List of variants in gene MYO7A reported as benign by PreventionGenetics, part of Exact Sciences

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_000260.4(MYO7A):c.6438+50A>T	rs2276289	0.86951
NM_000260.4(MYO7A):c.5743-12T>C	rs2276291	0.63742
NM_000260.4(MYO7A):c.4996A>T (p.Ser1666Cys)	rs2276288	0.59864
NM_000260.4(MYO7A):c.4323+35G>T	rs1109977	0.59156
NM_000260.4(MYO7A):c.5856+50G>A	rs2276290	0.56770
NM_000260.4(MYO7A):c.5715A>G (p.Lys1905=)	rs2276293	0.56709
NM_000260.4(MYO7A):c.6051+17T>A	rs1320702	0.56699
NM_000260.4(MYO7A):c.5857-7A>T	rs1320703	0.56654
NM_000260.4(MYO7A):c.1936-23G>A	rs2276283	0.52888
NM_000260.4(MYO7A):c.3924+12C>T	rs2276285	0.51057
NM_000260.4(MYO7A):c.783T>C (p.Gly261=)	rs762667	0.50077
NM_000260.4(MYO7A):c.4755C>T (p.Ser1585=)	rs7927472	0.47702
NM_000260.4(MYO7A):c.47T>C (p.Leu16Ser)	rs1052030	0.47208
NM_000260.4(MYO7A):c.6439-31G>A	rs883223	0.34445
NM_000260.4(MYO7A):c.6558+16G>A	rs883224	0.19125
NM_000260.4(MYO7A):c.736-47C>A	rs3737454	0.11805
NM_000260.4(MYO7A):c.1004-35C>G	rs2071151	0.09483
NM_000260.4(MYO7A):c.468C>T (p.Ile156=)	rs12420129	0.03116
NM_000260.4(MYO7A):c.5326+13C>T	rs114157944	0.02453
NM_000260.4(MYO7A):c.4589C>T (p.Ser1530Leu)	rs111033183	0.02384
NM_000260.4(MYO7A):c.3828G>A (p.Ser1276=)	rs78871677	0.02377
NM_000260.4(MYO7A):c.288G>A (p.Thr96=)	rs56023295	0.02179
NM_000260.4(MYO7A):c.3086A>G (p.His1029Arg)	rs60103800	0.00206
NM_000260.4(MYO7A):c.510G>A (p.Leu170=)	rs34477144	0.00138
NM_000260.4(MYO7A):c.4620G>A (p.Ala1540=)	rs41298745	0.00087
NM_000260.4(MYO7A):c.1726G>A (p.Asp576Asn)	rs187165412	0.00043
NM_000260.4(MYO7A):c.1343+8G>A	rs2276278
NM_000260.4(MYO7A):c.3375+33G>C	rs948972
NM_000260.4(MYO7A):c.3503+12_3503+33del	rs111033223
NM_000260.4(MYO7A):c.5860C>A (p.Leu1954Ile)	rs948962
NM_000260.4(MYO7A):c.6559-11C>T	rs34517202
NM_000260.4(MYO7A):c.93C>T (p.Cys31=)	rs35689081

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