Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583791C>ACA399477176KRT14c.896G>T (p.Arg299Leu)
n.346G>T
dbSNP gnomAD v3 gnomAD v4
17g.41583791C=CA2260085570KRT14c.896G= (p.Arg299=)
n.346G=
17g.41583791C>GCA399477179KRT14c.896G>C (p.Arg299Pro)
n.346G>C
17g.41583791C>TCA8562583KRT14c.896G>A (p.Arg299His)
n.346G>A
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583792G>ACA399477184KRT14c.895C>T (p.Arg299Cys)
n.345C>T
dbSNP gnomAD v4
17g.41583792G>CCA399477186KRT14c.895C>G (p.Arg299Gly)
n.345C>G
17g.41583792G=CA2260085571KRT14c.895C= (p.Arg299=)
n.345C=
17g.41583792G>TCA399477189KRT14c.895C>A (p.Arg299Ser)
n.345C>A
17g.41583793G>ACA500205468KRT14c.894C>T (p.Asn298=)
n.344C>T
gnomAD v4
17g.41583793G>CCA399477191KRT14c.894C>G (p.Asn298Lys)
n.344C>G
17g.41583793G>TCA399477192KRT14c.894C>A (p.Asn298Lys)
n.344C>A
17g.41583794T>ACA399477196KRT14c.893A>T (p.Asn298Ile)
n.343A>T
17g.41583794T>CCA399477198KRT14c.893A>G (p.Asn298Ser)
n.343A>G
17g.41583794T>GCA399477200KRT14c.893A>C (p.Asn298Thr)
n.343A>C
17g.41583795T>ACA399477209KRT14c.892A>T (p.Asn298Tyr)
n.342A>T
17g.41583795T>CCA399477207KRT14c.892A>G (p.Asn298Asp)
n.342A>G
17g.41583795T>GCA399477204KRT14c.892A>C (p.Asn298His)
n.342A>C
17g.41583796C>ACA399477212KRT14c.891G>T (p.Lys297Asn)
n.341G>T
17g.41583796C>GCA399477215KRT14c.891G>C (p.Lys297Asn)
n.341G>C
17g.41583796C>TCA500205470KRT14c.891G>A (p.Lys297=)
n.341G>A
17g.41583797T>ACA399477216KRT14c.890A>T (p.Lys297Met)
n.340A>T
17g.41583797T>CCA399477217KRT14c.890A>G (p.Lys297Arg)
n.340A>G
gnomAD v4
17g.41583797T>GCA399477218KRT14c.890A>C (p.Lys297Thr)
n.340A>C
17g.41583798T>ACA399477221KRT14c.889A>T (p.Lys297Ter)
n.339A>T
17g.41583798T>CCA399477223KRT14c.889A>G (p.Lys297Glu)
n.339A>G
17g.41583798T>GCA399477225KRT14c.889A>C (p.Lys297Gln)
n.339A>C
17g.41583799C>ACA399477228KRT14c.888G>T (p.Glu296Asp)
n.338G>T
COSMIC
17g.41583799C=CA2260085572KRT14c.888G= (p.Glu296=)
n.338G=
17g.41583799C>GCA399477230KRT14c.888G>C (p.Glu296Asp)
n.338G>C
17g.41583799C>TCA500205473KRT14c.888G>A (p.Glu296=)
n.338G>A
dbSNP
17g.41583800T>ACA399477233KRT14c.887A>T (p.Glu296Val)
n.337A>T
17g.41583800T>CCA399477235KRT14c.887A>G (p.Glu296Gly)
n.337A>G
17g.41583800T>GCA399477237KRT14c.887A>C (p.Glu296Ala)
n.337A>C
17g.41583801C>ACA399477241KRT14c.886G>T (p.Glu296Ter)
n.336G>T
17g.41583801C>GCA399477244KRT14c.886G>C (p.Glu296Gln)
n.336G>C
17g.41583801C>TCA399477240KRT14c.886G>A (p.Glu296Lys)
n.336G>A
gnomAD v4
17g.41583802T>ACA500205475KRT14c.885A>T (p.Ala295=)
n.335A>T
17g.41583802T>CCA500205476KRT14c.885A>G (p.Ala295=)
n.335A>G
17g.41583802T>GCA500205479KRT14c.885A>C (p.Ala295=)
n.335A>C
17g.41583803G>ACA399477250KRT14c.884C>T (p.Ala295Val)
n.334C>T
17g.41583803G>CCA399477248KRT14c.884C>G (p.Ala295Gly)
n.334C>G
17g.41583803G=CA2260085573KRT14c.884C= (p.Ala295=)
n.334C=
17g.41583803G>TCA399477252KRT14c.884C>A (p.Ala295Glu)
n.334C>A
dbSNP
17g.41583804C>ACA399477255KRT14c.883G>T (p.Ala295Ser)
n.333G>T
17g.41583804C>GCA399477257KRT14c.883G>C (p.Ala295Pro)
n.333G>C
17g.41583804C>TCA399477259KRT14c.883G>A (p.Ala295Thr)
n.333G>A
17g.41583805C>ACA399477263KRT14c.882G>T (p.Met294Ile)
n.332G>T
17g.41583805C>GCA399477265KRT14c.882G>C (p.Met294Ile)
n.332G>C
17g.41583805C>TCA399477267KRT14c.882G>A (p.Met294Ile)
n.332G>A
17g.41583806A=CA2260085574KRT14c.881T= (p.Met294=)
n.331T=
17g.41583806A>CCA399477275KRT14c.881T>G (p.Met294Arg)
n.331T>G
17g.41583806A>GCA8562584KRT14c.881T>C (p.Met294Thr)
n.331T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583806A>TCA399477273KRT14c.881T>A (p.Met294Lys)
n.331T>A
gnomAD v4
17g.41583807T>ACA399477278KRT14c.880A>T (p.Met294Leu)
n.330A>T
17g.41583807T>CCA399477280KRT14c.880A>G (p.Met294Val)
n.330A>G
dbSNP gnomAD v3 gnomAD v4
17g.41583807T>GCA399477282KRT14c.880A>C (p.Met294Leu)
n.330A>C
17g.41583807T=CA2260085575KRT14c.880A= (p.Met294=)
n.330A=
17g.41583808C>ACA399477284KRT14c.879G>T (p.Lys293Asn)
n.329G>T
17g.41583808C>GCA399477286KRT14c.879G>C (p.Lys293Asn)
n.329G>C
17g.41583808C>TCA500205492KRT14c.879G>A (p.Lys293=)
n.329G>A
17g.41583809T>ACA399477289KRT14c.878A>T (p.Lys293Met)
n.328A>T
17g.41583809T>CCA399477293KRT14c.878A>G (p.Lys293Arg)
n.328A>G
dbSNP gnomAD v2 gnomAD v4
17g.41583809T>GCA399477291KRT14c.878A>C (p.Lys293Thr)
n.328A>C
17g.41583809T=CA2260085576KRT14c.878A= (p.Lys293=)
n.328A=
17g.41583810T>ACA399477296KRT14c.877A>T (p.Lys293Ter)
n.327A>T
17g.41583810T>CCA399477297KRT14c.877A>G (p.Lys293Glu)
n.327A>G
gnomAD v4
17g.41583810T>GCA399477298KRT14c.877A>C (p.Lys293Gln)
n.327A>C
17g.41583811C>ACA399477301KRT14c.876G>T (p.Glu292Asp)
n.326G>T
17g.41583811C>GCA399477303KRT14c.876G>C (p.Glu292Asp)
n.326G>C
17g.41583811C>TCA500205498KRT14c.876G>A (p.Glu292=)
n.326G>A
gnomAD v4
17g.41583812T>ACA399477305KRT14c.875A>T (p.Glu292Val)
n.325A>T
17g.41583812T>CCA399477306KRT14c.875A>G (p.Glu292Gly)
n.325A>G
17g.41583812T>GCA399477308KRT14c.875A>C (p.Glu292Ala)
n.325A>C
17g.41583813C>ACA399477311KRT14c.874G>T (p.Glu292Ter)
n.324G>T
17g.41583813C=CA2260085577KRT14c.874G= (p.Glu292=)
n.324G=
17g.41583813C>GCA399477313KRT14c.874G>C (p.Glu292Gln)
n.324G>C
17g.41583813C>TCA8562585KRT14c.874G>A (p.Glu292Lys)
n.324G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583814A>CCA399477317KRT14c.873T>G (p.Tyr291Ter)
n.323T>G
17g.41583814A>GCA500205503KRT14c.873T>C (p.Tyr291=)
n.323T>C
gnomAD v4
17g.41583814A>TCA399477320KRT14c.873T>A (p.Tyr291Ter)
n.323T>A
17g.41583815T>ACA399477323KRT14c.872A>T (p.Tyr291Phe)
n.322A>T
17g.41583815T>CCA8562586KRT14c.872A>G (p.Tyr291Cys)
n.322A>G
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583815T>GCA399477327KRT14c.872A>C (p.Tyr291Ser)
n.322A>C
gnomAD v4
17g.41583815T=CA2260085578KRT14c.872A= (p.Tyr291=)
n.322A=
17g.41583816A>CCA399477330KRT14c.871T>G (p.Tyr291Asp)
n.321T>G
17g.41583816A>GCA399477332KRT14c.871T>C (p.Tyr291His)
n.321T>C
gnomAD v4
17g.41583816A>TCA399477334KRT14c.871T>A (p.Tyr291Asn)
n.321T>A
17g.41583817C>ACA399477336KRT14c.870G>T (p.Gln290His)
n.320G>T
17g.41583817C=CA2260085579KRT14c.870G= (p.Gln290=)
n.320G=
17g.41583817C>GCA399477337KRT14c.870G>C (p.Gln290His)
n.320G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583817C>TCA500205513KRT14c.870G>A (p.Gln290=)
n.320G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583818T>ACA8562587KRT14c.869A>T (p.Gln290Leu)
n.319A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583818T>CCA399477341KRT14c.869A>G (p.Gln290Arg)
n.319A>G
17g.41583818T>GCA399477343KRT14c.869A>C (p.Gln290Pro)
n.319A>C
17g.41583818T=CA2260085580KRT14c.869A= (p.Gln290=)
n.319A=
17g.41583819G>ACA399477347KRT14c.868C>T (p.Gln290Ter)
n.318C>T
17g.41583819G>CCA399477350KRT14c.868C>G (p.Gln290Glu)
n.318C>G
17g.41583819G>TCA399477352KRT14c.868C>A (p.Gln290Lys)
n.318C>A
17g.41583820G>ACA500205518KRT14c.867C>T (p.Asp289=)
n.317C>T
dbSNP
17g.41583820G>CCA399477355KRT14c.867C>G (p.Asp289Glu)
n.317C>G
17g.41583820G=CA2260085581KRT14c.867C= (p.Asp289=)
n.317C=
17g.41583820G>TCA399477357KRT14c.867C>A (p.Asp289Glu)
n.317C>A
17g.41583821T>ACA399477360KRT14c.866A>T (p.Asp289Val)
n.316A>T
17g.41583821T>CCA399477362KRT14c.866A>G (p.Asp289Gly)
n.316A>G
gnomAD v4
17g.41583821T>GCA399477364KRT14c.866A>C (p.Asp289Ala)
n.316A>C
17g.41583822C>ACA399477368KRT14c.865G>T (p.Asp289Tyr)
n.315G>T
17g.41583822C>GCA399477370KRT14c.865G>C (p.Asp289His)
n.315G>C
17g.41583822C>TCA399477372KRT14c.865G>A (p.Asp289Asn)
n.315G>A
17g.41583823A>CCA500205525KRT14c.864T>G (p.Arg288=)
n.314T>G
17g.41583823A>GCA500205526KRT14c.864T>C (p.Arg288=)
n.314T>C
17g.41583823A>TCA500205528KRT14c.864T>A (p.Arg288=)
n.314T>A
17g.41583824C>ACA399477373KRT14c.863G>T (p.Arg288Leu)
n.313G>T
ClinVar
17g.41583824C=CA2260085582KRT14c.863G= (p.Arg288=)
n.313G=
17g.41583824C>GCA399477376KRT14c.863G>C (p.Arg288Pro)
n.313G>C
17g.41583824C>TCA8562588KRT14c.863G>A (p.Arg288His)
n.313G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41583825G>ACA8562589KRT14c.862C>T (p.Arg288Cys)
n.312C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41583825G>CCA399477383KRT14c.862C>G (p.Arg288Gly)
n.312C>G
dbSNP gnomAD v4
17g.41583825G=CA2260085583KRT14c.862C= (p.Arg288=)
n.312C=
17g.41583825G>TCA399477385KRT14c.862C>A (p.Arg288Ser)
n.312C>A
gnomAD v4
17g.41583826C>ACA399477394KRT14c.861G>T (p.Met287Ile)
n.311G>T
17g.41583826C>GCA399477391KRT14c.861G>C (p.Met287Ile)
n.311G>C
gnomAD v4
17g.41583826C>TCA399477390KRT14c.861G>A (p.Met287Ile)
n.311G>A
gnomAD v4
17g.41583827A>CCA399477399KRT14c.860T>G (p.Met287Arg)
n.310T>G
17g.41583827A>GCA399477397KRT14c.860T>C (p.Met287Thr)
n.310T>C
17g.41583827A>TCA399477402KRT14c.860T>A (p.Met287Lys)
n.310T>A
17g.41583828T>ACA399477406KRT14c.859A>T (p.Met287Leu)
n.309A>T
17g.41583828T>CCA399477408KRT14c.859A>G (p.Met287Val)
n.309A>G
dbSNP gnomAD v2 gnomAD v4
17g.41583828T>GCA399477410KRT14c.859A>C (p.Met287Leu)
n.309A>C
17g.41583828T=CA2260085584KRT14c.859A= (p.Met287=)
n.309A=
17g.41583829C>ACA399477414KRT14c.858G>T (p.Glu286Asp)
n.308G>T
17g.41583829C>GCA399477415KRT14c.858G>C (p.Glu286Asp)
n.308G>C
17g.41583829C>TCA500205547KRT14c.858G>A (p.Glu286=)
n.308G>A
17g.41583830T>ACA399477418KRT14c.857A>T (p.Glu286Val)
n.307A>T
17g.41583830T>CCA399477420KRT14c.857A>G (p.Glu286Gly)
n.307A>G
dbSNP
17g.41583830T>GCA399477422KRT14c.857A>C (p.Glu286Ala)
n.307A>C
17g.41583831C>ACA399477425KRT14c.856G>T (p.Glu286Ter)
n.306G>T
COSMIC
17g.41583831C=CA2260085585KRT14c.856G= (p.Glu286=)
n.306G=
17g.41583831C>GCA8562590KRT14c.856G>C (p.Glu286Gln)
n.306G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583831C>TCA399477428KRT14c.856G>A (p.Glu286Lys)
n.306G>A
ClinVar dbSNP gnomAD v4 COSMIC
17g.41583832G>ACA8562591KRT14c.855C>T (p.Asn285=)
n.305C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583832G>CCA399477435KRT14c.855C>G (p.Asn285Lys)
n.305C>G
gnomAD v4
17g.41583832G=CA2260085586KRT14c.855C= (p.Asn285=)
n.305C=
17g.41583832G>TCA399477432KRT14c.855C>A (p.Asn285Lys)
n.305C>A
COSMIC
17g.41583833T>ACA399477440KRT14c.854A>T (p.Asn285Ile)
n.304A>T
17g.41583833T>CCA399477441KRT14c.854A>G (p.Asn285Ser)
n.304A>G
17g.41583833T>GCA399477442KRT14c.854A>C (p.Asn285Thr)
n.304A>C
ClinVar
17g.41583834T>ACA399477443KRT14c.853A>T (p.Asn285Tyr)
n.303A>T
17g.41583834T>CCA399477444KRT14c.853A>G (p.Asn285Asp)
n.303A>G
17g.41583834T>GCA399477445KRT14c.853A>C (p.Asn285His)
n.303A>C
17g.41583835C>ACA500205552KRT14c.852G>T (p.Leu284=)
n.302G>T
17g.41583835C>GCA500205553KRT14c.852G>C (p.Leu284=)
n.302G>C
17g.41583835C>TCA500205554KRT14c.852G>A (p.Leu284=)
n.302G>A
17g.41583836A>CCA399477446KRT14c.851T>G (p.Leu284Arg)
n.301T>G
17g.41583836A>GCA399477447KRT14c.851T>C (p.Leu284Pro)
n.301T>C
ClinVar dbSNP
17g.41583836A>TCA399477448KRT14c.851T>A (p.Leu284Gln)
n.301T>A
17g.41583837G>ACA500205555KRT14c.850C>T (p.Leu284=)
n.300C>T
17g.41583837G>CCA399477449KRT14c.850C>G (p.Leu284Val)
n.300C>G
17g.41583837G>TCA399477450KRT14c.850C>A (p.Leu284Met)
n.300C>A
17g.41583838A>CCA399477451KRT14c.849T>G (p.Ile283Met)
n.299T>G
17g.41583838A>GCA500205560KRT14c.849T>C (p.Ile283=)
n.299T>C
17g.41583838A>TCA500205557KRT14c.849T>A (p.Ile283=)
n.299T>A
17g.41583839A=CA2260085587KRT14c.848T= (p.Ile283=)
n.298T=
17g.41583839A>CCA399477453KRT14c.848T>G (p.Ile283Ser)
n.298T>G
17g.41583839A>GCA399477454KRT14c.848T>C (p.Ile283Thr)
n.298T>C
dbSNP
17g.41583839A>TCA399477452KRT14c.848T>A (p.Ile283Asn)
n.298T>A
17g.41583840T>ACA399477455KRT14c.847A>T (p.Ile283Phe)
n.297A>T
17g.41583840T>CCA399477456KRT14c.847A>G (p.Ile283Val)
n.297A>G
17g.41583840T>GCA399477457KRT14c.847A>C (p.Ile283Leu)
n.297A>C
17g.41583841G>ACA500205570KRT14c.846C>T (p.Arg282=)
n.296C>T
17g.41583841G>CCA500205566KRT14c.846C>G (p.Arg282=)
n.296C>G
17g.41583841G>TCA500205567KRT14c.846C>A (p.Arg282=)
n.296C>A
17g.41583842C>ACA8562593KRT14c.845G>T (p.Arg282Leu)
n.295G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583842C=CA2260085588KRT14c.845G= (p.Arg282=)
n.295G=
17g.41583842C>GCA399477458KRT14c.845G>C (p.Arg282Pro)
n.295G>C
17g.41583842C>TCA8562592KRT14c.845G>A (p.Arg282His)
n.295G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583843G>ACA8562594KRT14c.844C>T (p.Arg282Cys)
n.294C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583843G>CCA399477460KRT14c.844C>G (p.Arg282Gly)
n.294C>G
gnomAD v4
17g.41583843G=CA2260085589KRT14c.844C= (p.Arg282=)
n.294C=
17g.41583843G>TCA399477462KRT14c.844C>A (p.Arg282Ser)
n.294C>A
17g.41583844G>ACA500205580KRT14c.843C>T (p.Ser281=)
n.293C>T
gnomAD v4
17g.41583844G>CCA399477463KRT14c.843C>G (p.Ser281Arg)
n.293C>G
17g.41583844G>TCA399477464KRT14c.843C>A (p.Ser281Arg)
n.293C>A
17g.41583845C>ACA399477465KRT14c.842G>T (p.Ser281Ile)
n.292G>T
17g.41583845C>GCA399477466KRT14c.842G>C (p.Ser281Thr)
n.292G>C
17g.41583845C>TCA399477467KRT14c.842G>A (p.Ser281Asn)
n.292G>A
17g.41583846T>ACA399477468KRT14c.841A>T (p.Ser281Cys)
n.291A>T
17g.41583846T>CCA399477470KRT14c.841A>G (p.Ser281Gly)
n.291A>G
17g.41583846T>GCA399477469KRT14c.841A>C (p.Ser281Arg)
n.291A>C
17g.41583847C>ACA500205585KRT14c.840G>T (p.Leu280=)
n.290G>T
17g.41583847C>GCA500205586KRT14c.840G>C (p.Leu280=)
n.290G>C
gnomAD v4
17g.41583847C>TCA500205588KRT14c.840G>A (p.Leu280=)
n.290G>A
gnomAD v4
17g.41583848A>CCA399477471KRT14c.839T>G (p.Leu280Arg)
n.289T>G
17g.41583848A>GCA399477472KRT14c.839T>C (p.Leu280Pro)
n.289T>C
17g.41583848A>TCA399477473KRT14c.839T>A (p.Leu280Gln)
n.289T>A
17g.41583849G>ACA500205594KRT14c.838C>T (p.Leu280=)
n.288C>T
17g.41583849G>CCA399477474KRT14c.838C>G (p.Leu280Val)
n.288C>G
17g.41583849G=CA2260085590KRT14c.838C= (p.Leu280=)
n.288C=
17g.41583849G>TCA8562595KRT14c.838C>A (p.Leu280Met)
n.288C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583850G>ACA500205597KRT14c.837C>T (p.Asp279=)
n.287C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583850G>CCA399477475KRT14c.837C>G (p.Asp279Glu)
n.287C>G
17g.41583850G=CA2260085591KRT14c.837C= (p.Asp279=)
n.287C=
17g.41583850G>TCA399477476KRT14c.837C>A (p.Asp279Glu)
n.287C>A
17g.41583851T>ACA399477477KRT14c.836A>T (p.Asp279Val)
n.286A>T
17g.41583851T>CCA399477478KRT14c.836A>G (p.Asp279Gly)
n.286A>G
17g.41583851T>GCA399477479KRT14c.836A>C (p.Asp279Ala)
n.286A>C
17g.41583852C>ACA399477480KRT14c.835G>T (p.Asp279Tyr)
n.285G>T
17g.41583852C>GCA399477481KRT14c.835G>C (p.Asp279His)
n.285G>C
17g.41583852C>TCA399477482KRT14c.835G>A (p.Asp279Asn)
n.285G>A
17g.41583853C>ACA500205608KRT14c.834G>T (p.Val278=)
n.284G>T
17g.41583853C>GCA500205606KRT14c.834G>C (p.Val278=)
n.284G>C
17g.41583853C>TCA500205607KRT14c.834G>A (p.Val278=)
n.284G>A
COSMIC
17g.41583854A>CCA399477487KRT14c.833T>G (p.Val278Gly)
n.283T>G
17g.41583854A>GCA399477489KRT14c.833T>C (p.Val278Ala)
n.283T>C
17g.41583854A>TCA399477484KRT14c.833T>A (p.Val278Glu)
n.283T>A
17g.41583855C>ACA399477492KRT14c.832G>T (p.Val278Leu)
n.282G>T
gnomAD v4
17g.41583855C=CA2260085592KRT14c.832G= (p.Val278=)
n.282G=
17g.41583855C>GCA8562596KRT14c.832G>C (p.Val278Leu)
n.282G>C
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583855C>TCA8562597KRT14c.832G>A (p.Val278Met)
n.282G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583856G>ACA8562598KRT14c.831C>T (p.Gly277=)
n.281C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583856G>CCA500205613KRT14c.831C>G (p.Gly277=)
n.281C>G
17g.41583856G=CA2260085593KRT14c.831C= (p.Gly277=)
n.281C=
17g.41583856G>TCA500205614KRT14c.831C>A (p.Gly277=)
n.281C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583857C>ACA399477500KRT14c.830G>T (p.Gly277Val)
n.280G>T
ClinVar dbSNP
17g.41583857C>GCA399477502KRT14c.830G>C (p.Gly277Ala)
n.280G>C
17g.41583857C>TCA399477504KRT14c.830G>A (p.Gly277Asp)
n.280G>A
17g.41583858C>ACA399477507KRT14c.829G>T (p.Gly277Cys)
n.279G>T
17g.41583858C>GCA399477509KRT14c.829G>C (p.Gly277Arg)
n.279G>C
17g.41583858C>TCA399477512KRT14c.829G>A (p.Gly277Ser)
n.279G>A
17g.41583859A>CCA500205620KRT14c.828T>G (p.Pro276=)
n.278T>G
17g.41583859A>GCA500205621KRT14c.828T>C (p.Pro276=)
n.278T>C
gnomAD v4
17g.41583859A>TCA500205623KRT14c.828T>A (p.Pro276=)
n.278T>A
17g.41583859_41583860delinsAGCA2260085594KRT14c.827_828delinsCT (p.Pro276=)
n.277_278delinsCT
17g.41583860G>ACA399477515KRT14c.827C>T (p.Pro276Leu)
n.277C>T
17g.41583860G>CCA399477520KRT14c.827C>G (p.Pro276Arg)
n.277C>G
17g.41583860G>TCA399477518KRT14c.827C>A (p.Pro276His)
n.277C>A
17g.41583861delCA8562599KRT14c.827del (p.Pro276LeufsTer5)
n.277del
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583861G>ACA399477524KRT14c.826C>T (p.Pro276Ser)
n.276C>T
gnomAD v4
17g.41583861G>CCA399477526KRT14c.826C>G (p.Pro276Ala)
n.276C>G
17g.41583861G>TCA399477528KRT14c.826C>A (p.Pro276Thr)
n.276C>A
17g.41583862T>ACA500205629KRT14c.825A>T (p.Ala275=)
n.275A>T
17g.41583862T>CCA500205627KRT14c.825A>G (p.Ala275=)
n.275A>G
17g.41583862T>GCA500205628KRT14c.825A>C (p.Ala275=)
n.275A>C
dbSNP gnomAD v4
17g.41583862T=CA2260085595KRT14c.825A= (p.Ala275=)
n.275A=
17g.41583863G>ACA399477536KRT14c.824C>T (p.Ala275Val)
n.274C>T
COSMIC
17g.41583863G>CCA399477532KRT14c.824C>G (p.Ala275Gly)
n.274C>G
17g.41583863G>TCA399477534KRT14c.824C>A (p.Ala275Glu)
n.274C>A
17g.41583864C>ACA399477539KRT14c.823G>T (p.Ala275Ser)
n.273G>T
17g.41583864C>GCA399477541KRT14c.823G>C (p.Ala275Pro)
n.273G>C
17g.41583864C>TCA399477543KRT14c.823G>A (p.Ala275Thr)
n.273G>A
17g.41583865A>CCA500205638KRT14c.822T>G (p.Ala274=)
n.272T>G
17g.41583865A>GCA500205640KRT14c.822T>C (p.Ala274=)
n.272T>C
gnomAD v4
17g.41583865A>TCA500205641KRT14c.822T>A (p.Ala274=)
n.272T>A
17g.41583866G>ACA399477547KRT14c.821C>T (p.Ala274Val)
n.271C>T
17g.41583866G>CCA399477549KRT14c.821C>G (p.Ala274Gly)
n.271C>G
17g.41583866G=CA2260085596KRT14c.821C= (p.Ala274=)
n.271C=
17g.41583866G>TCA216986KRT14c.821C>A (p.Ala274Asp)
n.271C>A
ClinVar dbSNP
17g.41583867C>ACA399477554KRT14c.820G>T (p.Ala274Ser)
n.270G>T
17g.41583867C=CA2260085597KRT14c.820G= (p.Ala274=)
n.270G=
17g.41583867C>GCA399477556KRT14c.820G>C (p.Ala274Pro)
n.270G>C
17g.41583867C>TCA8562600KRT14c.820G>A (p.Ala274Thr)
n.270G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583868G>ACA8562601KRT14c.819C>T (p.Asp273=)
n.269C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583868G>CCA399477565KRT14c.819C>G (p.Asp273Glu)
n.269C>G
dbSNP gnomAD v4
17g.41583868G=CA2260085598KRT14c.819C= (p.Asp273=)
n.269C=
17g.41583868G>TCA399477567KRT14c.819C>A (p.Asp273Glu)
n.269C>A
17g.41583869T>ACA399477570KRT14c.818A>T (p.Asp273Val)
n.268A>T
17g.41583869T>CCA216984KRT14c.818A>G (p.Asp273Gly)
n.268A>G
ClinVar dbSNP
17g.41583869T>GCA399477572KRT14c.818A>C (p.Asp273Ala)
n.268A>C
17g.41583869T=CA2260085599KRT14c.818A= (p.Asp273=)
n.268A=
17g.41583870C>ACA399477576KRT14c.817G>T (p.Asp273Tyr)
n.267G>T
17g.41583870C=CA2260085600KRT14c.817G= (p.Asp273=)
n.267G=
17g.41583870C>GCA399477577KRT14c.817G>C (p.Asp273His)
n.267G>C
gnomAD v4
17g.41583870C>TCA399477578KRT14c.817G>A (p.Asp273Asn)
n.267G>A
dbSNP gnomAD v4 COSMIC
17g.41583871C>ACA399477582KRT14c.816G>T (p.Met272Ile)
n.266G>T
17g.41583871C>GCA399477584KRT14c.816G>C (p.Met272Ile)
n.266G>C
17g.41583871C>TCA399477586KRT14c.816G>A (p.Met272Ile)
n.266G>A
17g.41583880_41583893delCA2637835339KRT14c.803_816del (p.Val268GlyfsTer17)
n.253_266del
gnomAD v4
17g.41583872A=CA2260085601KRT14c.815T= (p.Met272=)
n.265T=
17g.41583872A>CCA216982KRT14c.815T>G (p.Met272Arg)
n.265T>G
ClinVar dbSNP
17g.41583872A>GCA216980KRT14c.815T>C (p.Met272Thr)
n.265T>C
ClinVar dbSNP
17g.41583872A>TCA399477592KRT14c.815T>A (p.Met272Lys)
n.265T>A
17g.41583873T>ACA399477596KRT14c.814A>T (p.Met272Leu)
n.264A>T
17g.41583873T>CCA399477598KRT14c.814A>G (p.Met272Val)
n.264A>G
17g.41583873T>GCA399477600KRT14c.814A>C (p.Met272Leu)
n.264A>C
17g.41583874C>ACA399477605KRT14c.813G>T (p.Glu271Asp)
n.263G>T
17g.41583874C>GCA399477603KRT14c.813G>C (p.Glu271Asp)
n.263G>C
17g.41583874C>TCA500205655KRT14c.813G>A (p.Glu271=)
n.263G>A
17g.41583875T>ACA399477608KRT14c.812A>T (p.Glu271Val)
n.262A>T
17g.41583875T>CCA399477610KRT14c.812A>G (p.Glu271Gly)
n.262A>G
17g.41583875T>GCA399477612KRT14c.812A>C (p.Glu271Ala)
n.262A>C
17g.41583876C>ACA399477615KRT14c.811G>T (p.Glu271Ter)
n.261G>T
17g.41583876C>GCA399477618KRT14c.811G>C (p.Glu271Gln)
n.261G>C
17g.41583876C>TCA399477619KRT14c.811G>A (p.Glu271Lys)
n.261G>A
17g.41583877C>ACA500205662KRT14c.810G>T (p.Val270=)
n.260G>T
17g.41583877C>GCA500205664KRT14c.810G>C (p.Val270=)
n.260G>C
17g.41583877C>TCA500205665KRT14c.810G>A (p.Val270=)
n.260G>A
17g.41583878A>CCA399477623KRT14c.809T>G (p.Val270Gly)
n.259T>G
17g.41583878A>GCA399477625KRT14c.809T>C (p.Val270Ala)
n.259T>C
17g.41583878A>TCA399477627KRT14c.809T>A (p.Val270Glu)
n.259T>A
17g.41583879C>ACA399477629KRT14c.808G>T (p.Val270Leu)
n.258G>T
17g.41583879C=CA2260085602KRT14c.808G= (p.Val270=)
n.258G=
17g.41583879C>GCA399477631KRT14c.808G>C (p.Val270Leu)
n.258G>C
17g.41583879C>TCA216978KRT14c.808G>A (p.Val270Met)
n.258G>A
ClinVar dbSNP
17g.41583880A=CA2260085603KRT14c.807T= (p.Asn269=)
n.257T=
17g.41583880A>CCA399477635KRT14c.807T>G (p.Asn269Lys)
n.257T>G
17g.41583880A>GCA8562602KRT14c.807T>C (p.Asn269=)
n.257T>C
dbSNP ExAC gnomAD v2
17g.41583880A>TCA399477634KRT14c.807T>A (p.Asn269Lys)
n.257T>A
17g.41583881T>ACA399477636KRT14c.806A>T (p.Asn269Ile)
n.256A>T
17g.41583881T>CCA399477637KRT14c.806A>G (p.Asn269Ser)
n.256A>G
dbSNP gnomAD v3 gnomAD v4
17g.41583881T>GCA399477638KRT14c.806A>C (p.Asn269Thr)
n.256A>C
17g.41583881T=CA2260085604KRT14c.806A= (p.Asn269=)
n.256A=
17g.41583882T>ACA399477639KRT14c.805A>T (p.Asn269Tyr)
n.255A>T
17g.41583882T>CCA399477640KRT14c.805A>G (p.Asn269Asp)
n.255A>G
17g.41583882T>GCA399477641KRT14c.805A>C (p.Asn269His)
n.255A>C
17g.41583883G>ACA500205678KRT14c.804C>T (p.Val268=)
n.254C>T
17g.41583883G>CCA500205680KRT14c.804C>G (p.Val268=)
n.254C>G
17g.41583883G>TCA500205679KRT14c.804C>A (p.Val268=)
n.254C>A
COSMIC
17g.41583884A=CA2260085605KRT14c.803T= (p.Val268=)
n.253T=
17g.41583884A>CCA399477643KRT14c.803T>G (p.Val268Gly)
n.253T>G
17g.41583884A>GCA399477642KRT14c.803T>C (p.Val268Ala)
n.253T>C
ClinVar
17g.41583884A>TCA216976KRT14c.803T>A (p.Val268Asp)
n.253T>A
ClinVar dbSNP
17g.41583885C>ACA399477644KRT14c.802G>T (p.Val268Phe)
n.252G>T
17g.41583885C=CA2260085606KRT14c.802G= (p.Val268=)
n.252G=
17g.41583885C>GCA399477645KRT14c.802G>C (p.Val268Leu)
n.252G>C
17g.41583885C>TCA399477646KRT14c.802G>A (p.Val268Ile)
n.252G>A
dbSNP
17g.41583886A=CA2260085607KRT14c.801T= (p.Asp267=)
n.251T=
17g.41583886A>CCA399477647KRT14c.801T>G (p.Asp267Glu)
n.251T>G
17g.41583886A>GCA8562603KRT14c.801T>C (p.Asp267=)
n.251T>C
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583886A>TCA399477648KRT14c.801T>A (p.Asp267Glu)
n.251T>A
17g.41583887T>ACA399477649KRT14c.800A>T (p.Asp267Val)
n.250A>T
17g.41583887T>CCA399477651KRT14c.800A>G (p.Asp267Gly)
n.250A>G
17g.41583887T>GCA399477650KRT14c.800A>C (p.Asp267Ala)
n.250A>C
17g.41583888C>ACA399477652KRT14c.799G>T (p.Asp267Tyr)
n.249G>T
17g.41583888C=CA2260085608KRT14c.799G= (p.Asp267=)
n.249G=
17g.41583888C>GCA399477653KRT14c.799G>C (p.Asp267His)
n.249G>C
gnomAD v4
17g.41583888C>TCA290665037KRT14c.799G>A (p.Asp267Asn)
n.249G>A
dbSNP
17g.41583889T>ACA500205696KRT14c.798A>T (p.Gly266=)
n.248A>T
17g.41583889T>CCA500205697KRT14c.798A>G (p.Gly266=)
n.248A>G
17g.41583889T>GCA500205701KRT14c.798A>C (p.Gly266=)
n.248A>C
17g.41583890C>ACA399477654KRT14c.797G>T (p.Gly266Val)
n.247G>T
gnomAD v4
17g.41583890C>GCA399477655KRT14c.797G>C (p.Gly266Ala)
n.247G>C
17g.41583890C>TCA399477656KRT14c.797G>A (p.Gly266Glu)
n.247G>A
17g.41583891C>ACA399477657KRT14c.796G>T (p.Gly266Ter)
n.246G>T
17g.41583891C>GCA399477658KRT14c.796G>C (p.Gly266Arg)
n.246G>C
17g.41583891C>TCA399477659KRT14c.796G>A (p.Gly266Arg)
n.246G>A
gnomAD v4 COSMIC

Number of alleles fetched