Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.42962823T>CCA551142760GRXCR1c.385-69T>C (n.385-69T>C)
c.22-69T>C (n.22-69T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962823T=CA1453073696GRXCR1c.385-69T= (n.385-69T=)
c.22-69T= (n.22-69T=)
4g.42962824delCA2670496452GRXCR1c.385-68del (n.385-68del)
c.22-68del (n.22-68del)
gnomAD v4
4g.42962824T>ACA2670496453GRXCR1c.385-68T>A (n.385-68T>A)
c.22-68T>A (n.22-68T>A)
gnomAD v4
4g.42962825G>ACA2670496454GRXCR1c.385-67G>A (n.385-67G>A)
c.22-67G>A (n.22-67G>A)
gnomAD v4
4g.42962825G>TCA2670496455GRXCR1c.385-67G>T (n.385-67G>T)
c.22-67G>T (n.22-67G>T)
gnomAD v4
4g.42962826T>CCA1453073698GRXCR1c.385-66T>C (n.385-66T>C)
c.22-66T>C (n.22-66T>C)
dbSNP
4g.42962826T=CA1453073697GRXCR1c.385-66T= (n.385-66T=)
c.22-66T= (n.22-66T=)
4g.42962827C>ACA2670496456GRXCR1c.385-65C>A (n.385-65C>A)
c.22-65C>A (n.22-65C>A)
gnomAD v4
4g.42962827C=CA1453073699GRXCR1c.385-65C= (n.385-65C=)
c.22-65C= (n.22-65C=)
4g.42962827C>GCA1453073700GRXCR1c.385-65C>G (n.385-65C>G)
c.22-65C>G (n.22-65C>G)
dbSNP
4g.42962827C>TCA2670496457GRXCR1c.385-65C>T (n.385-65C>T)
c.22-65C>T (n.22-65C>T)
gnomAD v4
4g.42962830A=CA1453073701GRXCR1c.385-62A= (n.385-62A=)
c.22-62A= (n.22-62A=)
4g.42962830A>GCA96311671GRXCR1c.385-62A>G (n.385-62A>G)
c.22-62A>G (n.22-62A>G)
dbSNP gnomAD v3 gnomAD v4
4g.42962833delCA2578076946GRXCR1c.385-59del (n.385-59del)
c.22-59del (n.22-59del)
4g.42962833A>GCA2670496458GRXCR1c.385-59A>G (n.385-59A>G)
c.22-59A>G (n.22-59A>G)
gnomAD v4
4g.42962834T>ACA2670496459GRXCR1c.385-58T>A (n.385-58T>A)
c.22-58T>A (n.22-58T>A)
gnomAD v4
4g.42962834T>CCA2578076947GRXCR1c.385-58T>C (n.385-58T>C)
c.22-58T>C (n.22-58T>C)
4g.42962835C>ACA2670496460GRXCR1c.385-57C>A (n.385-57C>A)
c.22-57C>A (n.22-57C>A)
gnomAD v4
4g.42962836A>GCA2670496461GRXCR1c.385-56A>G (n.385-56A>G)
c.22-56A>G (n.22-56A>G)
gnomAD v4
4g.42962837T>GCA2670496462GRXCR1c.385-55T>G (n.385-55T>G)
c.22-55T>G (n.22-55T>G)
gnomAD v4
4g.42962838A=CA1453073702GRXCR1c.385-54A= (n.385-54A=)
c.22-54A= (n.22-54A=)
4g.42962838A>GCA551142761GRXCR1c.385-54A>G (n.385-54A>G)
c.22-54A>G (n.22-54A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962840G>TCA649165699GRXCR1c.385-52G>T (n.385-52G>T)
c.22-52G>T (n.22-52G>T)
COSMIC
4g.42962841A>GCA2670496463GRXCR1c.385-51A>G (n.385-51A>G)
c.22-51A>G (n.22-51A>G)
gnomAD v4
4g.42962842C>ACA649165701GRXCR1c.385-50C>A (n.385-50C>A)
c.22-50C>A (n.22-50C>A)
COSMIC
4g.42962843A=CA1453073703GRXCR1c.385-49A= (n.385-49A=)
c.22-49A= (n.22-49A=)
4g.42962843A>GCA2904384GRXCR1c.385-49A>G (n.385-49A>G)
c.22-49A>G (n.22-49A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962844C>ACA2670496464GRXCR1c.385-48C>A (n.385-48C>A)
c.22-48C>A (n.22-48C>A)
gnomAD v4
4g.42962844C=CA1453073704GRXCR1c.385-48C= (n.385-48C=)
c.22-48C= (n.22-48C=)
4g.42962844C>TCA96311672GRXCR1c.385-48C>T (n.385-48C>T)
c.22-48C>T (n.22-48C>T)
dbSNP gnomAD v4
4g.42962848A=CA1453073705GRXCR1c.385-44A= (n.385-44A=)
c.22-44A= (n.22-44A=)
4g.42962848A>CCA2670496465GRXCR1c.385-44A>C (n.385-44A>C)
c.22-44A>C (n.22-44A>C)
gnomAD v4
4g.42962848A>GCA96311673GRXCR1c.385-44A>G (n.385-44A>G)
c.22-44A>G (n.22-44A>G)
dbSNP gnomAD v4 COSMIC
4g.42962849A=CA1453073707GRXCR1c.385-43A= (n.385-43A=)
c.22-43A= (n.22-43A=)
4g.42962849A>GCA1453073706GRXCR1c.385-43A>G (n.385-43A>G)
c.22-43A>G (n.22-43A>G)
dbSNP
4g.42962850A=CA1453073708GRXCR1c.385-42A= (n.385-42A=)
c.22-42A= (n.22-42A=)
4g.42962850A>GCA2904385GRXCR1c.385-42A>G (n.385-42A>G)
c.22-42A>G (n.22-42A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962851G>ACA2670496466GRXCR1c.385-41G>A (n.385-41G>A)
c.22-41G>A (n.22-41G>A)
gnomAD v4
4g.42962853A>GCA2670496467GRXCR1c.385-39A>G (n.385-39A>G)
c.22-39A>G (n.22-39A>G)
gnomAD v4
4g.42962856A=CA1453073709GRXCR1c.385-36A= (n.385-36A=)
c.22-36A= (n.22-36A=)
4g.42962856A>GCA96311674GRXCR1c.385-36A>G (n.385-36A>G)
c.22-36A>G (n.22-36A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962857G>ACA96311675GRXCR1c.385-35G>A (n.385-35G>A)
c.22-35G>A (n.22-35G>A)
dbSNP gnomAD v4
4g.42962857G=CA1453073710GRXCR1c.385-35G= (n.385-35G=)
c.22-35G= (n.22-35G=)
4g.42962858C=CA1453073711GRXCR1c.385-34C= (n.385-34C=)
c.22-34C= (n.22-34C=)
4g.42962858C>TCA2904386GRXCR1c.385-34C>T (n.385-34C>T)
c.22-34C>T (n.22-34C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962859A=CA1453073712GRXCR1c.385-33A= (n.385-33A=)
c.22-33A= (n.22-33A=)
4g.42962859A>GCA2904387GRXCR1c.385-33A>G (n.385-33A>G)
c.22-33A>G (n.22-33A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962861A=CA1453073713GRXCR1c.385-31A= (n.385-31A=)
c.22-31A= (n.22-31A=)
4g.42962861A>GCA551142766GRXCR1c.385-31A>G (n.385-31A>G)
c.22-31A>G (n.22-31A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962864T>GCA551142767GRXCR1c.385-28T>G (n.385-28T>G)
c.22-28T>G (n.22-28T>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962864T=CA1453073714GRXCR1c.385-28T= (n.385-28T=)
c.22-28T= (n.22-28T=)
4g.42962865T>GCA2670496468GRXCR1c.385-27T>G (n.385-27T>G)
c.22-27T>G (n.22-27T>G)
gnomAD v4
4g.42962866C>ACA2670496469GRXCR1c.385-26C>A (n.385-26C>A)
c.22-26C>A (n.22-26C>A)
gnomAD v4
4g.42962866C>GCA2596661327GRXCR1c.385-26C>G (n.385-26C>G)
c.22-26C>G (n.22-26C>G)
gnomAD v3 gnomAD v4
4g.42962867T>CCA2670496470GRXCR1c.385-25T>C (n.385-25T>C)
c.22-25T>C (n.22-25T>C)
gnomAD v4
4g.42962868T>ACA2670496471GRXCR1c.385-24T>A (n.385-24T>A)
c.22-24T>A (n.22-24T>A)
gnomAD v4
4g.42962869A=CA1453073715GRXCR1c.385-23A= (n.385-23A=)
c.22-23A= (n.22-23A=)
4g.42962869A>TCA96311676GRXCR1c.385-23A>T (n.385-23A>T)
c.22-23A>T (n.22-23A>T)
dbSNP gnomAD v2 gnomAD v4
4g.42962870C=CA1453073716GRXCR1c.385-22C= (n.385-22C=)
c.22-22C= (n.22-22C=)
4g.42962870C>TCA2904388GRXCR1c.385-22C>T (n.385-22C>T)
c.22-22C>T (n.22-22C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962872A=CA1453073717GRXCR1c.385-20A= (n.385-20A=)
c.22-20A= (n.22-20A=)
4g.42962872A>GCA1453073718GRXCR1c.385-20A>G (n.385-20A>G)
c.22-20A>G (n.22-20A>G)
dbSNP
4g.42962872A>TCA2670496472GRXCR1c.385-20A>T (n.385-20A>T)
c.22-20A>T (n.22-20A>T)
gnomAD v4
4g.42962873C>TCA2670496473GRXCR1c.385-19C>T (n.385-19C>T)
c.22-19C>T (n.22-19C>T)
gnomAD v4
4g.42962875C>ACA2904389GRXCR1c.385-17C>A (n.385-17C>A)
c.22-17C>A (n.22-17C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962875C=CA1453073719GRXCR1c.385-17C= (n.385-17C=)
c.22-17C= (n.22-17C=)
4g.42962876A=CA1453073720GRXCR1c.385-16A= (n.385-16A=)
c.22-16A= (n.22-16A=)
4g.42962876A>CCA2670496474GRXCR1c.385-16A>C (n.385-16A>C)
c.22-16A>C (n.22-16A>C)
gnomAD v4
4g.42962876A>GCA551142772GRXCR1c.385-16A>G (n.385-16A>G)
c.22-16A>G (n.22-16A>G)
dbSNP gnomAD v2 gnomAD v4
4g.42962877A=CA1453073721GRXCR1c.385-15A= (n.385-15A=)
c.22-15A= (n.22-15A=)
4g.42962877A>GCA2904390GRXCR1c.385-15A>G (n.385-15A>G)
c.22-15A>G (n.22-15A>G)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.42962878T>ACA2670496475GRXCR1c.385-14T>A (n.385-14T>A)
c.22-14T>A (n.22-14T>A)
gnomAD v4
4g.42962879G>ACA96311677GRXCR1c.385-13G>A (n.385-13G>A)
c.22-13G>A (n.22-13G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962879G=CA1453073722GRXCR1c.385-13G= (n.385-13G=)
c.22-13G= (n.22-13G=)
4g.42962880T>GCA2670496476GRXCR1c.385-12T>G (n.385-12T>G)
c.22-12T>G (n.22-12T>G)
gnomAD v4
4g.42962885C=CA1453073723GRXCR1c.385-7C= (n.385-7C=)
c.22-7C= (n.22-7C=)
4g.42962885C>TCA2904391GRXCR1c.385-7C>T (n.385-7C>T)
c.22-7C>T (n.22-7C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962886C>GCA2670496477GRXCR1c.385-6C>G (n.385-6C>G)
c.22-6C>G (n.22-6C>G)
gnomAD v4
4g.42962886C>TCA2670496478GRXCR1c.385-6C>T (n.385-6C>T)
c.22-6C>T (n.22-6C>T)
gnomAD v4
4g.42962889C>ACA2506588205GRXCR1c.385-3C>A (n.385-3C>A)
c.22-3C>A (n.22-3C>A)
4g.42962889C>GCA2670496479GRXCR1c.385-3C>G (n.385-3C>G)
c.22-3C>G (n.22-3C>G)
gnomAD v4
4g.42962890A=CA1453073724GRXCR1c.385-2A= (n.385-2A=)
c.22-2A= (n.22-2A=)
4g.42962890A>CCA356792090GRXCR1c.385-2A>C (n.385-2A>C)
c.22-2A>C (n.22-2A>C)
4g.42962890A>GCA2904392GRXCR1c.385-2A>G (n.385-2A>G)
c.22-2A>G (n.22-2A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962890A>TCA356792089GRXCR1c.385-2A>T (n.385-2A>T)
c.22-2A>T (n.22-2A>T)
4g.42962891G>ACA96311678GRXCR1c.385-1G>A (n.385-1G>A)
c.22-1G>A (n.22-1G>A)
dbSNP gnomAD v2 gnomAD v4
4g.42962891G>CCA356792091GRXCR1c.385-1G>C (n.385-1G>C)
c.22-1G>C (n.22-1G>C)
dbSNP gnomAD v4
4g.42962891G=CA1453073725GRXCR1c.385-1G= (n.385-1G=)
c.22-1G= (n.22-1G=)
4g.42962891G>TCA356792092GRXCR1c.385-1G>T (n.385-1G>T)
c.22-1G>T (n.22-1G>T)
COSMIC
4g.42962892C>ACA356792093GRXCR1c.385C>A (p.Gln129Lys)
c.22C>A (p.Gln8Lys)
4g.42962892C=CA1453073726GRXCR1c.385C= (p.Gln129=)
c.22C= (p.Gln8=)
4g.42962892C>GCA356792094GRXCR1c.385C>G (p.Gln129Glu)
c.22C>G (p.Gln8Glu)
4g.42962892C>TCA356792095GRXCR1c.385C>T (p.Gln129Ter)
c.22C>T (p.Gln8Ter)
dbSNP gnomAD v4 COSMIC
4g.42962893A=CA1453073727GRXCR1c.386A= (p.Gln129=)
c.23A= (p.Gln8=)
4g.42962893A>CCA356792096GRXCR1c.386A>C (p.Gln129Pro)
c.23A>C (p.Gln8Pro)
dbSNP
4g.42962893A>GCA96311679GRXCR1c.386A>G (p.Gln129Arg)
c.23A>G (p.Gln8Arg)
dbSNP
4g.42962893A>TCA356792097GRXCR1c.386A>T (p.Gln129Leu)
c.23A>T (p.Gln8Leu)
4g.42962894A=CA1453073728GRXCR1c.387A= (p.Gln129=)
c.24A= (p.Gln8=)
4g.42962894A>CCA356792098GRXCR1c.387A>C (p.Gln129His)
c.24A>C (p.Gln8His)
dbSNP
4g.42962894A>GCA439191461GRXCR1c.387A>G (p.Gln129=)
c.24A>G (p.Gln8=)
4g.42962894A>TCA356792099GRXCR1c.387A>T (p.Gln129His)
c.24A>T (p.Gln8His)
4g.42962895C>ACA2904393GRXCR1c.388C>A (p.Pro130Thr)
c.25C>A (p.Pro9Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962895C=CA1453073729GRXCR1c.388C= (p.Pro130=)
c.25C= (p.Pro9=)
4g.42962895C>GCA356792100GRXCR1c.388C>G (p.Pro130Ala)
c.25C>G (p.Pro9Ala)
4g.42962895C>TCA356792101GRXCR1c.388C>T (p.Pro130Ser)
c.25C>T (p.Pro9Ser)
4g.42962896dupCA795064995GRXCR1c.389dup (p.Ser131IlefsTer3)
c.26dup (p.Ser10IlefsTer3)
dbSNP
4g.42962896C>ACA356792102GRXCR1c.389C>A (p.Pro130Gln)
c.26C>A (p.Pro9Gln)
gnomAD v4
4g.42962896C=CA1453073730GRXCR1c.389C= (p.Pro130=)
c.26C= (p.Pro9=)
4g.42962896C>GCA356792103GRXCR1c.389C>G (p.Pro130Arg)
c.26C>G (p.Pro9Arg)
4g.42962896C>TCA356792104GRXCR1c.389C>T (p.Pro130Leu)
c.26C>T (p.Pro9Leu)
dbSNP gnomAD v4 COSMIC
4g.42962897A>CCA439191462GRXCR1c.390A>C (p.Pro130=)
c.27A>C (p.Pro9=)
