| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.18400779C>A | CA370636601 | NAT2 | c.776C>A (p.Thr259Asn) c.386C>A (p.Thr129Asn) | dbSNP |
| 8 | g.18400779C= | CA1768219147 | NAT2 | c.776C= (p.Thr259=) c.386C= (p.Thr129=) | |
| 8 | g.18400779C>G | CA370636602 | NAT2 | c.776C>G (p.Thr259Ser) c.386C>G (p.Thr129Ser) | |
| 8 | g.18400779C>T | CA370636603 | NAT2 | c.776C>T (p.Thr259Ile) c.386C>T (p.Thr129Ile) | dbSNP gnomAD v4 |
| 8 | g.18400780T>A | CA459699712 | NAT2 | c.777T>A (p.Thr259=) c.387T>A (p.Thr129=) | |
| 8 | g.18400780T>C | CA459699714 | NAT2 | c.777T>C (p.Thr259=) c.387T>C (p.Thr129=) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18400780T>G | CA459699716 | NAT2 | c.777T>G (p.Thr259=) c.387T>G (p.Thr129=) | gnomAD v4 |
| 8 | g.18400780T= | CA1768219148 | NAT2 | c.777T= (p.Thr259=) c.387T= (p.Thr129=) | |
| 8 | g.18400781G>A | CA4651699 | NAT2 | c.778G>A (p.Glu260Lys) c.388G>A (p.Glu130Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 8 | g.18400781G>C | CA370636604 | NAT2 | c.778G>C (p.Glu260Gln) c.388G>C (p.Glu130Gln) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18400781G= | CA1768219149 | NAT2 | c.778G= (p.Glu260=) c.388G= (p.Glu130=) | |
| 8 | g.18400781G>T | CA370636605 | NAT2 | c.778G>T (p.Glu260Ter) c.388G>T (p.Glu130Ter) | gnomAD v4 |
| 8 | g.18400782A= | CA1768219150 | NAT2 | c.779A= (p.Glu260=) c.389A= (p.Glu130=) | |
| 8 | g.18400782A>C | CA370636607 | NAT2 | c.779A>C (p.Glu260Ala) c.389A>C (p.Glu130Ala) | |
| 8 | g.18400782A>G | CA370636608 | NAT2 | c.779A>G (p.Glu260Gly) c.389A>G (p.Glu130Gly) | |
| 8 | g.18400782A>T | CA370636606 | NAT2 | c.779A>T (p.Glu260Val) c.389A>T (p.Glu130Val) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.18400783G>A | CA459699732 | NAT2 | c.780G>A (p.Glu260=) c.390G>A (p.Glu130=) | |
| 8 | g.18400783G>C | CA4651701 | NAT2 | c.780G>C (p.Glu260Asp) c.390G>C (p.Glu130Asp) | dbSNP ExAC gnomAD v2 |
| 8 | g.18400783G= | CA1768219151 | NAT2 | c.780G= (p.Glu260=) c.390G= (p.Glu130=) | |
| 8 | g.18400783G>T | CA370636609 | NAT2 | c.780G>T (p.Glu260Asp) c.390G>T (p.Glu130Asp) | |
| 8 | g.18400784dup | CA4651700 | NAT2 | c.781dup (p.Glu261GlyfsTer4) c.391dup (p.Glu131GlyfsTer4) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.18400784G>A | CA173519944 | NAT2 | c.781G>A (p.Glu261Lys) c.391G>A (p.Glu131Lys) | dbSNP |
| 8 | g.18400784G>C | CA370636610 | NAT2 | c.781G>C (p.Glu261Gln) c.391G>C (p.Glu131Gln) | |
| 8 | g.18400784G= | CA1768219152 | NAT2 | c.781G= (p.Glu261=) c.391G= (p.Glu131=) | |
| 8 | g.18400784G>T | CA370636611 | NAT2 | c.781G>T (p.Glu261Ter) c.391G>T (p.Glu131Ter) | gnomAD v4 |
| 8 | g.18400785A= | CA1768219153 | NAT2 | c.782A= (p.Glu261=) c.392A= (p.Glu131=) | |
| 8 | g.18400785A>C | CA370636614 | NAT2 | c.782A>C (p.Glu261Ala) c.392A>C (p.Glu131Ala) | |
| 8 | g.18400785A>G | CA370636612 | NAT2 | c.782A>G (p.Glu261Gly) c.392A>G (p.Glu131Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18400785A>T | CA370636613 | NAT2 | c.782A>T (p.Glu261Val) c.392A>T (p.Glu131Val) | |
| 8 | g.18400786A>C | CA370636615 | NAT2 | c.783A>C (p.Glu261Asp) c.393A>C (p.Glu131Asp) | |
| 8 | g.18400786A>G | CA459699751 | NAT2 | c.783A>G (p.Glu261=) c.393A>G (p.Glu131=) | |
| 8 | g.18400786A>T | CA370636616 | NAT2 | c.783A>T (p.Glu261Asp) c.393A>T (p.Glu131Asp) | |
| 8 | g.18400787G>A | CA370636617 | NAT2 | c.784G>A (p.Glu262Lys) c.394G>A (p.Glu132Lys) | gnomAD v4 |
| 8 | g.18400787G>C | CA370636618 | NAT2 | c.784G>C (p.Glu262Gln) c.394G>C (p.Glu132Gln) | |
| 8 | g.18400787G>T | CA370636619 | NAT2 | c.784G>T (p.Glu262Ter) c.394G>T (p.Glu132Ter) | |
| 8 | g.18400788del | CA2686326442 | NAT2 | c.785del (p.Glu262GlyfsTer6) c.395del (p.Glu132GlyfsTer6) | gnomAD v4 |
| 8 | g.18400788A>C | CA370636620 | NAT2 | c.785A>C (p.Glu262Ala) c.395A>C (p.Glu132Ala) | |
| 8 | g.18400788A>G | CA370636622 | NAT2 | c.785A>G (p.Glu262Gly) c.395A>G (p.Glu132Gly) | |
| 8 | g.18400788A>T | CA370636621 | NAT2 | c.785A>T (p.Glu262Val) c.395A>T (p.Glu132Val) | |
| 8 | g.18400789G>A | CA459699766 | NAT2 | c.786G>A (p.Glu262=) c.396G>A (p.Glu132=) | gnomAD v4 |
| 8 | g.18400789G>C | CA4651702 | NAT2 | c.786G>C (p.Glu262Asp) c.396G>C (p.Glu132Asp) | dbSNP ExAC |
| 8 | g.18400789G= | CA1768219154 | NAT2 | c.786G= (p.Glu262=) c.396G= (p.Glu132=) | |
| 8 | g.18400789G>T | CA370636623 | NAT2 | c.786G>T (p.Glu262Asp) c.396G>T (p.Glu132Asp) | |
| 8 | g.18400790G>A | CA370636624 | NAT2 | c.787G>A (p.Val263Ile) c.397G>A (p.Val133Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.18400790G>C | CA370636625 | NAT2 | c.787G>C (p.Val263Leu) c.397G>C (p.Val133Leu) | |
| 8 | g.18400790G= | CA1768219155 | NAT2 | c.787G= (p.Val263=) c.397G= (p.Val133=) | |
| 8 | g.18400790G>T | CA370636626 | NAT2 | c.787G>T (p.Val263Phe) c.397G>T (p.Val133Phe) | gnomAD v4 |
| 8 | g.18400791T>A | CA370636627 | NAT2 | c.788T>A (p.Val263Asp) c.398T>A (p.Val133Asp) | |
| 8 | g.18400791T>C | CA173519945 | NAT2 | c.788T>C (p.Val263Ala) c.398T>C (p.Val133Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.18400791T>G | CA370636628 | NAT2 | c.788T>G (p.Val263Gly) c.398T>G (p.Val133Gly) | gnomAD v4 |