UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.16948773T>A | CA398519804 | TNFRSF13B | c.410A>T (p.Gln137Leu) n.413A>T n.314A>T c.272A>T (p.Gln91Leu) | |
| 17 | g.16948773T>C | CA398519805 | TNFRSF13B | c.410A>G (p.Gln137Arg) n.413A>G n.314A>G c.272A>G (p.Gln91Arg) | ClinVar |
| 17 | g.16948773T>G | CA8414022 | TNFRSF13B | c.410A>C (p.Gln137Pro) n.413A>C n.314A>C c.272A>C (p.Gln91Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948773T= | CA2250304430 | TNFRSF13B | c.410A= (p.Gln137=) n.413A= n.314A= c.272A= (p.Gln91=) | |
| 17 | g.16948774G>A | CA398519807 | TNFRSF13B | c.409C>T (p.Gln137Ter) n.412C>T n.313C>T c.271C>T (p.Gln91Ter) | |
| 17 | g.16948774G>C | CA398519806 | TNFRSF13B | c.409C>G (p.Gln137Glu) n.412C>G n.313C>G c.271C>G (p.Gln91Glu) | |
| 17 | g.16948774G>T | CA398519808 | TNFRSF13B | c.409C>A (p.Gln137Lys) n.412C>A n.313C>A c.271C>A (p.Gln91Lys) | |
| 17 | g.16948775G>A | CA498420149 | TNFRSF13B | c.408C>T (p.Tyr136=) n.411C>T n.312C>T c.270C>T (p.Tyr90=) | dbSNP |
| 17 | g.16948775G>C | CA398519809 | TNFRSF13B | c.408C>G (p.Tyr136Ter) n.411C>G n.312C>G c.270C>G (p.Tyr90Ter) | |
| 17 | g.16948775G= | CA2250304440 | TNFRSF13B | c.408C= (p.Tyr136=) n.411C= n.312C= c.270C= (p.Tyr90=) | |
| 17 | g.16948775G>T | CA398519810 | TNFRSF13B | c.408C>A (p.Tyr136Ter) n.411C>A n.312C>A c.270C>A (p.Tyr90Ter) | |
| 17 | g.16948776T>A | CA398519811 | TNFRSF13B | c.407A>T (p.Tyr136Phe) n.410A>T n.311A>T c.269A>T (p.Tyr90Phe) | |
| 17 | g.16948776T>C | CA398519812 | TNFRSF13B | c.407A>G (p.Tyr136Cys) n.410A>G n.311A>G c.269A>G (p.Tyr90Cys) | |
| 17 | g.16948776T>G | CA288287935 | TNFRSF13B | c.407A>C (p.Tyr136Ser) n.410A>C n.311A>C c.269A>C (p.Tyr90Ser) | dbSNP |
| 17 | g.16948776T= | CA2250304446 | TNFRSF13B | c.407A= (p.Tyr136=) n.410A= n.311A= c.269A= (p.Tyr90=) | |
| 17 | g.16948776_16948785delinsTACCTTCCCG | CA2250304451 | TNFRSF13B | c.398_407delinsCGGGAAGGTA (p.Ser133=) n.401_410delinsCGGGAAGGTA n.302_311delinsCGGGAAGGTA c.260_269delinsCGGGAAGGTA (p.Ser87=) | |
| 17 | g.16948776_16948777insTGTCTGA | CA2576183882 | TNFRSF13B | c.406_407insTCAGACA (p.Tyr136PhefsTer?) n.409_410insTCAGACA n.310_311insTCAGACA c.268_269insTCAGACA (p.Tyr90PhefsTer?) | |
| 17 | g.16948777A>C | CA398519813 | TNFRSF13B | c.406T>G (p.Tyr136Asp) n.409T>G n.310T>G c.268T>G (p.Tyr90Asp) | |
| 17 | g.16948777A>G | CA398519814 | TNFRSF13B | c.406T>C (p.Tyr136His) n.409T>C n.310T>C c.268T>C (p.Tyr90His) | gnomAD v4 |
| 17 | g.16948777A>T | CA398519815 | TNFRSF13B | c.406T>A (p.Tyr136Asn) n.409T>A n.310T>A c.268T>A (p.Tyr90Asn) | |
| 17 | g.16948777_16948779del | CA2636329544 | TNFRSF13B | c.404_406del (p.Arg135_Tyr136delinsAsn) n.407_409del n.308_310del c.266_268del (p.Arg89_Tyr90delinsAsn) | gnomAD v4 |
| 17 | g.16948778_16948786del | CA981911096 | TNFRSF13B | c.398_406del (p.Ser133_Arg135del) n.401_409del n.302_310del c.260_268del (p.Ser87_Arg89del) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948778C>A | CA398519816 | TNFRSF13B | c.405G>T (p.Arg135Ser) n.408G>T n.309G>T c.267G>T (p.Arg89Ser) | |
| 17 | g.16948778C>G | CA398519817 | TNFRSF13B | c.405G>C (p.Arg135Ser) n.408G>C n.309G>C c.267G>C (p.Arg89Ser) | COSMIC COSMIC |
| 17 | g.16948778C>T | CA498420151 | TNFRSF13B | c.405G>A (p.Arg135=) n.408G>A n.309G>A c.267G>A (p.Arg89=) | gnomAD v4 |
| 17 | g.16948779C>A | CA398519818 | TNFRSF13B | c.404G>T (p.Arg135Met) n.407G>T n.308G>T c.266G>T (p.Arg89Met) | gnomAD v4 |
| 17 | g.16948779C>G | CA398519819 | TNFRSF13B | c.404G>C (p.Arg135Thr) n.407G>C n.308G>C c.266G>C (p.Arg89Thr) | |
| 17 | g.16948779C>T | CA398519820 | TNFRSF13B | c.404G>A (p.Arg135Lys) n.407G>A n.308G>A c.266G>A (p.Arg89Lys) | |
| 17 | g.16948780T>A | CA398519822 | TNFRSF13B | c.403A>T (p.Arg135Trp) n.406A>T n.307A>T c.265A>T (p.Arg89Trp) | |
| 17 | g.16948780T>C | CA398519821 | TNFRSF13B | c.403A>G (p.Arg135Gly) n.406A>G n.307A>G c.265A>G (p.Arg89Gly) | gnomAD v4 |
| 17 | g.16948780T>G | CA498420153 | TNFRSF13B | c.403A>C (p.Arg135=) n.406A>C n.307A>C c.265A>C (p.Arg89=) | |
| 17 | g.16948780_16948781insGTCTGAATTG | CA2636329570 | TNFRSF13B | c.402_403insCAATTCAGAC (p.Arg135GlnfsTer?) n.405_406insCAATTCAGAC n.306_307insCAATTCAGAC c.264_265insCAATTCAGAC (p.Arg89GlnfsTer?) | gnomAD v4 |
| 17 | g.16948781T>A | CA498420154 | TNFRSF13B | c.402A>T (p.Gly134=) n.405A>T n.306A>T c.264A>T (p.Gly88=) | |
| 17 | g.16948781T>C | CA498420155 | TNFRSF13B | c.402A>G (p.Gly134=) n.405A>G n.306A>G c.264A>G (p.Gly88=) | gnomAD v4 |
| 17 | g.16948781T>G | CA498420156 | TNFRSF13B | c.402A>C (p.Gly134=) n.405A>C n.306A>C c.264A>C (p.Gly88=) | |
| 17 | g.16948782C>A | CA398519823 | TNFRSF13B | c.401G>T (p.Gly134Val) n.404G>T n.305G>T c.263G>T (p.Gly88Val) | dbSNP gnomAD v4 |
| 17 | g.16948782C= | CA2250304474 | TNFRSF13B | c.401G= (p.Gly134=) n.404G= n.305G= c.263G= (p.Gly88=) | |
| 17 | g.16948782C>G | CA8414023 | TNFRSF13B | c.401G>C (p.Gly134Ala) n.404G>C n.305G>C c.263G>C (p.Gly88Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948782C>T | CA398519824 | TNFRSF13B | c.401G>A (p.Gly134Glu) n.404G>A n.305G>A c.263G>A (p.Gly88Glu) | |
| 17 | g.16948783C>A | CA398519825 | TNFRSF13B | c.400G>T (p.Gly134Ter) n.403G>T n.304G>T c.262G>T (p.Gly88Ter) | dbSNP gnomAD v4 |
| 17 | g.16948783C= | CA2250304482 | TNFRSF13B | c.400G= (p.Gly134=) n.403G= n.304G= c.262G= (p.Gly88=) | |
| 17 | g.16948783C>G | CA398519826 | TNFRSF13B | c.400G>C (p.Gly134Arg) n.403G>C n.304G>C c.262G>C (p.Gly88Arg) | |
| 17 | g.16948783C>T | CA398519827 | TNFRSF13B | c.400G>A (p.Gly134Arg) n.403G>A n.304G>A c.262G>A (p.Gly88Arg) | gnomAD v4 COSMIC COSMIC |
| 17 | g.16948784C>A | CA498420158 | TNFRSF13B | c.399G>T (p.Ser133=) n.402G>T n.303G>T c.261G>T (p.Ser87=) | gnomAD v4 |
| 17 | g.16948784C= | CA2250304493 | TNFRSF13B | c.399G= (p.Ser133=) n.402G= n.303G= c.261G= (p.Ser87=) | |
| 17 | g.16948784C>G | CA498420159 | TNFRSF13B | c.399G>C (p.Ser133=) n.402G>C n.303G>C c.261G>C (p.Ser87=) | |
| 17 | g.16948784C>T | CA288287943 | TNFRSF13B | c.399G>A (p.Ser133=) n.402G>A n.303G>A c.261G>A (p.Ser87=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948785G>A | CA8414024 | TNFRSF13B | c.398C>T (p.Ser133Leu) n.401C>T n.302C>T c.260C>T (p.Ser87Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.16948785G>C | CA398519828 | TNFRSF13B | c.398C>G (p.Ser133Trp) n.401C>G n.302C>G c.260C>G (p.Ser87Trp) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.16948785G= | CA2250304500 | TNFRSF13B | c.398C= (p.Ser133=) n.401C= n.302C= c.260C= (p.Ser87=) | |
| 17 | g.16948785G>T | CA398519829 | TNFRSF13B | c.398C>A (p.Ser133Ter) n.401C>A n.302C>A c.260C>A (p.Ser87Ter) | |
| 17 | g.16948786A>C | CA398519830 | TNFRSF13B | c.397T>G (p.Ser133Ala) n.400T>G n.301T>G c.259T>G (p.Ser87Ala) | |
| 17 | g.16948786A>G | CA398519831 | TNFRSF13B | c.397T>C (p.Ser133Pro) n.400T>C n.301T>C c.259T>C (p.Ser87Pro) | COSMIC COSMIC |
| 17 | g.16948786A>T | CA398519832 | TNFRSF13B | c.397T>A (p.Ser133Thr) n.400T>A n.301T>A c.259T>A (p.Ser87Thr) | |
| 17 | g.16948787G>A | CA498420162 | TNFRSF13B | c.396C>T (p.Asn132=) n.399C>T n.300C>T c.258C>T (p.Asn86=) | dbSNP |
| 17 | g.16948787G>C | CA398519833 | TNFRSF13B | c.396C>G (p.Asn132Lys) n.399C>G n.300C>G c.258C>G (p.Asn86Lys) | |
| 17 | g.16948787G= | CA2250304508 | TNFRSF13B | c.396C= (p.Asn132=) n.399C= n.300C= c.258C= (p.Asn86=) | |
| 17 | g.16948787G>T | CA398519834 | TNFRSF13B | c.396C>A (p.Asn132Lys) n.399C>A n.300C>A c.258C>A (p.Asn86Lys) | |
| 17 | g.16948788T>A | CA398519835 | TNFRSF13B | c.395A>T (p.Asn132Ile) n.398A>T n.299A>T c.257A>T (p.Asn86Ile) | |
| 17 | g.16948788T>C | CA398519836 | TNFRSF13B | c.395A>G (p.Asn132Ser) n.398A>G n.299A>G c.257A>G (p.Asn86Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.16948788T>G | CA398519837 | TNFRSF13B | c.395A>C (p.Asn132Thr) n.398A>C n.299A>C c.257A>C (p.Asn86Thr) | |
| 17 | g.16948788T= | CA2250304513 | TNFRSF13B | c.395A= (p.Asn132=) n.398A= n.299A= c.257A= (p.Asn86=) | |
| 17 | g.16948789T>A | CA398519838 | TNFRSF13B | c.394A>T (p.Asn132Tyr) n.397A>T n.298A>T c.256A>T (p.Asn86Tyr) | |
| 17 | g.16948789T>C | CA398519839 | TNFRSF13B | c.394A>G (p.Asn132Asp) n.397A>G n.298A>G c.256A>G (p.Asn86Asp) | |
| 17 | g.16948789T>G | CA398519840 | TNFRSF13B | c.394A>C (p.Asn132His) n.397A>C n.298A>C c.256A>C (p.Asn86His) | |
| 17 | g.16948790G>A | CA498420167 | TNFRSF13B | c.393C>T (p.Asp131=) n.396C>T n.297C>T c.255C>T (p.Asp85=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948790G>C | CA398519842 | TNFRSF13B | c.393C>G (p.Asp131Glu) n.396C>G n.297C>G c.255C>G (p.Asp85Glu) | |
| 17 | g.16948790G= | CA2250304525 | TNFRSF13B | c.393C= (p.Asp131=) n.396C= n.297C= c.255C= (p.Asp85=) | |
| 17 | g.16948790G>T | CA398519841 | TNFRSF13B | c.393C>A (p.Asp131Glu) n.396C>A n.297C>A c.255C>A (p.Asp85Glu) | |
| 17 | g.16948791T>A | CA398519843 | TNFRSF13B | c.392A>T (p.Asp131Val) n.395A>T n.296A>T c.254A>T (p.Asp85Val) | |
| 17 | g.16948791T>C | CA398519844 | TNFRSF13B | c.392A>G (p.Asp131Gly) n.395A>G n.296A>G c.254A>G (p.Asp85Gly) | |
| 17 | g.16948791T>G | CA398519845 | TNFRSF13B | c.392A>C (p.Asp131Ala) n.395A>C n.296A>C c.254A>C (p.Asp85Ala) | |
| 17 | g.16948792C>A | CA398519846 | TNFRSF13B | c.391G>T (p.Asp131Tyr) n.394G>T n.295G>T c.253G>T (p.Asp85Tyr) | |
| 17 | g.16948792C= | CA2250304527 | TNFRSF13B | c.391G= (p.Asp131=) n.394G= n.295G= c.253G= (p.Asp85=) | |
| 17 | g.16948792C>G | CA398519847 | TNFRSF13B | c.391G>C (p.Asp131His) n.394G>C n.295G>C c.253G>C (p.Asp85His) | |
| 17 | g.16948792C>T | CA398519848 | TNFRSF13B | c.391G>A (p.Asp131Asn) n.394G>A n.295G>A c.253G>A (p.Asp85Asn) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 17 | g.16948793T>A | CA498420170 | TNFRSF13B | c.390A>T (p.Ser130=) n.393A>T n.294A>T c.252A>T (p.Ser84=) | |
| 17 | g.16948793T>C | CA498420171 | TNFRSF13B | c.390A>G (p.Ser130=) n.393A>G n.294A>G c.252A>G (p.Ser84=) | |
| 17 | g.16948793T>G | CA498420173 | TNFRSF13B | c.390A>C (p.Ser130=) n.393A>C n.294A>C c.252A>C (p.Ser84=) | gnomAD v4 |
| 17 | g.16948794G>A | CA398519849 | TNFRSF13B | c.389C>T (p.Ser130Leu) n.392C>T n.293C>T c.251C>T (p.Ser84Leu) | |
| 17 | g.16948794G>C | CA398519851 | TNFRSF13B | c.389C>G (p.Ser130Ter) n.392C>G n.293C>G c.251C>G (p.Ser84Ter) | |
| 17 | g.16948794G>T | CA398519850 | TNFRSF13B | c.389C>A (p.Ser130Ter) n.392C>A n.293C>A c.251C>A (p.Ser84Ter) | |
| 17 | g.16948795A>C | CA398519852 | TNFRSF13B | c.388T>G (p.Ser130Ala) n.391T>G n.292T>G c.250T>G (p.Ser84Ala) | |
| 17 | g.16948795A>G | CA398519853 | TNFRSF13B | c.388T>C (p.Ser130Pro) n.391T>C n.292T>C c.250T>C (p.Ser84Pro) | |
| 17 | g.16948795A>T | CA398519854 | TNFRSF13B | c.388T>A (p.Ser130Thr) n.391T>A n.292T>A c.250T>A (p.Ser84Thr) | |
| 17 | g.16948796A>C | CA398519855 | TNFRSF13B | c.387T>G (p.Asn129Lys) n.390T>G n.291T>G c.249T>G (p.Asn83Lys) | |
| 17 | g.16948796A>G | CA498420176 | TNFRSF13B | c.387T>C (p.Asn129=) n.390T>C n.291T>C c.249T>C (p.Asn83=) | |
| 17 | g.16948796A>T | CA398519856 | TNFRSF13B | c.387T>A (p.Asn129Lys) n.390T>A n.291T>A c.249T>A (p.Asn83Lys) | |
| 17 | g.16948797T>A | CA398519857 | TNFRSF13B | c.386A>T (p.Asn129Ile) n.389A>T n.290A>T c.248A>T (p.Asn83Ile) | |
| 17 | g.16948797T>C | CA398519858 | TNFRSF13B | c.386A>G (p.Asn129Ser) n.389A>G n.290A>G c.248A>G (p.Asn83Ser) | gnomAD v4 |
| 17 | g.16948797T>G | CA398519859 | TNFRSF13B | c.386A>C (p.Asn129Thr) n.389A>C n.290A>C c.248A>C (p.Asn83Thr) | |
| 17 | g.16948798T>A | CA398519860 | TNFRSF13B | c.385A>T (p.Asn129Tyr) n.388A>T n.289A>T c.247A>T (p.Asn83Tyr) | |
| 17 | g.16948798T>C | CA398519861 | TNFRSF13B | c.385A>G (p.Asn129Asp) n.388A>G n.289A>G c.247A>G (p.Asn83Asp) | |
| 17 | g.16948798T>G | CA398519862 | TNFRSF13B | c.385A>C (p.Asn129His) n.388A>C n.289A>C c.247A>C (p.Asn83His) | |
| 17 | g.16948799G>A | CA8414025 | TNFRSF13B | c.384C>T (p.Asn128=) n.387C>T n.288C>T c.246C>T (p.Asn82=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948799G>C | CA398519864 | TNFRSF13B | c.384C>G (p.Asn128Lys) n.387C>G n.288C>G c.246C>G (p.Asn82Lys) | |
| 17 | g.16948799G= | CA2250304530 | TNFRSF13B | c.384C= (p.Asn128=) n.387C= n.288C= c.246C= (p.Asn82=) | |
| 17 | g.16948799G>T | CA398519863 | TNFRSF13B | c.384C>A (p.Asn128Lys) n.387C>A n.288C>A c.246C>A (p.Asn82Lys) | |
| 17 | g.16948799_16948807delinsGTTTTCAAC | CA2250304531 | TNFRSF13B | c.376_384delinsGTTGAAAAC (p.Val126=) n.379_387delinsGTTGAAAAC n.280_288delinsGTTGAAAAC c.238_246delinsGTTGAAAAC (p.Val80=) | |
| 17 | g.16948800T>A | CA398519865 | TNFRSF13B | c.383A>T (p.Asn128Ile) n.386A>T n.287A>T c.245A>T (p.Asn82Ile) | |
| 17 | g.16948800T>C | CA398519867 | TNFRSF13B | c.383A>G (p.Asn128Ser) n.386A>G n.287A>G c.245A>G (p.Asn82Ser) | gnomAD v4 |
| 17 | g.16948800T>G | CA398519866 | TNFRSF13B | c.383A>C (p.Asn128Thr) n.386A>C n.287A>C c.245A>C (p.Asn82Thr) | |
| 17 | g.16948802_16948809del | CA726576440 | TNFRSF13B | c.376_383del (p.Val126GlnfsTer?) n.379_386del n.280_287del c.238_245del (p.Val80GlnfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948801T>A | CA398519868 | TNFRSF13B | c.382A>T (p.Asn128Tyr) n.385A>T n.286A>T c.244A>T (p.Asn82Tyr) | |
| 17 | g.16948801T>C | CA398519869 | TNFRSF13B | c.382A>G (p.Asn128Asp) n.385A>G n.286A>G c.244A>G (p.Asn82Asp) | |
| 17 | g.16948801T>G | CA398519870 | TNFRSF13B | c.382A>C (p.Asn128His) n.385A>C n.286A>C c.244A>C (p.Asn82His) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.16948801T= | CA2250304532 | TNFRSF13B | c.382A= (p.Asn128=) n.385A= n.286A= c.244A= (p.Asn82=) | |
| 17 | g.16948802T>A | CA398519871 | TNFRSF13B | c.381A>T (p.Glu127Asp) n.384A>T n.285A>T c.243A>T (p.Glu81Asp) | |
| 17 | g.16948802T>C | CA498420183 | TNFRSF13B | c.381A>G (p.Glu127=) n.384A>G n.285A>G c.243A>G (p.Glu81=) | |
| 17 | g.16948802T>G | CA398519872 | TNFRSF13B | c.381A>C (p.Glu127Asp) n.384A>C n.285A>C c.243A>C (p.Glu81Asp) | |
| 17 | g.16948803T>A | CA398519873 | TNFRSF13B | c.380A>T (p.Glu127Val) n.383A>T n.284A>T c.242A>T (p.Glu81Val) | |
| 17 | g.16948803T>C | CA398519874 | TNFRSF13B | c.380A>G (p.Glu127Gly) n.383A>G n.284A>G c.242A>G (p.Glu81Gly) | |
| 17 | g.16948803T>G | CA398519875 | TNFRSF13B | c.380A>C (p.Glu127Ala) n.383A>C n.284A>C c.242A>C (p.Glu81Ala) | |
| 17 | g.16948804C>A | CA398519876 | TNFRSF13B | c.379G>T (p.Glu127Ter) n.382G>T n.283G>T c.241G>T (p.Glu81Ter) | |
| 17 | g.16948804C>G | CA398519877 | TNFRSF13B | c.379G>C (p.Glu127Gln) n.382G>C n.283G>C c.241G>C (p.Glu81Gln) | |
| 17 | g.16948804C>T | CA398519878 | TNFRSF13B | c.379G>A (p.Glu127Lys) n.382G>A n.283G>A c.241G>A (p.Glu81Lys) | COSMIC COSMIC |
| 17 | g.16948805A>C | CA498420187 | TNFRSF13B | c.378T>G (p.Val126=) n.381T>G n.282T>G c.240T>G (p.Val80=) | |
| 17 | g.16948805A>G | CA498420188 | TNFRSF13B | c.378T>C (p.Val126=) n.381T>C n.282T>C c.240T>C (p.Val80=) | |
| 17 | g.16948805A>T | CA498420189 | TNFRSF13B | c.378T>A (p.Val126=) n.381T>A n.282T>A c.240T>A (p.Val80=) | |
| 17 | g.16948806A= | CA2250304533 | TNFRSF13B | c.377T= (p.Val126=) n.380T= n.281T= c.239T= (p.Val80=) | |
| 17 | g.16948806A>C | CA398519881 | TNFRSF13B | c.377T>G (p.Val126Gly) n.380T>G n.281T>G c.239T>G (p.Val80Gly) | |
| 17 | g.16948806A>G | CA398519879 | TNFRSF13B | c.377T>C (p.Val126Ala) n.380T>C n.281T>C c.239T>C (p.Val80Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948806A>T | CA398519880 | TNFRSF13B | c.377T>A (p.Val126Asp) n.380T>A n.281T>A c.239T>A (p.Val80Asp) | |
| 17 | g.16948807C>A | CA398519882 | TNFRSF13B | c.376G>T (p.Val126Phe) n.379G>T n.280G>T c.238G>T (p.Val80Phe) | |
| 17 | g.16948807C>G | CA398519883 | TNFRSF13B | c.376G>C (p.Val126Leu) n.379G>C n.280G>C c.238G>C (p.Val80Leu) | |
| 17 | g.16948807C>T | CA398519884 | TNFRSF13B | c.376G>A (p.Val126Ile) n.379G>A n.280G>A c.238G>A (p.Val80Ile) | |
| 17 | g.16948808T>A | CA398519885 | TNFRSF13B | c.375A>T (p.Glu125Asp) n.378A>T n.279A>T c.237A>T (p.Glu79Asp) | |
| 17 | g.16948808T>C | CA498420190 | TNFRSF13B | c.375A>G (p.Glu125=) n.378A>G n.279A>G c.237A>G (p.Glu79=) | |
| 17 | g.16948808T>G | CA398519886 | TNFRSF13B | c.375A>C (p.Glu125Asp) n.378A>C n.279A>C c.237A>C (p.Glu79Asp) | |
| 17 | g.16948809T>A | CA398519887 | TNFRSF13B | c.374A>T (p.Glu125Val) n.377A>T n.278A>T c.236A>T (p.Glu79Val) | |
| 17 | g.16948809T>C | CA398519888 | TNFRSF13B | c.374A>G (p.Glu125Gly) n.377A>G n.278A>G c.236A>G (p.Glu79Gly) | |
| 17 | g.16948809T>G | CA398519889 | TNFRSF13B | c.374A>C (p.Glu125Ala) n.377A>C n.278A>C c.236A>C (p.Glu79Ala) | |
| 17 | g.16948810C>A | CA398519890 | TNFRSF13B | c.373G>T (p.Glu125Ter) n.376G>T n.277G>T c.235G>T (p.Glu79Ter) | |
| 17 | g.16948810C>G | CA398519891 | TNFRSF13B | c.373G>C (p.Glu125Gln) n.376G>C n.277G>C c.235G>C (p.Glu79Gln) | |
| 17 | g.16948810C>T | CA398519892 | TNFRSF13B | c.373G>A (p.Glu125Lys) n.376G>A n.277G>A c.235G>A (p.Glu79Lys) | |
| 17 | g.16948811T>A | CA498420195 | TNFRSF13B | c.372A>T (p.Gly124=) n.375A>T n.276A>T c.234A>T (p.Gly78=) | |
| 17 | g.16948811T>C | CA498420196 | TNFRSF13B | c.372A>G (p.Gly124=) n.375A>G n.276A>G c.234A>G (p.Gly78=) | |
| 17 | g.16948811T>G | CA498420197 | TNFRSF13B | c.372A>C (p.Gly124=) n.375A>C n.276A>C c.234A>C (p.Gly78=) | |
| 17 | g.16948812C>A | CA398519893 | TNFRSF13B | c.371G>T (p.Gly124Val) n.374G>T n.275G>T c.233G>T (p.Gly78Val) | |
| 17 | g.16948812C= | CA2250304534 | TNFRSF13B | c.371G= (p.Gly124=) n.374G= n.275G= c.233G= (p.Gly78=) | |
| 17 | g.16948812C>G | CA398519894 | TNFRSF13B | c.371G>C (p.Gly124Ala) n.374G>C n.275G>C c.233G>C (p.Gly78Ala) | |
| 17 | g.16948812C>T | CA288287954 | TNFRSF13B | c.371G>A (p.Gly124Glu) n.374G>A n.275G>A c.233G>A (p.Gly78Glu) | dbSNP gnomAD v4 |
| 17 | g.16948813C>A | CA398519895 | TNFRSF13B | c.370G>T (p.Gly124Ter) n.373G>T n.274G>T c.232G>T (p.Gly78Ter) | |
| 17 | g.16948813C>G | CA398519896 | TNFRSF13B | c.370G>C (p.Gly124Arg) n.373G>C n.274G>C c.232G>C (p.Gly78Arg) | |
| 17 | g.16948813C>T | CA398519897 | TNFRSF13B | c.370G>A (p.Gly124Arg) n.373G>A n.274G>A c.232G>A (p.Gly78Arg) | gnomAD v4 |
| 17 | g.16948814A= | CA2250304535 | TNFRSF13B | c.369T= (p.Ser123=) n.372T= n.273T= c.231T= (p.Ser77=) | |
| 17 | g.16948814A>C | CA398519898 | TNFRSF13B | c.369T>G (p.Ser123Arg) n.372T>G n.273T>G c.231T>G (p.Ser77Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948814A>G | CA498420199 | TNFRSF13B | c.369T>C (p.Ser123=) n.372T>C n.273T>C c.231T>C (p.Ser77=) | gnomAD v4 |
| 17 | g.16948814A>T | CA398519899 | TNFRSF13B | c.369T>A (p.Ser123Arg) n.372T>A n.273T>A c.231T>A (p.Ser77Arg) | |
| 17 | g.16948815C>A | CA398519900 | TNFRSF13B | c.368G>T (p.Ser123Ile) n.371G>T n.272G>T c.230G>T (p.Ser77Ile) | |
| 17 | g.16948815C= | CA2250304537 | TNFRSF13B | c.368G= (p.Ser123=) n.371G= n.272G= c.230G= (p.Ser77=) | |
| 17 | g.16948815C>G | CA398519901 | TNFRSF13B | c.368G>C (p.Ser123Thr) n.371G>C n.272G>C c.230G>C (p.Ser77Thr) | dbSNP gnomAD v4 |
| 17 | g.16948815C>T | CA398519902 | TNFRSF13B | c.368G>A (p.Ser123Asn) n.371G>A n.272G>A c.230G>A (p.Ser77Asn) | |
| 17 | g.16948816T>A | CA398519903 | TNFRSF13B | c.367A>T (p.Ser123Cys) n.370A>T n.271A>T c.229A>T (p.Ser77Cys) | |
| 17 | g.16948816T>C | CA398519904 | TNFRSF13B | c.367A>G (p.Ser123Gly) n.370A>G n.271A>G c.229A>G (p.Ser77Gly) | |
| 17 | g.16948816T>G | CA398519905 | TNFRSF13B | c.367A>C (p.Ser123Arg) n.370A>C n.271A>C c.229A>C (p.Ser77Arg) | |
| 17 | g.16948817C>A | CA8414026 | TNFRSF13B | c.366G>T (p.Arg122=) n.369G>T n.270G>T c.228G>T (p.Arg76=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948817C= | CA2250304541 | TNFRSF13B | c.366G= (p.Arg122=) n.369G= n.270G= c.228G= (p.Arg76=) | |
| 17 | g.16948817C>G | CA498420204 | TNFRSF13B | c.366G>C (p.Arg122=) n.369G>C n.270G>C c.228G>C (p.Arg76=) | |
| 17 | g.16948817C>T | CA498420201 | TNFRSF13B | c.366G>A (p.Arg122=) n.369G>A n.270G>A c.228G>A (p.Arg76=) | gnomAD v4 |
| 17 | g.16948818C>A | CA398519906 | TNFRSF13B | c.365G>T (p.Arg122Leu) n.368G>T n.269G>T c.227G>T (p.Arg76Leu) | dbSNP gnomAD v4 |
| 17 | g.16948818C= | CA2250304553 | TNFRSF13B | c.365G= (p.Arg122=) n.368G= n.269G= c.227G= (p.Arg76=) | |
| 17 | g.16948818C>G | CA398519907 | TNFRSF13B | c.365G>C (p.Arg122Pro) n.368G>C n.269G>C c.227G>C (p.Arg76Pro) | |
| 17 | g.16948818C>T | CA8414027 | TNFRSF13B | c.365G>A (p.Arg122Gln) n.368G>A n.269G>A c.227G>A (p.Arg76Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948819G>A | CA8414028 | TNFRSF13B | c.364C>T (p.Arg122Trp) n.367C>T n.268C>T c.226C>T (p.Arg76Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.16948819G>C | CA398519908 | TNFRSF13B | c.364C>G (p.Arg122Gly) n.367C>G n.268C>G c.226C>G (p.Arg76Gly) | |
| 17 | g.16948819G= | CA2250304567 | TNFRSF13B | c.364C= (p.Arg122=) n.367C= n.268C= c.226C= (p.Arg76=) | |
| 17 | g.16948819G>T | CA498420206 | TNFRSF13B | c.364C>A (p.Arg122=) n.367C>A n.268C>A c.226C>A (p.Arg76=) | |
| 17 | g.16948820C>A | CA398519909 | TNFRSF13B | c.363G>T (p.Gln121His) n.366G>T n.267G>T c.225G>T (p.Gln75His) | |
| 17 | g.16948820C= | CA2250304585 | TNFRSF13B | c.363G= (p.Gln121=) n.366G= n.267G= c.225G= (p.Gln75=) | |
| 17 | g.16948820C>G | CA288287973 | TNFRSF13B | c.363G>C (p.Gln121His) n.366G>C n.267G>C c.225G>C (p.Gln75His) | dbSNP |
| 17 | g.16948820C>T | CA498420208 | TNFRSF13B | c.363G>A (p.Gln121=) n.366G>A n.267G>A c.225G>A (p.Gln75=) | COSMIC COSMIC |
| 17 | g.16948821T>A | CA398519910 | TNFRSF13B | c.362A>T (p.Gln121Leu) n.365A>T n.266A>T c.224A>T (p.Gln75Leu) | |
| 17 | g.16948821T>C | CA398519911 | TNFRSF13B | c.362A>G (p.Gln121Arg) n.365A>G n.266A>G c.224A>G (p.Gln75Arg) | |
| 17 | g.16948821T>G | CA398519912 | TNFRSF13B | c.362A>C (p.Gln121Pro) n.365A>C n.266A>C c.224A>C (p.Gln75Pro) | |
| 17 | g.16948822G>A | CA8414029 | TNFRSF13B | c.361C>T (p.Gln121Ter) n.364C>T n.265C>T c.223C>T (p.Gln75Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948822G>C | CA398519914 | TNFRSF13B | c.361C>G (p.Gln121Glu) n.364C>G n.265C>G c.223C>G (p.Gln75Glu) | gnomAD v4 |
| 17 | g.16948822G= | CA2250304589 | TNFRSF13B | c.361C= (p.Gln121=) n.364C= n.265C= c.223C= (p.Gln75=) | |
| 17 | g.16948822G>T | CA398519913 | TNFRSF13B | c.361C>A (p.Gln121Lys) n.364C>A n.265C>A c.223C>A (p.Gln75Lys) | |
| 17 | g.16948823T>A | CA398519915 | TNFRSF13B | c.360A>T (p.Arg120Ser) n.363A>T n.264A>T c.222A>T (p.Arg74Ser) | |
| 17 | g.16948823T>C | CA498420214 | TNFRSF13B | c.360A>G (p.Arg120=) n.363A>G n.264A>G c.222A>G (p.Arg74=) | dbSNP gnomAD v4 |
| 17 | g.16948823T>G | CA398519916 | TNFRSF13B | c.360A>C (p.Arg120Ser) n.363A>C n.264A>C c.222A>C (p.Arg74Ser) | |
| 17 | g.16948823T= | CA2250304594 | TNFRSF13B | c.360A= (p.Arg120=) n.363A= n.264A= c.222A= (p.Arg74=) | |
| 17 | g.16948824C>A | CA398519917 | TNFRSF13B | c.359G>T (p.Arg120Ile) n.362G>T n.263G>T c.221G>T (p.Arg74Ile) | |
| 17 | g.16948824C>G | CA398519918 | TNFRSF13B | c.359G>C (p.Arg120Thr) n.362G>C n.263G>C c.221G>C (p.Arg74Thr) | |
| 17 | g.16948824C>T | CA398519919 | TNFRSF13B | c.359G>A (p.Arg120Lys) n.362G>A n.263G>A c.221G>A (p.Arg74Lys) | |
| 17 | g.16948824_16948825delinsCT | CA2250304611 | TNFRSF13B | c.358_359delinsAG (p.Arg120=) n.361_362delinsAG n.262_263delinsAG c.220_221delinsAG (p.Arg74=) | |
| 17 | g.16948825del | CA2250304613 | TNFRSF13B | c.358del (p.Arg120AspfsTer?) n.361del n.262del c.220del (p.Arg74AspfsTer?) | dbSNP gnomAD v4 |
| 17 | g.16948825T>A | CA398519920 | TNFRSF13B | c.358A>T (p.Arg120Ter) n.361A>T n.262A>T c.220A>T (p.Arg74Ter) | |
| 17 | g.16948825T>C | CA398519921 | TNFRSF13B | c.358A>G (p.Arg120Gly) n.361A>G n.262A>G c.220A>G (p.Arg74Gly) | |
| 17 | g.16948825T>G | CA498420215 | TNFRSF13B | c.358A>C (p.Arg120=) n.361A>C n.262A>C c.220A>C (p.Arg74=) | |
| 17 | g.16948826C>A | CA398519922 | TNFRSF13B | c.357G>T (p.Arg119Ser) n.360G>T n.261G>T c.219G>T (p.Arg73Ser) | |
| 17 | g.16948826C= | CA2250304618 | TNFRSF13B | c.357G= (p.Arg119=) n.360G= n.261G= c.219G= (p.Arg73=) | |
| 17 | g.16948826C>G | CA8414030 | TNFRSF13B | c.357G>C (p.Arg119Ser) n.360G>C n.261G>C c.219G>C (p.Arg73Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948826C>T | CA8414031 | TNFRSF13B | c.357G>A (p.Arg119=) n.360G>A n.261G>A c.219G>A (p.Arg73=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948826_16948833delinsCCTGAGCT | CA2250304622 | TNFRSF13B | c.350_357delinsAGCTCAGG (p.Glu117=) n.353_360delinsAGCTCAGG n.254_261delinsAGCTCAGG c.212_219delinsAGCTCAGG (p.Glu71=) | |
| 17 | g.16948827C>A | CA398519923 | TNFRSF13B | c.356G>T (p.Arg119Met) n.359G>T n.260G>T c.218G>T (p.Arg73Met) | |
| 17 | g.16948827C= | CA2250304638 | TNFRSF13B | c.356G= (p.Arg119=) n.359G= n.260G= c.218G= (p.Arg73=) | |
| 17 | g.16948827C>G | CA398519925 | TNFRSF13B | c.356G>C (p.Arg119Thr) n.359G>C n.260G>C c.218G>C (p.Arg73Thr) | |
| 17 | g.16948827C>T | CA398519924 | TNFRSF13B | c.356G>A (p.Arg119Lys) n.359G>A n.260G>A c.218G>A (p.Arg73Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948827_16948828delinsCT | CA2250304642 | TNFRSF13B | c.355_356delinsAG (p.Arg119=) n.358_359delinsAG n.259_260delinsAG c.217_218delinsAG (p.Arg73=) | |
| 17 | g.16948830_16948836del | CA726576493 | TNFRSF13B | c.350_356del (p.Glu117GlyfsTer?) n.353_359del n.254_260del c.212_218del (p.Glu71GlyfsTer?) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948828del | CA625313745 | TNFRSF13B | c.355del (p.Arg119GlyfsTer?) n.358del n.259del c.217del (p.Arg73GlyfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.16948828T>A | CA398519926 | TNFRSF13B | c.355A>T (p.Arg119Trp) n.358A>T n.259A>T c.217A>T (p.Arg73Trp) | |
| 17 | g.16948828T>C | CA398519927 | TNFRSF13B | c.355A>G (p.Arg119Gly) n.358A>G n.259A>G c.217A>G (p.Arg73Gly) | |
| 17 | g.16948828T>G | CA498420261 | TNFRSF13B | c.355A>C (p.Arg119=) n.358A>C n.259A>C c.217A>C (p.Arg73=) | COSMIC COSMIC |
| 17 | g.16948829G>A | CA498420262 | TNFRSF13B | c.354C>T (p.Leu118=) n.357C>T n.258C>T c.216C>T (p.Leu72=) | |
| 17 | g.16948829G>C | CA8414032 | TNFRSF13B | c.354C>G (p.Leu118=) n.357C>G n.258C>G c.216C>G (p.Leu72=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948829G= | CA2250304652 | TNFRSF13B | c.354C= (p.Leu118=) n.357C= n.258C= c.216C= (p.Leu72=) | |
| 17 | g.16948829G>T | CA498420263 | TNFRSF13B | c.354C>A (p.Leu118=) n.357C>A n.258C>A c.216C>A (p.Leu72=) | |
| 17 | g.16948830A>C | CA398519928 | TNFRSF13B | c.353T>G (p.Leu118Arg) n.356T>G n.257T>G c.215T>G (p.Leu72Arg) | |
| 17 | g.16948830A>G | CA398519929 | TNFRSF13B | c.353T>C (p.Leu118Pro) n.356T>C n.257T>C c.215T>C (p.Leu72Pro) | |
| 17 | g.16948830A>T | CA398519930 | TNFRSF13B | c.353T>A (p.Leu118His) n.356T>A n.257T>A c.215T>A (p.Leu72His) | |
| 17 | g.16948831G>A | CA398519933 | TNFRSF13B | c.352C>T (p.Leu118Phe) n.355C>T n.256C>T c.214C>T (p.Leu72Phe) | |
| 17 | g.16948831G>C | CA398519931 | TNFRSF13B | c.352C>G (p.Leu118Val) n.355C>G n.256C>G c.214C>G (p.Leu72Val) | ClinVar dbSNP gnomAD v4 |
| 17 | g.16948831G= | CA2250304659 | TNFRSF13B | c.352C= (p.Leu118=) n.355C= n.256C= c.214C= (p.Leu72=) | |
| 17 | g.16948831G>T | CA398519932 | TNFRSF13B | c.352C>A (p.Leu118Ile) n.355C>A n.256C>A c.214C>A (p.Leu72Ile) | gnomAD v4 |
| 17 | g.16948832C>A | CA398519934 | TNFRSF13B | c.351G>T (p.Glu117Asp) n.354G>T n.255G>T c.213G>T (p.Glu71Asp) | |
| 17 | g.16948832C= | CA2250304665 | TNFRSF13B | c.351G= (p.Glu117=) n.354G= n.255G= c.213G= (p.Glu71=) | |
| 17 | g.16948832C>G | CA398519935 | TNFRSF13B | c.351G>C (p.Glu117Asp) n.354G>C n.255G>C c.213G>C (p.Glu71Asp) | |
| 17 | g.16948832C>T | CA498420264 | TNFRSF13B | c.351G>A (p.Glu117=) n.354G>A n.255G>A c.213G>A (p.Glu71=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.16948833T>A | CA398519936 | TNFRSF13B | c.350A>T (p.Glu117Val) n.353A>T n.254A>T c.212A>T (p.Glu71Val) | |
| 17 | g.16948833T>C | CA398519937 | TNFRSF13B | c.350A>G (p.Glu117Gly) n.353A>G n.254A>G c.212A>G (p.Glu71Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948833T>G | CA398519938 | TNFRSF13B | c.350A>C (p.Glu117Ala) n.353A>C n.254A>C c.212A>C (p.Glu71Ala) | |
| 17 | g.16948833T= | CA2250304669 | TNFRSF13B | c.350A= (p.Glu117=) n.353A= n.254A= c.212A= (p.Glu71=) | |
| 17 | g.16948834C>A | CA398519941 | TNFRSF13B | c.349G>T (p.Glu117Ter) n.352G>T n.253G>T c.211G>T (p.Glu71Ter) | |
| 17 | g.16948834C>G | CA398519939 | TNFRSF13B | c.349G>C (p.Glu117Gln) n.352G>C n.253G>C c.211G>C (p.Glu71Gln) | |
| 17 | g.16948834C>T | CA398519940 | TNFRSF13B | c.349G>A (p.Glu117Lys) n.352G>A n.253G>A c.211G>A (p.Glu71Lys) | gnomAD v4 COSMIC COSMIC |
| 17 | g.16948835T>A | CA498420265 | TNFRSF13B | c.348A>T (p.Pro116=) n.351A>T n.252A>T c.210A>T (p.Pro70=) | |
| 17 | g.16948835T>C | CA498420266 | TNFRSF13B | c.348A>G (p.Pro116=) n.351A>G n.252A>G c.210A>G (p.Pro70=) | |
| 17 | g.16948835T>G | CA498420267 | TNFRSF13B | c.348A>C (p.Pro116=) n.351A>C n.252A>C c.210A>C (p.Pro70=) | gnomAD v4 |
| 17 | g.16948835dup | CA2576183895 | TNFRSF13B | c.348dup (p.Glu117ArgfsTer11) n.351dup n.252dup c.210dup (p.Glu71ArgfsTer11) | |
| 17 | g.16948836G>A | CA398519942 | TNFRSF13B | c.347C>T (p.Pro116Leu) n.350C>T n.251C>T c.209C>T (p.Pro70Leu) | |
| 17 | g.16948836G>C | CA398519943 | TNFRSF13B | c.347C>G (p.Pro116Arg) n.350C>G n.251C>G c.209C>G (p.Pro70Arg) | |
| 17 | g.16948836G>T | CA398519944 | TNFRSF13B | c.347C>A (p.Pro116Gln) n.350C>A n.251C>A c.209C>A (p.Pro70Gln) | |
| 17 | g.16948837G>A | CA398519945 | TNFRSF13B | c.346C>T (p.Pro116Ser) n.349C>T n.250C>T c.208C>T (p.Pro70Ser) | gnomAD v4 |
| 17 | g.16948837G>C | CA398519946 | TNFRSF13B | c.346C>G (p.Pro116Ala) n.349C>G n.250C>G c.208C>G (p.Pro70Ala) | |
| 17 | g.16948837G= | CA2250304677 | TNFRSF13B | c.346C= (p.Pro116=) n.349C= n.250C= c.208C= (p.Pro70=) | |
| 17 | g.16948837G>T | CA8414033 | TNFRSF13B | c.346C>A (p.Pro116Thr) n.349C>A n.250C>A c.208C>A (p.Pro70Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948838_16948839dup | CA2576183898 | TNFRSF13B | c.345_346dup (p.Pro116HisfsTer?) n.348_349dup n.249_250dup c.207_208dup (p.Pro70HisfsTer?) | |
| 17 | g.16948838T>A | CA498420270 | TNFRSF13B | c.345A>T (p.Pro115=) n.348A>T n.249A>T c.207A>T (p.Pro69=) | |
| 17 | g.16948838T>C | CA498420268 | TNFRSF13B | c.345A>G (p.Pro115=) n.348A>G n.249A>G c.207A>G (p.Pro69=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.16948838T>G | CA498420269 | TNFRSF13B | c.345A>C (p.Pro115=) n.348A>C n.249A>C c.207A>C (p.Pro69=) | |
| 17 | g.16948838T= | CA2250304687 | TNFRSF13B | c.345A= (p.Pro115=) n.348A= n.249A= c.207A= (p.Pro69=) | |
| 17 | g.16948841_16948852del | CA2636329826 | TNFRSF13B | c.334_345del (p.Val112_Pro115del) n.337_348del n.238_249del c.196_207del (p.Val66_Pro69del) | gnomAD v4 |
| 17 | g.16948839G>A | CA398519947 | TNFRSF13B | c.344C>T (p.Pro115Leu) n.347C>T n.248C>T c.206C>T (p.Pro69Leu) | COSMIC |
| 17 | g.16948839G>C | CA398519948 | TNFRSF13B | c.344C>G (p.Pro115Arg) n.347C>G n.248C>G c.206C>G (p.Pro69Arg) | |
| 17 | g.16948839G>T | CA398519949 | TNFRSF13B | c.344C>A (p.Pro115Gln) n.347C>A n.248C>A c.206C>A (p.Pro69Gln) | |
| 17 | g.16948841_16948844del | CA2636329830 | TNFRSF13B | c.341_344del (p.Leu114HisfsTer?) n.344_347del n.245_248del c.203_206del (p.Leu68HisfsTer?) | gnomAD v4 |
| 17 | g.16948840G>A | CA398519950 | TNFRSF13B | c.343C>T (p.Pro115Ser) n.346C>T n.247C>T c.205C>T (p.Pro69Ser) | COSMIC COSMIC |
| 17 | g.16948840G>C | CA398519951 | TNFRSF13B | c.343C>G (p.Pro115Ala) n.346C>G n.247C>G c.205C>G (p.Pro69Ala) | |
| 17 | g.16948840G>T | CA398519952 | TNFRSF13B | c.343C>A (p.Pro115Thr) n.346C>A n.247C>A c.205C>A (p.Pro69Thr) | |
| 17 | g.16948841A>C | CA498420271 | TNFRSF13B | c.342T>G (p.Leu114=) n.345T>G n.246T>G c.204T>G (p.Leu68=) | |
| 17 | g.16948841A>G | CA498420272 | TNFRSF13B | c.342T>C (p.Leu114=) n.345T>C n.246T>C c.204T>C (p.Leu68=) | |
| 17 | g.16948841A>T | CA498420273 | TNFRSF13B | c.342T>A (p.Leu114=) n.345T>A n.246T>A c.204T>A (p.Leu68=) | gnomAD v4 |
| 17 | g.16948842A>C | CA398519953 | TNFRSF13B | c.341T>G (p.Leu114Arg) n.344T>G n.245T>G c.203T>G (p.Leu68Arg) | |
| 17 | g.16948842A>G | CA398519955 | TNFRSF13B | c.341T>C (p.Leu114Pro) n.344T>C n.245T>C c.203T>C (p.Leu68Pro) | |
| 17 | g.16948842A>T | CA398519954 | TNFRSF13B | c.341T>A (p.Leu114His) n.344T>A n.245T>A c.203T>A (p.Leu68His) | |
| 17 | g.16948843G>A | CA398519956 | TNFRSF13B | c.340C>T (p.Leu114Phe) n.343C>T n.244C>T c.202C>T (p.Leu68Phe) | |
| 17 | g.16948843G>C | CA398519957 | TNFRSF13B | c.340C>G (p.Leu114Val) n.343C>G n.244C>G c.202C>G (p.Leu68Val) | |
| 17 | g.16948843G>T | CA398519958 | TNFRSF13B | c.340C>A (p.Leu114Ile) n.343C>A n.244C>A c.202C>A (p.Leu68Ile) | |
| 17 | g.16948843_16948844insCTT | CA2636329842 | TNFRSF13B | c.339_340insAAG (p.Asn113_Leu114insLys) n.342_343insAAG n.243_244insAAG c.201_202insAAG (p.Asn67_Leu68insLys) | gnomAD v4 |
| 17 | g.16948844G>A | CA498420274 | TNFRSF13B | c.339C>T (p.Asn113=) n.342C>T n.243C>T c.201C>T (p.Asn67=) | dbSNP |
| 17 | g.16948844G>C | CA398519959 | TNFRSF13B | c.339C>G (p.Asn113Lys) n.342C>G n.243C>G c.201C>G (p.Asn67Lys) | |
| 17 | g.16948844G= | CA2250304696 | TNFRSF13B | c.339C= (p.Asn113=) n.342C= n.243C= c.201C= (p.Asn67=) | |
| 17 | g.16948844G>T | CA398519960 | TNFRSF13B | c.339C>A (p.Asn113Lys) n.342C>A n.243C>A c.201C>A (p.Asn67Lys) | |
| 17 | g.16948845T>A | CA398519961 | TNFRSF13B | c.338A>T (p.Asn113Ile) n.341A>T n.242A>T c.200A>T (p.Asn67Ile) | |
| 17 | g.16948845T>C | CA398519962 | TNFRSF13B | c.338A>G (p.Asn113Ser) n.341A>G n.242A>G c.200A>G (p.Asn67Ser) | gnomAD v4 |
| 17 | g.16948845T>G | CA398519963 | TNFRSF13B | c.338A>C (p.Asn113Thr) n.341A>C n.242A>C c.200A>C (p.Asn67Thr) | |
| 17 | g.16948846T>A | CA288287993 | TNFRSF13B | c.337A>T (p.Asn113Tyr) n.340A>T n.241A>T c.199A>T (p.Asn67Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948846T>C | CA398519964 | TNFRSF13B | c.337A>G (p.Asn113Asp) n.340A>G n.241A>G c.199A>G (p.Asn67Asp) | |
| 17 | g.16948846T>G | CA398519965 | TNFRSF13B | c.337A>C (p.Asn113His) n.340A>C n.241A>C c.199A>C (p.Asn67His) | |
| 17 | g.16948846T= | CA2250304703 | TNFRSF13B | c.337A= (p.Asn113=) n.340A= n.241A= c.199A= (p.Asn67=) | |
| 17 | g.16948847C>A | CA498420275 | TNFRSF13B | c.336G>T (p.Val112=) n.339G>T n.240G>T c.198G>T (p.Val66=) | |
