ClinVar Miner

List of variants in gene MYH14 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.3033+11T>C rs930086 0.86981
NM_001145809.2(MYH14):c.5678+12C>T rs3826772 0.78229
NM_001145809.2(MYH14):c.2250A>G (p.Pro750=) rs1651553 0.74436
NM_001145809.2(MYH14):c.5469+16C>T rs3745510 0.64922
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509 0.63924
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822 0.56915
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504 0.53291
NM_001145809.2(MYH14):c.2355-14C>T rs12981413 0.46235
NM_001145809.2(MYH14):c.2205C>G (p.Arg735=) rs378811 0.38312
NM_001145809.2(MYH14):c.1114+13C>T rs11666328 0.32285
NM_001145809.2(MYH14):c.2355-17C>T rs28482851 0.23202
NM_001145809.2(MYH14):c.3680+9C>T rs76579307 0.20534
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722 0.14959
NM_001145809.2(MYH14):c.2827-9A>C rs3745503 0.14515
NM_001145809.2(MYH14):c.4752+16G>A rs10406788 0.14474
NM_001145809.2(MYH14):c.1483-10G>A rs73061136 0.09105
NM_001145809.2(MYH14):c.1755C>T (p.Gly585=) rs61731838 0.07411
NM_001145809.2(MYH14):c.1149T>C (p.Phe383=) rs61734424 0.06194
NM_001145809.2(MYH14):c.474T>C (p.Ile158=) rs34796700 0.02809
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034 0.02785
NM_001145809.2(MYH14):c.4753-9C>T rs45591233 0.02396
NM_001145809.2(MYH14):c.3468-3C>T rs78192108 0.01724
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457 0.01253
NM_001145809.2(MYH14):c.4741G>A (p.Val1581Ile) rs680446 0.01091
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624 0.00710
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400 0.00249
NM_001145809.2(MYH14):c.5533C>T (p.Arg1845Trp) rs199600574 0.00223
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646 0.00218
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363 0.00158
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073 0.00137
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324 0.00120
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met) rs112716976 0.00107
NM_001145809.2(MYH14):c.36G>A (p.Lys12=) rs372741317 0.00100
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011 0.00093
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) rs375866139 0.00075
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) rs199910006 0.00071
NM_001145809.2(MYH14):c.693+10C>T rs186027440 0.00057
NM_001145809.2(MYH14):c.1919G>A (p.Arg640Gln) rs199696801 0.00052
NM_001145809.2(MYH14):c.5778C>T (p.Leu1926=) rs201839634 0.00039
NM_001145809.2(MYH14):c.3850C>T (p.Arg1284Trp) rs201515738 0.00037
NM_001145809.2(MYH14):c.5960+8C>T rs373176553 0.00034
NM_001145809.2(MYH14):c.1026G>A (p.Pro342=) rs368124508 0.00029
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879 0.00024
NM_001145809.2(MYH14):c.1155C>T (p.Asn385=) rs558991834 0.00022
NM_001145809.2(MYH14):c.1133C>T (p.Ser378Leu) rs150806988 0.00011
NM_001145809.2(MYH14):c.1918C>T (p.Arg640Trp) rs376267080 0.00010
NM_001145809.2(MYH14):c.5447G>A (p.Arg1816His) rs201923258 0.00009
NM_001145809.2(MYH14):c.2921G>A (p.Arg974His) rs113993956 0.00008
NM_001145809.2(MYH14):c.5128-11G>A rs774151356 0.00006
NM_001145809.2(MYH14):c.3295+10C>T rs375601953 0.00004
NM_001145809.2(MYH14):c.3363G>C (p.Glu1121Asp) rs374915603 0.00004
NM_001145809.2(MYH14):c.543C>T (p.Ala181=) rs746669662 0.00004
NM_001145809.2(MYH14):c.68C>T (p.Ala23Val) rs765789880 0.00004
NM_001145809.2(MYH14):c.1251G>A (p.Thr417=) rs759132835 0.00002
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628 0.00002
NM_001145809.2(MYH14):c.4752+15C>T rs745696035 0.00002
NM_001145809.2(MYH14):c.5401G>A (p.Glu1801Lys) rs771246753 0.00002
NM_001145809.2(MYH14):c.1436C>A (p.Ala479Asp) rs886044300 0.00001
NM_001145809.2(MYH14):c.1995G>A (p.Ser665=) rs876657514 0.00001
NM_001145809.2(MYH14):c.5202G>A (p.Arg1734=) rs768918317 0.00001
NM_001145809.2(MYH14):c.1715C>T (p.Thr572Ile)
NM_001145809.2(MYH14):c.1835A>G (p.Asp612Gly)
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.2391C>G (p.Gly797=)
NM_001145809.2(MYH14):c.2681G>A (p.Arg894Gln)
NM_001145809.2(MYH14):c.2717C>T (p.Thr906Met) rs2035101711
NM_001145809.2(MYH14):c.2817A>T (p.Arg939=)
NM_001145809.2(MYH14):c.2932C>G (p.Leu978Val)
NM_001145809.2(MYH14):c.3247C>T (p.Leu1083Phe)
NM_001145809.2(MYH14):c.3300C>T (p.Arg1100=)
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.359C>T (p.Ser120Leu) rs119103281
NM_001145809.2(MYH14):c.4112C>G (p.Thr1371Arg)
NM_001145809.2(MYH14):c.4144C>G (p.Leu1382Val)
NM_001145809.2(MYH14):c.4355G>A (p.Arg1452Gln)
NM_001145809.2(MYH14):c.4412A>G (p.Glu1471Gly) rs2123423816
NM_001145809.2(MYH14):c.4625G>A (p.Arg1542Gln)
NM_001145809.2(MYH14):c.4853A>T (p.Asp1618Val)
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.5171C>T (p.Thr1724Ile)
NM_001145809.2(MYH14):c.5257-10A>G
NM_001145809.2(MYH14):c.5469+1G>T
NM_001145809.2(MYH14):c.5534G>C (p.Arg1845Pro)
NM_001145809.2(MYH14):c.5678+1G>A
NM_001145809.2(MYH14):c.5784C>T (p.Asp1928=)
NM_001145809.2(MYH14):c.5991_6004delinsTAGAGGAGGGCGTGGCA (p.Val1998_Phe2002delinsArgGlyGlyArgGlyIle)
NM_001145809.2(MYH14):c.5998del (p.Gln2000fs)
NM_001145809.2(MYH14):c.6090C>G (p.Ser2030=)
NM_001145809.2(MYH14):c.6093A>C (p.Pro2031=)
NM_001145809.2(MYH14):c.6096A>C (p.Pro2032=) rs2036794131
NM_001145809.2(MYH14):c.660G>T (p.Ser220=) rs201835322

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.