| 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) | |
| 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=) |