Related gene-specific medical variations for Gene (Select 10127) - ClinVar

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Links from Gene

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3177492	NM_033208.4(TIGD7):c.917C>T (p.Ser306Phe)	TIGD7, ZNF263 (S306F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177491	NM_033208.4(TIGD7):c.727A>C (p.Ser243Arg)	TIGD7, ZNF263 (S243R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177490	NM_033208.4(TIGD7):c.625A>T (p.Arg209Trp)	TIGD7, ZNF263 (R209W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177489	NM_033208.4(TIGD7):c.589G>A (p.Asp197Asn)	TIGD7, ZNF263 (D197N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177487	NM_033208.4(TIGD7):c.340T>A (p.Phe114Ile)	TIGD7, ZNF263 (F114I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177486	NM_033208.4(TIGD7):c.296G>A (p.Arg99Lys)	TIGD7, ZNF263 (R99K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177485	NM_033208.4(TIGD7):c.1314G>T (p.Arg438Ser)	TIGD7, ZNF263 (R438S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177484	NM_033208.4(TIGD7):c.1262G>C (p.Arg421Thr)	TIGD7, ZNF263 (R421T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622822	NM_033208.4(TIGD7):c.1371A>G (p.Ile457Met)	TIGD7, ZNF263 (I457M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598817	NM_033208.4(TIGD7):c.1494G>C (p.Gln498His)	TIGD7, ZNF263 (Q498H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2557403	NM_033208.4(TIGD7):c.824G>A (p.Arg275Gln)	TIGD7, ZNF263 (R275Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518888	NM_033208.4(TIGD7):c.122C>T (p.Thr41Ile)	TIGD7, ZNF263 (T41I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518744	NM_033208.4(TIGD7):c.627G>T (p.Arg209Ser)	TIGD7, ZNF263 (R209S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507931	NM_033208.4(TIGD7):c.334C>T (p.Arg112Trp)	TIGD7, ZNF263 (R112W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484354	NM_033208.4(TIGD7):c.751C>T (p.Pro251Ser)	TIGD7, ZNF263 (P251S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473381	NM_033208.4(TIGD7):c.1640C>A (p.Ser547Tyr)	TIGD7, ZNF263 (S547Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462682	NM_033208.4(TIGD7):c.157C>A (p.Leu53Met)	TIGD7, ZNF263 (L53M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402514	NM_033208.4(TIGD7):c.40G>A (p.Glu14Lys)	TIGD7, ZNF263 (E14K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393130	NM_033208.4(TIGD7):c.1619G>A (p.Ser540Asn)	TIGD7, ZNF263 (S540N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2388860	NM_033208.4(TIGD7):c.896C>T (p.Pro299Leu)	TIGD7, ZNF263 (P299L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386863	NM_033208.4(TIGD7):c.911C>G (p.Ser304Cys)	TIGD7, ZNF263 (S304C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366616	NM_033208.4(TIGD7):c.861G>C (p.Glu287Asp)	TIGD7, ZNF263 (E287D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363405	NM_033208.4(TIGD7):c.1151C>T (p.Ala384Val)	TIGD7, ZNF263 (A384V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358002	NM_033208.4(TIGD7):c.1576A>G (p.Ser526Gly)	TIGD7, ZNF263 (S526G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357737	NM_033208.4(TIGD7):c.1255G>C (p.Asp419His)	TIGD7, ZNF263 (D419H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342631	NM_033208.4(TIGD7):c.238G>C (p.Val80Leu)	TIGD7, ZNF263 (V80L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285610	NM_033208.4(TIGD7):c.199G>A (p.Glu67Lys)	TIGD7, ZNF263 (E67K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284083	NM_033208.4(TIGD7):c.1369A>G (p.Ile457Val)	TIGD7, ZNF263 (I457V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268355	NM_033208.4(TIGD7):c.794G>C (p.Trp265Ser)	TIGD7, ZNF263 (W265S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248520	NM_033208.4(TIGD7):c.1070G>A (p.Ser357Asn)	TIGD7, ZNF263 (S357N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235202	NM_033208.4(TIGD7):c.1450T>G (p.Leu484Val)	TIGD7, ZNF263 (L484V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233171	NM_033208.4(TIGD7):c.269A>G (p.Gln90Arg)	TIGD7, ZNF263 (Q90R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219790	NM_033208.4(TIGD7):c.574C>G (p.Gln192Glu)	TIGD7, ZNF263 (Q192E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213377	NM_033208.4(TIGD7):c.584G>A (p.Arg195Lys)	TIGD7, ZNF263 (R195K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768743	NM_033208.4(TIGD7):c.537A>G (p.Glu179=)	TIGD7, ZNF263	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 711959	NM_033208.4(TIGD7):c.435C>G (p.Val145=)	TIGD7, ZNF263	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 711958	NM_033208.4(TIGD7):c.1630A>G (p.Thr544Ala)	TIGD7, ZNF263 (T544A)	Single nucleotide variant (missense variant)	not provided	GBenign

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Links from Gene

Items: 37