ClinVar Miner

List of variants in gene SAMD9 reported as benign for not provided

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_017654.4(SAMD9):c.960T>C (p.Tyr320=) rs6965201 0.44772
NM_017654.4(SAMD9):c.428T>C (p.Ile143Thr) rs6969691 0.16513
NM_017654.4(SAMD9):c.1436C>T (p.Thr479Met) rs78564070 0.05927
NM_017654.4(SAMD9):c.1346A>G (p.Asn449Ser) rs10239435 0.05657
NM_017654.4(SAMD9):c.1360G>A (p.Ala454Thr) rs117649834 0.03101
NM_017654.4(SAMD9):c.2680A>G (p.Lys894Glu) rs79303965 0.02332
NM_017654.4(SAMD9):c.2642A>G (p.Asp881Gly) rs140921998 0.01659
NM_017654.4(SAMD9):c.3825T>C (p.Phe1275=) rs3802064 0.01446
NM_017654.4(SAMD9):c.995T>C (p.Ile332Thr) rs76377166 0.01341
NM_017654.4(SAMD9):c.4733T>C (p.Ile1578Thr) rs144380633 0.00655
NM_017654.4(SAMD9):c.1347T>C (p.Asn449=) rs150107667 0.00542
NM_017654.4(SAMD9):c.1398A>C (p.Pro466=) rs138066899 0.00533
NM_017654.4(SAMD9):c.4666G>A (p.Ala1556Thr) rs34896991 0.00462
NM_017654.4(SAMD9):c.257C>T (p.Ser86Phe) rs147157740 0.00428
NM_017654.4(SAMD9):c.1920C>T (p.Val640=) rs115425131 0.00377
NM_017654.4(SAMD9):c.4561G>A (p.Glu1521Lys) rs115350620 0.00320
NM_017654.4(SAMD9):c.3195A>G (p.Glu1065=) rs34256481 0.00081
NM_017654.4(SAMD9):c.1860A>G (p.Lys620=) rs77922936 0.00078
NM_017654.4(SAMD9):c.2374G>A (p.Val792Ile) rs147587391 0.00031
NM_017654.4(SAMD9):c.3171A>G (p.Ala1057=) rs202205898 0.00009
NM_017654.4(SAMD9):c.765T>C (p.Asp255=) rs201988689 0.00004
NM_017654.4(SAMD9):c.1645G>T (p.Val549Leu) rs10279499
NM_017654.4(SAMD9):c.1812A>G (p.Gln604=) rs181767582
NM_017654.4(SAMD9):c.223C>T (p.Arg75Trp) rs111780648
NM_017654.4(SAMD9):c.2854G>A (p.Gly952Arg)
NM_017654.4(SAMD9):c.2855G>C (p.Gly952Ala)
NM_017654.4(SAMD9):c.3651dup (p.Asp1218Ter) rs199887936
NM_017654.4(SAMD9):c.958T>G (p.Tyr320Asp)

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