"GeneDx"[submitter] AND "KLF9-DT"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2501854	NM_001366145.2(TRPM3):c.5123C>T (p.Thr1708Ile)	KLF9-DT, TRPM3 (T1533I +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3371817	NM_001366145.2(TRPM3):c.5044_5045delinsGA (p.Arg1682Glu)	KLF9-DT, TRPM3 (R1507E +9 more)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 1232067	NM_001366145.2(TRPM3):c.5045G>A (p.Arg1682Gln)	TRPM3, KLF9-DT (R1507Q +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3373241	NM_001366145.2(TRPM3):c.4933G>A (p.Glu1645Lys)	KLF9-DT, TRPM3 (E1470K +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3343527	NM_001366145.2(TRPM3):c.4780T>G (p.Cys1594Gly)	KLF9-DT, TRPM3 (C1419G +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3369979	NM_001366145.2(TRPM3):c.4718C>T (p.Ala1573Val)	TRPM3, KLF9-DT (A1398V +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1311789	NM_001366145.2(TRPM3):c.4637A>G (p.Asn1546Ser)	KLF9-DT, TRPM3 (N1371S +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3369049	NM_001366145.2(TRPM3):c.4540A>C (p.Ser1514Arg)	KLF9-DT, TRPM3 (S1339R +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1304822	NM_001366145.2(TRPM3):c.4314G>A (p.Leu1438=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1700844	NM_001366145.2(TRPM3):c.4261G>C (p.Glu1421Gln)	TRPM3, KLF9-DT (E1246Q +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1695667	NM_001366145.2(TRPM3):c.4229C>G (p.Ser1410Trp)	KLF9-DT, TRPM3 (S1235W +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2428865	NM_001366145.2(TRPM3):c.4220G>A (p.Arg1407Lys)	KLF9-DT, TRPM3 (R1232K +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1700411	NM_001366145.2(TRPM3):c.4187C>A (p.Ala1396Asp)	KLF9-DT, TRPM3 (A1221D +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2576899	NM_001366145.2(TRPM3):c.4100G>C (p.Ser1367Thr)	KLF9-DT, TRPM3 (S1192T +9 more)	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 1282840	NM_001366145.2(TRPM3):c.4059G>A (p.Ser1353=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3364206	NM_001366145.2(TRPM3):c.3873C>A (p.Asn1291Lys)	KLF9-DT, TRPM3 (N1116K +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365724	NM_001366145.2(TRPM3):c.3720G>A (p.Met1240Ile)	KLF9-DT, TRPM3 (M1065I +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343088	NM_001366145.2(TRPM3):c.3701C>T (p.Ser1234Leu)	KLF9-DT, TRPM3 (S1059L +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363628	NM_001366145.2(TRPM3):c.3680A>T (p.Asp1227Val)	KLF9-DT, TRPM3 (D1052V +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1329514	NM_001366145.2(TRPM3):c.3610C>T (p.His1204Tyr)	KLF9-DT, TRPM3 (H1029Y +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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Items: 20