C0796154[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1264219	NM_001448.3(GPC4):c.320-15del	GPC4	Deletion (intron variant)	Wilms tumor 1 +3 more	GBenign
Select item 761308	NM_004484.4(GPC3):c.1698C>T (p.Thr566=)	GPC3	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 543089	NM_004484.4(GPC3):c.1568T>C (p.Leu523Pro)	GPC3 (L523P +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 855265	NM_004484.4(GPC3):c.1562G>A (p.Arg521His)	GPC3 (R505H +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 1016304	NM_004484.4(GPC3):c.1292+6C>T	GPC3	Single nucleotide variant (intron variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 589096	NM_004484.4(GPC3):c.1277A>G (p.Gln426Arg)	GPC3 (Q426R +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +2 more	GUncertain significance
Select item 239935	NM_004484.4(GPC3):c.1232G>T (p.Ser411Ile)	GPC3 (S411I +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +3 more	GBenign/Likely benign
Select item 1054925	NM_004484.4(GPC3):c.1070A>G (p.Tyr357Cys)	GPC3 (Y303C +3 more)	Single nucleotide variant (missense variant)	GPC3-related disorder +2 more	GUncertain significance
Select item 1000238	NM_004484.4(GPC3):c.1051C>T (p.His351Tyr)	GPC3 (H297Y +3 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 415275	NM_004484.4(GPC3):c.1032+9C>T	GPC3	Single nucleotide variant (intron variant)	Wilms tumor 1 +1 more	GBenign/Likely benign
Select item 239947	NM_004484.4(GPC3):c.972T>C (p.Phe324=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1 +2 more	GBenign/Likely benign
Select item 1080524	NM_004484.4(GPC3):c.918T>C (p.Leu306=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1 +1 more	GLikely benign
Select item 575501	NM_004484.4(GPC3):c.913G>A (p.Glu305Lys)	GPC3 (E305K +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 1003335	NM_004484.4(GPC3):c.865G>A (p.Val289Met)	GPC3 (V235M +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 1103639	NM_004484.4(GPC3):c.696T>C (p.Ala232=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1 +1 more	GLikely benign
Select item 239944	NM_004484.4(GPC3):c.648G>C (p.Met216Ile)	GPC3 (M216I +2 more)	Single nucleotide variant (missense variant)	Wilms tumor 1 +3 more	GBenign/Likely benign
Select item 415277	NM_004484.4(GPC3):c.516C>T (p.Asp172=)	GPC3	Single nucleotide variant (synonymous variant)	Wilms tumor 1 +1 more	GLikely benign
Select item 1590763	NM_004484.4(GPC3):c.450A>G (p.Thr150=)	GPC3	Single nucleotide variant (synonymous variant)	Simpson-Golabi-Behmel syndrome type 1 +1 more	GLikely benign
Select item 1692814	NM_004484.4(GPC3):c.338-6_338-5dup	GPC3	Duplication (intron variant)	Simpson-Golabi-Behmel syndrome type 1 +2 more	GLikely benign
Select item 695314	NM_004484.4(GPC3):c.338-20dup	GPC3	Duplication (intron variant)	Wilms tumor 1 +2 more	GBenign/Likely benign
Select item 698976	NM_004484.4(GPC3):c.338-7_338-5del	GPC3	Deletion (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 218527	NM_004484.4(GPC3):c.338-5del	GPC3	Deletion (intron variant)	Wilms tumor 1 +5 more	GBenign/Likely benign
Select item 1663423	NM_004484.4(GPC3):c.175+12T>G	GPC3	Single nucleotide variant (intron variant)	Wilms tumor 1 +1 more	GLikely benign
Select item 860300	NM_004484.4(GPC3):c.140C>T (p.Pro47Leu)	GPC3 (P47L)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 1039655	NM_004484.4(GPC3):c.118T>C (p.Ser40Pro)	GPC3 (S40P)	Single nucleotide variant (missense variant)	Wilms tumor 1 +1 more	GUncertain significance
Select item 939060	NM_004484.4(GPC3):c.115C>T (p.Arg39Cys)	GPC3 (R39C)	Single nucleotide variant (missense variant)	Simpson-Golabi-Behmel syndrome type 1 +1 more	GUncertain significance

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Items: 26