Myl7 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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15 records found for search term Myl7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405725971	CV3321055	single nucleotide variant	NM_021223.3(MYL7):c.26G>A (p.Arg9Gln)	not specified [RCV004450426]	uncertain significance	7	44141052	44141052	Human		name
156345476	CV2356235	single nucleotide variant	NM_021223.3(MYL7):c.33G>T (p.Lys11Asn)	not specified [RCV004206050]	uncertain significance	7	44141045	44141045	Human		name
597664460	CV3564882	single nucleotide variant	NM_021223.3(MYL7):c.59G>A (p.Arg20His)	not specified [RCV004828916]	uncertain significance	7	44141019	44141019	Human		name
155964682	CV2210030	single nucleotide variant	NM_021223.3(MYL7):c.230T>C (p.Met77Thr)	not specified [RCV004076461]	uncertain significance	7	44140391	44140391	Human		name
405725897	CV3321048	single nucleotide variant	NM_021223.3(MYL7):c.239A>G (p.Glu80Gly)	not specified [RCV004450419]	uncertain significance	7	44140382	44140382	Human		name
407515160	CV3454547	single nucleotide variant	NM_021223.3(MYL7):c.199G>T (p.Val67Leu)	not specified [RCV004649804]	uncertain significance	7	44140422	44140422	Human		name
597664478	CV3564884	single nucleotide variant	NM_021223.3(MYL7):c.256A>C (p.Asn86His)	not specified [RCV004828918]	uncertain significance	7	44140365	44140365	Human		name
597664488	CV3564885	single nucleotide variant	NM_021223.3(MYL7):c.265G>A (p.Val89Ile)	not specified [RCV004828919]	uncertain significance	7	44140356	44140356	Human		name
598190195	CV3994071	single nucleotide variant	NM_021223.3(MYL7):c.191T>C (p.Leu64Pro)	not specified [RCV005374003]	uncertain significance	7	44140714	44140714	Human		name
598190201	CV3994072	single nucleotide variant	NM_021223.3(MYL7):c.226G>T (p.Ala76Ser)	not specified [RCV005374004]	uncertain significance	7	44140395	44140395	Human		name
405726119	CV3321071	single nucleotide variant	NM_021223.3(MYL7):c.351C>G (p.Ser117Arg)	not specified [RCV004450442]	uncertain significance	7	44139808	44139808	Human		name
597664452	CV3564881	single nucleotide variant	NM_021223.3(MYL7):c.385C>A (p.Gln129Lys)	not specified [RCV004828915]	uncertain significance	7	44139562	44139562	Human		name
597664494	CV3564886	single nucleotide variant	NM_021223.3(MYL7):c.493T>C (p.Tyr165His)	not specified [RCV004828920]	uncertain significance	7	44138956	44138956	Human		name
597664501	CV3564887	single nucleotide variant	NM_021223.3(MYL7):c.388C>T (p.Leu130Phe)	not specified [RCV004828921]	uncertain significance	7	44139559	44139559	Human		name
598190188	CV3994070	single nucleotide variant	NM_021223.3(MYL7):c.442G>T (p.Ala148Ser)	not specified [RCV005374002]	uncertain significance	7	44139007	44139007	Human		name