Transcript #00012807

Transcript name NLR family, CARD domain containing 3
Gene name NLRC3 (NLR family, CARD domain containing 3)
Chromosome 16
Transcript - NCBI ID NM_178844.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_849172.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

248 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-6G>A r.(=) p.(=)
?/? c.20G>T r.(?) p.(Arg7Leu)
?/? c.37G>A r.(?) p.(Gly13Ser)
?/? c.51T>C r.(=) p.(=)
?/? c.55G>A r.(?) p.(Gly19Ser)
?/? c.67G>A r.(?) p.(Glu23Lys)
?/? c.129G>A r.(=) p.(=)
?/? c.138G>C r.(=) p.(=)
?/? c.158C>T r.(?) p.(Pro53Leu)
?/? c.178+26C>T r.(=) p.(=)
?/? c.178+50T>C r.(=) p.(=)
?/? c.179-40C>A r.(=) p.(=)
?/? c.179-5C>T r.spl? p.?
?/? c.199C>T r.(?) p.(Arg67Cys)
?/? c.206C>T r.(?) p.(Ala69Val)
?/? c.244G>A r.(?) p.(Gly82Arg)
?/? c.325G>C r.(?) p.(Val109Leu)
?/? c.335C>T r.(?) p.(Thr112Ile)
?/? c.337C>T r.(?) p.(Arg113Cys)
?/? c.339C>T r.(=) p.(=)
?/? c.354C>T r.(=) p.(=)
?/? c.355G>A r.(?) p.(Ala119Thr)
?/? c.364G>A r.(?) p.(Val122Ile)
?/? c.367G>A r.(?) p.(Ala123Thr)
?/? c.398G>A r.(?) p.(Arg133Gln)
?/? c.409C>T r.(?) p.(Pro137Ser)
?/? c.417G>A r.(=) p.(=)
?/? c.431T>C r.(?) p.(Ile144Thr)
?/? c.439G>T r.(?) p.(Ala147Ser)
?/? c.458C>T r.(?) p.(Thr153Ile)
?/? c.459C>G r.(=) p.(=)
?/? c.478_479insC r.(?) p.(Arg160Profs*64)
?/? c.493G>A r.(?) p.(Gly165Arg)
?/? c.505A>C r.(?) p.(Lys169Gln)
?/? c.531G>C r.(=) p.(=)
?/? c.570C>T r.(=) p.(=)
?/? c.574C>A r.(=) p.(=)
?/? c.575G>A r.(?) p.(Arg192Gln)
?/? c.596C>T r.(?) p.(Pro199Leu)
?/? c.613A>G r.(?) p.(Ser205Gly)
?/? c.628G>A r.(?) p.(Val210Ile)
?/? c.657C>T r.(=) p.(=)
?/? c.678G>A r.(=) p.(=)
?/? c.700G>A r.(?) p.(Val234Met)
?/? c.711G>A r.(=) p.(=)
?/? c.717A>G r.(=) p.(=)
?/? c.753C>T r.(=) p.(=)
?/? c.795C>A r.(=) p.(=)
?/? c.802C>T r.(?) p.(Arg268Cys)
?/? c.830G>C r.(?) p.(Gly277Ala)
?/? c.844C>T r.(?) p.(Arg282Trp)
?/? c.845G>A r.(?) p.(Arg282Gln)
?/? c.848T>C r.(?) p.(Met283Thr)
?/? c.858C>G r.(?) p.(Ile286Met)
?/? c.860G>A r.(?) p.(Arg287Gln)
?/? c.877G>T r.(?) p.(Glu293*)
?/? c.879G>T r.(?) p.(Glu293Asp)
?/? c.906C>A r.(?) p.(Phe302Leu)
?/? c.909C>T r.(=) p.(=)
?/? c.977G>A r.(?) p.(Cys326Tyr)
?/? c.981C>T r.(=) p.(=)
?/? c.982G>A r.(?) p.(Val328Ile)
?/? c.995G>C r.(?) p.(Cys332Ser)
?/? c.1010T>C r.(?) p.(Met337Thr)
?/? c.1014G>T r.(=) p.(=)
?/? c.1027T>G r.(?) p.(Trp343Gly)
?/? c.1034G>C r.(?) p.(Ser345Thr)
?/? c.1041G>A r.(=) p.(=)
?/? c.1045C>T r.(?) p.(Pro349Ser)
?/? c.1062G>T r.(=) p.(=)
?/? c.1071G>A r.(=) p.(=)
?/? c.1090T>C r.(?) p.(Tyr364His)
?/? c.1101C>T r.(=) p.(=)
?/? c.1114del r.(?) p.(Leu372Serfs*49)
?/? c.1149C>T r.(=) p.(=)
?/? c.1154G>A r.(?) p.(Arg385His)
?/? c.1181G>A r.(?) p.(Arg394His)
?/? c.1198T>C r.(=) p.(=)
?/? c.1204C>T r.(?) p.(Arg402Cys)
?/? c.1218T>C r.(=) p.(=)
?/? c.1219G>A r.(?) p.(Gly407Arg)
?/? c.1223T>G r.(?) p.(Leu408Arg)
?/? c.1248C>T r.(=) p.(=)
?/? c.1268T>C r.(?) p.(Phe423Ser)
?/? c.1271G>A r.(?) p.(Gly424Asp)
?/? c.1281C>T r.(=) p.(=)
?/? c.1301C>T r.(?) p.(Pro434Leu)
?/? c.1321A>G r.(?) p.(Arg441Gly)
?/? c.1382T>C r.(?) p.(Phe461Ser)
?/? c.1385T>C r.(?) p.(Val462Ala)
?/? c.1420G>A r.(?) p.(Ala474Thr)
?/? c.1421C>A r.(?) p.(Ala474Asp)
?/? c.1445G>A r.(?) p.(Ser482Asn)
?/? c.1478C>T r.(?) p.(Thr493Met)
?/? c.1487G>A r.(?) p.(Arg496Lys)
?/? c.1492G>A r.(?) p.(Ala498Thr)
?/? c.1502G>A r.(?) p.(Arg501Gln)
?/? c.1521C>T r.(=) p.(=)
?/? c.1554C>A r.(=) p.(=)
?/? c.1559T>G r.(?) p.(Leu520Arg)
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