Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.855884_855894delinsCCCAACCCTGACA2317361534ELANEc.598-74_598-64delinsCCCAACCCTGA (n.598-74_598-64delinsCCCAACCCTGA)
19g.855886_855895delCA2317361537ELANEc.598-72_598-63del (n.598-72_598-63del)
dbSNP gnomAD v4
19g.855888A=CA2317361541ELANEc.598-70A= (n.598-70A=)
19g.855888A>CCA2576540523ELANEc.598-70A>C (n.598-70A>C)
19g.855888A>GCA303945180ELANEc.598-70A>G (n.598-70A>G)
dbSNP gnomAD v3 gnomAD v4
19g.855889C=CA2317361542ELANEc.598-69C= (n.598-69C=)
19g.855889C>TCA631295808ELANEc.598-69C>T (n.598-69C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855890C>TCA2587805372ELANEc.598-68C>T (n.598-68C>T)
gnomAD v4
19g.855891C>ACA2587805373ELANEc.598-67C>A (n.598-67C>A)
gnomAD v4
19g.855891_855892insGTTAACA2582306276ELANEc.598-67_598-66insGTTAA (n.598-67_598-66insGTTAA)
dbSNP gnomAD v3 gnomAD v4
19g.855892T>GCA2317361544ELANEc.598-66T>G (n.598-66T>G)
dbSNP
19g.855892T=CA2317361543ELANEc.598-66T= (n.598-66T=)
19g.855893G>ACA2317361546ELANEc.598-65G>A (n.598-65G>A)
dbSNP gnomAD v4
19g.855893G=CA2317361547ELANEc.598-65G= (n.598-65G=)
19g.855893G>TCA2317361545ELANEc.598-65G>T (n.598-65G>T)
dbSNP gnomAD v4
19g.855894A=CA2317361548ELANEc.598-64A= (n.598-64A=)
19g.855894A>CCA2317361549ELANEc.598-64A>C (n.598-64A>C)
dbSNP gnomAD v4
19g.855894A>TCA2317361550ELANEc.598-64A>T (n.598-64A>T)
dbSNP
19g.855894_855899delCA2582306277ELANEc.598-64_598-59del (n.598-64_598-59del)
gnomAD v3 gnomAD v4
19g.855895C>ACA2317361552ELANEc.598-63C>A (n.598-63C>A)
dbSNP
19g.855895C=CA2317361551ELANEc.598-63C= (n.598-63C=)
19g.855895C>GCA2587805374ELANEc.598-63C>G (n.598-63C>G)
gnomAD v4
19g.855897G=CA2317361553ELANEc.598-61G= (n.598-61G=)
19g.855897G>TCA2317361554ELANEc.598-61G>T (n.598-61G>T)
dbSNP
19g.855898G>ACA884315594ELANEc.598-60G>A (n.598-60G>A)
dbSNP gnomAD v4
19g.855898G=CA2317361555ELANEc.598-60G= (n.598-60G=)
19g.855898G>TCA2587805375ELANEc.598-60G>T (n.598-60G>T)
gnomAD v4
19g.855899C>ACA992487399ELANEc.598-59C>A (n.598-59C>A)
dbSNP gnomAD v3 gnomAD v4
19g.855899C=CA2317361556ELANEc.598-59C= (n.598-59C=)
19g.855899C>GCA2317361557ELANEc.598-59C>G (n.598-59C>G)
dbSNP
19g.855899C>TCA2502360425ELANEc.598-59C>T (n.598-59C>T)
gnomAD v4
19g.855900G>ACA303945182ELANEc.598-58G>A (n.598-58G>A)
dbSNP gnomAD v4
19g.855900G>CCA2576540524ELANEc.598-58G>C (n.598-58G>C)
gnomAD v4
19g.855900G=CA2317361558ELANEc.598-58G= (n.598-58G=)
19g.855900G>TCA2587805376ELANEc.598-58G>T (n.598-58G>T)
gnomAD v4
19g.855900_855901insACA2582306278ELANEc.598-58_598-57insA (n.598-58_598-57insA)
gnomAD v3 gnomAD v4
19g.855902C>ACA2587805377ELANEc.598-56C>A (n.598-56C>A)
gnomAD v4
19g.855902C=CA2317361559ELANEc.598-56C= (n.598-56C=)
19g.855902C>TCA657480008ELANEc.598-56C>T (n.598-56C>T)
dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.855903G>ACA303945184ELANEc.598-55G>A (n.598-55G>A)
dbSNP gnomAD v3 gnomAD v4
19g.855903G=CA2317361560ELANEc.598-55G= (n.598-55G=)
19g.855903G>TCA2587805378ELANEc.598-55G>T (n.598-55G>T)
gnomAD v4
19g.855904G>ACA2317361562ELANEc.598-54G>A (n.598-54G>A)
dbSNP
19g.855904G=CA2317361561ELANEc.598-54G= (n.598-54G=)
19g.855905G>ACA2587805379ELANEc.598-53G>A (n.598-53G>A)
gnomAD v4
19g.855906C>TCA657480009ELANEc.598-52C>T (n.598-52C>T)
COSMIC
19g.855907A>GCA2587805380ELANEc.598-51A>G (n.598-51A>G)
gnomAD v4
19g.855908G>ACA2587805381ELANEc.598-50G>A (n.598-50G>A)
gnomAD v4
19g.855909G>ACA631295809ELANEc.598-49G>A (n.598-49G>A)
dbSNP gnomAD v2 gnomAD v4
19g.855909G=CA2317361563ELANEc.598-49G= (n.598-49G=)
19g.855909G>TCA303945188ELANEc.598-49G>T (n.598-49G>T)
dbSNP gnomAD v2 gnomAD v4
19g.855911G>CCA2587805382ELANEc.598-47G>C (n.598-47G>C)
gnomAD v4
19g.855912G>ACA2587805383ELANEc.598-46G>A (n.598-46G>A)
gnomAD v4
19g.855912G>TCA2587805384ELANEc.598-46G>T (n.598-46G>T)
gnomAD v4
19g.855913G>ACA2317361565ELANEc.598-45G>A (n.598-45G>A)
dbSNP gnomAD v4
19g.855913G=CA2317361564ELANEc.598-45G= (n.598-45G=)
19g.855914C=CA2317361566ELANEc.598-44C= (n.598-44C=)
19g.855914C>GCA303945191ELANEc.598-44C>G (n.598-44C>G)
dbSNP gnomAD v4
19g.855914C>TCA2587805385ELANEc.598-44C>T (n.598-44C>T)
gnomAD v4
19g.855915A=CA2317361567ELANEc.598-43A= (n.598-43A=)
19g.855915A>CCA2317361568ELANEc.598-43A>C (n.598-43A>C)
dbSNP gnomAD v3 gnomAD v4
19g.855917G>ACA884315598ELANEc.598-41G>A (n.598-41G>A)
dbSNP gnomAD v3 gnomAD v4
19g.855917G=CA2317361569ELANEc.598-41G= (n.598-41G=)
19g.855918G>CCA2587805386ELANEc.598-40G>C (n.598-40G>C)
gnomAD v4
19g.855919C=CA2317361570ELANEc.598-39C= (n.598-39C=)
19g.855919C>TCA631295810ELANEc.598-39C>T (n.598-39C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855920C=CA2317361571ELANEc.598-38C= (n.598-38C=)
19g.855920C>GCA2317361572ELANEc.598-38C>G (n.598-38C>G)
dbSNP
19g.855920C>TCA2587805387ELANEc.598-38C>T (n.598-38C>T)
gnomAD v4
19g.855921T>ACA2317361574ELANEc.598-37T>A (n.598-37T>A)
dbSNP
19g.855921T=CA2317361573ELANEc.598-37T= (n.598-37T=)
19g.855922C=CA2317361575ELANEc.598-36C= (n.598-36C=)
19g.855922C>GCA9026112ELANEc.598-36C>G (n.598-36C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855922C>TCA631295811ELANEc.598-36C>T (n.598-36C>T)
dbSNP gnomAD v2 gnomAD v4
19g.855923G>ACA9026113ELANEc.598-35G>A (n.598-35G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855923G>CCA2317361577ELANEc.598-35G>C (n.598-35G>C)
dbSNP gnomAD v4
19g.855923G=CA2317361576ELANEc.598-35G= (n.598-35G=)
19g.855923G>TCA2587805388ELANEc.598-35G>T (n.598-35G>T)
gnomAD v4
19g.855924C>ACA9026114ELANEc.598-34C>A (n.598-34C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855924C=CA2317361578ELANEc.598-34C= (n.598-34C=)
19g.855926G>ACA631295813ELANEc.598-32G>A (n.598-32G>A)
dbSNP gnomAD v2
19g.855926G=CA2317361579ELANEc.598-32G= (n.598-32G=)
19g.855927T>CCA9026115ELANEc.598-31T>C (n.598-31T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855927T>GCA992487412ELANEc.598-31T>G (n.598-31T>G)
dbSNP gnomAD v3 gnomAD v4
19g.855927T=CA2317361580ELANEc.598-31T= (n.598-31T=)
19g.855928C>ACA2813227143ELANEc.598-30C>A (n.598-30C>A)
19g.855928C>GCA2587805389ELANEc.598-30C>G (n.598-30C>G)
gnomAD v4
19g.855928C>TCA2587805390ELANEc.598-30C>T (n.598-30C>T)
gnomAD v4
19g.855929C>TCA2587805391ELANEc.598-29C>T (n.598-29C>T)
gnomAD v4
19g.855930A>GCA2561095019ELANEc.598-28A>G (n.598-28A>G)
gnomAD v4
19g.855931G>ACA2587805392ELANEc.598-27G>A (n.598-27G>A)
gnomAD v4
19g.855931G>CCA2576540525ELANEc.598-27G>C (n.598-27G>C)
19g.855932_855933delinsCTCA2317361581ELANEc.598-26_598-25delinsCT (n.598-26_598-25delinsCT)
19g.855933T>GCA2587805393ELANEc.598-25T>G (n.598-25T>G)
gnomAD v4
19g.855934delCA2317361582ELANEc.598-24del (n.598-24del)
dbSNP
19g.855934_855935delinsTCCA2317361583ELANEc.598-24_598-23delinsTC (n.598-24_598-23delinsTC)
19g.855935C>ACA2576540526ELANEc.598-23C>A (n.598-23C>A)
19g.855935C=CA2317361584ELANEc.598-23C= (n.598-23C=)
19g.855935C>GCA2587805394ELANEc.598-23C>G (n.598-23C>G)
gnomAD v4
19g.855935C>TCA9026116ELANEc.598-23C>T (n.598-23C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855938delCA884315621ELANEc.598-20del (n.598-20del)
dbSNP
19g.855936C>ACA9026117ELANEc.598-22C>A (n.598-22C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855936C=CA2317361585ELANEc.598-22C= (n.598-22C=)
19g.855937C>ACA2576540527ELANEc.598-21C>A (n.598-21C>A)
19g.855937C>GCA2587805395ELANEc.598-21C>G (n.598-21C>G)
gnomAD v4
19g.855937C>TCA2587805396ELANEc.598-21C>T (n.598-21C>T)
gnomAD v4
19g.855939A=CA2317361586ELANEc.598-19A= (n.598-19A=)
19g.855939A>GCA303945207ELANEc.598-19A>G (n.598-19A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855939_855940delinsACCA2317361587ELANEc.598-19_598-18delinsAC (n.598-19_598-18delinsAC)
19g.855940C>ACA2587805397ELANEc.598-18C>A (n.598-18C>A)
gnomAD v4
19g.855941delCA2317361588ELANEc.598-17del (n.598-17del)
ClinVar dbSNP gnomAD v4
19g.855941C>ACA2587805398ELANEc.598-17C>A (n.598-17C>A)
gnomAD v4
19g.855941C>TCA2576540528ELANEc.598-17C>T (n.598-17C>T)
gnomAD v4
19g.855943T>GCA631295814ELANEc.598-15T>G (n.598-15T>G)
dbSNP gnomAD v2 gnomAD v4
19g.855943T=CA2317361589ELANEc.598-15T= (n.598-15T=)
19g.855944G>CCA2587805399ELANEc.598-14G>C (n.598-14G>C)
gnomAD v4
19g.855944G>TCA2587805400ELANEc.598-14G>T (n.598-14G>T)
gnomAD v4
19g.855945T>CCA631295815ELANEc.598-13T>C (n.598-13T>C)
dbSNP gnomAD v2 gnomAD v4
19g.855945T=CA2317361590ELANEc.598-13T= (n.598-13T=)
19g.855948G>ACA303945209ELANEc.598-10G>A (n.598-10G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855948G=CA2317361591ELANEc.598-10G= (n.598-10G=)
19g.855948G>TCA2587805401ELANEc.598-10G>T (n.598-10G>T)
gnomAD v4
19g.855950dupCA2587805402ELANEc.598-8dup (n.598-8dup)
gnomAD v4
19g.855950C=CA2317361592ELANEc.598-8C= (n.598-8C=)
19g.855950C>TCA9026118ELANEc.598-8C>T (n.598-8C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855952C>TCA2576540529ELANEc.598-6C>T (n.598-6C>T)
19g.855953C=CA2317361593ELANEc.598-5C= (n.598-5C=)
19g.855953C>TCA631295816ELANEc.598-5C>T (n.598-5C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855954A=CA2317361594ELANEc.598-4A= (n.598-4A=)
19g.855954A>GCA915951613ELANEc.598-4A>G (n.598-4A>G)
ClinVar dbSNP
19g.855955C=CA2317361595ELANEc.598-3C= (n.598-3C=)
19g.855955C>GCA346328ELANEc.598-3C>G (n.598-3C>G)
ClinVar dbSNP
19g.855956A=CA2317361596ELANEc.598-2A= (n.598-2A=)
19g.855956A>CCA16040333ELANEc.598-2A>C (n.598-2A>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855956A>GCA402918839ELANEc.598-2A>G (n.598-2A>G)
gnomAD v4
19g.855956A>TCA402918841ELANEc.598-2A>T (n.598-2A>T)
19g.855956_855957delCA2695227810ELANEc.598-2_598-1del (n.598-2_598-1del)
19g.855957G>ACA10577118ELANEc.598-1G>A (n.598-1G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855957G>CCA402918844ELANEc.598-1G>C (n.598-1G>C)
19g.855957G=CA2317361597ELANEc.598-1G= (n.598-1G=)
19g.855957G>TCA402918845ELANEc.598-1G>T (n.598-1G>T)
19g.855960_855961dupCA16043100ELANEc.600_601dup
ClinVar dbSNP
19g.855961delCA2695227811ELANEc.601del
19g.855958G>ACA402918847ELANEc.598G>A (p.Gly200Arg)
19g.855958G>CCA402918848ELANEc.598G>C (p.Gly200Arg)
19g.855958G=CA2317361598ELANEc.598G= (p.Gly200=)
19g.855958G>TCA9026119ELANEc.598G>T (p.Gly200Trp)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855959G>ACA402918850ELANEc.599G>A (p.Gly200Glu)
gnomAD v4
19g.855959G>CCA402918853ELANEc.599G>C (p.Gly200Ala)
19g.855959G>TCA402918851ELANEc.599G>T (p.Gly200Val)
19g.855961_855968dupCA2695227812ELANEc.601_608dup (p.Ser204ThrfsTer11)
19g.855960G>ACA9026120ELANEc.600G>A (p.Gly200=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855960G>CCA504686289ELANEc.600G>C (p.Gly200=)
19g.855960G=CA2317361599ELANEc.600G= (p.Gly200=)
19g.855960G>TCA504686291ELANEc.600G>T (p.Gly200=)
19g.855960_855961delinsAACA645613904ELANEc.600_601delinsAA (p.Asp201Asn)
COSMIC
19g.855962_855968delCA2695227813ELANEc.602_608del (p.Asp201AlafsTer9)
19g.855961G>ACA402918855ELANEc.601G>A (p.Asp201Asn)
gnomAD v4
19g.855961G>CCA402918857ELANEc.601G>C (p.Asp201His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855961G=CA2317361600ELANEc.601G= (p.Asp201=)
19g.855961G>TCA402918858ELANEc.601G>T (p.Asp201Tyr)
dbSNP gnomAD v4
19g.855961_855962delinsGACA2317361601ELANEc.601_602delinsGA (p.Asp201=)
19g.855962delCA1139770400ELANEc.602del (p.Asp201AlafsTer11)
ClinVar dbSNP
19g.855962A>CCA402918859ELANEc.602A>C (p.Asp201Ala)
gnomAD v4
19g.855962A>GCA402918861ELANEc.602A>G (p.Asp201Gly)
19g.855962A>TCA402918862ELANEc.602A>T (p.Asp201Val)
gnomAD v4
19g.855963C>ACA402918864ELANEc.603C>A (p.Asp201Glu)
19g.855963C>GCA402918865ELANEc.603C>G (p.Asp201Glu)
19g.855963C>TCA504686306ELANEc.603C>T (p.Asp201=)
19g.855964T>ACA402918869ELANEc.604T>A (p.Ser202Thr)
19g.855964T>CCA402918871ELANEc.604T>C (p.Ser202Pro)
19g.855964T>GCA402918867ELANEc.604T>G (p.Ser202Ala)
19g.855965C>ACA402918872ELANEc.605C>A (p.Ser202Tyr)
19g.855965C=CA2317361602ELANEc.605C= (p.Ser202=)
19g.855965C>GCA402918873ELANEc.605C>G (p.Ser202Cys)
19g.855965C>TCA10583965ELANEc.605C>T (p.Ser202Phe)
ClinVar dbSNP gnomAD v4
19g.855966C>ACA290722ELANEc.606C>A (p.Ser202=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855966C=CA2317361603ELANEc.606C= (p.Ser202=)
19g.855966C>GCA504686320ELANEc.606C>G (p.Ser202=)
dbSNP gnomAD v2 gnomAD v4
19g.855966C>TCA290725ELANEc.606C>T (p.Ser202=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855967G>ACA303945234ELANEc.607G>A (p.Gly203Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855967G>CCA402918877ELANEc.607G>C (p.Gly203Arg)
ClinVar dbSNP
19g.855967G=CA2317361604ELANEc.607G= (p.Gly203=)
19g.855967G>TCA402918878ELANEc.607G>T (p.Gly203Cys)
ClinVar dbSNP
19g.855968G>ACA402918879ELANEc.608G>A (p.Gly203Asp)
19g.855968G>CCA402918881ELANEc.608G>C (p.Gly203Ala)
19g.855968G>TCA402918883ELANEc.608G>T (p.Gly203Val)
19g.855969C>ACA504686342ELANEc.609C>A (p.Gly203=)
19g.855969C>GCA504686340ELANEc.609C>G (p.Gly203=)
19g.855969C>TCA504686337ELANEc.609C>T (p.Gly203=)
19g.855970A>CCA402918885ELANEc.610A>C (p.Ser204Arg)
19g.855970A>GCA402918887ELANEc.610A>G (p.Ser204Gly)
gnomAD v4
19g.855970A>TCA402918884ELANEc.610A>T (p.Ser204Cys)
19g.855971G>ACA402918889ELANEc.611G>A (p.Ser204Asn)
COSMIC
19g.855971G>CCA402918890ELANEc.611G>C (p.Ser204Thr)
19g.855971G>TCA402918892ELANEc.611G>T (p.Ser204Ile)
19g.855972C>ACA402918894ELANEc.612C>A (p.Ser204Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855972C=CA2317361605ELANEc.612C= (p.Ser204=)
19g.855972C>GCA402918896ELANEc.612C>G (p.Ser204Arg)
19g.855972C>TCA9026121ELANEc.612C>T (p.Ser204=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855975delCA2695227814ELANEc.615del (p.Leu206TrpfsTer6)
19g.855973C>ACA402918897ELANEc.613C>A (p.Pro205Thr)
19g.855973C=CA2317361606ELANEc.613C= (p.Pro205=)
19g.855973C>GCA402918901ELANEc.613C>G (p.Pro205Ala)
dbSNP gnomAD v2 gnomAD v4
19g.855973C>TCA402918898ELANEc.613C>T (p.Pro205Ser)
19g.855974C>ACA402918903ELANEc.614C>A (p.Pro205His)
19g.855974C=CA2317361607ELANEc.614C= (p.Pro205=)
19g.855974C>GCA402918904ELANEc.614C>G (p.Pro205Arg)
ClinVar dbSNP
19g.855974C>TCA402918906ELANEc.614C>T (p.Pro205Leu)
19g.855975C>ACA504686369ELANEc.615C>A (p.Pro205=)
19g.855975C>GCA504686371ELANEc.615C>G (p.Pro205=)
19g.855975C>TCA504686372ELANEc.615C>T (p.Pro205=)
gnomAD v4
19g.855975_855978delCA2695227815ELANEc.615_618del (p.Leu206SerfsTer5)
19g.855976T>ACA402918908ELANEc.616T>A (p.Leu206Met)
19g.855976T>CCA504686378ELANEc.616T>C (p.Leu206=)
gnomAD v4
19g.855976T>GCA402918910ELANEc.616T>G (p.Leu206Val)
19g.855977T>ACA402918914ELANEc.617T>A (p.Leu206Ter)
19g.855977T>CCA402918915ELANEc.617T>C (p.Leu206Ser)
19g.855977T>GCA402918912ELANEc.617T>G (p.Leu206Trp)
19g.855978G>ACA504686387ELANEc.618G>A (p.Leu206=)
ClinVar
19g.855978G>CCA402918918ELANEc.618G>C (p.Leu206Phe)
ClinVar dbSNP
19g.855978G=CA2317361608ELANEc.618G= (p.Leu206=)
19g.855978G>TCA281046ELANEc.618G>T (p.Leu206Phe)
ClinVar dbSNP
19g.855979G>ACA402918920ELANEc.619G>A (p.Val207Ile)
gnomAD v4 COSMIC
19g.855979G>CCA402918921ELANEc.619G>C (p.Val207Leu)
ClinVar dbSNP gnomAD v4
19g.855979G=CA2317361609ELANEc.619G= (p.Val207=)
19g.855979G>TCA402918924ELANEc.619G>T (p.Val207Phe)
ClinVar dbSNP
19g.855980T>ACA402918926ELANEc.620T>A (p.Val207Asp)
19g.855980T>CCA402918927ELANEc.620T>C (p.Val207Ala)
dbSNP
19g.855980T>GCA402918929ELANEc.620T>G (p.Val207Gly)
19g.855981C>ACA504686406ELANEc.621C>A (p.Val207=)
19g.855981C=CA2317361610ELANEc.621C= (p.Val207=)
19g.855981C>GCA504686408ELANEc.621C>G (p.Val207=)
dbSNP gnomAD v3 gnomAD v4
19g.855981C>TCA504686410ELANEc.621C>T (p.Val207=)
gnomAD v4
19g.855982T>ACA402918931ELANEc.622T>A (p.Cys208Ser)
19g.855982T>CCA402918932ELANEc.622T>C (p.Cys208Arg)
19g.855982T>GCA402918933ELANEc.622T>G (p.Cys208Gly)
ClinVar dbSNP
19g.855983G>ACA402918935ELANEc.623G>A (p.Cys208Tyr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855983G>CCA402918937ELANEc.623G>C (p.Cys208Ser)
19g.855983G=CA2317361611ELANEc.623G= (p.Cys208=)
19g.855983G>TCA402918939ELANEc.623G>T (p.Cys208Phe)
ClinVar dbSNP
19g.855984C>ACA402918940ELANEc.624C>A (p.Cys208Ter)
19g.855984C=CA2317361612ELANEc.624C= (p.Cys208=)
19g.855984C>GCA402918941ELANEc.624C>G (p.Cys208Trp)
19g.855984C>TCA504686421ELANEc.624C>T (p.Cys208=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855985A>CCA402918942ELANEc.625A>C (p.Asn209His)
19g.855985A>GCA402918943ELANEc.625A>G (p.Asn209Asp)
19g.855985A>TCA402918945ELANEc.625A>T (p.Asn209Tyr)
19g.855986A>CCA402918947ELANEc.626A>C (p.Asn209Thr)
19g.855986A>GCA402918948ELANEc.626A>G (p.Asn209Ser)
19g.855986A>TCA402918949ELANEc.626A>T (p.Asn209Ile)
COSMIC
19g.855987C>ACA402918950ELANEc.627C>A (p.Asn209Lys)
dbSNP
19g.855987C=CA2317361613ELANEc.627C= (p.Asn209=)
19g.855987C>GCA303945245ELANEc.627C>G (p.Asn209Lys)
dbSNP
19g.855987C>TCA9026122ELANEc.627C>T (p.Asn209=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855988G>ACA9026123ELANEc.628G>A (p.Gly210Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855988G>CCA402918954ELANEc.628G>C (p.Gly210Arg)
gnomAD v4
19g.855988G=CA2317361614ELANEc.628G= (p.Gly210=)
19g.855988G>TCA402918955ELANEc.628G>T (p.Gly210Trp)

Number of alleles fetched