Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.18400860G>A | CA114453 | NAT2 | c.857G>A (p.Gly286Glu) c.467G>A (p.Gly156Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400860G>C | CA370636771 | NAT2 | c.857G>C (p.Gly286Ala) c.467G>C (p.Gly156Ala) | dbSNP |
8 | g.18400860G= | CA1768219186 | NAT2 | c.857G= (p.Gly286=) c.467G= (p.Gly156=) | |
8 | g.18400860G>T | CA370636772 | NAT2 | c.857G>T (p.Gly286Val) c.467G>T (p.Gly156Val) | |
8 | g.18400861A= | CA1768219187 | NAT2 | c.858A= (p.Gly286=) c.468A= (p.Gly156=) | |
8 | g.18400861A>C | CA459700137 | NAT2 | c.858A>C (p.Gly286=) c.468A>C (p.Gly156=) | |
8 | g.18400861A>G | CA459700139 | NAT2 | c.858A>G (p.Gly286=) c.468A>G (p.Gly156=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400861A>T | CA459700142 | NAT2 | c.858A>T (p.Gly286=) c.468A>T (p.Gly156=) | |
8 | g.18400862del | CA2695208956 | NAT2 | c.859del (p.Ser287ProfsTer?) c.469del (p.Ser157ProfsTer?) | |
8 | g.18400862T>A | CA370636773 | NAT2 | c.859T>A (p.Ser287Thr) c.469T>A (p.Ser157Thr) | |
8 | g.18400862T>C | CA4651715 | NAT2 | c.859T>C (p.Ser287Pro) c.469T>C (p.Ser157Pro) | dbSNP ExAC gnomAD v4 |
8 | g.18400862T>G | CA370636774 | NAT2 | c.859T>G (p.Ser287Ala) c.469T>G (p.Ser157Ala) | |
8 | g.18400862T= | CA1768219188 | NAT2 | c.859T= (p.Ser287=) c.469T= (p.Ser157=) | |
8 | g.18400863C>A | CA370636775 | NAT2 | c.860C>A (p.Ser287Tyr) c.470C>A (p.Ser157Tyr) | |
8 | g.18400863C= | CA1768219189 | NAT2 | c.860C= (p.Ser287=) c.470C= (p.Ser157=) | |
8 | g.18400863C>G | CA370636776 | NAT2 | c.860C>G (p.Ser287Cys) c.470C>G (p.Ser157Cys) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.18400863C>T | CA370636777 | NAT2 | c.860C>T (p.Ser287Phe) c.470C>T (p.Ser157Phe) | COSMIC |
8 | g.18400864C>A | CA459700154 | NAT2 | c.861C>A (p.Ser287=) c.471C>A (p.Ser157=) | |
8 | g.18400864C= | CA1768219190 | NAT2 | c.861C= (p.Ser287=) c.471C= (p.Ser157=) | |
8 | g.18400864C>G | CA459700156 | NAT2 | c.861C>G (p.Ser287=) c.471C>G (p.Ser157=) | |
8 | g.18400864C>T | CA4651716 | NAT2 | c.861C>T (p.Ser287=) c.471C>T (p.Ser157=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400865C>A | CA370636778 | NAT2 | c.862C>A (p.Leu288Ile) c.472C>A (p.Leu158Ile) | |
8 | g.18400865C>G | CA370636779 | NAT2 | c.862C>G (p.Leu288Val) c.472C>G (p.Leu158Val) | |
8 | g.18400865C>T | CA370636780 | NAT2 | c.862C>T (p.Leu288Phe) c.472C>T (p.Leu158Phe) | gnomAD v4 |
8 | g.18400866T>A | CA370636781 | NAT2 | c.863T>A (p.Leu288His) c.473T>A (p.Leu158His) | |
8 | g.18400866T>C | CA370636782 | NAT2 | c.863T>C (p.Leu288Pro) c.473T>C (p.Leu158Pro) | |
8 | g.18400866T>G | CA370636783 | NAT2 | c.863T>G (p.Leu288Arg) c.473T>G (p.Leu158Arg) | |
8 | g.18400867T>A | CA459700168 | NAT2 | c.864T>A (p.Leu288=) c.474T>A (p.Leu158=) | |
8 | g.18400867T>C | CA459700170 | NAT2 | c.864T>C (p.Leu288=) c.474T>C (p.Leu158=) | |
8 | g.18400867T>G | CA459700172 | NAT2 | c.864T>G (p.Leu288=) c.474T>G (p.Leu158=) | |
8 | g.18400868A= | CA1768219191 | NAT2 | c.865A= (p.Thr289=) c.475A= (p.Thr159=) | |
8 | g.18400868A>C | CA370636784 | NAT2 | c.865A>C (p.Thr289Pro) c.475A>C (p.Thr159Pro) | dbSNP |
8 | g.18400868A>G | CA370636785 | NAT2 | c.865A>G (p.Thr289Ala) c.475A>G (p.Thr159Ala) | gnomAD v4 |
8 | g.18400868A>T | CA370636786 | NAT2 | c.865A>T (p.Thr289Ser) c.475A>T (p.Thr159Ser) | |
8 | g.18400869C>A | CA370636787 | NAT2 | c.866C>A (p.Thr289Asn) c.476C>A (p.Thr159Asn) | |
8 | g.18400869C>G | CA370636788 | NAT2 | c.866C>G (p.Thr289Ser) c.476C>G (p.Thr159Ser) | |
8 | g.18400869C>T | CA370636789 | NAT2 | c.866C>T (p.Thr289Ile) c.476C>T (p.Thr159Ile) | |
8 | g.18400870T>A | CA459700185 | NAT2 | c.867T>A (p.Thr289=) c.477T>A (p.Thr159=) | |
8 | g.18400870T>C | CA173519952 | NAT2 | c.867T>C (p.Thr289=) c.477T>C (p.Thr159=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400870T>G | CA459700188 | NAT2 | c.867T>G (p.Thr289=) c.477T>G (p.Thr159=) | |
8 | g.18400870T= | CA1768219192 | NAT2 | c.867T= (p.Thr289=) c.477T= (p.Thr159=) | |
8 | g.18400871A= | CA1768219193 | NAT2 | c.868A= (p.Ile290=) c.478A= (p.Ile160=) | |
8 | g.18400871A>C | CA370636792 | NAT2 | c.868A>C (p.Ile290Leu) c.478A>C (p.Ile160Leu) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.18400871A>G | CA370636791 | NAT2 | c.868A>G (p.Ile290Val) c.478A>G (p.Ile160Val) | |
8 | g.18400871A>T | CA370636790 | NAT2 | c.868A>T (p.Ile290Phe) c.478A>T (p.Ile160Phe) | |
8 | g.18400872T>A | CA370636793 | NAT2 | c.869T>A (p.Ile290Asn) c.479T>A (p.Ile160Asn) | |
8 | g.18400872T>C | CA4651717 | NAT2 | c.869T>C (p.Ile290Thr) c.479T>C (p.Ile160Thr) | dbSNP ExAC gnomAD v2 |
8 | g.18400872T>G | CA370636794 | NAT2 | c.869T>G (p.Ile290Ser) c.479T>G (p.Ile160Ser) | |
8 | g.18400872T= | CA1768219194 | NAT2 | c.869T= (p.Ile290=) c.479T= (p.Ile160=) | |
8 | g.18400873T>A | CA459700199 | NAT2 | c.870T>A (p.Ile290=) c.480T>A (p.Ile160=) |