Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.77917960A= | CA1148224369 | NEXN | c.220A= (p.Ile74=) c.28A= (p.Ile10=) | |
1 | g.77917960A>C | CA177484 | NEXN | c.220A>C (p.Ile74Leu) c.28A>C (p.Ile10Leu) | ClinVar dbSNP |
1 | g.77917960A>G | CA340886143 | NEXN | c.220A>G (p.Ile74Val) c.28A>G (p.Ile10Val) | |
1 | g.77917960A>T | CA340886144 | NEXN | c.220A>T (p.Ile74Phe) c.28A>T (p.Ile10Phe) | |
1 | g.77917961T>A | CA340886148 | NEXN | c.221T>A (p.Ile74Asn) c.29T>A (p.Ile10Asn) | |
1 | g.77917961T>C | CA340886152 | NEXN | c.221T>C (p.Ile74Thr) c.29T>C (p.Ile10Thr) | |
1 | g.77917961T>G | CA340886151 | NEXN | c.221T>G (p.Ile74Ser) c.29T>G (p.Ile10Ser) | |
1 | g.77917962T>A | CA418708964 | NEXN | c.222T>A (p.Ile74=) c.30T>A (p.Ile10=) | |
1 | g.77917962T>C | CA918597 | NEXN | c.222T>C (p.Ile74=) c.30T>C (p.Ile10=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77917962T>G | CA340886157 | NEXN | c.222T>G (p.Ile74Met) c.30T>G (p.Ile10Met) | |
1 | g.77917962T= | CA1177620256 | NEXN | c.222T= (p.Ile74=) c.30T= (p.Ile10=) | |
1 | g.77917963A>C | CA340886159 | NEXN | c.223A>C (p.Lys75Gln) c.31A>C (p.Lys11Gln) | |
1 | g.77917963A>G | CA340886161 | NEXN | c.223A>G (p.Lys75Glu) c.31A>G (p.Lys11Glu) | |
1 | g.77917963A>T | CA340886163 | NEXN | c.223A>T (p.Lys75Ter) c.31A>T (p.Lys11Ter) | |
1 | g.77917964A>C | CA340886166 | NEXN | c.224A>C (p.Lys75Thr) c.32A>C (p.Lys11Thr) | |
1 | g.77917964A>G | CA340886168 | NEXN | c.224A>G (p.Lys75Arg) c.32A>G (p.Lys11Arg) | |
1 | g.77917964A>T | CA340886173 | NEXN | c.224A>T (p.Lys75Ile) c.32A>T (p.Lys11Ile) | |
1 | g.77917965A>C | CA340886175 | NEXN | c.225A>C (p.Lys75Asn) c.33A>C (p.Lys11Asn) | |
1 | g.77917965A>G | CA418708970 | NEXN | c.225A>G (p.Lys75=) c.33A>G (p.Lys11=) | |
1 | g.77917965A>T | CA340886176 | NEXN | c.225A>T (p.Lys75Asn) c.33A>T (p.Lys11Asn) | |
1 | g.77917966G>A | CA340886179 | NEXN | c.226G>A (p.Glu76Lys) c.34G>A (p.Glu12Lys) | |
1 | g.77917966G>C | CA340886181 | NEXN | c.226G>C (p.Glu76Gln) c.34G>C (p.Glu12Gln) | |
1 | g.77917966G>T | CA340886182 | NEXN | c.226G>T (p.Glu76Ter) c.34G>T (p.Glu12Ter) | |
1 | g.77917967A= | CA1143588419 | NEXN | c.227A= (p.Glu76=) c.35A= (p.Glu12=) | |
1 | g.77917967A>C | CA340886186 | NEXN | c.227A>C (p.Glu76Ala) c.35A>C (p.Glu12Ala) | |
1 | g.77917967A>G | CA24705285 | NEXN | c.227A>G (p.Glu76Gly) c.35A>G (p.Glu12Gly) | ClinVar dbSNP gnomAD v4 |
1 | g.77917967A>T | CA340886184 | NEXN | c.227A>T (p.Glu76Val) c.35A>T (p.Glu12Val) | |
1 | g.77917968A>C | CA340886188 | NEXN | c.228A>C (p.Glu76Asp) c.36A>C (p.Glu12Asp) | |
1 | g.77917968A>G | CA418708973 | NEXN | c.228A>G (p.Glu76=) c.36A>G (p.Glu12=) | gnomAD v4 |
1 | g.77917968A>T | CA340886190 | NEXN | c.228A>T (p.Glu76Asp) c.36A>T (p.Glu12Asp) | |
1 | g.77917969A= | CA1177620257 | NEXN | c.229A= (p.Met77=) c.37A= (p.Met13=) | |
1 | g.77917969A>C | CA340886191 | NEXN | c.229A>C (p.Met77Leu) c.37A>C (p.Met13Leu) | |
1 | g.77917969A>G | CA340886193 | NEXN | c.229A>G (p.Met77Val) c.37A>G (p.Met13Val) | |
1 | g.77917969A>T | CA340886194 | NEXN | c.229A>T (p.Met77Leu) c.37A>T (p.Met13Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77917970T>A | CA340886196 | NEXN | c.230T>A (p.Met77Lys) c.38T>A (p.Met13Lys) | |
1 | g.77917970T>C | CA340886198 | NEXN | c.230T>C (p.Met77Thr) c.38T>C (p.Met13Thr) | |
1 | g.77917970T>G | CA340886200 | NEXN | c.230T>G (p.Met77Arg) c.38T>G (p.Met13Arg) | |
1 | g.77917971G>A | CA340886201 | NEXN | c.231G>A (p.Met77Ile) c.39G>A (p.Met13Ile) | |
1 | g.77917971G>C | CA340886202 | NEXN | c.231G>C (p.Met77Ile) c.39G>C (p.Met13Ile) | gnomAD v4 |
1 | g.77917971G>T | CA340886205 | NEXN | c.231G>T (p.Met77Ile) c.39G>T (p.Met13Ile) | |
1 | g.77917972C>A | CA340886207 | NEXN | c.232C>A (p.Leu78Ile) c.40C>A (p.Leu14Ile) | COSMIC COSMIC |
1 | g.77917972C= | CA1177620258 | NEXN | c.232C= (p.Leu78=) c.40C= (p.Leu14=) | |
1 | g.77917972C>G | CA340886208 | NEXN | c.232C>G (p.Leu78Val) c.40C>G (p.Leu14Val) | gnomAD v4 |
1 | g.77917972C>T | CA340886209 | NEXN | c.232C>T (p.Leu78Phe) c.40C>T (p.Leu14Phe) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77917973T>A | CA340886213 | NEXN | c.233T>A (p.Leu78His) c.41T>A (p.Leu14His) | |
1 | g.77917973T>C | CA340886214 | NEXN | c.233T>C (p.Leu78Pro) c.41T>C (p.Leu14Pro) | |
1 | g.77917973T>G | CA340886211 | NEXN | c.233T>G (p.Leu78Arg) c.41T>G (p.Leu14Arg) | |
1 | g.77917974T>A | CA418708980 | NEXN | c.234T>A (p.Leu78=) c.42T>A (p.Leu14=) | |
1 | g.77917974T>C | CA418708981 | NEXN | c.234T>C (p.Leu78=) c.42T>C (p.Leu14=) | |
1 | g.77917974T>G | CA418708982 | NEXN | c.234T>G (p.Leu78=) c.42T>G (p.Leu14=) | gnomAD v4 |