Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.30672006G>ACA351807948TGFBR2c.823G>A (p.Ala275Thr)
n.2419G>A
c.898G>A (p.Ala300Thr)
c.850G>A (p.Ala284Thr)
c.775G>A (p.Ala259Thr)
c.718G>A (p.Ala240Thr)
dbSNP
3g.30672006G>CCA351807949TGFBR2c.823G>C (p.Ala275Pro)
n.2419G>C
c.898G>C (p.Ala300Pro)
c.850G>C (p.Ala284Pro)
c.775G>C (p.Ala259Pro)
c.718G>C (p.Ala240Pro)
dbSNP
3g.30672006G=CA1354873087TGFBR2c.823G= (p.Ala275=)
n.2419G=
c.898G= (p.Ala300=)
c.850G= (p.Ala284=)
c.775G= (p.Ala259=)
c.718G= (p.Ala240=)
3g.30672006G>TCA049958TGFBR2c.823G>T (p.Ala275Ser)
n.2419G>T
c.898G>T (p.Ala300Ser)
c.850G>T (p.Ala284Ser)
c.775G>T (p.Ala259Ser)
c.718G>T (p.Ala240Ser)
ClinVar dbSNP ExAC gnomAD v2
3g.30672007C>ACA351807950TGFBR2c.824C>A (p.Ala275Glu)
n.2420C>A
c.899C>A (p.Ala300Glu)
c.851C>A (p.Ala284Glu)
c.776C>A (p.Ala259Glu)
c.719C>A (p.Ala240Glu)
dbSNP
3g.30672007C>GCA351807951TGFBR2c.824C>G (p.Ala275Gly)
n.2420C>G
c.899C>G (p.Ala300Gly)
c.851C>G (p.Ala284Gly)
c.776C>G (p.Ala259Gly)
c.719C>G (p.Ala240Gly)
dbSNP
3g.30672007C>TCA351807952TGFBR2c.824C>T (p.Ala275Val)
n.2420C>T
c.899C>T (p.Ala300Val)
c.851C>T (p.Ala284Val)
c.776C>T (p.Ala259Val)
c.719C>T (p.Ala240Val)
dbSNP gnomAD v4
3g.30672008A>CCA433058784TGFBR2c.825A>C (p.Ala275=)
n.2421A>C
c.900A>C (p.Ala300=)
c.852A>C (p.Ala284=)
c.777A>C (p.Ala259=)
c.720A>C (p.Ala240=)
3g.30672008A>GCA433058785TGFBR2c.825A>G (p.Ala275=)
n.2421A>G
c.900A>G (p.Ala300=)
c.852A>G (p.Ala284=)
c.777A>G (p.Ala259=)
c.720A>G (p.Ala240=)
ClinVar dbSNP
3g.30672008A>TCA433058786TGFBR2c.825A>T (p.Ala275=)
n.2421A>T
c.900A>T (p.Ala300=)
c.852A>T (p.Ala284=)
c.777A>T (p.Ala259=)
c.720A>T (p.Ala240=)
3g.30672009G>ACA351807955TGFBR2c.826G>A (p.Val276Ile)
n.2422G>A
c.901G>A (p.Val301Ile)
c.853G>A (p.Val285Ile)
c.778G>A (p.Val260Ile)
c.721G>A (p.Val241Ile)
dbSNP
3g.30672009G>CCA351807954TGFBR2c.826G>C (p.Val276Leu)
n.2422G>C
c.901G>C (p.Val301Leu)
c.853G>C (p.Val285Leu)
c.778G>C (p.Val260Leu)
c.721G>C (p.Val241Leu)
dbSNP
3g.30672009G=CA1354873088TGFBR2c.826G= (p.Val276=)
n.2422G=
c.901G= (p.Val301=)
c.853G= (p.Val285=)
c.778G= (p.Val260=)
c.721G= (p.Val241=)
3g.30672009G>TCA351807953TGFBR2c.826G>T (p.Val276Phe)
n.2422G>T
c.901G>T (p.Val301Phe)
c.853G>T (p.Val285Phe)
c.778G>T (p.Val260Phe)
c.721G>T (p.Val241Phe)
ClinVar dbSNP
3g.30672010T>ACA351807956TGFBR2c.827T>A (p.Val276Asp)
n.2423T>A
c.902T>A (p.Val301Asp)
c.854T>A (p.Val285Asp)
c.779T>A (p.Val260Asp)
c.722T>A (p.Val241Asp)
dbSNP
3g.30672010T>CCA351807957TGFBR2c.827T>C (p.Val276Ala)
n.2423T>C
c.902T>C (p.Val301Ala)
c.854T>C (p.Val285Ala)
c.779T>C (p.Val260Ala)
c.722T>C (p.Val241Ala)
3g.30672010T>GCA71528136TGFBR2c.827T>G (p.Val276Gly)
n.2423T>G
c.902T>G (p.Val301Gly)
c.854T>G (p.Val285Gly)
c.779T>G (p.Val260Gly)
c.722T>G (p.Val241Gly)
dbSNP gnomAD v2
3g.30672010T=CA1354873089TGFBR2c.827T= (p.Val276=)
n.2423T=
c.902T= (p.Val301=)
c.854T= (p.Val285=)
c.779T= (p.Val260=)
c.722T= (p.Val241=)
3g.30672011C>ACA433058787TGFBR2c.828C>A (p.Val276=)
n.2424C>A
c.903C>A (p.Val301=)
c.855C>A (p.Val285=)
c.780C>A (p.Val260=)
c.723C>A (p.Val241=)
3g.30672011C>GCA433058789TGFBR2c.828C>G (p.Val276=)
n.2424C>G
c.903C>G (p.Val301=)
c.855C>G (p.Val285=)
c.780C>G (p.Val260=)
c.723C>G (p.Val241=)
dbSNP
3g.30672011C>TCA433058788TGFBR2c.828C>T (p.Val276=)
n.2424C>T
c.903C>T (p.Val301=)
c.855C>T (p.Val285=)
c.780C>T (p.Val260=)
c.723C>T (p.Val241=)
dbSNP
3g.30672012A>CCA351807958TGFBR2c.829A>C (p.Lys277Gln)
n.2425A>C
c.904A>C (p.Lys302Gln)
c.856A>C (p.Lys286Gln)
c.781A>C (p.Lys261Gln)
c.724A>C (p.Lys242Gln)
3g.30672012A>GCA351807959TGFBR2c.829A>G (p.Lys277Glu)
n.2425A>G
c.904A>G (p.Lys302Glu)
c.856A>G (p.Lys286Glu)
c.781A>G (p.Lys261Glu)
c.724A>G (p.Lys242Glu)
COSMIC
3g.30672012A>TCA351807960TGFBR2c.829A>T (p.Lys277Ter)
n.2425A>T
c.904A>T (p.Lys302Ter)
c.856A>T (p.Lys286Ter)
c.781A>T (p.Lys261Ter)
c.724A>T (p.Lys242Ter)
dbSNP
3g.30672013A>CCA351807963TGFBR2c.830A>C (p.Lys277Thr)
n.2426A>C
c.905A>C (p.Lys302Thr)
c.857A>C (p.Lys286Thr)
c.782A>C (p.Lys261Thr)
c.725A>C (p.Lys242Thr)
3g.30672013A>GCA351807961TGFBR2c.830A>G (p.Lys277Arg)
n.2426A>G
c.905A>G (p.Lys302Arg)
c.857A>G (p.Lys286Arg)
c.782A>G (p.Lys261Arg)
c.725A>G (p.Lys242Arg)
COSMIC COSMIC
3g.30672013A>TCA351807962TGFBR2c.830A>T (p.Lys277Met)
n.2426A>T
c.905A>T (p.Lys302Met)
c.857A>T (p.Lys286Met)
c.782A>T (p.Lys261Met)
c.725A>T (p.Lys242Met)
dbSNP
3g.30672014G>ACA433058790TGFBR2c.831G>A (p.Lys277=)
n.2427G>A
c.906G>A (p.Lys302=)
c.858G>A (p.Lys286=)
c.783G>A (p.Lys261=)
c.726G>A (p.Lys242=)
dbSNP
3g.30672014G>CCA351807964TGFBR2c.831G>C (p.Lys277Asn)
n.2427G>C
c.906G>C (p.Lys302Asn)
c.858G>C (p.Lys286Asn)
c.783G>C (p.Lys261Asn)
c.726G>C (p.Lys242Asn)
ClinVar dbSNP
3g.30672014G=CA1354873090TGFBR2c.831G= (p.Lys277=)
n.2427G=
c.906G= (p.Lys302=)
c.858G= (p.Lys286=)
c.783G= (p.Lys261=)
c.726G= (p.Lys242=)
3g.30672014G>TCA10587565TGFBR2c.831G>T (p.Lys277Asn)
n.2427G>T
c.906G>T (p.Lys302Asn)
c.858G>T (p.Lys286Asn)
c.783G>T (p.Lys261Asn)
c.726G>T (p.Lys242Asn)
ClinVar dbSNP COSMIC COSMIC
3g.30672015A=CA1354873091TGFBR2c.832A= (p.Ile278=)
n.2428A=
c.907A= (p.Ile303=)
c.859A= (p.Ile287=)
c.784A= (p.Ile262=)
c.727A= (p.Ile243=)
3g.30672015A>CCA351807965TGFBR2c.832A>C (p.Ile278Leu)
n.2428A>C
c.907A>C (p.Ile303Leu)
c.859A>C (p.Ile287Leu)
c.784A>C (p.Ile262Leu)
c.727A>C (p.Ile243Leu)
3g.30672015A>GCA351807966TGFBR2c.832A>G (p.Ile278Val)
n.2428A>G
c.907A>G (p.Ile303Val)
c.859A>G (p.Ile287Val)
c.784A>G (p.Ile262Val)
c.727A>G (p.Ile243Val)
3g.30672015A>TCA351807967TGFBR2c.832A>T (p.Ile278Phe)
n.2428A>T
c.907A>T (p.Ile303Phe)
c.859A>T (p.Ile287Phe)
c.784A>T (p.Ile262Phe)
c.727A>T (p.Ile243Phe)
ClinVar dbSNP
3g.30672016T>ACA351807968TGFBR2c.833T>A (p.Ile278Asn)
n.2429T>A
c.908T>A (p.Ile303Asn)
c.860T>A (p.Ile287Asn)
c.785T>A (p.Ile262Asn)
c.728T>A (p.Ile243Asn)
3g.30672016T>CCA351807970TGFBR2c.833T>C (p.Ile278Thr)
n.2429T>C
c.908T>C (p.Ile303Thr)
c.860T>C (p.Ile287Thr)
c.785T>C (p.Ile262Thr)
c.728T>C (p.Ile243Thr)
3g.30672016T>GCA351807969TGFBR2c.833T>G (p.Ile278Ser)
n.2429T>G
c.908T>G (p.Ile303Ser)
c.860T>G (p.Ile287Ser)
c.785T>G (p.Ile262Ser)
c.728T>G (p.Ile243Ser)
3g.30672017C>ACA433058797TGFBR2c.834C>A (p.Ile278=)
n.2430C>A
c.909C>A (p.Ile303=)
c.861C>A (p.Ile287=)
c.786C>A (p.Ile262=)
c.729C>A (p.Ile243=)
dbSNP gnomAD v3 gnomAD v4
3g.30672017C=CA1354873092TGFBR2c.834C= (p.Ile278=)
n.2430C=
c.909C= (p.Ile303=)
c.861C= (p.Ile287=)
c.786C= (p.Ile262=)
c.729C= (p.Ile243=)
3g.30672017C>GCA351807971TGFBR2c.834C>G (p.Ile278Met)
n.2430C>G
c.909C>G (p.Ile303Met)
c.861C>G (p.Ile287Met)
c.786C>G (p.Ile262Met)
c.729C>G (p.Ile243Met)
dbSNP gnomAD v4
3g.30672017C>TCA049968TGFBR2c.834C>T (p.Ile278=)
n.2430C>T
c.909C>T (p.Ile303=)
c.861C>T (p.Ile287=)
c.786C>T (p.Ile262=)
c.729C>T (p.Ile243=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672018T>ACA351807972TGFBR2c.835T>A (p.Phe279Ile)
n.2431T>A
c.910T>A (p.Phe304Ile)
c.862T>A (p.Phe288Ile)
c.787T>A (p.Phe263Ile)
c.730T>A (p.Phe244Ile)
3g.30672018T>CCA049980TGFBR2c.835T>C (p.Phe279Leu)
n.2431T>C
c.910T>C (p.Phe304Leu)
c.862T>C (p.Phe288Leu)
c.787T>C (p.Phe263Leu)
c.730T>C (p.Phe244Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672018T>GCA351807973TGFBR2c.835T>G (p.Phe279Val)
n.2431T>G
c.910T>G (p.Phe304Val)
c.862T>G (p.Phe288Val)
c.787T>G (p.Phe263Val)
c.730T>G (p.Phe244Val)
3g.30672018T=CA1354873093TGFBR2c.835T= (p.Phe279=)
n.2431T=
c.910T= (p.Phe304=)
c.862T= (p.Phe288=)
c.787T= (p.Phe263=)
c.730T= (p.Phe244=)
3g.30672019T>ACA351807974TGFBR2c.836T>A (p.Phe279Tyr)
n.2432T>A
c.911T>A (p.Phe304Tyr)
c.863T>A (p.Phe288Tyr)
c.788T>A (p.Phe263Tyr)
c.731T>A (p.Phe244Tyr)
3g.30672019T>CCA351807975TGFBR2c.836T>C (p.Phe279Ser)
n.2432T>C
c.911T>C (p.Phe304Ser)
c.863T>C (p.Phe288Ser)
c.788T>C (p.Phe263Ser)
c.731T>C (p.Phe244Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672019T>GCA351807976TGFBR2c.836T>G (p.Phe279Cys)
n.2432T>G
c.911T>G (p.Phe304Cys)
c.863T>G (p.Phe288Cys)
c.788T>G (p.Phe263Cys)
c.731T>G (p.Phe244Cys)
3g.30672019T=CA1354873094TGFBR2c.836T= (p.Phe279=)
n.2432T=
c.911T= (p.Phe304=)
c.863T= (p.Phe288=)
c.788T= (p.Phe263=)
c.731T= (p.Phe244=)

Number of alleles fetched