TCEA2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2624374	NM_003195.6(TCEA2):c.94C>T (p.Arg32Trp)	TCEA2 (R5W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395718	NM_003195.6(TCEA2):c.107C>G (p.Ala36Gly)	TCEA2 (A36G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175041	NM_003195.6(TCEA2):c.269G>A (p.Arg90Gln)	TCEA2 (R90Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3324911	NM_003195.6(TCEA2):c.293C>T (p.Thr98Met)	TCEA2 (T71M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496240	NM_003195.6(TCEA2):c.307G>A (p.Ala103Thr)	TCEA2 (A76T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306934	NM_003195.6(TCEA2):c.332G>T (p.Arg111Leu)	TCEA2 (R111L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175043	NM_003195.6(TCEA2):c.336G>T (p.Lys112Asn)	TCEA2 (K112N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569924	NM_003195.6(TCEA2):c.389C>T (p.Pro130Leu)	TCEA2 (P103L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524073	NM_003195.6(TCEA2):c.442G>A (p.Ala148Thr)	TCEA2 (A121T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513834	NM_003195.6(TCEA2):c.467A>G (p.His156Arg)	TCEA2 (H129R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362322	NM_003195.6(TCEA2):c.469G>A (p.Val157Met)	TCEA2 (V157M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175044	NM_003195.6(TCEA2):c.510C>G (p.Ile170Met)	TCEA2 (I143M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364938	NM_003195.6(TCEA2):c.751A>G (p.Thr251Ala)	TCEA2 (T251A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324912	NM_003195.6(TCEA2):c.752C>A (p.Thr251Asn)	TCEA2 (T224N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528516	NM_003195.6(TCEA2):c.857T>A (p.Phe286Tyr)	TCEA2 (F286Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance