| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.154580323_154590216del | CA915940499 | |||
| 4 | g.154585792_154585810delinsGACTCAGTCTCACTGACAA | CA1504943192 | FGA | c.1619_1637delinsTTGTCAGTGAGACTGAGTC (p.Phe540=) c.644-100_644-82delinsTTGTCAGTGAGACTGAGTC (n.644-100_644-82delinsTTGTCAGTGAGACTGAGTC) | |
| 4 | g.154585797_154585814del | CA789378802 | FGA | c.1619_1636del (p.Phe540_Glu545del) c.644-100_644-83del (n.644-100_644-83del) | dbSNP |
| 4 | g.154585795T>A | CA126494 | FGA | c.1634A>T (p.Glu545Val) c.644-85A>T (n.644-85A>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585795T>C | CA358528033 | FGA | c.1634A>G (p.Glu545Gly) c.644-85A>G (n.644-85A>G) | gnomAD v4 |
| 4 | g.154585795T>G | CA358528036 | FGA | c.1634A>C (p.Glu545Ala) c.644-85A>C (n.644-85A>C) | |
| 4 | g.154585795T= | CA1504943194 | FGA | c.1634A= (p.Glu545=) c.644-85A= (n.644-85A=) | |
| 4 | g.154585796C>A | CA358528039 | FGA | c.1633G>T (p.Glu545Ter) c.644-86G>T (n.644-86G>T) | |
| 4 | g.154585796C= | CA1504943195 | FGA | c.1633G= (p.Glu545=) c.644-86G= (n.644-86G=) | |
| 4 | g.154585796C>G | CA358528041 | FGA | c.1633G>C (p.Glu545Gln) c.644-86G>C (n.644-86G>C) | |
| 4 | g.154585796C>T | CA3115061 | FGA | c.1633G>A (p.Glu545Lys) c.644-86G>A (n.644-86G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585797del | CA2695204024 | FGA | c.1632del (p.Glu545SerfsTer23) c.644-87del (n.644-87del) | |
| 4 | g.154585797A= | CA1504943196 | FGA | c.1632T= (p.Thr544=) c.644-87T= (n.644-87T=) | |
| 4 | g.154585797A>C | CA442013932 | FGA | c.1632T>G (p.Thr544=) c.644-87T>G (n.644-87T>G) | |
| 4 | g.154585797A>G | CA442013930 | FGA | c.1632T>C (p.Thr544=) c.644-87T>C (n.644-87T>C) | dbSNP |
| 4 | g.154585797A>T | CA442013931 | FGA | c.1632T>A (p.Thr544=) c.644-87T>A (n.644-87T>A) | gnomAD v4 |
| 4 | g.154585797_154585799delinsAGT | CA1504943197 | FGA | c.1630_1632delinsACT (p.Thr544=) c.644-89_644-87delinsACT (n.644-89_644-87delinsACT) | |
| 4 | g.154585798G>A | CA358528046 | FGA | c.1631C>T (p.Thr544Ile) c.644-88C>T (n.644-88C>T) | COSMIC COSMIC |
| 4 | g.154585798G>C | CA358528049 | FGA | c.1631C>G (p.Thr544Ser) c.644-88C>G (n.644-88C>G) | gnomAD v4 |
| 4 | g.154585798G>T | CA358528051 | FGA | c.1631C>A (p.Thr544Asn) c.644-88C>A (n.644-88C>A) | |
| 4 | g.154585798_154585799del | CA1504943198 | FGA | c.1630_1631del (p.Thr544Ter) c.644-89_644-88del (n.644-89_644-88del) | dbSNP |
| 4 | g.154585799T>A | CA358528070 | FGA | c.1630A>T (p.Thr544Ser) c.644-89A>T (n.644-89A>T) | |
| 4 | g.154585799T>C | CA358528066 | FGA | c.1630A>G (p.Thr544Ala) c.644-89A>G (n.644-89A>G) | |
| 4 | g.154585799T>G | CA358528064 | FGA | c.1630A>C (p.Thr544Pro) c.644-89A>C (n.644-89A>C) | |
| 4 | g.154585799_154585800delinsTC | CA1504943199 | FGA | c.1629_1630delinsGA (p.Glu543=) c.644-90_644-89delinsGA (n.644-90_644-89delinsGA) | |
| 4 | g.154585800del | CA126507 | FGA | c.1629del (p.Thr544LeufsTer24) c.644-90del (n.644-90del) | ClinVar dbSNP |
| 4 | g.154585800C>A | CA358528081 | FGA | c.1629G>T (p.Glu543Asp) c.644-90G>T (n.644-90G>T) | |
| 4 | g.154585800C>G | CA358528085 | FGA | c.1629G>C (p.Glu543Asp) c.644-90G>C (n.644-90G>C) | |
| 4 | g.154585800C>T | CA442013933 | FGA | c.1629G>A (p.Glu543=) c.644-90G>A (n.644-90G>A) | gnomAD v4 |
| 4 | g.154585802_154585805del | CA2695204025 | FGA | c.1626_1629del (p.Ser542ArgfsTer25) c.644-93_644-90del (n.644-93_644-90del) | |
| 4 | g.154585801T>A | CA358528090 | FGA | c.1628A>T (p.Glu543Val) c.644-91A>T (n.644-91A>T) | |
| 4 | g.154585801T>C | CA358528092 | FGA | c.1628A>G (p.Glu543Gly) c.644-91A>G (n.644-91A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.154585801T>G | CA358528094 | FGA | c.1628A>C (p.Glu543Ala) c.644-91A>C (n.644-91A>C) | |
| 4 | g.154585801T= | CA1504943200 | FGA | c.1628A= (p.Glu543=) c.644-91A= (n.644-91A=) | |
| 4 | g.154585801_154585803delinsTCA | CA1504943201 | FGA | c.1626_1628delinsTGA (p.Ser542=) c.644-93_644-91delinsTGA (n.644-93_644-91delinsTGA) | |
| 4 | g.154585802C>A | CA358528099 | FGA | c.1627G>T (p.Glu543Ter) c.644-92G>T (n.644-92G>T) | |
| 4 | g.154585802C>G | CA358528101 | FGA | c.1627G>C (p.Glu543Gln) c.644-92G>C (n.644-92G>C) | |
| 4 | g.154585802C>T | CA358528104 | FGA | c.1627G>A (p.Glu543Lys) c.644-92G>A (n.644-92G>A) | gnomAD v4 |
| 4 | g.154585803_154585804del | CA555971680 | FGA | c.1626_1627del (p.Ser542ArgfsTer3) c.644-93_644-92del (n.644-93_644-92del) | dbSNP gnomAD v2 |
| 4 | g.154585803A= | CA1504943202 | FGA | c.1626T= (p.Ser542=) c.644-93T= (n.644-93T=) | |
| 4 | g.154585803A>C | CA358528107 | FGA | c.1626T>G (p.Ser542Arg) c.644-93T>G (n.644-93T>G) | |
| 4 | g.154585803A>G | CA442013934 | FGA | c.1626T>C (p.Ser542=) c.644-93T>C (n.644-93T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.154585803A>T | CA358528109 | FGA | c.1626T>A (p.Ser542Arg) c.644-93T>A (n.644-93T>A) | |
| 4 | g.154585804C>A | CA358528111 | FGA | c.1625G>T (p.Ser542Ile) c.644-94G>T (n.644-94G>T) | COSMIC COSMIC |
| 4 | g.154585804C>G | CA358528115 | FGA | c.1625G>C (p.Ser542Thr) c.644-94G>C (n.644-94G>C) | |
| 4 | g.154585804C>T | CA358528118 | FGA | c.1625G>A (p.Ser542Asn) c.644-94G>A (n.644-94G>A) | |
| 4 | g.154585805T>A | CA358528126 | FGA | c.1624A>T (p.Ser542Cys) c.644-95A>T (n.644-95A>T) | |
| 4 | g.154585805T>C | CA358528124 | FGA | c.1624A>G (p.Ser542Gly) c.644-95A>G (n.644-95A>G) | |
| 4 | g.154585805T>G | CA358528122 | FGA | c.1624A>C (p.Ser542Arg) c.644-95A>C (n.644-95A>C) | |
| 4 | g.154585806G>A | CA442013937 | FGA | c.1623C>T (p.Val541=) c.644-96C>T (n.644-96C>T) |