UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.154580323_154590216del | CA915940499 | |||
| 4 | g.154585993_154586004del | CA2578217778 | FGA | c.1434_1445del (p.Thr479_Val482del) c.644-285_644-274del (n.644-285_644-274del) | gnomAD v4 |
| 4 | g.154585994T>A | CA358529052 | FGA | c.1435A>T (p.Thr479Ser) c.644-284A>T (n.644-284A>T) | |
| 4 | g.154585994T>C | CA358529054 | FGA | c.1435A>G (p.Thr479Ala) c.644-284A>G (n.644-284A>G) | |
| 4 | g.154585994T>G | CA358529055 | FGA | c.1435A>C (p.Thr479Pro) c.644-284A>C (n.644-284A>C) | |
| 4 | g.154585995A>C | CA442014036 | FGA | c.1434T>G (p.Val478=) c.644-285T>G (n.644-285T>G) | |
| 4 | g.154585995A>G | CA442014037 | FGA | c.1434T>C (p.Val478=) c.644-285T>C (n.644-285T>C) | gnomAD v4 |
| 4 | g.154585995A>T | CA442014038 | FGA | c.1434T>A (p.Val478=) c.644-285T>A (n.644-285T>A) | |
| 4 | g.154585996A>C | CA358529058 | FGA | c.1433T>G (p.Val478Gly) c.644-286T>G (n.644-286T>G) | |
| 4 | g.154585996A>G | CA358529062 | FGA | c.1433T>C (p.Val478Ala) c.644-286T>C (n.644-286T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585996A>T | CA358529060 | FGA | c.1433T>A (p.Val478Asp) c.644-286T>A (n.644-286T>A) | |
| 4 | g.154585997C>A | CA358529064 | FGA | c.1432G>T (p.Val478Phe) c.644-287G>T (n.644-287G>T) | |
| 4 | g.154585997C>G | CA358529066 | FGA | c.1432G>C (p.Val478Leu) c.644-287G>C (n.644-287G>C) | |
| 4 | g.154585997C>T | CA358529069 | FGA | c.1432G>A (p.Val478Ile) c.644-287G>A (n.644-287G>A) | |
| 4 | g.154585998T>A | CA358529071 | FGA | c.1431A>T (p.Glu477Asp) c.644-288A>T (n.644-288A>T) | |
| 4 | g.154585998T>C | CA442014040 | FGA | c.1431A>G (p.Glu477=) c.644-288A>G (n.644-288A>G) | |
| 4 | g.154585998T>G | CA358529073 | FGA | c.1431A>C (p.Glu477Asp) c.644-288A>C (n.644-288A>C) | |
| 4 | g.154585999T>A | CA358529076 | FGA | c.1430A>T (p.Glu477Val) c.644-289A>T (n.644-289A>T) | |
| 4 | g.154585999T>C | CA358529077 | FGA | c.1430A>G (p.Glu477Gly) c.644-289A>G (n.644-289A>G) | |
| 4 | g.154585999T>G | CA358529079 | FGA | c.1430A>C (p.Glu477Ala) c.644-289A>C (n.644-289A>C) | |
| 4 | g.154586000C>A | CA358529082 | FGA | c.1429G>T (p.Glu477Ter) c.644-290G>T (n.644-290G>T) | COSMIC COSMIC |
| 4 | g.154586000C= | CA1504943288 | FGA | c.1429G= (p.Glu477=) c.644-290G= (n.644-290G=) | |
| 4 | g.154586000C>G | CA358529083 | FGA | c.1429G>C (p.Glu477Gln) c.644-290G>C (n.644-290G>C) | dbSNP |
| 4 | g.154586000C>T | CA358529085 | FGA | c.1429G>A (p.Glu477Lys) c.644-290G>A (n.644-290G>A) | |
| 4 | g.154586001T>A | CA358529087 | FGA | c.1428A>T (p.Lys476Asn) c.644-291A>T (n.644-291A>T) | |
| 4 | g.154586001T>C | CA442014043 | FGA | c.1428A>G (p.Lys476=) c.644-291A>G (n.644-291A>G) | |
| 4 | g.154586001T>G | CA358529090 | FGA | c.1428A>C (p.Lys476Asn) c.644-291A>C (n.644-291A>C) | |
| 4 | g.154586002T>A | CA358529093 | FGA | c.1427A>T (p.Lys476Ile) c.644-292A>T (n.644-292A>T) | |
| 4 | g.154586002T>C | CA108761169 | FGA | c.1427A>G (p.Lys476Arg) c.644-292A>G (n.644-292A>G) | dbSNP |
| 4 | g.154586002T>G | CA358529095 | FGA | c.1427A>C (p.Lys476Thr) c.644-292A>C (n.644-292A>C) | |
| 4 | g.154586002T= | CA1504943289 | FGA | c.1427A= (p.Lys476=) c.644-292A= (n.644-292A=) | |
| 4 | g.154586003T>A | CA358529100 | FGA | c.1426A>T (p.Lys476Ter) c.644-293A>T (n.644-293A>T) | |
| 4 | g.154586003T>C | CA358529101 | FGA | c.1426A>G (p.Lys476Glu) c.644-293A>G (n.644-293A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586003T>G | CA358529103 | FGA | c.1426A>C (p.Lys476Gln) c.644-293A>C (n.644-293A>C) | |
| 4 | g.154586003T= | CA1504943290 | FGA | c.1426A= (p.Lys476=) c.644-293A= (n.644-293A=) | |
| 4 | g.154586004G>A | CA442014045 | FGA | c.1425C>T (p.His475=) c.644-294C>T (n.644-294C>T) | |
| 4 | g.154586004G>C | CA358529105 | FGA | c.1425C>G (p.His475Gln) c.644-294C>G (n.644-294C>G) | dbSNP gnomAD v4 |
| 4 | g.154586004G= | CA1504943291 | FGA | c.1425C= (p.His475=) c.644-294C= (n.644-294C=) | |
| 4 | g.154586004G>T | CA358529107 | FGA | c.1425C>A (p.His475Gln) c.644-294C>A (n.644-294C>A) | |
| 4 | g.154586005T>A | CA358529109 | FGA | c.1424A>T (p.His475Leu) c.644-295A>T (n.644-295A>T) | |
| 4 | g.154586005T>C | CA358529111 | FGA | c.1424A>G (p.His475Arg) c.644-295A>G (n.644-295A>G) | |
| 4 | g.154586005T>G | CA358529113 | FGA | c.1424A>C (p.His475Pro) c.644-295A>C (n.644-295A>C) | |
| 4 | g.154586006G>A | CA358529115 | FGA | c.1423C>T (p.His475Tyr) c.644-296C>T (n.644-296C>T) | |
| 4 | g.154586006G>C | CA358529117 | FGA | c.1423C>G (p.His475Asp) c.644-296C>G (n.644-296C>G) | |
| 4 | g.154586006G>T | CA358529119 | FGA | c.1423C>A (p.His475Asn) c.644-296C>A (n.644-296C>A) | |
| 4 | g.154586007A>C | CA442014047 | FGA | c.1422T>G (p.Gly474=) c.644-297T>G (n.644-297T>G) | |
| 4 | g.154586007A>G | CA442014048 | FGA | c.1422T>C (p.Gly474=) c.644-297T>C (n.644-297T>C) | dbSNP |
| 4 | g.154586007A>T | CA442014050 | FGA | c.1422T>A (p.Gly474=) c.644-297T>A (n.644-297T>A) | |
| 4 | g.154586008C>A | CA358529123 | FGA | c.1421G>T (p.Gly474Val) c.644-298G>T (n.644-298G>T) | |
| 4 | g.154586008C>G | CA358529125 | FGA | c.1421G>C (p.Gly474Ala) c.644-298G>C (n.644-298G>C) | |
| 4 | g.154586008C>T | CA358529121 | FGA | c.1421G>A (p.Gly474Asp) c.644-298G>A (n.644-298G>A) | gnomAD v4 |
| 4 | g.154586009del | CA2764115167 | FGA | c.1421del (p.Gly474ValfsTer10) c.644-298del (n.644-298del) | |
| 4 | g.154586009C>A | CA358529131 | FGA | c.1420G>T (p.Gly474Cys) c.644-299G>T (n.644-299G>T) | |
| 4 | g.154586009C= | CA1504943292 | FGA | c.1420G= (p.Gly474=) c.644-299G= (n.644-299G=) | |
| 4 | g.154586009C>G | CA108761171 | FGA | c.1420G>C (p.Gly474Arg) c.644-299G>C (n.644-299G>C) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586009C>T | CA358529129 | FGA | c.1420G>A (p.Gly474Ser) c.644-299G>A (n.644-299G>A) | COSMIC COSMIC |
| 4 | g.154586010A>C | CA358529133 | FGA | c.1419T>G (p.Asp473Glu) c.644-300T>G (n.644-300T>G) | |
| 4 | g.154586010A>G | CA442014055 | FGA | c.1419T>C (p.Asp473=) c.644-300T>C (n.644-300T>C) | |
| 4 | g.154586010A>T | CA358529134 | FGA | c.1419T>A (p.Asp473Glu) c.644-300T>A (n.644-300T>A) | |
| 4 | g.154586011T>A | CA358529138 | FGA | c.1418A>T (p.Asp473Val) c.644-301A>T (n.644-301A>T) | |
| 4 | g.154586011T>C | CA358529140 | FGA | c.1418A>G (p.Asp473Gly) c.644-301A>G (n.644-301A>G) | |
| 4 | g.154586011T>G | CA358529142 | FGA | c.1418A>C (p.Asp473Ala) c.644-301A>C (n.644-301A>C) | |
| 4 | g.154586012C>A | CA358529145 | FGA | c.1417G>T (p.Asp473Tyr) c.644-302G>T (n.644-302G>T) | |
| 4 | g.154586012C= | CA1504943293 | FGA | c.1417G= (p.Asp473=) c.644-302G= (n.644-302G=) | |
| 4 | g.154586012C>G | CA3115088 | FGA | c.1417G>C (p.Asp473His) c.644-302G>C (n.644-302G>C) | dbSNP ExAC |
| 4 | g.154586012C>T | CA3115087 | FGA | c.1417G>A (p.Asp473Asn) c.644-302G>A (n.644-302G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586013A= | CA1504943294 | FGA | c.1416T= (p.Pro472=) c.644-303T= (n.644-303T=) | |
| 4 | g.154586013A>C | CA442014058 | FGA | c.1416T>G (p.Pro472=) c.644-303T>G (n.644-303T>G) | gnomAD v4 |
| 4 | g.154586013A>G | CA442014059 | FGA | c.1416T>C (p.Pro472=) c.644-303T>C (n.644-303T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154586013A>T | CA442014060 | FGA | c.1416T>A (p.Pro472=) c.644-303T>A (n.644-303T>A) | |
| 4 | g.154586014G>A | CA358529149 | FGA | c.1415C>T (p.Pro472Leu) c.644-304C>T (n.644-304C>T) | gnomAD v4 |
| 4 | g.154586014G>C | CA358529152 | FGA | c.1415C>G (p.Pro472Arg) c.644-304C>G (n.644-304C>G) | |
| 4 | g.154586014G>T | CA358529154 | FGA | c.1415C>A (p.Pro472His) c.644-304C>A (n.644-304C>A) | dbSNP |
| 4 | g.154586015dup | CA915940508 | FGA | c.1415dup (p.Asp473Ter) c.644-304dup (n.644-304dup) | ClinVar |
| 4 | g.154586015G>A | CA358529156 | FGA | c.1414C>T (p.Pro472Ser) c.644-305C>T (n.644-305C>T) | |
| 4 | g.154586015G>C | CA358529161 | FGA | c.1414C>G (p.Pro472Ala) c.644-305C>G (n.644-305C>G) | |
| 4 | g.154586015G= | CA1504943295 | FGA | c.1414C= (p.Pro472=) c.644-305C= (n.644-305C=) | |
| 4 | g.154586015G>T | CA358529158 | FGA | c.1414C>A (p.Pro472Thr) c.644-305C>A (n.644-305C>A) | dbSNP gnomAD v4 |
| 4 | g.154586016A>C | CA442014062 | FGA | c.1413T>G (p.Gly471=) c.644-306T>G (n.644-306T>G) | |
| 4 | g.154586016A>G | CA442014063 | FGA | c.1413T>C (p.Gly471=) c.644-306T>C (n.644-306T>C) | |
| 4 | g.154586016A>T | CA442014064 | FGA | c.1413T>A (p.Gly471=) c.644-306T>A (n.644-306T>A) | |
| 4 | g.154586017C>A | CA358529164 | FGA | c.1412G>T (p.Gly471Val) c.644-307G>T (n.644-307G>T) | |
| 4 | g.154586017C= | CA1504943296 | FGA | c.1412G= (p.Gly471=) c.644-307G= (n.644-307G=) | |
| 4 | g.154586017C>G | CA358529166 | FGA | c.1412G>C (p.Gly471Ala) c.644-307G>C (n.644-307G>C) | |
| 4 | g.154586017C>T | CA358529168 | FGA | c.1412G>A (p.Gly471Asp) c.644-307G>A (n.644-307G>A) | dbSNP gnomAD v4 |
| 4 | g.154586018C>A | CA358529171 | FGA | c.1411G>T (p.Gly471Cys) c.644-308G>T (n.644-308G>T) | gnomAD v4 |
| 4 | g.154586018C= | CA1504943297 | FGA | c.1411G= (p.Gly471=) c.644-308G= (n.644-308G=) | |
| 4 | g.154586018C>G | CA358529172 | FGA | c.1411G>C (p.Gly471Arg) c.644-308G>C (n.644-308G>C) | |
| 4 | g.154586018C>T | CA358529173 | FGA | c.1411G>A (p.Gly471Ser) c.644-308G>A (n.644-308G>A) | |
| 4 | g.154586019A>C | CA358529174 | FGA | c.1410T>G (p.Ile470Met) c.644-309T>G (n.644-309T>G) | |
| 4 | g.154586019A>G | CA442014067 | FGA | c.1410T>C (p.Ile470=) c.644-309T>C (n.644-309T>C) | |
| 4 | g.154586019A>T | CA442014068 | FGA | c.1410T>A (p.Ile470=) c.644-309T>A (n.644-309T>A) | |
| 4 | g.154586020dup | CA3115089 | FGA | c.1410dup (p.Gly471TrpfsTer3) c.644-309dup (n.644-309dup) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586020A>C | CA358529177 | FGA | c.1409T>G (p.Ile470Ser) c.644-310T>G (n.644-310T>G) | |
| 4 | g.154586020A>G | CA358529178 | FGA | c.1409T>C (p.Ile470Thr) c.644-310T>C (n.644-310T>C) | dbSNP |
| 4 | g.154586020A>T | CA358529180 | FGA | c.1409T>A (p.Ile470Asn) c.644-310T>A (n.644-310T>A) | |
| 4 | g.154586021T>A | CA358529185 | FGA | c.1408A>T (p.Ile470Phe) c.644-311A>T (n.644-311A>T) | |
| 4 | g.154586021T>C | CA358529184 | FGA | c.1408A>G (p.Ile470Val) c.644-311A>G (n.644-311A>G) | dbSNP gnomAD v4 |
| 4 | g.154586021T>G | CA358529182 | FGA | c.1408A>C (p.Ile470Leu) c.644-311A>C (n.644-311A>C) | |
| 4 | g.154586022A= | CA1504943298 | FGA | c.1407T= (p.Val469=) c.644-312T= (n.644-312T=) | |
| 4 | g.154586022A>C | CA442014071 | FGA | c.1407T>G (p.Val469=) c.644-312T>G (n.644-312T>G) | |
| 4 | g.154586022A>G | CA442014069 | FGA | c.1407T>C (p.Val469=) c.644-312T>C (n.644-312T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154586022A>T | CA442014070 | FGA | c.1407T>A (p.Val469=) c.644-312T>A (n.644-312T>A) | |
| 4 | g.154586023A>C | CA358529191 | FGA | c.1406T>G (p.Val469Gly) c.644-313T>G (n.644-313T>G) | ClinVar dbSNP |
| 4 | g.154586023A>G | CA358529187 | FGA | c.1406T>C (p.Val469Ala) c.644-313T>C (n.644-313T>C) | |
| 4 | g.154586023A>T | CA358529189 | FGA | c.1406T>A (p.Val469Asp) c.644-313T>A (n.644-313T>A) | |
| 4 | g.154586024C>A | CA358529193 | FGA | c.1405G>T (p.Val469Phe) c.644-314G>T (n.644-314G>T) | dbSNP |
| 4 | g.154586024C= | CA1504943299 | FGA | c.1405G= (p.Val469=) c.644-314G= (n.644-314G=) | |
| 4 | g.154586024C>G | CA358529195 | FGA | c.1405G>C (p.Val469Leu) c.644-314G>C (n.644-314G>C) | |
| 4 | g.154586024C>T | CA108761183 | FGA | c.1405G>A (p.Val469Ile) c.644-314G>A (n.644-314G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586025A= | CA1504943300 | FGA | c.1404T= (p.Thr468=) c.644-315T= (n.644-315T=) | |
| 4 | g.154586025A>C | CA442014072 | FGA | c.1404T>G (p.Thr468=) c.644-315T>G (n.644-315T>G) | |
| 4 | g.154586025A>G | CA442014073 | FGA | c.1404T>C (p.Thr468=) c.644-315T>C (n.644-315T>C) | |
| 4 | g.154586025A>T | CA3115090 | FGA | c.1404T>A (p.Thr468=) c.644-315T>A (n.644-315T>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586026G>A | CA358529204 | FGA | c.1403C>T (p.Thr468Ile) c.644-316C>T (n.644-316C>T) | gnomAD v4 |
| 4 | g.154586026G>C | CA358529200 | FGA | c.1403C>G (p.Thr468Ser) c.644-316C>G (n.644-316C>G) | |
| 4 | g.154586026G>T | CA358529202 | FGA | c.1403C>A (p.Thr468Asn) c.644-316C>A (n.644-316C>A) | |
| 4 | g.154586027T>A | CA358529206 | FGA | c.1402A>T (p.Thr468Ser) c.644-317A>T (n.644-317A>T) | |
| 4 | g.154586027T>C | CA358529208 | FGA | c.1402A>G (p.Thr468Ala) c.644-317A>G (n.644-317A>G) | |
| 4 | g.154586027T>G | CA358529209 | FGA | c.1402A>C (p.Thr468Pro) c.644-317A>C (n.644-317A>C) | |
| 4 | g.154586028C>A | CA358529211 | FGA | c.1401G>T (p.Lys467Asn) c.644-318G>T (n.644-318G>T) | gnomAD v4 |
| 4 | g.154586028C>G | CA358529213 | FGA | c.1401G>C (p.Lys467Asn) c.644-318G>C (n.644-318G>C) | |
| 4 | g.154586028C>T | CA442014075 | FGA | c.1401G>A (p.Lys467=) c.644-318G>A (n.644-318G>A) | |
| 4 | g.154586029T>A | CA358529215 | FGA | c.1400A>T (p.Lys467Met) c.644-319A>T (n.644-319A>T) | |
| 4 | g.154586029T>C | CA358529218 | FGA | c.1400A>G (p.Lys467Arg) c.644-319A>G (n.644-319A>G) | |
| 4 | g.154586029T>G | CA358529216 | FGA | c.1400A>C (p.Lys467Thr) c.644-319A>C (n.644-319A>C) | |
| 4 | g.154586030T>A | CA358529221 | FGA | c.1399A>T (p.Lys467Ter) c.644-320A>T (n.644-320A>T) | |
| 4 | g.154586030T>C | CA358529222 | FGA | c.1399A>G (p.Lys467Glu) c.644-320A>G (n.644-320A>G) | gnomAD v4 |
| 4 | g.154586030T>G | CA358529224 | FGA | c.1399A>C (p.Lys467Gln) c.644-320A>C (n.644-320A>C) | dbSNP |
| 4 | g.154586031del | CA2695204034 | FGA | c.1398del (p.Lys467ArgfsTer17) c.644-321del (n.644-321del) | |
| 4 | g.154586031A= | CA1504943301 | FGA | c.1398T= (p.Thr466=) c.644-321T= (n.644-321T=) | |
| 4 | g.154586031A>C | CA442014076 | FGA | c.1398T>G (p.Thr466=) c.644-321T>G (n.644-321T>G) | |
| 4 | g.154586031A>G | CA442014077 | FGA | c.1398T>C (p.Thr466=) c.644-321T>C (n.644-321T>C) | dbSNP |
| 4 | g.154586031A>T | CA442014078 | FGA | c.1398T>A (p.Thr466=) c.644-321T>A (n.644-321T>A) | |
| 4 | g.154586032G>A | CA358529226 | FGA | c.1397C>T (p.Thr466Ile) c.644-322C>T (n.644-322C>T) | gnomAD v4 |
| 4 | g.154586032G>C | CA358529228 | FGA | c.1397C>G (p.Thr466Ser) c.644-322C>G (n.644-322C>G) | |
| 4 | g.154586032G>T | CA358529229 | FGA | c.1397C>A (p.Thr466Asn) c.644-322C>A (n.644-322C>A) | |
| 4 | g.154586033T>A | CA358529230 | FGA | c.1396A>T (p.Thr466Ser) c.644-323A>T (n.644-323A>T) | |
| 4 | g.154586033T>C | CA358529232 | FGA | c.1396A>G (p.Thr466Ala) c.644-323A>G (n.644-323A>G) | gnomAD v4 |
| 4 | g.154586033T>G | CA358529234 | FGA | c.1396A>C (p.Thr466Pro) c.644-323A>C (n.644-323A>C) | |
| 4 | g.154586034A= | CA1504943302 | FGA | c.1395T= (p.Val465=) c.644-324T= (n.644-324T=) | |
| 4 | g.154586034A>C | CA442014079 | FGA | c.1395T>G (p.Val465=) c.644-324T>G (n.644-324T>G) | |
| 4 | g.154586034A>G | CA442014080 | FGA | c.1395T>C (p.Val465=) c.644-324T>C (n.644-324T>C) | dbSNP |
| 4 | g.154586034A>T | CA442014081 | FGA | c.1395T>A (p.Val465=) c.644-324T>A (n.644-324T>A) | |
| 4 | g.154586035A>C | CA358529236 | FGA | c.1394T>G (p.Val465Gly) c.644-325T>G (n.644-325T>G) | |
| 4 | g.154586035A>G | CA358529238 | FGA | c.1394T>C (p.Val465Ala) c.644-325T>C (n.644-325T>C) | |
| 4 | g.154586035A>T | CA358529239 | FGA | c.1394T>A (p.Val465Asp) c.644-325T>A (n.644-325T>A) | |
| 4 | g.154586036C>A | CA358529243 | FGA | c.1393G>T (p.Val465Phe) c.644-326G>T (n.644-326G>T) | |
| 4 | g.154586036C= | CA1504943303 | FGA | c.1393G= (p.Val465=) c.644-326G= (n.644-326G=) | |
| 4 | g.154586036C>G | CA358529244 | FGA | c.1393G>C (p.Val465Leu) c.644-326G>C (n.644-326G>C) | gnomAD v4 |
| 4 | g.154586036C>T | CA3115091 | FGA | c.1393G>A (p.Val465Ile) c.644-326G>A (n.644-326G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586037G>A | CA442014082 | FGA | c.1392C>T (p.Thr464=) c.644-327C>T (n.644-327C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586037G>C | CA442014084 | FGA | c.1392C>G (p.Thr464=) c.644-327C>G (n.644-327C>G) | gnomAD v4 |
| 4 | g.154586037G= | CA1504943304 | FGA | c.1392C= (p.Thr464=) c.644-327C= (n.644-327C=) | |
| 4 | g.154586037G>T | CA3115092 | FGA | c.1392C>A (p.Thr464=) c.644-327C>A (n.644-327C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586037_154586038delinsTT | CA645540048 | FGA | c.1391_1392delinsAA (p.Thr464Lys) c.644-328_644-327delinsAA (n.644-328_644-327delinsAA) | COSMIC COSMIC |
| 4 | g.154586038G>A | CA358529247 | FGA | c.1391C>T (p.Thr464Ile) c.644-328C>T (n.644-328C>T) | |
| 4 | g.154586038G>C | CA358529249 | FGA | c.1391C>G (p.Thr464Ser) c.644-328C>G (n.644-328C>G) | |
| 4 | g.154586038G>T | CA358529251 | FGA | c.1391C>A (p.Thr464Asn) c.644-328C>A (n.644-328C>A) | |
| 4 | g.154586039T>A | CA358529253 | FGA | c.1390A>T (p.Thr464Ser) c.644-329A>T (n.644-329A>T) | |
| 4 | g.154586039T>C | CA358529254 | FGA | c.1390A>G (p.Thr464Ala) c.644-329A>G (n.644-329A>G) | |
| 4 | g.154586039T>G | CA358529255 | FGA | c.1390A>C (p.Thr464Pro) c.644-329A>C (n.644-329A>C) | |
| 4 | g.154586040T>A | CA358529257 | FGA | c.1389A>T (p.Lys463Asn) c.644-330A>T (n.644-330A>T) | |
| 4 | g.154586040T>C | CA442014087 | FGA | c.1389A>G (p.Lys463=) c.644-330A>G (n.644-330A>G) | |
| 4 | g.154586040T>G | CA358529256 | FGA | c.1389A>C (p.Lys463Asn) c.644-330A>C (n.644-330A>C) | |
| 4 | g.154586041T>A | CA358529258 | FGA | c.1388A>T (p.Lys463Ile) c.644-331A>T (n.644-331A>T) | |
| 4 | g.154586041T>C | CA358529259 | FGA | c.1388A>G (p.Lys463Arg) c.644-331A>G (n.644-331A>G) | |
| 4 | g.154586041T>G | CA358529260 | FGA | c.1388A>C (p.Lys463Thr) c.644-331A>C (n.644-331A>C) | |
| 4 | g.154586042T>A | CA358529261 | FGA | c.1387A>T (p.Lys463Ter) c.644-332A>T (n.644-332A>T) | |
| 4 | g.154586042T>C | CA358529262 | FGA | c.1387A>G (p.Lys463Glu) c.644-332A>G (n.644-332A>G) | gnomAD v4 |
| 4 | g.154586042T>G | CA358529263 | FGA | c.1387A>C (p.Lys463Gln) c.644-332A>C (n.644-332A>C) | COSMIC COSMIC |
| 4 | g.154586043A>C | CA442014091 | FGA | c.1386T>G (p.Ser462=) c.644-333T>G (n.644-333T>G) | |
| 4 | g.154586043A>G | CA442014093 | FGA | c.1386T>C (p.Ser462=) c.644-333T>C (n.644-333T>C) | |
| 4 | g.154586043A>T | CA442014095 | FGA | c.1386T>A (p.Ser462=) c.644-333T>A (n.644-333T>A) | |
| 4 | g.154586044G>A | CA358529264 | FGA | c.1385C>T (p.Ser462Phe) c.644-334C>T (n.644-334C>T) | |
| 4 | g.154586044G>C | CA358529266 | FGA | c.1385C>G (p.Ser462Cys) c.644-334C>G (n.644-334C>G) | |
| 4 | g.154586044G>T | CA358529265 | FGA | c.1385C>A (p.Ser462Tyr) c.644-334C>A (n.644-334C>A) | |
| 4 | g.154586045A>C | CA358529267 | FGA | c.1384T>G (p.Ser462Ala) c.644-335T>G (n.644-335T>G) | |
| 4 | g.154586045A>G | CA358529268 | FGA | c.1384T>C (p.Ser462Pro) c.644-335T>C (n.644-335T>C) | |
| 4 | g.154586045A>T | CA358529269 | FGA | c.1384T>A (p.Ser462Thr) c.644-335T>A (n.644-335T>A) | |
| 4 | g.154586046G>A | CA442014098 | FGA | c.1383C>T (p.Cys461=) c.644-336C>T (n.644-336C>T) | |
| 4 | g.154586046G>C | CA358529270 | FGA | c.1383C>G (p.Cys461Trp) c.644-336C>G (n.644-336C>G) | |
| 4 | g.154586046G>T | CA358529271 | FGA | c.1383C>A (p.Cys461Ter) c.644-336C>A (n.644-336C>A) | |
| 4 | g.154586047C>A | CA358529272 | FGA | c.1382G>T (p.Cys461Phe) c.644-337G>T (n.644-337G>T) | |
| 4 | g.154586047C>G | CA358529273 | FGA | c.1382G>C (p.Cys461Ser) c.644-337G>C (n.644-337G>C) | |
| 4 | g.154586047C>T | CA358529274 | FGA | c.1382G>A (p.Cys461Tyr) c.644-337G>A (n.644-337G>A) | gnomAD v4 |
| 4 | g.154586048A= | CA1504943305 | FGA | c.1381T= (p.Cys461=) c.644-338T= (n.644-338T=) | |
| 4 | g.154586048A>C | CA358529275 | FGA | c.1381T>G (p.Cys461Gly) c.644-338T>G (n.644-338T>G) | gnomAD v4 |
| 4 | g.154586048A>G | CA358529276 | FGA | c.1381T>C (p.Cys461Arg) c.644-338T>C (n.644-338T>C) | dbSNP gnomAD v4 |
| 4 | g.154586048A>T | CA358529277 | FGA | c.1381T>A (p.Cys461Ser) c.644-338T>A (n.644-338T>A) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586049T>A | CA442014104 | FGA | c.1380A>T (p.Ser460=) c.644-339A>T (n.644-339A>T) | |
| 4 | g.154586049T>C | CA442014102 | FGA | c.1380A>G (p.Ser460=) c.644-339A>G (n.644-339A>G) | gnomAD v4 |
| 4 | g.154586049T>G | CA3115093 | FGA | c.1380A>C (p.Ser460=) c.644-339A>C (n.644-339A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586049T= | CA1504943306 | FGA | c.1380A= (p.Ser460=) c.644-339A= (n.644-339A=) | |
| 4 | g.154586050G>A | CA358529278 | FGA | c.1379C>T (p.Ser460Leu) c.644-340C>T (n.644-340C>T) | COSMIC COSMIC |
| 4 | g.154586050G>C | CA358529280 | FGA | c.1379C>G (p.Ser460Ter) c.644-340C>G (n.644-340C>G) | gnomAD v4 |
| 4 | g.154586050G>T | CA358529279 | FGA | c.1379C>A (p.Ser460Ter) c.644-340C>A (n.644-340C>A) | |
| 4 | g.154586051A= | CA1504943307 | FGA | c.1378T= (p.Ser460=) c.644-341T= (n.644-341T=) | |
| 4 | g.154586051A>C | CA358529281 | FGA | c.1378T>G (p.Ser460Ala) c.644-341T>G (n.644-341T>G) | |
| 4 | g.154586051A>G | CA358529282 | FGA | c.1378T>C (p.Ser460Pro) c.644-341T>C (n.644-341T>C) | |
| 4 | g.154586051A>T | CA358529283 | FGA | c.1378T>A (p.Ser460Thr) c.644-341T>A (n.644-341T>A) | |
| 4 | g.154586052A>C | CA442014112 | FGA | c.1377T>G (p.Arg459=) c.644-342T>G (n.644-342T>G) | |
| 4 | g.154586052A>G | CA442014111 | FGA | c.1377T>C (p.Arg459=) c.644-342T>C (n.644-342T>C) | |
| 4 | g.154586052A>T | CA442014110 | FGA | c.1377T>A (p.Arg459=) c.644-342T>A (n.644-342T>A) | |
| 4 | g.154586055_154586057dup | CA1504943308 | FGA | c.1375_1377dup (p.Arg459_Ser460insArg) c.644-344_644-342dup (n.644-344_644-342dup) | dbSNP |
| 4 | g.154586053C>A | CA358529284 | FGA | c.1376G>T (p.Arg459Leu) c.644-343G>T (n.644-343G>T) | |
| 4 | g.154586053C= | CA1504943309 | FGA | c.1376G= (p.Arg459=) c.644-343G= (n.644-343G=) | |
| 4 | g.154586053C>G | CA358529285 | FGA | c.1376G>C (p.Arg459Pro) c.644-343G>C (n.644-343G>C) | |
| 4 | g.154586053C>T | CA3115094 | FGA | c.1376G>A (p.Arg459His) c.644-343G>A (n.644-343G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 4 | g.154586054G>A | CA358529286 | FGA | c.1375C>T (p.Arg459Cys) c.644-344C>T (n.644-344C>T) | COSMIC COSMIC |
| 4 | g.154586054G>C | CA358529287 | FGA | c.1375C>G (p.Arg459Gly) c.644-344C>G (n.644-344C>G) | |
| 4 | g.154586054G>T | CA358529288 | FGA | c.1375C>A (p.Arg459Ser) c.644-344C>A (n.644-344C>A) | |
| 4 | g.154586055A>C | CA442014115 | FGA | c.1374T>G (p.Arg458=) c.644-345T>G (n.644-345T>G) | |
| 4 | g.154586055A>G | CA442014119 | FGA | c.1374T>C (p.Arg458=) c.644-345T>C (n.644-345T>C) | |
| 4 | g.154586055A>T | CA442014117 | FGA | c.1374T>A (p.Arg458=) c.644-345T>A (n.644-345T>A) | |
| 4 | g.154586056C>A | CA358529289 | FGA | c.1373G>T (p.Arg458Leu) c.644-346G>T (n.644-346G>T) | |
| 4 | g.154586056C= | CA1504943310 | FGA | c.1373G= (p.Arg458=) c.644-346G= (n.644-346G=) | |
| 4 | g.154586056C>G | CA358529290 | FGA | c.1373G>C (p.Arg458Pro) c.644-346G>C (n.644-346G>C) | gnomAD v4 |
| 4 | g.154586056C>T | CA3115095 | FGA | c.1373G>A (p.Arg458His) c.644-346G>A (n.644-346G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586057G>A | CA16609673 | FGA | c.1372C>T (p.Arg458Cys) c.644-347C>T (n.644-347C>T) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 4 | g.154586057G>C | CA358529291 | FGA | c.1372C>G (p.Arg458Gly) c.644-347C>G (n.644-347C>G) | |
| 4 | g.154586057G= | CA1504943311 | FGA | c.1372C= (p.Arg458=) c.644-347C= (n.644-347C=) | |
| 4 | g.154586057G>T | CA358529292 | FGA | c.1372C>A (p.Arg458Ser) c.644-347C>A (n.644-347C>A) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154586058C>A | CA442014123 | FGA | c.1371G>T (p.Thr457=) c.644-348G>T (n.644-348G>T) | |
| 4 | g.154586058C= | CA1504943312 | FGA | c.1371G= (p.Thr457=) c.644-348G= (n.644-348G=) | |
| 4 | g.154586058C>G | CA3115097 | FGA | c.1371G>C (p.Thr457=) c.644-348G>C (n.644-348G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586058C>T | CA3115096 | FGA | c.1371G>A (p.Thr457=) c.644-348G>A (n.644-348G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586059G>A | CA3115098 | FGA | c.1370C>T (p.Thr457Met) c.644-349C>T (n.644-349C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 4 | g.154586059G>C | CA358529293 | FGA | c.1370C>G (p.Thr457Arg) c.644-349C>G (n.644-349C>G) | gnomAD v4 |
| 4 | g.154586059G= | CA1504943313 | FGA | c.1370C= (p.Thr457=) c.644-349C= (n.644-349C=) | |
| 4 | g.154586059G>T | CA358529294 | FGA | c.1370C>A (p.Thr457Lys) c.644-349C>A (n.644-349C>A) | |
| 4 | g.154586060T>A | CA358529295 | FGA | c.1369A>T (p.Thr457Ser) c.644-350A>T (n.644-350A>T) | |
| 4 | g.154586060T>C | CA3115099 | FGA | c.1369A>G (p.Thr457Ala) c.644-350A>G (n.644-350A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586060T>G | CA358529296 | FGA | c.1369A>C (p.Thr457Pro) c.644-350A>C (n.644-350A>C) | |
| 4 | g.154586060T= | CA1504943314 | FGA | c.1369A= (p.Thr457=) c.644-350A= (n.644-350A=) | |
| 4 | g.154586061G>A | CA442014127 | FGA | c.1368C>T (p.Thr456=) c.644-351C>T (n.644-351C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586061G>C | CA442014129 | FGA | c.1368C>G (p.Thr456=) c.644-351C>G (n.644-351C>G) | |
| 4 | g.154586061G= | CA1504943315 | FGA | c.1368C= (p.Thr456=) c.644-351C= (n.644-351C=) | |
| 4 | g.154586061G>T | CA442014130 | FGA | c.1368C>A (p.Thr456=) c.644-351C>A (n.644-351C>A) | |
| 4 | g.154586062del | CA2672444947 | FGA | c.1368del (p.Thr457ArgfsTer27) c.644-351del (n.644-351del) | gnomAD v4 |
| 4 | g.154586062G>A | CA108761252 | FGA | c.1367C>T (p.Thr456Ile) c.644-352C>T (n.644-352C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586062G>C | CA358529297 | FGA | c.1367C>G (p.Thr456Ser) c.644-352C>G (n.644-352C>G) | |
| 4 | g.154586062G= | CA1504943316 | FGA | c.1367C= (p.Thr456=) c.644-352C= (n.644-352C=) | |
| 4 | g.154586062G>T | CA358529298 | FGA | c.1367C>A (p.Thr456Asn) c.644-352C>A (n.644-352C>A) | gnomAD v4 |
| 4 | g.154586063T>A | CA358529300 | FGA | c.1366A>T (p.Thr456Ser) c.644-353A>T (n.644-353A>T) | |
| 4 | g.154586063T>C | CA3115100 | FGA | c.1366A>G (p.Thr456Ala) c.644-353A>G (n.644-353A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586063T>G | CA358529299 | FGA | c.1366A>C (p.Thr456Pro) c.644-353A>C (n.644-353A>C) | |
| 4 | g.154586063T= | CA1504943317 | FGA | c.1366A= (p.Thr456=) c.644-353A= (n.644-353A=) | |
| 4 | g.154586064G>A | CA442014134 | FGA | c.1365C>T (p.Thr455=) c.644-354C>T (n.644-354C>T) | |
| 4 | g.154586064G>C | CA442014135 | FGA | c.1365C>G (p.Thr455=) c.644-354C>G (n.644-354C>G) | |
| 4 | g.154586064G>T | CA442014136 | FGA | c.1365C>A (p.Thr455=) c.644-354C>A (n.644-354C>A) | |
| 4 | g.154586065G>A | CA358529301 | FGA | c.1364C>T (p.Thr455Ile) c.644-355C>T (n.644-355C>T) | gnomAD v4 |
| 4 | g.154586065G>C | CA358529303 | FGA | c.1364C>G (p.Thr455Ser) c.644-355C>G (n.644-355C>G) | dbSNP gnomAD v4 |
| 4 | g.154586065G= | CA1504943318 | FGA | c.1364C= (p.Thr455=) c.644-355C= (n.644-355C=) | |
| 4 | g.154586065G>T | CA358529302 | FGA | c.1364C>A (p.Thr455Asn) c.644-355C>A (n.644-355C>A) | |
| 4 | g.154586067_154586069del | CA2672444953 | FGA | c.1362_1364del (p.Thr455del) c.644-357_644-355del (n.644-357_644-355del) | gnomAD v4 |
| 4 | g.154586066T>A | CA358529304 | FGA | c.1363A>T (p.Thr455Ser) c.644-356A>T (n.644-356A>T) | |
| 4 | g.154586066T>C | CA358529306 | FGA | c.1363A>G (p.Thr455Ala) c.644-356A>G (n.644-356A>G) | |
| 4 | g.154586066T>G | CA358529305 | FGA | c.1363A>C (p.Thr455Pro) c.644-356A>C (n.644-356A>C) | |
| 4 | g.154586067T>A | CA442014138 | FGA | c.1362A>T (p.Thr454=) c.644-357A>T (n.644-357A>T) | |
| 4 | g.154586067T>C | CA442014140 | FGA | c.1362A>G (p.Thr454=) c.644-357A>G (n.644-357A>G) | |
| 4 | g.154586067T>G | CA442014142 | FGA | c.1362A>C (p.Thr454=) c.644-357A>C (n.644-357A>C) | |
| 4 | g.154586068G>A | CA358529307 | FGA | c.1361C>T (p.Thr454Ile) c.644-358C>T (n.644-358C>T) | |
| 4 | g.154586068G>C | CA358529309 | FGA | c.1361C>G (p.Thr454Arg) c.644-358C>G (n.644-358C>G) | |
| 4 | g.154586068G= | CA1504943319 | FGA | c.1361C= (p.Thr454=) c.644-358C= (n.644-358C=) | |
| 4 | g.154586068G>T | CA358529308 | FGA | c.1361C>A (p.Thr454Lys) c.644-358C>A (n.644-358C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586069T>A | CA358529310 | FGA | c.1360A>T (p.Thr454Ser) c.644-359A>T (n.644-359A>T) | |
| 4 | g.154586069T>C | CA358529311 | FGA | c.1360A>G (p.Thr454Ala) c.644-359A>G (n.644-359A>G) | |
| 4 | g.154586069T>G | CA3115101 | FGA | c.1360A>C (p.Thr454Pro) c.644-359A>C (n.644-359A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154586069T= | CA1504943320 | FGA | c.1360A= (p.Thr454=) c.644-359A= (n.644-359A=) | |
| 4 | g.154586070G>A | CA442014148 | FGA | c.1359C>T (p.Ser453=) c.644-360C>T (n.644-360C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586070G>C | CA358529312 | FGA | c.1359C>G (p.Ser453Arg) c.644-360C>G (n.644-360C>G) | |
| 4 | g.154586070G= | CA1504943321 | FGA | c.1359C= (p.Ser453=) c.644-360C= (n.644-360C=) | |
| 4 | g.154586070G>T | CA358529313 | FGA | c.1359C>A (p.Ser453Arg) c.644-360C>A (n.644-360C>A) | |
| 4 | g.154586071C>A | CA358529314 | FGA | c.1358G>T (p.Ser453Ile) c.644-361G>T (n.644-361G>T) | |
| 4 | g.154586071C= | CA1504943322 | FGA | c.1358G= (p.Ser453=) c.644-361G= (n.644-361G=) | |
| 4 | g.154586071C>G | CA358529315 | FGA | c.1358G>C (p.Ser453Thr) c.644-361G>C (n.644-361G>C) | |
| 4 | g.154586071C>T | CA126479 | FGA | c.1358G>A (p.Ser453Asn) c.644-361G>A (n.644-361G>A) | ClinVar dbSNP |
| 4 | g.154586072T>A | CA358529316 | FGA | c.1357A>T (p.Ser453Cys) c.644-362A>T (n.644-362A>T) | |
| 4 | g.154586072T>C | CA358529317 | FGA | c.1357A>G (p.Ser453Gly) c.644-362A>G (n.644-362A>G) | dbSNP gnomAD v4 |
| 4 | g.154586072T>G | CA358529318 | FGA | c.1357A>C (p.Ser453Arg) c.644-362A>C (n.644-362A>C) | |
| 4 | g.154586072T= | CA1504943323 | FGA | c.1357A= (p.Ser453=) c.644-362A= (n.644-362A=) | |
| 4 | g.154586073A>C | CA442014152 | FGA | c.1356T>G (p.Gly452=) c.644-363T>G (n.644-363T>G) | |
| 4 | g.154586073A>G | CA442014154 | FGA | c.1356T>C (p.Gly452=) c.644-363T>C (n.644-363T>C) | |
| 4 | g.154586073A>T | CA442014155 | FGA | c.1356T>A (p.Gly452=) c.644-363T>A (n.644-363T>A) | |
| 4 | g.154586076_154586085del | CA2672444954 | FGA | c.1347_1356del (p.Thr450AlafsTer?) c.644-372_644-363del (n.644-372_644-363del) | gnomAD v4 |
| 4 | g.154586074C>A | CA358529319 | FGA | c.1355G>T (p.Gly452Val) c.644-364G>T (n.644-364G>T) | COSMIC |
| 4 | g.154586074C= | CA1504943324 | FGA | c.1355G= (p.Gly452=) c.644-364G= (n.644-364G=) | |
| 4 | g.154586074C>G | CA358529320 | FGA | c.1355G>C (p.Gly452Ala) c.644-364G>C (n.644-364G>C) | dbSNP |
| 4 | g.154586074C>T | CA358529321 | FGA | c.1355G>A (p.Gly452Asp) c.644-364G>A (n.644-364G>A) | |
| 4 | g.154586075C>A | CA358529324 | FGA | c.1354G>T (p.Gly452Cys) c.644-365G>T (n.644-365G>T) | dbSNP |
| 4 | g.154586075C= | CA1504943325 | FGA | c.1354G= (p.Gly452=) c.644-365G= (n.644-365G=) | |
| 4 | g.154586075C>G | CA358529322 | FGA | c.1354G>C (p.Gly452Arg) c.644-365G>C (n.644-365G>C) | |
| 4 | g.154586075C>T | CA358529323 | FGA | c.1354G>A (p.Gly452Ser) c.644-365G>A (n.644-365G>A) | gnomAD v4 |
| 4 | g.154586076A>C | CA442014163 | FGA | c.1353T>G (p.Ser451=) c.644-366T>G (n.644-366T>G) | |
| 4 | g.154586076A>G | CA442014161 | FGA | c.1353T>C (p.Ser451=) c.644-366T>C (n.644-366T>C) | gnomAD v4 |
| 4 | g.154586076A>T | CA442014162 | FGA | c.1353T>A (p.Ser451=) c.644-366T>A (n.644-366T>A) | |
| 4 | g.154586077G>A | CA358529325 | FGA | c.1352C>T (p.Ser451Phe) c.644-367C>T (n.644-367C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586077G>C | CA358529326 | FGA | c.1352C>G (p.Ser451Cys) c.644-367C>G (n.644-367C>G) | |
| 4 | g.154586077G= | CA1504943326 | FGA | c.1352C= (p.Ser451=) c.644-367C= (n.644-367C=) | |
| 4 | g.154586077G>T | CA358529327 | FGA | c.1352C>A (p.Ser451Tyr) c.644-367C>A (n.644-367C>A) | |
| 4 | g.154586078A= | CA1504943327 | FGA | c.1351T= (p.Ser451=) c.644-368T= (n.644-368T=) | |
| 4 | g.154586078A>C | CA358529328 | FGA | c.1351T>G (p.Ser451Ala) c.644-368T>G (n.644-368T>G) | |
| 4 | g.154586078A>G | CA358529329 | FGA | c.1351T>C (p.Ser451Pro) c.644-368T>C (n.644-368T>C) | |
| 4 | g.154586078A>T | CA358529330 | FGA | c.1351T>A (p.Ser451Thr) c.644-368T>A (n.644-368T>A) | dbSNP |
| 4 | g.154586079G>A | CA108761276 | FGA | c.1350C>T (p.Thr450=) c.644-369C>T (n.644-369C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586079G>C | CA442014171 | FGA | c.1350C>G (p.Thr450=) c.644-369C>G (n.644-369C>G) | |
| 4 | g.154586079G= | CA1504943328 | FGA | c.1350C= (p.Thr450=) c.644-369C= (n.644-369C=) | |
| 4 | g.154586079G>T | CA442014174 | FGA | c.1350C>A (p.Thr450=) c.644-369C>A (n.644-369C>A) | |
| 4 | g.154586080G>A | CA358529331 | FGA | c.1349C>T (p.Thr450Ile) c.644-370C>T (n.644-370C>T) | |
| 4 | g.154586080G>C | CA358529332 | FGA | c.1349C>G (p.Thr450Ser) c.644-370C>G (n.644-370C>G) | |
| 4 | g.154586080G>T | CA358529333 | FGA | c.1349C>A (p.Thr450Asn) c.644-370C>A (n.644-370C>A) | |
| 4 | g.154586081T>A | CA358529336 | FGA | c.1348A>T (p.Thr450Ser) c.644-371A>T (n.644-371A>T) | |
| 4 | g.154586081T>C | CA358529335 | FGA | c.1348A>G (p.Thr450Ala) c.644-371A>G (n.644-371A>G) | |
| 4 | g.154586081T>G | CA358529334 | FGA | c.1348A>C (p.Thr450Pro) c.644-371A>C (n.644-371A>C) | |
| 4 | g.154586082G>A | CA3115102 | FGA | c.1347C>T (p.Val449=) c.644-372C>T (n.644-372C>T) | dbSNP ExAC |
| 4 | g.154586082G>C | CA442014182 | FGA | c.1347C>G (p.Val449=) c.644-372C>G (n.644-372C>G) | |
| 4 | g.154586082G= | CA1504943329 | FGA | c.1347C= (p.Val449=) c.644-372C= (n.644-372C=) | |
| 4 | g.154586082G>T | CA442014189 | FGA | c.1347C>A (p.Val449=) c.644-372C>A (n.644-372C>A) | gnomAD v3 gnomAD v4 |
| 4 | g.154586083A= | CA1504943330 | FGA | c.1346T= (p.Val449=) c.644-373T= (n.644-373T=) | |
| 4 | g.154586083A>C | CA358529337 | FGA | c.1346T>G (p.Val449Gly) c.644-373T>G (n.644-373T>G) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586083A>G | CA358529338 | FGA | c.1346T>C (p.Val449Ala) c.644-373T>C (n.644-373T>C) | |
| 4 | g.154586083A>T | CA358529339 | FGA | c.1346T>A (p.Val449Asp) c.644-373T>A (n.644-373T>A) | |
| 4 | g.154586084C>A | CA358529340 | FGA | c.1345G>T (p.Val449Phe) c.644-374G>T (n.644-374G>T) | |
| 4 | g.154586084C= | CA1504943331 | FGA | c.1345G= (p.Val449=) c.644-374G= (n.644-374G=) | |
| 4 | g.154586084C>G | CA358529341 | FGA | c.1345G>C (p.Val449Leu) c.644-374G>C (n.644-374G>C) | |
| 4 | g.154586084C>T | CA358529342 | FGA | c.1345G>A (p.Val449Ile) c.644-374G>A (n.644-374G>A) | dbSNP gnomAD v4 |
| 4 | g.154586085C>A | CA358529343 | FGA | c.1344G>T (p.Lys448Asn) c.644-375G>T (n.644-375G>T) | |
| 4 | g.154586085C= | CA1504943332 | FGA | c.1344G= (p.Lys448=) c.644-375G= (n.644-375G=) | |
| 4 | g.154586085C>G | CA358529344 | FGA | c.1344G>C (p.Lys448Asn) c.644-375G>C (n.644-375G>C) | |
| 4 | g.154586085C>T | CA108761283 | FGA | c.1344G>A (p.Lys448=) c.644-375G>A (n.644-375G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154586086T>A | CA358529345 | FGA | c.1343A>T (p.Lys448Met) c.644-376A>T (n.644-376A>T) | |
| 4 | g.154586086T>C | CA358529346 | FGA | c.1343A>G (p.Lys448Arg) c.644-376A>G (n.644-376A>G) | dbSNP |
| 4 | g.154586086T>G | CA358529347 | FGA | c.1343A>C (p.Lys448Thr) c.644-376A>C (n.644-376A>C) | |
| 4 | g.154586086T= | CA1504943333 | FGA | c.1343A= (p.Lys448=) c.644-376A= (n.644-376A=) | |
| 4 | g.154586087T>A | CA358529348 | FGA | c.1342A>T (p.Lys448Ter) c.644-377A>T (n.644-377A>T) | |
| 4 | g.154586087T>C | CA358529350 | FGA | c.1342A>G (p.Lys448Glu) c.644-377A>G (n.644-377A>G) | |
| 4 | g.154586087T>G | CA358529349 | FGA | c.1342A>C (p.Lys448Gln) c.644-377A>C (n.644-377A>C) | |
| 4 | g.154586088C>A | CA358529351 | FGA | c.1341G>T (p.Glu447Asp) c.644-378G>T (n.644-378G>T) | |
| 4 | g.154586088C= | CA1504943334 | FGA | c.1341G= (p.Glu447=) c.644-378G= (n.644-378G=) | |
| 4 | g.154586088C>G | CA3115103 | FGA | c.1341G>C (p.Glu447Asp) c.644-378G>C (n.644-378G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586088C>T | CA442014196 | FGA | c.1341G>A (p.Glu447=) c.644-378G>A (n.644-378G>A) | COSMIC COSMIC |
| 4 | g.154586089T>A | CA358529352 | FGA | c.1340A>T (p.Glu447Val) c.644-379A>T (n.644-379A>T) | |
| 4 | g.154586089T>C | CA358529353 | FGA | c.1340A>G (p.Glu447Gly) c.644-379A>G (n.644-379A>G) | |
| 4 | g.154586089T>G | CA358529354 | FGA | c.1340A>C (p.Glu447Ala) c.644-379A>C (n.644-379A>C) | |
| 4 | g.154586089_154586090delinsTC | CA1504943335 | FGA | c.1339_1340delinsGA (p.Glu447=) c.644-380_644-379delinsGA (n.644-380_644-379delinsGA) | |
| 4 | g.154586090del | CA1504943336 | FGA | c.1339del (p.Glu447ArgfsTer?) c.644-380del (n.644-380del) | dbSNP |
| 4 | g.154586090C>A | CA358529355 | FGA | c.1339G>T (p.Glu447Ter) c.644-380G>T (n.644-380G>T) | |
| 4 | g.154586090C= | CA1504943337 | FGA | c.1339G= (p.Glu447=) c.644-380G= (n.644-380G=) | |
| 4 | g.154586090C>G | CA3115104 | FGA | c.1339G>C (p.Glu447Gln) c.644-380G>C (n.644-380G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586090C>T | CA358529356 | FGA | c.1339G>A (p.Glu447Lys) c.644-380G>A (n.644-380G>A) | gnomAD v4 |
| 4 | g.154586091T>A | CA358529357 | FGA | c.1338A>T (p.Lys446Asn) c.644-381A>T (n.644-381A>T) | |
| 4 | g.154586091T>C | CA442014204 | FGA | c.1338A>G (p.Lys446=) c.644-381A>G (n.644-381A>G) | |
| 4 | g.154586091T>G | CA358529358 | FGA | c.1338A>C (p.Lys446Asn) c.644-381A>C (n.644-381A>C) | |
| 4 | g.154586092T>A | CA358529361 | FGA | c.1337A>T (p.Lys446Ile) c.644-382A>T (n.644-382A>T) | |
| 4 | g.154586092T>C | CA358529360 | FGA | c.1337A>G (p.Lys446Arg) c.644-382A>G (n.644-382A>G) | |
| 4 | g.154586092T>G | CA358529359 | FGA | c.1337A>C (p.Lys446Thr) c.644-382A>C (n.644-382A>C) | |
| 4 | g.154586093T>A | CA358529362 | FGA | c.1336A>T (p.Lys446Ter) c.644-383A>T (n.644-383A>T) | |
| 4 | g.154586093T>C | CA108761292 | FGA | c.1336A>G (p.Lys446Glu) c.644-383A>G (n.644-383A>G) | dbSNP |
| 4 | g.154586093T>G | CA358529363 | FGA | c.1336A>C (p.Lys446Gln) c.644-383A>C (n.644-383A>C) | |
| 4 | g.154586093T= | CA1504943338 | FGA | c.1336A= (p.Lys446=) c.644-383A= (n.644-383A=) | |
| 4 | g.154586094A>C | CA442014211 | FGA | c.1335T>G (p.Gly445=) c.644-384T>G (n.644-384T>G) | |
| 4 | g.154586094A>G | CA442014214 | FGA | c.1335T>C (p.Gly445=) c.644-384T>C (n.644-384T>C) | |
| 4 | g.154586094A>T | CA442014215 | FGA | c.1335T>A (p.Gly445=) c.644-384T>A (n.644-384T>A) |