| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.46357617T>A | CA433592577 | CCR2 | c.90T>A (p.Ala30=) n.315-500T>A | gnomAD v4 |
| 3 | g.46357617T>C | CA433592578 | CCR2 | c.90T>C (p.Ala30=) n.315-500T>C | |
| 3 | g.46357617T>G | CA433592579 | CCR2 | c.90T>G (p.Ala30=) n.315-500T>G | |
| 3 | g.46357618C>A | CA352466071 | CCR2 | c.91C>A (p.Pro31Thr) n.315-499C>A | |
| 3 | g.46357618C>G | CA352466069 | CCR2 | c.91C>G (p.Pro31Ala) n.315-499C>G | |
| 3 | g.46357618C>T | CA352466073 | CCR2 | c.91C>T (p.Pro31Ser) n.315-499C>T | gnomAD v4 |
| 3 | g.46357619_46357620del | CA433592580 | CCR2 | c.92_93del (p.Pro31LeufsTer3) n.315-498_315-497del | gnomAD v4 |
| 3 | g.46357619C>A | CA352466075 | CCR2 | c.92C>A (p.Pro31His) n.315-498C>A | |
| 3 | g.46357619C>G | CA352466078 | CCR2 | c.92C>G (p.Pro31Arg) n.315-498C>G | |
| 3 | g.46357619C>T | CA352466080 | CCR2 | c.92C>T (p.Pro31Leu) n.315-498C>T | |
| 3 | g.46357620C>A | CA433592581 | CCR2 | c.93C>A (p.Pro31=) n.315-497C>A | |
| 3 | g.46357620C>G | CA433592582 | CCR2 | c.93C>G (p.Pro31=) n.315-497C>G | |
| 3 | g.46357620C>T | CA433592583 | CCR2 | c.93C>T (p.Pro31=) n.315-497C>T | |
| 3 | g.46357621T>A | CA352466083 | CCR2 | c.94T>A (p.Cys32Ser) n.315-496T>A | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.46357621T>C | CA352466085 | CCR2 | c.94T>C (p.Cys32Arg) n.315-496T>C | |
| 3 | g.46357621T>G | CA352466086 | CCR2 | c.94T>G (p.Cys32Gly) n.315-496T>G | |
| 3 | g.46357621T= | CA1362075506 | CCR2 | c.94T= (p.Cys32=) n.315-496T= | |
| 3 | g.46357622G>A | CA352466092 | CCR2 | c.95G>A (p.Cys32Tyr) n.315-495G>A | |
| 3 | g.46357622G>C | CA352466088 | CCR2 | c.95G>C (p.Cys32Ser) n.315-495G>C | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.46357622G= | CA1362075507 | CCR2 | c.95G= (p.Cys32=) n.315-495G= | |
| 3 | g.46357622G>T | CA352466090 | CCR2 | c.95G>T (p.Cys32Phe) n.315-495G>T | |
| 3 | g.46357623T>A | CA352466094 | CCR2 | c.96T>A (p.Cys32Ter) n.315-494T>A | |
| 3 | g.46357623T>C | CA433592584 | CCR2 | c.96T>C (p.Cys32=) n.315-494T>C | |
| 3 | g.46357623T>G | CA352466096 | CCR2 | c.96T>G (p.Cys32Trp) n.315-494T>G | |
| 3 | g.46357624C>A | CA352466098 | CCR2 | c.97C>A (p.His33Asn) n.315-493C>A | |
| 3 | g.46357624C>G | CA352466100 | CCR2 | c.97C>G (p.His33Asp) n.315-493C>G | |
| 3 | g.46357624C>T | CA352466102 | CCR2 | c.97C>T (p.His33Tyr) n.315-493C>T | |
| 3 | g.46357625A>C | CA352466104 | CCR2 | c.98A>C (p.His33Pro) n.315-492A>C | |
| 3 | g.46357625A>G | CA352466108 | CCR2 | c.98A>G (p.His33Arg) n.315-492A>G | |
| 3 | g.46357625A>T | CA352466106 | CCR2 | c.98A>T (p.His33Leu) n.315-492A>T | |
| 3 | g.46357626T>A | CA352466110 | CCR2 | c.99T>A (p.His33Gln) n.315-491T>A | gnomAD v4 |
| 3 | g.46357626T>C | CA433592585 | CCR2 | c.99T>C (p.His33=) n.315-491T>C | gnomAD v4 |
| 3 | g.46357626T>G | CA352466112 | CCR2 | c.99T>G (p.His33Gln) n.315-491T>G | |
| 3 | g.46357627A>C | CA352466114 | CCR2 | c.100A>C (p.Lys34Gln) n.315-490A>C | |
| 3 | g.46357627A>G | CA352466116 | CCR2 | c.100A>G (p.Lys34Glu) n.315-490A>G | |
| 3 | g.46357627A>T | CA352466118 | CCR2 | c.100A>T (p.Lys34Ter) n.315-490A>T | |
| 3 | g.46357628A>C | CA352466120 | CCR2 | c.101A>C (p.Lys34Thr) n.315-489A>C | |
| 3 | g.46357628A>G | CA352466122 | CCR2 | c.101A>G (p.Lys34Arg) n.315-489A>G | |
| 3 | g.46357628A>T | CA352466124 | CCR2 | c.101A>T (p.Lys34Ile) n.315-489A>T | |
| 3 | g.46357629A>C | CA352466126 | CCR2 | c.102A>C (p.Lys34Asn) n.315-488A>C | |
| 3 | g.46357629A>G | CA433592586 | CCR2 | c.102A>G (p.Lys34=) n.315-488A>G | |
| 3 | g.46357629A>T | CA352466128 | CCR2 | c.102A>T (p.Lys34Asn) n.315-488A>T | |
| 3 | g.46357630T>A | CA352466135 | CCR2 | c.103T>A (p.Phe35Ile) n.315-487T>A | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.46357630T>C | CA352466132 | CCR2 | c.103T>C (p.Phe35Leu) n.315-487T>C | |
| 3 | g.46357630T>G | CA352466131 | CCR2 | c.103T>G (p.Phe35Val) n.315-487T>G | |
| 3 | g.46357630T= | CA1362075508 | CCR2 | c.103T= (p.Phe35=) n.315-487T= | |
| 3 | g.46357631T>A | CA352466137 | CCR2 | c.104T>A (p.Phe35Tyr) n.315-486T>A | |
| 3 | g.46357631T>C | CA352466139 | CCR2 | c.104T>C (p.Phe35Ser) n.315-486T>C | |
| 3 | g.46357631T>G | CA352466141 | CCR2 | c.104T>G (p.Phe35Cys) n.315-486T>G | gnomAD v4 |
| 3 | g.46357632T>A | CA352466143 | CCR2 | c.105T>A (p.Phe35Leu) n.315-485T>A |