.Phe130Cys)	rs727505071
NM_000432.4(MYL2):c.392C>G (p.Ser131Cys)	rs727504357
NM_000432.4(MYL2):c.402G>C (p.Glu134Asp)	rs727504408
NM_000432.4(MYL2):c.403-1G>T	rs199474813
NM_000432.4(MYL2):c.421G>A (p.Ala141Thr)	rs727504559
NM_000432.4(MYL2):c.470A>G (p.His157Arg)	rs730880951
NM_000432.4(MYL2):c.488A>C (p.Glu163Ala)	rs397516407
NM_000432.4(MYL2):c.488A>G (p.Glu163Gly)	rs397516407

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