Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44908595T>A | CA406303756 | APOE | c.299T>A (p.Leu100Gln) c.377T>A (p.Leu126Gln) | |
19 | g.44908595T>C | CA406303758 | APOE | c.299T>C (p.Leu100Pro) c.377T>C (p.Leu126Pro) | |
19 | g.44908595T>G | CA406303757 | APOE | c.299T>G (p.Leu100Arg) c.377T>G (p.Leu126Arg) | |
19 | g.44908596G>A | CA308885267 | APOE | c.300G>A (p.Leu100=) c.378G>A (p.Leu126=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44908596G>C | CA507947384 | APOE | c.300G>C (p.Leu100=) c.378G>C (p.Leu126=) | |
19 | g.44908596G= | CA2338167861 | APOE | c.300G= (p.Leu100=) c.378G= (p.Leu126=) | |
19 | g.44908596G>T | CA507947385 | APOE | c.300G>T (p.Leu100=) c.378G>T (p.Leu126=) | |
19 | g.44908597A>C | CA406303759 | APOE | c.301A>C (p.Thr101Pro) c.379A>C (p.Thr127Pro) | |
19 | g.44908597A>G | CA406303760 | APOE | c.301A>G (p.Thr101Ala) c.379A>G (p.Thr127Ala) | |
19 | g.44908597A>T | CA406303761 | APOE | c.301A>T (p.Thr101Ser) c.379A>T (p.Thr127Ser) | |
19 | g.44908598C>A | CA406303762 | APOE | c.302C>A (p.Thr101Asn) c.380C>A (p.Thr127Asn) | |
19 | g.44908598C= | CA2338167862 | APOE | c.302C= (p.Thr101=) c.380C= (p.Thr127=) | |
19 | g.44908598C>G | CA406303763 | APOE | c.302C>G (p.Thr101Ser) c.380C>G (p.Thr127Ser) | |
19 | g.44908598C>T | CA406303764 | APOE | c.302C>T (p.Thr101Ile) c.380C>T (p.Thr127Ile) | dbSNP |
19 | g.44908599C>A | CA507947388 | APOE | c.303C>A (p.Thr101=) c.381C>A (p.Thr127=) | |
19 | g.44908599C= | CA2338167385 | APOE | c.303C= (p.Thr101=) c.381C= (p.Thr127=) | |
19 | g.44908599C>G | CA507947387 | APOE | c.303C>G (p.Thr101=) c.381C>G (p.Thr127=) | |
19 | g.44908599C>T | CA507947389 | APOE | c.303C>T (p.Thr101=) c.381C>T (p.Thr127=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.44908600C>A | CA308885268 | APOE | c.304C>A (p.Pro102Thr) c.382C>A (p.Pro128Thr) | dbSNP gnomAD v4 |
19 | g.44908600C= | CA2338167389 | APOE | c.304C= (p.Pro102=) c.382C= (p.Pro128=) | |
19 | g.44908600C>G | CA406303765 | APOE | c.304C>G (p.Pro102Ala) c.382C>G (p.Pro128Ala) | |
19 | g.44908600C>T | CA406303766 | APOE | c.304C>T (p.Pro102Ser) c.382C>T (p.Pro128Ser) | |
19 | g.44908601C>A | CA308885274 | APOE | c.305C>A (p.Pro102Gln) c.383C>A (p.Pro128Gln) | dbSNP |
19 | g.44908601C= | CA2338167393 | APOE | c.305C= (p.Pro102=) c.383C= (p.Pro128=) | |
19 | g.44908601C>G | CA042073 | APOE | c.305C>G (p.Pro102Arg) c.383C>G (p.Pro128Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.[44908601C>G;44908684T>C] | CA042261 | APOE | c.[305C>G;388T>C] (p.[Pro102Arg;Cys130Arg]) c.[383C>G;466T>C] (p.[Pro128Arg;Cys156Arg]) | ClinVar |
19 | g.44908601C>T | CA308885271 | APOE | c.305C>T (p.Pro102Leu) c.383C>T (p.Pro128Leu) | dbSNP gnomAD v2 |
19 | g.44908602G>A | CA9506034 | APOE | c.306G>A (p.Pro102=) c.384G>A (p.Pro128=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44908602G>C | CA507947393 | APOE | c.306G>C (p.Pro102=) c.384G>C (p.Pro128=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.44908602G= | CA2338167397 | APOE | c.306G= (p.Pro102=) c.384G= (p.Pro128=) | |
19 | g.44908602G>T | CA507947395 | APOE | c.306G>T (p.Pro102=) c.384G>T (p.Pro128=) | |
19 | g.44908603G>A | CA406303767 | APOE | c.307G>A (p.Val103Met) c.385G>A (p.Val129Met) | gnomAD v4 |
19 | g.44908603G>C | CA406303768 | APOE | c.307G>C (p.Val103Leu) c.385G>C (p.Val129Leu) | dbSNP |
19 | g.44908603G= | CA2338167398 | APOE | c.307G= (p.Val103=) c.385G= (p.Val129=) | |
19 | g.44908603G>T | CA406303769 | APOE | c.307G>T (p.Val103Leu) c.385G>T (p.Val129Leu) | dbSNP gnomAD v2 |
19 | g.44908604T>A | CA406303770 | APOE | c.308T>A (p.Val103Glu) c.386T>A (p.Val129Glu) | |
19 | g.44908604T>C | CA406303771 | APOE | c.308T>C (p.Val103Ala) c.386T>C (p.Val129Ala) | gnomAD v4 |
19 | g.44908604T>G | CA406303772 | APOE | c.308T>G (p.Val103Gly) c.386T>G (p.Val129Gly) | |
19 | g.44908605G>A | CA507947397 | APOE | c.309G>A (p.Val103=) c.387G>A (p.Val129=) | |
19 | g.44908605G>C | CA507947399 | APOE | c.309G>C (p.Val103=) c.387G>C (p.Val129=) | |
19 | g.44908605G>T | CA507947398 | APOE | c.309G>T (p.Val103=) c.387G>T (p.Val129=) | |
19 | g.44908606G>A | CA9506035 | APOE | c.310G>A (p.Ala104Thr) c.388G>A (p.Ala130Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44908606G>C | CA406303773 | APOE | c.310G>C (p.Ala104Pro) c.388G>C (p.Ala130Pro) | |
19 | g.44908606G= | CA2338167400 | APOE | c.310G= (p.Ala104=) c.388G= (p.Ala130=) | |
19 | g.44908606G>T | CA406303774 | APOE | c.310G>T (p.Ala104Ser) c.388G>T (p.Ala130Ser) | |
19 | g.44908607C>A | CA406303775 | APOE | c.311C>A (p.Ala104Glu) c.389C>A (p.Ala130Glu) | |
19 | g.44908607C= | CA2338167402 | APOE | c.311C= (p.Ala104=) c.389C= (p.Ala130=) | |
19 | g.44908607C>G | CA406303776 | APOE | c.311C>G (p.Ala104Gly) c.389C>G (p.Ala130Gly) | |
19 | g.44908607C>T | CA406303777 | APOE | c.311C>T (p.Ala104Val) c.389C>T (p.Ala130Val) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.44908608G>A | CA9506036 | APOE | c.312G>A (p.Ala104=) c.390G>A (p.Ala130=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |