"Ambry Genetics"[submitter] AND "BOD1"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2613210	NM_138369.3(BOD1):c.541T>A (p.Ser181Thr)	BOD1 (S181T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3261313	NM_138369.3(BOD1):c.508C>T (p.Pro170Ser)	BOD1 (P170S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3261314	NM_138369.3(BOD1):c.506C>T (p.Pro169Leu)	BOD1 (P169L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2533848	NM_138369.3(BOD1):c.356T>C (p.Val119Ala)	BOD1 (V119A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261310	NM_138369.3(BOD1):c.314C>T (p.Thr105Met)	BOD1 (T105M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2228055	NM_138369.3(BOD1):c.124G>A (p.Ala42Thr)	BOD1 (A42T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321146	NM_138369.3(BOD1):c.94G>A (p.Ala32Thr)	BOD1 (A32T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622902	NM_138369.3(BOD1):c.70G>A (p.Gly24Arg)	BOD1 (G24R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272561	NM_138369.3(BOD1):c.61G>C (p.Ala21Pro)	BOD1 (A21P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261312	NM_138369.3(BOD1):c.11G>T (p.Gly4Val)	BOD1 (G4V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261311	NM_138369.3(BOD1):c.10G>C (p.Gly4Arg)	BOD1 (G4R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance