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.154585894C>A | CA358528621 | FGA | c.1535G>T (p.Arg512Met) c.644-184G>T (n.644-184G>T) | |
| 4 | g.154585894C>G | CA358528622 | FGA | c.1535G>C (p.Arg512Thr) c.644-184G>C (n.644-184G>C) | |
| 4 | g.154585894C>T | CA358528624 | FGA | c.1535G>A (p.Arg512Lys) c.644-184G>A (n.644-184G>A) | gnomAD v4 |
| 4 | g.154585895T>A | CA358528626 | FGA | c.1534A>T (p.Arg512Trp) c.644-185A>T (n.644-185A>T) | |
| 4 | g.154585895T>C | CA358528628 | FGA | c.1534A>G (p.Arg512Gly) c.644-185A>G (n.644-185A>G) | |
| 4 | g.154585895T>G | CA442013987 | FGA | c.1534A>C (p.Arg512=) c.644-185A>C (n.644-185A>C) | |
| 4 | g.154585896A>C | CA358528630 | FGA | c.1533T>G (p.His511Gln) c.644-186T>G (n.644-186T>G) | |
| 4 | g.154585896A>G | CA442013988 | FGA | c.1533T>C (p.His511=) c.644-186T>C (n.644-186T>C) | |
| 4 | g.154585896A>T | CA358528631 | FGA | c.1533T>A (p.His511Gln) c.644-186T>A (n.644-186T>A) | |
| 4 | g.154585897T>A | CA358528633 | FGA | c.1532A>T (p.His511Leu) c.644-187A>T (n.644-187A>T) | gnomAD v4 |
| 4 | g.154585897T>C | CA358528635 | FGA | c.1532A>G (p.His511Arg) c.644-187A>G (n.644-187A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585897T>G | CA358528636 | FGA | c.1532A>C (p.His511Pro) c.644-187A>C (n.644-187A>C) | |
| 4 | g.154585897T= | CA1504943244 | FGA | c.1532A= (p.His511=) c.644-187A= (n.644-187A=) | |
| 4 | g.154585897dup | CA2578217776 | FGA | c.1532dup (p.His511GlnfsTer2) c.644-187dup (n.644-187dup) | gnomAD v4 |
| 4 | g.154585898G>A | CA358528637 | FGA | c.1531C>T (p.His511Tyr) c.644-188C>T (n.644-188C>T) | |
| 4 | g.154585898G>C | CA358528638 | FGA | c.1531C>G (p.His511Asp) c.644-188C>G (n.644-188C>G) | |
| 4 | g.154585898G>T | CA358528640 | FGA | c.1531C>A (p.His511Asn) c.644-188C>A (n.644-188C>A) | |
| 4 | g.154585899G>A | CA442013989 | FGA | c.1530C>T (p.Arg510=) c.644-189C>T (n.644-189C>T) | |
| 4 | g.154585899G>C | CA442013990 | FGA | c.1530C>G (p.Arg510=) c.644-189C>G (n.644-189C>G) | |
| 4 | g.154585899G>T | CA442013991 | FGA | c.1530C>A (p.Arg510=) c.644-189C>A (n.644-189C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585900C>A | CA358528645 | FGA | c.1529G>T (p.Arg510Leu) c.644-190G>T (n.644-190G>T) | dbSNP gnomAD v4 |
| 4 | g.154585900C= | CA1504943245 | FGA | c.1529G= (p.Arg510=) c.644-190G= (n.644-190G=) | |
| 4 | g.154585900C>G | CA358528642 | FGA | c.1529G>C (p.Arg510Pro) c.644-190G>C (n.644-190G>C) | |
| 4 | g.154585900C>T | CA3115076 | FGA | c.1529G>A (p.Arg510His) c.644-190G>A (n.644-190G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585901G>A | CA358528650 | FGA | c.1528C>T (p.Arg510Cys) c.644-191C>T (n.644-191C>T) | gnomAD v4 |
| 4 | g.154585901G>C | CA358528648 | FGA | c.1528C>G (p.Arg510Gly) c.644-191C>G (n.644-191C>G) | |
| 4 | g.154585901G>T | CA358528653 | FGA | c.1528C>A (p.Arg510Ser) c.644-191C>A (n.644-191C>A) | |
| 4 | g.154585902G>A | CA442013992 | FGA | c.1527C>T (p.Phe509=) c.644-192C>T (n.644-192C>T) | COSMIC COSMIC |
| 4 | g.154585902G>C | CA358528655 | FGA | c.1527C>G (p.Phe509Leu) c.644-192C>G (n.644-192C>G) | |
| 4 | g.154585902G= | CA1504943246 | FGA | c.1527C= (p.Phe509=) c.644-192C= (n.644-192C=) | |
| 4 | g.154585902G>T | CA358528658 | FGA | c.1527C>A (p.Phe509Leu) c.644-192C>A (n.644-192C>A) | |
| 4 | g.154585903A>C | CA358528663 | FGA | c.1526T>G (p.Phe509Cys) c.644-193T>G (n.644-193T>G) | |
| 4 | g.154585903A>G | CA358528666 | FGA | c.1526T>C (p.Phe509Ser) c.644-193T>C (n.644-193T>C) | |
| 4 | g.154585903A>T | CA358528668 | FGA | c.1526T>A (p.Phe509Tyr) c.644-193T>A (n.644-193T>A) | COSMIC |
| 4 | g.154585904dup | CA555971681 | FGA | c.1526dup (p.Arg510ProfsTer3) c.644-193dup (n.644-193dup) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585904A>C | CA358528673 | FGA | c.1525T>G (p.Phe509Val) c.644-194T>G (n.644-194T>G) | |
| 4 | g.154585904A>G | CA358528674 | FGA | c.1525T>C (p.Phe509Leu) c.644-194T>C (n.644-194T>C) | gnomAD v4 |
| 4 | g.154585904A>T | CA358528677 | FGA | c.1525T>A (p.Phe509Ile) c.644-194T>A (n.644-194T>A) | |
| 4 | g.154585905C>A | CA442013993 | FGA | c.1524G>T (p.Gly508=) c.644-195G>T (n.644-195G>T) | |
| 4 | g.154585905C= | CA1504943247 | FGA | c.1524G= (p.Gly508=) c.644-195G= (n.644-195G=) | |
| 4 | g.154585905C>G | CA442013994 | FGA | c.1524G>C (p.Gly508=) c.644-195G>C (n.644-195G>C) | |
| 4 | g.154585905C>T | CA442013995 | FGA | c.1524G>A (p.Gly508=) c.644-195G>A (n.644-195G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585906C>A | CA358528680 | FGA | c.1523G>T (p.Gly508Val) c.644-196G>T (n.644-196G>T) | gnomAD v4 |
| 4 | g.154585906C>G | CA358528682 | FGA | c.1523G>C (p.Gly508Ala) c.644-196G>C (n.644-196G>C) | |
| 4 | g.154585906C>T | CA358528684 | FGA | c.1523G>A (p.Gly508Glu) c.644-196G>A (n.644-196G>A) | dbSNP |
| 4 | g.154585907C>A | CA358528693 | FGA | c.1522G>T (p.Gly508Trp) c.644-197G>T (n.644-197G>T) | |
| 4 | g.154585907C>G | CA358528690 | FGA | c.1522G>C (p.Gly508Arg) c.644-197G>C (n.644-197G>C) | |
| 4 | g.154585907C>T | CA358528688 | FGA | c.1522G>A (p.Gly508Arg) c.644-197G>A (n.644-197G>A) | gnomAD v4 |
| 4 | g.154585908A>C | CA358528696 | FGA | c.1521T>G (p.Asp507Glu) c.644-198T>G (n.644-198T>G) | |
| 4 | g.154585908A>G | CA442013996 | FGA | c.1521T>C (p.Asp507=) c.644-198T>C (n.644-198T>C) | |
| 4 | g.154585908A>T | CA358528698 | FGA | c.1521T>A (p.Asp507Glu) c.644-198T>A (n.644-198T>A) | |
| 4 | g.154585909T>A | CA358528703 | FGA | c.1520A>T (p.Asp507Val) c.644-199A>T (n.644-199A>T) | |
| 4 | g.154585909T>C | CA358528705 | FGA | c.1520A>G (p.Asp507Gly) c.644-199A>G (n.644-199A>G) | |
| 4 | g.154585909T>G | CA358528708 | FGA | c.1520A>C (p.Asp507Ala) c.644-199A>C (n.644-199A>C) | |
| 4 | g.154585910C>A | CA358528711 | FGA | c.1519G>T (p.Asp507Tyr) c.644-200G>T (n.644-200G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585910C= | CA1504943248 | FGA | c.1519G= (p.Asp507=) c.644-200G= (n.644-200G=) | |
| 4 | g.154585910C>G | CA358528714 | FGA | c.1519G>C (p.Asp507His) c.644-200G>C (n.644-200G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585910C>T | CA108761087 | FGA | c.1519G>A (p.Asp507Asn) c.644-200G>A (n.644-200G>A) | dbSNP gnomAD v4 |
| 4 | g.154585911C>A | CA108761091 | FGA | c.1518G>T (p.Leu506=) c.644-201G>T (n.644-201G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585911C= | CA1504943249 | FGA | c.1518G= (p.Leu506=) c.644-201G= (n.644-201G=) | |
| 4 | g.154585911C>G | CA442013998 | FGA | c.1518G>C (p.Leu506=) c.644-201G>C (n.644-201G>C) | |
| 4 | g.154585911C>T | CA442013997 | FGA | c.1518G>A (p.Leu506=) c.644-201G>A (n.644-201G>A) | COSMIC |
| 4 | g.154585912del | CA2695204032 | FGA | c.1517del (p.Leu506ArgfsTer?) c.644-202del (n.644-202del) | |
| 4 | g.154585912A>C | CA358528720 | FGA | c.1517T>G (p.Leu506Arg) c.644-202T>G (n.644-202T>G) | gnomAD v4 |
| 4 | g.154585912A>G | CA358528722 | FGA | c.1517T>C (p.Leu506Pro) c.644-202T>C (n.644-202T>C) | |
| 4 | g.154585912A>T | CA358528723 | FGA | c.1517T>A (p.Leu506Gln) c.644-202T>A (n.644-202T>A) | |
| 4 | g.154585913G>A | CA108761098 | FGA | c.1516C>T (p.Leu506=) c.644-203C>T (n.644-203C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585913G>C | CA358528725 | FGA | c.1516C>G (p.Leu506Val) c.644-203C>G (n.644-203C>G) | |
| 4 | g.154585913G= | CA1504943250 | FGA | c.1516C= (p.Leu506=) c.644-203C= (n.644-203C=) | |
| 4 | g.154585913G>T | CA358528726 | FGA | c.1516C>A (p.Leu506Met) c.644-203C>A (n.644-203C>A) | gnomAD v4 |
| 4 | g.154585914A>C | CA442013999 | FGA | c.1515T>G (p.Thr505=) c.644-204T>G (n.644-204T>G) | |
| 4 | g.154585914A>G | CA442014000 | FGA | c.1515T>C (p.Thr505=) c.644-204T>C (n.644-204T>C) | |
| 4 | g.154585914A>T | CA442014001 | FGA | c.1515T>A (p.Thr505=) c.644-204T>A (n.644-204T>A) | |
| 4 | g.154585915G>A | CA358528731 | FGA | c.1514C>T (p.Thr505Ile) c.644-205C>T (n.644-205C>T) | |
| 4 | g.154585915G>C | CA358528729 | FGA | c.1514C>G (p.Thr505Ser) c.644-205C>G (n.644-205C>G) | |
| 4 | g.154585915G= | CA1504943251 | FGA | c.1514C= (p.Thr505=) c.644-205C= (n.644-205C=) | |
| 4 | g.154585915G>T | CA358528728 | FGA | c.1514C>A (p.Thr505Asn) c.644-205C>A (n.644-205C>A) | |
| 4 | g.154585915_154585916insATT | CA917338622 | FGA | c.1513_1514insAAT (p.Thr505delinsLysSer) c.644-206_644-205insAAT (n.644-206_644-205insAAT) | dbSNP |
| 4 | g.154585916T>A | CA358528736 | FGA | c.1513A>T (p.Thr505Ser) c.644-206A>T (n.644-206A>T) | |
| 4 | g.154585916T>C | CA358528733 | FGA | c.1513A>G (p.Thr505Ala) c.644-206A>G (n.644-206A>G) | |
| 4 | g.154585916T>G | CA358528735 | FGA | c.1513A>C (p.Thr505Pro) c.644-206A>C (n.644-206A>C) | |
| 4 | g.154585917A= | CA1504943252 | FGA | c.1512T= (p.Gly504=) c.644-207T= (n.644-207T=) | |
| 4 | g.154585917A>C | CA442014002 | FGA | c.1512T>G (p.Gly504=) c.644-207T>G (n.644-207T>G) | |
| 4 | g.154585917A>G | CA442014003 | FGA | c.1512T>C (p.Gly504=) c.644-207T>C (n.644-207T>C) | |
| 4 | g.154585917A>T | CA442014004 | FGA | c.1512T>A (p.Gly504=) c.644-207T>A (n.644-207T>A) | |
| 4 | g.154585917_154585918insGCATGGCCTCTCTTGGTGCTATGTGTTCCTTCATGATCGGCTT | CA917338624 | FGA | c.1511_1512insAAGCCGATCATGAAGGAACACATAGCACCAAGAGAGGCCATGC (p.Thr505SerfsTer4) c.644-208_644-207insAAGCCGATCATGAAGGAACACATAGCACCAAGAGAGGCCATGC (n.644-208_644-207insAAGCCGATCATGAAGGAACACATAGCACCAAGAGAGGCCATGC) | dbSNP |
| 4 | g.154585918C>A | CA358528738 | FGA | c.1511G>T (p.Gly504Val) c.644-208G>T (n.644-208G>T) | |
| 4 | g.154585918C>G | CA358528739 | FGA | c.1511G>C (p.Gly504Ala) c.644-208G>C (n.644-208G>C) | gnomAD v4 |
| 4 | g.154585918C>T | CA358528741 | FGA | c.1511G>A (p.Gly504Asp) c.644-208G>A (n.644-208G>A) | |
| 4 | g.154585919C>A | CA358528743 | FGA | c.1510G>T (p.Gly504Cys) c.644-209G>T (n.644-209G>T) | |
| 4 | g.154585919C= | CA1504943253 | FGA | c.1510G= (p.Gly504=) c.644-209G= (n.644-209G=) | |
| 4 | g.154585919C>G | CA358528744 | FGA | c.1510G>C (p.Gly504Arg) c.644-209G>C (n.644-209G>C) | |
| 4 | g.154585919C>T | CA358528746 | FGA | c.1510G>A (p.Gly504Ser) c.644-209G>A (n.644-209G>A) | dbSNP |
| 4 | g.154585920T>A | CA442014005 | FGA | c.1509A>T (p.Ile503=) c.644-210A>T (n.644-210A>T) | |
| 4 | g.154585920T>C | CA358528748 | FGA | c.1509A>G (p.Ile503Met) c.644-210A>G (n.644-210A>G) | |
| 4 | g.154585920T>G | CA442014006 | FGA | c.1509A>C (p.Ile503=) c.644-210A>C (n.644-210A>C) | |
| 4 | g.154585921A= | CA1504943254 | FGA | c.1508T= (p.Ile503=) c.644-211T= (n.644-211T=) | |
| 4 | g.154585921A>C | CA358528750 | FGA | c.1508T>G (p.Ile503Arg) c.644-211T>G (n.644-211T>G) | |
| 4 | g.154585921A>G | CA358528751 | FGA | c.1508T>C (p.Ile503Thr) c.644-211T>C (n.644-211T>C) | dbSNP |
| 4 | g.154585921A>T | CA358528753 | FGA | c.1508T>A (p.Ile503Lys) c.644-211T>A (n.644-211T>A) | |
| 4 | g.154585922T>A | CA358528757 | FGA | c.1507A>T (p.Ile503Leu) c.644-212A>T (n.644-212A>T) | |
| 4 | g.154585922T>C | CA358528759 | FGA | c.1507A>G (p.Ile503Val) c.644-212A>G (n.644-212A>G) | |
| 4 | g.154585922T>G | CA358528755 | FGA | c.1507A>C (p.Ile503Leu) c.644-212A>C (n.644-212A>C) | |
| 4 | g.154585923G>A | CA442014007 | FGA | c.1506C>T (p.Gly502=) c.644-213C>T (n.644-213C>T) | dbSNP |
| 4 | g.154585923G>C | CA442014008 | FGA | c.1506C>G (p.Gly502=) c.644-213C>G (n.644-213C>G) | |
| 4 | g.154585923G= | CA1504943255 | FGA | c.1506C= (p.Gly502=) c.644-213C= (n.644-213C=) | |
| 4 | g.154585923G>T | CA442014009 | FGA | c.1506C>A (p.Gly502=) c.644-213C>A (n.644-213C>A) | |
| 4 | g.154585924C>A | CA358528761 | FGA | c.1505G>T (p.Gly502Val) c.644-214G>T (n.644-214G>T) | |
| 4 | g.154585924C>G | CA358528763 | FGA | c.1505G>C (p.Gly502Ala) c.644-214G>C (n.644-214G>C) | |
| 4 | g.154585924C>T | CA358528765 | FGA | c.1505G>A (p.Gly502Asp) c.644-214G>A (n.644-214G>A) | |
| 4 | g.154585925C>A | CA358528768 | FGA | c.1504G>T (p.Gly502Cys) c.644-215G>T (n.644-215G>T) | |
| 4 | g.154585925C>G | CA358528770 | FGA | c.1504G>C (p.Gly502Arg) c.644-215G>C (n.644-215G>C) | |
| 4 | g.154585925C>T | CA358528772 | FGA | c.1504G>A (p.Gly502Ser) c.644-215G>A (n.644-215G>A) | COSMIC COSMIC |
| 4 | g.154585926A>C | CA442014010 | FGA | c.1503T>G (p.Ser501=) c.644-216T>G (n.644-216T>G) | |
| 4 | g.154585926A>G | CA442014011 | FGA | c.1503T>C (p.Ser501=) c.644-216T>C (n.644-216T>C) | |
| 4 | g.154585926A>T | CA442014012 | FGA | c.1503T>A (p.Ser501=) c.644-216T>A (n.644-216T>A) | |
| 4 | g.154585927G>A | CA358528774 | FGA | c.1502C>T (p.Ser501Phe) c.644-217C>T (n.644-217C>T) | |
| 4 | g.154585927G>C | CA358528776 | FGA | c.1502C>G (p.Ser501Cys) c.644-217C>G (n.644-217C>G) | |
| 4 | g.154585927G>T | CA358528775 | FGA | c.1502C>A (p.Ser501Tyr) c.644-217C>A (n.644-217C>A) | |
| 4 | g.154585928A>C | CA358528777 | FGA | c.1501T>G (p.Ser501Ala) c.644-218T>G (n.644-218T>G) | |
| 4 | g.154585928A>G | CA358528778 | FGA | c.1501T>C (p.Ser501Pro) c.644-218T>C (n.644-218T>C) | |
| 4 | g.154585928A>T | CA358528780 | FGA | c.1501T>A (p.Ser501Thr) c.644-218T>A (n.644-218T>A) | gnomAD v4 |
| 4 | g.154585929C>A | CA3115077 | FGA | c.1500G>T (p.Leu500Phe) c.644-219G>T (n.644-219G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154585929C= | CA1504943256 | FGA | c.1500G= (p.Leu500=) c.644-219G= (n.644-219G=) | |
| 4 | g.154585929C>G | CA358528783 | FGA | c.1500G>C (p.Leu500Phe) c.644-219G>C (n.644-219G>C) | |
| 4 | g.154585929C>T | CA442014014 | FGA | c.1500G>A (p.Leu500=) c.644-219G>A (n.644-219G>A) | |
| 4 | g.154585930A>C | CA358528787 | FGA | c.1499T>G (p.Leu500Trp) c.644-220T>G (n.644-220T>G) | |
| 4 | g.154585930A>G | CA358528789 | FGA | c.1499T>C (p.Leu500Ser) c.644-220T>C (n.644-220T>C) | |
| 4 | g.154585930A>T | CA358528786 | FGA | c.1499T>A (p.Leu500Ter) c.644-220T>A (n.644-220T>A) | |
| 4 | g.154585931A= | CA1504943257 | FGA | c.1498T= (p.Leu500=) c.644-221T= (n.644-221T=) | |
| 4 | g.154585931A>C | CA358528791 | FGA | c.1498T>G (p.Leu500Val) c.644-221T>G (n.644-221T>G) | |
| 4 | g.154585931A>G | CA442014016 | FGA | c.1498T>C (p.Leu500=) c.644-221T>C (n.644-221T>C) | |
| 4 | g.154585931A>T | CA358528792 | FGA | c.1498T>A (p.Leu500Met) c.644-221T>A (n.644-221T>A) | dbSNP |
| 4 | g.154585931_154585932insCCCCAAACACACCCAACACA | CA2764115160 | FGA | c.1498_1499insGTGTTGGGTGTGTTTGGGGT (p.Leu500CysfsTer11) c.644-221_644-220insGTGTTGGGTGTGTTTGGGGT (n.644-221_644-220insGTGTTGGGTGTGTTTGGGGT) | |
| 4 | g.154585932T>A | CA442014017 | FGA | c.1497A>T (p.Thr499=) c.644-222A>T (n.644-222A>T) | |
| 4 | g.154585932T>C | CA3115078 | FGA | c.1497A>G (p.Thr499=) c.644-222A>G (n.644-222A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154585932T>G | CA442014018 | FGA | c.1497A>C (p.Thr499=) c.644-222A>C (n.644-222A>C) | |
| 4 | g.154585932T= | CA1504943258 | FGA | c.1497A= (p.Thr499=) c.644-222A= (n.644-222A=) | |
| 4 | g.154585934_154585948del | CA2564714257 | FGA | c.1483_1497del (p.Met495_Thr499del) c.644-236_644-222del (n.644-236_644-222del) | gnomAD v4 |
| 4 | g.154585933G>A | CA358528795 | FGA | c.1496C>T (p.Thr499Ile) c.644-223C>T (n.644-223C>T) | |
| 4 | g.154585933G>C | CA358528797 | FGA | c.1496C>G (p.Thr499Arg) c.644-223C>G (n.644-223C>G) | |
| 4 | g.154585933G>T | CA358528798 | FGA | c.1496C>A (p.Thr499Lys) c.644-223C>A (n.644-223C>A) | |
| 4 | g.154585934T>A | CA358528801 | FGA | c.1495A>T (p.Thr499Ser) c.644-224A>T (n.644-224A>T) | |
| 4 | g.154585934T>C | CA358528802 | FGA | c.1495A>G (p.Thr499Ala) c.644-224A>G (n.644-224A>G) | |
| 4 | g.154585934T>G | CA358528804 | FGA | c.1495A>C (p.Thr499Pro) c.644-224A>C (n.644-224A>C) | dbSNP gnomAD v4 |
| 4 | g.154585934T= | CA1504943259 | FGA | c.1495A= (p.Thr499=) c.644-224A= (n.644-224A=) | |
| 4 | g.154585939_154585951del | CA2672444883 | FGA | c.1483_1495del (p.Met495HisfsTer5) c.644-236_644-224del (n.644-236_644-224del) | ClinVar gnomAD v4 |
| 4 | g.154585935G>A | CA3115079 | FGA | c.1494C>T (p.Gly498=) c.644-225C>T (n.644-225C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 4 | g.154585935G>C | CA442014022 | FGA | c.1494C>G (p.Gly498=) c.644-225C>G (n.644-225C>G) | |
| 4 | g.154585935G= | CA1504943260 | FGA | c.1494C= (p.Gly498=) c.644-225C= (n.644-225C=) | |
| 4 | g.154585935G>T | CA442014023 | FGA | c.1494C>A (p.Gly498=) c.644-225C>A (n.644-225C>A) | |
| 4 | g.154585936C>A | CA358528807 | FGA | c.1493G>T (p.Gly498Val) c.644-226G>T (n.644-226G>T) | |
| 4 | g.154585936C= | CA1504943261 | FGA | c.1493G= (p.Gly498=) c.644-226G= (n.644-226G=) | |
| 4 | g.154585936C>G | CA358528809 | FGA | c.1493G>C (p.Gly498Ala) c.644-226G>C (n.644-226G>C) | |
| 4 | g.154585936C>T | CA3115080 | FGA | c.1493G>A (p.Gly498Asp) c.644-226G>A (n.644-226G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585936_154585937delinsAA | CA645540046 | FGA | c.1492_1493delinsTT (p.Gly498Phe) c.644-227_644-226delinsTT (n.644-227_644-226delinsTT) | COSMIC COSMIC |
| 4 | g.154585937C>A | CA358528815 | FGA | c.1492G>T (p.Gly498Cys) c.644-227G>T (n.644-227G>T) | |
| 4 | g.154585937C>G | CA358528813 | FGA | c.1492G>C (p.Gly498Arg) c.644-227G>C (n.644-227G>C) | |
| 4 | g.154585937C>T | CA358528812 | FGA | c.1492G>A (p.Gly498Ser) c.644-227G>A (n.644-227G>A) | |
| 4 | g.154585938T>A | CA358528817 | FGA | c.1491A>T (p.Leu497Phe) c.644-228A>T (n.644-228A>T) | |
| 4 | g.154585938T>C | CA442014026 | FGA | c.1491A>G (p.Leu497=) c.644-228A>G (n.644-228A>G) | |
| 4 | g.154585938T>G | CA358528819 | FGA | c.1491A>C (p.Leu497Phe) c.644-228A>C (n.644-228A>C) | |
| 4 | g.154585939A>C | CA358528821 | FGA | c.1490T>G (p.Leu497Ter) c.644-229T>G (n.644-229T>G) | |
| 4 | g.154585939A>G | CA358528822 | FGA | c.1490T>C (p.Leu497Ser) c.644-229T>C (n.644-229T>C) | |
| 4 | g.154585939A>T | CA358528824 | FGA | c.1490T>A (p.Leu497Ter) c.644-229T>A (n.644-229T>A) | |
| 4 | g.154585940A>C | CA358528826 | FGA | c.1489T>G (p.Leu497Val) c.644-230T>G (n.644-230T>G) | |
| 4 | g.154585940A>G | CA442014027 | FGA | c.1489T>C (p.Leu497=) c.644-230T>C (n.644-230T>C) | |
| 4 | g.154585940A>T | CA358528828 | FGA | c.1489T>A (p.Leu497Ile) c.644-230T>A (n.644-230T>A) | |
| 4 | g.154585941A= | CA1504943262 | FGA | c.1488T= (p.Asp496=) c.644-231T= (n.644-231T=) | |
| 4 | g.154585941A>C | CA3115081 | FGA | c.1488T>G (p.Asp496Glu) c.644-231T>G (n.644-231T>G) | dbSNP ExAC gnomAD v2 |
| 4 | g.154585941A>G | CA442014029 | FGA | c.1488T>C (p.Asp496=) c.644-231T>C (n.644-231T>C) | |
| 4 | g.154585941A>T | CA358528829 | FGA | c.1488T>A (p.Asp496Glu) c.644-231T>A (n.644-231T>A) | |
| 4 | g.154585942T>A | CA358528831 | FGA | c.1487A>T (p.Asp496Val) c.644-232A>T (n.644-232A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585942T>C | CA358528833 | FGA | c.1487A>G (p.Asp496Gly) c.644-232A>G (n.644-232A>G) | |
| 4 | g.154585942T>G | CA358528835 | FGA | c.1487A>C (p.Asp496Ala) c.644-232A>C (n.644-232A>C) | |
| 4 | g.154585942T= | CA1504943263 | FGA | c.1487A= (p.Asp496=) c.644-232A= (n.644-232A=) | |
| 4 | g.154585943C>A | CA358528839 | FGA | c.1486G>T (p.Asp496Tyr) c.644-233G>T (n.644-233G>T) | ClinVar dbSNP |
| 4 | g.154585943C>G | CA358528837 | FGA | c.1486G>C (p.Asp496His) c.644-233G>C (n.644-233G>C) | |
| 4 | g.154585943C>T | CA358528836 | FGA | c.1486G>A (p.Asp496Asn) c.644-233G>A (n.644-233G>A) | |
| 4 | g.154585944C>A | CA358528841 | FGA | c.1485G>T (p.Met495Ile) c.644-234G>T (n.644-234G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585944C= | CA1504943264 | FGA | c.1485G= (p.Met495=) c.644-234G= (n.644-234G=) | |
| 4 | g.154585944C>G | CA358528843 | FGA | c.1485G>C (p.Met495Ile) c.644-234G>C (n.644-234G>C) | |
| 4 | g.154585944C>T | CA108761119 | FGA | c.1485G>A (p.Met495Ile) c.644-234G>A (n.644-234G>A) | dbSNP |
| 4 | g.154585945A>C | CA358528846 | FGA | c.1484T>G (p.Met495Arg) c.644-235T>G (n.644-235T>G) | |
| 4 | g.154585945A>G | CA358528848 | FGA | c.1484T>C (p.Met495Thr) c.644-235T>C (n.644-235T>C) | |
| 4 | g.154585945A>T | CA358528850 | FGA | c.1484T>A (p.Met495Lys) c.644-235T>A (n.644-235T>A) | |
| 4 | g.154585946T>A | CA358528851 | FGA | c.1483A>T (p.Met495Leu) c.644-236A>T (n.644-236A>T) | |
| 4 | g.154585946T>C | CA108761121 | FGA | c.1483A>G (p.Met495Val) c.644-236A>G (n.644-236A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585946T>G | CA358528853 | FGA | c.1483A>C (p.Met495Leu) c.644-236A>C (n.644-236A>C) | |
| 4 | g.154585946T= | CA1504943265 | FGA | c.1483A= (p.Met495=) c.644-236A= (n.644-236A=) | |
| 4 | g.154585947T>A | CA442014034 | FGA | c.1482A>T (p.Ala494=) c.644-237A>T (n.644-237A>T) | |
| 4 | g.154585947T>C | CA108761125 | FGA | c.1482A>G (p.Ala494=) c.644-237A>G (n.644-237A>G) | dbSNP |
| 4 | g.154585947T>G | CA442014035 | FGA | c.1482A>C (p.Ala494=) c.644-237A>C (n.644-237A>C) | |
| 4 | g.154585947T= | CA1504943266 | FGA | c.1482A= (p.Ala494=) c.644-237A= (n.644-237A=) | |
| 4 | g.154585948G>A | CA358528856 | FGA | c.1481C>T (p.Ala494Val) c.644-238C>T (n.644-238C>T) | |
| 4 | g.154585948G>C | CA358528858 | FGA | c.1481C>G (p.Ala494Gly) c.644-238C>G (n.644-238C>G) | |
| 4 | g.154585948G>T | CA358528859 | FGA | c.1481C>A (p.Ala494Glu) c.644-238C>A (n.644-238C>A) | |
| 4 | g.154585949C>A | CA358528864 | FGA | c.1480G>T (p.Ala494Ser) c.644-239G>T (n.644-239G>T) | |
| 4 | g.154585949C>G | CA358528861 | FGA | c.1480G>C (p.Ala494Pro) c.644-239G>C (n.644-239G>C) | |
| 4 | g.154585949C>T | CA358528863 | FGA | c.1480G>A (p.Ala494Thr) c.644-239G>A (n.644-239G>A) | gnomAD v4 |
| 4 | g.154585950C>A | CA358528867 | FGA | c.1479G>T (p.Glu493Asp) c.644-240G>T (n.644-240G>T) | COSMIC COSMIC |
| 4 | g.154585950C= | CA1504943267 | FGA | c.1479G= (p.Glu493=) c.644-240G= (n.644-240G=) | |
| 4 | g.154585950C>G | CA358528868 | FGA | c.1479G>C (p.Glu493Asp) c.644-240G>C (n.644-240G>C) | |
| 4 | g.154585950C>T | CA442014039 | FGA | c.1479G>A (p.Glu493=) c.644-240G>A (n.644-240G>A) | dbSNP gnomAD v2 |
| 4 | g.154585951T>A | CA358528870 | FGA | c.1478A>T (p.Glu493Val) c.644-241A>T (n.644-241A>T) | |
| 4 | g.154585951T>C | CA358528872 | FGA | c.1478A>G (p.Glu493Gly) c.644-241A>G (n.644-241A>G) | |
| 4 | g.154585951T>G | CA358528874 | FGA | c.1478A>C (p.Glu493Ala) c.644-241A>C (n.644-241A>C) | |
| 4 | g.154585952C>A | CA358528875 | FGA | c.1477G>T (p.Glu493Ter) c.644-242G>T (n.644-242G>T) | |
| 4 | g.154585952C= | CA1504943268 | FGA | c.1477G= (p.Glu493=) c.644-242G= (n.644-242G=) | |
| 4 | g.154585952C>G | CA358528876 | FGA | c.1477G>C (p.Glu493Gln) c.644-242G>C (n.644-242G>C) | |
| 4 | g.154585952C>T | CA108761128 | FGA | c.1477G>A (p.Glu493Lys) c.644-242G>A (n.644-242G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585953G>A | CA3115082 | FGA | c.1476C>T (p.Pro492=) c.644-243C>T (n.644-243C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585953G>C | CA442014041 | FGA | c.1476C>G (p.Pro492=) c.644-243C>G (n.644-243C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585953G= | CA1504943269 | FGA | c.1476C= (p.Pro492=) c.644-243C= (n.644-243C=) | |
| 4 | g.154585953G>T | CA442014042 | FGA | c.1476C>A (p.Pro492=) c.644-243C>A (n.644-243C>A) | gnomAD v4 |
| 4 | g.154585954G>A | CA358528878 | FGA | c.1475C>T (p.Pro492Leu) c.644-244C>T (n.644-244C>T) | gnomAD v4 COSMIC COSMIC |
| 4 | g.154585954G>C | CA358528880 | FGA | c.1475C>G (p.Pro492Arg) c.644-244C>G (n.644-244C>G) | |
| 4 | g.154585954G>T | CA358528881 | FGA | c.1475C>A (p.Pro492His) c.644-244C>A (n.644-244C>A) | |
| 4 | g.154585955G>A | CA358528885 | FGA | c.1474C>T (p.Pro492Ser) c.644-245C>T (n.644-245C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 4 | g.154585955G>C | CA358528887 | FGA | c.1474C>G (p.Pro492Ala) c.644-245C>G (n.644-245C>G) | |
| 4 | g.154585955G= | CA1504943270 | FGA | c.1474C= (p.Pro492=) c.644-245C= (n.644-245C=) | |
| 4 | g.154585955G>T | CA358528883 | FGA | c.1474C>A (p.Pro492Thr) c.644-245C>A (n.644-245C>A) | |
| 4 | g.154585956A>C | CA358528889 | FGA | c.1473T>G (p.Cys491Trp) c.644-246T>G (n.644-246T>G) | |
| 4 | g.154585956A>G | CA442014044 | FGA | c.1473T>C (p.Cys491=) c.644-246T>C (n.644-246T>C) | |
| 4 | g.154585956A>T | CA358528890 | FGA | c.1473T>A (p.Cys491Ter) c.644-246T>A (n.644-246T>A) | |
| 4 | g.154585957C>A | CA358528892 | FGA | c.1472G>T (p.Cys491Phe) c.644-247G>T (n.644-247G>T) | |
| 4 | g.154585957C= | CA1504943271 | FGA | c.1472G= (p.Cys491=) c.644-247G= (n.644-247G=) | |
| 4 | g.154585957C>G | CA358528896 | FGA | c.1472G>C (p.Cys491Ser) c.644-247G>C (n.644-247G>C) | |
| 4 | g.154585957C>T | CA358528894 | FGA | c.1472G>A (p.Cys491Tyr) c.644-247G>A (n.644-247G>A) | ClinVar dbSNP gnomAD v4 |
| 4 | g.154585958A>C | CA358528898 | FGA | c.1471T>G (p.Cys491Gly) c.644-248T>G (n.644-248T>G) | |
| 4 | g.154585958A>G | CA358528900 | FGA | c.1471T>C (p.Cys491Arg) c.644-248T>C (n.644-248T>C) | |
| 4 | g.154585958A>T | CA358528902 | FGA | c.1471T>A (p.Cys491Ser) c.644-248T>A (n.644-248T>A) | |
| 4 | g.154585959G>A | CA442014046 | FGA | c.1470C>T (p.Asp490=) c.644-249C>T (n.644-249C>T) | |
| 4 | g.154585959G>C | CA358528903 | FGA | c.1470C>G (p.Asp490Glu) c.644-249C>G (n.644-249C>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585959G= | CA1504943272 | FGA | c.1470C= (p.Asp490=) c.644-249C= (n.644-249C=) | |
| 4 | g.154585959G>T | CA358528905 | FGA | c.1470C>A (p.Asp490Glu) c.644-249C>A (n.644-249C>A) | |
| 4 | g.154585960T>A | CA358528910 | FGA | c.1469A>T (p.Asp490Val) c.644-250A>T (n.644-250A>T) | dbSNP |
| 4 | g.154585960T>C | CA358528908 | FGA | c.1469A>G (p.Asp490Gly) c.644-250A>G (n.644-250A>G) | |
| 4 | g.154585960T>G | CA358528907 | FGA | c.1469A>C (p.Asp490Ala) c.644-250A>C (n.644-250A>C) | |
| 4 | g.154585960T= | CA1504943273 | FGA | c.1469A= (p.Asp490=) c.644-250A= (n.644-250A=) | |
| 4 | g.154585961C>A | CA358528912 | FGA | c.1468G>T (p.Asp490Tyr) c.644-251G>T (n.644-251G>T) | COSMIC COSMIC |
| 4 | g.154585961C= | CA1504943274 | FGA | c.1468G= (p.Asp490=) c.644-251G= (n.644-251G=) | |
| 4 | g.154585961C>G | CA358528914 | FGA | c.1468G>C (p.Asp490His) c.644-251G>C (n.644-251G>C) | |
| 4 | g.154585961C>T | CA358528916 | FGA | c.1468G>A (p.Asp490Asn) c.644-251G>A (n.644-251G>A) | dbSNP |
| 4 | g.154585962A>C | CA442014049 | FGA | c.1467T>G (p.Ser489=) c.644-252T>G (n.644-252T>G) | |
| 4 | g.154585962A>G | CA442014051 | FGA | c.1467T>C (p.Ser489=) c.644-252T>C (n.644-252T>C) | |
| 4 | g.154585962A>T | CA442014052 | FGA | c.1467T>A (p.Ser489=) c.644-252T>A (n.644-252T>A) | |
| 4 | g.154585963G>A | CA358528919 | FGA | c.1466C>T (p.Ser489Phe) c.644-253C>T (n.644-253C>T) | |
| 4 | g.154585963G>C | CA358528922 | FGA | c.1466C>G (p.Ser489Cys) c.644-253C>G (n.644-253C>G) | |
| 4 | g.154585963G>T | CA358528923 | FGA | c.1466C>A (p.Ser489Tyr) c.644-253C>A (n.644-253C>A) | |
| 4 | g.154585964A>C | CA358528926 | FGA | c.1465T>G (p.Ser489Ala) c.644-254T>G (n.644-254T>G) | |
| 4 | g.154585964A>G | CA358528929 | FGA | c.1465T>C (p.Ser489Pro) c.644-254T>C (n.644-254T>C) | |
| 4 | g.154585964A>T | CA358528928 | FGA | c.1465T>A (p.Ser489Thr) c.644-254T>A (n.644-254T>A) | |
| 4 | g.154585965A= | CA1504943275 | FGA | c.1464T= (p.Gly488=) c.644-255T= (n.644-255T=) | |
| 4 | g.154585965A>C | CA442014053 | FGA | c.1464T>G (p.Gly488=) c.644-255T>G (n.644-255T>G) | |
| 4 | g.154585965A>G | CA442014054 | FGA | c.1464T>C (p.Gly488=) c.644-255T>C (n.644-255T>C) | dbSNP gnomAD v4 |
| 4 | g.154585965A>T | CA442014056 | FGA | c.1464T>A (p.Gly488=) c.644-255T>A (n.644-255T>A) | |
| 4 | g.154585966C>A | CA358528932 | FGA | c.1463G>T (p.Gly488Val) c.644-256G>T (n.644-256G>T) | dbSNP gnomAD v4 |
| 4 | g.154585966C= | CA1504943276 | FGA | c.1463G= (p.Gly488=) c.644-256G= (n.644-256G=) | |
| 4 | g.154585966C>G | CA358528934 | FGA | c.1463G>C (p.Gly488Ala) c.644-256G>C (n.644-256G>C) | gnomAD v4 |
| 4 | g.154585966C>T | CA358528936 | FGA | c.1463G>A (p.Gly488Asp) c.644-256G>A (n.644-256G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585967C>A | CA358528938 | FGA | c.1462G>T (p.Gly488Cys) c.644-257G>T (n.644-257G>T) | |
| 4 | g.154585967C>G | CA358528939 | FGA | c.1462G>C (p.Gly488Arg) c.644-257G>C (n.644-257G>C) | |
| 4 | g.154585967C>T | CA358528941 | FGA | c.1462G>A (p.Gly488Ser) c.644-257G>A (n.644-257G>A) | |
| 4 | g.154585968A= | CA1504943277 | FGA | c.1461T= (p.Asp487=) c.644-258T= (n.644-258T=) | |
| 4 | g.154585968A>C | CA358528942 | FGA | c.1461T>G (p.Asp487Glu) c.644-258T>G (n.644-258T>G) | |
| 4 | g.154585968A>G | CA442014057 | FGA | c.1461T>C (p.Asp487=) c.644-258T>C (n.644-258T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585968A>T | CA358528943 | FGA | c.1461T>A (p.Asp487Glu) c.644-258T>A (n.644-258T>A) | |
| 4 | g.154585969T>A | CA358528945 | FGA | c.1460A>T (p.Asp487Val) c.644-259A>T (n.644-259A>T) | gnomAD v4 |
| 4 | g.154585969T>C | CA358528947 | FGA | c.1460A>G (p.Asp487Gly) c.644-259A>G (n.644-259A>G) | gnomAD v4 |
| 4 | g.154585969T>G | CA358528949 | FGA | c.1460A>C (p.Asp487Ala) c.644-259A>C (n.644-259A>C) | |
| 4 | g.154585970C>A | CA358528951 | FGA | c.1459G>T (p.Asp487Tyr) c.644-260G>T (n.644-260G>T) | gnomAD v4 |
| 4 | g.154585970C>G | CA358528953 | FGA | c.1459G>C (p.Asp487His) c.644-260G>C (n.644-260G>C) | |
| 4 | g.154585970C>T | CA358528952 | FGA | c.1459G>A (p.Asp487Asn) c.644-260G>A (n.644-260G>A) | |
| 4 | g.154585971T>A | CA358528954 | FGA | c.1458A>T (p.Glu486Asp) c.644-261A>T (n.644-261A>T) | |
| 4 | g.154585971T>C | CA442014061 | FGA | c.1458A>G (p.Glu486=) c.644-261A>G (n.644-261A>G) | |
| 4 | g.154585971T>G | CA358528956 | FGA | c.1458A>C (p.Glu486Asp) c.644-261A>C (n.644-261A>C) | |
| 4 | g.154585972T>A | CA358528959 | FGA | c.1457A>T (p.Glu486Val) c.644-262A>T (n.644-262A>T) | |
| 4 | g.154585972T>C | CA358528960 | FGA | c.1457A>G (p.Glu486Gly) c.644-262A>G (n.644-262A>G) | |
| 4 | g.154585972T>G | CA358528962 | FGA | c.1457A>C (p.Glu486Ala) c.644-262A>C (n.644-262A>C) | |
| 4 | g.154585973C>A | CA358528964 | FGA | c.1456G>T (p.Glu486Ter) c.644-263G>T (n.644-263G>T) | |
| 4 | g.154585973C= | CA1504943278 | FGA | c.1456G= (p.Glu486=) c.644-263G= (n.644-263G=) | |
| 4 | g.154585973C>G | CA358528965 | FGA | c.1456G>C (p.Glu486Gln) c.644-263G>C (n.644-263G>C) | |
| 4 | g.154585973C>T | CA108761138 | FGA | c.1456G>A (p.Glu486Lys) c.644-263G>A (n.644-263G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 4 | g.154585974G>A | CA3115083 | FGA | c.1455C>T (p.Ser485=) c.644-264C>T (n.644-264C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585974G>C | CA442014065 | FGA | c.1455C>G (p.Ser485=) c.644-264C>G (n.644-264C>G) | |
| 4 | g.154585974G= | CA1504943279 | FGA | c.1455C= (p.Ser485=) c.644-264C= (n.644-264C=) | |
| 4 | g.154585974G>T | CA442014066 | FGA | c.1455C>A (p.Ser485=) c.644-264C>A (n.644-264C>A) | |
| 4 | g.154585975G>A | CA358528968 | FGA | c.1454C>T (p.Ser485Phe) c.644-265C>T (n.644-265C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585975G>C | CA358528970 | FGA | c.1454C>G (p.Ser485Cys) c.644-265C>G (n.644-265C>G) | |
| 4 | g.154585975G= | CA1504943280 | FGA | c.1454C= (p.Ser485=) c.644-265C= (n.644-265C=) | |
| 4 | g.154585975G>T | CA358528972 | FGA | c.1454C>A (p.Ser485Tyr) c.644-265C>A (n.644-265C>A) | |
| 4 | g.154585976A= | CA1504943281 | FGA | c.1453T= (p.Ser485=) c.644-266T= (n.644-266T=) | |
| 4 | g.154585976A>C | CA358528979 | FGA | c.1453T>G (p.Ser485Ala) c.644-266T>G (n.644-266T>G) | |
| 4 | g.154585976A>G | CA108761145 | FGA | c.1453T>C (p.Ser485Pro) c.644-266T>C (n.644-266T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585976A>T | CA358528977 | FGA | c.1453T>A (p.Ser485Thr) c.644-266T>A (n.644-266T>A) | |
| 4 | g.154585977G>A | CA3115084 | FGA | c.1452C>T (p.Thr484=) c.644-267C>T (n.644-267C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 4 | g.154585977G>C | CA442014013 | FGA | c.1452C>G (p.Thr484=) c.644-267C>G (n.644-267C>G) | |
| 4 | g.154585977G= | CA1504943282 | FGA | c.1452C= (p.Thr484=) c.644-267C= (n.644-267C=) | |
| 4 | g.154585977G>T | CA442014015 | FGA | c.1452C>A (p.Thr484=) c.644-267C>A (n.644-267C>A) | |
| 4 | g.154585978del | CA2578217777 | FGA | c.1452del (p.Ser485ProfsTer13) c.644-267del (n.644-267del) | ClinVar gnomAD v4 |
| 4 | g.154585978G>A | CA3115085 | FGA | c.1451C>T (p.Thr484Ile) c.644-268C>T (n.644-268C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.154585978G>C | CA358528984 | FGA | c.1451C>G (p.Thr484Ser) c.644-268C>G (n.644-268C>G) | |
| 4 | g.154585978G= | CA1504943283 | FGA | c.1451C= (p.Thr484=) c.644-268C= (n.644-268C=) | |
| 4 | g.154585978G>T | CA358528986 | FGA | c.1451C>A (p.Thr484Asn) c.644-268C>A (n.644-268C>A) | |
| 4 | g.154585979T>A | CA358528988 | FGA | c.1450A>T (p.Thr484Ser) c.644-269A>T (n.644-269A>T) | |
| 4 | g.154585979T>C | CA358528989 | FGA | c.1450A>G (p.Thr484Ala) c.644-269A>G (n.644-269A>G) | dbSNP |
| 4 | g.154585979T>G | CA358528991 | FGA | c.1450A>C (p.Thr484Pro) c.644-269A>C (n.644-269A>C) | |
| 4 | g.154585980C>A | CA442014021 | FGA | c.1449G>T (p.Val483=) c.644-270G>T (n.644-270G>T) | |
| 4 | g.154585980C>G | CA442014020 | FGA | c.1449G>C (p.Val483=) c.644-270G>C (n.644-270G>C) | |
| 4 | g.154585980C>T | CA442014019 | FGA | c.1449G>A (p.Val483=) c.644-270G>A (n.644-270G>A) | |
| 4 | g.154585981A>C | CA358528993 | FGA | c.1448T>G (p.Val483Gly) c.644-271T>G (n.644-271T>G) | |
| 4 | g.154585981A>G | CA358528995 | FGA | c.1448T>C (p.Val483Ala) c.644-271T>C (n.644-271T>C) | |
| 4 | g.154585981A>T | CA358528997 | FGA | c.1448T>A (p.Val483Glu) c.644-271T>A (n.644-271T>A) | |
| 4 | g.154585982C>A | CA358529003 | FGA | c.1447G>T (p.Val483Leu) c.644-272G>T (n.644-272G>T) | gnomAD v4 |
| 4 | g.154585982C>G | CA358529001 | FGA | c.1447G>C (p.Val483Leu) c.644-272G>C (n.644-272G>C) | |
| 4 | g.154585982C>T | CA358528999 | FGA | c.1447G>A (p.Val483Met) c.644-272G>A (n.644-272G>A) | COSMIC COSMIC |
| 4 | g.154585983C>A | CA442014024 | FGA | c.1446G>T (p.Val482=) c.644-273G>T (n.644-273G>T) | |
| 4 | g.154585983C= | CA1504943284 | FGA | c.1446G= (p.Val482=) c.644-273G= (n.644-273G=) | |
| 4 | g.154585983C>G | CA442014025 | FGA | c.1446G>C (p.Val482=) c.644-273G>C (n.644-273G>C) | |
| 4 | g.154585983C>T | CA108761162 | FGA | c.1446G>A (p.Val482=) c.644-273G>A (n.644-273G>A) | dbSNP gnomAD v4 |
| 4 | g.154585984A= | CA1504943285 | FGA | c.1445T= (p.Val482=) c.644-274T= (n.644-274T=) | |
| 4 | g.154585984A>C | CA358529006 | FGA | c.1445T>G (p.Val482Gly) c.644-274T>G (n.644-274T>G) | |
| 4 | g.154585984A>G | CA358529008 | FGA | c.1445T>C (p.Val482Ala) c.644-274T>C (n.644-274T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585984A>T | CA358529010 | FGA | c.1445T>A (p.Val482Glu) c.644-274T>A (n.644-274T>A) | |
| 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.154585985C>A | CA358529012 | FGA | c.1444G>T (p.Val482Leu) c.644-275G>T (n.644-275G>T) | |
| 4 | g.154585985C= | CA1504943286 | FGA | c.1444G= (p.Val482=) c.644-275G= (n.644-275G=) | |
| 4 | g.154585985C>G | CA358529013 | FGA | c.1444G>C (p.Val482Leu) c.644-275G>C (n.644-275G>C) | |
| 4 | g.154585985C>T | CA3115086 | FGA | c.1444G>A (p.Val482Met) c.644-275G>A (n.644-275G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585986T>A | CA358529017 | FGA | c.1443A>T (p.Glu481Asp) c.644-276A>T (n.644-276A>T) | |
| 4 | g.154585986T>C | CA442014028 | FGA | c.1443A>G (p.Glu481=) c.644-276A>G (n.644-276A>G) | |
| 4 | g.154585986T>G | CA358529018 | FGA | c.1443A>C (p.Glu481Asp) c.644-276A>C (n.644-276A>C) | COSMIC COSMIC |
| 4 | g.154585987T>A | CA358529020 | FGA | c.1442A>T (p.Glu481Val) c.644-277A>T (n.644-277A>T) | gnomAD v4 |
| 4 | g.154585987T>C | CA358529022 | FGA | c.1442A>G (p.Glu481Gly) c.644-277A>G (n.644-277A>G) | |
| 4 | g.154585987T>G | CA358529023 | FGA | c.1442A>C (p.Glu481Ala) c.644-277A>C (n.644-277A>C) | |
| 4 | g.154585988del | CA2695204033 | FGA | c.1441del (p.Glu481LysfsTer3) c.644-278del (n.644-278del) | |
| 4 | g.154585988C>A | CA358529026 | FGA | c.1441G>T (p.Glu481Ter) c.644-278G>T (n.644-278G>T) | COSMIC COSMIC |
| 4 | g.154585988C>G | CA358529027 | FGA | c.1441G>C (p.Glu481Gln) c.644-278G>C (n.644-278G>C) | |
| 4 | g.154585988C>T | CA358529029 | FGA | c.1441G>A (p.Glu481Lys) c.644-278G>A (n.644-278G>A) | |
| 4 | g.154585989T>A | CA358529031 | FGA | c.1440A>T (p.Lys480Asn) c.644-279A>T (n.644-279A>T) | |
| 4 | g.154585989T>C | CA442014030 | FGA | c.1440A>G (p.Lys480=) c.644-279A>G (n.644-279A>G) | |
| 4 | g.154585989T>G | CA358529033 | FGA | c.1440A>C (p.Lys480Asn) c.644-279A>C (n.644-279A>C) | |
| 4 | g.154585991del | CA2578217779 | FGA | c.1440del (p.Glu481LysfsTer3) c.644-279del (n.644-279del) | |
| 4 | g.154585990T>A | CA358529036 | FGA | c.1439A>T (p.Lys480Ile) c.644-280A>T (n.644-280A>T) | |
| 4 | g.154585990T>C | CA358529037 | FGA | c.1439A>G (p.Lys480Arg) c.644-280A>G (n.644-280A>G) | gnomAD v4 |
| 4 | g.154585990T>G | CA358529039 | FGA | c.1439A>C (p.Lys480Thr) c.644-280A>C (n.644-280A>C) | |
| 4 | g.154585991T>A | CA126484 | FGA | c.1438A>T (p.Lys480Ter) c.644-281A>T (n.644-281A>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585991T>C | CA358529042 | FGA | c.1438A>G (p.Lys480Glu) c.644-281A>G (n.644-281A>G) | gnomAD v4 |
| 4 | g.154585991T>G | CA358529044 | FGA | c.1438A>C (p.Lys480Gln) c.644-281A>C (n.644-281A>C) | |
| 4 | g.154585991T= | CA1504943287 | FGA | c.1438A= (p.Lys480=) c.644-281A= (n.644-281A=) | |
| 4 | g.154585992G>A | CA442014031 | FGA | c.1437C>T (p.Thr479=) c.644-282C>T (n.644-282C>T) | |
| 4 | g.154585992G>C | CA442014033 | FGA | c.1437C>G (p.Thr479=) c.644-282C>G (n.644-282C>G) | |
| 4 | g.154585992G>T | CA442014032 | FGA | c.1437C>A (p.Thr479=) c.644-282C>A (n.644-282C>A) | |
| 4 | g.154585993G>A | CA358529047 | FGA | c.1436C>T (p.Thr479Ile) c.644-283C>T (n.644-283C>T) | gnomAD v4 COSMIC COSMIC |
| 4 | g.154585993G>C | CA358529048 | FGA | c.1436C>G (p.Thr479Ser) c.644-283C>G (n.644-283C>G) | |
| 4 | g.154585993G>T | CA358529049 | FGA | c.1436C>A (p.Thr479Asn) c.644-283C>A (n.644-283C>A) | 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) |