"Ambry Genetics"[submitter] AND "TFDP2"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2602930	NM_001178139.2(TFDP2):c.1292A>G (p.Asn431Ser)	TFDP2 (N295S +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176499	NM_001178139.2(TFDP2):c.1277C>A (p.Thr426Asn)	TFDP2 (T365N +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283966	NM_001178139.2(TFDP2):c.1179G>T (p.Leu393Phe)	TFDP2 (L333F +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218606	NM_001178139.2(TFDP2):c.1159G>A (p.Val387Ile)	TFDP2 (V359I +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176498	NM_001178139.2(TFDP2):c.1132A>G (p.Thr378Ala)	TFDP2 (T318A +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325624	NM_001178139.2(TFDP2):c.1040G>T (p.Gly347Val)	TFDP2 (G211V +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558163	NM_001178139.2(TFDP2):c.950G>A (p.Arg317Gln)	TFDP2 (R257Q +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508321	NM_001178139.2(TFDP2):c.949C>T (p.Arg317Trp)	TFDP2 (R204W +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541235	NM_001178139.2(TFDP2):c.797C>A (p.Pro266Gln)	TFDP2 (P244Q +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176504	NM_001178139.2(TFDP2):c.739G>A (p.Ala247Thr)	TFDP2 (A230T +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176503	NM_001178139.2(TFDP2):c.677G>A (p.Arg226Lys)	TFDP2 (R209K +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325625	NM_001178139.2(TFDP2):c.646G>C (p.Glu216Gln)	TFDP2 (E103Q +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176502	NM_001178139.2(TFDP2):c.496A>G (p.Asn166Asp)	TFDP2 (N138D +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213006	NM_001178139.2(TFDP2):c.376G>A (p.Asp126Asn)	TFDP2 (D104N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176501	NM_001178139.2(TFDP2):c.362G>A (p.Arg121Gln)	TFDP2 (R104Q +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176500	NM_001178139.2(TFDP2):c.173T>C (p.Val58Ala)	TFDP2 (V41A +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2518951	NM_001178139.2(TFDP2):c.136A>G (p.Ile46Val)	TFDP2 (I46V +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2613712	NM_001178139.2(TFDP2):c.119C>T (p.Thr40Ile)	TFDP2 (T23I +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2529407	NM_001178139.2(TFDP2):c.86A>G (p.Asn29Ser)	TFDP2 (N12S +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance