Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.47566625C>ACA2693580417ARAFc.558-14C>A (n.558-14C>A)
c.567-14C>A (n.567-14C>A)
c.559C>A (p.Leu187Ile)
c.-100-14C>A (n.-100-14C>A)
 gnomAD v4
Xg.47566625C=CA2427968692ARAFc.558-14C= (n.558-14C=)
c.567-14C= (n.567-14C=)
c.559C= (p.Leu187=)
c.-100-14C= (n.-100-14C=)
Xg.47566625C>TCA329053039ARAFc.558-14C>T (n.558-14C>T)
c.567-14C>T (n.567-14C>T)
c.559C>T (p.Leu187Phe)
c.-100-14C>T (n.-100-14C>T)
 dbSNP
Xg.47566626T>CCA2693580419ARAFc.558-13T>C (n.558-13T>C)
c.567-13T>C (n.567-13T>C)
c.560T>C (p.Leu187Pro)
c.-100-13T>C (n.-100-13T>C)
 gnomAD v4
Xg.47566628delCA2693580418ARAFc.558-11del (n.558-11del)
c.567-11del (n.567-11del)
c.562del (p.Ser188ProfsTer?)
c.-100-11del (n.-100-11del)
 gnomAD v4
Xg.47566627T>GCA2693580420ARAFc.558-12T>G (n.558-12T>G)
c.567-12T>G (n.567-12T>G)
c.561T>G (p.Leu187=)
c.-100-12T>G (n.-100-12T>G)
 gnomAD v4
Xg.47566628T>CCA2693580421ARAFc.558-11T>C (n.558-11T>C)
c.567-11T>C (n.567-11T>C)
c.562T>C (p.Ser188Pro)
c.-100-11T>C (n.-100-11T>C)
 gnomAD v4
Xg.47566629C>ACA2693580423ARAFc.558-10C>A (n.558-10C>A)
c.567-10C>A (n.567-10C>A)
c.563C>A (p.Ser188Tyr)
c.-100-10C>A (n.-100-10C>A)
 gnomAD v4
Xg.47566629C=CA2427968693ARAFc.558-10C= (n.558-10C=)
c.567-10C= (n.567-10C=)
c.563C= (p.Ser188=)
c.-100-10C= (n.-100-10C=)
Xg.47566629C>TCA10398037ARAFc.558-10C>T (n.558-10C>T)
c.567-10C>T (n.567-10C>T)
c.563C>T (p.Ser188Phe)
c.-100-10C>T (n.-100-10C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566632delCA2693580422ARAFc.558-7del (n.558-7del)
c.567-7del (n.567-7del)
c.566del (p.Pro189LeufsTer?)
c.-100-7del (n.-100-7del)
 gnomAD v4
Xg.47566630C>ACA2693580424ARAFc.558-9C>A (n.558-9C>A)
c.567-9C>A (n.567-9C>A)
c.564C>A (p.Ser188=)
c.-100-9C>A (n.-100-9C>A)
 gnomAD v4
Xg.47566630C=CA2427968694ARAFc.558-9C= (n.558-9C=)
c.567-9C= (n.567-9C=)
c.564C= (p.Ser188=)
c.-100-9C= (n.-100-9C=)
Xg.47566630C>TCA10398038ARAFc.558-9C>T (n.558-9C>T)
c.567-9C>T (n.567-9C>T)
c.564C>T (p.Ser188=)
c.-100-9C>T (n.-100-9C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566631C=CA2427968695ARAFc.558-8C= (n.558-8C=)
c.567-8C= (n.567-8C=)
c.565C= (p.Pro189=)
c.-100-8C= (n.-100-8C=)
Xg.47566631C>TCA10398039ARAFc.558-8C>T (n.558-8C>T)
c.567-8C>T (n.567-8C>T)
c.565C>T (p.Pro189Ser)
c.-100-8C>T (n.-100-8C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566632C>ACA2738526282ARAFc.558-7C>A (n.558-7C>A)
c.567-7C>A (n.567-7C>A)
c.566C>A (p.Pro189His)
c.-100-7C>A (n.-100-7C>A)
 dbSNP
Xg.47566632C>TCA2693580425ARAFc.558-7C>T (n.558-7C>T)
c.567-7C>T (n.567-7C>T)
c.566C>T (p.Pro189Leu)
c.-100-7C>T (n.-100-7C>T)
 gnomAD v4
Xg.47566633T>CCA2693580426ARAFc.558-6T>C (n.558-6T>C)
c.567-6T>C (n.567-6T>C)
c.567T>C (p.Pro189=)
c.-100-6T>C (n.-100-6T>C)
 gnomAD v4
Xg.47566634G>ACA2693580427ARAFc.558-5G>A (n.558-5G>A)
c.567-5G>A (n.567-5G>A)
c.568G>A (p.Gly190Ser)
c.-100-5G>A (n.-100-5G>A)
 gnomAD v4
Xg.47566635G>ACA2579596414ARAFc.558-4G>A (n.558-4G>A)
c.567-4G>A (n.567-4G>A)
c.569G>A (p.Gly190Asp)
c.-100-4G>A (n.-100-4G>A)
 dbSNP gnomAD v4
Xg.47566635G>CCA875843334ARAFc.558-4G>C (n.558-4G>C)
c.567-4G>C (n.567-4G>C)
c.569G>C (p.Gly190Ala)
c.-100-4G>C (n.-100-4G>C)
 dbSNP
Xg.47566635G=CA2427968696ARAFc.558-4G= (n.558-4G=)
c.567-4G= (n.567-4G=)
c.569G= (p.Gly190=)
c.-100-4G= (n.-100-4G=)
Xg.47566635G>TCA2693580428ARAFc.558-4G>T (n.558-4G>T)
c.567-4G>T (n.567-4G>T)
c.569G>T (p.Gly190Val)
c.-100-4G>T (n.-100-4G>T)
 gnomAD v4
Xg.47566636C>ACA2693580429ARAFc.558-3C>A (n.558-3C>A)
c.567-3C>A (n.567-3C>A)
c.570C>A (p.Gly190=)
c.-100-3C>A (n.-100-3C>A)
 gnomAD v4
Xg.47566636C=CA2427968697ARAFc.558-3C= (n.558-3C=)
c.567-3C= (n.567-3C=)
c.570C= (p.Gly190=)
c.-100-3C= (n.-100-3C=)
Xg.47566636C>TCA641482344ARAFc.558-3C>T (n.558-3C>T)
c.567-3C>T (n.567-3C>T)
c.570C>T (p.Gly190=)
c.-100-3C>T (n.-100-3C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566637A>CCA412813157ARAFc.558-2A>C (n.558-2A>C)
c.567-2A>C (n.567-2A>C)
c.571A>C (p.Ser191Arg)
c.-100-2A>C (n.-100-2A>C)
Xg.47566637A>GCA412813154ARAFc.558-2A>G (n.558-2A>G)
c.567-2A>G (n.567-2A>G)
c.571A>G (p.Ser191Gly)
c.-100-2A>G (n.-100-2A>G)
 gnomAD v4
Xg.47566637A>TCA412813156ARAFc.558-2A>T (n.558-2A>T)
c.567-2A>T (n.567-2A>T)
c.571A>T (p.Ser191Cys)
c.-100-2A>T (n.-100-2A>T)
Xg.47566638G>ACA412813159ARAFc.558-1G>A (n.558-1G>A)
c.567-1G>A (n.567-1G>A)
c.572G>A (p.Ser191Asn)
c.-100-1G>A (n.-100-1G>A)
 gnomAD v4
Xg.47566638G>CCA412813160ARAFc.558-1G>C (n.558-1G>C)
c.567-1G>C (n.567-1G>C)
c.572G>C (p.Ser191Thr)
c.-100-1G>C (n.-100-1G>C)
Xg.47566638G>TCA412813162ARAFc.558-1G>T (n.558-1G>T)
c.567-1G>T (n.567-1G>T)
c.572G>T (p.Ser191Ile)
c.-100-1G>T (n.-100-1G>T)
 gnomAD v4
Xg.47566639C>ACA10398040ARAFc.558C>A (p.Ser186Arg)
c.567C>A (p.Ser189Arg)
c.573C>A (p.Ser191Arg)
c.-100C>A (n.-100C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566639C=CA2427968698ARAFc.558C= (p.Ser186=)
c.567C= (p.Ser189=)
c.573C= (p.Ser191=)
c.-100C= (n.-100C=)
Xg.47566639C>GCA412813164ARAFc.558C>G (p.Ser186Arg)
c.567C>G (p.Ser189Arg)
c.573C>G (p.Ser191Arg)
c.-100C>G (n.-100C>G)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566639C>TCA515989036ARAFc.558C>T (p.Ser186=)
c.567C>T (p.Ser189=)
c.573C>T (p.Ser191=)
c.-100C>T (n.-100C>T)
 dbSNP gnomAD v4
Xg.47566643delCA2693580430ARAFc.562del (p.Arg188AlafsTer?)
c.571del (p.Arg191AlafsTer?)
c.577del (p.Arg193AlafsTer?)
c.-96del (n.-96del)
 gnomAD v4
Xg.47566640C>ACA412813166ARAFc.559C>A (p.Pro187Thr)
c.568C>A (p.Pro190Thr)
c.574C>A (p.Pro192Thr)
c.-99C>A (n.-99C>A)
Xg.47566640C=CA2427968699ARAFc.559C= (p.Pro187=)
c.568C= (p.Pro190=)
c.574C= (p.Pro192=)
c.-99C= (n.-99C=)
Xg.47566640C>GCA412813168ARAFc.559C>G (p.Pro187Ala)
c.568C>G (p.Pro190Ala)
c.574C>G (p.Pro192Ala)
c.-99C>G (n.-99C>G)
Xg.47566640C>TCA10398041ARAFc.559C>T (p.Pro187Ser)
c.568C>T (p.Pro190Ser)
c.574C>T (p.Pro192Ser)
c.-99C>T (n.-99C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566641C>ACA412813170ARAFc.560C>A (p.Pro187His)
c.569C>A (p.Pro190His)
c.575C>A (p.Pro192His)
c.-98C>A (n.-98C>A)
Xg.47566641C>GCA412813172ARAFc.560C>G (p.Pro187Arg)
c.569C>G (p.Pro190Arg)
c.575C>G (p.Pro192Arg)
c.-98C>G (n.-98C>G)
Xg.47566641C>TCA412813173ARAFc.560C>T (p.Pro187Leu)
c.569C>T (p.Pro190Leu)
c.575C>T (p.Pro192Leu)
c.-98C>T (n.-98C>T)
Xg.47566642C>ACA515989043ARAFc.561C>A (p.Pro187=)
c.570C>A (p.Pro190=)
c.576C>A (p.Pro192=)
c.-97C>A (n.-97C>A)
 gnomAD v4
Xg.47566642C=CA2427968700ARAFc.561C= (p.Pro187=)
c.570C= (p.Pro190=)
c.576C= (p.Pro192=)
c.-97C= (n.-97C=)
Xg.47566642C>GCA515989044ARAFc.561C>G (p.Pro187=)
c.570C>G (p.Pro190=)
c.576C>G (p.Pro192=)
c.-97C>G (n.-97C>G)
Xg.47566642C>TCA515989045ARAFc.561C>T (p.Pro187=)
c.570C>T (p.Pro190=)
c.576C>T (p.Pro192=)
c.-97C>T (n.-97C>T)
 dbSNP gnomAD v4
Xg.47566643C>ACA10398043ARAFc.562C>A (p.Arg188Ser)
c.571C>A (p.Arg191Ser)
c.577C>A (p.Arg193Ser)
c.-96C>A (n.-96C>A)
 dbSNP ExAC gnomAD v4
Xg.47566643C=CA2427968701ARAFc.562C= (p.Arg188=)
c.571C= (p.Arg191=)
c.577C= (p.Arg193=)
c.-96C= (n.-96C=)
Xg.47566643C>GCA412813175ARAFc.562C>G (p.Arg188Gly)
c.571C>G (p.Arg191Gly)
c.577C>G (p.Arg193Gly)
c.-96C>G (n.-96C>G)
 gnomAD v4
Xg.47566643C>TCA10398042ARAFc.562C>T (p.Arg188Cys)
c.571C>T (p.Arg191Cys)
c.577C>T (p.Arg193Cys)
c.-96C>T (n.-96C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566644G>ACA10398044ARAFc.563G>A (p.Arg188His)
c.572G>A (p.Arg191His)
c.578G>A (p.Arg193His)
c.-95G>A (n.-95G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.47566644G>CCA412813179ARAFc.563G>C (p.Arg188Pro)
c.572G>C (p.Arg191Pro)
c.578G>C (p.Arg193Pro)
c.-95G>C (n.-95G>C)
 dbSNP
Xg.47566644G=CA2427968702ARAFc.563G= (p.Arg188=)
c.572G= (p.Arg191=)
c.578G= (p.Arg193=)
c.-95G= (n.-95G=)
Xg.47566644G>TCA412813180ARAFc.563G>T (p.Arg188Leu)
c.572G>T (p.Arg191Leu)
c.578G>T (p.Arg193Leu)
c.-95G>T (n.-95G>T)
 dbSNP gnomAD v4
Xg.47566645C>ACA515989051ARAFc.564C>A (p.Arg188=)
c.573C>A (p.Arg191=)
c.579C>A (p.Arg193=)
c.-94C>A (n.-94C>A)
 dbSNP gnomAD v4
Xg.47566645C=CA2427968703ARAFc.564C= (p.Arg188=)
c.573C= (p.Arg191=)
c.579C= (p.Arg193=)
c.-94C= (n.-94C=)
Xg.47566645C>GCA515989055ARAFc.564C>G (p.Arg188=)
c.573C>G (p.Arg191=)
c.579C>G (p.Arg193=)
c.-94C>G (n.-94C>G)
Xg.47566645C>TCA515989053ARAFc.564C>T (p.Arg188=)
c.573C>T (p.Arg191=)
c.579C>T (p.Arg193=)
c.-94C>T (n.-94C>T)
 gnomAD v4
Xg.47566646A>CCA412813181ARAFc.565A>C (p.Thr189Pro)
c.574A>C (p.Thr192Pro)
c.580A>C (p.Thr194Pro)
c.-93A>C (n.-93A>C)
 dbSNP gnomAD v4
Xg.47566646A>GCA412813182ARAFc.565A>G (p.Thr189Ala)
c.574A>G (p.Thr192Ala)
c.580A>G (p.Thr194Ala)
c.-93A>G (n.-93A>G)
Xg.47566646A>TCA412813184ARAFc.565A>T (p.Thr189Ser)
c.574A>T (p.Thr192Ser)
c.580A>T (p.Thr194Ser)
c.-93A>T (n.-93A>T)
Xg.47566647C>ACA412813186ARAFc.566C>A (p.Thr189Asn)
c.575C>A (p.Thr192Asn)
c.581C>A (p.Thr194Asn)
c.-92C>A (n.-92C>A)
 gnomAD v4
Xg.47566647C>GCA412813187ARAFc.566C>G (p.Thr189Ser)
c.575C>G (p.Thr192Ser)
c.581C>G (p.Thr194Ser)
c.-92C>G (n.-92C>G)
Xg.47566647C>TCA412813189ARAFc.566C>T (p.Thr189Ile)
c.575C>T (p.Thr192Ile)
c.581C>T (p.Thr194Ile)
c.-92C>T (n.-92C>T)
 gnomAD v4
Xg.47566648C>ACA515989061ARAFc.567C>A (p.Thr189=)
c.576C>A (p.Thr192=)
c.582C>A (p.Thr194=)
c.-91C>A (n.-91C>A)
 gnomAD v4
Xg.47566648C=CA2427968704ARAFc.567C= (p.Thr189=)
c.576C= (p.Thr192=)
c.582C= (p.Thr194=)
c.-91C= (n.-91C=)
Xg.47566648C>GCA515989062ARAFc.567C>G (p.Thr189=)
c.576C>G (p.Thr192=)
c.582C>G (p.Thr194=)
c.-91C>G (n.-91C>G)
Xg.47566648C>TCA10398045ARAFc.567C>T (p.Thr189=)
c.576C>T (p.Thr192=)
c.582C>T (p.Thr194=)
c.-91C>T (n.-91C>T)
 dbSNP ExAC gnomAD v2
Xg.47566649C>ACA412813191ARAFc.568C>A (p.Gln190Lys)
c.577C>A (p.Gln193Lys)
c.583C>A (p.Gln195Lys)
c.-90C>A (n.-90C>A)
 gnomAD v4
Xg.47566649C>GCA412813193ARAFc.568C>G (p.Gln190Glu)
c.577C>G (p.Gln193Glu)
c.583C>G (p.Gln195Glu)
c.-90C>G (n.-90C>G)
Xg.47566649C>TCA412813195ARAFc.568C>T (p.Gln190Ter)
c.577C>T (p.Gln193Ter)
c.583C>T (p.Gln195Ter)
c.-90C>T (n.-90C>T)
Xg.47566650A=CA2427968705ARAFc.569A= (p.Gln190=)
c.578A= (p.Gln193=)
c.584A= (p.Gln195=)
c.-89A= (n.-89A=)
Xg.47566650A>CCA329053084ARAFc.569A>C (p.Gln190Pro)
c.578A>C (p.Gln193Pro)
c.584A>C (p.Gln195Pro)
c.-89A>C (n.-89A>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566650A>GCA412813198ARAFc.569A>G (p.Gln190Arg)
c.578A>G (p.Gln193Arg)
c.584A>G (p.Gln195Arg)
c.-89A>G (n.-89A>G)
Xg.47566650A>TCA412813196ARAFc.569A>T (p.Gln190Leu)
c.578A>T (p.Gln193Leu)
c.584A>T (p.Gln195Leu)
c.-89A>T (n.-89A>T)
Xg.47566651G>ACA515989064ARAFc.570G>A (p.Gln190=)
c.579G>A (p.Gln193=)
c.585G>A (p.Gln195=)
c.-88G>A (n.-88G>A)
 gnomAD v4
Xg.47566651G>CCA412813200ARAFc.570G>C (p.Gln190His)
c.579G>C (p.Gln193His)
c.585G>C (p.Gln195His)
c.-88G>C (n.-88G>C)
Xg.47566651G=CA2427968706ARAFc.570G= (p.Gln190=)
c.579G= (p.Gln193=)
c.585G= (p.Gln195=)
c.-88G= (n.-88G=)
Xg.47566651G>TCA10398046ARAFc.570G>T (p.Gln190His)
c.579G>T (p.Gln193His)
c.585G>T (p.Gln195His)
c.-88G>T (n.-88G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566652C>ACA412813202ARAFc.571C>A (p.His191Asn)
c.580C>A (p.His194Asn)
c.586C>A (p.His196Asn)
c.-87C>A (n.-87C>A)
 dbSNP
Xg.47566652C=CA2427968707ARAFc.571C= (p.His191=)
c.580C= (p.His194=)
c.586C= (p.His196=)
c.-87C= (n.-87C=)
Xg.47566652C>GCA412813204ARAFc.571C>G (p.His191Asp)
c.580C>G (p.His194Asp)
c.586C>G (p.His196Asp)
c.-87C>G (n.-87C>G)
Xg.47566652C>TCA10398047ARAFc.571C>T (p.His191Tyr)
c.580C>T (p.His194Tyr)
c.586C>T (p.His196Tyr)
c.-87C>T (n.-87C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566653A>CCA412813206ARAFc.572A>C (p.His191Pro)
c.581A>C (p.His194Pro)
c.587A>C (p.His196Pro)
c.-86A>C (n.-86A>C)
Xg.47566653A>GCA412813207ARAFc.572A>G (p.His191Arg)
c.581A>G (p.His194Arg)
c.587A>G (p.His196Arg)
c.-86A>G (n.-86A>G)
Xg.47566653A>TCA412813209ARAFc.572A>T (p.His191Leu)
c.581A>T (p.His194Leu)
c.587A>T (p.His196Leu)
c.-86A>T (n.-86A>T)
Xg.47566654C>ACA412813211ARAFc.573C>A (p.His191Gln)
c.582C>A (p.His194Gln)
c.588C>A (p.His196Gln)
c.-85C>A (n.-85C>A)
Xg.47566654C>GCA412813213ARAFc.573C>G (p.His191Gln)
c.582C>G (p.His194Gln)
c.588C>G (p.His196Gln)
c.-85C>G (n.-85C>G)
Xg.47566654C>TCA515989072ARAFc.573C>T (p.His191=)
c.582C>T (p.His194=)
c.588C>T (p.His196=)
c.-85C>T (n.-85C>T)
Xg.47566655T>ACA412813214ARAFc.574T>A (p.Cys192Ser)
c.583T>A (p.Cys195Ser)
c.589T>A (p.Cys197Ser)
c.-84T>A (n.-84T>A)
Xg.47566655T>CCA412813216ARAFc.574T>C (p.Cys192Arg)
c.583T>C (p.Cys195Arg)
c.589T>C (p.Cys197Arg)
c.-84T>C (n.-84T>C)
Xg.47566655T>GCA412813218ARAFc.574T>G (p.Cys192Gly)
c.583T>G (p.Cys195Gly)
c.589T>G (p.Cys197Gly)
c.-84T>G (n.-84T>G)
Xg.47566656G>ACA412813219ARAFc.575G>A (p.Cys192Tyr)
c.584G>A (p.Cys195Tyr)
c.590G>A (p.Cys197Tyr)
c.-83G>A (n.-83G>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566656G>CCA412813221ARAFc.575G>C (p.Cys192Ser)
c.584G>C (p.Cys195Ser)
c.590G>C (p.Cys197Ser)
c.-83G>C (n.-83G>C)
Xg.47566656G=CA2427968708ARAFc.575G= (p.Cys192=)
c.584G= (p.Cys195=)
c.590G= (p.Cys197=)
c.-83G= (n.-83G=)
Xg.47566656G>TCA412813220ARAFc.575G>T (p.Cys192Phe)
c.584G>T (p.Cys195Phe)
c.590G>T (p.Cys197Phe)
c.-83G>T (n.-83G>T)
Xg.47566657T>ACA412813223ARAFc.576T>A (p.Cys192Ter)
c.585T>A (p.Cys195Ter)
c.591T>A (p.Cys197Ter)
c.-82T>A (n.-82T>A)
Xg.47566657T>CCA515989077ARAFc.576T>C (p.Cys192=)
c.585T>C (p.Cys195=)
c.591T>C (p.Cys197=)
c.-82T>C (n.-82T>C)
Xg.47566657T>GCA412813225ARAFc.576T>G (p.Cys192Trp)
c.585T>G (p.Cys195Trp)
c.591T>G (p.Cys197Trp)
c.-82T>G (n.-82T>G)
Xg.47566658G>ACA412813227ARAFc.577G>A (p.Asp193Asn)
c.586G>A (p.Asp196Asn)
c.592G>A (p.Asp198Asn)
c.-81G>A (n.-81G>A)
Xg.47566658G>CCA412813228ARAFc.577G>C (p.Asp193His)
c.586G>C (p.Asp196His)
c.592G>C (p.Asp198His)
c.-81G>C (n.-81G>C)
 gnomAD v4
Xg.47566658G>TCA412813230ARAFc.577G>T (p.Asp193Tyr)
c.586G>T (p.Asp196Tyr)
c.592G>T (p.Asp198Tyr)
c.-81G>T (n.-81G>T)
Xg.47566659A>CCA412813231ARAFc.578A>C (p.Asp193Ala)
c.587A>C (p.Asp196Ala)
c.593A>C (p.Asp198Ala)
c.-80A>C (n.-80A>C)
 dbSNP
Xg.47566659A>GCA412813233ARAFc.578A>G (p.Asp193Gly)
c.587A>G (p.Asp196Gly)
c.593A>G (p.Asp198Gly)
c.-80A>G (n.-80A>G)
Xg.47566659A>TCA412813235ARAFc.578A>T (p.Asp193Val)
c.587A>T (p.Asp196Val)
c.593A>T (p.Asp198Val)
c.-80A>T (n.-80A>T)
 dbSNP
Xg.47566660C>ACA412813236ARAFc.579C>A (p.Asp193Glu)
c.588C>A (p.Asp196Glu)
c.594C>A (p.Asp198Glu)
c.-79C>A (n.-79C>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566660C=CA2427968709ARAFc.579C= (p.Asp193=)
c.588C= (p.Asp196=)
c.594C= (p.Asp198=)
c.-79C= (n.-79C=)
Xg.47566660C>GCA412813237ARAFc.579C>G (p.Asp193Glu)
c.588C>G (p.Asp196Glu)
c.594C>G (p.Asp198Glu)
c.-79C>G (n.-79C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566660C>TCA515989080ARAFc.579C>T (p.Asp193=)
c.588C>T (p.Asp196=)
c.594C>T (p.Asp198=)
c.-79C>T (n.-79C>T)
Xg.47566661C>ACA412813241ARAFc.580C>A (p.Pro194Thr)
c.589C>A (p.Pro197Thr)
c.595C>A (p.Pro199Thr)
c.-78C>A (n.-78C>A)
 gnomAD v4
Xg.47566661C>GCA412813242ARAFc.580C>G (p.Pro194Ala)
c.589C>G (p.Pro197Ala)
c.595C>G (p.Pro199Ala)
c.-78C>G (n.-78C>G)
Xg.47566661C>TCA412813240ARAFc.580C>T (p.Pro194Ser)
c.589C>T (p.Pro197Ser)
c.595C>T (p.Pro199Ser)
c.-78C>T (n.-78C>T)
Xg.47566662C>ACA412813247ARAFc.581C>A (p.Pro194Gln)
c.590C>A (p.Pro197Gln)
c.596C>A (p.Pro199Gln)
c.-77C>A (n.-77C>A)
 gnomAD v4
Xg.47566662C=CA2427968710ARAFc.581C= (p.Pro194=)
c.590C= (p.Pro197=)
c.596C= (p.Pro199=)
c.-77C= (n.-77C=)
Xg.47566662C>GCA412813244ARAFc.581C>G (p.Pro194Arg)
c.590C>G (p.Pro197Arg)
c.596C>G (p.Pro199Arg)
c.-77C>G (n.-77C>G)
Xg.47566662C>TCA10398048ARAFc.581C>T (p.Pro194Leu)
c.590C>T (p.Pro197Leu)
c.596C>T (p.Pro199Leu)
c.-77C>T (n.-77C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566663G>ACA515989082ARAFc.582G>A (p.Pro194=)
c.591G>A (p.Pro197=)
c.597G>A (p.Pro199=)
c.-76G>A (n.-76G>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566663G>CCA515989083ARAFc.582G>C (p.Pro194=)
c.591G>C (p.Pro197=)
c.597G>C (p.Pro199=)
c.-76G>C (n.-76G>C)
 dbSNP
Xg.47566663G=CA2427968711ARAFc.582G= (p.Pro194=)
c.591G= (p.Pro197=)
c.597G= (p.Pro199=)
c.-76G= (n.-76G=)
Xg.47566663G>TCA515989084ARAFc.582G>T (p.Pro194=)
c.591G>T (p.Pro197=)
c.597G>T (p.Pro199=)
c.-76G>T (n.-76G>T)
Xg.47566664G>ACA412813248ARAFc.583G>A (p.Glu195Lys)
c.592G>A (p.Glu198Lys)
c.598G>A (p.Glu200Lys)
c.-75G>A (n.-75G>A)
 gnomAD v4
Xg.47566664G>CCA412813249ARAFc.583G>C (p.Glu195Gln)
c.592G>C (p.Glu198Gln)
c.598G>C (p.Glu200Gln)
c.-75G>C (n.-75G>C)
Xg.47566664G>TCA412813250ARAFc.583G>T (p.Glu195Ter)
c.592G>T (p.Glu198Ter)
c.598G>T (p.Glu200Ter)
c.-75G>T (n.-75G>T)
Xg.47566665A>CCA412813252ARAFc.584A>C (p.Glu195Ala)
c.593A>C (p.Glu198Ala)
c.599A>C (p.Glu200Ala)
c.-74A>C (n.-74A>C)
Xg.47566665A>GCA412813253ARAFc.584A>G (p.Glu195Gly)
c.593A>G (p.Glu198Gly)
c.599A>G (p.Glu200Gly)
c.-74A>G (n.-74A>G)
 dbSNP gnomAD v4
Xg.47566665A>TCA412813255ARAFc.584A>T (p.Glu195Val)
c.593A>T (p.Glu198Val)
c.599A>T (p.Glu200Val)
c.-74A>T (n.-74A>T)
Xg.47566666G>ACA515989086ARAFc.585G>A (p.Glu195=)
c.594G>A (p.Glu198=)
c.600G>A (p.Glu200=)
c.-73G>A (n.-73G>A)
Xg.47566666G>CCA412813256ARAFc.585G>C (p.Glu195Asp)
c.594G>C (p.Glu198Asp)
c.600G>C (p.Glu200Asp)
c.-73G>C (n.-73G>C)
Xg.47566666G>TCA412813257ARAFc.585G>T (p.Glu195Asp)
c.594G>T (p.Glu198Asp)
c.600G>T (p.Glu200Asp)
c.-73G>T (n.-73G>T)
Xg.47566667C>ACA412813259ARAFc.586C>A (p.His196Asn)
c.595C>A (p.His199Asn)
c.601C>A (p.His201Asn)
c.-72C>A (n.-72C>A)
 gnomAD v4
Xg.47566667C>GCA412813260ARAFc.586C>G (p.His196Asp)
c.595C>G (p.His199Asp)
c.601C>G (p.His201Asp)
c.-72C>G (n.-72C>G)
Xg.47566667C>TCA412813262ARAFc.586C>T (p.His196Tyr)
c.595C>T (p.His199Tyr)
c.601C>T (p.His201Tyr)
c.-72C>T (n.-72C>T)
 dbSNP gnomAD v4
Xg.47566668A>CCA412813264ARAFc.587A>C (p.His196Pro)
c.596A>C (p.His199Pro)
c.602A>C (p.His201Pro)
c.-71A>C (n.-71A>C)
Xg.47566668A>GCA412813266ARAFc.587A>G (p.His196Arg)
c.596A>G (p.His199Arg)
c.602A>G (p.His201Arg)
c.-71A>G (n.-71A>G)
Xg.47566668A>TCA412813265ARAFc.587A>T (p.His196Leu)
c.596A>T (p.His199Leu)
c.602A>T (p.His201Leu)
c.-71A>T (n.-71A>T)
Xg.47566669C>ACA412813268ARAFc.588C>A (p.His196Gln)
c.597C>A (p.His199Gln)
c.603C>A (p.His201Gln)
c.-70C>A (n.-70C>A)
 gnomAD v4
Xg.47566669C=CA2427968712ARAFc.588C= (p.His196=)
c.597C= (p.His199=)
c.603C= (p.His201=)
c.-70C= (n.-70C=)
Xg.47566669C>GCA412813270ARAFc.588C>G (p.His196Gln)
c.597C>G (p.His199Gln)
c.603C>G (p.His201Gln)
c.-70C>G (n.-70C>G)
Xg.47566669C>TCA10398049ARAFc.588C>T (p.His196=)
c.597C>T (p.His199=)
c.603C>T (p.His201=)
c.-70C>T (n.-70C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566670T>ACA412813272ARAFc.589T>A (p.Phe197Ile)
c.598T>A (p.Phe200Ile)
c.604T>A (p.Phe202Ile)
c.-69T>A (n.-69T>A)
Xg.47566670T>CCA412813273ARAFc.589T>C (p.Phe197Leu)
c.598T>C (p.Phe200Leu)
c.604T>C (p.Phe202Leu)
c.-69T>C (n.-69T>C)
 dbSNP gnomAD v4
Xg.47566670T>GCA412813275ARAFc.589T>G (p.Phe197Val)
c.598T>G (p.Phe200Val)
c.604T>G (p.Phe202Val)
c.-69T>G (n.-69T>G)
Xg.47566671T>ACA412813277ARAFc.590T>A (p.Phe197Tyr)
c.599T>A (p.Phe200Tyr)
c.605T>A (p.Phe202Tyr)
c.-68T>A (n.-68T>A)
Xg.47566671T>CCA412813278ARAFc.590T>C (p.Phe197Ser)
c.599T>C (p.Phe200Ser)
c.605T>C (p.Phe202Ser)
c.-68T>C (n.-68T>C)
 gnomAD v4
Xg.47566671T>GCA412813279ARAFc.590T>G (p.Phe197Cys)
c.599T>G (p.Phe200Cys)
c.605T>G (p.Phe202Cys)
c.-68T>G (n.-68T>G)
Xg.47566672C>ACA412813281ARAFc.591C>A (p.Phe197Leu)
c.600C>A (p.Phe200Leu)
c.606C>A (p.Phe202Leu)
c.-67C>A (n.-67C>A)
 gnomAD v4
Xg.47566672C>GCA412813283ARAFc.591C>G (p.Phe197Leu)
c.600C>G (p.Phe200Leu)
c.606C>G (p.Phe202Leu)
c.-67C>G (n.-67C>G)
Xg.47566672C>TCA515989092ARAFc.591C>T (p.Phe197=)
c.600C>T (p.Phe200=)
c.606C>T (p.Phe202=)
c.-67C>T (n.-67C>T)
Xg.47566675delCA515989093ARAFc.594del (p.Phe199SerfsTer?)
c.603del (p.Phe202SerfsTer?)
c.609del (p.Phe204SerfsTer?)
c.-64del (n.-64del)
 COSMIC
Xg.47566673C>ACA412813286ARAFc.592C>A (p.Pro198Thr)
c.601C>A (p.Pro201Thr)
c.607C>A (p.Pro203Thr)
c.-66C>A (n.-66C>A)
 gnomAD v4
Xg.47566673C>GCA412813287ARAFc.592C>G (p.Pro198Ala)
c.601C>G (p.Pro201Ala)
c.607C>G (p.Pro203Ala)
c.-66C>G (n.-66C>G)
Xg.47566673C>TCA412813285ARAFc.592C>T (p.Pro198Ser)
c.601C>T (p.Pro201Ser)
c.607C>T (p.Pro203Ser)
c.-66C>T (n.-66C>T)
 gnomAD v4
Xg.47566674C>ACA412813290ARAFc.593C>A (p.Pro198His)
c.602C>A (p.Pro201His)
c.608C>A (p.Pro203His)
c.-65C>A (n.-65C>A)
 gnomAD v4
Xg.47566674C>GCA412813291ARAFc.593C>G (p.Pro198Arg)
c.602C>G (p.Pro201Arg)
c.608C>G (p.Pro203Arg)
c.-65C>G (n.-65C>G)
Xg.47566674C>TCA412813293ARAFc.593C>T (p.Pro198Leu)
c.602C>T (p.Pro201Leu)
c.608C>T (p.Pro203Leu)
c.-65C>T (n.-65C>T)
 dbSNP gnomAD v4
Xg.47566675C>ACA515989095ARAFc.594C>A (p.Pro198=)
c.603C>A (p.Pro201=)
c.609C>A (p.Pro203=)
c.-64C>A (n.-64C>A)
 gnomAD v4
Xg.47566675C>GCA515989096ARAFc.594C>G (p.Pro198=)
c.603C>G (p.Pro201=)
c.609C>G (p.Pro203=)
c.-64C>G (n.-64C>G)
Xg.47566675C>TCA515989097ARAFc.594C>T (p.Pro198=)
c.603C>T (p.Pro201=)
c.609C>T (p.Pro203=)
c.-64C>T (n.-64C>T)
Xg.47566676T>ACA412813294ARAFc.595T>A (p.Phe199Ile)
c.604T>A (p.Phe202Ile)
c.610T>A (p.Phe204Ile)
c.-63T>A (n.-63T>A)
Xg.47566676T>CCA412813295ARAFc.595T>C (p.Phe199Leu)
c.604T>C (p.Phe202Leu)
c.610T>C (p.Phe204Leu)
c.-63T>C (n.-63T>C)
 dbSNP gnomAD v4
Xg.47566676T>GCA412813296ARAFc.595T>G (p.Phe199Val)
c.604T>G (p.Phe202Val)
c.610T>G (p.Phe204Val)
c.-63T>G (n.-63T>G)
Xg.47566677delCA2693580431ARAFc.596del (p.Phe199SerfsTer?)
c.605del (p.Phe202SerfsTer?)
c.611del (p.Phe204SerfsTer?)
c.-62del (n.-62del)
 gnomAD v4
Xg.47566677T>ACA412813301ARAFc.596T>A (p.Phe199Tyr)
c.605T>A (p.Phe202Tyr)
c.611T>A (p.Phe204Tyr)
c.-62T>A (n.-62T>A)
Xg.47566677T>CCA412813298ARAFc.596T>C (p.Phe199Ser)
c.605T>C (p.Phe202Ser)
c.611T>C (p.Phe204Ser)
c.-62T>C (n.-62T>C)
 gnomAD v4
Xg.47566677T>GCA412813300ARAFc.596T>G (p.Phe199Cys)
c.605T>G (p.Phe202Cys)
c.611T>G (p.Phe204Cys)
c.-62T>G (n.-62T>G)
Xg.47566678C>ACA412813303ARAFc.597C>A (p.Phe199Leu)
c.606C>A (p.Phe202Leu)
c.612C>A (p.Phe204Leu)
c.-61C>A (n.-61C>A)
Xg.47566678C=CA2427968713ARAFc.597C= (p.Phe199=)
c.606C= (p.Phe202=)
c.612C= (p.Phe204=)
c.-61C= (n.-61C=)
Xg.47566678C>GCA412813304ARAFc.597C>G (p.Phe199Leu)
c.606C>G (p.Phe202Leu)
c.612C>G (p.Phe204Leu)
c.-61C>G (n.-61C>G)
Xg.47566678C>TCA515989101ARAFc.597C>T (p.Phe199=)
c.606C>T (p.Phe202=)
c.612C>T (p.Phe204=)
c.-61C>T (n.-61C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.47566679C>ACA412813306ARAFc.598C>A (p.Pro200Thr)
c.607C>A (p.Pro203Thr)
c.613C>A (p.Pro205Thr)
c.-60C>A (n.-60C>A)
 gnomAD v4
Xg.47566679C>GCA412813307ARAFc.598C>G (p.Pro200Ala)
c.607C>G (p.Pro203Ala)
c.613C>G (p.Pro205Ala)
c.-60C>G (n.-60C>G)
Xg.47566679C>TCA412813308ARAFc.598C>T (p.Pro200Ser)
c.607C>T (p.Pro203Ser)
c.613C>T (p.Pro205Ser)
c.-60C>T (n.-60C>T)
Xg.47566680C>ACA412813309ARAFc.599C>A (p.Pro200His)
c.608C>A (p.Pro203His)
c.614C>A (p.Pro205His)
c.-59C>A (n.-59C>A)
 gnomAD v4
Xg.47566680C=CA2427968714ARAFc.599C= (p.Pro200=)
c.608C= (p.Pro203=)
c.614C= (p.Pro205=)
c.-59C= (n.-59C=)
Xg.47566680C>GCA10398050ARAFc.599C>G (p.Pro200Arg)
c.608C>G (p.Pro203Arg)
c.614C>G (p.Pro205Arg)
c.-59C>G (n.-59C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.47566680C>TCA412813310ARAFc.599C>T (p.Pro200Leu)
c.608C>T (p.Pro203Leu)
c.614C>T (p.Pro205Leu)
c.-59C>T (n.-59C>T)
Xg.47566681T>ACA515989102ARAFc.600T>A (p.Pro200=)
c.609T>A (p.Pro203=)
c.615T>A (p.Pro205=)
c.-58T>A (n.-58T>A)
Xg.47566681T>CCA515989104ARAFc.600T>C (p.Pro200=)
c.609T>C (p.Pro203=)
c.615T>C (p.Pro205=)
c.-58T>C (n.-58T>C)
 gnomAD v4
Xg.47566681T>GCA515989103ARAFc.600T>G (p.Pro200=)
c.609T>G (p.Pro203=)
c.615T>G (p.Pro205=)
c.-58T>G (n.-58T>G)
Xg.47566682G>ACA412813312ARAFc.601G>A (p.Ala201Thr)
c.610G>A (p.Ala204Thr)
c.616G>A (p.Ala206Thr)
c.-57G>A (n.-57G>A)
Xg.47566682G>CCA412813313ARAFc.601G>C (p.Ala201Pro)
c.610G>C (p.Ala204Pro)
c.616G>C (p.Ala206Pro)
c.-57G>C (n.-57G>C)
 dbSNP
Xg.47566682G>TCA412813314ARAFc.601G>T (p.Ala201Ser)
c.610G>T (p.Ala204Ser)
c.616G>T (p.Ala206Ser)
c.-57G>T (n.-57G>T)
 gnomAD v4
Xg.47566683C>ACA412813315ARAFc.602C>A (p.Ala201Asp)
c.611C>A (p.Ala204Asp)
c.617C>A (p.Ala206Asp)
c.-56C>A (n.-56C>A)
 gnomAD v4
Xg.47566683C>GCA412813316ARAFc.602C>G (p.Ala201Gly)
c.611C>G (p.Ala204Gly)
c.617C>G (p.Ala206Gly)
c.-56C>G (n.-56C>G)
Xg.47566683C>TCA412813317ARAFc.602C>T (p.Ala201Val)
c.611C>T (p.Ala204Val)
c.617C>T (p.Ala206Val)
c.-56C>T (n.-56C>T)
 dbSNP gnomAD v4
Xg.47566686delCA2693580433ARAFc.605del (p.Pro202GlnfsTer?)
c.614del (p.Pro205GlnfsTer?)
c.620del (p.Pro207GlnfsTer?)
c.-53del (n.-53del)
 gnomAD v4
Xg.47566687_47566699delCA2693580432ARAFc.606_618del (p.Ala203TyrfsTer?)
c.615_627del (p.Ala206TyrfsTer?)
c.621_633del (p.Ala208TyrfsTer?)
c.-52_-40del (n.-52_-40del)
 gnomAD v4
Xg.47566684C>ACA515989108ARAFc.603C>A (p.Ala201=)
c.612C>A (p.Ala204=)
c.618C>A (p.Ala206=)
c.-55C>A (n.-55C>A)
 gnomAD v4
Xg.47566684C>GCA515989109ARAFc.603C>G (p.Ala201=)
c.612C>G (p.Ala204=)
c.618C>G (p.Ala206=)
c.-55C>G (n.-55C>G)
Xg.47566684C>TCA515989110ARAFc.603C>T (p.Ala201=)
c.612C>T (p.Ala204=)
c.618C>T (p.Ala206=)
c.-55C>T (n.-55C>T)
 gnomAD v4
Xg.47566685C>ACA412813318ARAFc.604C>A (p.Pro202Thr)
c.613C>A (p.Pro205Thr)
c.619C>A (p.Pro207Thr)
c.-54C>A (n.-54C>A)
 gnomAD v4
Xg.47566685C>GCA412813319ARAFc.604C>G (p.Pro202Ala)
c.613C>G (p.Pro205Ala)
c.619C>G (p.Pro207Ala)
c.-54C>G (n.-54C>G)
Xg.47566685C>TCA412813320ARAFc.604C>T (p.Pro202Ser)
c.613C>T (p.Pro205Ser)
c.619C>T (p.Pro207Ser)
c.-54C>T (n.-54C>T)
 dbSNP gnomAD v4
Xg.47566686C>ACA412813321ARAFc.605C>A (p.Pro202Gln)
c.614C>A (p.Pro205Gln)
c.620C>A (p.Pro207Gln)
c.-53C>A (n.-53C>A)
 gnomAD v4
Xg.47566686C>GCA412813322ARAFc.605C>G (p.Pro202Arg)
c.614C>G (p.Pro205Arg)
c.620C>G (p.Pro207Arg)
c.-53C>G (n.-53C>G)
Xg.47566686C>TCA412813323ARAFc.605C>T (p.Pro202Leu)
c.614C>T (p.Pro205Leu)
c.620C>T (p.Pro207Leu)
c.-53C>T (n.-53C>T)
 gnomAD v4
Xg.47566687A>CCA515989112ARAFc.606A>C (p.Pro202=)
c.615A>C (p.Pro205=)
c.621A>C (p.Pro207=)
c.-52A>C (n.-52A>C)
 dbSNP
Xg.47566687A>GCA515989113ARAFc.606A>G (p.Pro202=)
c.615A>G (p.Pro205=)
c.621A>G (p.Pro207=)
c.-52A>G (n.-52A>G)
Xg.47566687A>TCA515989114ARAFc.606A>T (p.Pro202=)
c.615A>T (p.Pro205=)
c.621A>T (p.Pro207=)
c.-52A>T (n.-52A>T)
Xg.47566688G>ACA329053113ARAFc.607G>A (p.Ala203Thr)
c.616G>A (p.Ala206Thr)
c.622G>A (p.Ala208Thr)
c.-51G>A (n.-51G>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566688G>CCA412813325ARAFc.607G>C (p.Ala203Pro)
c.616G>C (p.Ala206Pro)
c.622G>C (p.Ala208Pro)
c.-51G>C (n.-51G>C)
 dbSNP
Xg.47566688G=CA2427968715ARAFc.607G= (p.Ala203=)
c.616G= (p.Ala206=)
c.622G= (p.Ala208=)
c.-51G= (n.-51G=)
Xg.47566688G>TCA412813324ARAFc.607G>T (p.Ala203Ser)
c.616G>T (p.Ala206Ser)
c.622G>T (p.Ala208Ser)
c.-51G>T (n.-51G>T)
 gnomAD v4
Xg.47566689C>ACA412813326ARAFc.608C>A (p.Ala203Asp)
c.617C>A (p.Ala206Asp)
c.623C>A (p.Ala208Asp)
c.-50C>A (n.-50C>A)
 gnomAD v4
Xg.47566689C>GCA412813327ARAFc.608C>G (p.Ala203Gly)
c.617C>G (p.Ala206Gly)
c.623C>G (p.Ala208Gly)
c.-50C>G (n.-50C>G)
Xg.47566689C>TCA412813328ARAFc.608C>T (p.Ala203Val)
c.617C>T (p.Ala206Val)
c.623C>T (p.Ala208Val)
c.-50C>T (n.-50C>T)
 dbSNP
Xg.47566690C>ACA515989119ARAFc.609C>A (p.Ala203=)
c.618C>A (p.Ala206=)
c.624C>A (p.Ala208=)
c.-49C>A (n.-49C>A)
 gnomAD v4
Xg.47566690C>GCA515989120ARAFc.609C>G (p.Ala203=)
c.618C>G (p.Ala206=)
c.624C>G (p.Ala208=)
c.-49C>G (n.-49C>G)
Xg.47566690C>TCA515989117ARAFc.609C>T (p.Ala203=)
c.618C>T (p.Ala206=)
c.624C>T (p.Ala208=)
c.-49C>T (n.-49C>T)
Xg.47566691A>CCA412813329ARAFc.610A>C (p.Asn204His)
c.619A>C (p.Asn207His)
c.625A>C (p.Asn209His)
c.-48A>C (n.-48A>C)
 dbSNP
Xg.47566691A>GCA412813330ARAFc.610A>G (p.Asn204Asp)
c.619A>G (p.Asn207Asp)
c.625A>G (p.Asn209Asp)
c.-48A>G (n.-48A>G)
Xg.47566691A>TCA412813331ARAFc.610A>T (p.Asn204Tyr)
c.619A>T (p.Asn207Tyr)
c.625A>T (p.Asn209Tyr)
c.-48A>T (n.-48A>T)
Xg.47566692A>CCA412813332ARAFc.611A>C (p.Asn204Thr)
c.620A>C (p.Asn207Thr)
c.626A>C (p.Asn209Thr)
c.-47A>C (n.-47A>C)
Xg.47566692A>GCA412813333ARAFc.611A>G (p.Asn204Ser)
c.620A>G (p.Asn207Ser)
c.626A>G (p.Asn209Ser)
c.-47A>G (n.-47A>G)
 gnomAD v4
Xg.47566692A>TCA412813334ARAFc.611A>T (p.Asn204Ile)
c.620A>T (p.Asn207Ile)
c.626A>T (p.Asn209Ile)
c.-47A>T (n.-47A>T)
Xg.47566693T>ACA412813335ARAFc.612T>A (p.Asn204Lys)
c.621T>A (p.Asn207Lys)
c.627T>A (p.Asn209Lys)
c.-46T>A (n.-46T>A)
Xg.47566693T>CCA515989121ARAFc.612T>C (p.Asn204=)
c.621T>C (p.Asn207=)
c.627T>C (p.Asn209=)
c.-46T>C (n.-46T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566693T>GCA412813336ARAFc.612T>G (p.Asn204Lys)
c.621T>G (p.Asn207Lys)
c.627T>G (p.Asn209Lys)
c.-46T>G (n.-46T>G)
Xg.47566693T=CA2427968716ARAFc.612T= (p.Asn204=)
c.621T= (p.Asn207=)
c.627T= (p.Asn209=)
c.-46T= (n.-46T=)
Xg.47566694G>ACA412813337ARAFc.613G>A (p.Ala205Thr)
c.622G>A (p.Ala208Thr)
c.628G>A (p.Ala210Thr)
c.-45G>A (n.-45G>A)
 gnomAD v4
Xg.47566694G>CCA412813338ARAFc.613G>C (p.Ala205Pro)
c.622G>C (p.Ala208Pro)
c.628G>C (p.Ala210Pro)
c.-45G>C (n.-45G>C)
 dbSNP
Xg.47566694G=CA2427968717ARAFc.613G= (p.Ala205=)
c.622G= (p.Ala208=)
c.628G= (p.Ala210=)
c.-45G= (n.-45G=)
Xg.47566694G>TCA412813339ARAFc.613G>T (p.Ala205Ser)
c.622G>T (p.Ala208Ser)
c.628G>T (p.Ala210Ser)
c.-45G>T (n.-45G>T)
Xg.47566695C>ACA412813342ARAFc.614C>A (p.Ala205Asp)
c.623C>A (p.Ala208Asp)
c.629C>A (p.Ala210Asp)
c.-44C>A (n.-44C>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566695C=CA2427968718ARAFc.614C= (p.Ala205=)
c.623C= (p.Ala208=)
c.629C= (p.Ala210=)
c.-44C= (n.-44C=)
Xg.47566695C>GCA412813341ARAFc.614C>G (p.Ala205Gly)
c.623C>G (p.Ala208Gly)
c.629C>G (p.Ala210Gly)
c.-44C>G (n.-44C>G)
Xg.47566695C>TCA412813340ARAFc.614C>T (p.Ala205Val)
c.623C>T (p.Ala208Val)
c.629C>T (p.Ala210Val)
c.-44C>T (n.-44C>T)
 dbSNP gnomAD v4
Xg.47566700dupCA641482345ARAFc.619dup (p.Leu207ProfsTer?)
c.628dup (p.Leu210ProfsTer?)
c.634dup (p.Leu212ProfsTer?)
c.-39dup (n.-39dup)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566700delCA515989124ARAFc.619del (p.Leu207TyrfsTer?)
c.628del (p.Leu210TyrfsTer?)
c.634del (p.Leu212TyrfsTer?)
c.-39del (n.-39del)
 gnomAD v4 COSMIC
Xg.47566696C>ACA10398052ARAFc.615C>A (p.Ala205=)
c.624C>A (p.Ala208=)
c.630C>A (p.Ala210=)
c.-43C>A (n.-43C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.47566696C=CA2427968719ARAFc.615C= (p.Ala205=)
c.624C= (p.Ala208=)
c.630C= (p.Ala210=)
c.-43C= (n.-43C=)
Xg.47566696C>GCA10398051ARAFc.615C>G (p.Ala205=)
c.624C>G (p.Ala208=)
c.630C>G (p.Ala210=)
c.-43C>G (n.-43C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566696C>TCA515989126ARAFc.615C>T (p.Ala205=)
c.624C>T (p.Ala208=)
c.630C>T (p.Ala210=)
c.-43C>T (n.-43C>T)
 gnomAD v4
Xg.47566697C>ACA412813343ARAFc.616C>A (p.Pro206Thr)
c.625C>A (p.Pro209Thr)
c.631C>A (p.Pro211Thr)
c.-42C>A (n.-42C>A)
 gnomAD v4
Xg.47566697C=CA2427968720ARAFc.616C= (p.Pro206=)
c.625C= (p.Pro209=)
c.631C= (p.Pro211=)
c.-42C= (n.-42C=)
Xg.47566697C>GCA412813344ARAFc.616C>G (p.Pro206Ala)
c.625C>G (p.Pro209Ala)
c.631C>G (p.Pro211Ala)
c.-42C>G (n.-42C>G)
Xg.47566697C>TCA412813345ARAFc.616C>T (p.Pro206Ser)
c.625C>T (p.Pro209Ser)
c.631C>T (p.Pro211Ser)
c.-42C>T (n.-42C>T)
 dbSNP gnomAD v4
Xg.47566698C>ACA412813346ARAFc.617C>A (p.Pro206His)
c.626C>A (p.Pro209His)
c.632C>A (p.Pro211His)
c.-41C>A (n.-41C>A)
Xg.47566698C>GCA412813347ARAFc.617C>G (p.Pro206Arg)
c.626C>G (p.Pro209Arg)
c.632C>G (p.Pro211Arg)
c.-41C>G (n.-41C>G)
Xg.47566698C>TCA412813348ARAFc.617C>T (p.Pro206Leu)
c.626C>T (p.Pro209Leu)
c.632C>T (p.Pro211Leu)
c.-41C>T (n.-41C>T)
 gnomAD v4
Xg.47566699C>ACA515989127ARAFc.618C>A (p.Pro206=)
c.627C>A (p.Pro209=)
c.633C>A (p.Pro211=)
c.-40C>A (n.-40C>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566699C=CA2427968721ARAFc.618C= (p.Pro206=)
c.627C= (p.Pro209=)
c.633C= (p.Pro211=)
c.-40C= (n.-40C=)
Xg.47566699C>GCA515989128ARAFc.618C>G (p.Pro206=)
c.627C>G (p.Pro209=)
c.633C>G (p.Pro211=)
c.-40C>G (n.-40C>G)
Xg.47566699C>TCA10398053ARAFc.618C>T (p.Pro206=)
c.627C>T (p.Pro209=)
c.633C>T (p.Pro211=)
c.-40C>T (n.-40C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566700C>ACA412813349ARAFc.619C>A (p.Leu207Ile)
c.628C>A (p.Leu210Ile)
c.634C>A (p.Leu212Ile)
c.-39C>A (n.-39C>A)
 gnomAD v4
Xg.47566700C>GCA412813350ARAFc.619C>G (p.Leu207Val)
c.628C>G (p.Leu210Val)
c.634C>G (p.Leu212Val)
c.-39C>G (n.-39C>G)
 gnomAD v4
Xg.47566700C>TCA515989129ARAFc.619C>T (p.Leu207=)
c.628C>T (p.Leu210=)
c.634C>T (p.Leu212=)
c.-39C>T (n.-39C>T)
 gnomAD v4
Xg.47566701T>ACA412813351ARAFc.620T>A (p.Leu207Gln)
c.629T>A (p.Leu210Gln)
c.635T>A (p.Leu212Gln)
c.-38T>A (n.-38T>A)
Xg.47566701T>CCA412813352ARAFc.620T>C (p.Leu207Pro)
c.629T>C (p.Leu210Pro)
c.635T>C (p.Leu212Pro)
c.-38T>C (n.-38T>C)
Xg.47566701T>GCA412813353ARAFc.620T>G (p.Leu207Arg)
c.629T>G (p.Leu210Arg)
c.635T>G (p.Leu212Arg)
c.-38T>G (n.-38T>G)
Xg.47566702A>CCA515989131ARAFc.621A>C (p.Leu207=)
c.630A>C (p.Leu210=)
c.636A>C (p.Leu212=)
c.-37A>C (n.-37A>C)
Xg.47566702A>GCA515989132ARAFc.621A>G (p.Leu207=)
c.630A>G (p.Leu210=)
c.636A>G (p.Leu212=)
c.-37A>G (n.-37A>G)
 gnomAD v4
Xg.47566702A>TCA515989133ARAFc.621A>T (p.Leu207=)
c.630A>T (p.Leu210=)
c.636A>T (p.Leu212=)
c.-37A>T (n.-37A>T)
Xg.47566703C>ACA412813356ARAFc.622C>A (p.Gln208Lys)
c.631C>A (p.Gln211Lys)
c.637C>A (p.Gln213Lys)
c.-36C>A (n.-36C>A)
 gnomAD v4
Xg.47566703C>GCA412813355ARAFc.622C>G (p.Gln208Glu)
c.631C>G (p.Gln211Glu)
c.637C>G (p.Gln213Glu)
c.-36C>G (n.-36C>G)
Xg.47566703C>TCA412813354ARAFc.622C>T (p.Gln208Ter)
c.631C>T (p.Gln211Ter)
c.637C>T (p.Gln213Ter)
c.-36C>T (n.-36C>T)
Xg.47566704A=CA2427968722ARAFc.623A= (p.Gln208=)
c.632A= (p.Gln211=)
c.638A= (p.Gln213=)
c.-35A= (n.-35A=)
Xg.47566704A>CCA412813357ARAFc.623A>C (p.Gln208Pro)
c.632A>C (p.Gln211Pro)
c.638A>C (p.Gln213Pro)
c.-35A>C (n.-35A>C)
Xg.47566704A>GCA412813358ARAFc.623A>G (p.Gln208Arg)
c.632A>G (p.Gln211Arg)
c.638A>G (p.Gln213Arg)
c.-35A>G (n.-35A>G)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566704A>TCA412813359ARAFc.623A>T (p.Gln208Leu)
c.632A>T (p.Gln211Leu)
c.638A>T (p.Gln213Leu)
c.-35A>T (n.-35A>T)
Xg.47566705G>ACA515989137ARAFc.624G>A (p.Gln208=)
c.633G>A (p.Gln211=)
c.639G>A (p.Gln213=)
c.-34G>A (n.-34G>A)
 dbSNP
Xg.47566705G>CCA10398054ARAFc.624G>C (p.Gln208His)
c.633G>C (p.Gln211His)
c.639G>C (p.Gln213His)
c.-34G>C (n.-34G>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566705G=CA2427968723ARAFc.624G= (p.Gln208=)
c.633G= (p.Gln211=)
c.639G= (p.Gln213=)
c.-34G= (n.-34G=)
Xg.47566705G>TCA412813360ARAFc.624G>T (p.Gln208His)
c.633G>T (p.Gln211His)
c.639G>T (p.Gln213His)
c.-34G>T (n.-34G>T)
Xg.47566706C>ACA412813363ARAFc.625C>A (p.Arg209Ser)
c.634C>A (p.Arg212Ser)
c.640C>A (p.Arg214Ser)
c.-33C>A (n.-33C>A)
Xg.47566706C>GCA412813362ARAFc.625C>G (p.Arg209Gly)
c.634C>G (p.Arg212Gly)
c.640C>G (p.Arg214Gly)
c.-33C>G (n.-33C>G)
Xg.47566706C>TCA412813361ARAFc.625C>T (p.Arg209Cys)
c.634C>T (p.Arg212Cys)
c.640C>T (p.Arg214Cys)
c.-33C>T (n.-33C>T)
 dbSNP gnomAD v4 COSMIC
Xg.47566707G>ACA412813364ARAFc.626G>A (p.Arg209His)
c.635G>A (p.Arg212His)
c.641G>A (p.Arg214His)
c.-32G>A (n.-32G>A)
 dbSNP gnomAD v4
Xg.47566707G>CCA412813365ARAFc.626G>C (p.Arg209Pro)
c.635G>C (p.Arg212Pro)
c.641G>C (p.Arg214Pro)
c.-32G>C (n.-32G>C)
 dbSNP
Xg.47566707G>TCA412813366ARAFc.626G>T (p.Arg209Leu)
c.635G>T (p.Arg212Leu)
c.641G>T (p.Arg214Leu)
c.-32G>T (n.-32G>T)
Xg.47566708C>ACA515989143ARAFc.627C>A (p.Arg209=)
c.636C>A (p.Arg212=)
c.642C>A (p.Arg214=)
c.-31C>A (n.-31C>A)
Xg.47566708C>GCA515989144ARAFc.627C>G (p.Arg209=)
c.636C>G (p.Arg212=)
c.642C>G (p.Arg214=)
c.-31C>G (n.-31C>G)
Xg.47566708C>TCA515989145ARAFc.627C>T (p.Arg209=)
c.636C>T (p.Arg212=)
c.642C>T (p.Arg214=)
c.-31C>T (n.-31C>T)
Xg.47566709A=CA2427968724ARAFc.628A= (p.Ile210=)
c.637A= (p.Ile213=)
c.643A= (p.Ile215=)
c.-30A= (n.-30A=)
Xg.47566709A>CCA412813367ARAFc.628A>C (p.Ile210Leu)
c.637A>C (p.Ile213Leu)
c.643A>C (p.Ile215Leu)
c.-30A>C (n.-30A>C)
Xg.47566709A>GCA412813368ARAFc.628A>G (p.Ile210Val)
c.637A>G (p.Ile213Val)
c.643A>G (p.Ile215Val)
c.-30A>G (n.-30A>G)
 dbSNP gnomAD v2 gnomAD v4
Xg.47566709A>TCA412813369ARAFc.628A>T (p.Ile210Phe)
c.637A>T (p.Ile213Phe)
c.643A>T (p.Ile215Phe)
c.-30A>T (n.-30A>T)
Xg.47566710T>ACA412813372ARAFc.629T>A (p.Ile210Asn)
c.638T>A (p.Ile213Asn)
c.644T>A (p.Ile215Asn)
c.-29T>A (n.-29T>A)
Xg.47566710T>CCA412813370ARAFc.629T>C (p.Ile210Thr)
c.638T>C (p.Ile213Thr)
c.644T>C (p.Ile215Thr)
c.-29T>C (n.-29T>C)
Xg.47566710T>GCA412813371ARAFc.629T>G (p.Ile210Ser)
c.638T>G (p.Ile213Ser)
c.644T>G (p.Ile215Ser)
c.-29T>G (n.-29T>G)
Xg.47566711C>ACA515989149ARAFc.630C>A (p.Ile210=)
c.639C>A (p.Ile213=)
c.645C>A (p.Ile215=)
c.-28C>A (n.-28C>A)
Xg.47566711C>GCA412813373ARAFc.630C>G (p.Ile210Met)
c.639C>G (p.Ile213Met)
c.645C>G (p.Ile215Met)
c.-28C>G (n.-28C>G)
Xg.47566711C>TCA515989150ARAFc.630C>T (p.Ile210=)
c.639C>T (p.Ile213=)
c.645C>T (p.Ile215=)
c.-28C>T (n.-28C>T)
 gnomAD v4
Xg.47566712C>ACA412813374ARAFc.631C>A (p.Arg211Ser)
c.640C>A (p.Arg214Ser)
c.646C>A (p.Arg216Ser)
c.-27C>A (n.-27C>A)
Xg.47566712C=CA2427968725ARAFc.631C= (p.Arg211=)
c.640C= (p.Arg214=)
c.646C= (p.Arg216=)
c.-27C= (n.-27C=)
Xg.47566712C>GCA412813375ARAFc.631C>G (p.Arg211Gly)
c.640C>G (p.Arg214Gly)
c.646C>G (p.Arg216Gly)
c.-27C>G (n.-27C>G)
Xg.47566712C>TCA412813376ARAFc.631C>T (p.Arg211Cys)
c.640C>T (p.Arg214Cys)
c.646C>T (p.Arg216Cys)
c.-27C>T (n.-27C>T)
 dbSNP gnomAD v4
Xg.47566713G>ACA329053170ARAFc.632G>A (p.Arg211His)
c.641G>A (p.Arg214His)
c.647G>A (p.Arg216His)
c.-26G>A (n.-26G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566713G>CCA412813377ARAFc.632G>C (p.Arg211Pro)
c.641G>C (p.Arg214Pro)
c.647G>C (p.Arg216Pro)
c.-26G>C (n.-26G>C)
 dbSNP
Xg.47566713G=CA2427968726ARAFc.632G= (p.Arg211=)
c.641G= (p.Arg214=)
c.647G= (p.Arg216=)
c.-26G= (n.-26G=)
Xg.47566713G>TCA412813378ARAFc.632G>T (p.Arg211Leu)
c.641G>T (p.Arg214Leu)
c.647G>T (p.Arg216Leu)
c.-26G>T (n.-26G>T)
 gnomAD v4
Xg.47566713_47566728delinsGCTCCACGTCCACTCCCA2427968727ARAFc.632_647delinsGCTCCACGTCCACTCC (p.Arg211=)
c.641_656delinsGCTCCACGTCCACTCC (p.Arg214=)
c.647_662delinsGCTCCACGTCCACTCC (p.Arg216=)
c.-26_-11delinsGCTCCACGTCCACTCC (n.-26_-11delinsGCTCCACGTCCACTCC)
Xg.47566714C>ACA515989156ARAFc.633C>A (p.Arg211=)
c.642C>A (p.Arg214=)
c.648C>A (p.Arg216=)
c.-25C>A (n.-25C>A)
Xg.47566714C>GCA515989158ARAFc.633C>G (p.Arg211=)
c.642C>G (p.Arg214=)
c.648C>G (p.Arg216=)
c.-25C>G (n.-25C>G)
Xg.47566714C>TCA515989161ARAFc.633C>T (p.Arg211=)
c.642C>T (p.Arg214=)
c.648C>T (p.Arg216=)
c.-25C>T (n.-25C>T)
 dbSNP gnomAD v4
Xg.47566715_47566729delCA875843492ARAFc.634_648del (p.Ser212_Pro216del)
c.643_657del (p.Ser215_Pro219del)
c.649_663del (p.Ser217_Pro221del)
c.-24_-10del (n.-24_-10del)
 dbSNP gnomAD v3 gnomAD v4
Xg.47566715T>ACA412813379ARAFc.634T>A (p.Ser212Thr)
c.643T>A (p.Ser215Thr)
c.649T>A (p.Ser217Thr)
c.-24T>A (n.-24T>A)
Xg.47566715T>CCA412813380ARAFc.634T>C (p.Ser212Pro)
c.643T>C (p.Ser215Pro)
c.649T>C (p.Ser217Pro)
c.-24T>C (n.-24T>C)
 gnomAD v4
Xg.47566715T>GCA412813381ARAFc.634T>G (p.Ser212Ala)
c.643T>G (p.Ser215Ala)
c.649T>G (p.Ser217Ala)
c.-24T>G (n.-24T>G)
Xg.47566716C>ACA412813382ARAFc.635C>A (p.Ser212Tyr)
c.644C>A (p.Ser215Tyr)
c.650C>A (p.Ser217Tyr)
c.-23C>A (n.-23C>A)
 gnomAD v4
Xg.47566716C>GCA412813383ARAFc.635C>G (p.Ser212Cys)
c.644C>G (p.Ser215Cys)
c.650C>G (p.Ser217Cys)
c.-23C>G (n.-23C>G)
Xg.47566716C>TCA412813384ARAFc.635C>T (p.Ser212Phe)
c.644C>T (p.Ser215Phe)
c.650C>T (p.Ser217Phe)
c.-23C>T (n.-23C>T)
Xg.47566717C>ACA515989163ARAFc.636C>A (p.Ser212=)
c.645C>A (p.Ser215=)
c.651C>A (p.Ser217=)
c.-22C>A (n.-22C>A)
Xg.47566717C>GCA515989165ARAFc.636C>G (p.Ser212=)
c.645C>G (p.Ser215=)
c.651C>G (p.Ser217=)
c.-22C>G (n.-22C>G)
Xg.47566717C>TCA515989166ARAFc.636C>T (p.Ser212=)
c.645C>T (p.Ser215=)
c.651C>T (p.Ser217=)
c.-22C>T (n.-22C>T)
Xg.47566718A>CCA412813385ARAFc.637A>C (p.Thr213Pro)
c.646A>C (p.Thr216Pro)
c.652A>C (p.Thr218Pro)
c.-21A>C (n.-21A>C)
 dbSNP gnomAD v4
Xg.47566718A>GCA412813387ARAFc.637A>G (p.Thr213Ala)
c.646A>G (p.Thr216Ala)
c.652A>G (p.Thr218Ala)
c.-21A>G (n.-21A>G)
Xg.47566718A>TCA412813386ARAFc.637A>T (p.Thr213Ser)
c.646A>T (p.Thr216Ser)
c.652A>T (p.Thr218Ser)
c.-21A>T (n.-21A>T)
Xg.47566719C>ACA412813388ARAFc.638C>A (p.Thr213Lys)
c.647C>A (p.Thr216Lys)
c.653C>A (p.Thr218Lys)
c.-20C>A (n.-20C>A)
Xg.47566719C=CA2427968728ARAFc.638C= (p.Thr213=)
c.647C= (p.Thr216=)
c.653C= (p.Thr218=)
c.-20C= (n.-20C=)
Xg.47566719C>GCA412813390ARAFc.638C>G (p.Thr213Arg)
c.647C>G (p.Thr216Arg)
c.653C>G (p.Thr218Arg)
c.-20C>G (n.-20C>G)
Xg.47566719C>TCA412813389ARAFc.638C>T (p.Thr213Met)
c.647C>T (p.Thr216Met)
c.653C>T (p.Thr218Met)
c.-20C>T (n.-20C>T)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
Xg.47566720G>ACA10398055ARAFc.639G>A (p.Thr213=)
c.648G>A (p.Thr216=)
c.654G>A (p.Thr218=)
c.-19G>A (n.-19G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566720G>CCA515989171ARAFc.639G>C (p.Thr213=)
c.648G>C (p.Thr216=)
c.654G>C (p.Thr218=)
c.-19G>C (n.-19G>C)
 dbSNP
Xg.47566720G=CA2427968729ARAFc.639G= (p.Thr213=)
c.648G= (p.Thr216=)
c.654G= (p.Thr218=)
c.-19G= (n.-19G=)
Xg.47566720G>TCA515989173ARAFc.639G>T (p.Thr213=)
c.648G>T (p.Thr216=)
c.654G>T (p.Thr218=)
c.-19G>T (n.-19G>T)
Xg.47566721T>ACA412813391ARAFc.640T>A (p.Ser214Thr)
c.649T>A (p.Ser217Thr)
c.655T>A (p.Ser219Thr)
c.-18T>A (n.-18T>A)
 dbSNP COSMIC
Xg.47566721T>CCA412813392ARAFc.640T>C (p.Ser214Pro)
c.649T>C (p.Ser217Pro)
c.655T>C (p.Ser219Pro)
c.-18T>C (n.-18T>C)
Xg.47566721T>GCA16602806ARAFc.640T>G (p.Ser214Ala)
c.649T>G (p.Ser217Ala)
c.655T>G (p.Ser219Ala)
c.-18T>G (n.-18T>G)
 ClinVar dbSNP COSMIC
Xg.47566721T=CA2427968730ARAFc.640T= (p.Ser214=)
c.649T= (p.Ser217=)
c.655T= (p.Ser219=)
c.-18T= (n.-18T=)
Xg.47566722C>ACA412813393ARAFc.641C>A (p.Ser214Tyr)
c.650C>A (p.Ser217Tyr)
c.656C>A (p.Ser219Tyr)
c.-17C>A (n.-17C>A)
 dbSNP COSMIC
Xg.47566722C=CA2427968731ARAFc.641C= (p.Ser214=)
c.650C= (p.Ser217=)
c.656C= (p.Ser219=)
c.-17C= (n.-17C=)
Xg.47566722C>GCA16602595ARAFc.641C>G (p.Ser214Cys)
c.650C>G (p.Ser217Cys)
c.656C>G (p.Ser219Cys)
c.-17C>G (n.-17C>G)
 ClinVar dbSNP COSMIC
Xg.47566722C>TCA16602805ARAFc.641C>T (p.Ser214Phe)
c.650C>T (p.Ser217Phe)
c.656C>T (p.Ser219Phe)
c.-17C>T (n.-17C>T)
 ClinVar dbSNP gnomAD v4 COSMIC
Xg.47566722_47566723delinsGTCA645603172ARAFc.641_642delinsGT (p.Ser214Cys)
c.650_651delinsGT (p.Ser217Cys)
c.656_657delinsGT (p.Ser219Cys)
c.-17_-16delinsGT (n.-17_-16delinsGT)
 COSMIC
Xg.47566723C>ACA10398056ARAFc.642C>A (p.Ser214=)
c.651C>A (p.Ser217=)
c.657C>A (p.Ser219=)
c.-16C>A (n.-16C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.47566723C=CA2427968732ARAFc.642C= (p.Ser214=)
c.651C= (p.Ser217=)
c.657C= (p.Ser219=)
c.-16C= (n.-16C=)
Xg.47566723C>GCA515989177ARAFc.642C>G (p.Ser214=)
c.651C>G (p.Ser217=)
c.657C>G (p.Ser219=)
c.-16C>G (n.-16C>G)
 gnomAD v4
Xg.47566723C>TCA515989176ARAFc.642C>T (p.Ser214=)
c.651C>T (p.Ser217=)
c.657C>T (p.Ser219=)
c.-16C>T (n.-16C>T)
 dbSNP
Xg.47566724A>CCA412813394ARAFc.643A>C (p.Thr215Pro)
c.652A>C (p.Thr218Pro)
c.658A>C (p.Thr220Pro)
c.-15A>C (n.-15A>C)
Xg.47566724A>GCA412813395ARAFc.643A>G (p.Thr215Ala)
c.652A>G (p.Thr218Ala)
c.658A>G (p.Thr220Ala)
c.-15A>G (n.-15A>G)
Xg.47566724A>TCA412813396ARAFc.643A>T (p.Thr215Ser)
c.652A>T (p.Thr218Ser)
c.658A>T (p.Thr220Ser)
c.-15A>T (n.-15A>T)
Xg.47566725C>ACA412813399ARAFc.644C>A (p.Thr215Asn)
c.653C>A (p.Thr218Asn)
c.659C>A (p.Thr220Asn)
c.-14C>A (n.-14C>A)
Xg.47566725C>GCA412813398ARAFc.644C>G (p.Thr215Ser)
c.653C>G (p.Thr218Ser)
c.659C>G (p.Thr220Ser)
c.-14C>G (n.-14C>G)
Xg.47566725C>TCA412813397ARAFc.644C>T (p.Thr215Ile)
c.653C>T (p.Thr218Ile)
c.659C>T (p.Thr220Ile)
c.-14C>T (n.-14C>T)
 dbSNP

Number of alleles fetched