| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.93585388G>A | CA360526118 | NR2F1 | c.290G>A (p.Cys97Tyr) c.365G>A (p.Cys122Tyr) c.212G>A (p.Cys71Tyr) | ClinVar |
| 5 | g.93585388G>C | CA16604998 | NR2F1 | c.290G>C (p.Cys97Ser) c.365G>C (p.Cys122Ser) c.212G>C (p.Cys71Ser) | ClinVar dbSNP |
| 5 | g.93585388G= | CA1564182847 | NR2F1 | c.290G= (p.Cys97=) c.365G= (p.Cys122=) c.212G= (p.Cys71=) | |
| 5 | g.93585388G>T | CA360526119 | NR2F1 | c.290G>T (p.Cys97Phe) c.365G>T (p.Cys122Phe) c.212G>T (p.Cys71Phe) | |
| 5 | g.93585389C>A | CA360526120 | NR2F1 | c.291C>A (p.Cys97Ter) c.366C>A (p.Cys122Ter) c.213C>A (p.Cys71Ter) | |
| 5 | g.93585389C>G | CA360526121 | NR2F1 | c.291C>G (p.Cys97Trp) c.366C>G (p.Cys122Trp) c.213C>G (p.Cys71Trp) | |
| 5 | g.93585389C>T | CA445569987 | NR2F1 | c.291C>T (p.Cys97=) c.366C>T (p.Cys122=) c.213C>T (p.Cys71=) | |
| 5 | g.93585390C>A | CA360526124 | NR2F1 | c.292C>A (p.Arg98Ser) c.367C>A (p.Arg123Ser) c.214C>A (p.Arg72Ser) | |
| 5 | g.93585390C= | CA1564182848 | NR2F1 | c.292C= (p.Arg98=) c.367C= (p.Arg123=) c.214C= (p.Arg72=) | |
| 5 | g.93585390C>G | CA360526123 | NR2F1 | c.292C>G (p.Arg98Gly) c.367C>G (p.Arg123Gly) c.214C>G (p.Arg72Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.93585390C>T | CA360526122 | NR2F1 | c.292C>T (p.Arg98Cys) c.367C>T (p.Arg123Cys) c.214C>T (p.Arg72Cys) | |
| 5 | g.93585391G>A | CA360526125 | NR2F1 | c.293G>A (p.Arg98His) c.368G>A (p.Arg123His) c.215G>A (p.Arg72His) | |
| 5 | g.93585391G>C | CA360526127 | NR2F1 | c.293G>C (p.Arg98Pro) c.368G>C (p.Arg123Pro) c.215G>C (p.Arg72Pro) | |
| 5 | g.93585391G>T | CA360526126 | NR2F1 | c.293G>T (p.Arg98Leu) c.368G>T (p.Arg123Leu) c.215G>T (p.Arg72Leu) | |
| 5 | g.93585392T>A | CA445569991 | NR2F1 | c.294T>A (p.Arg98=) c.369T>A (p.Arg123=) c.216T>A (p.Arg72=) | |
| 5 | g.93585392T>C | CA445569989 | NR2F1 | c.294T>C (p.Arg98=) c.369T>C (p.Arg123=) c.216T>C (p.Arg72=) | |
| 5 | g.93585392T>G | CA445569990 | NR2F1 | c.294T>G (p.Arg98=) c.369T>G (p.Arg123=) c.216T>G (p.Arg72=) | |
| 5 | g.93585393G>A | CA360526128 | NR2F1 | c.295G>A (p.Ala99Thr) c.370G>A (p.Ala124Thr) c.217G>A (p.Ala73Thr) | |
| 5 | g.93585393G>C | CA360526129 | NR2F1 | c.295G>C (p.Ala99Pro) c.370G>C (p.Ala124Pro) c.217G>C (p.Ala73Pro) | |
| 5 | g.93585393G>T | CA360526130 | NR2F1 | c.295G>T (p.Ala99Ser) c.370G>T (p.Ala124Ser) c.217G>T (p.Ala73Ser) | |
| 5 | g.93585394C>A | CA360526131 | NR2F1 | c.296C>A (p.Ala99Asp) c.371C>A (p.Ala124Asp) c.218C>A (p.Ala73Asp) | |
| 5 | g.93585394C= | CA1564182849 | NR2F1 | c.296C= (p.Ala99=) c.371C= (p.Ala124=) c.218C= (p.Ala73=) | |
| 5 | g.93585394C>G | CA360526132 | NR2F1 | c.296C>G (p.Ala99Gly) c.371C>G (p.Ala124Gly) c.218C>G (p.Ala73Gly) | |
| 5 | g.93585394C>T | CA360526133 | NR2F1 | c.296C>T (p.Ala99Val) c.371C>T (p.Ala124Val) c.218C>T (p.Ala73Val) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 5 | g.93585395C>A | CA445569992 | NR2F1 | c.297C>A (p.Ala99=) c.372C>A (p.Ala124=) c.219C>A (p.Ala73=) | |
| 5 | g.93585395C= | CA1564182850 | NR2F1 | c.297C= (p.Ala99=) c.372C= (p.Ala124=) c.219C= (p.Ala73=) | |
| 5 | g.93585395C>G | CA445569993 | NR2F1 | c.297C>G (p.Ala99=) c.372C>G (p.Ala124=) c.219C>G (p.Ala73=) | dbSNP gnomAD v4 |
| 5 | g.93585395C>T | CA445569994 | NR2F1 | c.297C>T (p.Ala99=) c.372C>T (p.Ala124=) c.219C>T (p.Ala73=) | |
| 5 | g.93585396A>C | CA360526134 | NR2F1 | c.298A>C (p.Asn100His) c.373A>C (p.Asn125His) c.220A>C (p.Asn74His) | |
| 5 | g.93585396A>G | CA360526135 | NR2F1 | c.298A>G (p.Asn100Asp) c.373A>G (p.Asn125Asp) c.220A>G (p.Asn74Asp) | |
| 5 | g.93585396A>T | CA360526136 | NR2F1 | c.298A>T (p.Asn100Tyr) c.373A>T (p.Asn125Tyr) c.220A>T (p.Asn74Tyr) | |
| 5 | g.93585397A= | CA1564182851 | NR2F1 | c.299A= (p.Asn100=) c.374A= (p.Asn125=) c.221A= (p.Asn74=) | |
| 5 | g.93585397A>C | CA360526137 | NR2F1 | c.299A>C (p.Asn100Thr) c.374A>C (p.Asn125Thr) c.221A>C (p.Asn74Thr) | |
| 5 | g.93585397A>G | CA123266256 | NR2F1 | c.299A>G (p.Asn100Ser) c.374A>G (p.Asn125Ser) c.221A>G (p.Asn74Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.93585397A>T | CA360526138 | NR2F1 | c.299A>T (p.Asn100Ile) c.374A>T (p.Asn125Ile) c.221A>T (p.Asn74Ile) | |
| 5 | g.93585398C>A | CA360526139 | NR2F1 | c.300C>A (p.Asn100Lys) c.375C>A (p.Asn125Lys) c.222C>A (p.Asn74Lys) | |
| 5 | g.93585398C>G | CA360526140 | NR2F1 | c.300C>G (p.Asn100Lys) c.375C>G (p.Asn125Lys) c.222C>G (p.Asn74Lys) | |
| 5 | g.93585398C>T | CA445569995 | NR2F1 | c.300C>T (p.Asn100=) c.375C>T (p.Asn125=) c.222C>T (p.Asn74=) | |
| 5 | g.93585399A>C | CA445569996 | NR2F1 | c.301A>C (p.Arg101=) c.376A>C (p.Arg126=) c.223A>C (p.Arg75=) | ClinVar dbSNP |
| 5 | g.93585399A>G | CA360526141 | NR2F1 | c.301A>G (p.Arg101Gly) c.376A>G (p.Arg126Gly) c.223A>G (p.Arg75Gly) | |
| 5 | g.93585399A>T | CA360526142 | NR2F1 | c.301A>T (p.Arg101Trp) c.376A>T (p.Arg126Trp) c.223A>T (p.Arg75Trp) | |
| 5 | g.93585400G>A | CA360526143 | NR2F1 | c.302G>A (p.Arg101Lys) c.377G>A (p.Arg126Lys) c.224G>A (p.Arg75Lys) | dbSNP gnomAD v4 |
| 5 | g.93585400G>C | CA360526144 | NR2F1 | c.302G>C (p.Arg101Thr) c.377G>C (p.Arg126Thr) c.224G>C (p.Arg75Thr) | |
| 5 | g.93585400G= | CA1564182852 | NR2F1 | c.302G= (p.Arg101=) c.377G= (p.Arg126=) c.224G= (p.Arg75=) | |
| 5 | g.93585400G>T | CA360526145 | NR2F1 | c.302G>T (p.Arg101Met) c.377G>T (p.Arg126Met) c.224G>T (p.Arg75Met) | |
| 5 | g.93585401del | CA2674596793 | NR2F1 | c.303del (p.Asn102ThrfsTer25) c.378del (p.Asn127ThrfsTer25) c.225del (p.Asn76ThrfsTer25) | gnomAD v4 |
| 5 | g.93585401G>A | CA445569997 | NR2F1 | c.303G>A (p.Arg101=) c.378G>A (p.Arg126=) c.225G>A (p.Arg75=) | COSMIC |
| 5 | g.93585401G>C | CA360526146 | NR2F1 | c.303G>C (p.Arg101Ser) c.378G>C (p.Arg126Ser) c.225G>C (p.Arg75Ser) | |
| 5 | g.93585401G>T | CA360526147 | NR2F1 | c.303G>T (p.Arg101Ser) c.378G>T (p.Arg126Ser) c.225G>T (p.Arg75Ser) | gnomAD v4 |
| 5 | g.93585402A>C | CA360526148 | NR2F1 | c.304A>C (p.Asn102His) c.379A>C (p.Asn127His) c.226A>C (p.Asn76His) |