ClinVar Miner

List of variants in gene RAI1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_030665.4(RAI1):c.1992G>A (p.Pro664=) rs8067439 0.58185
NM_030665.4(RAI1):c.269G>C (p.Gly90Ala) rs3803763 0.43727
NM_030665.4(RAI1):c.5601T>C (p.Ile1867=) rs3818717 0.42485
NM_030665.4(RAI1):c.493C>A (p.Pro165Thr) rs11649804 0.35747
NM_030665.4(RAI1):c.4311T>C (p.Pro1437=) rs4925112 0.11504
NM_030665.4(RAI1):c.4530C>T (p.Pro1510=) rs35686634 0.09361
NM_030665.4(RAI1):c.264G>A (p.Gln88=) rs61999281 0.02170
NM_030665.4(RAI1):c.301G>A (p.Gly101Ser) rs145801481 0.00078
NM_030665.4(RAI1):c.5036C>T (p.Ala1679Val) rs142981643 0.00066
NM_030665.4(RAI1):c.3650G>A (p.Arg1217Gln) rs142415050 0.00063
NM_030665.4(RAI1):c.4676G>A (p.Arg1559Gln) rs141317462 0.00060
NM_030665.4(RAI1):c.1941C>T (p.Ser647=) rs140198185 0.00041
NM_030665.4(RAI1):c.1476C>T (p.Pro492=) rs200887225 0.00016
NM_030665.4(RAI1):c.5254G>A (p.Gly1752Arg) rs755572135 0.00013
NM_030665.4(RAI1):c.1925C>T (p.Ser642Leu) rs200061071 0.00009
NM_030665.4(RAI1):c.5366G>A (p.Arg1789Gln) rs368587743 0.00009
NM_030665.4(RAI1):c.486C>T (p.Ala162=) rs748628863 0.00008
NM_030665.4(RAI1):c.1904A>T (p.Asp635Val) rs200517965 0.00007
NM_030665.4(RAI1):c.3158C>T (p.Pro1053Leu) rs748386061 0.00007
NM_030665.4(RAI1):c.2669C>T (p.Pro890Leu) rs745320469 0.00006
NM_030665.4(RAI1):c.1276C>T (p.Leu426=) rs747528529 0.00005
NM_030665.4(RAI1):c.387A>G (p.Pro129=) rs199605856 0.00005
NM_030665.4(RAI1):c.925G>A (p.Ala309Thr) rs542056789 0.00005
NM_030665.4(RAI1):c.187G>A (p.Ala63Thr) rs758424396 0.00004
NM_030665.4(RAI1):c.776C>T (p.Pro259Leu) rs758661378 0.00003
NM_030665.4(RAI1):c.4096C>T (p.Arg1366Cys) rs375295086 0.00002
NM_030665.4(RAI1):c.5264C>A (p.Pro1755His) rs750872928 0.00002
NM_030665.4(RAI1):c.1110T>G (p.Phe370Leu) rs754037858 0.00001
NM_030665.4(RAI1):c.1850C>A (p.Ala617Asp) rs549244691 0.00001
NM_030665.4(RAI1):c.3270C>G (p.Ala1090=) rs398124416
NM_030665.4(RAI1):c.453G>C (p.Val151=) rs767613627
NM_030665.4(RAI1):c.5470G>C (p.Val1824Leu) rs778040446
NM_030665.4(RAI1):c.834GCA[17] (p.Gln288_Gln291dup) rs371983878
NM_030665.4(RAI1):c.834GCA[9] (p.Gln288_Gln291del) rs371983878
NM_030665.4(RAI1):c.838_839insCAGCAG (p.Gln280delinsProAlaGlu) rs1555565014
NM_030665.4(RAI1):c.980C>G (p.Ala327Gly) rs1555565043

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