"Fulgent Genetics, Fulgent Genetics"[submitter] AND "WNT5A"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1053536	NM_003392.7(WNT5A):c.1005C>T (p.Cys335=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided +1 more	GUncertain significance
Select item 1487547	NM_003392.7(WNT5A):c.937G>A (p.Glu313Lys)	WNT5A (E313K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 346267	NM_003392.7(WNT5A):c.807G>A (p.Lys269=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1224446	NM_003392.7(WNT5A):c.685A>G (p.Thr229Ala)	WNT5A (T229A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1633369	NM_003392.7(WNT5A):c.684+18C>A	WNT5A	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1046361	NM_003392.7(WNT5A):c.634G>A (p.Glu212Lys)	WNT5A (E212K +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant Robinow syndrome 1 +1 more	GUncertain significance
Select item 1362244	NM_003392.7(WNT5A):c.554A>G (p.Asn185Ser)	WNT5A (N170S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1567377	NM_003392.7(WNT5A):c.522G>T (p.Pro174=)	WNT5A	Single nucleotide variant (synonymous variant)	Autosomal dominant Robinow syndrome 1 +1 more	GLikely benign
Select item 775880	NM_003392.7(WNT5A):c.502G>A (p.Ala168Thr)	WNT5A (A168T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1441429	NM_003392.7(WNT5A):c.448A>G (p.Met150Val)	WNT5A (M135V +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant Robinow syndrome 1 +1 more	GUncertain significance
Select item 731899	NM_003392.7(WNT5A):c.291G>A (p.Ala97=)	WNT5A	Single nucleotide variant (synonymous variant)	Autosomal dominant Robinow syndrome 1 +1 more	GLikely benign
Select item 1413528	NM_003392.7(WNT5A):c.290C>T (p.Ala97Val)	WNT5A (A82V +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant Robinow syndrome 1 +1 more	GUncertain significance
Select item 977082	NM_003392.7(WNT5A):c.115G>C (p.Val39Leu)	WNT5A (V24L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 287634	NM_003392.7(WNT5A):c.14T>C (p.Ile5Thr)	WNT5A (I5T)	Single nucleotide variant (5 prime UTR variant +1 more)	Autosomal dominant Robinow syndrome 1 +2 more	GBenign/Likely benign
Select item 1621125	NM_003392.7(WNT5A):c.6+18T>A	WNT5A	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1311644	NM_003392.7(WNT5A):c.-6C>A	WNT5A	Single nucleotide variant (5 prime UTR variant)	Autosomal dominant Robinow syndrome 1 +1 more	GUncertain significance