Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.16948776_16948785delinsTACCTTCCCG | CA2250304451 | TNFRSF13B | c.398_407delinsCGGGAAGGTA (p.Ser133=) n.401_410delinsCGGGAAGGTA n.302_311delinsCGGGAAGGTA c.260_269delinsCGGGAAGGTA (p.Ser87=) | |
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.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) |