| 17 | g.16948847C= | CA2250304707 | TNFRSF13B | c.336G= (p.Val112=) n.339G= n.240G= c.198G= (p.Val66=) | |
| 17 | g.16948847C>G | CA498420276 | TNFRSF13B | c.336G>C (p.Val112=) n.339G>C n.240G>C c.198G>C (p.Val66=) | |
| 17 | g.16948847C>T | CA498420277 | TNFRSF13B | c.336G>A (p.Val112=) n.339G>A n.240G>A c.198G>A (p.Val66=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948848A= | CA2250304711 | TNFRSF13B | c.335T= (p.Val112=) n.338T= n.239T= c.197T= (p.Val66=) | |
| 17 | g.16948848A>C | CA398519967 | TNFRSF13B | c.335T>G (p.Val112Gly) n.338T>G n.239T>G c.197T>G (p.Val66Gly) | |
| 17 | g.16948848A>G | CA8414034 | TNFRSF13B | c.335T>C (p.Val112Ala) n.338T>C n.239T>C c.197T>C (p.Val66Ala) | dbSNP ExAC gnomAD v4 |
| 17 | g.16948848A>T | CA398519966 | TNFRSF13B | c.335T>A (p.Val112Glu) n.338T>A n.239T>A c.197T>A (p.Val66Glu) | |
| 17 | g.16948849C>A | CA398519968 | TNFRSF13B | c.334G>T (p.Val112Leu) n.337G>T n.238G>T c.196G>T (p.Val66Leu) | |
| 17 | g.16948849C>G | CA398519969 | TNFRSF13B | c.334G>C (p.Val112Leu) n.337G>C n.238G>C c.196G>C (p.Val66Leu) | |
| 17 | g.16948849C>T | CA398519970 | TNFRSF13B | c.334G>A (p.Val112Met) n.337G>A n.238G>A c.196G>A (p.Val66Met) | |
| 17 | g.16948850T>A | CA498420278 | TNFRSF13B | c.333A>T (p.Pro111=) n.336A>T n.237A>T c.195A>T (p.Pro65=) | |
| 17 | g.16948850T>C | CA498420279 | TNFRSF13B | c.333A>G (p.Pro111=) n.336A>G n.237A>G c.195A>G (p.Pro65=) | dbSNP gnomAD v4 |
| 17 | g.16948850T>G | CA498420280 | TNFRSF13B | c.333A>C (p.Pro111=) n.336A>C n.237A>C c.195A>C (p.Pro65=) | |
| 17 | g.16948850T= | CA2250304712 | TNFRSF13B | c.333A= (p.Pro111=) n.336A= n.237A= c.195A= (p.Pro65=) | |
| 17 | g.16948851G>A | CA398519971 | TNFRSF13B | c.332C>T (p.Pro111Leu) n.335C>T n.236C>T c.194C>T (p.Pro65Leu) | gnomAD v4 |
| 17 | g.16948851G>C | CA8414035 | TNFRSF13B | c.332C>G (p.Pro111Arg) n.335C>G n.236C>G c.194C>G (p.Pro65Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948851G= | CA2250304717 | TNFRSF13B | c.332C= (p.Pro111=) n.335C= n.236C= c.194C= (p.Pro65=) | |
| 17 | g.16948851G>T | CA398519972 | TNFRSF13B | c.332C>A (p.Pro111Gln) n.335C>A n.236C>A c.194C>A (p.Pro65Gln) | |
| 17 | g.16948852G>A | CA398519973 | TNFRSF13B | c.331C>T (p.Pro111Ser) n.334C>T n.235C>T c.193C>T (p.Pro65Ser) | |
| 17 | g.16948852G>C | CA398519974 | TNFRSF13B | c.331C>G (p.Pro111Ala) n.334C>G n.235C>G c.193C>G (p.Pro65Ala) | |
| 17 | g.16948852G>T | CA398519975 | TNFRSF13B | c.331C>A (p.Pro111Thr) n.334C>A n.235C>A c.193C>A (p.Pro65Thr) | |
| 17 | g.16948853G>A | CA498420281 | TNFRSF13B | c.330C>T (p.Ser110=) n.333C>T n.234C>T c.192C>T (p.Ser64=) | |
| 17 | g.16948853G>C | CA398519976 | TNFRSF13B | c.330C>G (p.Ser110Arg) n.333C>G n.234C>G c.192C>G (p.Ser64Arg) | |
| 17 | g.16948853G>T | CA398519977 | TNFRSF13B | c.330C>A (p.Ser110Arg) n.333C>A n.234C>A c.192C>A (p.Ser64Arg) | |
| 17 | g.16948854C>A | CA8414037 | TNFRSF13B | c.329G>T (p.Ser110Ile) n.332G>T n.233G>T c.191G>T (p.Ser64Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948854C= | CA2250304736 | TNFRSF13B | c.329G= (p.Ser110=) n.332G= n.233G= c.191G= (p.Ser64=) | |
| 17 | g.16948854C>G | CA398519978 | TNFRSF13B | c.329G>C (p.Ser110Thr) n.332G>C n.233G>C c.191G>C (p.Ser64Thr) | dbSNP gnomAD v4 |
| 17 | g.16948854C>T | CA8414036 | TNFRSF13B | c.329G>A (p.Ser110Asn) n.332G>A n.233G>A c.191G>A (p.Ser64Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948855T>A | CA398519979 | TNFRSF13B | c.328A>T (p.Ser110Cys) n.331A>T n.232A>T c.190A>T (p.Ser64Cys) | |
| 17 | g.16948855T>C | CA398519981 | TNFRSF13B | c.328A>G (p.Ser110Gly) n.331A>G n.232A>G c.190A>G (p.Ser64Gly) | |
| 17 | g.16948855T>G | CA398519980 | TNFRSF13B | c.328A>C (p.Ser110Arg) n.331A>C n.232A>C c.190A>C (p.Ser64Arg) | |
| 17 | g.16948856C>A | CA398519982 | TNFRSF13B | c.327G>T (p.Arg109Ser) n.330G>T n.231G>T c.189G>T (p.Arg63Ser) | |
| 17 | g.16948856C= | CA2250304740 | TNFRSF13B | c.327G= (p.Arg109=) n.330G= n.231G= c.189G= (p.Arg63=) | |
| 17 | g.16948856C>G | CA8414038 | TNFRSF13B | c.327G>C (p.Arg109Ser) n.330G>C n.231G>C c.189G>C (p.Arg63Ser) | dbSNP ExAC |
| 17 | g.16948856C>T | CA288288025 | TNFRSF13B | c.327G>A (p.Arg109=) n.330G>A n.231G>A c.189G>A (p.Arg63=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948857C>A | CA398519983 | TNFRSF13B | c.326G>T (p.Arg109Met) n.329G>T n.230G>T c.188G>T (p.Arg63Met) | |
| 17 | g.16948857C>G | CA398519984 | TNFRSF13B | c.326G>C (p.Arg109Thr) n.329G>C n.230G>C c.188G>C (p.Arg63Thr) | |
| 17 | g.16948857C>T | CA398519985 | TNFRSF13B | c.326G>A (p.Arg109Lys) n.329G>A n.230G>A c.188G>A (p.Arg63Lys) | gnomAD v4 |
| 17 | g.16948858T>A | CA398519986 | TNFRSF13B | c.325A>T (p.Arg109Trp) n.328A>T n.229A>T c.187A>T (p.Arg63Trp) | |
| 17 | g.16948858T>C | CA398519987 | TNFRSF13B | c.325A>G (p.Arg109Gly) n.328A>G n.229A>G c.187A>G (p.Arg63Gly) | |
| 17 | g.16948858T>G | CA498420282 | TNFRSF13B | c.325A>C (p.Arg109=) n.328A>C n.229A>C c.187A>C (p.Arg63=) | |
| 17 | g.16948859G>A | CA498420285 | TNFRSF13B | c.324C>T (p.Leu108=) n.327C>T n.228C>T c.186C>T (p.Leu62=) | |
| 17 | g.16948859G>C | CA498420284 | TNFRSF13B | c.324C>G (p.Leu108=) n.327C>G n.228C>G c.186C>G (p.Leu62=) | |
| 17 | g.16948859G>T | CA498420283 | TNFRSF13B | c.324C>A (p.Leu108=) n.327C>A n.228C>A c.186C>A (p.Leu62=) | |
| 17 | g.16948860A>C | CA398519988 | TNFRSF13B | c.323T>G (p.Leu108Arg) n.326T>G n.227T>G c.185T>G (p.Leu62Arg) | |
| 17 | g.16948860A>G | CA398519989 | TNFRSF13B | c.323T>C (p.Leu108Pro) n.326T>C n.227T>C c.185T>C (p.Leu62Pro) | |
| 17 | g.16948860A>T | CA398519990 | TNFRSF13B | c.323T>A (p.Leu108His) n.326T>A n.227T>A c.185T>A (p.Leu62His) | |
| 17 | g.16948861G>A | CA398519991 | TNFRSF13B | c.322C>T (p.Leu108Phe) n.325C>T n.226C>T c.184C>T (p.Leu62Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948861G>C | CA398519992 | TNFRSF13B | c.322C>G (p.Leu108Val) n.325C>G n.226C>G c.184C>G (p.Leu62Val) | |
| 17 | g.16948861G= | CA2250304747 | TNFRSF13B | c.322C= (p.Leu108=) n.325C= n.226C= c.184C= (p.Leu62=) | |
| 17 | g.16948861G>T | CA398519993 | TNFRSF13B | c.322C>A (p.Leu108Ile) n.325C>A n.226C>A c.184C>A (p.Leu62Ile) | gnomAD v4 |
| 17 | g.16948862C>A | CA398519994 | TNFRSF13B | c.321G>T (p.Lys107Asn) n.324G>T n.225G>T c.183G>T (p.Lys61Asn) | |
| 17 | g.16948862C>G | CA398519995 | TNFRSF13B | c.321G>C (p.Lys107Asn) n.324G>C n.225G>C c.183G>C (p.Lys61Asn) | |
| 17 | g.16948862C>T | CA498420286 | TNFRSF13B | c.321G>A (p.Lys107=) n.324G>A n.225G>A c.183G>A (p.Lys61=) | |
| 17 | g.16948863T>A | CA398519996 | TNFRSF13B | c.320A>T (p.Lys107Met) n.323A>T n.224A>T c.182A>T (p.Lys61Met) | |
| 17 | g.16948863T>C | CA398519997 | TNFRSF13B | c.320A>G (p.Lys107Arg) n.323A>G n.224A>G c.182A>G (p.Lys61Arg) | dbSNP |
| 17 | g.16948863T>G | CA398519998 | TNFRSF13B | c.320A>C (p.Lys107Thr) n.323A>C n.224A>C c.182A>C (p.Lys61Thr) | |
| 17 | g.16948863T= | CA2250304760 | TNFRSF13B | c.320A= (p.Lys107=) n.323A= n.224A= c.182A= (p.Lys61=) | |
| 17 | g.16948864T>A | CA398519999 | TNFRSF13B | c.319A>T (p.Lys107Ter) n.322A>T n.223A>T c.181A>T (p.Lys61Ter) | |
| 17 | g.16948864T>C | CA398520000 | TNFRSF13B | c.319A>G (p.Lys107Glu) n.322A>G n.223A>G c.181A>G (p.Lys61Glu) | |
| 17 | g.16948864T>G | CA398520001 | TNFRSF13B | c.319A>C (p.Lys107Gln) n.322A>C n.223A>C c.181A>C (p.Lys61Gln) | |
| 17 | g.16948865G>A | CA498420287 | TNFRSF13B | c.318C>T (p.Asn106=) n.321C>T n.222C>T c.180C>T (p.Asn60=) | ClinVar dbSNP |
| 17 | g.16948865G>C | CA398520002 | TNFRSF13B | c.318C>G (p.Asn106Lys) n.321C>G n.222C>G c.180C>G (p.Asn60Lys) | |
| 17 | g.16948865G>T | CA398520003 | TNFRSF13B | c.318C>A (p.Asn106Lys) n.321C>A n.222C>A c.180C>A (p.Asn60Lys) | |
| 17 | g.16948866T>A | CA398520004 | TNFRSF13B | c.317A>T (p.Asn106Ile) n.320A>T n.221A>T c.179A>T (p.Asn60Ile) | |
| 17 | g.16948866T>C | CA398520005 | TNFRSF13B | c.317A>G (p.Asn106Ser) n.320A>G n.221A>G c.179A>G (p.Asn60Ser) | ClinVar dbSNP |
| 17 | g.16948866T>G | CA398520006 | TNFRSF13B | c.317A>C (p.Asn106Thr) n.320A>C n.221A>C c.179A>C (p.Asn60Thr) | |
| 17 | g.16948866T= | CA2250304770 | TNFRSF13B | c.317A= (p.Asn106=) n.320A= n.221A= c.179A= (p.Asn60=) | |
| 17 | g.16948867T>A | CA398520009 | TNFRSF13B | c.316A>T (p.Asn106Tyr) n.319A>T n.220A>T c.178A>T (p.Asn60Tyr) | |
| 17 | g.16948867T>C | CA398520008 | TNFRSF13B | c.316A>G (p.Asn106Asp) n.319A>G n.220A>G c.178A>G (p.Asn60Asp) | |
| 17 | g.16948867T>G | CA398520007 | TNFRSF13B | c.316A>C (p.Asn106His) n.319A>C n.220A>C c.178A>C (p.Asn60His) | |
| 17 | g.16948868C>A | CA398520010 | TNFRSF13B | c.315G>T (p.Glu105Asp) n.318G>T n.219G>T c.177G>T (p.Glu59Asp) | |
| 17 | g.16948868C= | CA2250304786 | TNFRSF13B | c.315G= (p.Glu105=) n.318G= n.219G= c.177G= (p.Glu59=) | |
| 17 | g.16948868C>G | CA398520011 | TNFRSF13B | c.315G>C (p.Glu105Asp) n.318G>C n.219G>C c.177G>C (p.Glu59Asp) | gnomAD v4 |
| 17 | g.16948868C>T | CA288288048 | TNFRSF13B | c.315G>A (p.Glu105=) n.318G>A n.219G>A c.177G>A (p.Glu59=) | dbSNP |
| 17 | g.16948869T>A | CA398520012 | TNFRSF13B | c.314A>T (p.Glu105Val) n.317A>T n.218A>T c.176A>T (p.Glu59Val) | |
| 17 | g.16948869T>C | CA398520013 | TNFRSF13B | c.314A>G (p.Glu105Gly) n.317A>G n.218A>G c.176A>G (p.Glu59Gly) | |
| 17 | g.16948869T>G | CA398520014 | TNFRSF13B | c.314A>C (p.Glu105Ala) n.317A>C n.218A>C c.176A>C (p.Glu59Ala) | |
| 17 | g.16948870C>A | CA398520015 | TNFRSF13B | c.313G>T (p.Glu105Ter) n.316G>T n.217G>T c.175G>T (p.Glu59Ter) | |
| 17 | g.16948870C= | CA2250304794 | TNFRSF13B | c.313G= (p.Glu105=) n.316G= n.217G= c.175G= (p.Glu59=) | |
| 17 | g.16948870C>G | CA398520016 | TNFRSF13B | c.313G>C (p.Glu105Gln) n.316G>C n.217G>C c.175G>C (p.Glu59Gln) | |
| 17 | g.16948870C>T | CA8414039 | TNFRSF13B | c.313G>A (p.Glu105Lys) n.316G>A n.217G>A c.175G>A (p.Glu59Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948871A= | CA2250304798 | TNFRSF13B | c.312T= (p.Cys104=) n.315T= n.216T= c.174T= (p.Cys58=) | |
| 17 | g.16948871A>C | CA398520017 | TNFRSF13B | c.312T>G (p.Cys104Trp) n.315T>G n.216T>G c.174T>G (p.Cys58Trp) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948871A>G | CA498420288 | TNFRSF13B | c.312T>C (p.Cys104=) n.315T>C n.216T>C c.174T>C (p.Cys58=) | |
| 17 | g.16948871A>T | CA398520018 | TNFRSF13B | c.312T>A (p.Cys104Ter) n.315T>A n.216T>A c.174T>A (p.Cys58Ter) | |
| 17 | g.16948872C>A | CA398520019 | TNFRSF13B | c.311G>T (p.Cys104Phe) n.314G>T n.215G>T c.173G>T (p.Cys58Phe) | |
| 17 | g.16948872C= | CA2250304804 | TNFRSF13B | c.311G= (p.Cys104=) n.314G= n.215G= c.173G= (p.Cys58=) | |
| 17 | g.16948872C>G | CA398520020 | TNFRSF13B | c.311G>C (p.Cys104Ser) n.314G>C n.215G>C c.173G>C (p.Cys58Ser) | |
| 17 | g.16948872C>T | CA8414040 | TNFRSF13B | c.311G>A (p.Cys104Tyr) n.314G>A n.215G>A c.173G>A (p.Cys58Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948873A= | CA2250304812 | TNFRSF13B | c.310T= (p.Cys104=) n.313T= n.214T= c.172T= (p.Cys58=) | |
| 17 | g.16948873A>C | CA398520022 | TNFRSF13B | c.310T>G (p.Cys104Gly) n.313T>G n.214T>G c.172T>G (p.Cys58Gly) | |
| 17 | g.16948873A>G | CA117387 | TNFRSF13B | c.310T>C (p.Cys104Arg) n.313T>C n.214T>C c.172T>C (p.Cys58Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948873A>T | CA398520021 | TNFRSF13B | c.310T>A (p.Cys104Ser) n.313T>A n.214T>A c.172T>A (p.Cys58Ser) |