Related gene-specific medical variations for Gene (Select 143941) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3184335	NM_001080441.4(TTC36):c.424G>A (p.Ala142Thr)	TTC36, TTC36-AS1 (A142T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184334	NM_001080441.4(TTC36):c.352C>T (p.Arg118Trp)	LOC130006846, TTC36 +1 more (R59W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184332	NM_001080441.4(TTC36):c.311C>T (p.Ala104Val)	LOC130006846, TTC36 +1 more (A104V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184331	NM_001080441.4(TTC36):c.172G>C (p.Gly58Arg)	TTC36, TTC36-AS1 (G58R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3184330	NM_001080441.4(TTC36):c.119A>T (p.Asp40Val)	TTC36, TTC36-AS1 (D40V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2528202	NM_001080441.4(TTC36):c.284G>A (p.Arg95Gln)	TTC36, TTC36-AS1 (R95Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528135	NM_001080441.4(TTC36):c.353G>T (p.Arg118Leu)	LOC130006846, TTC36 +1 more (R118L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2397921	NM_001080441.4(TTC36):c.518G>T (p.Arg173Leu)	TTC36, TTC36-AS1 (R81L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396708	NM_001080441.4(TTC36):c.556C>T (p.Arg186Cys)	LOC130006847, TTC36 +1 more (R94C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393387	NM_001080441.4(TTC36):c.88G>A (p.Glu30Lys)	TTC36, TTC36-AS1 (E30K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354143	NM_001080441.4(TTC36):c.101A>C (p.Lys34Thr)	TTC36, TTC36-AS1 (K34T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325818	NM_001080441.4(TTC36):c.473G>A (p.Arg158Gln)	TTC36, TTC36-AS1 (R158Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277059	NM_001080441.4(TTC36):c.19C>G (p.Gln7Glu)	TTC36, TTC36-AS1 (Q7E)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2273263	NM_001080441.4(TTC36):c.16G>A (p.Asp6Asn)	TTC36, TTC36-AS1 (D6N)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2270539	NM_001080441.4(TTC36):c.214G>A (p.Glu72Lys)	TTC36, TTC36-AS1 (E13K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226045	NM_001080441.4(TTC36):c.152C>T (p.Ser51Phe)	TTC36, TTC36-AS1 (S51F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221571	NM_001080441.4(TTC36):c.85G>A (p.Gly29Arg)	TTC36, TTC36-AS1 (G29R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance