"TDRD9-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045991	NM_153046.3(TDRD9):c.144C>T (p.Pro48=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition	GLikely benign
Select item 718196	NM_153046.3(TDRD9):c.332C>T (p.Pro111Leu)	TDRD9 (P111L)	Single nucleotide variant (missense variant)	TDRD9-related condition +1 more	GBenign
Select item 3035459	NM_153046.3(TDRD9):c.421-3T>C	TDRD9	Single nucleotide variant (intron variant)	TDRD9-related condition	GLikely benign
Select item 3049271	NM_153046.3(TDRD9):c.531C>T (p.Ser177=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition	GLikely benign
Select item 3041885	NM_153046.3(TDRD9):c.624A>T (p.Gly208=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition	GLikely benign
Select item 3038035	NM_153046.3(TDRD9):c.642+8T>G	TDRD9	Single nucleotide variant (intron variant)	TDRD9-related condition	GLikely benign
Select item 3040471	NM_153046.3(TDRD9):c.907G>C (p.Val303Leu)	TDRD9 (V303L)	Single nucleotide variant (missense variant)	TDRD9-related condition	GBenign
Select item 3049822	NM_153046.3(TDRD9):c.1103T>C (p.Met368Thr)	TDRD9 (M368T)	Single nucleotide variant (missense variant)	TDRD9-related condition	GLikely benign
Select item 3034799	NM_153046.3(TDRD9):c.2223+3G>A	TDRD9	Single nucleotide variant (intron variant)	TDRD9-related condition	GLikely benign
Select item 3052446	NM_153046.3(TDRD9):c.2607-5T>C	TDRD9	Single nucleotide variant (intron variant)	TDRD9-related condition	GBenign
Select item 3058205	NM_153046.3(TDRD9):c.2719-5T>G	TDRD9	Single nucleotide variant (intron variant)	TDRD9-related condition	GLikely benign
Select item 787417	NM_153046.3(TDRD9):c.2808G>C (p.Leu936=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition +1 more	GBenign
Select item 3039126	NM_153046.3(TDRD9):c.3118C>T (p.Leu1040=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition	GLikely benign
Select item 3044698	NM_153046.3(TDRD9):c.3261G>A (p.Thr1087=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition	GLikely benign
Select item 3038382	NM_153046.3(TDRD9):c.3514G>A (p.Val1172Ile)	TDRD9 (V1172I)	Single nucleotide variant (missense variant)	TDRD9-related condition	GLikely benign
Select item 3055404	NM_153046.3(TDRD9):c.3626C>T (p.Thr1209Met)	TDRD9 (T1209M)	Single nucleotide variant (missense variant)	TDRD9-related condition	GLikely benign
Select item 3059627	NM_153046.3(TDRD9):c.3833T>G (p.Phe1278Cys)	TDRD9 (F1278C)	Single nucleotide variant (missense variant)	TDRD9-related condition	GBenign
Select item 3056462	NM_153046.3(TDRD9):c.3957C>T (p.Ala1319=)	TDRD9	Single nucleotide variant (synonymous variant)	TDRD9-related condition	GLikely benign
Select item 3057823	NM_153046.3(TDRD9):c.3975-7A>T	TDRD9	Single nucleotide variant (intron variant)	TDRD9-related condition	GLikely benign
Select item 3055448	NM_153046.3(TDRD9):c.*1G>A	TDRD9	Single nucleotide variant (3 prime UTR variant)	TDRD9-related condition	GBenign

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Items: 20