Related gene-specific medical variations for Gene (Select 49861) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3145490	NM_001001346.3(CLDN20):c.431T>C (p.Ile144Thr)	CLDN20, TFB1M (I144T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145489	NM_001001346.3(CLDN20):c.164C>T (p.Thr55Met)	CLDN20, TFB1M (T55M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623520	NM_001001346.3(CLDN20):c.632C>A (p.Ser211Tyr)	CLDN20, TFB1M (S211Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517453	NM_001001346.3(CLDN20):c.644T>C (p.Leu215Pro)	CLDN20, TFB1M (L215P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494344	NM_001001346.3(CLDN20):c.455T>C (p.Val152Ala)	CLDN20, TFB1M (V152A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455703	NM_001001346.3(CLDN20):c.239C>T (p.Ala80Val)	CLDN20, TFB1M (A80V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387440	NM_001001346.3(CLDN20):c.404C>T (p.Ser135Leu)	CLDN20, TFB1M (S135L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357769	NM_001001346.3(CLDN20):c.115A>G (p.Asn39Asp)	CLDN20, TFB1M (N39D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355178	NM_001001346.3(CLDN20):c.137A>G (p.Gln46Arg)	CLDN20, TFB1M (Q46R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284870	NM_001001346.3(CLDN20):c.145G>A (p.Gly49Arg)	CLDN20, TFB1M (G49R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance