Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.98707879_98707880delinsCG | CA2199177506 | IGF1R | c.412_413delinsCG (p.Arg138=) c.49_50delinsCG (p.Arg17=) n.412_413delinsCG c.487_488delinsCG (p.Arg163=) | |
15 | g.98707880G>A | CA124307 | IGF1R | c.413G>A (p.Arg138Gln) c.50G>A (p.Arg17Gln) n.413G>A c.488G>A (p.Arg163Gln) | ClinVar dbSNP |
15 | g.98707880G>C | CA393697222 | IGF1R | c.413G>C (p.Arg138Pro) c.50G>C (p.Arg17Pro) n.413G>C c.488G>C (p.Arg163Pro) | |
15 | g.98707880G= | CA2199177508 | IGF1R | c.413G= (p.Arg138=) c.50G= (p.Arg17=) n.413G= c.488G= (p.Arg163=) | |
15 | g.98707880G>T | CA7751791 | IGF1R | c.413G>T (p.Arg138Leu) c.50G>T (p.Arg17Leu) n.413G>T c.488G>T (p.Arg163Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.98707885dup | CA7751789 | IGF1R | c.418dup (p.Ala140GlyfsTer5) c.55dup (p.Ala19GlyfsTer5) n.418dup c.493dup (p.Ala165GlyfsTer5) | ClinVar dbSNP ExAC |
15 | g.98707885del | CA7751790 | IGF1R | c.418del (p.Ala140ProfsTer20) c.55del (p.Ala19ProfsTer20) n.418del c.493del (p.Ala165ProfsTer20) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
15 | g.98707881G>A | CA492686352 | IGF1R | c.414G>A (p.Arg138=) c.51G>A (p.Arg17=) n.414G>A c.489G>A (p.Arg163=) | gnomAD v4 |
15 | g.98707881G>C | CA492686353 | IGF1R | c.414G>C (p.Arg138=) c.51G>C (p.Arg17=) n.414G>C c.489G>C (p.Arg163=) | |
15 | g.98707881G>T | CA492686354 | IGF1R | c.414G>T (p.Arg138=) c.51G>T (p.Arg17=) n.414G>T c.489G>T (p.Arg163=) | |
15 | g.98707882G>A | CA393697225 | IGF1R | c.415G>A (p.Gly139Arg) c.52G>A (p.Gly18Arg) n.415G>A c.490G>A (p.Gly164Arg) | |
15 | g.98707882G>C | CA393697223 | IGF1R | c.415G>C (p.Gly139Arg) c.52G>C (p.Gly18Arg) n.415G>C c.490G>C (p.Gly164Arg) | |
15 | g.98707882G>T | CA393697224 | IGF1R | c.415G>T (p.Gly139Trp) c.52G>T (p.Gly18Trp) n.415G>T c.490G>T (p.Gly164Trp) | |
15 | g.98707883G>A | CA393697226 | IGF1R | c.416G>A (p.Gly139Glu) c.53G>A (p.Gly18Glu) n.416G>A c.491G>A (p.Gly164Glu) | dbSNP |
15 | g.98707883G>C | CA393697227 | IGF1R | c.416G>C (p.Gly139Ala) c.53G>C (p.Gly18Ala) n.416G>C c.491G>C (p.Gly164Ala) | |
15 | g.98707883G>T | CA393697228 | IGF1R | c.416G>T (p.Gly139Val) c.53G>T (p.Gly18Val) n.416G>T c.491G>T (p.Gly164Val) | |
15 | g.98707884G>A | CA492686356 | IGF1R | c.417G>A (p.Gly139=) c.54G>A (p.Gly18=) n.417G>A c.492G>A (p.Gly164=) | dbSNP gnomAD v4 |
15 | g.98707884G>C | CA492686359 | IGF1R | c.417G>C (p.Gly139=) c.54G>C (p.Gly18=) n.417G>C c.492G>C (p.Gly164=) | |
15 | g.98707884G>T | CA492686357 | IGF1R | c.417G>T (p.Gly139=) c.54G>T (p.Gly18=) n.417G>T c.492G>T (p.Gly164=) | |
15 | g.98707885G>A | CA393697229 | IGF1R | c.418G>A (p.Ala140Thr) c.55G>A (p.Ala19Thr) n.418G>A c.493G>A (p.Ala165Thr) | dbSNP gnomAD v4 |
15 | g.98707885G>C | CA393697230 | IGF1R | c.418G>C (p.Ala140Pro) c.55G>C (p.Ala19Pro) n.418G>C c.493G>C (p.Ala165Pro) | dbSNP |
15 | g.98707885G= | CA2199177509 | IGF1R | c.418G= (p.Ala140=) c.55G= (p.Ala19=) n.418G= c.493G= (p.Ala165=) | |
15 | g.98707885G>T | CA393697231 | IGF1R | c.418G>T (p.Ala140Ser) c.55G>T (p.Ala19Ser) n.418G>T c.493G>T (p.Ala165Ser) | |
15 | g.98707886C>A | CA393697232 | IGF1R | c.419C>A (p.Ala140Asp) c.56C>A (p.Ala19Asp) n.419C>A c.494C>A (p.Ala165Asp) | gnomAD v4 |
15 | g.98707886C= | CA2199177510 | IGF1R | c.419C= (p.Ala140=) c.56C= (p.Ala19=) n.419C= c.494C= (p.Ala165=) | |
15 | g.98707886C>G | CA393697233 | IGF1R | c.419C>G (p.Ala140Gly) c.56C>G (p.Ala19Gly) n.419C>G c.494C>G (p.Ala165Gly) | dbSNP |
15 | g.98707886C>T | CA275819421 | IGF1R | c.419C>T (p.Ala140Val) c.56C>T (p.Ala19Val) n.419C>T c.494C>T (p.Ala165Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.98707887del | CA2695221147 | IGF1R | c.420del (p.Ile141SerfsTer19) c.57del (p.Ile20SerfsTer19) n.420del c.495del (p.Ile166SerfsTer19) | |
15 | g.98707887C>A | CA492686378 | IGF1R | c.420C>A (p.Ala140=) c.57C>A (p.Ala19=) n.420C>A c.495C>A (p.Ala165=) | |
15 | g.98707887C>G | CA492686381 | IGF1R | c.420C>G (p.Ala140=) c.57C>G (p.Ala19=) n.420C>G c.495C>G (p.Ala165=) | |
15 | g.98707887C>T | CA492686383 | IGF1R | c.420C>T (p.Ala140=) c.57C>T (p.Ala19=) n.420C>T c.495C>T (p.Ala165=) | |
15 | g.98707888A>C | CA393697236 | IGF1R | c.421A>C (p.Ile141Leu) c.58A>C (p.Ile20Leu) n.421A>C c.496A>C (p.Ile166Leu) | |
15 | g.98707888A>G | CA393697235 | IGF1R | c.421A>G (p.Ile141Val) c.58A>G (p.Ile20Val) n.421A>G c.496A>G (p.Ile166Val) | |
15 | g.98707888A>T | CA393697234 | IGF1R | c.421A>T (p.Ile141Phe) c.58A>T (p.Ile20Phe) n.421A>T c.496A>T (p.Ile166Phe) | |
15 | g.98707889T>A | CA393697237 | IGF1R | c.422T>A (p.Ile141Asn) c.59T>A (p.Ile20Asn) n.422T>A c.497T>A (p.Ile166Asn) | |
15 | g.98707889T>C | CA393697238 | IGF1R | c.422T>C (p.Ile141Thr) c.59T>C (p.Ile20Thr) n.422T>C c.497T>C (p.Ile166Thr) | |
15 | g.98707889T>G | CA393697239 | IGF1R | c.422T>G (p.Ile141Ser) c.59T>G (p.Ile20Ser) n.422T>G c.497T>G (p.Ile166Ser) | |
15 | g.98707890C>A | CA492686387 | IGF1R | c.423C>A (p.Ile141=) c.60C>A (p.Ile20=) n.423C>A c.498C>A (p.Ile166=) | |
15 | g.98707890C= | CA2199177511 | IGF1R | c.423C= (p.Ile141=) c.60C= (p.Ile20=) n.423C= c.498C= (p.Ile166=) | |
15 | g.98707890C>G | CA393697240 | IGF1R | c.423C>G (p.Ile141Met) c.60C>G (p.Ile20Met) n.423C>G c.498C>G (p.Ile166Met) | dbSNP |
15 | g.98707890C>T | CA7751792 | IGF1R | c.423C>T (p.Ile141=) c.60C>T (p.Ile20=) n.423C>T c.498C>T (p.Ile166=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.98707891A>C | CA492686388 | IGF1R | c.424A>C (p.Arg142=) c.61A>C (p.Arg21=) n.424A>C c.499A>C (p.Arg167=) | |
15 | g.98707891A>G | CA393697241 | IGF1R | c.424A>G (p.Arg142Gly) c.61A>G (p.Arg21Gly) n.424A>G c.499A>G (p.Arg167Gly) | |
15 | g.98707891A>T | CA393697242 | IGF1R | c.424A>T (p.Arg142Trp) c.61A>T (p.Arg21Trp) n.424A>T c.499A>T (p.Arg167Trp) | |
15 | g.98707892G>A | CA393697243 | IGF1R | c.425G>A (p.Arg142Lys) c.62G>A (p.Arg21Lys) n.425G>A c.500G>A (p.Arg167Lys) | dbSNP |
15 | g.98707892G>C | CA393697244 | IGF1R | c.425G>C (p.Arg142Thr) c.62G>C (p.Arg21Thr) n.425G>C c.500G>C (p.Arg167Thr) | dbSNP |
15 | g.98707892G>T | CA393697245 | IGF1R | c.425G>T (p.Arg142Met) c.62G>T (p.Arg21Met) n.425G>T c.500G>T (p.Arg167Met) | |
15 | g.98707893G>A | CA492686391 | IGF1R | c.426G>A (p.Arg142=) c.63G>A (p.Arg21=) n.426G>A c.501G>A (p.Arg167=) | dbSNP |
15 | g.98707893G>C | CA393697246 | IGF1R | c.426G>C (p.Arg142Ser) c.63G>C (p.Arg21Ser) n.426G>C c.501G>C (p.Arg167Ser) | |
15 | g.98707893G>T | CA393697247 | IGF1R | c.426G>T (p.Arg142Ser) c.63G>T (p.Arg21Ser) n.426G>T c.501G>T (p.Arg167Ser) |