C5193005[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 581334	NM_006206.6(PDGFRA):c.11C>A (p.Ser4Tyr)	PDGFRA (S4Y +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 458990	NM_006206.6(PDGFRA):c.11C>T (p.Ser4Phe)	PDGFRA (S4F +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 855876	NM_006206.6(PDGFRA):c.40C>T (p.Leu14Phe)	PDGFRA (L27F +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 459107	NM_006206.6(PDGFRA):c.50G>T (p.Gly17Val)	PDGFRA (G17V +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 407376	NM_006206.6(PDGFRA):c.88A>G (p.Ile30Val)	PDGFRA (I30V +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GConflicting classifications of pathogenicity
Select item 407378	NM_006206.6(PDGFRA):c.94C>A (p.Pro32Thr)	PDGFRA (P32T +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 407434	NM_006206.6(PDGFRA):c.133T>C (p.Phe45Leu)	PDGFRA (F45L +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 2587716	NM_006206.6(PDGFRA):c.145T>C (p.Cys49Arg)	PDGFRA (C74R +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 843187	NM_006206.6(PDGFRA):c.206T>C (p.Val69Ala)	PDGFRA (V94A +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 528558	NM_006206.6(PDGFRA):c.230A>G (p.Asn77Ser)	PDGFRA (N77S +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 528578	NM_006206.6(PDGFRA):c.235G>A (p.Gly79Ser)	PDGFRA (G79S +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 407420	NM_006206.6(PDGFRA):c.248C>T (p.Thr83Met)	PDGFRA (T83M +2 more)	Single nucleotide variant (missense variant)	Ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 459067	NM_006206.6(PDGFRA):c.272C>T (p.Ser91Leu)	PDGFRA (S91L +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 528495	NM_006206.6(PDGFRA):c.275C>T (p.Ala92Val)	PDGFRA (A92V +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 528601	NM_006206.6(PDGFRA):c.282C>A (p.His94Gln)	PDGFRA (H94Q +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 839446	NM_006206.6(PDGFRA):c.295A>G (p.Thr99Ala)	PDGFRA (T112A +2 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 2677587	NM_006206.6(PDGFRA):c.309_310delinsAA (p.Asn103_His104delinsLysAsn)	PDGFRA	Indel (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 240348	NM_006206.6(PDGFRA):c.322G>A (p.Glu108Lys)	PDGFRA (E108K +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GConflicting classifications of pathogenicity
Select item 3240065	NM_006206.6(PDGFRA):c.404A>G (p.Asp135Gly)	PDGFRA (D135G +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 528567	NM_006206.6(PDGFRA):c.418G>A (p.Val140Met)	PDGFRA (V140M +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 3240062	NM_006206.6(PDGFRA):c.431A>T (p.Asp144Val)	PDGFRA (D144V +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 802074	NM_006206.6(PDGFRA):c.451C>T (p.Arg151Cys)	PDGFRA (R151C +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GConflicting classifications of pathogenicity
Select item 3240059	NM_006206.6(PDGFRA):c.461A>G (p.Asp154Gly)	PDGFRA (D154G +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 2677583	NM_006206.6(PDGFRA):c.502G>T (p.Val168Leu)	PDGFRA (V168L +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 1007897	NM_006206.6(PDGFRA):c.502G>A (p.Val168Ile)	PDGFRA (V168I +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 567533	NM_006206.6(PDGFRA):c.502G>C (p.Val168Leu)	PDGFRA (V168L +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 648175	NM_006206.6(PDGFRA):c.517G>C (p.Asp173His)	PDGFRA (D173H +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GConflicting classifications of pathogenicity
Select item 240352	NM_006206.6(PDGFRA):c.517G>A (p.Asp173Asn)	PDGFRA (D173N +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GConflicting classifications of pathogenicity
Select item 528618	NM_006206.6(PDGFRA):c.527A>G (p.Gln176Arg)	PDGFRA (Q176R +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GConflicting classifications of pathogenicity
Select item 1002030	NM_006206.6(PDGFRA):c.541A>T (p.Thr181Ser)	PDGFRA (T181S +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 846650	NM_006206.6(PDGFRA):c.568G>A (p.Glu190Lys)	PDGFRA (E190K +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 660967	NM_006206.6(PDGFRA):c.581A>G (p.Lys194Arg)	PDGFRA (K219R +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1003659	NM_006206.6(PDGFRA):c.592T>A (p.Phe198Ile)	PDGFRA (F198I +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 568919	NM_006206.6(PDGFRA):c.632C>T (p.Thr211Ile)	PDGFRA (T211I +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 240358	NM_006206.6(PDGFRA):c.721G>A (p.Glu241Lys)	PDGFRA (E241K +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 1512628	NM_006206.6(PDGFRA):c.730G>A (p.Asp244Asn)	PDGFRA (D244N +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 1362887	NM_006206.6(PDGFRA):c.760A>G (p.Lys254Glu)	PDGFRA (K279E +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 459123	NM_006206.6(PDGFRA):c.799C>T (p.Pro267Ser)	PDGFRA (P267S +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 459124	NM_006206.6(PDGFRA):c.820A>T (p.Thr274Ser)	PDGFRA (T274S +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 407381	NM_006206.6(PDGFRA):c.838G>T (p.Ala280Ser)	PDGFRA (A280S +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 407386	NM_006206.6(PDGFRA):c.877C>T (p.Arg293Cys)	PDGFRA (R293C +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 567433	NM_006206.6(PDGFRA):c.916A>G (p.Thr306Ala)	PDGFRA (T306A +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 3240057	NM_006206.6(PDGFRA):c.929A>G (p.His310Arg)	PDGFRA (H310R +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 572635	NM_006206.6(PDGFRA):c.986T>C (p.Leu329Pro)	PDGFRA (L329P +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 459134	NM_006206.6(PDGFRA):c.988C>T (p.His330Tyr)	PDGFRA (H330Y +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 1047778	NM_006206.6(PDGFRA):c.1000C>T (p.His334Tyr)	PDGFRA (H347Y +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 407382	NM_006206.6(PDGFRA):c.1018C>T (p.Arg340Trp)	PDGFRA (R340W +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 2677594	NM_006206.6(PDGFRA):c.1102G>A (p.Glu368Lys)	PDGFRA (E368K +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 220810	NM_006206.6(PDGFRA):c.1133A>T (p.Lys378Ile)	PDGFRA (K378I +2 more)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 3240063	NM_006206.6(PDGFRA):c.1181T>C (p.Ile394Thr)	PDGFRA (I394T +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 3240056	NM_006206.6(PDGFRA):c.1212C>G (p.Ser404Arg)	PDGFRA (S404R +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 528600	NM_006206.6(PDGFRA):c.1214A>G (p.Tyr405Cys)	PDGFRA (Y405C +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 458994	NM_006206.6(PDGFRA):c.1273C>T (p.His425Tyr)	PDGFRA (H425Y +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 407410	NM_006206.6(PDGFRA):c.1274A>G (p.His425Arg)	PDGFRA (H425R +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +4 more	GUncertain significance
Select item 240301	NM_006206.6(PDGFRA):c.1283C>T (p.Thr428Ile)	PDGFRA (T428I +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GConflicting classifications of pathogenicity
Select item 970829	NM_006206.6(PDGFRA):c.1298T>C (p.Val433Ala)	PDGFRA (V433A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 407443	NM_006206.6(PDGFRA):c.1357A>G (p.Ile453Val)	PDGFRA (I453V +2 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 407425	NM_006206.6(PDGFRA):c.1424A>C (p.Glu475Ala)	PDGFRA (E475A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 407379	NM_006206.6(PDGFRA):c.1425G>T (p.Glu475Asp)	PDGFRA (E475D +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GConflicting classifications of pathogenicity
Select item 459001	NM_006206.6(PDGFRA):c.1438G>A (p.Asp480Asn)	PDGFRA (D480N +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 407406	NM_006206.6(PDGFRA):c.1459C>T (p.Arg487Cys)	PDGFRA (R487C +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 528508	NM_006206.6(PDGFRA):c.1460G>A (p.Arg487His)	PDGFRA (R487H +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GConflicting classifications of pathogenicity
Select item 407416	NM_006206.6(PDGFRA):c.1475A>C (p.Lys492Thr)	PDGFRA (K492T +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 407407	NM_006206.6(PDGFRA):c.1492G>A (p.Ala498Thr)	PDGFRA (A498T +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +3 more	GUncertain significance
Select item 407385	NM_006206.6(PDGFRA):c.1522G>A (p.Gly508Arg)	PDGFRA (G508R +2 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2677592	NM_006206.6(PDGFRA):c.1556C>A (p.Pro519His)	PDGFRA (P519H +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 528506	NM_006206.6(PDGFRA):c.1565G>A (p.Arg522His)	PDGFRA (R522H +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 459010	NM_006206.6(PDGFRA):c.1567T>A (p.Ser523Thr)	PDGFRA (S523T +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 577591	NM_006206.6(PDGFRA):c.1577C>T (p.Thr526Met)	PDGFRA (T526M +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 528559	NM_006206.6(PDGFRA):c.1580T>C (p.Val527Ala)	PDGFRA (V527A +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 2677589	NM_006206.6(PDGFRA):c.1589C>T (p.Ala530Val)	PDGFRA (A530V +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 407402	NM_006206.6(PDGFRA):c.1605G>T (p.Leu535Phe)	PDGFRA (L535F +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 971935	NM_006206.6(PDGFRA):c.1610T>C (p.Ile537Thr)	PDGFRA (I562T +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 2677584	NM_006206.6(PDGFRA):c.1616T>A (p.Ile539Asn)	PDGFRA (I539N +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 1776846	NM_006206.6(PDGFRA):c.1631T>G (p.Val544Gly)	PDGFRA (V557G +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 459014	NM_006206.6(PDGFRA):c.1642A>G (p.Ile548Val)	PDGFRA (I548V +2 more)	Single nucleotide variant (missense variant)	PDGFRA-related disorder +3 more	GUncertain significance
Select item 1006898	NM_006206.6(PDGFRA):c.1694T>C (p.Ile565Thr)	PDGFRA (I565T +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 41795	NM_006206.6(PDGFRA):c.1700C>T (p.Pro567Leu)	PDGFRA (P567L +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 662983	NM_006206.6(PDGFRA):c.1721A>T (p.Tyr574Phe)	PDGFRA (Y587F +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +2 more	GUncertain significance
Select item 2677586	NM_006206.6(PDGFRA):c.1736A>G (p.Gln579Arg)	PDGFRA (Q579R +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 1413496	NM_006206.6(PDGFRA):c.1780G>C (p.Val594Leu)	PDGFRA (V607L +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1035452	NM_006206.6(PDGFRA):c.1792G>A (p.Val598Ile)	PDGFRA (V598I +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 407429	NM_006206.6(PDGFRA):c.1822G>A (p.Val608Ile)	PDGFRA (V608I +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +3 more	GUncertain significance
Select item 240318	NM_006206.6(PDGFRA):c.1849C>T (p.Arg617Trp)	PDGFRA (R617W +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 459030	NM_006206.6(PDGFRA):c.1895C>T (p.Thr632Met)	PDGFRA (T632M +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +3 more	GUncertain significance
Select item 1354785	NM_006206.6(PDGFRA):c.1907G>C (p.Ser636Thr)	PDGFRA (S649T +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1379958	NM_006206.6(PDGFRA):c.1962T>A (p.His654Gln)	PDGFRA (H654Q +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 846986	NM_006206.6(PDGFRA):c.2014A>G (p.Ile672Val)	PDGFRA (I672V +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 2677588	NM_006206.6(PDGFRA):c.2054A>G (p.Tyr685Cys)	PDGFRA (Y685C +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 643860	NM_006206.6(PDGFRA):c.2069G>T (p.Arg690Met)	PDGFRA (R715M +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 407422	NM_006206.6(PDGFRA):c.2075G>A (p.Ser692Asn)	PDGFRA (S692N +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 1786183	NM_006206.6(PDGFRA):c.2116G>T (p.Asp706Tyr)	PDGFRA (D706Y +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 2677591	NM_006206.6(PDGFRA):c.2120T>G (p.Ile707Ser)	PDGFRA (I707S +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 407393	NM_006206.6(PDGFRA):c.2153G>A (p.Arg718Gln)	PDGFRA (R718Q +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 2677579	NM_006206.6(PDGFRA):c.2186G>A (p.Gly729Asp)	PDGFRA (G729D +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 639421	NM_006206.6(PDGFRA):c.2215A>G (p.Thr739Ala)	PDGFRA (T739A +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 660989	NM_006206.6(PDGFRA):c.2234T>C (p.Met745Thr)	PDGFRA (M758T +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2677593	NM_006206.6(PDGFRA):c.2235G>T (p.Met745Ile)	PDGFRA (M745I +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal +1 more	GUncertain significance
Select item 3240064	NM_006206.6(PDGFRA):c.2237T>C (p.Leu746Pro)	PDGFRA (L746P +2 more)	Single nucleotide variant (missense variant)	Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	GUncertain significance
Select item 348905	NM_006206.6(PDGFRA):c.2266G>A (p.Asp756Asn)	PDGFRA (D756N +2 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor +3 more	GConflicting classifications of pathogenicity

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