ClinVar Miner

List of variants in gene RAI1 reported as benign by Eurofins NTD LLC (GA)

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Total variants: 23
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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.837_838del (p.Gln280fs) rs35068024 0.37587
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.1044C>T (p.Arg348=) rs142316059 0.00634
NM_030665.4(RAI1):c.4512G>T (p.Leu1504=) rs117995220 0.00559
NM_030665.4(RAI1):c.1142C>T (p.Ala381Val) rs113208290 0.00400
NM_030665.4(RAI1):c.837G>A (p.Gln279=) rs11078398 0.00357
NM_030665.4(RAI1):c.725C>T (p.Pro242Leu) rs150563155 0.00220
NM_030665.4(RAI1):c.840G>A (p.Gln280=) rs398124421 0.00123
NM_030665.4(RAI1):c.972G>A (p.Pro324=) rs138675466 0.00113
NM_030665.4(RAI1):c.3357C>T (p.Ser1119=) rs139448147 0.00076
NM_030665.4(RAI1):c.4438A>G (p.Arg1480Gly) rs139684843 0.00053
NM_030665.4(RAI1):c.3778GAG[1] (p.Glu1261del) rs149716029
NM_030665.4(RAI1):c.834GCA[10] (p.Gln289_Gln291del) rs371983878
NM_030665.4(RAI1):c.834GCA[11] (p.Gln290_Gln291del) rs371983878
NM_030665.4(RAI1):c.834GCA[12] (p.Gln291del) rs371983878
NM_030665.4(RAI1):c.834GCA[14] (p.Gln291dup) rs371983878
NM_030665.4(RAI1):c.834GCA[9] (p.Gln288_Gln291del) rs371983878

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