"Ambry Genetics"[submitter] AND "TTC4"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2285989	NM_004623.5(TTC4):c.19G>A (p.Asp7Asn)	MROH7-TTC4, TTC4 (D7N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296736	NM_004623.5(TTC4):c.88T>A (p.Phe30Ile)	MROH7-TTC4, TTC4 (F30I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619555	NM_004623.5(TTC4):c.103T>C (p.Trp35Arg)	MROH7-TTC4, TTC4 (W35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3329904	NM_004623.5(TTC4):c.154G>A (p.Glu52Lys)	MROH7-TTC4, TTC4 (E52K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184365	NM_004623.5(TTC4):c.233A>G (p.Gln78Arg)	MROH7-TTC4, TTC4 (Q78R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184366	NM_004623.5(TTC4):c.335A>G (p.Asp112Gly)	MROH7-TTC4, TTC4 (D112G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184367	NM_004623.5(TTC4):c.377C>T (p.Ala126Val)	MROH7-TTC4, TTC4 (A126V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2254226	NM_004623.5(TTC4):c.683C>T (p.Ala228Val)	MROH7-TTC4, TTC4 (A228V)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2526267	NM_004623.5(TTC4):c.686G>C (p.Arg229Thr)	MROH7-TTC4, TTC4 (R229T)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2542980	NM_004623.5(TTC4):c.779A>T (p.Asn260Ile)	MROH7-TTC4, TTC4 (N260I)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3184368	NM_004623.5(TTC4):c.786T>A (p.His262Gln)	MROH7-TTC4, TTC4 (H262Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3184369	NM_004623.5(TTC4):c.817A>G (p.Arg273Gly)	MROH7-TTC4, TTC4 (R273G)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2460783	NM_004623.5(TTC4):c.863C>T (p.Ser288Leu)	MROH7-TTC4, TTC4 (S288L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2543303	NM_004623.5(TTC4):c.979G>C (p.Val327Leu)	MROH7-TTC4, TTC4 (V228L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3329903	NM_004623.5(TTC4):c.1006G>C (p.Glu336Gln)	MROH7-TTC4, TTC4 (E237Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184364	NM_004623.5(TTC4):c.1102G>A (p.Val368Ile)	MROH7-TTC4, TTC4 (V368I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance