Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.101599079T>ACA371645328GRHL2c.1026T>A (p.Asn342Lys)
c.978T>A (p.Asn326Lys)
8g.101599079T>CCA462238438GRHL2c.1026T>C (p.Asn342=)
c.978T>C (p.Asn326=)
8g.101599079T>GCA371645329GRHL2c.1026T>G (p.Asn342Lys)
c.978T>G (p.Asn326Lys)
8g.101599080A>CCA371645330GRHL2c.1027A>C (p.Thr343Pro)
c.979A>C (p.Thr327Pro)
8g.101599080A>GCA371645331GRHL2c.1027A>G (p.Thr343Ala)
c.979A>G (p.Thr327Ala)
8g.101599080A>TCA371645332GRHL2c.1027A>T (p.Thr343Ser)
c.979A>T (p.Thr327Ser)
8g.101599081C>ACA371645333GRHL2c.1028C>A (p.Thr343Lys)
c.980C>A (p.Thr327Lys)
gnomAD v4
8g.101599081C=CA1806401557GRHL2c.1028C= (p.Thr343=)
c.980C= (p.Thr327=)
8g.101599081C>GCA371645334GRHL2c.1028C>G (p.Thr343Arg)
c.980C>G (p.Thr327Arg)
dbSNP
8g.101599081C>TCA4830464GRHL2c.1028C>T (p.Thr343Met)
c.980C>T (p.Thr327Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.101599082G>ACA4830465GRHL2c.1029G>A (p.Thr343=)
c.981G>A (p.Thr327=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.101599082G>CCA462238439GRHL2c.1029G>C (p.Thr343=)
c.981G>C (p.Thr327=)
8g.101599082G=CA1806401558GRHL2c.1029G= (p.Thr343=)
c.981G= (p.Thr327=)
8g.101599082G>TCA182753078GRHL2c.1029G>T (p.Thr343=)
c.981G>T (p.Thr327=)
dbSNP gnomAD v3 gnomAD v4
8g.101599083A>CCA371645335GRHL2c.1030A>C (p.Ile344Leu)
c.982A>C (p.Ile328Leu)
8g.101599083A>GCA371645336GRHL2c.1030A>G (p.Ile344Val)
c.982A>G (p.Ile328Val)
8g.101599083A>TCA371645337GRHL2c.1030A>T (p.Ile344Phe)
c.982A>T (p.Ile328Phe)
8g.101599084T>ACA371645338GRHL2c.1031T>A (p.Ile344Asn)
c.983T>A (p.Ile328Asn)
8g.101599084T>CCA371645339GRHL2c.1031T>C (p.Ile344Thr)
c.983T>C (p.Ile328Thr)
dbSNP gnomAD v3 gnomAD v4
8g.101599084T>GCA371645340GRHL2c.1031T>G (p.Ile344Ser)
c.983T>G (p.Ile328Ser)
8g.101599084T=CA1806401559GRHL2c.1031T= (p.Ile344=)
c.983T= (p.Ile328=)
8g.101599085T>ACA462238440GRHL2c.1032T>A (p.Ile344=)
c.984T>A (p.Ile328=)
8g.101599085T>CCA4830466GRHL2c.1032T>C (p.Ile344=)
c.984T>C (p.Ile328=)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.101599085T>GCA371645341GRHL2c.1032T>G (p.Ile344Met)
c.984T>G (p.Ile328Met)
8g.101599085T=CA1806401560GRHL2c.1032T= (p.Ile344=)
c.984T= (p.Ile328=)
8g.101599086G>ACA371645342GRHL2c.1033G>A (p.Gly345Arg)
c.985G>A (p.Gly329Arg)
8g.101599086G>CCA371645343GRHL2c.1033G>C (p.Gly345Arg)
c.985G>C (p.Gly329Arg)
8g.101599086G>TCA371645344GRHL2c.1033G>T (p.Gly345Ter)
c.985G>T (p.Gly329Ter)
8g.101599087G>ACA4830467GRHL2c.1034G>A (p.Gly345Glu)
c.986G>A (p.Gly329Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.101599087G>CCA371645345GRHL2c.1034G>C (p.Gly345Ala)
c.986G>C (p.Gly329Ala)
8g.101599087G=CA1806401561GRHL2c.1034G= (p.Gly345=)
c.986G= (p.Gly329=)
8g.101599087G>TCA371645346GRHL2c.1034G>T (p.Gly345Val)
c.986G>T (p.Gly329Val)
8g.101599088A>CCA462238443GRHL2c.1035A>C (p.Gly345=)
c.987A>C (p.Gly329=)
8g.101599088A>GCA462238441GRHL2c.1035A>G (p.Gly345=)
c.987A>G (p.Gly329=)
8g.101599088A>TCA462238442GRHL2c.1035A>T (p.Gly345=)
c.987A>T (p.Gly329=)
8g.101599089A>CCA371645347GRHL2c.1036A>C (p.Asn346His)
c.988A>C (p.Asn330His)
8g.101599089A>GCA371645348GRHL2c.1036A>G (p.Asn346Asp)
c.988A>G (p.Asn330Asp)
8g.101599089A>TCA371645349GRHL2c.1036A>T (p.Asn346Tyr)
c.988A>T (p.Asn330Tyr)
8g.101599090A>CCA371645350GRHL2c.1037A>C (p.Asn346Thr)
c.989A>C (p.Asn330Thr)
8g.101599090A>GCA371645351GRHL2c.1037A>G (p.Asn346Ser)
c.989A>G (p.Asn330Ser)
8g.101599090A>TCA371645352GRHL2c.1037A>T (p.Asn346Ile)
c.989A>T (p.Asn330Ile)
8g.101599091C>ACA371645354GRHL2c.1038C>A (p.Asn346Lys)
c.990C>A (p.Asn330Lys)
8g.101599091C>GCA371645353GRHL2c.1038C>G (p.Asn346Lys)
c.990C>G (p.Asn330Lys)
8g.101599091C>TCA462238444GRHL2c.1038C>T (p.Asn346=)
c.990C>T (p.Asn330=)
8g.101599092A=CA1806401562GRHL2c.1039A= (p.Ile347=)
c.991A= (p.Ile331=)
8g.101599092A>CCA371645355GRHL2c.1039A>C (p.Ile347Leu)
c.991A>C (p.Ile331Leu)
8g.101599092A>GCA4830468GRHL2c.1039A>G (p.Ile347Val)
c.991A>G (p.Ile331Val)
dbSNP ExAC gnomAD v3 gnomAD v4
8g.101599092A>TCA371645356GRHL2c.1039A>T (p.Ile347Phe)
c.991A>T (p.Ile331Phe)
8g.101599093T>ACA371645357GRHL2c.1040T>A (p.Ile347Asn)
c.992T>A (p.Ile331Asn)
8g.101599093T>CCA371645358GRHL2c.1040T>C (p.Ile347Thr)
c.992T>C (p.Ile331Thr)

Number of alleles fetched