Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.51806761A>C | CA384885136 | SCN8A | c.5275A>C (p.Asn1759His) c.3339A>C c.5152A>C (p.Asn1718His) c.5308A>C (p.Asn1770His) | |
12 | g.51806761A>G | CA384885137 | SCN8A | c.5275A>G (p.Asn1759Asp) c.3339A>G c.5152A>G (p.Asn1718Asp) c.5308A>G (p.Asn1770Asp) | |
12 | g.51806761A>T | CA384885138 | SCN8A | c.5275A>T (p.Asn1759Tyr) c.3339A>T c.5152A>T (p.Asn1718Tyr) c.5308A>T (p.Asn1770Tyr) | |
12 | g.51806762A= | CA2036193679 | SCN8A | c.5276A= (p.Asn1759=) c.3340A= c.5153A= (p.Asn1718=) c.5309A= (p.Asn1770=) | |
12 | g.51806762A>C | CA384885145 | SCN8A | c.5276A>C (p.Asn1759Thr) c.3340A>C c.5153A>C (p.Asn1718Thr) c.5309A>C (p.Asn1770Thr) | |
12 | g.51806762A>G | CA354191 | SCN8A | c.5276A>G (p.Asn1759Ser) c.3340A>G c.5153A>G (p.Asn1718Ser) c.5309A>G (p.Asn1770Ser) | ClinVar dbSNP |
12 | g.51806762A>T | CA384885143 | SCN8A | c.5276A>T (p.Asn1759Ile) c.3340A>T c.5153A>T (p.Asn1718Ile) c.5309A>T (p.Asn1770Ile) | |
12 | g.51806763C>A | CA384885150 | SCN8A | c.5277C>A (p.Asn1759Lys) c.3341C>A c.5154C>A (p.Asn1718Lys) c.5310C>A (p.Asn1770Lys) | |
12 | g.51806763C>G | CA384885151 | SCN8A | c.5277C>G (p.Asn1759Lys) c.3341C>G c.5154C>G (p.Asn1718Lys) c.5310C>G (p.Asn1770Lys) | |
12 | g.51806763C>T | CA480061934 | SCN8A | c.5277C>T (p.Asn1759=) c.3341C>T c.5154C>T (p.Asn1718=) c.5310C>T (p.Asn1770=) | |
12 | g.51806764A= | CA2036193689 | SCN8A | c.5278A= (p.Met1760=) c.3342A= c.5155A= (p.Met1719=) c.5311A= (p.Met1771=) | |
12 | g.51806764A>C | CA384885152 | SCN8A | c.5278A>C (p.Met1760Leu) c.3342A>C c.5155A>C (p.Met1719Leu) c.5311A>C (p.Met1771Leu) | |
12 | g.51806764A>G | CA384885154 | SCN8A | c.5278A>G (p.Met1760Val) c.3342A>G c.5155A>G (p.Met1719Val) c.5311A>G (p.Met1771Val) | ClinVar dbSNP |
12 | g.51806764A>T | CA384885156 | SCN8A | c.5278A>T (p.Met1760Leu) c.3342A>T c.5155A>T (p.Met1719Leu) c.5311A>T (p.Met1771Leu) | |
12 | g.51806765T>A | CA384885157 | SCN8A | c.5279T>A (p.Met1760Lys) c.3343T>A c.5156T>A (p.Met1719Lys) c.5312T>A (p.Met1771Lys) | |
12 | g.51806765T>C | CA384885161 | SCN8A | c.5279T>C (p.Met1760Thr) c.3343T>C c.5156T>C (p.Met1719Thr) c.5312T>C (p.Met1771Thr) | ClinVar dbSNP |
12 | g.51806765T>G | CA384885158 | SCN8A | c.5279T>G (p.Met1760Arg) c.3343T>G c.5156T>G (p.Met1719Arg) c.5312T>G (p.Met1771Arg) | |
12 | g.51806765T= | CA2036193699 | SCN8A | c.5279T= (p.Met1760=) c.3343T= c.5156T= (p.Met1719=) c.5312T= (p.Met1771=) | |
12 | g.51806766G>A | CA384885163 | SCN8A | c.5280G>A (p.Met1760Ile) c.3344G>A c.5157G>A (p.Met1719Ile) c.5313G>A (p.Met1771Ile) | ClinVar dbSNP |
12 | g.51806766G>C | CA384885164 | SCN8A | c.5280G>C (p.Met1760Ile) c.3344G>C c.5157G>C (p.Met1719Ile) c.5313G>C (p.Met1771Ile) | COSMIC COSMIC |
12 | g.51806766G= | CA2036193711 | SCN8A | c.5280G= (p.Met1760=) c.3344G= c.5157G= (p.Met1719=) c.5313G= (p.Met1771=) | |
12 | g.51806766G>T | CA384885165 | SCN8A | c.5280G>T (p.Met1760Ile) c.3344G>T c.5157G>T (p.Met1719Ile) c.5313G>T (p.Met1771Ile) | |
12 | g.51806767T>A | CA384885168 | SCN8A | c.5281T>A (p.Tyr1761Asn) c.3345T>A c.5158T>A (p.Tyr1720Asn) c.5314T>A (p.Tyr1772Asn) | |
12 | g.51806767T>C | CA384885170 | SCN8A | c.5281T>C (p.Tyr1761His) c.3345T>C c.5158T>C (p.Tyr1720His) c.5314T>C (p.Tyr1772His) | |
12 | g.51806767T>G | CA384885171 | SCN8A | c.5281T>G (p.Tyr1761Asp) c.3345T>G c.5158T>G (p.Tyr1720Asp) c.5314T>G (p.Tyr1772Asp) | |
12 | g.51806768A>C | CA384885172 | SCN8A | c.5282A>C (p.Tyr1761Ser) c.3346A>C c.5159A>C (p.Tyr1720Ser) c.5315A>C (p.Tyr1772Ser) | |
12 | g.51806768A>G | CA384885173 | SCN8A | c.5282A>G (p.Tyr1761Cys) c.3346A>G c.5159A>G (p.Tyr1720Cys) c.5315A>G (p.Tyr1772Cys) | gnomAD v4 |
12 | g.51806768A>T | CA384885174 | SCN8A | c.5282A>T (p.Tyr1761Phe) c.3346A>T c.5159A>T (p.Tyr1720Phe) c.5315A>T (p.Tyr1772Phe) | |
12 | g.51806769C>A | CA384885177 | SCN8A | c.5283C>A (p.Tyr1761Ter) c.3347C>A c.5160C>A (p.Tyr1720Ter) c.5316C>A (p.Tyr1772Ter) | |
12 | g.51806769C= | CA2036193718 | SCN8A | c.5283C= (p.Tyr1761=) c.3347C= c.5160C= (p.Tyr1720=) c.5316C= (p.Tyr1772=) | |
12 | g.51806769C>G | CA384885179 | SCN8A | c.5283C>G (p.Tyr1761Ter) c.3347C>G c.5160C>G (p.Tyr1720Ter) c.5316C>G (p.Tyr1772Ter) | |
12 | g.51806769C>T | CA6571905 | SCN8A | c.5283C>T (p.Tyr1761=) c.3347C>T c.5160C>T (p.Tyr1720=) c.5316C>T (p.Tyr1772=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.51806770A>C | CA384885184 | SCN8A | c.5284A>C (p.Ile1762Leu) c.3348A>C c.5161A>C (p.Ile1721Leu) c.5317A>C (p.Ile1773Leu) | ClinVar |
12 | g.51806770A>G | CA384885188 | SCN8A | c.5284A>G (p.Ile1762Val) c.3348A>G c.5161A>G (p.Ile1721Val) c.5317A>G (p.Ile1773Val) | ClinVar |
12 | g.51806770A>T | CA384885186 | SCN8A | c.5284A>T (p.Ile1762Phe) c.3348A>T c.5161A>T (p.Ile1721Phe) c.5317A>T (p.Ile1773Phe) | ClinVar dbSNP |
12 | g.51806771T>A | CA384885191 | SCN8A | c.5285T>A (p.Ile1762Asn) c.3349T>A c.5162T>A (p.Ile1721Asn) c.5318T>A (p.Ile1773Asn) | |
12 | g.51806771T>C | CA384885193 | SCN8A | c.5285T>C (p.Ile1762Thr) c.3349T>C c.5162T>C (p.Ile1721Thr) c.5318T>C (p.Ile1773Thr) | |
12 | g.51806771T>G | CA384885192 | SCN8A | c.5285T>G (p.Ile1762Ser) c.3349T>G c.5162T>G (p.Ile1721Ser) c.5318T>G (p.Ile1773Ser) | |
12 | g.51806772T>A | CA480061948 | SCN8A | c.5286T>A (p.Ile1762=) c.3350T>A c.5163T>A (p.Ile1721=) c.5319T>A (p.Ile1773=) | |
12 | g.51806772T>C | CA480061950 | SCN8A | c.5286T>C (p.Ile1762=) c.3350T>C c.5163T>C (p.Ile1721=) c.5319T>C (p.Ile1773=) | |
12 | g.51806772T>G | CA384885194 | SCN8A | c.5286T>G (p.Ile1762Met) c.3350T>G c.5163T>G (p.Ile1721Met) c.5319T>G (p.Ile1773Met) | |
12 | g.51806773G>A | CA384885195 | SCN8A | c.5287G>A (p.Ala1763Thr) c.3351G>A c.5164G>A (p.Ala1722Thr) c.5320G>A (p.Ala1774Thr) | |
12 | g.51806773G>C | CA384885196 | SCN8A | c.5287G>C (p.Ala1763Pro) c.3351G>C c.5164G>C (p.Ala1722Pro) c.5320G>C (p.Ala1774Pro) | |
12 | g.51806773G>T | CA384885197 | SCN8A | c.5287G>T (p.Ala1763Ser) c.3351G>T c.5164G>T (p.Ala1722Ser) c.5320G>T (p.Ala1774Ser) | |
12 | g.51806774C>A | CA384885198 | SCN8A | c.5288C>A (p.Ala1763Asp) c.3352C>A c.5165C>A (p.Ala1722Asp) c.5321C>A (p.Ala1774Asp) | |
12 | g.51806774C>G | CA384885199 | SCN8A | c.5288C>G (p.Ala1763Gly) c.3352C>G c.5165C>G (p.Ala1722Gly) c.5321C>G (p.Ala1774Gly) | |
12 | g.51806774C>T | CA384885200 | SCN8A | c.5288C>T (p.Ala1763Val) c.3352C>T c.5165C>T (p.Ala1722Val) c.5321C>T (p.Ala1774Val) | |
12 | g.51806775C>A | CA480061956 | SCN8A | c.5289C>A (p.Ala1763=) c.3353C>A c.5166C>A (p.Ala1722=) c.5322C>A (p.Ala1774=) | |
12 | g.51806775C>G | CA480061954 | SCN8A | c.5289C>G (p.Ala1763=) c.3353C>G c.5166C>G (p.Ala1722=) c.5322C>G (p.Ala1774=) | |
12 | g.51806775C>T | CA480061955 | SCN8A | c.5289C>T (p.Ala1763=) c.3353C>T c.5166C>T (p.Ala1722=) c.5322C>T (p.Ala1774=) | gnomAD v4 |