| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) | |
| 17 | g.16948874G>A | CA498420289 | TNFRSF13B | c.309C>T (p.Phe103=) n.312C>T n.213C>T c.171C>T (p.Phe57=) | |
| 17 | g.16948874G>C | CA398520023 | TNFRSF13B | c.309C>G (p.Phe103Leu) n.312C>G n.213C>G c.171C>G (p.Phe57Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.16948874G= | CA2250304822 | TNFRSF13B | c.309C= (p.Phe103=) n.312C= n.213C= c.171C= (p.Phe57=) | |
| 17 | g.16948874G>T | CA398520024 | TNFRSF13B | c.309C>A (p.Phe103Leu) n.312C>A n.213C>A c.171C>A (p.Phe57Leu) | |
| 17 | g.16948874_16948875delinsGA | CA2250304826 | TNFRSF13B | c.308_309delinsTC (p.Phe103=) n.311_312delinsTC n.212_213delinsTC c.170_171delinsTC (p.Phe57=) | |
| 17 | g.16948875A= | CA2250304833 | TNFRSF13B | c.308T= (p.Phe103=) n.311T= n.212T= c.170T= (p.Phe57=) | |
| 17 | g.16948875A>C | CA398520025 | TNFRSF13B | c.308T>G (p.Phe103Cys) n.311T>G n.212T>G c.170T>G (p.Phe57Cys) | |
| 17 | g.16948875A>G | CA8414041 | TNFRSF13B | c.308T>C (p.Phe103Ser) n.311T>C n.212T>C c.170T>C (p.Phe57Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948875A>T | CA398520026 | TNFRSF13B | c.308T>A (p.Phe103Tyr) n.311T>A n.212T>A c.170T>A (p.Phe57Tyr) | |
| 17 | g.16948876del | CA625313746 | TNFRSF13B | c.308del (p.Phe103SerfsTer10) n.311del n.212del c.170del (p.Phe57SerfsTer10) | dbSNP gnomAD v2 |
| 17 | g.16948876A>C | CA398520027 | TNFRSF13B | c.307T>G (p.Phe103Val) n.310T>G n.211T>G c.169T>G (p.Phe57Val) | |
| 17 | g.16948876A>G | CA398520028 | TNFRSF13B | c.307T>C (p.Phe103Leu) n.310T>C n.211T>C c.169T>C (p.Phe57Leu) | |
| 17 | g.16948876A>T | CA398520029 | TNFRSF13B | c.307T>A (p.Phe103Ile) n.310T>A n.211T>A c.169T>A (p.Phe57Ile) | |
| 17 | g.16948876_16948877del | CA2695224526 | TNFRSF13B | c.306_307del (p.Phe103LeufsTer2) n.309_310del n.210_211del c.168_169del (p.Phe57LeufsTer2) | |
| 17 | g.16948876_16948877delinsAG | CA2250304839 | TNFRSF13B | c.306_307delinsCT (p.Tyr102=) n.309_310delinsCT n.210_211delinsCT c.168_169delinsCT (p.Tyr56=) | |
| 17 | g.16948877del | CA8414042 | TNFRSF13B | c.306del (p.Phe103SerfsTer10) n.309del n.210del c.168del (p.Phe57SerfsTer10) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948877G>A | CA498420290 | TNFRSF13B | c.306C>T (p.Tyr102=) n.309C>T n.210C>T c.168C>T (p.Tyr56=) | gnomAD v4 |
| 17 | g.16948877G>C | CA398520030 | TNFRSF13B | c.306C>G (p.Tyr102Ter) n.309C>G n.210C>G c.168C>G (p.Tyr56Ter) | |
| 17 | g.16948877G= | CA2250304844 | TNFRSF13B | c.306C= (p.Tyr102=) n.309C= n.210C= c.168C= (p.Tyr56=) | |
| 17 | g.16948877G>T | CA8414043 | TNFRSF13B | c.306C>A (p.Tyr102Ter) n.309C>A n.210C>A c.168C>A (p.Tyr56Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948877_16948880delinsCAA | CA2695201252 | TNFRSF13B | c.303_306delinsTTG (p.Tyr102CysfsTer11) n.306_309delinsTTG n.207_210delinsTTG c.165_168delinsTTG (p.Tyr56CysfsTer11) | ClinVar |
| 17 | g.16948878_16948881dup | CA2576183922 | TNFRSF13B | c.303_306dup (p.Phe103IlefsTer4) n.306_309dup n.207_210dup c.165_168dup (p.Phe57IlefsTer4) | gnomAD v4 |
| 17 | g.16948878T>A | CA398520032 | TNFRSF13B | c.305A>T (p.Tyr102Phe) n.308A>T n.209A>T c.167A>T (p.Tyr56Phe) | |
| 17 | g.16948878T>C | CA8414044 | TNFRSF13B | c.305A>G (p.Tyr102Cys) n.308A>G n.209A>G c.167A>G (p.Tyr56Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948878T>G | CA398520031 | TNFRSF13B | c.305A>C (p.Tyr102Ser) n.308A>C n.209A>C c.167A>C (p.Tyr56Ser) | |
| 17 | g.16948878T= | CA2250304857 | TNFRSF13B | c.305A= (p.Tyr102=) n.308A= n.209A= c.167A= (p.Tyr56=) | |
| 17 | g.16948879A= | CA2250304858 | TNFRSF13B | c.304T= (p.Tyr102=) n.307T= n.208T= c.166T= (p.Tyr56=) | |
| 17 | g.16948879A>C | CA398520033 | TNFRSF13B | c.304T>G (p.Tyr102Asp) n.307T>G n.208T>G c.166T>G (p.Tyr56Asp) | |
| 17 | g.16948879A>G | CA398520034 | TNFRSF13B | c.304T>C (p.Tyr102His) n.307T>C n.208T>C c.166T>C (p.Tyr56His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948879A>T | CA8414045 | TNFRSF13B | c.304T>A (p.Tyr102Asn) n.307T>A n.208T>A c.166T>A (p.Tyr56Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.16948880T>A | CA8414046 | TNFRSF13B | c.303A>T (p.Ala101=) n.306A>T n.207A>T c.165A>T (p.Ala55=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 17 | g.16948880T>C | CA498420292 | TNFRSF13B | c.303A>G (p.Ala101=) n.306A>G n.207A>G c.165A>G (p.Ala55=) | |
| 17 | g.16948880T>G | CA498420291 | TNFRSF13B | c.303A>C (p.Ala101=) n.306A>C n.207A>C c.165A>C (p.Ala55=) | ClinVar |
| 17 | g.16948880T= | CA2250304862 | TNFRSF13B | c.303A= (p.Ala101=) n.306A= n.207A= c.165A= (p.Ala55=) | |
| 17 | g.16948881G>A | CA398520035 | TNFRSF13B | c.302C>T (p.Ala101Val) n.305C>T n.206C>T c.164C>T (p.Ala55Val) | dbSNP |
| 17 | g.16948881G>C | CA398520036 | TNFRSF13B | c.302C>G (p.Ala101Gly) n.305C>G n.206C>G c.164C>G (p.Ala55Gly) | |
| 17 | g.16948881G= | CA2250304872 | TNFRSF13B | c.302C= (p.Ala101=) n.305C= n.206C= c.164C= (p.Ala55=) | |
| 17 | g.16948881G>T | CA398520037 | TNFRSF13B | c.302C>A (p.Ala101Glu) n.305C>A n.206C>A c.164C>A (p.Ala55Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.16948882C>A | CA398520038 | TNFRSF13B | c.301G>T (p.Ala101Ser) n.304G>T n.205G>T c.163G>T (p.Ala55Ser) | dbSNP gnomAD v4 |
| 17 | g.16948882C= | CA2250304877 | TNFRSF13B | c.301G= (p.Ala101=) n.304G= n.205G= c.163G= (p.Ala55=) | |
| 17 | g.16948882C>G | CA398520039 | TNFRSF13B | c.301G>C (p.Ala101Pro) n.304G>C n.205G>C c.163G>C (p.Ala55Pro) | |
| 17 | g.16948882C>T | CA398520040 | TNFRSF13B | c.301G>A (p.Ala101Thr) n.304G>A n.205G>A c.163G>A (p.Ala55Thr) | dbSNP |
| 17 | g.16948883A= | CA2250304883 | TNFRSF13B | c.300T= (p.Cys100=) n.303T= n.204T= c.162T= (p.Cys54=) | |
| 17 | g.16948883A>C | CA398520041 | TNFRSF13B | c.300T>G (p.Cys100Trp) n.303T>G n.204T>G c.162T>G (p.Cys54Trp) | |
| 17 | g.16948883A>G | CA498420293 | TNFRSF13B | c.300T>C (p.Cys100=) n.303T>C n.204T>C c.162T>C (p.Cys54=) | dbSNP gnomAD v4 |
| 17 | g.16948883A>T | CA398520042 | TNFRSF13B | c.300T>A (p.Cys100Ter) n.303T>A n.204T>A c.162T>A (p.Cys54Ter) |