ClinVar Miner

List of variants in gene RAI1 reported by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 29
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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.4512G>T (p.Leu1504=) rs117995220 0.00559
NM_030665.4(RAI1):c.725C>T (p.Pro242Leu) rs150563155 0.00220
NM_030665.4(RAI1):c.4526A>G (p.Gln1509Arg) rs140063274 0.00073
NM_030665.4(RAI1):c.4039A>G (p.Lys1347Glu) rs34521483 0.00070
NM_030665.4(RAI1):c.1941C>T (p.Ser647=) rs140198185 0.00041
NM_030665.4(RAI1):c.4652C>T (p.Ser1551Leu) rs202158738 0.00032
NM_030665.4(RAI1):c.5079G>A (p.Pro1693=) rs748845443 0.00032
NM_030665.4(RAI1):c.2728T>G (p.Ser910Ala) rs745515458 0.00030
NM_030665.4(RAI1):c.3589G>C (p.Gly1197Arg) rs200719553 0.00024
NM_030665.4(RAI1):c.214G>A (p.Ala72Thr) rs370671656 0.00016
NM_030665.4(RAI1):c.4693G>A (p.Val1565Met) rs368106957 0.00016
NM_030665.4(RAI1):c.1503G>A (p.Pro501=) rs374194622 0.00006
NM_030665.4(RAI1):c.3543C>T (p.Ser1181=) rs773430101 0.00004
NM_030665.4(RAI1):c.4251A>G (p.Lys1417=) rs556223883 0.00003
NM_030665.4(RAI1):c.1274A>G (p.Asn425Ser) rs1054337797 0.00001
NM_030665.4(RAI1):c.4681C>A (p.Arg1561=) rs750728463 0.00001
NM_030665.4(RAI1):c.1321C>T (p.Gln441Ter) rs1555565108
NM_030665.4(RAI1):c.1915C>T (p.Pro639Ser) rs1030615093
NM_030665.4(RAI1):c.3112A>G (p.Met1038Val)
NM_030665.4(RAI1):c.3430A>G (p.Met1144Val) rs1198803613
NM_030665.4(RAI1):c.3769G>T (p.Asp1257Tyr)
NM_030665.4(RAI1):c.3778GAG[1] (p.Glu1261del) rs149716029

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