SESN3[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2350786	NM_144665.4(SESN3):c.1454G>A (p.Arg485His)	SESN3 (R346H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 711066	NM_144665.4(SESN3):c.1197C>T (p.Thr399=)	SESN3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2237447	NM_144665.4(SESN3):c.971T>C (p.Val324Ala)	SESN3 (V185A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329925	NM_144665.4(SESN3):c.962C>T (p.Thr321Ile)	SESN3 (T182I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2567764	NM_144665.4(SESN3):c.865C>T (p.Arg289Cys)	SESN3 (R289C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160555	NM_144665.4(SESN3):c.815T>C (p.Leu272Pro)	SESN3 (L133P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285904	NM_144665.4(SESN3):c.732G>C (p.Glu244Asp)	SESN3 (E105D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317671	NM_144665.4(SESN3):c.700G>A (p.Val234Ile)	SESN3 (V234I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376658	NM_144665.4(SESN3):c.661T>G (p.Ser221Ala)	SESN3 (S221A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306348	NM_144665.4(SESN3):c.494G>A (p.Arg165Gln)	SESN3 (R165Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213974	NM_144665.4(SESN3):c.437A>G (p.Glu146Gly)	SESN3 (E146G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621141	NM_144665.4(SESN3):c.384T>A (p.His128Gln)	SESN3 (H128Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317672	NM_144665.4(SESN3):c.295A>G (p.Met99Val)	SESN3 (M99V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558393	NM_144665.4(SESN3):c.166G>A (p.Asp56Asn)	SESN3 (D56N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 594353	NM_144665.4(SESN3):c.161C>G (p.Thr54Arg)	SESN3 (T54R)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 787096	NM_144665.4(SESN3):c.145-10T>G	SESN3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2358261	NM_144665.4(SESN3):c.110C>A (p.Thr37Lys)	SESN3 (T37K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2550205	NM_144665.4(SESN3):c.80A>G (p.Asp27Gly)	SESN3 (D27G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance