| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.77917594C>A | CA340885039 | NEXN | c.56C>A (p.Pro19Gln) c.28-366C>A (n.28-366C>A) | |
| 1 | g.77917594C>G | CA340885043 | NEXN | c.56C>G (p.Pro19Arg) c.28-366C>G (n.28-366C>G) | |
| 1 | g.77917594C>T | CA340885036 | NEXN | c.56C>T (p.Pro19Leu) c.28-366C>T (n.28-366C>T) | gnomAD v4 |
| 1 | g.77917594_77917595del | CA2572913996 | NEXN | c.56_57del (p.Pro19GlnfsTer11) c.28-366_28-365del (n.28-366_28-365del) | |
| 1 | g.77917595A>C | CA418571011 | NEXN | c.57A>C (p.Pro19=) c.28-365A>C (n.28-365A>C) | |
| 1 | g.77917595A>G | CA418571012 | NEXN | c.57A>G (p.Pro19=) c.28-365A>G (n.28-365A>G) | |
| 1 | g.77917595A>T | CA418571013 | NEXN | c.57A>T (p.Pro19=) c.28-365A>T (n.28-365A>T) | |
| 1 | g.77917599del | CA2565589958 | NEXN | c.61del (p.Thr21ProfsTer11) c.28-361del (n.28-361del) | gnomAD v4 |
| 1 | g.77917596A>C | CA340885047 | NEXN | c.58A>C (p.Lys20Gln) c.28-364A>C (n.28-364A>C) | |
| 1 | g.77917596A>G | CA340885045 | NEXN | c.58A>G (p.Lys20Glu) c.28-364A>G (n.28-364A>G) | |
| 1 | g.77917596A>T | CA340885050 | NEXN | c.58A>T (p.Lys20Ter) c.28-364A>T (n.28-364A>T) | |
| 1 | g.77917597A>C | CA340885052 | NEXN | c.59A>C (p.Lys20Thr) c.28-363A>C (n.28-363A>C) | |
| 1 | g.77917597A>G | CA340885053 | NEXN | c.59A>G (p.Lys20Arg) c.28-363A>G (n.28-363A>G) | |
| 1 | g.77917597A>T | CA340885054 | NEXN | c.59A>T (p.Lys20Ile) c.28-363A>T (n.28-363A>T) | |
| 1 | g.77917598A= | CA1177620123 | NEXN | c.60A= (p.Lys20=) c.28-362A= (n.28-362A=) | |
| 1 | g.77917598A>C | CA340885055 | NEXN | c.60A>C (p.Lys20Asn) c.28-362A>C (n.28-362A>C) | ClinVar dbSNP |
| 1 | g.77917598A>G | CA418571017 | NEXN | c.60A>G (p.Lys20=) c.28-362A>G (n.28-362A>G) | |
| 1 | g.77917598A>T | CA340885056 | NEXN | c.60A>T (p.Lys20Asn) c.28-362A>T (n.28-362A>T) | |
| 1 | g.77917599A= | CA1177620124 | NEXN | c.61A= (p.Thr21=) c.28-361A= (n.28-361A=) | |
| 1 | g.77917599A>C | CA340885059 | NEXN | c.61A>C (p.Thr21Pro) c.28-361A>C (n.28-361A>C) | |
| 1 | g.77917599A>G | CA340885061 | NEXN | c.61A>G (p.Thr21Ala) c.28-361A>G (n.28-361A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77917599A>T | CA340885072 | NEXN | c.61A>T (p.Thr21Ser) c.28-361A>T (n.28-361A>T) | |
| 1 | g.77917599_77917600insGT | CA2562331965 | NEXN | c.61_62insGT (p.Thr21SerfsTer12) c.28-361_28-360insGT (n.28-361_28-360insGT) | |
| 1 | g.77917600C>A | CA340885074 | NEXN | c.62C>A (p.Thr21Asn) c.28-360C>A (n.28-360C>A) | |
| 1 | g.77917600C= | CA1177620125 | NEXN | c.62C= (p.Thr21=) c.28-360C= (n.28-360C=) | |
| 1 | g.77917600C>G | CA340885079 | NEXN | c.62C>G (p.Thr21Ser) c.28-360C>G (n.28-360C>G) | dbSNP |
| 1 | g.77917600C>T | CA335382 | NEXN | c.62C>T (p.Thr21Ile) c.28-360C>T (n.28-360C>T) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77917601C>A | CA418571021 | NEXN | c.63C>A (p.Thr21=) c.28-359C>A (n.28-359C>A) | |
| 1 | g.77917601C>G | CA418571022 | NEXN | c.63C>G (p.Thr21=) c.28-359C>G (n.28-359C>G) | gnomAD v4 |
| 1 | g.77917601C>T | CA418571023 | NEXN | c.63C>T (p.Thr21=) c.28-359C>T (n.28-359C>T) | |
| 1 | g.77917602T>A | CA340885084 | NEXN | c.64T>A (p.Tyr22Asn) c.28-358T>A (n.28-358T>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77917602T>C | CA340885083 | NEXN | c.64T>C (p.Tyr22His) c.28-358T>C (n.28-358T>C) | |
| 1 | g.77917602T>G | CA340885082 | NEXN | c.64T>G (p.Tyr22Asp) c.28-358T>G (n.28-358T>G) | |
| 1 | g.77917602T= | CA1177620126 | NEXN | c.64T= (p.Tyr22=) c.28-358T= (n.28-358T=) | |
| 1 | g.77917603A= | CA1177620127 | NEXN | c.65A= (p.Tyr22=) c.28-357A= (n.28-357A=) | |
| 1 | g.77917603A>C | CA340885085 | NEXN | c.65A>C (p.Tyr22Ser) c.28-357A>C (n.28-357A>C) | |
| 1 | g.77917603A>G | CA16042401 | NEXN | c.65A>G (p.Tyr22Cys) c.28-357A>G (n.28-357A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 1 | g.77917603A>T | CA340885086 | NEXN | c.65A>T (p.Tyr22Phe) c.28-357A>T (n.28-357A>T) | |
| 1 | g.77917604T>A | CA340885087 | NEXN | c.66T>A (p.Tyr22Ter) c.28-356T>A (n.28-356T>A) | |
| 1 | g.77917604T>C | CA918558 | NEXN | c.66T>C (p.Tyr22=) c.28-356T>C (n.28-356T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917604T>G | CA340885089 | NEXN | c.66T>G (p.Tyr22Ter) c.28-356T>G (n.28-356T>G) | |
| 1 | g.77917604T= | CA1149071512 | NEXN | c.66T= (p.Tyr22=) c.28-356T= (n.28-356T=) | |
| 1 | g.77917605G>A | CA24705157 | NEXN | c.67G>A (p.Val23Ile) c.28-355G>A (n.28-355G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77917605G>C | CA340885098 | NEXN | c.67G>C (p.Val23Leu) c.28-355G>C (n.28-355G>C) | |
| 1 | g.77917605G= | CA1147623050 | NEXN | c.67G= (p.Val23=) c.28-355G= (n.28-355G=) | |
| 1 | g.77917605G>T | CA340885101 | NEXN | c.67G>T (p.Val23Leu) c.28-355G>T (n.28-355G>T) | |
| 1 | g.77917606T>A | CA340885105 | NEXN | c.68T>A (p.Val23Glu) c.28-354T>A (n.28-354T>A) | |
| 1 | g.77917606T>C | CA340885108 | NEXN | c.68T>C (p.Val23Ala) c.28-354T>C (n.28-354T>C) | COSMIC COSMIC |
| 1 | g.77917606T>G | CA340885111 | NEXN | c.68T>G (p.Val23Gly) c.28-354T>G (n.28-354T>G) | |
| 1 | g.77917607A>C | CA418571028 | NEXN | c.69A>C (p.Val23=) c.28-353A>C (n.28-353A>C) |