Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.12192868A>C | CA338454909 | TNFRSF1B | c.557A>C (p.Asn186Thr) n.269A>C n.546A>C c.536A>C (p.Asn179Thr) c.-29A>C (n.-29A>C) | gnomAD v4 |
1 | g.12192868A>G | CA338454911 | TNFRSF1B | c.557A>G (p.Asn186Ser) n.269A>G n.546A>G c.536A>G (p.Asn179Ser) c.-29A>G (n.-29A>G) | |
1 | g.12192868A>T | CA338454910 | TNFRSF1B | c.557A>T (p.Asn186Ile) n.269A>T n.546A>T c.536A>T (p.Asn179Ile) c.-29A>T (n.-29A>T) | |
1 | g.12192869C>A | CA338454912 | TNFRSF1B | c.558C>A (p.Asn186Lys) n.270C>A n.547C>A c.537C>A (p.Asn179Lys) c.-28C>A (n.-28C>A) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192869C= | CA1144966229 | TNFRSF1B | c.558C= (p.Asn186=) n.270C= n.547C= c.537C= (p.Asn179=) c.-28C= (n.-28C=) | |
1 | g.12192869C>G | CA338454913 | TNFRSF1B | c.558C>G (p.Asn186Lys) n.270C>G n.547C>G c.537C>G (p.Asn179Lys) c.-28C>G (n.-28C>G) | |
1 | g.12192869C>T | CA600824 | TNFRSF1B | c.558C>T (p.Asn186=) n.270C>T n.547C>T c.537C>T (p.Asn179=) c.-28C>T (n.-28C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192869_12192872delinsCGTG | CA1154001412 | TNFRSF1B | c.558_561delinsCGTG (p.Asn186=) n.270_273delinsCGTG n.547_550delinsCGTG c.537_540delinsCGTG (p.Asn179=) c.-28_-25delinsCGTG (n.-28_-25delinsCGTG) | |
1 | g.12192870G>A | CA600826 | TNFRSF1B | c.559G>A (p.Val187Met) n.271G>A n.548G>A c.538G>A (p.Val180Met) c.-27G>A (n.-27G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192870G>C | CA338454914 | TNFRSF1B | c.559G>C (p.Val187Leu) n.271G>C n.548G>C c.538G>C (p.Val180Leu) c.-27G>C (n.-27G>C) | |
1 | g.12192870G= | CA1139921333 | TNFRSF1B | c.559G= (p.Val187=) n.271G= n.548G= c.538G= (p.Val180=) c.-27G= (n.-27G=) | |
1 | g.12192870G>T | CA338454915 | TNFRSF1B | c.559G>T (p.Val187Leu) n.271G>T n.548G>T c.538G>T (p.Val180Leu) c.-27G>T (n.-27G>T) | |
1 | g.12192874_12192876del | CA600825 | TNFRSF1B | c.563_565del (p.Val188del) n.275_277del n.552_554del c.542_544del (p.Val181del) c.-23_-21del (n.-23_-21del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192871T>A | CA338454916 | TNFRSF1B | c.560T>A (p.Val187Glu) n.272T>A n.549T>A c.539T>A (p.Val180Glu) c.-26T>A (n.-26T>A) | dbSNP gnomAD v4 |
1 | g.12192871T>C | CA600827 | TNFRSF1B | c.560T>C (p.Val187Ala) n.272T>C n.549T>C c.539T>C (p.Val180Ala) c.-26T>C (n.-26T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192871T>G | CA338454917 | TNFRSF1B | c.560T>G (p.Val187Gly) n.272T>G n.549T>G c.539T>G (p.Val180Gly) c.-26T>G (n.-26T>G) | |
1 | g.12192871T= | CA1148263909 | TNFRSF1B | c.560T= (p.Val187=) n.272T= n.549T= c.539T= (p.Val180=) c.-26T= (n.-26T=) | |
1 | g.12192872G>A | CA416364709 | TNFRSF1B | c.561G>A (p.Val187=) n.273G>A n.550G>A c.540G>A (p.Val180=) c.-25G>A (n.-25G>A) | |
1 | g.12192872G>C | CA416364710 | TNFRSF1B | c.561G>C (p.Val187=) n.273G>C n.550G>C c.540G>C (p.Val180=) c.-25G>C (n.-25G>C) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192872G= | CA1154001413 | TNFRSF1B | c.561G= (p.Val187=) n.273G= n.550G= c.540G= (p.Val180=) c.-25G= (n.-25G=) | |
1 | g.12192872G>T | CA416364711 | TNFRSF1B | c.561G>T (p.Val187=) n.273G>T n.550G>T c.540G>T (p.Val180=) c.-25G>T (n.-25G>T) | |
1 | g.12192873G>A | CA338454919 | TNFRSF1B | c.562G>A (p.Val188Met) n.274G>A n.551G>A c.541G>A (p.Val181Met) c.-24G>A (n.-24G>A) | |
1 | g.12192873G>C | CA338454920 | TNFRSF1B | c.562G>C (p.Val188Leu) n.274G>C n.551G>C c.541G>C (p.Val181Leu) c.-24G>C (n.-24G>C) | |
1 | g.12192873G>T | CA338454918 | TNFRSF1B | c.562G>T (p.Val188Leu) n.274G>T n.551G>T c.541G>T (p.Val181Leu) c.-24G>T (n.-24G>T) | |
1 | g.12192874T>A | CA338454921 | TNFRSF1B | c.563T>A (p.Val188Glu) n.275T>A n.552T>A c.542T>A (p.Val181Glu) c.-23T>A (n.-23T>A) | |
1 | g.12192874T>C | CA338454922 | TNFRSF1B | c.563T>C (p.Val188Ala) n.275T>C n.552T>C c.542T>C (p.Val181Ala) c.-23T>C (n.-23T>C) | |
1 | g.12192874T>G | CA338454923 | TNFRSF1B | c.563T>G (p.Val188Gly) n.275T>G n.552T>G c.542T>G (p.Val181Gly) c.-23T>G (n.-23T>G) | |
1 | g.12192875G>A | CA416364712 | TNFRSF1B | c.564G>A (p.Val188=) n.276G>A n.553G>A c.543G>A (p.Val181=) c.-22G>A (n.-22G>A) | |
1 | g.12192875G>C | CA416364713 | TNFRSF1B | c.564G>C (p.Val188=) n.276G>C n.553G>C c.543G>C (p.Val181=) c.-22G>C (n.-22G>C) | |
1 | g.12192875G>T | CA416364714 | TNFRSF1B | c.564G>T (p.Val188=) n.276G>T n.553G>T c.543G>T (p.Val181=) c.-22G>T (n.-22G>T) | |
1 | g.12192876G>A | CA600828 | TNFRSF1B | c.565G>A (p.Ala189Thr) n.277G>A n.554G>A c.544G>A (p.Ala182Thr) c.-21G>A (n.-21G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192876G>C | CA338454924 | TNFRSF1B | c.565G>C (p.Ala189Pro) n.277G>C n.554G>C c.544G>C (p.Ala182Pro) c.-21G>C (n.-21G>C) | |
1 | g.12192876G= | CA1143405249 | TNFRSF1B | c.565G= (p.Ala189=) n.277G= n.554G= c.544G= (p.Ala182=) c.-21G= (n.-21G=) | |
1 | g.12192876G>T | CA338454925 | TNFRSF1B | c.565G>T (p.Ala189Ser) n.277G>T n.554G>T c.544G>T (p.Ala182Ser) c.-21G>T (n.-21G>T) | dbSNP |
1 | g.12192877C>A | CA338454926 | TNFRSF1B | c.566C>A (p.Ala189Asp) n.278C>A n.555C>A c.545C>A (p.Ala182Asp) c.-20C>A (n.-20C>A) | gnomAD v4 |
1 | g.12192877C>G | CA338454927 | TNFRSF1B | c.566C>G (p.Ala189Gly) n.278C>G n.555C>G c.545C>G (p.Ala182Gly) c.-20C>G (n.-20C>G) | |
1 | g.12192877C>T | CA338454928 | TNFRSF1B | c.566C>T (p.Ala189Val) n.278C>T n.555C>T c.545C>T (p.Ala182Val) c.-20C>T (n.-20C>T) | gnomAD v4 |
1 | g.12192878C>A | CA416364717 | TNFRSF1B | c.567C>A (p.Ala189=) n.279C>A n.556C>A c.546C>A (p.Ala182=) c.-19C>A (n.-19C>A) | |
1 | g.12192878C>G | CA416364716 | TNFRSF1B | c.567C>G (p.Ala189=) n.279C>G n.556C>G c.546C>G (p.Ala182=) c.-19C>G (n.-19C>G) | |
1 | g.12192878C>T | CA416364715 | TNFRSF1B | c.567C>T (p.Ala189=) n.279C>T n.556C>T c.546C>T (p.Ala182=) c.-19C>T (n.-19C>T) | |
1 | g.12192879A>C | CA338454929 | TNFRSF1B | c.568A>C (p.Ile190Leu) n.280A>C n.557A>C c.547A>C (p.Ile183Leu) c.-18A>C (n.-18A>C) | |
1 | g.12192879A>G | CA338454930 | TNFRSF1B | c.568A>G (p.Ile190Val) n.280A>G n.557A>G c.547A>G (p.Ile183Val) c.-18A>G (n.-18A>G) | |
1 | g.12192879A>T | CA338454931 | TNFRSF1B | c.568A>T (p.Ile190Phe) n.280A>T n.557A>T c.547A>T (p.Ile183Phe) c.-18A>T (n.-18A>T) | |
1 | g.12192880T>A | CA338454933 | TNFRSF1B | c.569T>A (p.Ile190Asn) n.281T>A n.558T>A c.548T>A (p.Ile183Asn) c.-17T>A (n.-17T>A) | gnomAD v4 |
