"Ambry Genetics"[submitter] AND "TEX38"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3176408	NM_001145474.4(TEX38):c.18G>C (p.Glu6Asp)	TEX38 (E6D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3325577	NM_001145474.4(TEX38):c.31C>T (p.Pro11Ser)	TEX38 (P11S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355752	NM_001145474.4(TEX38):c.39G>C (p.Met13Ile)	TEX38 (M13I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321347	NM_001145474.4(TEX38):c.110A>G (p.His37Arg)	TEX38 (H37R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329204	NM_001145474.4(TEX38):c.112T>C (p.Trp38Arg)	TEX38 (W38R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390922	NM_001145474.4(TEX38):c.154G>A (p.Val52Met)	TEX38 (V52M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2411218	NM_001145474.4(TEX38):c.167G>C (p.Arg56Thr)	TEX38 (R56T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176407	NM_001145474.4(TEX38):c.187A>T (p.Ser63Cys)	TEX38 (S9C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350370	NM_001145474.4(TEX38):c.217C>T (p.Arg73Trp)	TEX38 (R19W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460615	NM_001145474.4(TEX38):c.221G>A (p.Arg74His)	TEX38 (R20H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2358828	NM_001145474.4(TEX38):c.275C>T (p.Thr92Ile)	TEX38 (T38I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371318	NM_001145474.4(TEX38):c.286G>T (p.Val96Phe)	TEX38 (V20F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406356	NM_001145474.4(TEX38):c.325G>A (p.Glu109Lys)	TEX38 (E33K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273693	NM_001145474.4(TEX38):c.359C>T (p.Pro120Leu)	TEX38 (P66L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510179	NM_001145474.4(TEX38):c.457G>A (p.Val153Met)	TEX38 (V153M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395349	NM_001145474.4(TEX38):c.544G>A (p.Val182Ile)	TEX38 (V182I +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2322192	NM_001145474.4(TEX38):c.590T>G (p.Phe197Cys)	TEX38 (F143C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance