Related gene-specific medical variations for Gene (Select 94241) - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328223	NM_033285.4(TP53INP1):c.233A>G (p.Asp78Gly)	NDUFAF6, TP53INP1 (D78G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328222	NM_033285.4(TP53INP1):c.641T>G (p.Leu214Arg)	NDUFAF6, TP53INP1 (L214R)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3328221	NM_033285.4(TP53INP1):c.568C>T (p.Arg190Cys)	NDUFAF6, TP53INP1 (R190C)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181443	NM_033285.4(TP53INP1):c.670A>C (p.Lys224Gln)	NDUFAF6, TP53INP1 (K224Q)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181442	NM_033285.4(TP53INP1):c.632G>A (p.Arg211His)	NDUFAF6, TP53INP1 (R211H)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181441	NM_033285.4(TP53INP1):c.629G>C (p.Arg210Pro)	NDUFAF6, TP53INP1 (R210P)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181440	NM_033285.4(TP53INP1):c.608C>T (p.Pro203Leu)	NDUFAF6, TP53INP1 (P203L)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181439	NM_033285.4(TP53INP1):c.569G>A (p.Arg190His)	NDUFAF6, TP53INP1 (R190H)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181438	NM_033285.4(TP53INP1):c.54C>G (p.Asn18Lys)	NDUFAF6, TP53INP1 (N18K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612727	NM_033285.4(TP53INP1):c.71A>G (p.Asn24Ser)	NDUFAF6, TP53INP1 (N24S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2610975	NM_033285.4(TP53INP1):c.304C>T (p.Pro102Ser)	NDUFAF6, TP53INP1 (P102S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535424	NM_033285.4(TP53INP1):c.224G>T (p.Cys75Phe)	NDUFAF6, TP53INP1 (C75F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510010	NM_033285.4(TP53INP1):c.304C>G (p.Pro102Ala)	NDUFAF6, TP53INP1 (P102A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463932	NM_033285.4(TP53INP1):c.631C>T (p.Arg211Cys)	NDUFAF6, TP53INP1 (R211C)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2390195	NM_033285.4(TP53INP1):c.295A>G (p.Thr99Ala)	NDUFAF6, TP53INP1 (T99A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369095	NM_033285.4(TP53INP1):c.209C>T (p.Pro70Leu)	NDUFAF6, TP53INP1 (P70L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317294	NM_033285.4(TP53INP1):c.713A>G (p.Tyr238Cys)	NDUFAF6, TP53INP1 (Y238C)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2311866	NM_033285.4(TP53INP1):c.175C>T (p.Pro59Ser)	NDUFAF6, TP53INP1 (P59S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300294	NM_033285.4(TP53INP1):c.503A>G (p.His168Arg)	NDUFAF6, TP53INP1 (H168R)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2291717	NM_033285.4(TP53INP1):c.395A>G (p.Tyr132Cys)	NDUFAF6, TP53INP1 (Y132C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261579	NM_033285.4(TP53INP1):c.314C>T (p.Thr105Ile)	NDUFAF6, TP53INP1 (T105I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241310	NM_033285.4(TP53INP1):c.624C>G (p.Ser208Arg)	NDUFAF6, TP53INP1 (S208R)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2229822	NM_033285.4(TP53INP1):c.707G>A (p.Arg236His)	NDUFAF6, TP53INP1 (R236H)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 23