1 | g.12192880T>C | CA338454934 | TNFRSF1B | c.569T>C (p.Ile190Thr) n.281T>C n.558T>C c.548T>C (p.Ile183Thr) c.-17T>C (n.-17T>C) | |
1 | g.12192880T>G | CA338454932 | TNFRSF1B | c.569T>G (p.Ile190Ser) n.281T>G n.558T>G c.548T>G (p.Ile183Ser) c.-17T>G (n.-17T>G) | |
1 | g.12192881C>A | CA416364718 | TNFRSF1B | c.570C>A (p.Ile190=) n.282C>A n.559C>A c.549C>A (p.Ile183=) c.-16C>A (n.-16C>A) | |
1 | g.12192881C= | CA1154001414 | TNFRSF1B | c.570C= (p.Ile190=) n.282C= n.559C= c.549C= (p.Ile183=) c.-16C= (n.-16C=) | |
1 | g.12192881C>G | CA338454935 | TNFRSF1B | c.570C>G (p.Ile190Met) n.282C>G n.559C>G c.549C>G (p.Ile183Met) c.-16C>G (n.-16C>G) | |
1 | g.12192881C>T | CA416364719 | TNFRSF1B | c.570C>T (p.Ile190=) n.282C>T n.559C>T c.549C>T (p.Ile183=) c.-16C>T (n.-16C>T) | dbSNP gnomAD v2 |
1 | g.12192882C>A | CA338454936 | TNFRSF1B | c.571C>A (p.Pro191Thr) n.283C>A n.560C>A c.550C>A (p.Pro184Thr) c.-15C>A (n.-15C>A) | |
1 | g.12192882C= | CA1154001415 | TNFRSF1B | c.571C= (p.Pro191=) n.283C= n.560C= c.550C= (p.Pro184=) c.-15C= (n.-15C=) | |
1 | g.12192882C>G | CA600829 | TNFRSF1B | c.571C>G (p.Pro191Ala) n.283C>G n.560C>G c.550C>G (p.Pro184Ala) c.-15C>G (n.-15C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.12192882C>T | CA338454937 | TNFRSF1B | c.571C>T (p.Pro191Ser) n.283C>T n.560C>T c.550C>T (p.Pro184Ser) c.-15C>T (n.-15C>T) | |
1 | g.12192883C>A | CA338454940 | TNFRSF1B | c.572C>A (p.Pro191His) n.284C>A n.561C>A c.551C>A (p.Pro184His) c.-14C>A (n.-14C>A) | |
1 | g.12192883C>G | CA338454939 | TNFRSF1B | c.572C>G (p.Pro191Arg) n.284C>G n.561C>G c.551C>G (p.Pro184Arg) c.-14C>G (n.-14C>G) | |
1 | g.12192883C>T | CA338454938 | TNFRSF1B | c.572C>T (p.Pro191Leu) n.284C>T n.561C>T c.551C>T (p.Pro184Leu) c.-14C>T (n.-14C>T) | |
1 | g.12192884T>A | CA416364720 | TNFRSF1B | c.573T>A (p.Pro191=) n.285T>A n.562T>A c.552T>A (p.Pro184=) c.-13T>A (n.-13T>A) | |
1 | g.12192884T>C | CA416364721 | TNFRSF1B | c.573T>C (p.Pro191=) n.285T>C n.562T>C c.552T>C (p.Pro184=) c.-13T>C (n.-13T>C) | gnomAD v4 |
1 | g.12192884T>G | CA18022029 | TNFRSF1B | c.573T>G (p.Pro191=) n.285T>G n.562T>G c.552T>G (p.Pro184=) c.-13T>G (n.-13T>G) | dbSNP gnomAD v4 |
1 | g.12192884T= | CA1144994179 | TNFRSF1B | c.573T= (p.Pro191=) n.285T= n.562T= c.552T= (p.Pro184=) c.-13T= (n.-13T=) | |
1 | g.12192885G>A | CA338454941 | TNFRSF1B | c.574G>A (p.Gly192Arg) n.286G>A n.563G>A c.553G>A (p.Gly185Arg) c.-12G>A (n.-12G>A) | |
1 | g.12192885G>C | CA338454942 | TNFRSF1B | c.574G>C (p.Gly192Arg) n.286G>C n.563G>C c.553G>C (p.Gly185Arg) c.-12G>C (n.-12G>C) | |
1 | g.12192885G>T | CA338454943 | TNFRSF1B | c.574G>T (p.Gly192Trp) n.286G>T n.563G>T c.553G>T (p.Gly185Trp) c.-12G>T (n.-12G>T) | |
1 | g.12192886G>A | CA338454944 | TNFRSF1B | c.575G>A (p.Gly192Glu) n.287G>A n.564G>A c.554G>A (p.Gly185Glu) c.-11G>A (n.-11G>A) | |
1 | g.12192886G>C | CA338454945 | TNFRSF1B | c.575G>C (p.Gly192Ala) n.287G>C n.564G>C c.554G>C (p.Gly185Ala) c.-11G>C (n.-11G>C) | |
1 | g.12192886G>T | CA338454946 | TNFRSF1B | c.575G>T (p.Gly192Val) n.287G>T n.564G>T c.554G>T (p.Gly185Val) c.-11G>T (n.-11G>T) | |
1 | g.12192887G>A | CA416364724 | TNFRSF1B | c.576G>A (p.Gly192=) n.288G>A n.565G>A c.555G>A (p.Gly185=) c.-10G>A (n.-10G>A) | gnomAD v4 |
1 | g.12192887G>C | CA416364723 | TNFRSF1B | c.576G>C (p.Gly192=) n.288G>C n.565G>C c.555G>C (p.Gly185=) c.-10G>C (n.-10G>C) | |
1 | g.12192887G>T | CA416364722 | TNFRSF1B | c.576G>T (p.Gly192=) n.288G>T n.565G>T c.555G>T (p.Gly185=) c.-10G>T (n.-10G>T) | |
1 | g.12192888A>C | CA338454948 | TNFRSF1B | c.577A>C (p.Asn193His) n.289A>C n.566A>C c.556A>C (p.Asn186His) c.-9A>C (n.-9A>C) | |
1 | g.12192888A>G | CA338454949 | TNFRSF1B | c.577A>G (p.Asn193Asp) n.289A>G n.566A>G c.556A>G (p.Asn186Asp) c.-9A>G (n.-9A>G) | |
1 | g.12192888A>T | CA338454947 | TNFRSF1B | c.577A>T (p.Asn193Tyr) n.289A>T n.566A>T c.556A>T (p.Asn186Tyr) c.-9A>T (n.-9A>T) | |
1 | g.12192889A>C | CA338454951 | TNFRSF1B | c.578A>C (p.Asn193Thr) n.290A>C n.567A>C c.557A>C (p.Asn186Thr) c.-8A>C (n.-8A>C) | gnomAD v4 |
1 | g.12192889A>G | CA338454950 | TNFRSF1B | c.578A>G (p.Asn193Ser) n.290A>G n.567A>G c.557A>G (p.Asn186Ser) c.-8A>G (n.-8A>G) | |
1 | g.12192889A>T | CA338454952 | TNFRSF1B | c.578A>T (p.Asn193Ile) n.290A>T n.567A>T c.557A>T (p.Asn186Ile) c.-8A>T (n.-8A>T) | |
1 | g.12192890T>A | CA338454953 | TNFRSF1B | c.579T>A (p.Asn193Lys) n.291T>A n.568T>A c.558T>A (p.Asn186Lys) c.-7T>A (n.-7T>A) | |
1 | g.12192890T>C | CA416364725 | TNFRSF1B | c.579T>C (p.Asn193=) n.291T>C n.568T>C c.558T>C (p.Asn186=) c.-7T>C (n.-7T>C) | |
1 | g.12192890T>G | CA338454954 | TNFRSF1B | c.579T>G (p.Asn193Lys) n.291T>G n.568T>G c.558T>G (p.Asn186Lys) c.-7T>G (n.-7T>G) | gnomAD v4 |
1 | g.12192891G>A | CA338454955 | TNFRSF1B | c.580G>A (p.Ala194Thr) n.292G>A n.569G>A c.559G>A (p.Ala187Thr) c.-6G>A (n.-6G>A) | |
1 | g.12192891G>C | CA338454957 | TNFRSF1B | c.580G>C (p.Ala194Pro) n.292G>C n.569G>C c.559G>C (p.Ala187Pro) c.-6G>C (n.-6G>C) | |
1 | g.12192891G>T | CA338454956 | TNFRSF1B | c.580G>T (p.Ala194Ser) n.292G>T n.569G>T c.559G>T (p.Ala187Ser) c.-6G>T (n.-6G>T) | |
1 | g.12192892C>A | CA338454958 | TNFRSF1B | c.581C>A (p.Ala194Glu) n.293C>A n.570C>A c.560C>A (p.Ala187Glu) c.-5C>A (n.-5C>A) | |
1 | g.12192892C>G | CA338454960 | TNFRSF1B | c.581C>G (p.Ala194Gly) n.293C>G n.570C>G c.560C>G (p.Ala187Gly) c.-5C>G (n.-5C>G) | |
1 | g.12192892C>T | CA338454959 | TNFRSF1B | c.581C>T (p.Ala194Val) n.293C>T n.570C>T c.560C>T (p.Ala187Val) c.-5C>T (n.-5C>T) | gnomAD v4 |
1 | g.12192893A>C | CA416364726 | TNFRSF1B | c.582A>C (p.Ala194=) n.294A>C n.571A>C c.561A>C (p.Ala187=) c.-4A>C (n.-4A>C) | |
1 | g.12192893A>G | CA416364727 | TNFRSF1B | c.582A>G (p.Ala194=) n.294A>G n.571A>G c.561A>G (p.Ala187=) c.-4A>G (n.-4A>G) | |
1 | g.12192893A>T | CA416364728 | TNFRSF1B | c.582A>T (p.Ala194=) n.294A>T n.571A>T c.561A>T (p.Ala187=) c.-4A>T (n.-4A>T) | |
1 | g.12192894A>C | CA338454961 | TNFRSF1B | c.583A>C (p.Ser195Arg) n.295A>C n.572A>C c.562A>C (p.Ser188Arg) c.-3A>C (n.-3A>C) | |
1 | g.12192894A>G | CA338454963 | TNFRSF1B | c.583A>G (p.Ser195Gly) n.295A>G n.572A>G c.562A>G (p.Ser188Gly) c.-3A>G (n.-3A>G) | |
1 | g.12192894A>T | CA338454962 | TNFRSF1B | c.583A>T (p.Ser195Cys) n.295A>T n.572A>T c.562A>T (p.Ser188Cys) c.-3A>T (n.-3A>T) | |
1 | g.12192895G>A | CA338454964 | TNFRSF1B | c.584G>A (p.Ser195Asn) n.296G>A n.573G>A c.563G>A (p.Ser188Asn) c.-2G>A (n.-2G>A) | |
1 | g.12192895G>C | CA338454968 | TNFRSF1B | c.584G>C (p.Ser195Thr) n.296G>C n.573G>C c.563G>C (p.Ser188Thr) c.-2G>C (n.-2G>C) | |
1 | g.12192895G>T | CA338454966 | TNFRSF1B | c.584G>T (p.Ser195Ile) n.296G>T n.573G>T c.563G>T (p.Ser188Ile) c.-2G>T (n.-2G>T) | |
1 | g.12192896C>A | CA338454970 | TNFRSF1B | c.585C>A (p.Ser195Arg) n.297C>A n.574C>A c.564C>A (p.Ser188Arg) c.-1C>A (n.-1C>A) | |
1 | g.12192896C= | CA1154001416 | TNFRSF1B | c.585C= (p.Ser195=) n.297C= n.574C= c.564C= (p.Ser188=) c.-1C= (n.-1C=) | |
1 | g.12192896C>G | CA338454971 | TNFRSF1B | c.585C>G (p.Ser195Arg) n.297C>G n.574C>G c.564C>G (p.Ser188Arg) c.-1C>G (n.-1C>G) | |
1 | g.12192896C>T | CA18022034 | TNFRSF1B | c.585C>T (p.Ser195=) n.297C>T n.574C>T c.564C>T (p.Ser188=) c.-1C>T (n.-1C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192897A= | CA1154001417 | TNFRSF1B | c.586A= (p.Met196=) n.298A= n.575A= c.565A= (p.Met189=) c.1A= (p.Met1=) | |
1 | g.12192897A>C | CA338454974 | TNFRSF1B | c.586A>C (p.Met196Leu) n.298A>C n.575A>C c.565A>C (p.Met189Leu) c.1A>C (p.Met1Leu) | dbSNP gnomAD v4 |
1 | g.12192897A>G | CA338454976 | TNFRSF1B | c.586A>G (p.Met196Val) n.298A>G n.575A>G c.565A>G (p.Met189Val) c.1A>G (p.Met1Val) | |
1 | g.12192897A>T | CA338454978 | TNFRSF1B | c.586A>T (p.Met196Leu) n.298A>T n.575A>T c.565A>T (p.Met189Leu) c.1A>T (p.Met1Leu) | |
1 | g.12192898T>A | CA338454980 | TNFRSF1B | c.587T>A (p.Met196Lys) n.299T>A n.576T>A c.566T>A (p.Met189Lys) c.2T>A (p.Met1Lys) | |
1 | g.12192898T>C | CA338454982 | TNFRSF1B | c.587T>C (p.Met196Thr) n.299T>C n.576T>C c.566T>C (p.Met189Thr) c.2T>C (p.Met1Thr) | |
1 | g.12192898T>G | CA600830 | TNFRSF1B | c.587T>G (p.Met196Arg) n.299T>G n.576T>G c.566T>G (p.Met189Arg) c.2T>G (p.Met1Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192898T= | CA1139849752 | TNFRSF1B | c.587T= (p.Met196=) n.299T= n.576T= c.566T= (p.Met189=) c.2T= (p.Met1=) | |
1 | g.12192899G>A | CA600831 | TNFRSF1B | c.588G>A (p.Met196Ile) n.300G>A n.577G>A c.567G>A (p.Met189Ile) c.3G>A (p.Met1Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192899G>C | CA338454987 | TNFRSF1B | c.588G>C (p.Met196Ile) n.300G>C n.577G>C c.567G>C (p.Met189Ile) c.3G>C (p.Met1Ile) | |
1 | g.12192899G= | CA1154001418 | TNFRSF1B | c.588G= (p.Met196=) n.300G= n.577G= c.567G= (p.Met189=) c.3G= (p.Met1=) | |
1 | g.12192899G>T | CA338454990 | TNFRSF1B | c.588G>T (p.Met196Ile) n.300G>T n.577G>T c.567G>T (p.Met189Ile) c.3G>T (p.Met1Ile) | |
1 | g.12192900G>A | CA338454997 | TNFRSF1B | c.589G>A (p.Asp197Asn) n.301G>A n.578G>A c.568G>A (p.Asp190Asn) c.4G>A (p.Asp2Asn) | |
1 | g.12192900G>C | CA338454995 | TNFRSF1B | c.589G>C (p.Asp197His) n.301G>C n.578G>C c.568G>C (p.Asp190His) c.4G>C (p.Asp2His) | |
1 | g.12192900G>T | CA338454992 | TNFRSF1B | c.589G>T (p.Asp197Tyr) n.301G>T n.578G>T c.568G>T (p.Asp190Tyr) c.4G>T (p.Asp2Tyr) | |
1 | g.12192901A= | CA1154001419 | TNFRSF1B | c.590A= (p.Asp197=) n.302A= n.579A= c.569A= (p.Asp190=) c.5A= (p.Asp2=) | |
1 | g.12192901A>C | CA338455000 | TNFRSF1B | c.590A>C (p.Asp197Ala) n.302A>C n.579A>C c.569A>C (p.Asp190Ala) c.5A>C (p.Asp2Ala) | |
1 | g.12192901A>G | CA338455002 | TNFRSF1B | c.590A>G (p.Asp197Gly) n.302A>G n.579A>G c.569A>G (p.Asp190Gly) c.5A>G (p.Asp2Gly) | gnomAD v4 |
1 | g.12192901A>T | CA338455004 | TNFRSF1B | c.590A>T (p.Asp197Val) n.302A>T n.579A>T c.569A>T (p.Asp190Val) c.5A>T (p.Asp2Val) | dbSNP gnomAD v4 |
1 | g.12192902T>A | CA338455006 | TNFRSF1B | c.591T>A (p.Asp197Glu) n.303T>A n.580T>A c.570T>A (p.Asp190Glu) c.6T>A (p.Asp2Glu) | gnomAD v4 |
1 | g.12192902T>C | CA416364729 | TNFRSF1B | c.591T>C (p.Asp197=) n.303T>C n.580T>C c.570T>C (p.Asp190=) c.6T>C (p.Asp2=) | |
1 | g.12192902T>G | CA338455007 | TNFRSF1B | c.591T>G (p.Asp197Glu) n.303T>G n.580T>G c.570T>G (p.Asp190Glu) c.6T>G (p.Asp2Glu) | |
1 | g.12192903G>A | CA338455009 | TNFRSF1B | c.592G>A (p.Ala198Thr) n.304G>A n.581G>A c.571G>A (p.Ala191Thr) c.7G>A (p.Ala3Thr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192903G>C | CA338455011 | TNFRSF1B | c.592G>C (p.Ala198Pro) n.304G>C n.581G>C c.571G>C (p.Ala191Pro) c.7G>C (p.Ala3Pro) | |
1 | g.12192903G= | CA1154001420 | TNFRSF1B | c.592G= (p.Ala198=) n.304G= n.581G= c.571G= (p.Ala191=) c.7G= (p.Ala3=) | |
1 | g.12192903G>T | CA338455012 | TNFRSF1B | c.592G>T (p.Ala198Ser) n.304G>T n.581G>T c.571G>T (p.Ala191Ser) c.7G>T (p.Ala3Ser) | |
1 | g.12192904C>A | CA338455015 | TNFRSF1B | c.593C>A (p.Ala198Glu) n.305C>A n.582C>A c.572C>A (p.Ala191Glu) c.8C>A (p.Ala3Glu) | |
1 | g.12192904C= | CA1154001421 | TNFRSF1B | c.593C= (p.Ala198=) n.305C= n.582C= c.572C= (p.Ala191=) c.8C= (p.Ala3=) | |
1 | g.12192904C>G | CA338455017 | TNFRSF1B | c.593C>G (p.Ala198Gly) n.305C>G n.582C>G c.572C>G (p.Ala191Gly) c.8C>G (p.Ala3Gly) | |
1 | g.12192904C>T | CA18022060 | TNFRSF1B | c.593C>T (p.Ala198Val) n.305C>T n.582C>T c.572C>T (p.Ala191Val) c.8C>T (p.Ala3Val) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192905A>C | CA416364730 | TNFRSF1B | c.594A>C (p.Ala198=) n.306A>C n.583A>C c.573A>C (p.Ala191=) c.9A>C (p.Ala3=) | |
1 | g.12192905A>G | CA416364732 | TNFRSF1B | c.594A>G (p.Ala198=) n.306A>G n.583A>G c.573A>G (p.Ala191=) c.9A>G (p.Ala3=) | |
1 | g.12192905A>T | CA416364731 | TNFRSF1B | c.594A>T (p.Ala198=) n.306A>T n.583A>T c.573A>T (p.Ala191=) c.9A>T (p.Ala3=) | |
1 | g.12192906G>A | CA338455022 | TNFRSF1B | c.595G>A (p.Val199Ile) n.307G>A n.584G>A c.574G>A (p.Val192Ile) c.10G>A (p.Val4Ile) | |
1 | g.12192906G>C | CA338455021 | TNFRSF1B | c.595G>C (p.Val199Leu) n.307G>C n.584G>C c.574G>C (p.Val192Leu) c.10G>C (p.Val4Leu) | |
1 | g.12192906G>T | CA338455019 | TNFRSF1B | c.595G>T (p.Val199Phe) n.307G>T n.584G>T c.574G>T (p.Val192Phe) c.10G>T (p.Val4Phe) | |
1 | g.12192907T>A | CA338455026 | TNFRSF1B | c.596T>A (p.Val199Asp) n.308T>A n.585T>A c.575T>A (p.Val192Asp) c.11T>A (p.Val4Asp) | |
1 | g.12192907T>C | CA338455027 | TNFRSF1B | c.596T>C (p.Val199Ala) n.308T>C n.585T>C c.575T>C (p.Val192Ala) c.11T>C (p.Val4Ala) | |
1 | g.12192907T>G | CA338455029 | TNFRSF1B | c.596T>G (p.Val199Gly) n.308T>G n.585T>G c.575T>G (p.Val192Gly) c.11T>G (p.Val4Gly) | |
1 | g.12192908C>A | CA416364733 | TNFRSF1B | c.597C>A (p.Val199=) n.309C>A n.586C>A c.576C>A (p.Val192=) c.12C>A (p.Val4=) | |
1 | g.12192908C>G | CA416364734 | TNFRSF1B | c.597C>G (p.Val199=) n.309C>G n.586C>G c.576C>G (p.Val192=) c.12C>G (p.Val4=) | |
1 | g.12192908C>T | CA416364735 | TNFRSF1B | c.597C>T (p.Val199=) n.309C>T n.586C>T c.576C>T (p.Val192=) c.12C>T (p.Val4=) | |
1 | g.12192909T>A | CA338455032 | TNFRSF1B | c.598T>A (p.Cys200Ser) n.310T>A n.587T>A c.577T>A (p.Cys193Ser) c.13T>A (p.Cys5Ser) | |
1 | g.12192909T>C | CA338455033 | TNFRSF1B | c.598T>C (p.Cys200Arg) n.310T>C n.587T>C c.577T>C (p.Cys193Arg) c.13T>C (p.Cys5Arg) | |
1 | g.12192909T>G | CA338455035 | TNFRSF1B | c.598T>G (p.Cys200Gly) n.310T>G n.587T>G c.577T>G (p.Cys193Gly) c.13T>G (p.Cys5Gly) | |
1 | g.12192910G>A | CA338455037 | TNFRSF1B | c.599G>A (p.Cys200Tyr) n.311G>A n.588G>A c.578G>A (p.Cys193Tyr) c.14G>A (p.Cys5Tyr) | |
1 | g.12192910G>C | CA338455038 | TNFRSF1B | c.599G>C (p.Cys200Ser) n.311G>C n.588G>C c.578G>C (p.Cys193Ser) c.14G>C (p.Cys5Ser) | |
1 | g.12192910G>T | CA338455039 | TNFRSF1B | c.599G>T (p.Cys200Phe) n.311G>T n.588G>T c.578G>T (p.Cys193Phe) c.14G>T (p.Cys5Phe) | |
1 | g.12192911C>A | CA338455040 | TNFRSF1B | c.600C>A (p.Cys200Ter) n.312C>A n.589C>A c.579C>A (p.Cys193Ter) c.15C>A (p.Cys5Ter) | |
1 | g.12192911C>G | CA338455042 | TNFRSF1B | c.600C>G (p.Cys200Trp) n.312C>G n.589C>G c.579C>G (p.Cys193Trp) c.15C>G (p.Cys5Trp) | |
1 | g.12192911C>T | CA416364736 | TNFRSF1B | c.600C>T (p.Cys200=) n.312C>T n.589C>T c.579C>T (p.Cys193=) c.15C>T (p.Cys5=) | COSMIC |
1 | g.12192912A>C | CA338455049 | TNFRSF1B | c.601A>C (p.Thr201Pro) n.313A>C n.590A>C c.580A>C (p.Thr194Pro) c.16A>C (p.Thr6Pro) | |
1 | g.12192912A>G | CA338455047 | TNFRSF1B | c.601A>G (p.Thr201Ala) n.313A>G n.590A>G c.580A>G (p.Thr194Ala) c.16A>G (p.Thr6Ala) | |
1 | g.12192912A>T | CA338455045 | TNFRSF1B | c.601A>T (p.Thr201Ser) n.313A>T n.590A>T c.580A>T (p.Thr194Ser) c.16A>T (p.Thr6Ser) | |
1 | g.12192913C>A | CA338455051 | TNFRSF1B | c.602C>A (p.Thr201Lys) n.314C>A n.591C>A c.581C>A (p.Thr194Lys) c.17C>A (p.Thr6Lys) | |
1 | g.12192913C= | CA1154001422 | TNFRSF1B | c.602C= (p.Thr201=) n.314C= n.591C= c.581C= (p.Thr194=) c.17C= (p.Thr6=) | |
1 | g.12192913C>G | CA338455053 | TNFRSF1B | c.602C>G (p.Thr201Arg) n.314C>G n.591C>G c.581C>G (p.Thr194Arg) c.17C>G (p.Thr6Arg) | ClinVar gnomAD v4 |
1 | g.12192913C>T | CA18022061 | TNFRSF1B | c.602C>T (p.Thr201Met) n.314C>T n.591C>T c.581C>T (p.Thr194Met) c.17C>T (p.Thr6Met) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.12192914G>A | CA416364737 | TNFRSF1B | c.603G>A (p.Thr201=) n.315G>A n.592G>A c.582G>A (p.Thr194=) c.18G>A (p.Thr6=) | dbSNP gnomAD v4 COSMIC |
1 | g.12192914G>C | CA416364738 | TNFRSF1B | c.603G>C (p.Thr201=) n.315G>C n.592G>C c.582G>C (p.Thr194=) c.18G>C (p.Thr6=) | |
1 | g.12192914G= | CA1154001423 | TNFRSF1B | c.603G= (p.Thr201=) n.315G= n.592G= c.582G= (p.Thr194=) c.18G= (p.Thr6=) | |
1 | g.12192914G>T | CA416364739 | TNFRSF1B | c.603G>T (p.Thr201=) n.315G>T n.592G>T c.582G>T (p.Thr194=) c.18G>T (p.Thr6=) | |
1 | g.12192915T>A | CA338455062 | TNFRSF1B | c.604T>A (p.Ser202Thr) n.316T>A n.593T>A c.583T>A (p.Ser195Thr) c.19T>A (p.Ser7Thr) | |
1 | g.12192915T>C | CA338455064 | TNFRSF1B | c.604T>C (p.Ser202Pro) n.316T>C n.593T>C c.583T>C (p.Ser195Pro) c.19T>C (p.Ser7Pro) | |
1 | g.12192915T>G | CA338455066 | TNFRSF1B | c.604T>G (p.Ser202Ala) n.316T>G n.593T>G c.583T>G (p.Ser195Ala) c.19T>G (p.Ser7Ala) | |
1 | g.12192916C>A | CA338455073 | TNFRSF1B | c.605C>A (p.Ser202Tyr) n.317C>A n.594C>A c.584C>A (p.Ser195Tyr) c.20C>A (p.Ser7Tyr) | |
1 | g.12192916C>G | CA338455074 | TNFRSF1B | c.605C>G (p.Ser202Cys) n.317C>G n.594C>G c.584C>G (p.Ser195Cys) c.20C>G (p.Ser7Cys) | |
1 | g.12192916C>T | CA338455077 | TNFRSF1B | c.605C>T (p.Ser202Phe) n.317C>T n.594C>T c.584C>T (p.Ser195Phe) c.20C>T (p.Ser7Phe) | |
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.12192917C>A | CA416364740 | TNFRSF1B | c.606C>A (p.Ser202=) n.318C>A n.595C>A c.585C>A (p.Ser195=) c.21C>A (p.Ser7=) | |
1 | g.12192917C= | CA1154001424 | TNFRSF1B | c.606C= (p.Ser202=) n.318C= n.595C= c.585C= (p.Ser195=) c.21C= (p.Ser7=) | |
1 | g.12192917C>G | CA416364741 | TNFRSF1B | c.606C>G (p.Ser202=) n.318C>G n.595C>G c.585C>G (p.Ser195=) c.21C>G (p.Ser7=) | |
1 | g.12192917C>T | CA416364742 | TNFRSF1B | c.606C>T (p.Ser202=) n.318C>T n.595C>T c.585C>T (p.Ser195=) c.21C>T (p.Ser7=) | dbSNP |
1 | g.12192918A>C | CA338455079 | TNFRSF1B | c.607A>C (p.Thr203Pro) n.319A>C n.596A>C c.586A>C (p.Thr196Pro) c.22A>C (p.Thr8Pro) | |
1 | g.12192918A>G | CA338455084 | TNFRSF1B | c.607A>G (p.Thr203Ala) n.319A>G n.596A>G c.586A>G (p.Thr196Ala) c.22A>G (p.Thr8Ala) | |
1 | g.12192918A>T | CA338455086 | TNFRSF1B | c.607A>T (p.Thr203Ser) n.319A>T n.596A>T c.586A>T (p.Thr196Ser) c.22A>T (p.Thr8Ser) | |
1 | g.12192919C>A | CA338455100 | TNFRSF1B | c.608C>A (p.Thr203Lys) n.320C>A n.597C>A c.587C>A (p.Thr196Lys) c.23C>A (p.Thr8Lys) | |
1 | g.12192919C= | CA1143379683 | TNFRSF1B | c.608C= (p.Thr203=) n.320C= n.597C= c.587C= (p.Thr196=) c.23C= (p.Thr8=) | |
1 | g.12192919C>G | CA338455098 | TNFRSF1B | c.608C>G (p.Thr203Arg) n.320C>G n.597C>G c.587C>G (p.Thr196Arg) c.23C>G (p.Thr8Arg) | |
1 | g.12192919C>T | CA600832 | TNFRSF1B | c.608C>T (p.Thr203Met) n.320C>T n.597C>T c.587C>T (p.Thr196Met) c.23C>T (p.Thr8Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.12192920G>A | CA600833 | TNFRSF1B | c.609G>A (p.Thr203=) n.321G>A n.598G>A c.588G>A (p.Thr196=) c.24G>A (p.Thr8=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.12192920G>C | CA416364743 | TNFRSF1B | c.609G>C (p.Thr203=) n.321G>C n.598G>C c.588G>C (p.Thr196=) c.24G>C (p.Thr8=) | |
1 | g.12192920G= | CA1154001425 | TNFRSF1B | c.609G= (p.Thr203=) n.321G= n.598G= c.588G= (p.Thr196=) c.24G= (p.Thr8=) | |
1 | g.12192920G>T | CA416364744 | TNFRSF1B | c.609G>T (p.Thr203=) n.321G>T n.598G>T c.588G>T (p.Thr196=) c.24G>T (p.Thr8=) | COSMIC |
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.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=) |