4g.42962897A>GCA439191463GRXCR1c.390A>G (p.Pro130=)
c.27A>G (p.Pro9=)
gnomAD v4
4g.42962897A>TCA439191464GRXCR1c.390A>T (p.Pro130=)
c.27A>T (p.Pro9=)
4g.42962898T>ACA356792105GRXCR1c.391T>A (p.Ser131Thr)
c.28T>A (p.Ser10Thr)
4g.42962898T>CCA356792106GRXCR1c.391T>C (p.Ser131Pro)
c.28T>C (p.Ser10Pro)
gnomAD v4
4g.42962898T>GCA356792107GRXCR1c.391T>G (p.Ser131Ala)
c.28T>G (p.Ser10Ala)
4g.42962899C>ACA356792108GRXCR1c.392C>A (p.Ser131Ter)
c.29C>A (p.Ser10Ter)
gnomAD v4
4g.42962899C=CA1453073732GRXCR1c.392C= (p.Ser131=)
c.29C= (p.Ser10=)
4g.42962899C>GCA356792109GRXCR1c.392C>G (p.Ser131Ter)
c.29C>G (p.Ser10Ter)
dbSNP gnomAD v2 gnomAD v4
4g.42962899C>TCA356792110GRXCR1c.392C>T (p.Ser131Leu)
c.29C>T (p.Ser10Leu)
gnomAD v4
4g.42962899_42962908delinsCAACTGATCTCA1453073731GRXCR1c.392_401delinsCAACTGATCT (p.Ser131=)
c.29_38delinsCAACTGATCT (p.Ser10=)
4g.42962900A>CCA439191466GRXCR1c.393A>C (p.Ser131=)
c.30A>C (p.Ser10=)
4g.42962900A>GCA439191467GRXCR1c.393A>G (p.Ser131=)
c.30A>G (p.Ser10=)
4g.42962900A>TCA439191468GRXCR1c.393A>T (p.Ser131=)
c.30A>T (p.Ser10=)
4g.42962901_42962909delCA795065018GRXCR1c.394_402del (p.Thr132_Leu134del)
c.31_39del (p.Thr11_Leu13del)
dbSNP
4g.42962901A=CA1453073733GRXCR1c.394A= (p.Thr132=)
c.31A= (p.Thr11=)
4g.42962901A>CCA356792111GRXCR1c.394A>C (p.Thr132Pro)
c.31A>C (p.Thr11Pro)
4g.42962901A>GCA2904394GRXCR1c.394A>G (p.Thr132Ala)
c.31A>G (p.Thr11Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962901A>TCA356792112GRXCR1c.394A>T (p.Thr132Ser)
c.31A>T (p.Thr11Ser)
4g.42962902C>ACA96311680GRXCR1c.395C>A (p.Thr132Asn)
c.32C>A (p.Thr11Asn)
dbSNP gnomAD v4
4g.42962902C=CA1453073734GRXCR1c.395C= (p.Thr132=)
c.32C= (p.Thr11=)
4g.42962902C>GCA356792113GRXCR1c.395C>G (p.Thr132Ser)
c.32C>G (p.Thr11Ser)
4g.42962902C>TCA2904395GRXCR1c.395C>T (p.Thr132Ile)
c.32C>T (p.Thr11Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962903T>ACA439191470GRXCR1c.396T>A (p.Thr132=)
c.33T>A (p.Thr11=)
4g.42962903T>CCA439191471GRXCR1c.396T>C (p.Thr132=)
c.33T>C (p.Thr11=)
gnomAD v4
4g.42962903T>GCA439191472GRXCR1c.396T>G (p.Thr132=)
c.33T>G (p.Thr11=)
4g.42962904G>ACA356792114GRXCR1c.397G>A (p.Asp133Asn)
c.34G>A (p.Asp12Asn)
4g.42962904G>CCA356792116GRXCR1c.397G>C (p.Asp133His)
c.34G>C (p.Asp12His)
4g.42962904G>TCA356792115GRXCR1c.397G>T (p.Asp133Tyr)
c.34G>T (p.Asp12Tyr)
4g.42962905A=CA1453073735GRXCR1c.398A= (p.Asp133=)
c.35A= (p.Asp12=)
4g.42962905A>CCA356792117GRXCR1c.398A>C (p.Asp133Ala)
c.35A>C (p.Asp12Ala)
dbSNP gnomAD v3 gnomAD v4
4g.42962905A>GCA356792118GRXCR1c.398A>G (p.Asp133Gly)
c.35A>G (p.Asp12Gly)
4g.42962905A>TCA356792119GRXCR1c.398A>T (p.Asp133Val)
c.35A>T (p.Asp12Val)
4g.42962906T>ACA356792120GRXCR1c.399T>A (p.Asp133Glu)
c.36T>A (p.Asp12Glu)
4g.42962906T>CCA439191475GRXCR1c.399T>C (p.Asp133=)
c.36T>C (p.Asp12=)
4g.42962906T>GCA356792121GRXCR1c.399T>G (p.Asp133Glu)
c.36T>G (p.Asp12Glu)
dbSNP gnomAD v3 gnomAD v4
4g.42962906T=CA1453073736GRXCR1c.399T= (p.Asp133=)
c.36T= (p.Asp12=)
4g.42962907C>ACA356792122GRXCR1c.400C>A (p.Leu134Ile)
c.37C>A (p.Leu13Ile)
4g.42962907C>GCA356792123GRXCR1c.400C>G (p.Leu134Val)
c.37C>G (p.Leu13Val)
gnomAD v4
4g.42962907C>TCA439191476GRXCR1c.400C>T (p.Leu134=)
c.37C>T (p.Leu13=)
4g.42962908T>ACA356792124GRXCR1c.401T>A (p.Leu134Gln)
c.38T>A (p.Leu13Gln)
gnomAD v4
4g.42962908T>CCA356792125GRXCR1c.401T>C (p.Leu134Pro)
c.38T>C (p.Leu13Pro)
4g.42962908T>GCA356792126GRXCR1c.401T>G (p.Leu134Arg)
c.38T>G (p.Leu13Arg)
4g.42962909A>CCA439191477GRXCR1c.402A>C (p.Leu134=)
c.39A>C (p.Leu13=)
4g.42962909A>GCA439191478GRXCR1c.402A>G (p.Leu134=)
c.39A>G (p.Leu13=)
4g.42962909A>TCA439191479GRXCR1c.402A>T (p.Leu134=)
c.39A>T (p.Leu13=)
4g.42962910G>ACA356792127GRXCR1c.403G>A (p.Glu135Lys)
c.40G>A (p.Glu14Lys)
COSMIC
4g.42962910G>CCA2904396GRXCR1c.403G>C (p.Glu135Gln)
c.40G>C (p.Glu14Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962910G=CA1453073737GRXCR1c.403G= (p.Glu135=)
c.40G= (p.Glu14=)
4g.42962910G>TCA356792128GRXCR1c.403G>T (p.Glu135Ter)
c.40G>T (p.Glu14Ter)
dbSNP gnomAD v3 gnomAD v4
4g.42962911A>CCA356792131GRXCR1c.404A>C (p.Glu135Ala)
c.41A>C (p.Glu14Ala)
4g.42962911A>GCA356792130GRXCR1c.404A>G (p.Glu135Gly)
c.41A>G (p.Glu14Gly)
gnomAD v4
4g.42962911A>TCA356792129GRXCR1c.404A>T (p.Glu135Val)
c.41A>T (p.Glu14Val)
4g.42962912A>CCA356792132GRXCR1c.405A>C (p.Glu135Asp)
c.42A>C (p.Glu14Asp)
4g.42962912A>GCA439191482GRXCR1c.405A>G (p.Glu135=)
c.42A>G (p.Glu14=)
4g.42962912A>TCA356792133GRXCR1c.405A>T (p.Glu135Asp)
c.42A>T (p.Glu14Asp)
4g.42962913T>ACA356792134GRXCR1c.406T>A (p.Phe136Ile)
c.43T>A (p.Phe15Ile)
4g.42962913T>CCA356792135GRXCR1c.406T>C (p.Phe136Leu)
c.43T>C (p.Phe15Leu)
gnomAD v4
4g.42962913T>GCA356792136GRXCR1c.406T>G (p.Phe136Val)
c.43T>G (p.Phe15Val)
4g.42962914T>ACA356792137GRXCR1c.407T>A (p.Phe136Tyr)
c.44T>A (p.Phe15Tyr)
4g.42962914T>CCA356792138GRXCR1c.407T>C (p.Phe136Ser)
c.44T>C (p.Phe15Ser)
4g.42962914T>GCA356792139GRXCR1c.407T>G (p.Phe136Cys)
c.44T>G (p.Phe15Cys)
4g.42962915T>ACA356792140GRXCR1c.408T>A (p.Phe136Leu)
c.45T>A (p.Phe15Leu)
4g.42962915T>CCA96311681GRXCR1c.408T>C (p.Phe136=)
c.45T>C (p.Phe15=)
dbSNP gnomAD v4
4g.42962915T>GCA356792141GRXCR1c.408T>G (p.Phe136Leu)
c.45T>G (p.Phe15Leu)
4g.42962915T=CA1453073738GRXCR1c.408T= (p.Phe136=)
c.45T= (p.Phe15=)
4g.42962916G>ACA356792142GRXCR1c.409G>A (p.Asp137Asn)
c.46G>A (p.Asp16Asn)
COSMIC
4g.42962916G>CCA356792143GRXCR1c.409G>C (p.Asp137His)
c.46G>C (p.Asp16His)
4g.42962916G>TCA356792144GRXCR1c.409G>T (p.Asp137Tyr)
c.46G>T (p.Asp16Tyr)
gnomAD v4 COSMIC
4g.42962917A>CCA356792146GRXCR1c.410A>C (p.Asp137Ala)
c.47A>C (p.Asp16Ala)
4g.42962917A>GCA356792147GRXCR1c.410A>G (p.Asp137Gly)
c.47A>G (p.Asp16Gly)
4g.42962917A>TCA356792145GRXCR1c.410A>T (p.Asp137Val)
c.47A>T (p.Asp16Val)
4g.42962918C>ACA356792148GRXCR1c.411C>A (p.Asp137Glu)
c.48C>A (p.Asp16Glu)
4g.42962918C=CA1453073739GRXCR1c.411C= (p.Asp137=)
c.48C= (p.Asp16=)
4g.42962918C>GCA356792149GRXCR1c.411C>G (p.Asp137Glu)
c.48C>G (p.Asp16Glu)
4g.42962918C>TCA439191487GRXCR1c.411C>T (p.Asp137=)
c.48C>T (p.Asp16=)
dbSNP gnomAD v3 gnomAD v4
4g.42962919C>ACA356792150GRXCR1c.412C>A (p.Arg138Ser)
c.49C>A (p.Arg17Ser)
4g.42962919C=CA1453073740GRXCR1c.412C= (p.Arg138=)
c.49C= (p.Arg17=)
4g.42962919C>GCA356792151GRXCR1c.412C>G (p.Arg138Gly)
c.49C>G (p.Arg17Gly)
4g.42962919C>TCA114035GRXCR1c.412C>T (p.Arg138Cys)
c.49C>T (p.Arg17Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962920G>ACA2904397GRXCR1c.413G>A (p.Arg138His)
c.50G>A (p.Arg17His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962920G>CCA356792152GRXCR1c.413G>C (p.Arg138Pro)
c.50G>C (p.Arg17Pro)
4g.42962920G=CA1453073741GRXCR1c.413G= (p.Arg138=)
c.50G= (p.Arg17=)
4g.42962920G>TCA356792153GRXCR1c.413G>T (p.Arg138Leu)
c.50G>T (p.Arg17Leu)
4g.42962921T>ACA439191491GRXCR1c.414T>A (p.Arg138=)
c.51T>A (p.Arg17=)
4g.42962921T>CCA439191492GRXCR1c.414T>C (p.Arg138=)
c.51T>C (p.Arg17=)
dbSNP gnomAD v3 gnomAD v4
4g.42962921T>GCA439191493GRXCR1c.414T>G (p.Arg138=)
c.51T>G (p.Arg17=)
4g.42962921T=CA1453073742GRXCR1c.414T= (p.Arg138=)
c.51T= (p.Arg17=)
4g.42962922G>ACA356792154GRXCR1c.415G>A (p.Val139Ile)
c.52G>A (p.Val18Ile)
dbSNP gnomAD v3 gnomAD v4
4g.42962922G>CCA356792155GRXCR1c.415G>C (p.Val139Leu)
c.52G>C (p.Val18Leu)
4g.42962922G=CA1453073743GRXCR1c.415G= (p.Val139=)
c.52G= (p.Val18=)
4g.42962922G>TCA356792156GRXCR1c.415G>T (p.Val139Leu)
c.52G>T (p.Val18Leu)
COSMIC
4g.42962923T>ACA356792159GRXCR1c.416T>A (p.Val139Glu)
c.53T>A (p.Val18Glu)
4g.42962923T>CCA356792158GRXCR1c.416T>C (p.Val139Ala)
c.53T>C (p.Val18Ala)
gnomAD v4
4g.42962923T>GCA356792157GRXCR1c.416T>G (p.Val139Gly)
c.53T>G (p.Val18Gly)

Number of alleles fetched