List of variants in gene combination MYH8, MYHAS reported as uncertain significance for not provided

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_002472.3(MYH8):c.1209C>A (p.Cys403Ter)	rs144321381	0.00124
NM_002472.3(MYH8):c.4878T>C (p.Asn1626=)	rs202123184	0.00055
NM_002472.3(MYH8):c.59G>A (p.Arg20Gln)	rs201580344	0.00026
NM_002472.3(MYH8):c.3874C>T (p.Arg1292Ter)	rs150008607	0.00024
NM_002472.3(MYH8):c.277A>G (p.Met93Val)	rs144036067	0.00021
NM_002472.3(MYH8):c.320A>G (p.Asn107Ser)	rs139192237	0.00008
NM_002472.3(MYH8):c.-7C>T	rs201919885	0.00006
NM_002472.3(MYH8):c.4470del (p.Tyr1491fs)	rs1060499730	0.00004
NM_002472.3(MYH8):c.2557G>A (p.Ala853Thr)	rs1319449107	0.00003
NM_002472.3(MYH8):c.5140G>A (p.Glu1714Lys)	rs553069572	0.00003
NM_002472.3(MYH8):c.5789T>G (p.Val1930Gly)	rs1346984851	0.00003
NM_002472.3(MYH8):c.1268T>G (p.Val423Gly)	rs747960533	0.00001
NM_002472.3(MYH8):c.1966-2A>G	rs747170484	0.00001
NM_002472.3(MYH8):c.2465G>A (p.Arg822His)	rs776002223	0.00001
NM_002472.3(MYH8):c.4089G>A (p.Ala1363=)	rs369923394	0.00001
NM_002472.3(MYH8):c.4253A>C (p.Glu1418Ala)	rs2508027162	0.00001
NM_002472.3(MYH8):c.447G>A (p.Lys149=)	rs1202079116	0.00001
NM_002472.3(MYH8):c.4543C>A (p.Leu1515Ile)	rs34564342	0.00001
NM_002472.3(MYH8):c.4846A>T (p.Arg1616Ter)	rs778961328	0.00001
NM_002472.3(MYH8):c.551G>C (p.Gly184Ala)	rs1472258546	0.00001
NM_002472.3(MYH8):c.5743A>G (p.Ile1915Val)	rs1216879928	0.00001
NM_002472.3(MYH8):c.629A>G (p.Asp210Gly)	rs963790352	0.00001
NM_002472.3(MYH8):c.11G>A (p.Ser4Asn)	rs1555558639
NM_002472.3(MYH8):c.1408del (p.Ile470fs)	rs1060499728
NM_002472.3(MYH8):c.1475del (p.Phe492fs)	rs781085472
NM_002472.3(MYH8):c.1667A>C (p.Tyr556Ser)	rs1380658768
NM_002472.3(MYH8):c.1759G>A (p.Gly587Ser)
NM_002472.3(MYH8):c.1966-1G>T	rs561214803
NM_002472.3(MYH8):c.1996A>T (p.Arg666Trp)
NM_002472.3(MYH8):c.2128A>T (p.Lys710Ter)	rs1060499731
NM_002472.3(MYH8):c.2230G>A (p.Ala744Thr)	rs2072193064
NM_002472.3(MYH8):c.2234C>T (p.Ser745Phe)	rs1555556803
NM_002472.3(MYH8):c.2691A>G (p.Glu897=)	rs1567684537
NM_002472.3(MYH8):c.2746dup (p.Ile916fs)	rs1555556193
NM_002472.3(MYH8):c.372C>G (p.Phe124Leu)
NM_002472.3(MYH8):c.3790A>G (p.Thr1264Ala)	rs2508037401
NM_002472.3(MYH8):c.3803A>T (p.Glu1268Val)	rs2072115603
NM_002472.3(MYH8):c.3860C>T (p.Ala1287Val)	rs1268282594
NM_002472.3(MYH8):c.3980A>C (p.Lys1327Thr)	rs2508033257
NM_002472.3(MYH8):c.398G>T (p.Trp133Leu)	rs483352720
NM_002472.3(MYH8):c.4172A>G (p.Glu1391Gly)	rs2508031752
NM_002472.3(MYH8):c.4649C>G (p.Ala1550Gly)	rs1344875858
NM_002472.3(MYH8):c.5623C>T (p.Gln1875Ter)	rs1060499727
NM_002472.3(MYH8):c.847G>T (p.Glu283Ter)

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