"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "WNT7A"[ - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1570439	NM_004625.4(WNT7A):c.1029G>A (p.Thr343=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 497790	NM_004625.4(WNT7A):c.1028C>T (p.Thr343Met)	WNT7A (T343M)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 749690	NM_004625.4(WNT7A):c.942C>T (p.Asn314=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1922392	NM_004625.4(WNT7A):c.937T>C (p.Tyr313His)	WNT7A (Y313H)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 197238	NM_004625.4(WNT7A):c.861G>A (p.Val287=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1635400	NM_004625.4(WNT7A):c.777G>A (p.Ser259=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1634278	NM_004625.4(WNT7A):c.747C>A (p.Pro249=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 787253	NM_004625.4(WNT7A):c.681G>A (p.Val227=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 743183	NM_004625.4(WNT7A):c.624G>A (p.Ser208=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 792987	NM_004625.4(WNT7A):c.571-9C>G	WNT7A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3020334	NM_004625.4(WNT7A):c.571-15C>T	WNT7A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 500584	NM_004625.4(WNT7A):c.555C>T (p.Asn185=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 2713473	NM_004625.4(WNT7A):c.474C>T (p.Tyr158=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1050186	NM_004625.4(WNT7A):c.470G>A (p.Arg157His)	LOC126806608, WNT7A (R157H)	Single nucleotide variant (missense variant)	Fuhrmann syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1291668	NM_004625.4(WNT7A):c.459T>C (p.Ser153=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 288358	NM_004625.4(WNT7A):c.399C>T (p.Cys133=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 732506	NM_004625.4(WNT7A):c.387C>T (p.Ser129=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1278485	NM_004625.4(WNT7A):c.315G>A (p.Ala105=)	LOC126806608, WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 748820	NM_004625.4(WNT7A):c.259C>T (p.Leu87=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 497708	NM_004625.4(WNT7A):c.213C>T (p.Asp71=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 726320	NM_004625.4(WNT7A):c.171C>T (p.Asp57=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1921035	NM_004625.4(WNT7A):c.145C>T (p.Arg49Trp)	WNT7A (R49W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 725462	NM_004625.4(WNT7A):c.145C>A (p.Arg49=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2084552	NM_004625.4(WNT7A):c.99C>T (p.Gly33=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 719319	NM_004625.4(WNT7A):c.81C>T (p.Ser27=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 281770	NM_004625.4(WNT7A):c.75C>T (p.Gly25=)	WNT7A	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 785034	NM_004625.4(WNT7A):c.72-10C>T	WNT7A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 787254	NM_004625.4(WNT7A):c.60C>T (p.Tyr20=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2066787	NM_004625.4(WNT7A):c.25C>T (p.Leu9=)	WNT7A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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Items: 29