Related gene-specific medical variations for Gene (Select 151648) - ClinVar - NCBI

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Links from Gene

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059284	NM_001199251.3(SGO1):c.504A>T (p.Thr168=)	SGO1, SGO1-AS1	Single nucleotide variant (synonymous variant +2 more)	SGO1-related condition	GBenign
Select item 3038529	NM_001199251.3(SGO1):c.1151C>T (p.Pro384Leu)	SGO1, SGO1-AS1 (P384L)	Single nucleotide variant (non-coding transcript variant +2 more)	SGO1-related condition	GLikely benign
Select item 2435915	NM_001199251.3(SGO1):c.1178C>G (p.Thr393Arg)	SGO1, SGO1-AS1 (T393R)	Single nucleotide variant (non-coding transcript variant +2 more)	Chronic atrial and intestinal dysrhythmia	GUncertain significance
Select item 2281372	NM_001199251.3(SGO1):c.539C>T (p.Ser180Phe)	SGO1, SGO1-AS1 (S180F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 791914	NM_001199251.3(SGO1):c.965A>C (p.Gln322Pro)	SGO1, SGO1-AS1 (Q322P)	Single nucleotide variant (missense variant +1 more)	SGO1-related condition +1 more	GBenign
Select item 787255	NM_001199251.3(SGO1):c.926A>G (p.Tyr309Cys)	SGO1, SGO1-AS1 (Y309C)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 760207	NM_001199251.3(SGO1):c.30C>A (p.Ser10=)	SGO1, SGO1-AS1	Single nucleotide variant (synonymous variant +1 more)	SGO1-related condition +1 more	GBenign
Select item 714173	NM_001199251.3(SGO1):c.654G>A (p.Gly218=)	SGO1, SGO1-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 382303	NM_001199251.3(SGO1):c.512T>C (p.Val171Ala)	SGO1, SGO1-AS1 (V171A)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 162627	NM_001199251.3(SGO1):c.67A>G (p.Lys23Glu)	SGO1, SGO1-AS1 (K23E)	Single nucleotide variant (missense variant +1 more)	Chronic atrial and intestinal dysrhythmia +1 more	GPathogenic