Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.12192920_12192928dup | CA2643340370 | TNFRSF1B | c.609_617dup (p.Thr206_Arg207insSerProThr) n.321_329dup n.598_606dup c.588_596dup (p.Thr199_Arg200insSerProThr) c.24_32dup (p.Thr11_Arg12insSerProThr) | gnomAD v4 |
1 | g.12192921T>A | CA338455113 | TNFRSF1B | c.610T>A (p.Ser204Thr) n.322T>A n.599T>A c.589T>A (p.Ser197Thr) c.25T>A (p.Ser9Thr) | |
1 | g.12192921T>C | CA338455107 | TNFRSF1B | c.610T>C (p.Ser204Pro) n.322T>C n.599T>C c.589T>C (p.Ser197Pro) c.25T>C (p.Ser9Pro) | dbSNP gnomAD v2 |
1 | g.12192921T>G | CA338455109 | TNFRSF1B | c.610T>G (p.Ser204Ala) n.322T>G n.599T>G c.589T>G (p.Ser197Ala) c.25T>G (p.Ser9Ala) | |
1 | g.12192921T= | CA1154001426 | TNFRSF1B | c.610T= (p.Ser204=) n.322T= n.599T= c.589T= (p.Ser197=) c.25T= (p.Ser9=) | |
1 | g.12192922C>A | CA338455117 | TNFRSF1B | c.611C>A (p.Ser204Tyr) n.323C>A n.600C>A c.590C>A (p.Ser197Tyr) c.26C>A (p.Ser9Tyr) | |
1 | g.12192922C>G | CA338455120 | TNFRSF1B | c.611C>G (p.Ser204Cys) n.323C>G n.600C>G c.590C>G (p.Ser197Cys) c.26C>G (p.Ser9Cys) | |
1 | g.12192922C>T | CA338455123 | TNFRSF1B | c.611C>T (p.Ser204Phe) n.323C>T n.600C>T c.590C>T (p.Ser197Phe) c.26C>T (p.Ser9Phe) | |
1 | g.12192923C>A | CA416364745 | TNFRSF1B | c.612C>A (p.Ser204=) n.324C>A n.601C>A c.591C>A (p.Ser197=) c.27C>A (p.Ser9=) | |
1 | g.12192923C>G | CA416364746 | TNFRSF1B | c.612C>G (p.Ser204=) n.324C>G n.601C>G c.591C>G (p.Ser197=) c.27C>G (p.Ser9=) | |
1 | g.12192923C>T | CA416364747 | TNFRSF1B | c.612C>T (p.Ser204=) n.324C>T n.601C>T c.591C>T (p.Ser197=) c.27C>T (p.Ser9=) | |
1 | g.12192924C>A | CA338455129 | TNFRSF1B | c.613C>A (p.Pro205Thr) n.325C>A n.602C>A c.592C>A (p.Pro198Thr) c.28C>A (p.Pro10Thr) | gnomAD v4 |
1 | g.12192924C= | CA1143489384 | TNFRSF1B | c.613C= (p.Pro205=) n.325C= n.602C= c.592C= (p.Pro198=) c.28C= (p.Pro10=) | |
1 | g.12192924C>G | CA600834 | TNFRSF1B | c.613C>G (p.Pro205Ala) n.325C>G n.602C>G c.592C>G (p.Pro198Ala) c.28C>G (p.Pro10Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192924C>T | CA338455145 | TNFRSF1B | c.613C>T (p.Pro205Ser) n.325C>T n.602C>T c.592C>T (p.Pro198Ser) c.28C>T (p.Pro10Ser) | |
1 | g.12192925C>A | CA338455151 | TNFRSF1B | c.614C>A (p.Pro205His) n.326C>A n.603C>A c.593C>A (p.Pro198His) c.29C>A (p.Pro10His) | |
1 | g.12192925C= | CA1154001427 | TNFRSF1B | c.614C= (p.Pro205=) n.326C= n.603C= c.593C= (p.Pro198=) c.29C= (p.Pro10=) | |
1 | g.12192925C>G | CA600835 | TNFRSF1B | c.614C>G (p.Pro205Arg) n.326C>G n.603C>G c.593C>G (p.Pro198Arg) c.29C>G (p.Pro10Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192925C>T | CA338455158 | TNFRSF1B | c.614C>T (p.Pro205Leu) n.326C>T n.603C>T c.593C>T (p.Pro198Leu) c.29C>T (p.Pro10Leu) | |
1 | g.12192926C>A | CA600836 | TNFRSF1B | c.615C>A (p.Pro205=) n.327C>A n.604C>A c.594C>A (p.Pro198=) c.30C>A (p.Pro10=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192926C= | CA1154001428 | TNFRSF1B | c.615C= (p.Pro205=) n.327C= n.604C= c.594C= (p.Pro198=) c.30C= (p.Pro10=) | |
1 | g.12192926C>G | CA416364748 | TNFRSF1B | c.615C>G (p.Pro205=) n.327C>G n.604C>G c.594C>G (p.Pro198=) c.30C>G (p.Pro10=) | gnomAD v4 |
1 | g.12192926C>T | CA416364749 | TNFRSF1B | c.615C>T (p.Pro205=) n.327C>T n.604C>T c.594C>T (p.Pro198=) c.30C>T (p.Pro10=) | |
1 | g.12192927A>C | CA338455171 | TNFRSF1B | c.616A>C (p.Thr206Pro) n.328A>C n.605A>C c.595A>C (p.Thr199Pro) c.31A>C (p.Thr11Pro) | |
1 | g.12192927A>G | CA338455165 | TNFRSF1B | c.616A>G (p.Thr206Ala) n.328A>G n.605A>G c.595A>G (p.Thr199Ala) c.31A>G (p.Thr11Ala) | |
1 | g.12192927A>T | CA338455167 | TNFRSF1B | c.616A>T (p.Thr206Ser) n.328A>T n.605A>T c.595A>T (p.Thr199Ser) c.31A>T (p.Thr11Ser) | |
1 | g.12192928C>A | CA338455172 | TNFRSF1B | c.617C>A (p.Thr206Asn) n.329C>A n.606C>A c.596C>A (p.Thr199Asn) c.32C>A (p.Thr11Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192928C= | CA1154001429 | TNFRSF1B | c.617C= (p.Thr206=) n.329C= n.606C= c.596C= (p.Thr199=) c.32C= (p.Thr11=) | |
1 | g.12192928C>G | CA338455179 | TNFRSF1B | c.617C>G (p.Thr206Ser) n.329C>G n.606C>G c.596C>G (p.Thr199Ser) c.32C>G (p.Thr11Ser) | |
1 | g.12192928C>T | CA338455183 | TNFRSF1B | c.617C>T (p.Thr206Ile) n.329C>T n.606C>T c.596C>T (p.Thr199Ile) c.32C>T (p.Thr11Ile) | |
1 | g.12192930dup | CA2838979534 | TNFRSF1B | c.619dup (p.Arg207ProfsTer?) n.331dup n.608dup c.598dup (p.Arg200ProfsTer?) c.34dup (p.Arg12ProfsTer?) | |
1 | g.12192929C>A | CA416364750 | TNFRSF1B | c.618C>A (p.Thr206=) n.330C>A n.607C>A c.597C>A (p.Thr199=) c.33C>A (p.Thr11=) | dbSNP |
1 | g.12192929C= | CA1154001430 | TNFRSF1B | c.618C= (p.Thr206=) n.330C= n.607C= c.597C= (p.Thr199=) c.33C= (p.Thr11=) | |
1 | g.12192929C>G | CA416364751 | TNFRSF1B | c.618C>G (p.Thr206=) n.330C>G n.607C>G c.597C>G (p.Thr199=) c.33C>G (p.Thr11=) | |
1 | g.12192929C>T | CA416364752 | TNFRSF1B | c.618C>T (p.Thr206=) n.330C>T n.607C>T c.597C>T (p.Thr199=) c.33C>T (p.Thr11=) | |
1 | g.12192930C>A | CA416364753 | TNFRSF1B | c.619C>A (p.Arg207=) n.331C>A n.608C>A c.598C>A (p.Arg200=) c.34C>A (p.Arg12=) | |
1 | g.12192930C= | CA1141768164 | TNFRSF1B | c.619C= (p.Arg207=) n.331C= n.608C= c.598C= (p.Arg200=) c.34C= (p.Arg12=) | |
1 | g.12192930C>G | CA338455187 | TNFRSF1B | c.619C>G (p.Arg207Gly) n.331C>G n.608C>G c.598C>G (p.Arg200Gly) c.34C>G (p.Arg12Gly) | dbSNP |
1 | g.12192930C>T | CA600837 | TNFRSF1B | c.619C>T (p.Arg207Trp) n.331C>T n.608C>T c.598C>T (p.Arg200Trp) c.34C>T (p.Arg12Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192931G>A | CA600838 | TNFRSF1B | c.620G>A (p.Arg207Gln) n.332G>A n.609G>A c.599G>A (p.Arg200Gln) c.35G>A (p.Arg12Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192931G>C | CA338455212 | TNFRSF1B | c.620G>C (p.Arg207Pro) n.332G>C n.609G>C c.599G>C (p.Arg200Pro) c.35G>C (p.Arg12Pro) | |
1 | g.12192931G= | CA1145935286 | TNFRSF1B | c.620G= (p.Arg207=) n.332G= n.609G= c.599G= (p.Arg200=) c.35G= (p.Arg12=) | |
1 | g.12192931G>T | CA338455217 | TNFRSF1B | c.620G>T (p.Arg207Leu) n.332G>T n.609G>T c.599G>T (p.Arg200Leu) c.35G>T (p.Arg12Leu) | |
