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32 records found for search term Tigit
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8577826CV112203single nucleotide variantNM_173799.3(TIGIT):c.-871G>ALung cancer [RCV000092726]uncertain significance3114293191114293191Humanname
156032050CV2218191single nucleotide variantNM_173799.4(TIGIT):c.4C>T (p.Arg2Cys)not specified [RCV004088397]uncertain significance3114294065114294065Humanname
407520397CV3475671single nucleotide variantNM_173799.4(TIGIT):c.5G>A (p.Arg2His)not specified [RCV004676943]uncertain significance3114294066114294066Humanname
156369327CV2193949single nucleotide variantNM_173799.4(TIGIT):c.41G>A (p.Arg14Lys)not specified [RCV004074678]uncertain significance3114294102114294102Humanname
156041097CV2342102single nucleotide variantNM_173799.4(TIGIT):c.89C>T (p.Thr30Met)not specified [RCV004191697]likely benign3114295572114295572Humanname
156063500CV2349626single nucleotide variantNM_173799.4(TIGIT):c.99T>G (p.Ile33Met)not specified [RCV004204047]uncertain significance3114295582114295582Humanname
401760519CV2695069single nucleotide variantNM_173799.4(TIGIT):c.55G>A (p.Ala19Thr)not specified [RCV004303227]likely benign3114294116114294116Humanname
597764613CV3613434single nucleotide variantNM_173799.4(TIGIT):c.80T>C (p.Ile27Thr)not specified [RCV004870116]uncertain significance3114295563114295563Humanname
598197622CV3924223single nucleotide variantNM_173799.4(TIGIT):c.660C>T (p.Ala220=)not specified [RCV005289604]likely benign3114308056114308056Humanname
156057014CV2343517single nucleotide variantNM_173799.4(TIGIT):c.106G>A (p.Glu36Lys)not specified [RCV004190556]likely benign3114295589114295589Humanname
329382767CV2424548single nucleotide variantNM_173799.4(TIGIT):c.245A>T (p.Lys82Met)not specified [RCV004254049]uncertain significance3114295728114295728Humanname
597764753CV3613431single nucleotide variantNM_173799.4(TIGIT):c.152C>T (p.Thr51Met)not specified [RCV004870113]likely benign3114295635114295635Humanname
597764745CV3613433single nucleotide variantNM_173799.4(TIGIT):c.268G>A (p.Gly90Ser)not specified [RCV004870115]uncertain significance3114295751114295751Humanname
597764429CV3613436single nucleotide variantNM_173799.4(TIGIT):c.260C>T (p.Pro87Leu)not specified [RCV004870118]uncertain significance3114295743114295743Humanname
8577827CV112204single nucleotide variantNM_173799.3(TIGIT):c.298G>A (p.Val100Met)Lung cancer [RCV000092727]uncertain significance3114295781114295781Humanname
156130335CV2238608single nucleotide variantNM_173799.4(TIGIT):c.392T>A (p.Val131Glu)not specified [RCV004107216]uncertain significance3114299597114299597Humanname
155988142CV2285315single nucleotide variantNM_173799.4(TIGIT):c.304G>A (p.Asp102Asn)not specified [RCV004139194]uncertain significance3114295787114295787Humanname
156388264CV2380252single nucleotide variantNM_173799.4(TIGIT):c.403G>A (p.Gly135Ser)not specified [RCV004224610]likely benign3114299608114299608Humanname
156226755CV2401239single nucleotide variantNM_173799.4(TIGIT):c.434C>T (p.Ala145Val)not specified [RCV004245790]uncertain significance3114299639114299639Humanname
329391499CV2448630single nucleotide variantNM_173799.4(TIGIT):c.350C>T (p.Thr117Met)not specified [RCV004259300]uncertain significance3114295833114295833Humanname
401735387CV2687570single nucleotide variantNM_173799.4(TIGIT):c.333C>G (p.His111Gln)not specified [RCV004300795]uncertain significance3114295816114295816Humanname
405752636CV3335919single nucleotide variantNM_173799.4(TIGIT):c.442G>A (p.Ala148Thr)not specified [RCV004467337]likely benign3114299647114299647Humanname
405752643CV3335920single nucleotide variantNM_173799.4(TIGIT):c.530G>A (p.Gly177Asp)not specified [RCV004467338]uncertain significance3114307926114307926Humanname
405752648CV3335921single nucleotide variantNM_173799.4(TIGIT):c.569G>A (p.Ser190Asn)not specified [RCV004467339]uncertain significance3114307965114307965Humanname
405752653CV3335922single nucleotide variantNM_173799.4(TIGIT):c.611A>T (p.Glu204Val)not specified [RCV004467340]uncertain significance3114308007114308007Humanname
405752663CV3335923single nucleotide variantNM_173799.4(TIGIT):c.680A>G (p.Asn227Ser)not specified [RCV004467341]uncertain significance3114308076114308076Humanname
405752669CV3335924single nucleotide variantNM_173799.4(TIGIT):c.731G>A (p.Gly244Asp)not specified [RCV004467342]uncertain significance3114308127114308127Humanname
407520400CV3475672single nucleotide variantNM_173799.4(TIGIT):c.446C>A (p.Thr149Lys)not specified [RCV004676944]uncertain significance3114299651114299651Humanname
597764757CV3613430single nucleotide variantNM_173799.4(TIGIT):c.644G>A (p.Arg215Gln)not specified [RCV004870112]likely benign3114308040114308040Humanname
597764749CV3613432single nucleotide variantNM_173799.4(TIGIT):c.386G>T (p.Ser129Ile)not specified [RCV004870114]uncertain significance3114295869114295869Humanname
597764513CV3613435single nucleotide variantNM_173799.4(TIGIT):c.538A>G (p.Arg180Gly)not specified [RCV004870117]likely benign3114307934114307934Humanname
598176582CV3924221single nucleotide variantNM_173799.4(TIGIT):c.454G>A (p.Val152Ile)not specified [RCV005285662]uncertain significance3114299659114299659Humanname