C4748924[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 644129	NM_177438.3(DICER1):c.5761A>C (p.Asn1921His)	DICER1 (N1921H)	Single nucleotide variant (3 prime UTR variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1025708	NM_177438.3(DICER1):c.5728C>T (p.Arg1910Ter)	DICER1 (R1910*)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2674809	NM_177438.3(DICER1):c.5632G>A (p.Val1878Ile)	DICER1 (V1317I +4 more)	Single nucleotide variant (missense variant +2 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 412160	NM_177438.3(DICER1):c.5623G>A (p.Asp1875Asn)	DICER1 (D1875N)	Single nucleotide variant (synonymous variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 825817	NM_177438.3(DICER1):c.5542A>G (p.Asn1848Asp)	DICER1 (N1848D)	Single nucleotide variant (synonymous variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +1 more	GUncertain significance
Select item 242139	NM_177438.3(DICER1):c.5524A>G (p.Ile1842Val)	DICER1 (I1842V)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 133976	NM_177438.3(DICER1):c.5516G>A (p.Arg1839Gln)	DICER1 (R1839Q)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 412116	NM_177438.3(DICER1):c.5504A>G (p.Tyr1835Cys)	DICER1 (Y1835C)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 1022345	NM_177438.3(DICER1):c.5483A>T (p.Glu1828Val)	DICER1 (E1828V)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +1 more	GUncertain significance
Select item 3241326	NM_177438.3(DICER1):c.5479C>G (p.Leu1827Val)	DICER1 (L1266V +4 more)	Single nucleotide variant (missense variant +2 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 647583	NM_177438.3(DICER1):c.5471G>A (p.Gly1824Glu)	DICER1 (G1824E)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 412057	NM_177438.3(DICER1):c.5471G>T (p.Gly1824Val)	DICER1 (G1824V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 412149	NM_177438.3(DICER1):c.5461A>G (p.Met1821Val)	DICER1 (M1821V)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 2566169	NM_177438.3(DICER1):c.5450G>A (p.Gly1817Asp)	DICER1 (G1682D +4 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 661301	NM_177438.3(DICER1):c.5425G>A (p.Gly1809Arg)	DICER1 (G1809R)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition	GPathogenic FDA Recognized database
Select item 579687	NM_177438.3(DICER1):c.5330T>A (p.Leu1777His)	DICER1 (L1777H)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +3 more	GConflicting classifications of pathogenicity
Select item 1475164	NM_177438.3(DICER1):c.5300A>G (p.His1767Arg)	DICER1 (H1767R)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 1934672	NM_177438.3(DICER1):c.5287C>T (p.Pro1763Ser)	DICER1 (P1628S +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +1 more	GUncertain significance
Select item 477251	NM_177438.3(DICER1):c.5257G>A (p.Asp1753Asn)	DICER1 (D1753N)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 3241321	NM_177438.3(DICER1):c.5181C>G (p.His1727Gln)	DICER1 (H1166Q +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 652143	NM_177438.3(DICER1):c.5173C>T (p.Arg1725Trp)	DICER1 (R1725W)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 690455	NM_177438.3(DICER1):c.5171C>T (p.Pro1724Leu)	DICER1 (P1724L)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 477240	NM_177438.3(DICER1):c.5089A>G (p.Ile1697Val)	DICER1 (I1697V)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 3241320	NM_177438.3(DICER1):c.5065C>G (p.His1689Asp)	DICER1 (H1128D +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 483436	NM_177438.3(DICER1):c.5041G>T (p.Ala1681Ser)	DICER1 (A1681S)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 848706	NM_177438.3(DICER1):c.5027G>A (p.Arg1676Lys)	DICER1 (R1676K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 483415	NM_177438.3(DICER1):c.5027G>C (p.Arg1676Thr)	DICER1 (R1676T)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 477232	NM_177438.3(DICER1):c.5016A>T (p.Lys1672Asn)	DICER1 (K1672N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1361992	NM_177438.3(DICER1):c.5013G>T (p.Lys1671Asn)	DICER1 (K1671N)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +3 more	GUncertain significance
Select item 543632	NM_177438.3(DICER1):c.5013G>C (p.Lys1671Asn)	DICER1 (K1671N)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 825366	NM_177438.3(DICER1):c.5007T>G (p.Phe1669Leu)	DICER1 (F1669L)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 412095	NM_177438.3(DICER1):c.4991C>T (p.Ser1664Leu)	DICER1 (S1664L)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 477231	NM_177438.3(DICER1):c.4987A>G (p.Ile1663Val)	DICER1 (I1663V)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 2674838	NM_177438.3(DICER1):c.4979_4982dup (p.His1661fs)	DICER1 (H1100fs +4 more)	Duplication (frameshift variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GLikely pathogenic
Select item 2674804	NM_177438.3(DICER1):c.4957C>G (p.Pro1653Ala)	DICER1 (P1092A +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 477229	NM_177438.3(DICER1):c.4954C>T (p.His1652Tyr)	DICER1 (H1652Y)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 412129	NM_177438.3(DICER1):c.4945A>G (p.Met1649Val)	DICER1 (M1649V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 3241323	NM_177438.3(DICER1):c.4926G>C (p.Leu1642Phe)	DICER1 (L1081F +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 133973	NM_177438.3(DICER1):c.4923T>G (p.Cys1641Trp)	DICER1 (C1641W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 412102	NM_177438.3(DICER1):c.4894T>C (p.Ser1632Pro)	DICER1 (S1632P)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +3 more	GConflicting classifications of pathogenicity
Select item 477226	NM_177438.3(DICER1):c.4889G>A (p.Arg1630His)	DICER1 (R1630H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 412061	NM_177438.3(DICER1):c.4888C>T (p.Arg1630Cys)	DICER1 (R1630C)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +3 more	GConflicting classifications of pathogenicity
Select item 220773	NM_177438.3(DICER1):c.4874C>A (p.Ser1625Tyr)	DICER1 (S1625Y)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 483414	NM_177438.3(DICER1):c.4870G>C (p.Ala1624Pro)	DICER1 (A1624P)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1047183	NM_177438.3(DICER1):c.4868C>T (p.Ala1623Val)	DICER1 (A1623V)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 242122	NM_177438.3(DICER1):c.4853C>T (p.Ser1618Leu)	DICER1 (S1618L)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 483406	NM_177438.3(DICER1):c.4838A>T (p.Gln1613Leu)	DICER1 (Q1613L)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1743451	NM_177438.3(DICER1):c.4834A>G (p.Ser1612Gly)	DICER1 (S1051G +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 2674829	NM_177438.3(DICER1):c.4828T>A (p.Phe1610Ile)	DICER1 (F1049I +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 412153	NM_177438.3(DICER1):c.4820G>A (p.Arg1607Gln)	DICER1 (R1607Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 2674833	NM_177438.3(DICER1):c.4814del (p.Pro1605fs)	DICER1 (P1044fs +4 more)	Deletion (frameshift variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GLikely pathogenic
Select item 825200	NM_177438.3(DICER1):c.4814C>T (p.Pro1605Leu)	DICER1 (P1605L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 477219	NM_177438.3(DICER1):c.4796G>T (p.Arg1599Leu)	DICER1 (R1599L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 133972	NM_177438.3(DICER1):c.4795C>T (p.Arg1599Trp)	DICER1 (R1599W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 841449	NM_177438.3(DICER1):c.4780A>G (p.Ile1594Val)	DICER1 (I1594V)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 225883	NM_177438.3(DICER1):c.4754C>G (p.Ser1585Ter)	DICER1 (S1585*)	Single nucleotide variant (nonsense)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GPathogenic
Select item 2674821	NM_177438.3(DICER1):c.4748T>C (p.Leu1583Pro)	DICER1 (L1022P +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 856552	NM_177438.3(DICER1):c.4732G>A (p.Ala1578Thr)	DICER1 (A1578T)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 1040976	NM_177438.3(DICER1):c.4652A>G (p.Glu1551Gly)	DICER1 (E1551G)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +1 more	GUncertain significance
Select item 947239	NM_177438.3(DICER1):c.4639G>A (p.Asp1547Asn)	DICER1 (D1547N)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 412088	NM_177438.3(DICER1):c.4616C>A (p.Thr1539Lys)	DICER1 (T1539K)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 1499379	NM_177438.3(DICER1):c.4532A>G (p.Tyr1511Cys)	DICER1 (Y1511C)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +1 more	GUncertain significance
Select item 1715642	NM_177438.3(DICER1):c.4525A>G (p.Met1509Val)	DICER1 (M1320V +4 more)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 2195728	NM_177438.3(DICER1):c.4508A>G (p.Tyr1503Cys)	DICER1 (Y1503C +4 more)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 483407	NM_177438.3(DICER1):c.4475T>C (p.Met1492Thr)	DICER1 (M1492T)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 577152	NM_177438.3(DICER1):c.4449G>A (p.Met1483Ile)	DICER1 (M1483I)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 477202	NM_177438.3(DICER1):c.4406T>C (p.Leu1469Pro)	DICER1 (L1469P)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +4 more	GConflicting classifications of pathogenicity
Select item 412062	NM_177438.3(DICER1):c.4405C>A (p.Leu1469Ile)	DICER1 (L1469I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 1983636	NM_177438.3(DICER1):c.4382G>C (p.Gly1461Ala)	DICER1 (G1272A +4 more)	Single nucleotide variant (missense variant +1 more)	DICER1-related tumor predisposition +1 more	GUncertain significance
Select item 543597	NM_177438.3(DICER1):c.4376G>A (p.Gly1459Glu)	DICER1 (G1459E)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 660437	NM_177438.3(DICER1):c.4374G>A (p.Met1458Ile)	DICER1 (M1458I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 654992	NM_177438.3(DICER1):c.4366A>G (p.Met1456Val)	DICER1 (M1456V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 242108	NM_177438.3(DICER1):c.4364A>C (p.Asn1455Thr)	DICER1 (N1455T)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 2007403	NM_177438.3(DICER1):c.4348_4354del (p.Ile1450fs)	DICER1 (I1450fs +4 more)	Deletion (frameshift variant +1 more)	DICER1-related tumor predisposition +1 more	GPathogenic/Likely pathogenic
Select item 1739886	NM_177438.3(DICER1):c.4346A>G (p.His1449Arg)	DICER1 (H1355R +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 641766	NM_177438.3(DICER1):c.4336G>A (p.Asp1446Asn)	DICER1 (D1446N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 957097	NM_177438.3(DICER1):c.4332G>C (p.Glu1444Asp)	DICER1 (E1444D)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 2674813	NM_177438.3(DICER1):c.4313A>T (p.Tyr1438Phe)	DICER1 (Y1249F +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 939082	NM_177438.3(DICER1):c.4313A>G (p.Tyr1438Cys)	DICER1 (Y1438C)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 412140	NM_177438.3(DICER1):c.4307C>A (p.Ala1436Asp)	DICER1 (A1436D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 477200	NM_177438.3(DICER1):c.4295C>T (p.Pro1432Leu)	DICER1 (P1432L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 649571	NM_177438.3(DICER1):c.4267G>A (p.Glu1423Lys)	DICER1 (E1423K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1739089	NM_177438.3(DICER1):c.4250A>T (p.Tyr1417Phe)	DICER1 (Y1323F +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GConflicting classifications of pathogenicity
Select item 824694	NM_177438.3(DICER1):c.4226C>G (p.Ala1409Gly)	DICER1 (A1409G)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 412047	NM_177438.3(DICER1):c.4221G>T (p.Met1407Ile)	DICER1 (M1407I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 579670	NM_177438.3(DICER1):c.4201G>A (p.Glu1401Lys)	DICER1 (E1401K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 242101	NM_177438.3(DICER1):c.4189T>C (p.Trp1397Arg)	DICER1 (W1397R)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 242100	NM_177438.3(DICER1):c.4178_4180dup (p.Asn1393dup)	DICER1	Duplication (inframe_insertion)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 3241330	NM_177438.3(DICER1):c.4163A>G (p.Asn1388Ser)	DICER1 (N1199S +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 1973827	NM_177438.3(DICER1):c.4154A>G (p.Tyr1385Cys)	DICER1 (Y1196C +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GUncertain significance
Select item 242099	NM_177438.3(DICER1):c.4102C>T (p.Arg1368Cys)	DICER1 (R1368C)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +4 more	GConflicting classifications of pathogenicity
Select item 477181	NM_177438.3(DICER1):c.4093C>A (p.Leu1365Ile)	DICER1 (L1365I)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +3 more	GUncertain significance
Select item 477180	NM_177438.3(DICER1):c.4091G>C (p.Gly1364Ala)	DICER1 (G1364A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 952254	NM_177438.3(DICER1):c.4085del (p.Lys1362fs)	DICER1 (K1362fs)	Deletion (frameshift variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +2 more	GPathogenic/Likely pathogenic
Select item 3241333	NM_177438.3(DICER1):c.4079G>C (p.Gly1360Ala)	DICER1 (G1171A +4 more)	Single nucleotide variant (missense variant +1 more)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome	GUncertain significance
Select item 479650	NM_177438.3(DICER1):c.4072C>T (p.Arg1358Cys)	DICER1 (R1358C)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 477176	NM_177438.3(DICER1):c.4060T>A (p.Cys1354Ser)	DICER1 (C1354S)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 570935	NM_177438.3(DICER1):c.4036A>G (p.Met1346Val)	DICER1 (M1346V)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 1401908	NM_177438.3(DICER1):c.3941G>A (p.Arg1314Gln)	DICER1 (R1314Q)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +2 more	GUncertain significance
Select item 477168	NM_177438.3(DICER1):c.3878A>G (p.Asn1293Ser)	DICER1 (N1293S)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +3 more	GUncertain significance

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