1 | g.12192932G>A | CA416364754 | TNFRSF1B | c.621G>A (p.Arg207=) n.333G>A n.610G>A c.600G>A (p.Arg200=) c.36G>A (p.Arg12=) | gnomAD v4 |
1 | g.12192932G>C | CA416364755 | TNFRSF1B | c.621G>C (p.Arg207=) n.333G>C n.610G>C c.600G>C (p.Arg200=) c.36G>C (p.Arg12=) | |
1 | g.12192932G>T | CA416364756 | TNFRSF1B | c.621G>T (p.Arg207=) n.333G>T n.610G>T c.600G>T (p.Arg200=) c.36G>T (p.Arg12=) | |
1 | g.12192933A= | CA1154001431 | TNFRSF1B | c.622A= (p.Ser208=) n.334A= n.611A= c.601A= (p.Ser201=) c.37A= (p.Ser13=) | |
1 | g.12192933A>C | CA600839 | TNFRSF1B | c.622A>C (p.Ser208Arg) n.334A>C n.611A>C c.601A>C (p.Ser201Arg) c.37A>C (p.Ser13Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192933A>G | CA338455220 | TNFRSF1B | c.622A>G (p.Ser208Gly) n.334A>G n.611A>G c.601A>G (p.Ser201Gly) c.37A>G (p.Ser13Gly) | |
1 | g.12192933A>T | CA338455221 | TNFRSF1B | c.622A>T (p.Ser208Cys) n.334A>T n.611A>T c.601A>T (p.Ser201Cys) c.37A>T (p.Ser13Cys) | |
1 | g.12192934G>A | CA338455230 | TNFRSF1B | c.623G>A (p.Ser208Asn) n.335G>A n.612G>A c.602G>A (p.Ser201Asn) c.38G>A (p.Ser13Asn) | |
1 | g.12192934G>C | CA338455225 | TNFRSF1B | c.623G>C (p.Ser208Thr) n.335G>C n.612G>C c.602G>C (p.Ser201Thr) c.38G>C (p.Ser13Thr) | dbSNP |
1 | g.12192934G= | CA1154001432 | TNFRSF1B | c.623G= (p.Ser208=) n.335G= n.612G= c.602G= (p.Ser201=) c.38G= (p.Ser13=) | |
1 | g.12192934G>T | CA338455223 | TNFRSF1B | c.623G>T (p.Ser208Ile) n.335G>T n.612G>T c.602G>T (p.Ser201Ile) c.38G>T (p.Ser13Ile) | |
1 | g.12192935T>A | CA338455233 | TNFRSF1B | c.624T>A (p.Ser208Arg) n.336T>A n.613T>A c.603T>A (p.Ser201Arg) c.39T>A (p.Ser13Arg) | |
1 | g.12192935T>C | CA416364757 | TNFRSF1B | c.624T>C (p.Ser208=) n.336T>C n.613T>C c.603T>C (p.Ser201=) c.39T>C (p.Ser13=) | |
1 | g.12192935T>G | CA338455234 | TNFRSF1B | c.624T>G (p.Ser208Arg) n.336T>G n.613T>G c.603T>G (p.Ser201Arg) c.39T>G (p.Ser13Arg) | |
1 | g.12192936A>C | CA338455236 | TNFRSF1B | c.625A>C (p.Met209Leu) n.337A>C n.614A>C c.604A>C (p.Met202Leu) c.40A>C (p.Met14Leu) | |
1 | g.12192936A>G | CA338455240 | TNFRSF1B | c.625A>G (p.Met209Val) n.337A>G n.614A>G c.604A>G (p.Met202Val) c.40A>G (p.Met14Val) | gnomAD v4 |
1 | g.12192936A>T | CA338455242 | TNFRSF1B | c.625A>T (p.Met209Leu) n.337A>T n.614A>T c.604A>T (p.Met202Leu) c.40A>T (p.Met14Leu) | |
1 | g.12192937T>A | CA338455260 | TNFRSF1B | c.626T>A (p.Met209Lys) n.338T>A n.615T>A c.605T>A (p.Met202Lys) c.41T>A (p.Met14Lys) | |
1 | g.12192937T>C | CA338455253 | TNFRSF1B | c.626T>C (p.Met209Thr) n.338T>C n.615T>C c.605T>C (p.Met202Thr) c.41T>C (p.Met14Thr) | |
1 | g.12192937T>G | CA338455249 | TNFRSF1B | c.626T>G (p.Met209Arg) n.338T>G n.615T>G c.605T>G (p.Met202Arg) c.41T>G (p.Met14Arg) | |
1 | g.12192938G>A | CA338455268 | TNFRSF1B | c.627G>A (p.Met209Ile) n.339G>A n.616G>A c.606G>A (p.Met202Ile) c.42G>A (p.Met14Ile) | |
1 | g.12192938G>C | CA338455275 | TNFRSF1B | c.627G>C (p.Met209Ile) n.339G>C n.616G>C c.606G>C (p.Met202Ile) c.42G>C (p.Met14Ile) | |
1 | g.12192938G>T | CA338455280 | TNFRSF1B | c.627G>T (p.Met209Ile) n.339G>T n.616G>T c.606G>T (p.Met202Ile) c.42G>T (p.Met14Ile) | |
1 | g.12192939G>A | CA338455283 | TNFRSF1B | c.628G>A (p.Ala210Thr) n.340G>A n.617G>A c.607G>A (p.Ala203Thr) c.43G>A (p.Ala15Thr) | gnomAD v4 |
1 | g.12192939G>C | CA338455284 | TNFRSF1B | c.628G>C (p.Ala210Pro) n.340G>C n.617G>C c.607G>C (p.Ala203Pro) c.43G>C (p.Ala15Pro) | |
1 | g.12192939G= | CA1154001433 | TNFRSF1B | c.628G= (p.Ala210=) n.340G= n.617G= c.607G= (p.Ala203=) c.43G= (p.Ala15=) | |
1 | g.12192939G>T | CA338455285 | TNFRSF1B | c.628G>T (p.Ala210Ser) n.340G>T n.617G>T c.607G>T (p.Ala203Ser) c.43G>T (p.Ala15Ser) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192940C>A | CA338455288 | TNFRSF1B | c.629C>A (p.Ala210Asp) n.341C>A n.618C>A c.608C>A (p.Ala203Asp) c.44C>A (p.Ala15Asp) | |
1 | g.12192940C= | CA1154001434 | TNFRSF1B | c.629C= (p.Ala210=) n.341C= n.618C= c.608C= (p.Ala203=) c.44C= (p.Ala15=) | |
1 | g.12192940C>G | CA338455296 | TNFRSF1B | c.629C>G (p.Ala210Gly) n.341C>G n.618C>G c.608C>G (p.Ala203Gly) c.44C>G (p.Ala15Gly) | |
1 | g.12192940C>T | CA338455291 | TNFRSF1B | c.629C>T (p.Ala210Val) n.341C>T n.618C>T c.608C>T (p.Ala203Val) c.44C>T (p.Ala15Val) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12192941C>A | CA416364760 | TNFRSF1B | c.630C>A (p.Ala210=) n.342C>A n.619C>A c.609C>A (p.Ala203=) c.45C>A (p.Ala15=) | |
1 | g.12192941C>G | CA416364759 | TNFRSF1B | c.630C>G (p.Ala210=) n.342C>G n.619C>G c.609C>G (p.Ala203=) c.45C>G (p.Ala15=) | |
1 | g.12192941C>T | CA416364758 | TNFRSF1B | c.630C>T (p.Ala210=) n.342C>T n.619C>T c.609C>T (p.Ala203=) c.45C>T (p.Ala15=) | |
1 | g.12192942C>A | CA338455309 | TNFRSF1B | c.631C>A (p.Pro211Thr) n.343C>A n.620C>A c.610C>A (p.Pro204Thr) c.46C>A (p.Pro16Thr) | |
1 | g.12192942C>G | CA338455313 | TNFRSF1B | c.631C>G (p.Pro211Ala) n.343C>G n.620C>G c.610C>G (p.Pro204Ala) c.46C>G (p.Pro16Ala) | |
1 | g.12192942C>T | CA338455316 | TNFRSF1B | c.631C>T (p.Pro211Ser) n.343C>T n.620C>T c.610C>T (p.Pro204Ser) c.46C>T (p.Pro16Ser) | |
1 | g.12192943C>A | CA338455321 | TNFRSF1B | c.632C>A (p.Pro211Gln) n.344C>A n.621C>A c.611C>A (p.Pro204Gln) c.47C>A (p.Pro16Gln) | |
1 | g.12192943C>G | CA338455327 | TNFRSF1B | c.632C>G (p.Pro211Arg) n.344C>G n.621C>G c.611C>G (p.Pro204Arg) c.47C>G (p.Pro16Arg) | |
1 | g.12192943C>T | CA338455331 | TNFRSF1B | c.632C>T (p.Pro211Leu) n.344C>T n.621C>T c.611C>T (p.Pro204Leu) c.47C>T (p.Pro16Leu) | |
1 | g.12192944A= | CA1154001435 | TNFRSF1B | c.633A= (p.Pro211=) n.345A= n.622A= c.612A= (p.Pro204=) c.48A= (p.Pro16=) | |
1 | g.12192944A>C | CA416364761 | TNFRSF1B | c.633A>C (p.Pro211=) n.345A>C n.622A>C c.612A>C (p.Pro204=) c.48A>C (p.Pro16=) | |
1 | g.12192944A>G | CA600840 | TNFRSF1B | c.633A>G (p.Pro211=) n.345A>G n.622A>G c.612A>G (p.Pro204=) c.48A>G (p.Pro16=) | dbSNP ExAC gnomAD v2 |
1 | g.12192944A>T | CA416364762 | TNFRSF1B | c.633A>T (p.Pro211=) n.345A>T n.622A>T c.612A>T (p.Pro204=) c.48A>T (p.Pro16=) | |
1 | g.12192945G>A | CA338455350 | TNFRSF1B | c.634G>A (p.Gly212Arg) n.346G>A n.623G>A c.613G>A (p.Gly205Arg) c.49G>A (p.Gly17Arg) | |
1 | g.12192945G>C | CA600841 | TNFRSF1B | c.634G>C (p.Gly212Arg) n.346G>C n.623G>C c.613G>C (p.Gly205Arg) c.49G>C (p.Gly17Arg) | dbSNP ExAC gnomAD v2 |
1 | g.12192945G= | CA1154001436 | TNFRSF1B | c.634G= (p.Gly212=) n.346G= n.623G= c.613G= (p.Gly205=) c.49G= (p.Gly17=) | |
1 | g.12192945G>T | CA338455359 | TNFRSF1B | c.634G>T (p.Gly212Trp) n.346G>T n.623G>T c.613G>T (p.Gly205Trp) c.49G>T (p.Gly17Trp) | |
1 | g.12192946G>A | CA338455368 | TNFRSF1B | c.635G>A (p.Gly212Glu) n.347G>A n.624G>A c.614G>A (p.Gly205Glu) c.50G>A (p.Gly17Glu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12192946G>C | CA338455367 | TNFRSF1B | c.635G>C (p.Gly212Ala) n.347G>C n.624G>C c.614G>C (p.Gly205Ala) c.50G>C (p.Gly17Ala) | |
1 | g.12192946G= | CA1154001437 | TNFRSF1B | c.635G= (p.Gly212=) n.347G= n.624G= c.614G= (p.Gly205=) c.50G= (p.Gly17=) | |
1 | g.12192946G>T | CA338455363 | TNFRSF1B | c.635G>T (p.Gly212Val) n.347G>T n.624G>T c.614G>T (p.Gly205Val) c.50G>T (p.Gly17Val) | |
1 | g.12192947G>A | CA416364763 | TNFRSF1B | c.636G>A (p.Gly212=) n.348G>A n.625G>A c.615G>A (p.Gly205=) c.51G>A (p.Gly17=) | |
1 | g.12192947G>C | CA416364764 | TNFRSF1B | c.636G>C (p.Gly212=) n.348G>C n.625G>C c.615G>C (p.Gly205=) c.51G>C (p.Gly17=) | |
1 | g.12192947G>T | CA416364765 | TNFRSF1B | c.636G>T (p.Gly212=) n.348G>T n.625G>T c.615G>T (p.Gly205=) c.51G>T (p.Gly17=) | |
1 | g.12192948G>A | CA338455371 | TNFRSF1B | c.637G>A (p.Ala213Thr) n.349G>A n.626G>A c.616G>A (p.Ala206Thr) c.52G>A (p.Ala18Thr) | |
1 | g.12192948G>C | CA338455376 | TNFRSF1B | c.637G>C (p.Ala213Pro) n.349G>C n.626G>C c.616G>C (p.Ala206Pro) c.52G>C (p.Ala18Pro) | COSMIC |
1 | g.12192948G>T | CA338455382 | TNFRSF1B | c.637G>T (p.Ala213Ser) n.349G>T n.626G>T c.616G>T (p.Ala206Ser) c.52G>T (p.Ala18Ser) | |
1 | g.12192949C>A | CA338455387 | TNFRSF1B | c.638C>A (p.Ala213Glu) n.350C>A n.627C>A c.617C>A (p.Ala206Glu) c.53C>A (p.Ala18Glu) | |
1 | g.12192949C>G | CA338455388 | TNFRSF1B | c.638C>G (p.Ala213Gly) n.350C>G n.627C>G c.617C>G (p.Ala206Gly) c.53C>G (p.Ala18Gly) | |
1 | g.12192949C>T | CA338455389 | TNFRSF1B | c.638C>T (p.Ala213Val) n.350C>T n.627C>T c.617C>T (p.Ala206Val) c.53C>T (p.Ala18Val) | gnomAD v4 |
1 | g.12192950A>C | CA416364766 | TNFRSF1B | c.639A>C (p.Ala213=) n.351A>C n.628A>C c.618A>C (p.Ala206=) c.54A>C (p.Ala18=) | |
1 | g.12192950A>G | CA416364767 | TNFRSF1B | c.639A>G (p.Ala213=) n.351A>G n.628A>G c.618A>G (p.Ala206=) c.54A>G (p.Ala18=) | |
1 | g.12192950A>T | CA416364768 | TNFRSF1B | c.639A>T (p.Ala213=) n.351A>T n.628A>T c.618A>T (p.Ala206=) c.54A>T (p.Ala18=) | |
1 | g.12192951G>A | CA338455396 | TNFRSF1B | c.640G>A (p.Val214Ile) n.352G>A n.629G>A c.619G>A (p.Val207Ile) c.55G>A (p.Val19Ile) | gnomAD v4 |
1 | g.12192951G>C | CA338455395 | TNFRSF1B | c.640G>C (p.Val214Leu) n.352G>C n.629G>C c.619G>C (p.Val207Leu) c.55G>C (p.Val19Leu) | |
1 | g.12192951G>T | CA338455392 | TNFRSF1B | c.640G>T (p.Val214Leu) n.352G>T n.629G>T c.619G>T (p.Val207Leu) c.55G>T (p.Val19Leu) | |
1 | g.12192952T>A | CA338455397 | TNFRSF1B | c.641T>A (p.Val214Glu) n.353T>A n.630T>A c.620T>A (p.Val207Glu) c.56T>A (p.Val19Glu) | |
1 | g.12192952T>C | CA338455400 | TNFRSF1B | c.641T>C (p.Val214Ala) n.353T>C n.630T>C c.620T>C (p.Val207Ala) c.56T>C (p.Val19Ala) | gnomAD v4 COSMIC |
1 | g.12192952T>G | CA338455408 | TNFRSF1B | c.641T>G (p.Val214Gly) n.353T>G n.630T>G c.620T>G (p.Val207Gly) c.56T>G (p.Val19Gly) | |
1 | g.12192953A= | CA1154001438 | TNFRSF1B | c.642A= (p.Val214=) n.354A= n.631A= c.621A= (p.Val207=) c.57A= (p.Val19=) | |
1 | g.12192953A>C | CA416364769 | TNFRSF1B | c.642A>C (p.Val214=) n.354A>C n.631A>C c.621A>C (p.Val207=) c.57A>C (p.Val19=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192953A>G | CA416364770 | TNFRSF1B | c.642A>G (p.Val214=) n.354A>G n.631A>G c.621A>G (p.Val207=) c.57A>G (p.Val19=) | |
1 | g.12192953A>T | CA416364771 | TNFRSF1B | c.642A>T (p.Val214=) n.354A>T n.631A>T c.621A>T (p.Val207=) c.57A>T (p.Val19=) | |
1 | g.12192954C>A | CA338455422 | TNFRSF1B | c.643C>A (p.His215Asn) n.355C>A n.632C>A c.622C>A (p.His208Asn) c.58C>A (p.His20Asn) | |
1 | g.12192954C>G | CA338455429 | TNFRSF1B | c.643C>G (p.His215Asp) n.355C>G n.632C>G c.622C>G (p.His208Asp) c.58C>G (p.His20Asp) | |
1 | g.12192954C>T | CA338455439 | TNFRSF1B | c.643C>T (p.His215Tyr) n.355C>T n.632C>T c.622C>T (p.His208Tyr) c.58C>T (p.His20Tyr) | COSMIC |
1 | g.12192955A>C | CA338455449 | TNFRSF1B | c.644A>C (p.His215Pro) n.356A>C n.633A>C c.623A>C (p.His208Pro) c.59A>C (p.His20Pro) | |
1 | g.12192955A>G | CA338455455 | TNFRSF1B | c.644A>G (p.His215Arg) n.356A>G n.633A>G c.623A>G (p.His208Arg) c.59A>G (p.His20Arg) | gnomAD v4 |
1 | g.12192955A>T | CA338455454 | TNFRSF1B | c.644A>T (p.His215Leu) n.356A>T n.633A>T c.623A>T (p.His208Leu) c.59A>T (p.His20Leu) | |
1 | g.12192956C>A | CA338455458 | TNFRSF1B | c.645C>A (p.His215Gln) n.357C>A n.634C>A c.624C>A (p.His208Gln) c.60C>A (p.His20Gln) | |
1 | g.12192956C>G | CA338455462 | TNFRSF1B | c.645C>G (p.His215Gln) n.357C>G n.634C>G c.624C>G (p.His208Gln) c.60C>G (p.His20Gln) | |
1 | g.12192956C>T | CA416364772 | TNFRSF1B | c.645C>T (p.His215=) n.357C>T n.634C>T c.624C>T (p.His208=) c.60C>T (p.His20=) | |
1 | g.12192957T>A | CA338455468 | TNFRSF1B | c.646T>A (p.Leu216Ile) n.358T>A n.635T>A c.625T>A (p.Leu209Ile) c.61T>A (p.Leu21Ile) | |
1 | g.12192957T>C | CA416364773 | TNFRSF1B | c.646T>C (p.Leu216=) n.358T>C n.635T>C c.625T>C (p.Leu209=) c.61T>C (p.Leu21=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192957T>G | CA338455470 | TNFRSF1B | c.646T>G (p.Leu216Val) n.358T>G n.635T>G c.625T>G (p.Leu209Val) c.61T>G (p.Leu21Val) | |
1 | g.12192957T= | CA1154001439 | TNFRSF1B | c.646T= (p.Leu216=) n.358T= n.635T= c.625T= (p.Leu209=) c.61T= (p.Leu21=) | |
1 | g.12192958T>A | CA338455473 | TNFRSF1B | c.647T>A (p.Leu216Ter) n.359T>A n.636T>A c.626T>A (p.Leu209Ter) c.62T>A (p.Leu21Ter) | |
1 | g.12192958T>C | CA338455478 | TNFRSF1B | c.647T>C (p.Leu216Ser) n.359T>C n.636T>C c.626T>C (p.Leu209Ser) c.62T>C (p.Leu21Ser) | |
1 | g.12192958T>G | CA338455479 | TNFRSF1B | c.647T>G (p.Leu216Ter) n.359T>G n.636T>G c.626T>G (p.Leu209Ter) c.62T>G (p.Leu21Ter) | |
1 | g.12192959A= | CA1154001440 | TNFRSF1B | c.648A= (p.Leu216=) n.360A= n.637A= c.627A= (p.Leu209=) c.63A= (p.Leu21=) | |
1 | g.12192959A>C | CA600842 | TNFRSF1B | c.648A>C (p.Leu216Phe) n.360A>C n.637A>C c.627A>C (p.Leu209Phe) c.63A>C (p.Leu21Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192959A>G | CA416364774 | TNFRSF1B | c.648A>G (p.Leu216=) n.360A>G n.637A>G c.627A>G (p.Leu209=) c.63A>G (p.Leu21=) | |
1 | g.12192959A>T | CA338455482 | TNFRSF1B | c.648A>T (p.Leu216Phe) n.360A>T n.637A>T c.627A>T (p.Leu209Phe) c.63A>T (p.Leu21Phe) | |
1 | g.12192960C>A | CA338455487 | TNFRSF1B | c.649C>A (p.Pro217Thr) n.361C>A n.638C>A c.628C>A (p.Pro210Thr) c.64C>A (p.Pro22Thr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192960C= | CA1154001441 | TNFRSF1B | c.649C= (p.Pro217=) n.361C= n.638C= c.628C= (p.Pro210=) c.64C= (p.Pro22=) | |
1 | g.12192960C>G | CA338455488 | TNFRSF1B | c.649C>G (p.Pro217Ala) n.361C>G n.638C>G c.628C>G (p.Pro210Ala) c.64C>G (p.Pro22Ala) | gnomAD v4 |
1 | g.12192960C>T | CA338455489 | TNFRSF1B | c.649C>T (p.Pro217Ser) n.361C>T n.638C>T c.628C>T (p.Pro210Ser) c.64C>T (p.Pro22Ser) | |
1 | g.12192961C>A | CA338455504 | TNFRSF1B | c.650C>A (p.Pro217His) n.362C>A n.639C>A c.629C>A (p.Pro210His) c.65C>A (p.Pro22His) | |
1 | g.12192961C= | CA1154001442 | TNFRSF1B | c.650C= (p.Pro217=) n.362C= n.639C= c.629C= (p.Pro210=) c.65C= (p.Pro22=) | |
1 | g.12192961C>G | CA338455495 | TNFRSF1B | c.650C>G (p.Pro217Arg) n.362C>G n.639C>G c.629C>G (p.Pro210Arg) c.65C>G (p.Pro22Arg) | |
1 | g.12192961C>T | CA338455498 | TNFRSF1B | c.650C>T (p.Pro217Leu) n.362C>T n.639C>T c.629C>T (p.Pro210Leu) c.65C>T (p.Pro22Leu) | dbSNP gnomAD v4 |
1 | g.12192962C>A | CA416364777 | TNFRSF1B | c.651C>A (p.Pro217=) n.363C>A n.640C>A c.630C>A (p.Pro210=) c.66C>A (p.Pro22=) | |
1 | g.12192962C>G | CA416364776 | TNFRSF1B | c.651C>G (p.Pro217=) n.363C>G n.640C>G c.630C>G (p.Pro210=) c.66C>G (p.Pro22=) | gnomAD v4 |
1 | g.12192962C>T | CA416364775 | TNFRSF1B | c.651C>T (p.Pro217=) n.363C>T n.640C>T c.630C>T (p.Pro210=) c.66C>T (p.Pro22=) | |
1 | g.12192963C>A | CA338455506 | TNFRSF1B | c.652C>A (p.Gln218Lys) n.364C>A n.641C>A c.631C>A (p.Gln211Lys) c.67C>A (p.Gln23Lys) | |
1 | g.12192963C>G | CA338455509 | TNFRSF1B | c.652C>G (p.Gln218Glu) n.364C>G n.641C>G c.631C>G (p.Gln211Glu) c.67C>G (p.Gln23Glu) | |
1 | g.12192963C>T | CA338455513 | TNFRSF1B | c.652C>T (p.Gln218Ter) n.364C>T n.641C>T c.631C>T (p.Gln211Ter) c.67C>T (p.Gln23Ter) | |
1 | g.12192964A>C | CA338455517 | TNFRSF1B | c.653A>C (p.Gln218Pro) n.365A>C n.642A>C c.632A>C (p.Gln211Pro) c.68A>C (p.Gln23Pro) | |
1 | g.12192964A>G | CA338455518 | TNFRSF1B | c.653A>G (p.Gln218Arg) n.365A>G n.642A>G c.632A>G (p.Gln211Arg) c.68A>G (p.Gln23Arg) | |
1 | g.12192964A>T | CA338455519 | TNFRSF1B | c.653A>T (p.Gln218Leu) n.365A>T n.642A>T c.632A>T (p.Gln211Leu) c.68A>T (p.Gln23Leu) | |
1 | g.12192965G>A | CA416364778 | TNFRSF1B | c.654G>A (p.Gln218=) n.366G>A n.643G>A c.633G>A (p.Gln211=) c.69G>A (p.Gln23=) | |
1 | g.12192965G>C | CA600843 | TNFRSF1B | c.654G>C (p.Gln218His) n.366G>C n.643G>C c.633G>C (p.Gln211His) c.69G>C (p.Gln23His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192965G= | CA1154001443 | TNFRSF1B | c.654G= (p.Gln218=) n.366G= n.643G= c.633G= (p.Gln211=) c.69G= (p.Gln23=) | |
1 | g.12192965G>T | CA338455523 | TNFRSF1B | c.654G>T (p.Gln218His) n.366G>T n.643G>T c.633G>T (p.Gln211His) c.69G>T (p.Gln23His) | gnomAD v4 |
1 | g.12192965_12192973del | CA2742494883 | TNFRSF1B | c.654_662del (p.Gln218_Ser221delinsHis) n.366_374del n.643_651del c.633_641del (p.Gln211_Ser214delinsHis) c.69_77del (p.Gln23_Ser26delinsHis) | |
1 | g.12192966C>A | CA338455527 | TNFRSF1B | c.655C>A (p.Pro219Thr) n.367C>A n.644C>A c.634C>A (p.Pro212Thr) c.70C>A (p.Pro24Thr) | dbSNP |
1 | g.12192966C>G | CA338455528 | TNFRSF1B | c.655C>G (p.Pro219Ala) n.367C>G n.644C>G c.634C>G (p.Pro212Ala) c.70C>G (p.Pro24Ala) | |
1 | g.12192966C>T | CA338455530 | TNFRSF1B | c.655C>T (p.Pro219Ser) n.367C>T n.644C>T c.634C>T (p.Pro212Ser) c.70C>T (p.Pro24Ser) | |
1 | g.12192967C>A | CA338455536 | TNFRSF1B | c.656C>A (p.Pro219Gln) n.368C>A n.645C>A c.635C>A (p.Pro212Gln) c.71C>A (p.Pro24Gln) | |
1 | g.12192967C>G | CA338455547 | TNFRSF1B | c.656C>G (p.Pro219Arg) n.368C>G n.645C>G c.635C>G (p.Pro212Arg) c.71C>G (p.Pro24Arg) | |
1 | g.12192967C>T | CA338455560 | TNFRSF1B | c.656C>T (p.Pro219Leu) n.368C>T n.645C>T c.635C>T (p.Pro212Leu) c.71C>T (p.Pro24Leu) | |
1 | g.12192968A= | CA1154001444 | TNFRSF1B | c.657A= (p.Pro219=) n.369A= n.646A= c.636A= (p.Pro212=) c.72A= (p.Pro24=) | |
1 | g.12192968A>C | CA416364779 | TNFRSF1B | c.657A>C (p.Pro219=) n.369A>C n.646A>C c.636A>C (p.Pro212=) c.72A>C (p.Pro24=) | |
1 | g.12192968A>G | CA416364781 | TNFRSF1B | c.657A>G (p.Pro219=) n.369A>G n.646A>G c.636A>G (p.Pro212=) c.72A>G (p.Pro24=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12192968A>T | CA416364780 | TNFRSF1B | c.657A>T (p.Pro219=) n.369A>T n.646A>T c.636A>T (p.Pro212=) c.72A>T (p.Pro24=) | |
1 | g.12192969G>A | CA338455592 | TNFRSF1B | c.658G>A (p.Val220Met) n.370G>A n.647G>A c.637G>A (p.Val213Met) c.73G>A (p.Val25Met) | |
1 | g.12192969G>C | CA338455564 | TNFRSF1B | c.658G>C (p.Val220Leu) n.370G>C n.647G>C c.637G>C (p.Val213Leu) c.73G>C (p.Val25Leu) | |
1 | g.12192969G>T | CA338455587 | TNFRSF1B | c.658G>T (p.Val220Leu) n.370G>T n.647G>T c.637G>T (p.Val213Leu) c.73G>T (p.Val25Leu) | |
1 | g.12192970T>A | CA338455597 | TNFRSF1B | c.659T>A (p.Val220Glu) n.371T>A n.648T>A c.638T>A (p.Val213Glu) c.74T>A (p.Val25Glu) | |
1 | g.12192970T>C | CA600844 | TNFRSF1B | c.659T>C (p.Val220Ala) n.371T>C n.648T>C c.638T>C (p.Val213Ala) c.74T>C (p.Val25Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192970T>G | CA600845 | TNFRSF1B | c.659T>G (p.Val220Gly) n.371T>G n.648T>G c.638T>G (p.Val213Gly) c.74T>G (p.Val25Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192970T= | CA1148254969 | TNFRSF1B | c.659T= (p.Val220=) n.371T= n.648T= c.638T= (p.Val213=) c.74T= (p.Val25=) | |
1 | g.12192971G>A | CA416364782 | TNFRSF1B | c.660G>A (p.Val220=) n.372G>A n.649G>A c.639G>A (p.Val213=) c.75G>A (p.Val25=) | |
1 | g.12192971G>C | CA416364783 | TNFRSF1B | c.660G>C (p.Val220=) n.372G>C n.649G>C c.639G>C (p.Val213=) c.75G>C (p.Val25=) | |
1 | g.12192971G>T | CA416364784 | TNFRSF1B | c.660G>T (p.Val220=) n.372G>T n.649G>T c.639G>T (p.Val213=) c.75G>T (p.Val25=) | |
1 | g.12192972T>A | CA338455608 | TNFRSF1B | c.661T>A (p.Ser221Thr) n.373T>A n.650T>A c.640T>A (p.Ser214Thr) c.76T>A (p.Ser26Thr) | |
1 | g.12192972T>C | CA338455613 | TNFRSF1B | c.661T>C (p.Ser221Pro) n.373T>C n.650T>C c.640T>C (p.Ser214Pro) c.76T>C (p.Ser26Pro) | |
1 | g.12192972T>G | CA338455616 | TNFRSF1B | c.661T>G (p.Ser221Ala) n.373T>G n.650T>G c.640T>G (p.Ser214Ala) c.76T>G (p.Ser26Ala) | |
1 | g.12192973C>A | CA338455625 | TNFRSF1B | c.662C>A (p.Ser221Tyr) n.374C>A n.651C>A c.641C>A (p.Ser214Tyr) c.77C>A (p.Ser26Tyr) | |
1 | g.12192973C>G | CA338455626 | TNFRSF1B | c.662C>G (p.Ser221Cys) n.374C>G n.651C>G c.641C>G (p.Ser214Cys) c.77C>G (p.Ser26Cys) | |
1 | g.12192973C>T | CA338455627 | TNFRSF1B | c.662C>T (p.Ser221Phe) n.374C>T n.651C>T c.641C>T (p.Ser214Phe) c.77C>T (p.Ser26Phe) | |
1 | g.12192974C>A | CA416364785 | TNFRSF1B | c.663C>A (p.Ser221=) n.375C>A n.652C>A c.642C>A (p.Ser214=) c.78C>A (p.Ser26=) | |
1 | g.12192974C= | CA1154001445 | TNFRSF1B | c.663C= (p.Ser221=) n.375C= n.652C= c.642C= (p.Ser214=) c.78C= (p.Ser26=) | |
1 | g.12192974C>G | CA416364786 | TNFRSF1B | c.663C>G (p.Ser221=) n.375C>G n.652C>G c.642C>G (p.Ser214=) c.78C>G (p.Ser26=) | |
1 | g.12192974C>T | CA416364787 | TNFRSF1B | c.663C>T (p.Ser221=) n.375C>T n.652C>T c.642C>T (p.Ser214=) c.78C>T (p.Ser26=) | dbSNP |
1 | g.12192975A= | CA1154001446 | TNFRSF1B | c.664A= (p.Thr222=) n.376A= n.653A= c.643A= (p.Thr215=) c.79A= (p.Thr27=) | |
1 | g.12192975A>C | CA338455628 | TNFRSF1B | c.664A>C (p.Thr222Pro) n.376A>C n.653A>C c.643A>C (p.Thr215Pro) c.79A>C (p.Thr27Pro) | COSMIC |
1 | g.12192975A>G | CA600846 | TNFRSF1B | c.664A>G (p.Thr222Ala) n.376A>G n.653A>G c.643A>G (p.Thr215Ala) c.79A>G (p.Thr27Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192975A>T | CA338455634 | TNFRSF1B | c.664A>T (p.Thr222Ser) n.376A>T n.653A>T c.643A>T (p.Thr215Ser) c.79A>T (p.Thr27Ser) | |
1 | g.12192976C>A | CA338455636 | TNFRSF1B | c.665C>A (p.Thr222Lys) n.377C>A n.654C>A c.644C>A (p.Thr215Lys) c.80C>A (p.Thr27Lys) | |
1 | g.12192976C= | CA1154001447 | TNFRSF1B | c.665C= (p.Thr222=) n.377C= n.654C= c.644C= (p.Thr215=) c.80C= (p.Thr27=) | |
1 | g.12192976C>G | CA338455644 | TNFRSF1B | c.665C>G (p.Thr222Arg) n.377C>G n.654C>G c.644C>G (p.Thr215Arg) c.80C>G (p.Thr27Arg) | COSMIC |
1 | g.12192976C>T | CA338455640 | TNFRSF1B | c.665C>T (p.Thr222Ile) n.377C>T n.654C>T c.644C>T (p.Thr215Ile) c.80C>T (p.Thr27Ile) | dbSNP gnomAD v4 |
1 | g.12192977del | CA2526561950 | TNFRSF1B | c.666del (p.Arg223AspfsTer?) n.378del n.655del c.645del (p.Arg216AspfsTer?) c.81del (p.Arg28AspfsTer?) | |
1 | g.12192977A>C | CA416364788 | TNFRSF1B | c.666A>C (p.Thr222=) n.378A>C n.655A>C c.645A>C (p.Thr215=) c.81A>C (p.Thr27=) | |
1 | g.12192977A>G | CA416364789 | TNFRSF1B | c.666A>G (p.Thr222=) n.378A>G n.655A>G c.645A>G (p.Thr215=) c.81A>G (p.Thr27=) | gnomAD v4 |
1 | g.12192977A>T | CA416364790 | TNFRSF1B | c.666A>T (p.Thr222=) n.378A>T n.655A>T c.645A>T (p.Thr215=) c.81A>T (p.Thr27=) | |
1 | g.12192978C>A | CA416364791 | TNFRSF1B | c.667C>A (p.Arg223=) n.379C>A n.656C>A c.646C>A (p.Arg216=) c.82C>A (p.Arg28=) | |
1 | g.12192978C= | CA1154001448 | TNFRSF1B | c.667C= (p.Arg223=) n.379C= n.656C= c.646C= (p.Arg216=) c.82C= (p.Arg28=) | |
1 | g.12192978C>G | CA338455653 | TNFRSF1B | c.667C>G (p.Arg223Gly) n.379C>G n.656C>G c.646C>G (p.Arg216Gly) c.82C>G (p.Arg28Gly) | gnomAD v4 |
1 | g.12192978C>T | CA338455678 | TNFRSF1B | c.667C>T (p.Arg223Ter) n.379C>T n.656C>T c.646C>T (p.Arg216Ter) c.82C>T (p.Arg28Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192979_12192982del | CA2742494884 | TNFRSF1B | c.668_671del (p.Arg223ProfsTer?) n.380_383del n.657_660del c.647_650del (p.Arg216ProfsTer?) c.83_86del (p.Arg28ProfsTer?) | |
1 | g.12192979G>A | CA600847 | TNFRSF1B | c.668G>A (p.Arg223Gln) n.380G>A n.657G>A c.647G>A (p.Arg216Gln) c.83G>A (p.Arg28Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192979G>C | CA338455687 | TNFRSF1B | c.668G>C (p.Arg223Pro) n.380G>C n.657G>C c.647G>C (p.Arg216Pro) c.83G>C (p.Arg28Pro) | |
1 | g.12192979G= | CA1149067258 | TNFRSF1B | c.668G= (p.Arg223=) n.380G= n.657G= c.647G= (p.Arg216=) c.83G= (p.Arg28=) | |
1 | g.12192979G>T | CA338455688 | TNFRSF1B | c.668G>T (p.Arg223Leu) n.380G>T n.657G>T c.647G>T (p.Arg216Leu) c.83G>T (p.Arg28Leu) | gnomAD v4 |
1 | g.12192979_12192980dup | CA2527604623 | TNFRSF1B | c.668_669dup (p.Ser224AspfsTer?) n.380_381dup n.657_658dup c.647_648dup (p.Ser217AspfsTer?) c.83_84dup (p.Ser29AspfsTer?) | |
1 | g.12192980A= | CA1154001449 | TNFRSF1B | c.669A= (p.Arg223=) n.381A= n.658A= c.648A= (p.Arg216=) c.84A= (p.Arg28=) | |
1 | g.12192980A>C | CA416364792 | TNFRSF1B | c.669A>C (p.Arg223=) n.381A>C n.658A>C c.648A>C (p.Arg216=) c.84A>C (p.Arg28=) | |
1 | g.12192980A>G | CA18022185 | TNFRSF1B | c.669A>G (p.Arg223=) n.381A>G n.658A>G c.648A>G (p.Arg216=) c.84A>G (p.Arg28=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12192980A>T | CA416364793 | TNFRSF1B | c.669A>T (p.Arg223=) n.381A>T n.658A>T c.648A>T (p.Arg216=) c.84A>T (p.Arg28=) | |
1 | g.12192980_12192981insACCCAAACAC | CA2742494885 | TNFRSF1B | c.669_670insACCCAAACAC (p.Ser224ThrfsTer32) n.381_382insACCCAAACAC n.658_659insACCCAAACAC c.648_649insACCCAAACAC (p.Ser217ThrfsTer32) c.84_85insACCCAAACAC (p.Ser29ThrfsTer32) | |
1 | g.12192981T>A | CA338455689 | TNFRSF1B | c.670T>A (p.Ser224Thr) n.382T>A n.659T>A c.649T>A (p.Ser217Thr) c.85T>A (p.Ser29Thr) | |
1 | g.12192981T>C | CA338455692 | TNFRSF1B | c.670T>C (p.Ser224Pro) n.382T>C n.659T>C c.649T>C (p.Ser217Pro) c.85T>C (p.Ser29Pro) | ClinVar |
1 | g.12192981T>G | CA338455694 | TNFRSF1B | c.670T>G (p.Ser224Ala) n.382T>G n.659T>G c.649T>G (p.Ser217Ala) c.85T>G (p.Ser29Ala) | |
1 | g.12192982C>A | CA338455699 | TNFRSF1B | c.671C>A (p.Ser224Tyr) n.383C>A n.660C>A c.650C>A (p.Ser217Tyr) c.86C>A (p.Ser29Tyr) | |
1 | g.12192982C= | CA1142071941 | TNFRSF1B | c.671C= (p.Ser224=) n.383C= n.660C= c.650C= (p.Ser217=) c.86C= (p.Ser29=) | |
1 | g.12192982C>G | CA600848 | TNFRSF1B | c.671C>G (p.Ser224Cys) n.383C>G n.660C>G c.650C>G (p.Ser217Cys) c.86C>G (p.Ser29Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192982C>T | CA338455709 | TNFRSF1B | c.671C>T (p.Ser224Phe) n.383C>T n.660C>T c.650C>T (p.Ser217Phe) c.86C>T (p.Ser29Phe) | gnomAD v4 COSMIC |
1 | g.12192983_12192984del | CA2514160120 | TNFRSF1B | c.672_673del (p.Gln225ThrfsTer27) n.384_385del n.661_662del c.651_652del (p.Gln218ThrfsTer27) c.87_88del (p.Gln30ThrfsTer27) | |
1 | g.12192983C>A | CA416364794 | TNFRSF1B | c.672C>A (p.Ser224=) n.384C>A n.661C>A c.651C>A (p.Ser217=) c.87C>A (p.Ser29=) | |
1 | g.12192983C>G | CA416364795 | TNFRSF1B | c.672C>G (p.Ser224=) n.384C>G n.661C>G c.651C>G (p.Ser217=) c.87C>G (p.Ser29=) | |
1 | g.12192983C>T | CA416364796 | TNFRSF1B | c.672C>T (p.Ser224=) n.384C>T n.661C>T c.651C>T (p.Ser217=) c.87C>T (p.Ser29=) | |
1 | g.12192984C>A | CA338455711 | TNFRSF1B | c.673C>A (p.Gln225Lys) n.385C>A n.662C>A c.652C>A (p.Gln218Lys) c.88C>A (p.Gln30Lys) | |
1 | g.12192984C>G | CA338455712 | TNFRSF1B | c.673C>G (p.Gln225Glu) n.385C>G n.662C>G c.652C>G (p.Gln218Glu) c.88C>G (p.Gln30Glu) | gnomAD v4 |
1 | g.12192984C>T | CA338455713 | TNFRSF1B | c.673C>T (p.Gln225Ter) n.385C>T n.662C>T c.652C>T (p.Gln218Ter) c.88C>T (p.Gln30Ter) | |
1 | g.12192985A>C | CA338455717 | TNFRSF1B | c.674A>C (p.Gln225Pro) n.386A>C n.663A>C c.653A>C (p.Gln218Pro) c.89A>C (p.Gln30Pro) | |
1 | g.12192985A>G | CA338455721 | TNFRSF1B | c.674A>G (p.Gln225Arg) n.386A>G n.663A>G c.653A>G (p.Gln218Arg) c.89A>G (p.Gln30Arg) | |
1 | g.12192985A>T | CA338455718 | TNFRSF1B | c.674A>T (p.Gln225Leu) n.386A>T n.663A>T c.653A>T (p.Gln218Leu) c.89A>T (p.Gln30Leu) | |
1 | g.12192986A>C | CA338455724 | TNFRSF1B | c.675A>C (p.Gln225His) n.387A>C n.664A>C c.654A>C (p.Gln218His) c.90A>C (p.Gln30His) | |
1 | g.12192986A>G | CA416364797 | TNFRSF1B | c.675A>G (p.Gln225=) n.387A>G n.664A>G c.654A>G (p.Gln218=) c.90A>G (p.Gln30=) | |
1 | g.12192986A>T | CA338455725 | TNFRSF1B | c.675A>T (p.Gln225His) n.387A>T n.664A>T c.654A>T (p.Gln218His) c.90A>T (p.Gln30His) | |
1 | g.12192987C>A | CA600849 | TNFRSF1B | c.676C>A (p.His226Asn) n.388C>A n.665C>A c.655C>A (p.His219Asn) c.91C>A (p.His31Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192987C= | CA1154001450 | TNFRSF1B | c.676C= (p.His226=) n.388C= n.665C= c.655C= (p.His219=) c.91C= (p.His31=) | |
1 | g.12192987C>G | CA338455729 | TNFRSF1B | c.676C>G (p.His226Asp) n.388C>G n.665C>G c.655C>G (p.His219Asp) c.91C>G (p.His31Asp) | |
1 | g.12192987C>T | CA338455731 | TNFRSF1B | c.676C>T (p.His226Tyr) n.388C>T n.665C>T c.655C>T (p.His219Tyr) c.91C>T (p.His31Tyr) | gnomAD v4 |
1 | g.12192988A>C | CA338455737 | TNFRSF1B | c.677A>C (p.His226Pro) n.389A>C n.666A>C c.656A>C (p.His219Pro) c.92A>C (p.His31Pro) | |
1 | g.12192988A>G | CA338455738 | TNFRSF1B | c.677A>G (p.His226Arg) n.389A>G n.666A>G c.656A>G (p.His219Arg) c.92A>G (p.His31Arg) | |
1 | g.12192988A>T | CA338455739 | TNFRSF1B | c.677A>T (p.His226Leu) n.389A>T n.666A>T c.656A>T (p.His219Leu) c.92A>T (p.His31Leu) | |
1 | g.12192989C>A | CA338455740 | TNFRSF1B | c.678C>A (p.His226Gln) n.390C>A n.667C>A c.657C>A (p.His219Gln) c.93C>A (p.His31Gln) | |
1 | g.12192989C>G | CA338455742 | TNFRSF1B | c.678C>G (p.His226Gln) n.390C>G n.667C>G c.657C>G (p.His219Gln) c.93C>G (p.His31Gln) | |
1 | g.12192989C>T | CA416364798 | TNFRSF1B | c.678C>T (p.His226=) n.390C>T n.667C>T c.657C>T (p.His219=) c.93C>T (p.His31=) | gnomAD v4 |
1 | g.12192990A>C | CA338455752 | TNFRSF1B | c.679A>C (p.Thr227Pro) n.391A>C n.668A>C c.658A>C (p.Thr220Pro) c.94A>C (p.Thr32Pro) | |
1 | g.12192990A>G | CA338455754 | TNFRSF1B | c.679A>G (p.Thr227Ala) n.391A>G n.668A>G c.658A>G (p.Thr220Ala) c.94A>G (p.Thr32Ala) | |
1 | g.12192990A>T | CA338455748 | TNFRSF1B | c.679A>T (p.Thr227Ser) n.391A>T n.668A>T c.658A>T (p.Thr220Ser) c.94A>T (p.Thr32Ser) | |
1 | g.12192991C>A | CA338455758 | TNFRSF1B | c.680C>A (p.Thr227Lys) n.392C>A n.669C>A c.659C>A (p.Thr220Lys) c.95C>A (p.Thr32Lys) | |
1 | g.12192991C= | CA1154001451 | TNFRSF1B | c.680C= (p.Thr227=) n.392C= n.669C= c.659C= (p.Thr220=) c.95C= (p.Thr32=) | |
1 | g.12192991C>G | CA338455760 | TNFRSF1B | c.680C>G (p.Thr227Arg) n.392C>G n.669C>G c.659C>G (p.Thr220Arg) c.95C>G (p.Thr32Arg) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192991C>T | CA600850 | TNFRSF1B | c.680C>T (p.Thr227Met) n.392C>T n.669C>T c.659C>T (p.Thr220Met) c.95C>T (p.Thr32Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192992G>A | CA600851 | TNFRSF1B | c.681G>A (p.Thr227=) n.393G>A n.670G>A c.660G>A (p.Thr220=) c.96G>A (p.Thr32=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192992G>C | CA416364800 | TNFRSF1B | c.681G>C (p.Thr227=) n.393G>C n.670G>C c.660G>C (p.Thr220=) c.96G>C (p.Thr32=) | gnomAD v4 |
1 | g.12192992G= | CA1154001452 | TNFRSF1B | c.681G= (p.Thr227=) n.393G= n.670G= c.660G= (p.Thr220=) c.96G= (p.Thr32=) | |
1 | g.12192992G>T | CA416364799 | TNFRSF1B | c.681G>T (p.Thr227=) n.393G>T n.670G>T c.660G>T (p.Thr220=) c.96G>T (p.Thr32=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12192993C>A | CA338455770 | TNFRSF1B | c.682C>A (p.Gln228Lys) n.394C>A n.671C>A c.661C>A (p.Gln221Lys) c.97C>A (p.Gln33Lys) | |
1 | g.12192993C>G | CA338455773 | TNFRSF1B | c.682C>G (p.Gln228Glu) n.394C>G n.671C>G c.661C>G (p.Gln221Glu) c.97C>G (p.Gln33Glu) | |
1 | g.12192993C>T | CA338455780 | TNFRSF1B | c.682C>T (p.Gln228Ter) n.394C>T n.671C>T c.661C>T (p.Gln221Ter) c.97C>T (p.Gln33Ter) | |
1 | g.12192994A>C | CA338455784 | TNFRSF1B | c.683A>C (p.Gln228Pro) n.395A>C n.672A>C c.662A>C (p.Gln221Pro) c.98A>C (p.Gln33Pro) | |
1 | g.12192994A>G | CA338455785 | TNFRSF1B | c.683A>G (p.Gln228Arg) n.395A>G n.672A>G c.662A>G (p.Gln221Arg) c.98A>G (p.Gln33Arg) | |
1 | g.12192994A>T | CA338455788 | TNFRSF1B | c.683A>T (p.Gln228Leu) n.395A>T n.672A>T c.662A>T (p.Gln221Leu) c.98A>T (p.Gln33Leu) | |
1 | g.12192995G>A | CA416364801 | TNFRSF1B | c.684G>A (p.Gln228=) n.396G>A n.673G>A c.663G>A (p.Gln221=) c.99G>A (p.Gln33=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12192995G>C | CA338455791 | TNFRSF1B | c.684G>C (p.Gln228His) n.396G>C n.673G>C c.663G>C (p.Gln221His) c.99G>C (p.Gln33His) | |
1 | g.12192995G= | CA1154001453 | TNFRSF1B | c.684G= (p.Gln228=) n.396G= n.673G= c.663G= (p.Gln221=) c.99G= (p.Gln33=) | |
1 | g.12192995G>T | CA338455796 | TNFRSF1B | c.684G>T (p.Gln228His) n.396G>T n.673G>T c.663G>T (p.Gln221His) c.99G>T (p.Gln33His) | |
1 | g.12192996C>A | CA338455800 | TNFRSF1B | c.685C>A (p.Pro229Thr) n.397C>A n.674C>A c.664C>A (p.Pro222Thr) c.100C>A (p.Pro34Thr) | |
1 | g.12192996C= | CA1154001454 | TNFRSF1B | c.685C= (p.Pro229=) n.397C= n.674C= c.664C= (p.Pro222=) c.100C= (p.Pro34=) | |
1 | g.12192996C>G | CA338455801 | TNFRSF1B | c.685C>G (p.Pro229Ala) n.397C>G n.674C>G c.664C>G (p.Pro222Ala) c.100C>G (p.Pro34Ala) | gnomAD v4 |
1 | g.12192996C>T | CA338455799 | TNFRSF1B | c.685C>T (p.Pro229Ser) n.397C>T n.674C>T c.664C>T (p.Pro222Ser) c.100C>T (p.Pro34Ser) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192997C>A | CA338455804 | TNFRSF1B | c.686C>A (p.Pro229Gln) n.398C>A n.675C>A c.665C>A (p.Pro222Gln) c.101C>A (p.Pro34Gln) | |
1 | g.12192997C>G | CA338455807 | TNFRSF1B | c.686C>G (p.Pro229Arg) n.398C>G n.675C>G c.665C>G (p.Pro222Arg) c.101C>G (p.Pro34Arg) | |
1 | g.12192997C>T | CA338455813 | TNFRSF1B | c.686C>T (p.Pro229Leu) n.398C>T n.675C>T c.665C>T (p.Pro222Leu) c.101C>T (p.Pro34Leu) | gnomAD v4 |
1 | g.12192998A>C | CA416364802 | TNFRSF1B | c.687A>C (p.Pro229=) n.399A>C n.676A>C c.666A>C (p.Pro222=) c.102A>C (p.Pro34=) | |
1 | g.12192998A>G | CA416364803 | TNFRSF1B | c.687A>G (p.Pro229=) n.399A>G n.676A>G c.666A>G (p.Pro222=) c.102A>G (p.Pro34=) | |
1 | g.12192998A>T | CA416364804 | TNFRSF1B | c.687A>T (p.Pro229=) n.399A>T n.676A>T c.666A>T (p.Pro222=) c.102A>T (p.Pro34=) | |
1 | g.12192999A>C | CA338455823 | TNFRSF1B | c.688A>C (p.Thr230Pro) n.400A>C n.677A>C c.667A>C (p.Thr223Pro) c.103A>C (p.Thr35Pro) | |
1 | g.12192999A>G | CA338455824 | TNFRSF1B | c.688A>G (p.Thr230Ala) n.400A>G n.677A>G c.667A>G (p.Thr223Ala) c.103A>G (p.Thr35Ala) | |
1 | g.12192999A>T | CA338455827 | TNFRSF1B | c.688A>T (p.Thr230Ser) n.400A>T n.677A>T c.667A>T (p.Thr223Ser) c.103A>T (p.Thr35Ser) | |
1 | g.12193000C>A | CA338455835 | TNFRSF1B | c.689C>A (p.Thr230Asn) n.401C>A n.678C>A c.668C>A (p.Thr223Asn) c.104C>A (p.Thr35Asn) | |
1 | g.12193000C>G | CA338455841 | TNFRSF1B | c.689C>G (p.Thr230Ser) n.401C>G n.678C>G c.668C>G (p.Thr223Ser) c.104C>G (p.Thr35Ser) | gnomAD v4 |
1 | g.12193000C>T | CA338455840 | TNFRSF1B | c.689C>T (p.Thr230Ile) n.401C>T n.678C>T c.668C>T (p.Thr223Ile) c.104C>T (p.Thr35Ile) | gnomAD v4 |
1 | g.12193001T>A | CA600852 | TNFRSF1B | c.690T>A (p.Thr230=) n.402T>A n.679T>A c.669T>A (p.Thr223=) c.105T>A (p.Thr35=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12193001T>C | CA416364805 | TNFRSF1B | c.690T>C (p.Thr230=) n.402T>C n.679T>C c.669T>C (p.Thr223=) c.105T>C (p.Thr35=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12193001T>G | CA416364806 | TNFRSF1B | c.690T>G (p.Thr230=) n.402T>G n.679T>G c.669T>G (p.Thr223=) c.105T>G (p.Thr35=) | |
1 | g.12193001T= | CA1154001455 | TNFRSF1B | c.690T= (p.Thr230=) n.402T= n.679T= c.669T= (p.Thr223=) c.105T= (p.Thr35=) | |
1 | g.12193002C>A | CA338455844 | TNFRSF1B | c.691C>A (p.Pro231Thr) n.403C>A n.680C>A c.670C>A (p.Pro224Thr) c.106C>A (p.Pro36Thr) | |
1 | g.12193002C= | CA1154001456 | TNFRSF1B | c.691C= (p.Pro231=) n.403C= n.680C= c.670C= (p.Pro224=) c.106C= (p.Pro36=) | |
1 | g.12193002C>G | CA338455845 | TNFRSF1B | c.691C>G (p.Pro231Ala) n.403C>G n.680C>G c.670C>G (p.Pro224Ala) c.106C>G (p.Pro36Ala) | |
1 | g.12193002C>T | CA338455847 | TNFRSF1B | c.691C>T (p.Pro231Ser) n.403C>T n.680C>T c.670C>T (p.Pro224Ser) c.106C>T (p.Pro36Ser) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12193003C>A | CA338455856 | TNFRSF1B | c.692C>A (p.Pro231Gln) n.404C>A n.681C>A c.671C>A (p.Pro224Gln) c.107C>A (p.Pro36Gln) | |
1 | g.12193003C>G | CA338455853 | TNFRSF1B | c.692C>G (p.Pro231Arg) n.404C>G n.681C>G c.671C>G (p.Pro224Arg) c.107C>G (p.Pro36Arg) | |
1 | g.12193003C>T | CA338455851 | TNFRSF1B | c.692C>T (p.Pro231Leu) n.404C>T n.681C>T c.671C>T (p.Pro224Leu) c.107C>T (p.Pro36Leu) | gnomAD v4 |
1 | g.12193004A>C | CA416364807 | TNFRSF1B | c.693A>C (p.Pro231=) n.405A>C n.682A>C c.672A>C (p.Pro224=) c.108A>C (p.Pro36=) | |
1 | g.12193004A>G | CA416364808 | TNFRSF1B | c.693A>G (p.Pro231=) n.405A>G n.682A>G c.672A>G (p.Pro224=) c.108A>G (p.Pro36=) | gnomAD v4 |
1 | g.12193004A>T | CA416364809 | TNFRSF1B | c.693A>T (p.Pro231=) n.405A>T n.682A>T c.672A>T (p.Pro224=) c.108A>T (p.Pro36=) | |
1 | g.12193005G>A | CA600853 | TNFRSF1B | c.694G>A (p.Glu232Lys) n.406G>A n.683G>A c.673G>A (p.Glu225Lys) c.109G>A (p.Glu37Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12193005G>C | CA338455857 | TNFRSF1B | c.694G>C (p.Glu232Gln) n.406G>C n.683G>C c.673G>C (p.Glu225Gln) c.109G>C (p.Glu37Gln) | |
1 | g.12193005G= | CA1140055749 | TNFRSF1B | c.694G= (p.Glu232=) n.406G= n.683G= c.673G= (p.Glu225=) c.109G= (p.Glu37=) | |
1 | g.12193005G>T | CA338455860 | TNFRSF1B | c.694G>T (p.Glu232Ter) n.406G>T n.683G>T c.673G>T (p.Glu225Ter) c.109G>T (p.Glu37Ter) | |
1 | g.12193006A>C | CA338455863 | TNFRSF1B | c.695A>C (p.Glu232Ala) n.407A>C n.684A>C c.674A>C (p.Glu225Ala) c.110A>C (p.Glu37Ala) | |
1 | g.12193006A>G | CA338455864 | TNFRSF1B | c.695A>G (p.Glu232Gly) n.407A>G n.684A>G c.674A>G (p.Glu225Gly) c.110A>G (p.Glu37Gly) | |
1 | g.12193006A>T | CA338455866 | TNFRSF1B | c.695A>T (p.Glu232Val) n.407A>T n.684A>T c.674A>T (p.Glu225Val) c.110A>T (p.Glu37Val) | |
1 | g.12193007A>C | CA338455869 | TNFRSF1B | c.696A>C (p.Glu232Asp) n.408A>C n.685A>C c.675A>C (p.Glu225Asp) c.111A>C (p.Glu37Asp) | |
1 | g.12193007A>G | CA416364810 | TNFRSF1B | c.696A>G (p.Glu232=) n.408A>G n.685A>G c.675A>G (p.Glu225=) c.111A>G (p.Glu37=) | |
1 | g.12193007A>T | CA338455870 | TNFRSF1B | c.696A>T (p.Glu232Asp) n.408A>T n.685A>T c.675A>T (p.Glu225Asp) c.111A>T (p.Glu37Asp) | |
1 | g.12193008C>A | CA338455874 | TNFRSF1B | c.697C>A (p.Pro233Thr) n.409C>A n.686C>A c.676C>A (p.Pro226Thr) c.112C>A (p.Pro38Thr) | |
1 | g.12193008C>G | CA338455892 | TNFRSF1B | c.697C>G (p.Pro233Ala) n.409C>G n.686C>G c.676C>G (p.Pro226Ala) c.112C>G (p.Pro38Ala) | |
1 | g.12193008C>T | CA338455900 | TNFRSF1B | c.697C>T (p.Pro233Ser) n.409C>T n.686C>T c.676C>T (p.Pro226Ser) c.112C>T (p.Pro38Ser) | |
1 | g.12193009C>A | CA338455905 | TNFRSF1B | c.698C>A (p.Pro233His) n.687C>A c.677C>A (p.Pro226His) c.113C>A (p.Pro38His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.12193009C= | CA1154001457 | TNFRSF1B | c.698C= (p.Pro233=) n.687C= c.677C= (p.Pro226=) c.113C= (p.Pro38=) | |
1 | g.12193009C>G | CA338455913 | TNFRSF1B | c.698C>G (p.Pro233Arg) n.687C>G c.677C>G (p.Pro226Arg) c.113C>G (p.Pro38Arg) | |
1 | g.12193009C>T | CA338455934 | TNFRSF1B | c.698C>T (p.Pro233Leu) n.687C>T c.677C>T (p.Pro226Leu) c.113C>T (p.Pro38Leu) | dbSNP gnomAD v4 |
1 | g.12193010C>A | CA416364812 | TNFRSF1B | c.699C>A (p.Pro233=) n.688C>A c.678C>A (p.Pro226=) c.114C>A (p.Pro38=) | |
1 | g.12193010C>G | CA416364813 | TNFRSF1B | c.699C>G (p.Pro233=) n.688C>G c.678C>G (p.Pro226=) c.114C>G (p.Pro38=) | |
1 | g.12193010C>T | CA416364811 | TNFRSF1B | c.699C>T (p.Pro233=) n.688C>T c.678C>T (p.Pro226=) c.114C>T (p.Pro38=) | |
1 | g.12193011A>C | CA338455949 | TNFRSF1B | c.700A>C (p.Ser234Arg) n.689A>C c.679A>C (p.Ser227Arg) c.115A>C (p.Ser39Arg) | gnomAD v4 |
1 | g.12193011A>G | CA338455947 | TNFRSF1B | c.700A>G (p.Ser234Gly) n.689A>G c.679A>G (p.Ser227Gly) c.115A>G (p.Ser39Gly) | |
1 | g.12193011A>T | CA338455945 | TNFRSF1B | c.700A>T (p.Ser234Cys) n.689A>T c.679A>T (p.Ser227Cys) c.115A>T (p.Ser39Cys) | |
1 | g.12193012G>A | CA600854 | TNFRSF1B | c.701G>A (p.Ser234Asn) n.690G>A c.680G>A (p.Ser227Asn) c.116G>A (p.Ser39Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12193012G>C | CA338455954 | TNFRSF1B | c.701G>C (p.Ser234Thr) n.690G>C c.680G>C (p.Ser227Thr) c.116G>C (p.Ser39Thr) | |
1 | g.12193012G= | CA1154001458 | TNFRSF1B | c.701G= (p.Ser234=) n.690G= c.680G= (p.Ser227=) c.116G= (p.Ser39=) | |
1 | g.12193012G>T | CA338455965 | TNFRSF1B | c.701G>T (p.Ser234Ile) n.690G>T c.680G>T (p.Ser227Ile) c.116G>T (p.Ser39Ile) | |
1 | g.12193013C>A | CA338455972 | TNFRSF1B | c.702C>A (p.Ser234Arg) n.691C>A c.681C>A (p.Ser227Arg) c.117C>A (p.Ser39Arg) | |
1 | g.12193013C>G | CA338455977 | TNFRSF1B | c.702C>G (p.Ser234Arg) n.691C>G c.681C>G (p.Ser227Arg) c.117C>G (p.Ser39Arg) | |
1 | g.12193013C>T | CA416364814 | TNFRSF1B | c.702C>T (p.Ser234=) n.691C>T c.681C>T (p.Ser227=) c.117C>T (p.Ser39=) | |
1 | g.12193014A>C | CA338455984 | TNFRSF1B | c.703A>C (p.Thr235Pro) n.692A>C c.682A>C (p.Thr228Pro) c.118A>C (p.Thr40Pro) | |
1 | g.12193014A>G | CA338455987 | TNFRSF1B | c.703A>G (p.Thr235Ala) n.692A>G c.682A>G (p.Thr228Ala) c.118A>G (p.Thr40Ala) | |
1 | g.12193014A>T | CA338455995 | TNFRSF1B | c.703A>T (p.Thr235Ser) n.692A>T c.682A>T (p.Thr228Ser) c.118A>T (p.Thr40Ser) | |
1 | g.12193015C>A | CA338456009 | TNFRSF1B | c.704C>A (p.Thr235Asn) n.693C>A c.683C>A (p.Thr228Asn) c.119C>A (p.Thr40Asn) | |
1 | g.12193015C= | CA1154001459 | TNFRSF1B | c.704C= (p.Thr235=) n.693C= c.683C= (p.Thr228=) c.119C= (p.Thr40=) | |
1 | g.12193015C>G | CA338456010 | TNFRSF1B | c.704C>G (p.Thr235Ser) n.693C>G c.683C>G (p.Thr228Ser) c.119C>G (p.Thr40Ser) | |
1 | g.12193015C>T | CA338456011 | TNFRSF1B | c.704C>T (p.Thr235Ile) n.693C>T c.683C>T (p.Thr228Ile) c.119C>T (p.Thr40Ile) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.12193016T>A | CA416364815 | TNFRSF1B | c.705T>A (p.Thr235=) n.694T>A c.684T>A (p.Thr228=) c.120T>A (p.Thr40=) | |
1 | g.12193016T>C | CA416364817 | TNFRSF1B | c.705T>C (p.Thr235=) n.694T>C c.684T>C (p.Thr228=) c.120T>C (p.Thr40=) | |
1 | g.12193016T>G | CA416364816 | TNFRSF1B | c.705T>G (p.Thr235=) n.694T>G c.684T>G (p.Thr228=) c.120T>G (p.Thr40=) | |
1 | g.12193017G>A | CA600855 | TNFRSF1B | c.706G>A (p.Ala236Thr) n.695G>A c.685G>A (p.Ala229Thr) c.121G>A (p.Ala41Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12193017G>C | CA338456015 | TNFRSF1B | c.706G>C (p.Ala236Pro) n.695G>C c.685G>C (p.Ala229Pro) c.121G>C (p.Ala41Pro) | |
1 | g.12193017G= | CA1140055750 | TNFRSF1B | c.706G= (p.Ala236=) n.695G= c.685G= (p.Ala229=) c.121G= (p.Ala41=) | |
1 | g.12193017G>T | CA338456017 | TNFRSF1B | c.706G>T (p.Ala236Ser) n.695G>T c.685G>T (p.Ala229Ser) c.121G>T (p.Ala41Ser) | |
1 | g.12193018C>A | CA338456028 | TNFRSF1B | c.707C>A (p.Ala236Asp) n.696C>A c.686C>A (p.Ala229Asp) c.122C>A (p.Ala41Asp) | |
1 | g.12193018C>G | CA338456033 | TNFRSF1B | c.707C>G (p.Ala236Gly) n.696C>G c.686C>G (p.Ala229Gly) c.122C>G (p.Ala41Gly) | |
1 | g.12193018C>T | CA338456025 | TNFRSF1B | c.707C>T (p.Ala236Val) n.696C>T c.686C>T (p.Ala229Val) c.122C>T (p.Ala41Val) | COSMIC |
1 | g.12193019T>A | CA416364818 | TNFRSF1B | c.708T>A (p.Ala236=) n.697T>A c.687T>A (p.Ala229=) c.123T>A (p.Ala41=) | |
1 | g.12193019T>C | CA416364819 | TNFRSF1B | c.708T>C (p.Ala236=) n.697T>C c.687T>C (p.Ala229=) c.123T>C (p.Ala41=) | gnomAD v4 |
1 | g.12193019T>G | CA416364820 | TNFRSF1B | c.708T>G (p.Ala236=) n.697T>G c.687T>G (p.Ala229=) c.123T>G (p.Ala41=) | |
1 | g.12193020C>A | CA338456036 | TNFRSF1B | c.709C>A (p.Pro237Thr) n.698C>A c.688C>A (p.Pro230Thr) c.124C>A (p.Pro42Thr) | |
1 | g.12193020C>G | CA338456038 | TNFRSF1B | c.709C>G (p.Pro237Ala) n.698C>G c.688C>G (p.Pro230Ala) c.124C>G (p.Pro42Ala) | |
1 | g.12193020C>T | CA338456043 | TNFRSF1B | c.709C>T (p.Pro237Ser) n.698C>T c.688C>T (p.Pro230Ser) c.124C>T (p.Pro42Ser) | |
1 | g.12193021C>A | CA338456051 | TNFRSF1B | c.710C>A (p.Pro237Gln) n.699C>A c.689C>A (p.Pro230Gln) c.125C>A (p.Pro42Gln) | |
1 | g.12193021C>G | CA338456052 | TNFRSF1B | c.710C>G (p.Pro237Arg) n.699C>G c.689C>G (p.Pro230Arg) c.125C>G (p.Pro42Arg) | |
1 | g.12193021C>T | CA338456053 | TNFRSF1B | c.710C>T (p.Pro237Leu) n.699C>T c.689C>T (p.Pro230Leu) c.125C>T (p.Pro42Leu) |