"Ambry Genetics"[submitter] AND "AIG1"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2297783	NM_016108.4(AIG1):c.7C>T (p.Leu3Phe)	AIG1 (L3F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102768	NM_016108.4(AIG1):c.19C>A (p.Gln7Lys)	AIG1 (Q7K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2358327	NM_016108.4(AIG1):c.94C>T (p.His32Tyr)	AIG1 (H22Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279001	NM_016108.4(AIG1):c.277T>G (p.Leu93Val)	AIG1 (L140V +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102774	NM_016108.4(AIG1):c.349T>C (p.Tyr117His)	AIG1 (Y164H +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2518551	NM_016108.4(AIG1):c.353C>T (p.Pro118Leu)	AIG1 (P114L +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2331953	NM_016108.4(AIG1):c.443C>T (p.Ser148Leu)	AIG1 (S138L +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2371155	NM_016108.4(AIG1):c.446A>G (p.His149Arg)	AIG1 (H115R +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3278990	NM_016108.4(AIG1):c.460A>G (p.Ser154Gly)	AIG1 (S150G +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2245987	NM_016108.4(AIG1):c.510A>G (p.Ile170Met)	AIG1 (I136M +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2316339	NM_016108.4(AIG1):c.535G>A (p.Val179Ile)	AIG1, LOC126859817 (C164Y +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530464	NM_016108.4(AIG1):c.572T>C (p.Ile191Thr)	AIG1, LOC126859817 (I215T +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3278995	NM_016108.4(AIG1):c.610A>G (p.Thr204Ala)	AIG1, LOC126859817 (N165S +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance