"GeneDx"[submitter] AND "ST3GAL3"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1261624	NM_006279.5(ST3GAL3):c.166+206_166+207dup	ST3GAL3	Duplication (intron variant)	not provided	GBenign
Select item 1236159	NM_006279.5(ST3GAL3):c.166+220A>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241211	NM_006279.5(ST3GAL3):c.167-182A>T	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229033	NM_006279.5(ST3GAL3):c.167-138T>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 130378	NM_006279.5(ST3GAL3):c.209+9925A>G	ST3GAL3 (T128A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GBenign
Select item 1246788	NM_006279.5(ST3GAL3):c.210-211_210-181del	ST3GAL3	Deletion (intron variant)	not provided	GBenign
Select item 1253557	NM_006279.5(ST3GAL3):c.210-148C>T	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1218049	NM_006279.5(ST3GAL3):c.303-226C>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1181960	NM_006279.5(ST3GAL3):c.397+180dup	ST3GAL3	Duplication (intron variant)	not provided	GLikely benign
Select item 1707323	NM_006279.5(ST3GAL3):c.397+172T>C	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1296229	NM_006279.5(ST3GAL3):c.397+172T>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283068	NM_006279.5(ST3GAL3):c.398-284C>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262588	NM_006279.5(ST3GAL3):c.398-197T>C	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1687684	NM_006279.5(ST3GAL3):c.398-153C>A	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1314922	NM_006279.5(ST3GAL3):c.608C>T (p.Thr203Met)	ST3GAL3 (T110M +8 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1179655	NM_006279.5(ST3GAL3):c.685G>C (p.Ala229Pro)	ST3GAL3 (A136P +8 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1255174	NM_006279.5(ST3GAL3):c.744+55C>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233138	NM_006279.5(ST3GAL3):c.744+58A>G	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275447	NM_006279.5(ST3GAL3):c.744+130G>A	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228590	NM_006279.5(ST3GAL3):c.745-304C>T	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1452219	NM_006279.5(ST3GAL3):c.781C>T (p.Arg261Ter)	ST3GAL3 (R168* +7 more)	Single nucleotide variant (nonsense +2 more)	Inborn genetic diseases +4 more	GPathogenic/Likely pathogenic
Select item 1700265	NM_006279.5(ST3GAL3):c.808C>T (p.Arg270Ter)	ST3GAL3 (R177* +7 more)	Single nucleotide variant (nonsense +2 more)	not provided	GPathogenic
Select item 450214	NM_006279.5(ST3GAL3):c.887G>A (p.Arg296Gln)	ST3GAL3 (R296Q +8 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 1259769	NM_006279.5(ST3GAL3):c.891+83C>T	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 130375	NM_006279.5(ST3GAL3):c.892-9G>A	ST3GAL3	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1261387	NM_006279.5(ST3GAL3):c.1038+42G>C	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1255027	NM_006279.5(ST3GAL3):c.1039-288C>A	LOC112590792, ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 504155	NM_006279.5(ST3GAL3):c.1068dup (p.Glu357fs)	ST3GAL3 (R143fs +20 more)	Duplication (frameshift variant +2 more)	not provided	GUncertain significance
Select item 450235	NM_006279.5(ST3GAL3):c.1120G>T (p.Gly374Cys)	ST3GAL3 (G374C +11 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance

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Items: 29