Chr Mutation (hg38) CAid Gene Transcript Linkouts
Yg.20759791G>TCA923789750RPS4Y2c.82-77G>T (n.82-77G>T)
c.31-77G>T (n.31-77G>T)
Yg.20759807A>CCA923789776RPS4Y2c.82-61A>C (n.82-61A>C)
c.31-61A>C (n.31-61A>C)
Yg.20759811T>CCA337511148RPS4Y2c.82-57T>C (n.82-57T>C)
c.31-57T>C (n.31-57T>C)
dbSNP
Yg.20759811T=CA2471054479RPS4Y2c.82-57T= (n.82-57T=)
c.31-57T= (n.31-57T=)
Yg.20759816A>TCA2579749852RPS4Y2c.82-52A>T (n.82-52A>T)
c.31-52A>T (n.31-52A>T)
Yg.20759817T>GCA645235425RPS4Y2c.82-51T>G (n.82-51T>G)
c.31-51T>G (n.31-51T>G)
dbSNP gnomAD v2
Yg.20759817T=CA2471054480RPS4Y2c.82-51T= (n.82-51T=)
c.31-51T= (n.31-51T=)
Yg.20759820A=CA2471054481RPS4Y2c.82-48A= (n.82-48A=)
c.31-48A= (n.31-48A=)
Yg.20759820A>GCA10575176RPS4Y2c.82-48A>G (n.82-48A>G)
c.31-48A>G (n.31-48A>G)
dbSNP ExAC gnomAD v2
Yg.20759821_20759822delinsAGCA2471054482RPS4Y2c.82-47_82-46delinsAG (n.82-47_82-46delinsAG)
c.31-47_31-46delinsAG (n.31-47_31-46delinsAG)
Yg.20759822G=CA2471054483RPS4Y2c.82-46G= (n.82-46G=)
c.31-46G= (n.31-46G=)
Yg.20759822G>TCA10575178RPS4Y2c.82-46G>T (n.82-46G>T)
c.31-46G>T (n.31-46G>T)
dbSNP ExAC gnomAD v2
Yg.20759825delCA10575177RPS4Y2c.82-43del (n.82-43del)
c.31-43del (n.31-43del)
dbSNP ExAC gnomAD v2
Yg.20759826C=CA2471054484RPS4Y2c.82-42C= (n.82-42C=)
c.31-42C= (n.31-42C=)
Yg.20759826C>TCA10575179RPS4Y2c.82-42C>T (n.82-42C>T)
c.31-42C>T (n.31-42C>T)
dbSNP ExAC gnomAD v2
Yg.20759827G>ACA10575180RPS4Y2c.82-41G>A (n.82-41G>A)
c.31-41G>A (n.31-41G>A)
dbSNP ExAC gnomAD v2
Yg.20759827G=CA2471054485RPS4Y2c.82-41G= (n.82-41G=)
c.31-41G= (n.31-41G=)
Yg.20759839_20759840delinsATCA2471054486RPS4Y2c.82-29_82-28delinsAT (n.82-29_82-28delinsAT)
c.31-29_31-28delinsAT (n.31-29_31-28delinsAT)
Yg.20759841delCA10575181RPS4Y2c.82-27del (n.82-27del)
c.31-27del (n.31-27del)
dbSNP ExAC gnomAD v2
Yg.20759841T>GCA10575182RPS4Y2c.82-27T>G (n.82-27T>G)
c.31-27T>G (n.31-27T>G)
dbSNP ExAC gnomAD v2
Yg.20759841T=CA2471054487RPS4Y2c.82-27T= (n.82-27T=)
c.31-27T= (n.31-27T=)
Yg.20759849C=CA2471054488RPS4Y2c.82-19C= (n.82-19C=)
c.31-19C= (n.31-19C=)
Yg.20759849C>TCA10575183RPS4Y2c.82-19C>T (n.82-19C>T)
c.31-19C>T (n.31-19C>T)
dbSNP ExAC gnomAD v2
Yg.20759850delCA2579749853RPS4Y2c.82-18del (n.82-18del)
c.31-18del (n.31-18del)
Yg.20759859C>GCA645614636RPS4Y2c.82-9C>G (n.82-9C>G)
c.31-9C>G (n.31-9C>G)
COSMIC
Yg.20759866A=CA2471054489RPS4Y2c.82-2A= (n.82-2A=)
c.31-2A= (n.31-2A=)
Yg.20759866A>CCA414858139RPS4Y2c.82-2A>C (n.82-2A>C)
c.31-2A>C (n.31-2A>C)
Yg.20759866A>GCA414858136RPS4Y2c.82-2A>G (n.82-2A>G)
c.31-2A>G (n.31-2A>G)
dbSNP
Yg.20759866A>TCA414858138RPS4Y2c.82-2A>T (n.82-2A>T)
c.31-2A>T (n.31-2A>T)
Yg.20759867G>ACA414858142RPS4Y2c.82-1G>A (n.82-1G>A)
c.31-1G>A (n.31-1G>A)
Yg.20759867G>CCA414858143RPS4Y2c.82-1G>C (n.82-1G>C)
c.31-1G>C (n.31-1G>C)
Yg.20759867G>TCA414858144RPS4Y2c.82-1G>T (n.82-1G>T)
c.31-1G>T (n.31-1G>T)
Yg.20759868G>ACA414858147RPS4Y2c.82G>A (p.Ala28Thr)
c.31G>A (p.Ala11Thr)
Yg.20759868G>CCA414858149RPS4Y2c.82G>C (p.Ala28Pro)
c.31G>C (p.Ala11Pro)
Yg.20759868G>TCA414858150RPS4Y2c.82G>T (p.Ala28Ser)
c.31G>T (p.Ala11Ser)
Yg.20759869C>ACA414858152RPS4Y2c.83C>A (p.Ala28Glu)
c.32C>A (p.Ala11Glu)
dbSNP gnomAD v2
Yg.20759869C=CA2471054490RPS4Y2c.83C= (p.Ala28=)
c.32C= (p.Ala11=)
Yg.20759869C>GCA414858154RPS4Y2c.83C>G (p.Ala28Gly)
c.32C>G (p.Ala11Gly)
Yg.20759869C>TCA414858156RPS4Y2c.83C>T (p.Ala28Val)
c.32C>T (p.Ala11Val)
Yg.20759870A>CCA520176160RPS4Y2c.84A>C (p.Ala28=)
c.33A>C (p.Ala11=)
Yg.20759870A>GCA520176162RPS4Y2c.84A>G (p.Ala28=)
c.33A>G (p.Ala11=)
Yg.20759870A>TCA520176163RPS4Y2c.84A>T (p.Ala28=)
c.33A>T (p.Ala11=)
Yg.20759871C>ACA414858158RPS4Y2c.85C>A (p.Pro29Thr)
c.34C>A (p.Pro12Thr)
Yg.20759871C>GCA414858160RPS4Y2c.85C>G (p.Pro29Ala)
c.34C>G (p.Pro12Ala)
Yg.20759871C>TCA414858161RPS4Y2c.85C>T (p.Pro29Ser)
c.34C>T (p.Pro12Ser)
Yg.20759872C>ACA414858167RPS4Y2c.86C>A (p.Pro29His)
c.35C>A (p.Pro12His)
Yg.20759872C>GCA414858165RPS4Y2c.86C>G (p.Pro29Arg)
c.35C>G (p.Pro12Arg)
Yg.20759872C>TCA414858163RPS4Y2c.86C>T (p.Pro29Leu)
c.35C>T (p.Pro12Leu)
Yg.20759873T>ACA520176182RPS4Y2c.87T>A (p.Pro29=)
c.36T>A (p.Pro12=)
Yg.20759873T>CCA520176186RPS4Y2c.87T>C (p.Pro29=)
c.36T>C (p.Pro12=)

Number of alleles fetched