Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.98707879_98707880delinsCGCA2199177506IGF1Rc.412_413delinsCG (p.Arg138=)
c.49_50delinsCG (p.Arg17=)
n.412_413delinsCG
c.487_488delinsCG (p.Arg163=)
15g.98707880G>ACA124307IGF1Rc.413G>A (p.Arg138Gln)
c.50G>A (p.Arg17Gln)
n.413G>A
c.488G>A (p.Arg163Gln)
ClinVar dbSNP
15g.98707880G>CCA393697222IGF1Rc.413G>C (p.Arg138Pro)
c.50G>C (p.Arg17Pro)
n.413G>C
c.488G>C (p.Arg163Pro)
15g.98707880G=CA2199177508IGF1Rc.413G= (p.Arg138=)
c.50G= (p.Arg17=)
n.413G=
c.488G= (p.Arg163=)
15g.98707880G>TCA7751791IGF1Rc.413G>T (p.Arg138Leu)
c.50G>T (p.Arg17Leu)
n.413G>T
c.488G>T (p.Arg163Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.98707885dupCA7751789IGF1Rc.418dup (p.Ala140GlyfsTer5)
c.55dup (p.Ala19GlyfsTer5)
n.418dup
c.493dup (p.Ala165GlyfsTer5)
ClinVar dbSNP ExAC
15g.98707885delCA7751790IGF1Rc.418del (p.Ala140ProfsTer20)
c.55del (p.Ala19ProfsTer20)
n.418del
c.493del (p.Ala165ProfsTer20)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
15g.98707881G>ACA492686352IGF1Rc.414G>A (p.Arg138=)
c.51G>A (p.Arg17=)
n.414G>A
c.489G>A (p.Arg163=)
gnomAD v4
15g.98707881G>CCA492686353IGF1Rc.414G>C (p.Arg138=)
c.51G>C (p.Arg17=)
n.414G>C
c.489G>C (p.Arg163=)
15g.98707881G>TCA492686354IGF1Rc.414G>T (p.Arg138=)
c.51G>T (p.Arg17=)
n.414G>T
c.489G>T (p.Arg163=)
15g.98707882G>ACA393697225IGF1Rc.415G>A (p.Gly139Arg)
c.52G>A (p.Gly18Arg)
n.415G>A
c.490G>A (p.Gly164Arg)
15g.98707882G>CCA393697223IGF1Rc.415G>C (p.Gly139Arg)
c.52G>C (p.Gly18Arg)
n.415G>C
c.490G>C (p.Gly164Arg)
15g.98707882G>TCA393697224IGF1Rc.415G>T (p.Gly139Trp)
c.52G>T (p.Gly18Trp)
n.415G>T
c.490G>T (p.Gly164Trp)
15g.98707883G>ACA393697226IGF1Rc.416G>A (p.Gly139Glu)
c.53G>A (p.Gly18Glu)
n.416G>A
c.491G>A (p.Gly164Glu)
dbSNP
15g.98707883G>CCA393697227IGF1Rc.416G>C (p.Gly139Ala)
c.53G>C (p.Gly18Ala)
n.416G>C
c.491G>C (p.Gly164Ala)
15g.98707883G>TCA393697228IGF1Rc.416G>T (p.Gly139Val)
c.53G>T (p.Gly18Val)
n.416G>T
c.491G>T (p.Gly164Val)
15g.98707884G>ACA492686356IGF1Rc.417G>A (p.Gly139=)
c.54G>A (p.Gly18=)
n.417G>A
c.492G>A (p.Gly164=)
dbSNP gnomAD v4
15g.98707884G>CCA492686359IGF1Rc.417G>C (p.Gly139=)
c.54G>C (p.Gly18=)
n.417G>C
c.492G>C (p.Gly164=)
15g.98707884G>TCA492686357IGF1Rc.417G>T (p.Gly139=)
c.54G>T (p.Gly18=)
n.417G>T
c.492G>T (p.Gly164=)
15g.98707885G>ACA393697229IGF1Rc.418G>A (p.Ala140Thr)
c.55G>A (p.Ala19Thr)
n.418G>A
c.493G>A (p.Ala165Thr)
dbSNP gnomAD v4
15g.98707885G>CCA393697230IGF1Rc.418G>C (p.Ala140Pro)
c.55G>C (p.Ala19Pro)
n.418G>C
c.493G>C (p.Ala165Pro)
dbSNP
15g.98707885G=CA2199177509IGF1Rc.418G= (p.Ala140=)
c.55G= (p.Ala19=)
n.418G=
c.493G= (p.Ala165=)
15g.98707885G>TCA393697231IGF1Rc.418G>T (p.Ala140Ser)
c.55G>T (p.Ala19Ser)
n.418G>T
c.493G>T (p.Ala165Ser)
15g.98707886C>ACA393697232IGF1Rc.419C>A (p.Ala140Asp)
c.56C>A (p.Ala19Asp)
n.419C>A
c.494C>A (p.Ala165Asp)
gnomAD v4
15g.98707886C=CA2199177510IGF1Rc.419C= (p.Ala140=)
c.56C= (p.Ala19=)
n.419C=
c.494C= (p.Ala165=)
15g.98707886C>GCA393697233IGF1Rc.419C>G (p.Ala140Gly)
c.56C>G (p.Ala19Gly)
n.419C>G
c.494C>G (p.Ala165Gly)
dbSNP
15g.98707886C>TCA275819421IGF1Rc.419C>T (p.Ala140Val)
c.56C>T (p.Ala19Val)
n.419C>T
c.494C>T (p.Ala165Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
15g.98707887delCA2695221147IGF1Rc.420del (p.Ile141SerfsTer19)
c.57del (p.Ile20SerfsTer19)
n.420del
c.495del (p.Ile166SerfsTer19)
15g.98707887C>ACA492686378IGF1Rc.420C>A (p.Ala140=)
c.57C>A (p.Ala19=)
n.420C>A
c.495C>A (p.Ala165=)
15g.98707887C>GCA492686381IGF1Rc.420C>G (p.Ala140=)
c.57C>G (p.Ala19=)
n.420C>G
c.495C>G (p.Ala165=)
15g.98707887C>TCA492686383IGF1Rc.420C>T (p.Ala140=)
c.57C>T (p.Ala19=)
n.420C>T
c.495C>T (p.Ala165=)
15g.98707888A>CCA393697236IGF1Rc.421A>C (p.Ile141Leu)
c.58A>C (p.Ile20Leu)
n.421A>C
c.496A>C (p.Ile166Leu)
15g.98707888A>GCA393697235IGF1Rc.421A>G (p.Ile141Val)
c.58A>G (p.Ile20Val)
n.421A>G
c.496A>G (p.Ile166Val)
15g.98707888A>TCA393697234IGF1Rc.421A>T (p.Ile141Phe)
c.58A>T (p.Ile20Phe)
n.421A>T
c.496A>T (p.Ile166Phe)
15g.98707889T>ACA393697237IGF1Rc.422T>A (p.Ile141Asn)
c.59T>A (p.Ile20Asn)
n.422T>A
c.497T>A (p.Ile166Asn)
15g.98707889T>CCA393697238IGF1Rc.422T>C (p.Ile141Thr)
c.59T>C (p.Ile20Thr)
n.422T>C
c.497T>C (p.Ile166Thr)
15g.98707889T>GCA393697239IGF1Rc.422T>G (p.Ile141Ser)
c.59T>G (p.Ile20Ser)
n.422T>G
c.497T>G (p.Ile166Ser)
15g.98707890C>ACA492686387IGF1Rc.423C>A (p.Ile141=)
c.60C>A (p.Ile20=)
n.423C>A
c.498C>A (p.Ile166=)
15g.98707890C=CA2199177511IGF1Rc.423C= (p.Ile141=)
c.60C= (p.Ile20=)
n.423C=
c.498C= (p.Ile166=)
15g.98707890C>GCA393697240IGF1Rc.423C>G (p.Ile141Met)
c.60C>G (p.Ile20Met)
n.423C>G
c.498C>G (p.Ile166Met)
dbSNP
15g.98707890C>TCA7751792IGF1Rc.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
15g.98707891A>CCA492686388IGF1Rc.424A>C (p.Arg142=)
c.61A>C (p.Arg21=)
n.424A>C
c.499A>C (p.Arg167=)
15g.98707891A>GCA393697241IGF1Rc.424A>G (p.Arg142Gly)
c.61A>G (p.Arg21Gly)
n.424A>G
c.499A>G (p.Arg167Gly)
15g.98707891A>TCA393697242IGF1Rc.424A>T (p.Arg142Trp)
c.61A>T (p.Arg21Trp)
n.424A>T
c.499A>T (p.Arg167Trp)
15g.98707892G>ACA393697243IGF1Rc.425G>A (p.Arg142Lys)
c.62G>A (p.Arg21Lys)
n.425G>A
c.500G>A (p.Arg167Lys)
dbSNP
15g.98707892G>CCA393697244IGF1Rc.425G>C (p.Arg142Thr)
c.62G>C (p.Arg21Thr)
n.425G>C
c.500G>C (p.Arg167Thr)
dbSNP
15g.98707892G>TCA393697245IGF1Rc.425G>T (p.Arg142Met)
c.62G>T (p.Arg21Met)
n.425G>T
c.500G>T (p.Arg167Met)
15g.98707893G>ACA492686391IGF1Rc.426G>A (p.Arg142=)
c.63G>A (p.Arg21=)
n.426G>A
c.501G>A (p.Arg167=)
dbSNP
15g.98707893G>CCA393697246IGF1Rc.426G>C (p.Arg142Ser)
c.63G>C (p.Arg21Ser)
n.426G>C
c.501G>C (p.Arg167Ser)
15g.98707893G>TCA393697247IGF1Rc.426G>T (p.Arg142Ser)
c.63G>T (p.Arg21Ser)
n.426G>T
c.501G>T (p.Arg167Ser)

Number of alleles fetched