ClinVar Miner

List of variants in gene SHROOM4 reported as benign by Ambry Genetics

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_020717.5(SHROOM4):c.3468A>G (p.Glu1156=) rs3747282 0.29345
NM_020717.5(SHROOM4):c.3414A>G (p.Glu1138=) rs6614552 0.06860
NM_020717.5(SHROOM4):c.3168T>C (p.Arg1056=) rs61753881 0.04533
NM_020717.5(SHROOM4):c.1627A>T (p.Thr543Ser) rs61748324 0.01731
NM_020717.5(SHROOM4):c.439C>T (p.His147Tyr) rs111940781 0.01702
NM_020717.5(SHROOM4):c.2497G>A (p.Ala833Thr) rs61751944 0.01613
NM_020717.5(SHROOM4):c.3734C>T (p.Ser1245Leu) rs12689863 0.01172
NM_020717.5(SHROOM4):c.3147G>A (p.Met1049Ile) rs61753876 0.01148
NM_020717.5(SHROOM4):c.4101G>T (p.Leu1367Phe) rs28362302 0.00632
NM_020717.5(SHROOM4):c.3611A>G (p.Glu1204Gly) rs148721221 0.00172
NM_020717.5(SHROOM4):c.266G>A (p.Arg89Lys) rs148911180 0.00105
NM_020717.5(SHROOM4):c.4066G>A (p.Val1356Ile) rs137923286 0.00105
NM_020717.5(SHROOM4):c.1053C>A (p.Ser351Arg) rs59595864 0.00095
NM_020717.5(SHROOM4):c.1288G>T (p.Gly430Cys)
NM_020717.5(SHROOM4):c.1541G>T (p.Arg514Ile)
NM_020717.5(SHROOM4):c.2821C>T (p.Pro941Ser)
NM_020717.5(SHROOM4):c.3372_3383dup (p.Gln1125_Gln1128dup) rs201922875
NM_020717.5(SHROOM4):c.3384G>A (p.Gln1128=)
NM_020717.5(SHROOM4):c.3385A>C (p.Lys1129Gln)
NM_020717.5(SHROOM4):c.3393GGA[6] (p.Glu1151del) rs143151534
NM_020717.5(SHROOM4):c.3393GGA[8] (p.Glu1151dup) rs143151534
NM_020717.5(SHROOM4):c.3393_3394insCAGAAGCAACAGGAG (p.Gln1131_Glu1132insGlnLysGlnGlnGlu)
NM_020717.5(SHROOM4):c.3440AGG[6] (p.Glu1151dup) rs782326752

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