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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.44351655A>C | CA399765433 | GRN | c.1039A>C (p.Lys347Gln) c.480A>C c.568A>C (p.Lys190Gln) n.297A>C | |
| 17 | g.44351655A>G | CA399765435 | GRN | c.1039A>G (p.Lys347Glu) c.480A>G c.568A>G (p.Lys190Glu) n.297A>G | dbSNP gnomAD v4 COSMIC |
| 17 | g.44351655A>T | CA399765439 | GRN | c.1039A>T (p.Lys347Ter) c.480A>T c.568A>T (p.Lys190Ter) n.297A>T | |
| 17 | g.44351656dup | CA2638209691 | GRN | c.1040dup (p.Ala348GlyfsTer20) c.481dup c.569dup (p.Ala191GlyfsTer20) n.298dup | gnomAD v4 |
| 17 | g.44351656A= | CA2261354260 | GRN | c.1040A= (p.Lys347=) c.481A= c.569A= (p.Lys190=) n.298A= | |
| 17 | g.44351656A>C | CA399765449 | GRN | c.1040A>C (p.Lys347Thr) c.481A>C c.569A>C (p.Lys190Thr) n.298A>C | |
| 17 | g.44351656A>G | CA399765446 | GRN | c.1040A>G (p.Lys347Arg) c.481A>G c.569A>G (p.Lys190Arg) n.298A>G | dbSNP gnomAD v4 |
| 17 | g.44351656A>T | CA399765444 | GRN | c.1040A>T (p.Lys347Met) c.481A>T c.569A>T (p.Lys190Met) n.298A>T | |
| 17 | g.44351657G>A | CA8602092 | GRN | c.1041G>A (p.Lys347=) c.482G>A c.570G>A (p.Lys190=) n.299G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351657G>C | CA399765455 | GRN | c.1041G>C (p.Lys347Asn) c.482G>C c.570G>C (p.Lys190Asn) n.299G>C | |
| 17 | g.44351657G= | CA2261354261 | GRN | c.1041G= (p.Lys347=) c.482G= c.570G= (p.Lys190=) n.299G= | |
| 17 | g.44351657G>T | CA399765457 | GRN | c.1041G>T (p.Lys347Asn) c.482G>T c.570G>T (p.Lys190Asn) n.299G>T | |
| 17 | g.44351658G>A | CA399765462 | GRN | c.1042G>A (p.Ala348Thr) c.483G>A c.571G>A (p.Ala191Thr) n.300G>A | |
| 17 | g.44351658G>C | CA399765465 | GRN | c.1042G>C (p.Ala348Pro) c.483G>C c.571G>C (p.Ala191Pro) n.300G>C | |
| 17 | g.44351658G>T | CA399765466 | GRN | c.1042G>T (p.Ala348Ser) c.483G>T c.571G>T (p.Ala191Ser) n.300G>T | |
| 17 | g.44351659C>A | CA399765471 | GRN | c.1043C>A (p.Ala348Asp) c.484C>A c.572C>A (p.Ala191Asp) n.301C>A | |
| 17 | g.44351659C>G | CA399765474 | GRN | c.1043C>G (p.Ala348Gly) c.484C>G c.572C>G (p.Ala191Gly) n.301C>G | |
| 17 | g.44351659C>T | CA399765476 | GRN | c.1043C>T (p.Ala348Val) c.484C>T c.572C>T (p.Ala191Val) n.301C>T | gnomAD v4 |
| 17 | g.44351660C>A | CA500622036 | GRN | c.1044C>A (p.Ala348=) c.485C>A c.573C>A (p.Ala191=) n.302C>A | |
| 17 | g.44351660C>G | CA500622037 | GRN | c.1044C>G (p.Ala348=) c.485C>G c.573C>G (p.Ala191=) n.302C>G | |
| 17 | g.44351660C>T | CA500622038 | GRN | c.1044C>T (p.Ala348=) c.485C>T c.573C>T (p.Ala191=) n.302C>T | |
| 17 | g.44351661C>A | CA399765480 | GRN | c.1045C>A (p.Pro349Thr) c.486C>A c.574C>A (p.Pro192Thr) n.303C>A | |
| 17 | g.44351661C>G | CA399765483 | GRN | c.1045C>G (p.Pro349Ala) c.486C>G c.574C>G (p.Pro192Ala) n.303C>G | |
| 17 | g.44351661C>T | CA399765485 | GRN | c.1045C>T (p.Pro349Ser) c.486C>T c.574C>T (p.Pro192Ser) n.303C>T | |
| 17 | g.44351662C>A | CA399765496 | GRN | c.1046C>A (p.Pro349Gln) c.487C>A c.575C>A (p.Pro192Gln) n.304C>A | |
| 17 | g.44351662C>G | CA399765494 | GRN | c.1046C>G (p.Pro349Arg) c.487C>G c.575C>G (p.Pro192Arg) n.304C>G | |
| 17 | g.44351662C>T | CA399765490 | GRN | c.1046C>T (p.Pro349Leu) c.487C>T c.575C>T (p.Pro192Leu) n.304C>T | |
| 17 | g.44351663A= | CA2261354262 | GRN | c.1047A= (p.Pro349=) c.488A= c.576A= (p.Pro192=) n.305A= | |
| 17 | g.44351663A>C | CA500622042 | GRN | c.1047A>C (p.Pro349=) c.488A>C c.576A>C (p.Pro192=) n.305A>C | |
| 17 | g.44351663A>G | CA8602093 | GRN | c.1047A>G (p.Pro349=) c.488A>G c.576A>G (p.Pro192=) n.305A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351663A>T | CA500622044 | GRN | c.1047A>T (p.Pro349=) c.488A>T c.576A>T (p.Pro192=) n.305A>T | |
| 17 | g.44351664G>A | CA399765507 | GRN | c.1048G>A (p.Ala350Thr) c.489G>A c.577G>A (p.Ala193Thr) n.306G>A | |
| 17 | g.44351664G>C | CA399765505 | GRN | c.1048G>C (p.Ala350Pro) c.489G>C c.577G>C (p.Ala193Pro) n.306G>C | |
| 17 | g.44351664G>T | CA399765509 | GRN | c.1048G>T (p.Ala350Ser) c.489G>T c.577G>T (p.Ala193Ser) n.306G>T | |
| 17 | g.44351664dup | CA2638209702 | GRN | c.1048dup (p.Ala350GlyfsTer18) c.489dup c.577dup (p.Ala193GlyfsTer18) n.306dup | gnomAD v4 |
| 17 | g.44351665C>A | CA399765513 | GRN | c.1049C>A (p.Ala350Asp) c.490C>A c.578C>A (p.Ala193Asp) n.307C>A | |
| 17 | g.44351665C= | CA2261354263 | GRN | c.1049C= (p.Ala350=) c.490C= c.578C= (p.Ala193=) n.307C= | |
| 17 | g.44351665C>G | CA399765521 | GRN | c.1049C>G (p.Ala350Gly) c.490C>G c.578C>G (p.Ala193Gly) n.307C>G | |
| 17 | g.44351665C>T | CA399765516 | GRN | c.1049C>T (p.Ala350Val) c.490C>T c.578C>T (p.Ala193Val) n.307C>T | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351666T>A | CA500622046 | GRN | c.1050T>A (p.Ala350=) c.491T>A c.579T>A (p.Ala193=) n.308T>A | |
| 17 | g.44351666T>C | CA500622047 | GRN | c.1050T>C (p.Ala350=) c.491T>C c.579T>C (p.Ala193=) n.308T>C | |
| 17 | g.44351666T>G | CA500622048 | GRN | c.1050T>G (p.Ala350=) c.491T>G c.579T>G (p.Ala193=) n.308T>G | |
| 17 | g.44351667C>A | CA399765525 | GRN | c.1051C>A (p.His351Asn) c.492C>A c.580C>A (p.His194Asn) n.309C>A | |
| 17 | g.44351667C>G | CA399765528 | GRN | c.1051C>G (p.His351Asp) c.492C>G c.580C>G (p.His194Asp) n.309C>G | |
| 17 | g.44351667C>T | CA399765526 | GRN | c.1051C>T (p.His351Tyr) c.492C>T c.580C>T (p.His194Tyr) n.309C>T | |
| 17 | g.44351668A= | CA2261354264 | GRN | c.1052A= (p.His351=) c.493A= c.581A= (p.His194=) n.310A= | |
| 17 | g.44351668A>C | CA399765531 | GRN | c.1052A>C (p.His351Pro) c.493A>C c.581A>C (p.His194Pro) n.310A>C | dbSNP |
| 17 | g.44351668A>G | CA399765534 | GRN | c.1052A>G (p.His351Arg) c.493A>G c.581A>G (p.His194Arg) n.310A>G | |
| 17 | g.44351668A>T | CA399765536 | GRN | c.1052A>T (p.His351Leu) c.493A>T c.581A>T (p.His194Leu) n.310A>T | |
| 17 | g.44351669C>A | CA399765539 | GRN | c.1053C>A (p.His351Gln) c.494C>A c.582C>A (p.His194Gln) n.311C>A | |
| 17 | g.44351669C>G | CA399765541 | GRN | c.1053C>G (p.His351Gln) c.494C>G c.582C>G (p.His194Gln) n.311C>G | |
| 17 | g.44351669C>T | CA500622051 | GRN | c.1053C>T (p.His351=) c.494C>T c.582C>T (p.His194=) n.311C>T | gnomAD v4 |
| 17 | g.44351670_44351676dup | CA2832528778 | GRN | c.1054_1060dup (p.Leu354ProfsTer16) c.495_501dup c.583_589dup (p.Leu197ProfsTer16) n.312_318dup | |
| 17 | g.44351670C>A | CA399765546 | GRN | c.1054C>A (p.Leu352Ile) c.495C>A c.583C>A (p.Leu195Ile) n.312C>A | |
| 17 | g.44351670C>G | CA399765548 | GRN | c.1054C>G (p.Leu352Val) c.495C>G c.583C>G (p.Leu195Val) n.312C>G | |
| 17 | g.44351670C>T | CA399765552 | GRN | c.1054C>T (p.Leu352Phe) c.495C>T c.583C>T (p.Leu195Phe) n.312C>T | gnomAD v4 |
| 17 | g.44351671T>A | CA399765562 | GRN | c.1055T>A (p.Leu352His) c.496T>A c.584T>A (p.Leu195His) n.313T>A | |
| 17 | g.44351671T>C | CA399765565 | GRN | c.1055T>C (p.Leu352Pro) c.496T>C c.584T>C (p.Leu195Pro) n.313T>C | |
| 17 | g.44351671T>G | CA399765569 | GRN | c.1055T>G (p.Leu352Arg) c.496T>G c.584T>G (p.Leu195Arg) n.313T>G | |
| 17 | g.44351672C>A | CA500622052 | GRN | c.1056C>A (p.Leu352=) c.497C>A c.585C>A (p.Leu195=) n.314C>A | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351672C= | CA2261354265 | GRN | c.1056C= (p.Leu352=) c.497C= c.585C= (p.Leu195=) n.314C= | |
| 17 | g.44351672C>G | CA500622053 | GRN | c.1056C>G (p.Leu352=) c.497C>G c.585C>G (p.Leu195=) n.314C>G | |
| 17 | g.44351672C>T | CA500622054 | GRN | c.1056C>T (p.Leu352=) c.497C>T c.585C>T (p.Leu195=) n.314C>T | |
| 17 | g.44351672dup | CA2638209707 | GRN | c.1056dup (p.Ser353GlnfsTer15) c.497dup c.585dup (p.Ser196GlnfsTer15) n.314dup | gnomAD v4 |
| 17 | g.44351673A>C | CA399765581 | GRN | c.1057A>C (p.Ser353Arg) c.498A>C c.586A>C (p.Ser196Arg) n.315A>C | |
| 17 | g.44351673A>G | CA399765577 | GRN | c.1057A>G (p.Ser353Gly) c.498A>G c.586A>G (p.Ser196Gly) n.315A>G | |
| 17 | g.44351673A>T | CA399765572 | GRN | c.1057A>T (p.Ser353Cys) c.498A>T c.586A>T (p.Ser196Cys) n.315A>T | |
| 17 | g.44351674G>A | CA399765587 | GRN | c.1058G>A (p.Ser353Asn) c.499G>A c.587G>A (p.Ser196Asn) n.316G>A | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351674G>C | CA399765590 | GRN | c.1058G>C (p.Ser353Thr) c.499G>C c.587G>C (p.Ser196Thr) n.316G>C | |
| 17 | g.44351674G= | CA2261354266 | GRN | c.1058G= (p.Ser353=) c.499G= c.587G= (p.Ser196=) n.316G= | |
| 17 | g.44351674G>T | CA399765594 | GRN | c.1058G>T (p.Ser353Ile) c.499G>T c.587G>T (p.Ser196Ile) n.316G>T | |
| 17 | g.44351675C>A | CA399765596 | GRN | c.1059C>A (p.Ser353Arg) c.500C>A c.588C>A (p.Ser196Arg) n.317C>A | gnomAD v4 |
| 17 | g.44351675C= | CA2261354267 | GRN | c.1059C= (p.Ser353=) c.500C= c.588C= (p.Ser196=) n.317C= | |
| 17 | g.44351675C>G | CA399765600 | GRN | c.1059C>G (p.Ser353Arg) c.500C>G c.588C>G (p.Ser196Arg) n.317C>G | ClinVar dbSNP |
| 17 | g.44351675C>T | CA500622055 | GRN | c.1059C>T (p.Ser353=) c.500C>T c.588C>T (p.Ser196=) n.317C>T | dbSNP gnomAD v2 |
| 17 | g.44351676C>A | CA399765606 | GRN | c.1060C>A (p.Leu354Met) c.501C>A c.589C>A (p.Leu197Met) n.318C>A | |
| 17 | g.44351676C= | CA2261354268 | GRN | c.1060C= (p.Leu354=) c.501C= c.589C= (p.Leu197=) n.318C= | |
| 17 | g.44351676C>G | CA399765610 | GRN | c.1060C>G (p.Leu354Val) c.501C>G c.589C>G (p.Leu197Val) n.318C>G | COSMIC |
| 17 | g.44351676C>T | CA8602094 | GRN | c.1060C>T (p.Leu354=) c.501C>T c.589C>T (p.Leu197=) n.318C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351677T>A | CA399765619 | GRN | c.1061T>A (p.Leu354Gln) c.502T>A c.590T>A (p.Leu197Gln) n.319T>A | gnomAD v4 |
| 17 | g.44351677T>C | CA399765623 | GRN | c.1061T>C (p.Leu354Pro) c.502T>C c.590T>C (p.Leu197Pro) n.319T>C | |
| 17 | g.44351677T>G | CA399765627 | GRN | c.1061T>G (p.Leu354Arg) c.502T>G c.590T>G (p.Leu197Arg) n.319T>G | |
| 17 | g.44351678G>A | CA500622058 | GRN | c.1062G>A (p.Leu354=) c.503G>A c.591G>A (p.Leu197=) n.320G>A | |
| 17 | g.44351678G>C | CA500622060 | GRN | c.1062G>C (p.Leu354=) c.503G>C c.591G>C (p.Leu197=) n.320G>C | |
| 17 | g.44351678G>T | CA500622061 | GRN | c.1062G>T (p.Leu354=) c.503G>T c.591G>T (p.Leu197=) n.320G>T | |
| 17 | g.44351679C>A | CA399765636 | GRN | c.1063C>A (p.Pro355Thr) c.504C>A c.592C>A (p.Pro198Thr) n.321C>A | |
| 17 | g.44351679C= | CA2261354269 | GRN | c.1063C= (p.Pro355=) c.504C= c.592C= (p.Pro198=) n.321C= | |
| 17 | g.44351679C>G | CA399765634 | GRN | c.1063C>G (p.Pro355Ala) c.504C>G c.592C>G (p.Pro198Ala) n.321C>G | |
| 17 | g.44351679C>T | CA399765631 | GRN | c.1063C>T (p.Pro355Ser) c.504C>T c.592C>T (p.Pro198Ser) n.321C>T | dbSNP |
| 17 | g.44351679_44351680del | CA2809588843 | GRN | c.1063_1064del (p.Pro355ArgfsTer12) c.504_505del c.592_593del (p.Pro198ArgfsTer12) n.321_322del | |
| 17 | g.44351680C>A | CA399765642 | GRN | c.1064C>A (p.Pro355Gln) c.505C>A c.593C>A (p.Pro198Gln) n.322C>A | |
| 17 | g.44351680C>G | CA399765646 | GRN | c.1064C>G (p.Pro355Arg) c.505C>G c.593C>G (p.Pro198Arg) n.322C>G | |
| 17 | g.44351680C>T | CA399765647 | GRN | c.1064C>T (p.Pro355Leu) c.505C>T c.593C>T (p.Pro198Leu) n.322C>T | |
| 17 | g.44351681A>C | CA500622062 | GRN | c.1065A>C (p.Pro355=) c.506A>C c.594A>C (p.Pro198=) n.323A>C | |
| 17 | g.44351681A>G | CA500622063 | GRN | c.1065A>G (p.Pro355=) c.506A>G c.594A>G (p.Pro198=) n.323A>G | |
| 17 | g.44351681A>T | CA500622064 | GRN | c.1065A>T (p.Pro355=) c.506A>T c.594A>T (p.Pro198=) n.323A>T | |
| 17 | g.44351682G>A | CA399765654 | GRN | c.1066G>A (p.Asp356Asn) c.507G>A c.595G>A (p.Asp199Asn) n.324G>A | |
| 17 | g.44351682G>C | CA399765657 | GRN | c.1066G>C (p.Asp356His) c.507G>C c.595G>C (p.Asp199His) n.324G>C | |
| 17 | g.44351682G>T | CA399765660 | GRN | c.1066G>T (p.Asp356Tyr) c.507G>T c.595G>T (p.Asp199Tyr) n.324G>T | |
| 17 | g.44351683A= | CA2261354270 | GRN | c.1067A= (p.Asp356=) c.508A= c.596A= (p.Asp199=) n.325A= | |
| 17 | g.44351683A>C | CA399765667 | GRN | c.1067A>C (p.Asp356Ala) c.508A>C c.596A>C (p.Asp199Ala) n.325A>C | |
| 17 | g.44351683A>G | CA399765670 | GRN | c.1067A>G (p.Asp356Gly) c.508A>G c.596A>G (p.Asp199Gly) n.325A>G | dbSNP |
| 17 | g.44351683A>T | CA399765672 | GRN | c.1067A>T (p.Asp356Val) c.508A>T c.596A>T (p.Asp199Val) n.325A>T | |
| 17 | g.44351684C>A | CA399765678 | GRN | c.1068C>A (p.Asp356Glu) c.509C>A c.597C>A (p.Asp199Glu) n.326C>A | |
| 17 | g.44351684C= | CA2261354271 | GRN | c.1068C= (p.Asp356=) c.509C= c.597C= (p.Asp199=) n.326C= | |
| 17 | g.44351684C>G | CA399765682 | GRN | c.1068C>G (p.Asp356Glu) c.509C>G c.597C>G (p.Asp199Glu) n.326C>G | |
| 17 | g.44351684C>T | CA500622068 | GRN | c.1068C>T (p.Asp356=) c.509C>T c.597C>T (p.Asp199=) n.326C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351686del | CA2638209726 | GRN | c.1070del (p.Pro357HisfsTer4) c.511del c.599del (p.Pro200HisfsTer4) n.328del | gnomAD v4 |
| 17 | g.44351685C>A | CA399765692 | GRN | c.1069C>A (p.Pro357Thr) c.510C>A c.598C>A (p.Pro200Thr) n.327C>A | |
| 17 | g.44351685C= | CA2261354272 | GRN | c.1069C= (p.Pro357=) c.510C= c.598C= (p.Pro200=) n.327C= | |
| 17 | g.44351685C>G | CA399765691 | GRN | c.1069C>G (p.Pro357Ala) c.510C>G c.598C>G (p.Pro200Ala) n.327C>G | |
| 17 | g.44351685C>T | CA399765687 | GRN | c.1069C>T (p.Pro357Ser) c.510C>T c.598C>T (p.Pro200Ser) n.327C>T | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351686C>A | CA399765693 | GRN | c.1070C>A (p.Pro357Gln) c.511C>A c.599C>A (p.Pro200Gln) n.328C>A | |
| 17 | g.44351686C= | CA2261354273 | GRN | c.1070C= (p.Pro357=) c.511C= c.599C= (p.Pro200=) n.328C= | |
| 17 | g.44351686C>G | CA399765694 | GRN | c.1070C>G (p.Pro357Arg) c.511C>G c.599C>G (p.Pro200Arg) n.328C>G | |
| 17 | g.44351686C>T | CA399765695 | GRN | c.1070C>T (p.Pro357Leu) c.511C>T c.599C>T (p.Pro200Leu) n.328C>T | dbSNP gnomAD v4 |
| 17 | g.44351687A= | CA2261354274 | GRN | c.1071A= (p.Pro357=) c.512A= c.600A= (p.Pro200=) n.329A= | |
| 17 | g.44351687A>C | CA8602095 | GRN | c.1071A>C (p.Pro357=) c.512A>C c.600A>C (p.Pro200=) n.329A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351687A>G | CA500622069 | GRN | c.1071A>G (p.Pro357=) c.512A>G c.600A>G (p.Pro200=) n.329A>G | |
| 17 | g.44351687A>T | CA500622070 | GRN | c.1071A>T (p.Pro357=) c.512A>T c.600A>T (p.Pro200=) n.329A>T | ClinVar dbSNP gnomAD v4 |
| 17 | g.44351688C>A | CA399765699 | GRN | c.1072C>A (p.Gln358Lys) c.513C>A c.601C>A (p.Gln201Lys) n.330C>A | |
| 17 | g.44351688C= | CA2261354275 | GRN | c.1072C= (p.Gln358=) c.513C= c.601C= (p.Gln201=) n.330C= | |
| 17 | g.44351688C>G | CA399765700 | GRN | c.1072C>G (p.Gln358Glu) c.513C>G c.601C>G (p.Gln201Glu) n.330C>G | gnomAD v4 |
| 17 | g.44351688C>T | CA399765702 | GRN | c.1072C>T (p.Gln358Ter) c.513C>T c.601C>T (p.Gln201Ter) n.330C>T | ClinVar dbSNP gnomAD v4 |
| 17 | g.44351689A= | CA2261354276 | GRN | c.1073A= (p.Gln358=) c.514A= c.602A= (p.Gln201=) n.331A= | |
| 17 | g.44351689A>C | CA399765705 | GRN | c.1073A>C (p.Gln358Pro) c.514A>C c.602A>C (p.Gln201Pro) n.331A>C | |
| 17 | g.44351689A>G | CA399765707 | GRN | c.1073A>G (p.Gln358Arg) c.514A>G c.602A>G (p.Gln201Arg) n.331A>G | dbSNP gnomAD v4 |
| 17 | g.44351689A>T | CA399765710 | GRN | c.1073A>T (p.Gln358Leu) c.514A>T c.602A>T (p.Gln201Leu) n.331A>T | |
| 17 | g.44351689_44351690dup | CA891843550 | GRN | c.1073_1074dup (p.Ala359LysfsTer3) c.514_515dup c.602_603dup (p.Ala202LysfsTer3) n.331_332dup | ClinVar dbSNP |
| 17 | g.44351690A>C | CA399765714 | GRN | c.1074A>C (p.Gln358His) c.515A>C c.603A>C (p.Gln201His) n.332A>C | |
| 17 | g.44351690A>G | CA500622071 | GRN | c.1074A>G (p.Gln358=) c.515A>G c.603A>G (p.Gln201=) n.332A>G | |
| 17 | g.44351690A>T | CA399765717 | GRN | c.1074A>T (p.Gln358His) c.515A>T c.603A>T (p.Gln201His) n.332A>T | |
| 17 | g.44351691G>A | CA399765729 | GRN | c.1075G>A (p.Ala359Thr) c.516G>A c.604G>A (p.Ala202Thr) n.333G>A | gnomAD v4 |
| 17 | g.44351691G>C | CA399765726 | GRN | c.1075G>C (p.Ala359Pro) c.516G>C c.604G>C (p.Ala202Pro) n.333G>C | |
| 17 | g.44351691G>T | CA399765722 | GRN | c.1075G>T (p.Ala359Ser) c.516G>T c.604G>T (p.Ala202Ser) n.333G>T | |
| 17 | g.44351692C>A | CA399765734 | GRN | c.1076C>A (p.Ala359Asp) c.517C>A c.605C>A (p.Ala202Asp) n.334C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351692C= | CA2261354277 | GRN | c.1076C= (p.Ala359=) c.517C= c.605C= (p.Ala202=) n.334C= | |
| 17 | g.44351692C>G | CA399765739 | GRN | c.1076C>G (p.Ala359Gly) c.517C>G c.605C>G (p.Ala202Gly) n.334C>G | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351692C>T | CA8602096 | GRN | c.1076C>T (p.Ala359Val) c.517C>T c.605C>T (p.Ala202Val) n.334C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351693C>A | CA500622073 | GRN | c.1077C>A (p.Ala359=) c.518C>A c.606C>A (p.Ala202=) n.335C>A | |
| 17 | g.44351693C>G | CA500622075 | GRN | c.1077C>G (p.Ala359=) c.518C>G c.606C>G (p.Ala202=) n.335C>G | |
| 17 | g.44351693C>T | CA500622076 | GRN | c.1077C>T (p.Ala359=) c.518C>T c.606C>T (p.Ala202=) n.335C>T | |
| 17 | g.44351694T>A | CA399765743 | GRN | c.1078T>A (p.Leu360Met) c.519T>A c.607T>A (p.Leu203Met) n.336T>A | |
| 17 | g.44351694T>C | CA8602097 | GRN | c.1078T>C (p.Leu360=) c.519T>C c.607T>C (p.Leu203=) n.336T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351694T>G | CA399765749 | GRN | c.1078T>G (p.Leu360Val) c.519T>G c.607T>G (p.Leu203Val) n.336T>G | gnomAD v4 |
| 17 | g.44351694T= | CA2261354278 | GRN | c.1078T= (p.Leu360=) c.519T= c.607T= (p.Leu203=) n.336T= | |
| 17 | g.44351695T>A | CA399765753 | GRN | c.1079T>A (p.Leu360Ter) c.520T>A c.608T>A (p.Leu203Ter) n.337T>A | |
| 17 | g.44351695T>C | CA399765756 | GRN | c.1079T>C (p.Leu360Ser) c.520T>C c.608T>C (p.Leu203Ser) n.337T>C | |
| 17 | g.44351695T>G | CA399765759 | GRN | c.1079T>G (p.Leu360Trp) c.520T>G c.608T>G (p.Leu203Trp) n.337T>G | |
| 17 | g.44351696G>A | CA500622077 | GRN | c.1080G>A (p.Leu360=) c.521G>A c.609G>A (p.Leu203=) n.338G>A | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.44351696G>C | CA399765765 | GRN | c.1080G>C (p.Leu360Phe) c.521G>C c.609G>C (p.Leu203Phe) n.338G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351696G= | CA2261354279 | GRN | c.1080G= (p.Leu360=) c.521G= c.609G= (p.Leu203=) n.338G= | |
| 17 | g.44351696G>T | CA399765770 | GRN | c.1080G>T (p.Leu360Phe) c.521G>T c.609G>T (p.Leu203Phe) n.338G>T | |
| 17 | g.44351697A= | CA2261354281 | GRN | c.1081A= (p.Lys361=) c.522A= c.610A= (p.Lys204=) n.339A= | |
| 17 | g.44351697A>C | CA399765773 | GRN | c.1081A>C (p.Lys361Gln) c.522A>C c.610A>C (p.Lys204Gln) n.339A>C | |
| 17 | g.44351697A>G | CA399765775 | GRN | c.1081A>G (p.Lys361Glu) c.522A>G c.610A>G (p.Lys204Glu) n.339A>G | dbSNP |
| 17 | g.44351697A>T | CA399765778 | GRN | c.1081A>T (p.Lys361Ter) c.522A>T c.610A>T (p.Lys204Ter) n.339A>T | |
| 17 | g.44351697_44351699delinsAAG | CA2261354280 | GRN | c.1081_1083delinsAAG (p.Lys361=) c.522_524delinsAAG c.610_612delinsAAG (p.Lys204=) n.339_341delinsAAG | |
| 17 | g.44351698A>C | CA399765791 | GRN | c.1082A>C (p.Lys361Thr) c.523A>C c.611A>C (p.Lys204Thr) n.340A>C | |
| 17 | g.44351698A>G | CA399765786 | GRN | c.1082A>G (p.Lys361Arg) c.523A>G c.611A>G (p.Lys204Arg) n.340A>G | gnomAD v4 |
| 17 | g.44351698A>T | CA399765784 | GRN | c.1082A>T (p.Lys361Met) c.523A>T c.611A>T (p.Lys204Met) n.340A>T | |
| 17 | g.44351703_44351704del | CA913191166 | GRN | c.1087_1088del (p.Asp363CysfsTer4) c.528_529del c.616_617del (p.Asp206CysfsTer4) n.345_346del | ClinVar dbSNP gnomAD v4 |
| 17 | g.44351699G>A | CA500622078 | GRN | c.1083G>A (p.Lys361=) c.524G>A c.612G>A (p.Lys204=) n.341G>A | |
| 17 | g.44351699G>C | CA399765796 | GRN | c.1083G>C (p.Lys361Asn) c.524G>C c.612G>C (p.Lys204Asn) n.341G>C | gnomAD v4 |
| 17 | g.44351699G= | CA2261354282 | GRN | c.1083G= (p.Lys361=) c.524G= c.612G= (p.Lys204=) n.341G= | |
| 17 | g.44351699G>T | CA399765800 | GRN | c.1083G>T (p.Lys361Asn) c.524G>T c.612G>T (p.Lys204Asn) n.341G>T | dbSNP |
| 17 | g.44351700A>C | CA500622079 | GRN | c.1084A>C (p.Arg362=) c.525A>C c.613A>C (p.Arg205=) n.342A>C | |
| 17 | g.44351700A>G | CA399765806 | GRN | c.1084A>G (p.Arg362Gly) c.525A>G c.613A>G (p.Arg205Gly) n.342A>G | |
| 17 | g.44351700A>T | CA399765808 | GRN | c.1084A>T (p.Arg362Ter) c.525A>T c.613A>T (p.Arg205Ter) n.342A>T | |
| 17 | g.44351701G>A | CA399765813 | GRN | c.1085G>A (p.Arg362Lys) c.526G>A c.614G>A (p.Arg205Lys) n.343G>A | |
| 17 | g.44351701G>C | CA399765817 | GRN | c.1085G>C (p.Arg362Thr) c.526G>C c.614G>C (p.Arg205Thr) n.343G>C | |
| 17 | g.44351701G>T | CA399765820 | GRN | c.1085G>T (p.Arg362Ile) c.526G>T c.614G>T (p.Arg205Ile) n.343G>T | |
| 17 | g.44351702A= | CA2261354283 | GRN | c.1086A= (p.Arg362=) c.527A= c.615A= (p.Arg205=) n.344A= | |
| 17 | g.44351702A>C | CA399765824 | GRN | c.1086A>C (p.Arg362Ser) c.527A>C c.615A>C (p.Arg205Ser) n.344A>C | dbSNP |
| 17 | g.44351702A>G | CA500622080 | GRN | c.1086A>G (p.Arg362=) c.527A>G c.615A>G (p.Arg205=) n.344A>G | gnomAD v4 |
| 17 | g.44351702A>T | CA399765828 | GRN | c.1086A>T (p.Arg362Ser) c.527A>T c.615A>T (p.Arg205Ser) n.344A>T | |
| 17 | g.44351704_44351728del | CA2576290524 | GRN | c.1088_1112del (p.Asp363AlafsTer?) c.529_553del c.617_641del (p.Asp206AlafsTer?) n.346_370del | |
| 17 | g.44351703G>A | CA399765835 | GRN | c.1087G>A (p.Asp363Asn) c.528G>A c.616G>A (p.Asp206Asn) n.345G>A | |
| 17 | g.44351703G>C | CA399765839 | GRN | c.1087G>C (p.Asp363His) c.528G>C c.616G>C (p.Asp206His) n.345G>C | |
| 17 | g.44351703G>T | CA399765843 | GRN | c.1087G>T (p.Asp363Tyr) c.528G>T c.616G>T (p.Asp206Tyr) n.345G>T | |
| 17 | g.44351704A>C | CA399765855 | GRN | c.1088A>C (p.Asp363Ala) c.529A>C c.617A>C (p.Asp206Ala) n.346A>C | |
| 17 | g.44351704A>G | CA399765851 | GRN | c.1088A>G (p.Asp363Gly) c.529A>G c.617A>G (p.Asp206Gly) n.346A>G | gnomAD v4 |
| 17 | g.44351704A>T | CA399765847 | GRN | c.1088A>T (p.Asp363Val) c.529A>T c.617A>T (p.Asp206Val) n.346A>T | |
| 17 | g.44351705T>A | CA399765858 | GRN | c.1089T>A (p.Asp363Glu) c.530T>A c.618T>A (p.Asp206Glu) n.347T>A | |
| 17 | g.44351705T>C | CA500622082 | GRN | c.1089T>C (p.Asp363=) c.530T>C c.618T>C (p.Asp206=) n.347T>C | dbSNP gnomAD v4 |
| 17 | g.44351705T>G | CA399765871 | GRN | c.1089T>G (p.Asp363Glu) c.530T>G c.618T>G (p.Asp206Glu) n.347T>G | |
| 17 | g.44351705T= | CA2261354284 | GRN | c.1089T= (p.Asp363=) c.530T= c.618T= (p.Asp206=) n.347T= | |
| 17 | g.44351706G>A | CA399765874 | GRN | c.1090G>A (p.Val364Ile) c.531G>A c.619G>A (p.Val207Ile) n.348G>A | |
| 17 | g.44351706G>C | CA399765876 | GRN | c.1090G>C (p.Val364Leu) c.531G>C c.619G>C (p.Val207Leu) n.348G>C | |
| 17 | g.44351706G>T | CA399765881 | GRN | c.1090G>T (p.Val364Phe) c.531G>T c.619G>T (p.Val207Phe) n.348G>T | |
| 17 | g.44351707T>A | CA399765885 | GRN | c.1091T>A (p.Val364Asp) c.532T>A c.620T>A (p.Val207Asp) n.349T>A | |
| 17 | g.44351707T>C | CA399765888 | GRN | c.1091T>C (p.Val364Ala) c.532T>C c.620T>C (p.Val207Ala) n.349T>C | |
| 17 | g.44351707T>G | CA399765892 | GRN | c.1091T>G (p.Val364Gly) c.532T>G c.620T>G (p.Val207Gly) n.349T>G | |
| 17 | g.44351708C>A | CA500622085 | GRN | c.1092C>A (p.Val364=) c.533C>A c.621C>A (p.Val207=) n.350C>A | |
| 17 | g.44351708C= | CA2261354285 | GRN | c.1092C= (p.Val364=) c.533C= c.621C= (p.Val207=) n.350C= | |
| 17 | g.44351708C>G | CA500622087 | GRN | c.1092C>G (p.Val364=) c.533C>G c.621C>G (p.Val207=) n.350C>G | |
| 17 | g.44351708C>T | CA8602098 | GRN | c.1092C>T (p.Val364=) c.533C>T c.621C>T (p.Val207=) n.350C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351709C>A | CA399765901 | GRN | c.1093C>A (p.Pro365Thr) c.534C>A c.622C>A (p.Pro208Thr) n.351C>A | |
| 17 | g.44351709C>G | CA399765908 | GRN | c.1093C>G (p.Pro365Ala) c.534C>G c.622C>G (p.Pro208Ala) n.351C>G | |
| 17 | g.44351709C>T | CA399765910 | GRN | c.1093C>T (p.Pro365Ser) c.534C>T c.622C>T (p.Pro208Ser) n.351C>T | |
| 17 | g.44351710C>A | CA399765917 | GRN | c.1094C>A (p.Pro365His) c.535C>A c.623C>A (p.Pro208His) n.352C>A | |
| 17 | g.44351710C>G | CA399765914 | GRN | c.1094C>G (p.Pro365Arg) c.535C>G c.623C>G (p.Pro208Arg) n.352C>G | |
| 17 | g.44351710C>T | CA399765912 | GRN | c.1094C>T (p.Pro365Leu) c.535C>T c.623C>T (p.Pro208Leu) n.352C>T | |
| 17 | g.44351710_44351712delinsCCT | CA2261354286 | GRN | c.1094_1096delinsCCT (p.Pro365=) c.535_537delinsCCT c.623_625delinsCCT (p.Pro208=) n.352_354delinsCCT | |
| 17 | g.44351711C>A | CA500622088 | GRN | c.1095C>A (p.Pro365=) c.536C>A c.624C>A (p.Pro208=) n.353C>A | |
| 17 | g.44351711C>G | CA500622089 | GRN | c.1095C>G (p.Pro365=) c.536C>G c.624C>G (p.Pro208=) n.353C>G | |
| 17 | g.44351711C>T | CA500622090 | GRN | c.1095C>T (p.Pro365=) c.536C>T c.624C>T (p.Pro208=) n.353C>T | gnomAD v4 |
| 17 | g.44351711_44351712del | CA225523 | GRN | c.1095_1096del (p.Cys366Ter) c.536_537del c.624_625del (p.Cys209Ter) n.353_354del | ClinVar dbSNP gnomAD v4 |
| 17 | g.44351712T>A | CA399765927 | GRN | c.1096T>A (p.Cys366Ser) c.537T>A c.625T>A (p.Cys209Ser) n.354T>A | |
| 17 | g.44351712T>C | CA399765930 | GRN | c.1096T>C (p.Cys366Arg) c.537T>C c.625T>C (p.Cys209Arg) n.354T>C | |
| 17 | g.44351712T>G | CA399765933 | GRN | c.1096T>G (p.Cys366Gly) c.537T>G c.625T>G (p.Cys209Gly) n.354T>G | |
| 17 | g.44351713G>A | CA290926425 | GRN | c.1097G>A (p.Cys366Tyr) c.538G>A c.626G>A (p.Cys209Tyr) n.355G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.44351713G>C | CA399765943 | GRN | c.1097G>C (p.Cys366Ser) c.538G>C c.626G>C (p.Cys209Ser) n.355G>C | |
| 17 | g.44351713G= | CA2261354287 | GRN | c.1097G= (p.Cys366=) c.538G= c.626G= (p.Cys209=) n.355G= | |
| 17 | g.44351713G>T | CA399765946 | GRN | c.1097G>T (p.Cys366Phe) c.538G>T c.626G>T (p.Cys209Phe) n.355G>T | gnomAD v4 |
| 17 | g.44351714T>A | CA399765950 | GRN | c.1098T>A (p.Cys366Ter) c.539T>A c.627T>A (p.Cys209Ter) n.356T>A | |
| 17 | g.44351714T>C | CA500622091 | GRN | c.1098T>C (p.Cys366=) c.539T>C c.627T>C (p.Cys209=) n.356T>C | |
| 17 | g.44351714T>G | CA399765956 | GRN | c.1098T>G (p.Cys366Trp) c.539T>G c.627T>G (p.Cys209Trp) n.356T>G | |
| 17 | g.44351715G>A | CA399765960 | GRN | c.1099G>A (p.Asp367Asn) c.540G>A c.628G>A (p.Asp210Asn) n.357G>A | |
| 17 | g.44351715G>C | CA399765963 | GRN | c.1099G>C (p.Asp367His) c.540G>C c.628G>C (p.Asp210His) n.357G>C | gnomAD v4 |
| 17 | g.44351715G>T | CA399765966 | GRN | c.1099G>T (p.Asp367Tyr) c.540G>T c.628G>T (p.Asp210Tyr) n.357G>T | |
| 17 | g.44351715_44351718delinsGATA | CA2261354288 | GRN | c.1099_1102delinsGATA (p.Asp367=) c.540_543delinsGATA c.628_631delinsGATA (p.Asp210=) n.357_360delinsGATA | |
| 17 | g.44351716A= | CA2261354289 | GRN | c.1100A= (p.Asp367=) c.541A= c.629A= (p.Asp210=) n.358A= | |
| 17 | g.44351716A>C | CA399765975 | GRN | c.1100A>C (p.Asp367Ala) c.541A>C c.629A>C (p.Asp210Ala) n.358A>C | |
| 17 | g.44351716A>G | CA399765971 | GRN | c.1100A>G (p.Asp367Gly) c.541A>G c.629A>G (p.Asp210Gly) n.358A>G | |
| 17 | g.44351716A>T | CA8602099 | GRN | c.1100A>T (p.Asp367Val) c.541A>T c.629A>T (p.Asp210Val) n.358A>T | dbSNP ExAC gnomAD v2 |
| 17 | g.44351718_44351720del | CA626224175 | GRN | c.1102_1104del (p.Asn368del) c.543_545del c.631_633del (p.Asn211del) n.360_362del | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.44351717T>A | CA399765978 | GRN | c.1101T>A (p.Asp367Glu) c.542T>A c.630T>A (p.Asp210Glu) n.359T>A | |
| 17 | g.44351717T>C | CA8602100 | GRN | c.1101T>C (p.Asp367=) c.542T>C c.630T>C (p.Asp210=) n.359T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351717T>G | CA399765981 | GRN | c.1101T>G (p.Asp367Glu) c.542T>G c.630T>G (p.Asp210Glu) n.359T>G | |
| 17 | g.44351717T= | CA2261354290 | GRN | c.1101T= (p.Asp367=) c.542T= c.630T= (p.Asp210=) n.359T= | |
| 17 | g.44351718A= | CA2261354291 | GRN | c.1102A= (p.Asn368=) c.543A= c.631A= (p.Asn211=) n.360A= | |
| 17 | g.44351718A>C | CA399765987 | GRN | c.1102A>C (p.Asn368His) c.543A>C c.631A>C (p.Asn211His) n.360A>C | |
| 17 | g.44351718A>G | CA399765991 | GRN | c.1102A>G (p.Asn368Asp) c.543A>G c.631A>G (p.Asn211Asp) n.360A>G | dbSNP |
| 17 | g.44351718A>T | CA399765994 | GRN | c.1102A>T (p.Asn368Tyr) c.543A>T c.631A>T (p.Asn211Tyr) n.360A>T | |
| 17 | g.44351719A= | CA2261354292 | GRN | c.1103A= (p.Asn368=) c.544A= c.632A= (p.Asn211=) n.361A= | |
| 17 | g.44351719A>C | CA399765997 | GRN | c.1103A>C (p.Asn368Thr) c.544A>C c.632A>C (p.Asn211Thr) n.361A>C | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351719A>G | CA399766000 | GRN | c.1103A>G (p.Asn368Ser) c.544A>G c.632A>G (p.Asn211Ser) n.361A>G | |
| 17 | g.44351719A>T | CA399766003 | GRN | c.1103A>T (p.Asn368Ile) c.544A>T c.632A>T (p.Asn211Ile) n.361A>T | |
| 17 | g.44351720T>A | CA399766008 | GRN | c.1104T>A (p.Asn368Lys) c.545T>A c.633T>A (p.Asn211Lys) n.362T>A | |
| 17 | g.44351720T>C | CA500622095 | GRN | c.1104T>C (p.Asn368=) c.545T>C c.633T>C (p.Asn211=) n.362T>C | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.44351720T>G | CA399766007 | GRN | c.1104T>G (p.Asn368Lys) c.545T>G c.633T>G (p.Asn211Lys) n.362T>G | |
| 17 | g.44351720T= | CA2261354293 | GRN | c.1104T= (p.Asn368=) c.545T= c.633T= (p.Asn211=) n.362T= | |
| 17 | g.44351721G>A | CA399766012 | GRN | c.1105G>A (p.Val369Ile) c.546G>A c.634G>A (p.Val212Ile) n.363G>A | gnomAD v4 |
| 17 | g.44351721G>C | CA399766015 | GRN | c.1105G>C (p.Val369Leu) c.546G>C c.634G>C (p.Val212Leu) n.363G>C | |
| 17 | g.44351721G= | CA2261354294 | GRN | c.1105G= (p.Val369=) c.546G= c.634G= (p.Val212=) n.363G= | |
| 17 | g.44351721G>T | CA399766017 | GRN | c.1105G>T (p.Val369Phe) c.546G>T c.634G>T (p.Val212Phe) n.363G>T | dbSNP gnomAD v2 |
| 17 | g.44351722T>A | CA399766021 | GRN | c.1106T>A (p.Val369Asp) c.547T>A c.635T>A (p.Val212Asp) n.364T>A | |
| 17 | g.44351722T>C | CA399766024 | GRN | c.1106T>C (p.Val369Ala) c.547T>C c.635T>C (p.Val212Ala) n.364T>C | |
| 17 | g.44351722T>G | CA399766026 | GRN | c.1106T>G (p.Val369Gly) c.547T>G c.635T>G (p.Val212Gly) n.364T>G | |
| 17 | g.44351723C>A | CA500622099 | GRN | c.1107C>A (p.Val369=) c.548C>A c.636C>A (p.Val212=) n.365C>A | |
| 17 | g.44351723C>G | CA500622097 | GRN | c.1107C>G (p.Val369=) c.548C>G c.636C>G (p.Val212=) n.365C>G | |
| 17 | g.44351723C>T | CA500622098 | GRN | c.1107C>T (p.Val369=) c.548C>T c.636C>T (p.Val212=) n.365C>T | |
| 17 | g.44351724A= | CA2261354295 | GRN | c.1108A= (p.Ser370=) c.549A= c.637A= (p.Ser213=) n.366A= | |
| 17 | g.44351724A>C | CA399766029 | GRN | c.1108A>C (p.Ser370Arg) c.549A>C c.637A>C (p.Ser213Arg) n.366A>C | |
| 17 | g.44351724A>G | CA399766031 | GRN | c.1108A>G (p.Ser370Gly) c.549A>G c.637A>G (p.Ser213Gly) n.366A>G | |
| 17 | g.44351724A>T | CA399766030 | GRN | c.1108A>T (p.Ser370Cys) c.549A>T c.637A>T (p.Ser213Cys) n.366A>T | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351725G>A | CA399766032 | GRN | c.1109G>A (p.Ser370Asn) c.550G>A c.638G>A (p.Ser213Asn) n.367G>A | |
| 17 | g.44351725G>C | CA399766033 | GRN | c.1109G>C (p.Ser370Thr) c.550G>C c.638G>C (p.Ser213Thr) n.367G>C | |
| 17 | g.44351725G>T | CA399766034 | GRN | c.1109G>T (p.Ser370Ile) c.550G>T c.638G>T (p.Ser213Ile) n.367G>T | |
| 17 | g.44351726C>A | CA399766036 | GRN | c.1110C>A (p.Ser370Arg) c.551C>A c.639C>A (p.Ser213Arg) n.368C>A | |
| 17 | g.44351726C>G | CA399766038 | GRN | c.1110C>G (p.Ser370Arg) c.551C>G c.639C>G (p.Ser213Arg) n.368C>G | |
| 17 | g.44351726C>T | CA500622100 | GRN | c.1110C>T (p.Ser370=) c.551C>T c.639C>T (p.Ser213=) n.368C>T | COSMIC |
| 17 | g.44351727A>C | CA399766041 | GRN | c.1111A>C (p.Ser371Arg) c.552A>C c.640A>C (p.Ser214Arg) n.369A>C | |
| 17 | g.44351727A>G | CA399766044 | GRN | c.1111A>G (p.Ser371Gly) c.552A>G c.640A>G (p.Ser214Gly) n.369A>G | |
| 17 | g.44351727A>T | CA399766045 | GRN | c.1111A>T (p.Ser371Cys) c.552A>T c.640A>T (p.Ser214Cys) n.369A>T | |
| 17 | g.44351727_44351729delinsAGC | CA2261354296 | GRN | c.1111_1113delinsAGC (p.Ser371=) c.552_554delinsAGC c.640_642delinsAGC (p.Ser214=) n.369_371delinsAGC | |
| 17 | g.44351728G>A | CA399766046 | GRN | c.1112G>A (p.Ser371Asn) c.553G>A c.641G>A (p.Ser214Asn) n.370G>A | gnomAD v4 |
| 17 | g.44351728G>C | CA8602101 | GRN | c.1112G>C (p.Ser371Thr) c.553G>C c.641G>C (p.Ser214Thr) n.370G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351728G= | CA2261354297 | GRN | c.1112G= (p.Ser371=) c.553G= c.641G= (p.Ser214=) n.370G= | |
| 17 | g.44351728G>T | CA399766050 | GRN | c.1112G>T (p.Ser371Ile) c.553G>T c.641G>T (p.Ser214Ile) n.370G>T | |
| 17 | g.44351728_44351729del | CA626224176 | GRN | c.1112_1113del (p.Ser371MetfsTer?) c.1112_1113del (p.Ser371MetfsTer28) c.553_554del c.641_642del (p.Ser214MetfsTer?) n.370_371del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351729C>A | CA399766053 | GRN | c.1113C>A (p.Ser371Arg) c.554C>A c.642C>A (p.Ser214Arg) n.371C>A | |
| 17 | g.44351729C>G | CA399766055 | GRN | c.1113C>G (p.Ser371Arg) c.554C>G c.642C>G (p.Ser214Arg) n.371C>G | |
| 17 | g.44351729C>T | CA500622101 | GRN | c.1113C>T (p.Ser371=) c.554C>T c.642C>T (p.Ser214=) n.371C>T | |
| 17 | g.44351730T>A | CA399766058 | GRN | c.1114T>A (p.Cys372Ser) c.555T>A c.643T>A (p.Cys215Ser) n.372T>A | |
| 17 | g.44351730T>C | CA399766060 | GRN | c.1114T>C (p.Cys372Arg) c.555T>C c.643T>C (p.Cys215Arg) n.372T>C | |
| 17 | g.44351730T>G | CA399766072 | GRN | c.1114T>G (p.Cys372Gly) c.555T>G c.643T>G (p.Cys215Gly) n.372T>G | |
| 17 | g.44351730_44351731delinsTG | CA2261354298 | GRN | c.1114_1115delinsTG (p.Cys372=) c.555_556delinsTG c.643_644delinsTG (p.Cys215=) n.372_373delinsTG | |
| 17 | g.44351731del | CA626224177 | GRN | c.1115del (p.Cys372PhefsTer?) c.556del c.644del (p.Cys215PhefsTer?) n.373del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351731G>A | CA399766078 | GRN | c.1115G>A (p.Cys372Tyr) c.556G>A c.644G>A (p.Cys215Tyr) n.373G>A | COSMIC |
| 17 | g.44351731G>C | CA399766081 | GRN | c.1115G>C (p.Cys372Ser) c.556G>C c.644G>C (p.Cys215Ser) n.373G>C | |
| 17 | g.44351731G>T | CA399766084 | GRN | c.1115G>T (p.Cys372Phe) c.556G>T c.644G>T (p.Cys215Phe) n.373G>T | |
| 17 | g.44351732T>A | CA399766088 | GRN | c.1116T>A (p.Cys372Ter) c.557T>A c.645T>A (p.Cys215Ter) n.374T>A | |
| 17 | g.44351732T>C | CA500622102 | GRN | c.1116T>C (p.Cys372=) c.557T>C c.645T>C (p.Cys215=) n.374T>C | dbSNP |
| 17 | g.44351732T>G | CA399766091 | GRN | c.1116T>G (p.Cys372Trp) c.557T>G c.645T>G (p.Cys215Trp) n.374T>G | |
| 17 | g.44351732T= | CA2261354300 | GRN | c.1116T= (p.Cys372=) c.557T= c.645T= (p.Cys215=) n.374T= | |
| 17 | g.44351732_44351742delinsTCCCTCCTCCG | CA2261354299 | GRN | c.1116_1126delinsTCCCTCCTCCG (p.Cys372=) c.557_567delinsTCCCTCCTCCG c.645_655delinsTCCCTCCTCCG (p.Cys215=) n.374_384delinsTCCCTCCTCCG | |
| 17 | g.44351733C>A | CA8602102 | GRN | c.1117C>A (p.Pro373Thr) c.558C>A c.646C>A (p.Pro216Thr) n.375C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351733C= | CA2261354301 | GRN | c.1117C= (p.Pro373=) c.558C= c.646C= (p.Pro216=) n.375C= | |
| 17 | g.44351733C>G | CA399766101 | GRN | c.1117C>G (p.Pro373Ala) c.558C>G c.646C>G (p.Pro216Ala) n.375C>G | |
| 17 | g.44351733C>T | CA290926429 | GRN | c.1117C>T (p.Pro373Ser) c.558C>T c.646C>T (p.Pro216Ser) n.375C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351733_44351736delinsCCCT | CA2261354302 | GRN | c.1117_1120delinsCCCT (p.Pro373=) c.558_561delinsCCCT c.646_649delinsCCCT (p.Pro216=) n.375_378delinsCCCT | |
| 17 | g.44351733_44351742del | CA626224178 | GRN | c.1117_1126del (p.Pro373IlefsTer?) c.558_567del c.646_655del (p.Pro216IlefsTer?) n.375_384del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351734C>A | CA399766110 | GRN | c.1118C>A (p.Pro373His) c.559C>A c.647C>A (p.Pro216His) n.376C>A | |
| 17 | g.44351734C>G | CA399766112 | GRN | c.1118C>G (p.Pro373Arg) c.559C>G c.647C>G (p.Pro216Arg) n.376C>G | |
| 17 | g.44351734C>T | CA399766116 | GRN | c.1118C>T (p.Pro373Leu) c.559C>T c.647C>T (p.Pro216Leu) n.376C>T | |
| 17 | g.44351734_44351735delinsG | CA2695226231 | GRN | c.1118_1119delinsG (p.Pro373ArgfsTer?) c.559_560delinsG c.647_648delinsG (p.Pro216ArgfsTer?) n.376_377delinsG | |
| 17 | g.44351739_44351741del | CA8602103 | GRN | c.1123_1125del (p.Ser375del) c.564_566del c.652_654del (p.Ser218del) n.381_383del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351735C>A | CA500622103 | GRN | c.1119C>A (p.Pro373=) c.560C>A c.648C>A (p.Pro216=) n.377C>A | |
| 17 | g.44351735C= | CA2261354303 | GRN | c.1119C= (p.Pro373=) c.560C= c.648C= (p.Pro216=) n.377C= | |
| 17 | g.44351735C>G | CA500622104 | GRN | c.1119C>G (p.Pro373=) c.560C>G c.648C>G (p.Pro216=) n.377C>G | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.44351735C>T | CA500622105 | GRN | c.1119C>T (p.Pro373=) c.560C>T c.648C>T (p.Pro216=) n.377C>T | |
| 17 | g.44351736T>A | CA399766128 | GRN | c.1120T>A (p.Ser374Thr) c.561T>A c.649T>A (p.Ser217Thr) n.378T>A | |
| 17 | g.44351736T>C | CA399766134 | GRN | c.1120T>C (p.Ser374Pro) c.561T>C c.649T>C (p.Ser217Pro) n.378T>C | |
| 17 | g.44351736T>G | CA399766131 | GRN | c.1120T>G (p.Ser374Ala) c.561T>G c.649T>G (p.Ser217Ala) n.378T>G | gnomAD v4 |
| 17 | g.44351737C>A | CA399766138 | GRN | c.1121C>A (p.Ser374Tyr) c.562C>A c.650C>A (p.Ser217Tyr) n.379C>A | |
| 17 | g.44351737C>G | CA399766141 | GRN | c.1121C>G (p.Ser374Cys) c.562C>G c.650C>G (p.Ser217Cys) n.379C>G | |
| 17 | g.44351737C>T | CA399766145 | GRN | c.1121C>T (p.Ser374Phe) c.562C>T c.650C>T (p.Ser217Phe) n.379C>T | |
| 17 | g.44351738C>A | CA500622106 | GRN | c.1122C>A (p.Ser374=) c.563C>A c.651C>A (p.Ser217=) n.380C>A | |
| 17 | g.44351738C>G | CA500622107 | GRN | c.1122C>G (p.Ser374=) c.563C>G c.651C>G (p.Ser217=) n.380C>G | |
| 17 | g.44351738C>T | CA500622108 | GRN | c.1122C>T (p.Ser374=) c.563C>T c.651C>T (p.Ser217=) n.380C>T | |
| 17 | g.44351739T>A | CA399766149 | GRN | c.1123T>A (p.Ser375Thr) c.564T>A c.652T>A (p.Ser218Thr) n.381T>A | |
| 17 | g.44351739T>C | CA399766153 | GRN | c.1123T>C (p.Ser375Pro) c.564T>C c.652T>C (p.Ser218Pro) n.381T>C | |
| 17 | g.44351739T>G | CA399766157 | GRN | c.1123T>G (p.Ser375Ala) c.564T>G c.652T>G (p.Ser218Ala) n.381T>G | |
| 17 | g.44351740C>A | CA399766161 | GRN | c.1124C>A (p.Ser375Tyr) c.565C>A c.653C>A (p.Ser218Tyr) n.382C>A | dbSNP gnomAD v4 |
| 17 | g.44351740C= | CA2261354304 | GRN | c.1124C= (p.Ser375=) c.565C= c.653C= (p.Ser218=) n.382C= | |
| 17 | g.44351740C>G | CA399766163 | GRN | c.1124C>G (p.Ser375Cys) c.565C>G c.653C>G (p.Ser218Cys) n.382C>G | ClinVar |
| 17 | g.44351740C>T | CA399766168 | GRN | c.1124C>T (p.Ser375Phe) c.565C>T c.653C>T (p.Ser218Phe) n.382C>T | |
| 17 | g.44351741C>A | CA500622109 | GRN | c.1125C>A (p.Ser375=) c.566C>A c.654C>A (p.Ser218=) n.383C>A | |
| 17 | g.44351741C= | CA2261354305 | GRN | c.1125C= (p.Ser375=) c.566C= c.654C= (p.Ser218=) n.383C= | |
| 17 | g.44351741C>G | CA500622110 | GRN | c.1125C>G (p.Ser375=) c.566C>G c.654C>G (p.Ser218=) n.383C>G | |
| 17 | g.44351741C>T | CA8602104 | GRN | c.1125C>T (p.Ser375=) c.566C>T c.654C>T (p.Ser218=) n.383C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351742G>A | CA8602105 | GRN | c.1126G>A (p.Asp376Asn) c.567G>A c.655G>A (p.Asp219Asn) n.384G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351742G>C | CA399766182 | GRN | c.1126G>C (p.Asp376His) c.567G>C c.655G>C (p.Asp219His) n.384G>C | |
| 17 | g.44351742G= | CA2261354306 | GRN | c.1126G= (p.Asp376=) c.567G= c.655G= (p.Asp219=) n.384G= | |
| 17 | g.44351742G>T | CA399766179 | GRN | c.1126G>T (p.Asp376Tyr) c.567G>T c.655G>T (p.Asp219Tyr) n.384G>T | |
| 17 | g.44351743A>C | CA399766190 | GRN | c.1127A>C (p.Asp376Ala) c.568A>C c.656A>C (p.Asp219Ala) n.385A>C | |
| 17 | g.44351743A>G | CA399766197 | GRN | c.1127A>G (p.Asp376Gly) c.568A>G c.656A>G (p.Asp219Gly) n.385A>G | |
| 17 | g.44351743A>T | CA399766193 | GRN | c.1127A>T (p.Asp376Val) c.568A>T c.656A>T (p.Asp219Val) n.385A>T | |
| 17 | g.44351744T>A | CA399766206 | GRN | c.1128T>A (p.Asp376Glu) c.569T>A c.657T>A (p.Asp219Glu) n.386T>A | |
| 17 | g.44351744T>C | CA500622117 | GRN | c.1128T>C (p.Asp376=) c.569T>C c.657T>C (p.Asp219=) n.386T>C | |
| 17 | g.44351744T>G | CA399766208 | GRN | c.1128T>G (p.Asp376Glu) c.569T>G c.657T>G (p.Asp219Glu) n.386T>G | |
| 17 | g.44351744_44351753delinsTACCTGCTGC | CA2261354307 | GRN | c.1128_1137delinsTACCTGCTGC (p.Asp376=) c.1128_1136+1delinsTACCTGCTGC c.569_578delinsTACCTGCTGC c.657_666delinsTACCTGCTGC (p.Asp219=) n.386_395delinsTACCTGCTGC | |
| 17 | g.44351745A= | CA2261354308 | GRN | c.1129A= (p.Thr377=) c.570A= c.658A= (p.Thr220=) n.387A= | |
| 17 | g.44351745A>C | CA399766211 | GRN | c.1129A>C (p.Thr377Pro) c.570A>C c.658A>C (p.Thr220Pro) n.387A>C | dbSNP |
| 17 | g.44351745A>G | CA399766215 | GRN | c.1129A>G (p.Thr377Ala) c.570A>G c.658A>G (p.Thr220Ala) n.387A>G | |
| 17 | g.44351745A>T | CA399766232 | GRN | c.1129A>T (p.Thr377Ser) c.570A>T c.658A>T (p.Thr220Ser) n.387A>T | |
| 17 | g.44351745_44351753del | CA626224179 | GRN | c.1129_1137del (p.Thr377_Cys379del) c.1129_1136+1del c.570_578del c.658_666del (p.Thr220_Cys222del) n.387_395del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351746C>A | CA290926436 | GRN | c.1130C>A (p.Thr377Asn) c.571C>A c.659C>A (p.Thr220Asn) n.388C>A | dbSNP gnomAD v4 |
| 17 | g.44351746C= | CA2261354309 | GRN | c.1130C= (p.Thr377=) c.571C= c.659C= (p.Thr220=) n.388C= | |
| 17 | g.44351746C>G | CA399766244 | GRN | c.1130C>G (p.Thr377Ser) c.571C>G c.659C>G (p.Thr220Ser) n.388C>G | |
| 17 | g.44351746C>T | CA399766246 | GRN | c.1130C>T (p.Thr377Ile) c.571C>T c.659C>T (p.Thr220Ile) n.388C>T | |
| 17 | g.44351746_44351747insA | CA2809588844 | GRN | c.1130_1131insA (p.Cys378LeufsTer?) c.1130_1131insA (p.Cys378LeufsTer22) c.571_572insA c.659_660insA (p.Cys221LeufsTer?) n.388_389insA | |
| 17 | g.44351747C>A | CA500622119 | GRN | c.1131C>A (p.Thr377=) c.572C>A c.660C>A (p.Thr220=) n.389C>A | gnomAD v4 |
| 17 | g.44351747C= | CA2261354310 | GRN | c.1131C= (p.Thr377=) c.572C= c.660C= (p.Thr220=) n.389C= | |
| 17 | g.44351747C>G | CA290926438 | GRN | c.1131C>G (p.Thr377=) c.572C>G c.660C>G (p.Thr220=) n.389C>G | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.44351747C>T | CA500622118 | GRN | c.1131C>T (p.Thr377=) c.572C>T c.660C>T (p.Thr220=) n.389C>T | gnomAD v4 |
| 17 | g.44351748T>A | CA399766254 | GRN | c.1132T>A (p.Cys378Ser) c.573T>A c.661T>A (p.Cys221Ser) n.390T>A | |
| 17 | g.44351748T>C | CA399766258 | GRN | c.1132T>C (p.Cys378Arg) c.573T>C c.661T>C (p.Cys221Arg) n.390T>C | dbSNP gnomAD v4 |
| 17 | g.44351748T>G | CA399766263 | GRN | c.1132T>G (p.Cys378Gly) c.573T>G c.661T>G (p.Cys221Gly) n.390T>G | |
| 17 | g.44351748T= | CA2261354311 | GRN | c.1132T= (p.Cys378=) c.573T= c.661T= (p.Cys221=) n.390T= | |
| 17 | g.44351749G>A | CA399766274 | GRN | c.1133G>A (p.Cys378Tyr) c.574G>A c.662G>A (p.Cys221Tyr) n.391G>A | COSMIC |
| 17 | g.44351749G>C | CA399766272 | GRN | c.1133G>C (p.Cys378Ser) c.574G>C c.662G>C (p.Cys221Ser) n.391G>C | gnomAD v4 |
| 17 | g.44351749G>T | CA399766268 | GRN | c.1133G>T (p.Cys378Phe) c.574G>T c.662G>T (p.Cys221Phe) n.391G>T | |
| 17 | g.44351750C>A | CA399766279 | GRN | c.1134C>A (p.Cys378Ter) c.575C>A c.663C>A (p.Cys221Ter) n.392C>A | |
| 17 | g.44351750C= | CA2261354312 | GRN | c.1134C= (p.Cys378=) c.575C= c.663C= (p.Cys221=) n.392C= | |
| 17 | g.44351750C>G | CA399766282 | GRN | c.1134C>G (p.Cys378Trp) c.575C>G c.663C>G (p.Cys221Trp) n.392C>G | |
| 17 | g.44351750C>T | CA8602106 | GRN | c.1134C>T (p.Cys378=) c.575C>T c.663C>T (p.Cys221=) n.392C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44351751T>A | CA399766294 | GRN | c.1135T>A (p.Cys379Ser) c.576T>A c.664T>A (p.Cys222Ser) n.393T>A | |
| 17 | g.44351751T>C | CA399766296 | GRN | c.1135T>C (p.Cys379Arg) c.576T>C c.664T>C (p.Cys222Arg) n.393T>C | |
| 17 | g.44351751T>G | CA399766299 | GRN | c.1135T>G (p.Cys379Gly) c.576T>G c.664T>G (p.Cys222Gly) n.393T>G | |
| 17 | g.44351752G>A | CA399766304 | GRN | c.1136G>A (p.Cys379Tyr) c.577G>A c.665G>A (p.Cys222Tyr) n.394G>A | gnomAD v4 |
| 17 | g.44351752G>C | CA399766308 | GRN | c.1136G>C (p.Cys379Ser) c.577G>C c.665G>C (p.Cys222Ser) n.394G>C | |
| 17 | g.44351752G>T | CA399766311 | GRN | c.1136G>T (p.Cys379Phe) c.577G>T c.665G>T (p.Cys222Phe) n.394G>T | |
| 17 | g.44351753C>A | CA399766316 | GRN | c.1137C>A (p.Cys379Ter) c.1136+1C>A (n.1136+1C>A) c.578C>A c.666C>A (p.Cys222Ter) n.395C>A | COSMIC |
| 17 | g.44351753C>G | CA399766323 | GRN | c.1137C>G (p.Cys379Trp) c.1136+1C>G (n.1136+1C>G) c.578C>G c.666C>G (p.Cys222Trp) n.395C>G | |
| 17 | g.44351753C>T | CA500622126 | GRN | c.1137C>T (p.Cys379=) c.1136+1C>T (n.1136+1C>T) c.578C>T c.666C>T (p.Cys222=) n.395C>T | |
| 17 | g.44351754C>A | CA399766334 | GRN | c.1138C>A (p.Gln380Lys) c.1136+2C>A (n.1136+2C>A) c.579C>A c.667C>A (p.Gln223Lys) n.396C>A | |
| 17 | g.44351754C= | CA2261354313 | GRN | c.1138C= (p.Gln380=) c.1136+2C= (n.1136+2C=) c.579C= c.667C= (p.Gln223=) n.396C= | |
| 17 | g.44351754C>G | CA8602107 | GRN | c.1138C>G (p.Gln380Glu) c.1136+2C>G (n.1136+2C>G) c.579C>G c.667C>G (p.Gln223Glu) n.396C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44351754C>T | CA399766328 | GRN | c.1138C>T (p.Gln380Ter) c.1136+2C>T (n.1136+2C>T) c.579C>T c.667C>T (p.Gln223Ter) n.396C>T | |
| 17 | g.44351755A= | CA2261354315 | GRN | c.1139A= (p.Gln380=) c.1136+3A= (n.1136+3A=) c.580A= c.668A= (p.Gln223=) n.397A= | |
| 17 | g.44351755A>C | CA399766339 | GRN | c.1139A>C (p.Gln380Pro) c.1136+3A>C (n.1136+3A>C) c.580A>C c.668A>C (p.Gln223Pro) n.397A>C | dbSNP |
| 17 | g.44351755A>G | CA399766343 | GRN | c.1139A>G (p.Gln380Arg) c.1136+3A>G (n.1136+3A>G) c.580A>G c.668A>G (p.Gln223Arg) n.397A>G | |
| 17 | g.44351755A>T | CA399766346 | GRN | c.1139A>T (p.Gln380Leu) c.1136+3A>T (n.1136+3A>T) c.580A>T c.668A>T (p.Gln223Leu) n.397A>T | |
| 17 | g.44351755_44351758delinsAACT | CA2261354314 | GRN | c.1139_1142delinsAACT (p.Gln380=) c.1136+3_1136+6delinsAACT (n.1136+3_1136+6delinsAACT) c.580_583delinsAACT c.668_671delinsAACT (p.Gln223=) n.397_400delinsAACT |