Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.47574082_47574194del | CA2580101019 | SYN1 | c.1794_1906del (p.Thr601GlufsTer?) c.70+498_70+610del (n.70+498_70+610del) | ClinVar |
X | g.47574093G>A | CA412822250 | SYN1 | c.1891C>T (p.Arg631Cys) c.70+595C>T (n.70+595C>T) | gnomAD v4 |
X | g.47574093G>C | CA412822251 | SYN1 | c.1891C>G (p.Arg631Gly) c.70+595C>G (n.70+595C>G) | |
X | g.47574093G>T | CA412822252 | SYN1 | c.1891C>A (p.Arg631Ser) c.70+595C>A (n.70+595C>A) | gnomAD v4 |
X | g.47574094T>A | CA516353319 | SYN1 | c.1890A>T (p.Gly630=) c.70+594A>T (n.70+594A>T) | |
X | g.47574094T>C | CA516353320 | SYN1 | c.1890A>G (p.Gly630=) c.70+594A>G (n.70+594A>G) | gnomAD v4 |
X | g.47574094T>G | CA516353321 | SYN1 | c.1890A>C (p.Gly630=) c.70+594A>C (n.70+594A>C) | |
X | g.47574095C>A | CA412822253 | SYN1 | c.1889G>T (p.Gly630Val) c.70+593G>T (n.70+593G>T) | gnomAD v4 |
X | g.47574095C>G | CA412822254 | SYN1 | c.1889G>C (p.Gly630Ala) c.70+593G>C (n.70+593G>C) | |
X | g.47574095C>T | CA412822255 | SYN1 | c.1889G>A (p.Gly630Glu) c.70+593G>A (n.70+593G>A) | gnomAD v4 |
X | g.47574096C>A | CA412822256 | SYN1 | c.1888G>T (p.Gly630Ter) c.70+592G>T (n.70+592G>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47574096C= | CA2427971182 | SYN1 | c.1888G= (p.Gly630=) c.70+592G= (n.70+592G=) | |
X | g.47574096C>G | CA412822257 | SYN1 | c.1888G>C (p.Gly630Arg) c.70+592G>C (n.70+592G>C) | gnomAD v4 |
X | g.47574096C>T | CA412822258 | SYN1 | c.1888G>A (p.Gly630Arg) c.70+592G>A (n.70+592G>A) | gnomAD v4 |
X | g.47574097A= | CA2427971183 | SYN1 | c.1887T= (p.Ala629=) c.70+591T= (n.70+591T=) | |
X | g.47574097A>C | CA516353324 | SYN1 | c.1887T>G (p.Ala629=) c.70+591T>G (n.70+591T>G) | |
X | g.47574097A>G | CA516353325 | SYN1 | c.1887T>C (p.Ala629=) c.70+591T>C (n.70+591T>C) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47574097A>T | CA516353323 | SYN1 | c.1887T>A (p.Ala629=) c.70+591T>A (n.70+591T>A) | gnomAD v4 |
X | g.47574098G>A | CA412822261 | SYN1 | c.1886C>T (p.Ala629Val) c.70+590C>T (n.70+590C>T) | gnomAD v4 |
X | g.47574098G>C | CA412822260 | SYN1 | c.1886C>G (p.Ala629Gly) c.70+590C>G (n.70+590C>G) | |
X | g.47574098G>T | CA412822259 | SYN1 | c.1886C>A (p.Ala629Asp) c.70+590C>A (n.70+590C>A) | gnomAD v4 |
X | g.47574099C>A | CA412822262 | SYN1 | c.1885G>T (p.Ala629Ser) c.70+589G>T (n.70+589G>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47574099C= | CA2427971184 | SYN1 | c.1885G= (p.Ala629=) c.70+589G= (n.70+589G=) | |
X | g.47574099C>G | CA412822263 | SYN1 | c.1885G>C (p.Ala629Pro) c.70+589G>C (n.70+589G>C) | gnomAD v4 |
X | g.47574099C>T | CA412822264 | SYN1 | c.1885G>A (p.Ala629Thr) c.70+589G>A (n.70+589G>A) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47574100G>A | CA516353327 | SYN1 | c.1884C>T (p.Pro628=) c.70+588C>T (n.70+588C>T) | ClinVar dbSNP gnomAD v4 |
X | g.47574100G>C | CA516353328 | SYN1 | c.1884C>G (p.Pro628=) c.70+588C>G (n.70+588C>G) | |
X | g.47574100G>T | CA516353329 | SYN1 | c.1884C>A (p.Pro628=) c.70+588C>A (n.70+588C>A) | gnomAD v4 |
X | g.47574103del | CA2523321858 | SYN1 | c.1884del (p.Ala629LeufsTer?) c.70+588del (n.70+588del) | gnomAD v4 |
X | g.47574102_47574103del | CA2579596676 | SYN1 | c.1883_1884del (p.Pro628ArgfsTer?) c.70+587_70+588del (n.70+587_70+588del) | gnomAD v4 |
X | g.47574101G>A | CA412822265 | SYN1 | c.1883C>T (p.Pro628Leu) c.70+587C>T (n.70+587C>T) | gnomAD v4 |
X | g.47574101G>C | CA412822266 | SYN1 | c.1883C>G (p.Pro628Arg) c.70+587C>G (n.70+587C>G) | |
X | g.47574101G>T | CA412822267 | SYN1 | c.1883C>A (p.Pro628His) c.70+587C>A (n.70+587C>A) | gnomAD v4 |
X | g.47574102G>A | CA412822268 | SYN1 | c.1882C>T (p.Pro628Ser) c.70+586C>T (n.70+586C>T) | gnomAD v4 |
X | g.47574102G>C | CA412822269 | SYN1 | c.1882C>G (p.Pro628Ala) c.70+586C>G (n.70+586C>G) | |
X | g.47574102G>T | CA412822270 | SYN1 | c.1882C>A (p.Pro628Thr) c.70+586C>A (n.70+586C>A) | gnomAD v4 |
X | g.47574103G>A | CA10398345 | SYN1 | c.1881C>T (p.Gly627=) c.70+585C>T (n.70+585C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.47574103G>C | CA516353331 | SYN1 | c.1881C>G (p.Gly627=) c.70+585C>G (n.70+585C>G) | |
X | g.47574103G= | CA2427971185 | SYN1 | c.1881C= (p.Gly627=) c.70+585C= (n.70+585C=) | |
X | g.47574103G>T | CA516353330 | SYN1 | c.1881C>A (p.Gly627=) c.70+585C>A (n.70+585C>A) | gnomAD v4 |
X | g.47574104C>A | CA412822272 | SYN1 | c.1880G>T (p.Gly627Val) c.70+584G>T (n.70+584G>T) | gnomAD v4 |
X | g.47574104C>G | CA412822273 | SYN1 | c.1880G>C (p.Gly627Ala) c.70+584G>C (n.70+584G>C) | |
X | g.47574104C>T | CA412822274 | SYN1 | c.1880G>A (p.Gly627Asp) c.70+584G>A (n.70+584G>A) | gnomAD v4 |
X | g.47574106del | CA2693584636 | SYN1 | c.1880del (p.Gly627AlafsTer?) c.70+584del (n.70+584del) | gnomAD v4 |
X | g.47574105C>A | CA412822278 | SYN1 | c.1879G>T (p.Gly627Cys) c.70+583G>T (n.70+583G>T) | gnomAD v4 |
X | g.47574105C>G | CA412822276 | SYN1 | c.1879G>C (p.Gly627Arg) c.70+583G>C (n.70+583G>C) | |
X | g.47574105C>T | CA412822277 | SYN1 | c.1879G>A (p.Gly627Ser) c.70+583G>A (n.70+583G>A) | gnomAD v4 |
X | g.47574106C>A | CA516353332 | SYN1 | c.1878G>T (p.Pro626=) c.70+582G>T (n.70+582G>T) | gnomAD v4 |
X | g.47574106C= | CA2427971186 | SYN1 | c.1878G= (p.Pro626=) c.70+582G= (n.70+582G=) | |
X | g.47574106C>G | CA516353333 | SYN1 | c.1878G>C (p.Pro626=) c.70+582G>C (n.70+582G>C) | gnomAD v4 |
X | g.47574106C>T | CA516353334 | SYN1 | c.1878G>A (p.Pro626=) c.70+582G>A (n.70+582G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47574107G>A | CA412822280 | SYN1 | c.1877C>T (p.Pro626Leu) c.70+581C>T (n.70+581C>T) | gnomAD v4 |
X | g.47574107G>C | CA412822281 | SYN1 | c.1877C>G (p.Pro626Arg) c.70+581C>G (n.70+581C>G) | |
X | g.47574107G>T | CA412822282 | SYN1 | c.1877C>A (p.Pro626Gln) c.70+581C>A (n.70+581C>A) | gnomAD v4 |
X | g.47574108G>A | CA412822284 | SYN1 | c.1876C>T (p.Pro626Ser) c.70+580C>T (n.70+580C>T) | |
X | g.47574108G>C | CA412822285 | SYN1 | c.1876C>G (p.Pro626Ala) c.70+580C>G (n.70+580C>G) | |
X | g.47574108G>T | CA412822287 | SYN1 | c.1876C>A (p.Pro626Thr) c.70+580C>A (n.70+580C>A) | gnomAD v4 |
X | g.47574109G>A | CA516353337 | SYN1 | c.1875C>T (p.Gly625=) c.70+579C>T (n.70+579C>T) | gnomAD v4 |
X | g.47574109G>C | CA516353338 | SYN1 | c.1875C>G (p.Gly625=) c.70+579C>G (n.70+579C>G) | |
X | g.47574109G>T | CA516353339 | SYN1 | c.1875C>A (p.Gly625=) c.70+579C>A (n.70+579C>A) | gnomAD v4 |
X | g.47574110C>A | CA412822289 | SYN1 | c.1874G>T (p.Gly625Val) c.70+578G>T (n.70+578G>T) | gnomAD v4 |
X | g.47574110C>G | CA412822291 | SYN1 | c.1874G>C (p.Gly625Ala) c.70+578G>C (n.70+578G>C) | |
X | g.47574110C>T | CA412822292 | SYN1 | c.1874G>A (p.Gly625Asp) c.70+578G>A (n.70+578G>A) | gnomAD v4 |
X | g.47574110_47574111dup | CA2579596677 | SYN1 | c.1873_1874dup (p.Pro626AlafsTer?) c.70+577_70+578dup (n.70+577_70+578dup) | gnomAD v4 |
X | g.47574111C>A | CA412822294 | SYN1 | c.1873G>T (p.Gly625Cys) c.70+577G>T (n.70+577G>T) | gnomAD v4 |
X | g.47574111C>G | CA412822296 | SYN1 | c.1873G>C (p.Gly625Arg) c.70+577G>C (n.70+577G>C) | |
X | g.47574111C>T | CA412822297 | SYN1 | c.1873G>A (p.Gly625Ser) c.70+577G>A (n.70+577G>A) | gnomAD v4 |
X | g.47574112G>A | CA516353343 | SYN1 | c.1872C>T (p.Ser624=) c.70+576C>T (n.70+576C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47574112G>C | CA412822299 | SYN1 | c.1872C>G (p.Ser624Arg) c.70+576C>G (n.70+576C>G) | gnomAD v4 |
X | g.47574112G= | CA2427971187 | SYN1 | c.1872C= (p.Ser624=) c.70+576C= (n.70+576C=) | |
X | g.47574112G>T | CA412822300 | SYN1 | c.1872C>A (p.Ser624Arg) c.70+576C>A (n.70+576C>A) | gnomAD v4 |
X | g.47574113C>A | CA412822302 | SYN1 | c.1871G>T (p.Ser624Ile) c.70+575G>T (n.70+575G>T) | gnomAD v4 |
X | g.47574113C>G | CA412822306 | SYN1 | c.1871G>C (p.Ser624Thr) c.70+575G>C (n.70+575G>C) | |
X | g.47574113C>T | CA412822304 | SYN1 | c.1871G>A (p.Ser624Asn) c.70+575G>A (n.70+575G>A) | gnomAD v4 |
X | g.47574114T>A | CA412822307 | SYN1 | c.1870A>T (p.Ser624Cys) c.70+574A>T (n.70+574A>T) | |
X | g.47574114T>C | CA412822308 | SYN1 | c.1870A>G (p.Ser624Gly) c.70+574A>G (n.70+574A>G) | gnomAD v4 |
X | g.47574114T>G | CA412822309 | SYN1 | c.1870A>C (p.Ser624Arg) c.70+574A>C (n.70+574A>C) | |
X | g.47574115G>A | CA516353347 | SYN1 | c.1869C>T (p.Pro623=) c.70+573C>T (n.70+573C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.47574115G>C | CA516353348 | SYN1 | c.1869C>G (p.Pro623=) c.70+573C>G (n.70+573C>G) | |
X | g.47574115G= | CA2427971188 | SYN1 | c.1869C= (p.Pro623=) c.70+573C= (n.70+573C=) | |
X | g.47574115G>T | CA516353349 | SYN1 | c.1869C>A (p.Pro623=) c.70+573C>A (n.70+573C>A) | gnomAD v4 |
X | g.47574116G>A | CA412822310 | SYN1 | c.1868C>T (p.Pro623Leu) c.70+572C>T (n.70+572C>T) | gnomAD v4 |
X | g.47574116G>C | CA412822312 | SYN1 | c.1868C>G (p.Pro623Arg) c.70+572C>G (n.70+572C>G) | |
X | g.47574116G= | CA2427971189 | SYN1 | c.1868C= (p.Pro623=) c.70+572C= (n.70+572C=) | |
X | g.47574116G>T | CA412822314 | SYN1 | c.1868C>A (p.Pro623His) c.70+572C>A (n.70+572C>A) | dbSNP gnomAD v4 |
X | g.47574117G>A | CA329057197 | SYN1 | c.1867C>T (p.Pro623Ser) c.70+571C>T (n.70+571C>T) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47574117G>C | CA412822316 | SYN1 | c.1867C>G (p.Pro623Ala) c.70+571C>G (n.70+571C>G) | |
X | g.47574117G= | CA2427971190 | SYN1 | c.1867C= (p.Pro623=) c.70+571C= (n.70+571C=) | |
X | g.47574117G>T | CA412822317 | SYN1 | c.1867C>A (p.Pro623Thr) c.70+571C>A (n.70+571C>A) | gnomAD v4 |
X | g.47574118C>A | CA516353353 | SYN1 | c.1866G>T (p.Arg622=) c.70+570G>T (n.70+570G>T) | gnomAD v4 |
X | g.47574118C= | CA2427971191 | SYN1 | c.1866G= (p.Arg622=) c.70+570G= (n.70+570G=) | |
X | g.47574118C>G | CA516353352 | SYN1 | c.1866G>C (p.Arg622=) c.70+570G>C (n.70+570G>C) | gnomAD v4 |
X | g.47574118C>T | CA516353351 | SYN1 | c.1866G>A (p.Arg622=) c.70+570G>A (n.70+570G>A) | dbSNP gnomAD v4 |
X | g.47574119C>A | CA412822319 | SYN1 | c.1865G>T (p.Arg622Leu) c.70+569G>T (n.70+569G>T) | gnomAD v4 |
X | g.47574119C>G | CA412822320 | SYN1 | c.1865G>C (p.Arg622Pro) c.70+569G>C (n.70+569G>C) | |
X | g.47574119C>T | CA412822321 | SYN1 | c.1865G>A (p.Arg622Gln) c.70+569G>A (n.70+569G>A) | gnomAD v4 |
X | g.47574120G>A | CA412822323 | SYN1 | c.1864C>T (p.Arg622Trp) c.70+568C>T (n.70+568C>T) | ClinVar gnomAD v4 |
X | g.47574120G>C | CA412822324 | SYN1 | c.1864C>G (p.Arg622Gly) c.70+568C>G (n.70+568C>G) | |
X | g.47574120G>T | CA516353354 | SYN1 | c.1864C>A (p.Arg622=) c.70+568C>A (n.70+568C>A) | gnomAD v4 |
X | g.47574121A>C | CA516353358 | SYN1 | c.1863T>G (p.Pro621=) c.70+567T>G (n.70+567T>G) | |
X | g.47574121A>G | CA516353357 | SYN1 | c.1863T>C (p.Pro621=) c.70+567T>C (n.70+567T>C) | gnomAD v4 |
X | g.47574121A>T | CA516353355 | SYN1 | c.1863T>A (p.Pro621=) c.70+567T>A (n.70+567T>A) | |
X | g.47574122G>A | CA412822326 | SYN1 | c.1862C>T (p.Pro621Leu) c.70+566C>T (n.70+566C>T) | |
X | g.47574122G>C | CA412822328 | SYN1 | c.1862C>G (p.Pro621Arg) c.70+566C>G (n.70+566C>G) | |
X | g.47574122G>T | CA412822329 | SYN1 | c.1862C>A (p.Pro621His) c.70+566C>A (n.70+566C>A) | gnomAD v4 |
X | g.47574123G>A | CA412822331 | SYN1 | c.1861C>T (p.Pro621Ser) c.70+565C>T (n.70+565C>T) | gnomAD v4 |
X | g.47574123G>C | CA412822332 | SYN1 | c.1861C>G (p.Pro621Ala) c.70+565C>G (n.70+565C>G) | |
X | g.47574123G>T | CA412822333 | SYN1 | c.1861C>A (p.Pro621Thr) c.70+565C>A (n.70+565C>A) | gnomAD v4 |
X | g.47574124C>A | CA412822335 | SYN1 | c.1860G>T (p.Gln620His) c.70+564G>T (n.70+564G>T) | gnomAD v4 |
X | g.47574124C>G | CA412822336 | SYN1 | c.1860G>C (p.Gln620His) c.70+564G>C (n.70+564G>C) | |
X | g.47574124C>T | CA516353362 | SYN1 | c.1860G>A (p.Gln620=) c.70+564G>A (n.70+564G>A) | gnomAD v4 |
X | g.47574125T>A | CA412822338 | SYN1 | c.1859A>T (p.Gln620Leu) c.70+563A>T (n.70+563A>T) | |
X | g.47574125T>C | CA412822340 | SYN1 | c.1859A>G (p.Gln620Arg) c.70+563A>G (n.70+563A>G) | |
X | g.47574125T>G | CA412822342 | SYN1 | c.1859A>C (p.Gln620Pro) c.70+563A>C (n.70+563A>C) | |
X | g.47574126G>A | CA412822345 | SYN1 | c.1858C>T (p.Gln620Ter) c.70+562C>T (n.70+562C>T) | gnomAD v4 |
X | g.47574126G>C | CA412822347 | SYN1 | c.1858C>G (p.Gln620Glu) c.70+562C>G (n.70+562C>G) | |
X | g.47574126G>T | CA412822343 | SYN1 | c.1858C>A (p.Gln620Lys) c.70+562C>A (n.70+562C>A) | gnomAD v4 |
X | g.47574127C>A | CA412822348 | SYN1 | c.1857G>T (p.Gln619His) c.70+561G>T (n.70+561G>T) | gnomAD v4 |
X | g.47574127C>G | CA412822349 | SYN1 | c.1857G>C (p.Gln619His) c.70+561G>C (n.70+561G>C) | |
X | g.47574127C>T | CA516353364 | SYN1 | c.1857G>A (p.Gln619=) c.70+561G>A (n.70+561G>A) | gnomAD v4 |
X | g.47574128T>A | CA412822352 | SYN1 | c.1856A>T (p.Gln619Leu) c.70+560A>T (n.70+560A>T) | gnomAD v4 |
X | g.47574128T>C | CA412822354 | SYN1 | c.1856A>G (p.Gln619Arg) c.70+560A>G (n.70+560A>G) | gnomAD v4 |
X | g.47574128T>G | CA412822355 | SYN1 | c.1856A>C (p.Gln619Pro) c.70+560A>C (n.70+560A>C) | |
X | g.47574129G>A | CA412822360 | SYN1 | c.1855C>T (p.Gln619Ter) c.70+559C>T (n.70+559C>T) | gnomAD v4 |
X | g.47574129G>C | CA412822359 | SYN1 | c.1855C>G (p.Gln619Glu) c.70+559C>G (n.70+559C>G) | |
X | g.47574129G= | CA2427971192 | SYN1 | c.1855C= (p.Gln619=) c.70+559C= (n.70+559C=) | |
X | g.47574129G>T | CA412822357 | SYN1 | c.1855C>A (p.Gln619Lys) c.70+559C>A (n.70+559C>A) | ClinVar dbSNP gnomAD v4 |
X | g.47574130C>A | CA516353368 | SYN1 | c.1854G>T (p.Thr618=) c.70+558G>T (n.70+558G>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47574130C= | CA2427971193 | SYN1 | c.1854G= (p.Thr618=) c.70+558G= (n.70+558G=) | |
X | g.47574130C>G | CA516353369 | SYN1 | c.1854G>C (p.Thr618=) c.70+558G>C (n.70+558G>C) | |
X | g.47574130C>T | CA516353371 | SYN1 | c.1854G>A (p.Thr618=) c.70+558G>A (n.70+558G>A) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47574131G>A | CA412822362 | SYN1 | c.1853C>T (p.Thr618Met) c.70+557C>T (n.70+557C>T) | gnomAD v4 |
X | g.47574131G>C | CA412822363 | SYN1 | c.1853C>G (p.Thr618Arg) c.70+557C>G (n.70+557C>G) | |
X | g.47574131G>T | CA412822365 | SYN1 | c.1853C>A (p.Thr618Lys) c.70+557C>A (n.70+557C>A) | gnomAD v4 COSMIC COSMIC |
X | g.47574132T>A | CA412822367 | SYN1 | c.1852A>T (p.Thr618Ser) c.70+556A>T (n.70+556A>T) | |
X | g.47574132T>C | CA412822369 | SYN1 | c.1852A>G (p.Thr618Ala) c.70+556A>G (n.70+556A>G) | gnomAD v4 |
X | g.47574132T>G | CA412822370 | SYN1 | c.1852A>C (p.Thr618Pro) c.70+556A>C (n.70+556A>C) | |
X | g.47574133G>A | CA516353374 | SYN1 | c.1851C>T (p.Thr617=) c.70+555C>T (n.70+555C>T) | gnomAD v4 |
X | g.47574133G>C | CA516353376 | SYN1 | c.1851C>G (p.Thr617=) c.70+555C>G (n.70+555C>G) | |
X | g.47574133G>T | CA516353378 | SYN1 | c.1851C>A (p.Thr617=) c.70+555C>A (n.70+555C>A) | ClinVar dbSNP gnomAD v4 |
X | g.47574134G>A | CA412822371 | SYN1 | c.1850C>T (p.Thr617Ile) c.70+554C>T (n.70+554C>T) | gnomAD v4 |
X | g.47574134G>C | CA412822374 | SYN1 | c.1850C>G (p.Thr617Ser) c.70+554C>G (n.70+554C>G) | gnomAD v4 |
X | g.47574134G>T | CA412822372 | SYN1 | c.1850C>A (p.Thr617Asn) c.70+554C>A (n.70+554C>A) | |
X | g.47574135T>A | CA412822375 | SYN1 | c.1849A>T (p.Thr617Ser) c.70+553A>T (n.70+553A>T) | |
X | g.47574135T>C | CA412822376 | SYN1 | c.1849A>G (p.Thr617Ala) c.70+553A>G (n.70+553A>G) | gnomAD v4 |
X | g.47574135T>G | CA412822377 | SYN1 | c.1849A>C (p.Thr617Pro) c.70+553A>C (n.70+553A>C) | |
X | g.47574136G>A | CA516353379 | SYN1 | c.1848C>T (p.Pro616=) c.70+552C>T (n.70+552C>T) | gnomAD v4 |
X | g.47574136G>C | CA516353381 | SYN1 | c.1848C>G (p.Pro616=) c.70+552C>G (n.70+552C>G) | |
X | g.47574136G>T | CA516353382 | SYN1 | c.1848C>A (p.Pro616=) c.70+552C>A (n.70+552C>A) | gnomAD v4 |
X | g.47574137G>A | CA412822380 | SYN1 | c.1847C>T (p.Pro616Leu) c.70+551C>T (n.70+551C>T) | |
X | g.47574137G>C | CA412822381 | SYN1 | c.1847C>G (p.Pro616Arg) c.70+551C>G (n.70+551C>G) | |
X | g.47574137G>T | CA412822383 | SYN1 | c.1847C>A (p.Pro616His) c.70+551C>A (n.70+551C>A) | gnomAD v4 |
X | g.47574138G>A | CA412822384 | SYN1 | c.1846C>T (p.Pro616Ser) c.70+550C>T (n.70+550C>T) | gnomAD v4 |
X | g.47574138G>C | CA412822385 | SYN1 | c.1846C>G (p.Pro616Ala) c.70+550C>G (n.70+550C>G) | |
X | g.47574138G>T | CA412822386 | SYN1 | c.1846C>A (p.Pro616Thr) c.70+550C>A (n.70+550C>A) | gnomAD v4 |
X | g.47574139T>A | CA516353386 | SYN1 | c.1845A>T (p.Pro615=) c.70+549A>T (n.70+549A>T) | |
X | g.47574139T>C | CA516353385 | SYN1 | c.1845A>G (p.Pro615=) c.70+549A>G (n.70+549A>G) | gnomAD v4 |
X | g.47574139T>G | CA516353384 | SYN1 | c.1845A>C (p.Pro615=) c.70+549A>C (n.70+549A>C) | |
X | g.47574140G>A | CA412822388 | SYN1 | c.1844C>T (p.Pro615Leu) c.70+548C>T (n.70+548C>T) | |
X | g.47574140G>C | CA412822390 | SYN1 | c.1844C>G (p.Pro615Arg) c.70+548C>G (n.70+548C>G) | |
X | g.47574140G>T | CA412822391 | SYN1 | c.1844C>A (p.Pro615Gln) c.70+548C>A (n.70+548C>A) | gnomAD v4 |
X | g.47574141G>A | CA412822393 | SYN1 | c.1843C>T (p.Pro615Ser) c.70+547C>T (n.70+547C>T) | gnomAD v4 |
X | g.47574141G>C | CA412822396 | SYN1 | c.1843C>G (p.Pro615Ala) c.70+547C>G (n.70+547C>G) | gnomAD v4 |
X | g.47574141G>T | CA412822394 | SYN1 | c.1843C>A (p.Pro615Thr) c.70+547C>A (n.70+547C>A) | gnomAD v4 |
X | g.47574142C>A | CA516353388 | SYN1 | c.1842G>T (p.Gly614=) c.70+546G>T (n.70+546G>T) | gnomAD v4 |
X | g.47574142C>G | CA516353389 | SYN1 | c.1842G>C (p.Gly614=) c.70+546G>C (n.70+546G>C) | |
X | g.47574142C>T | CA516353390 | SYN1 | c.1842G>A (p.Gly614=) c.70+546G>A (n.70+546G>A) | gnomAD v4 |
X | g.47574144del | CA2551079782 | SYN1 | c.1842del (p.Pro615HisfsTer?) c.70+546del (n.70+546del) | gnomAD v4 |
X | g.47574143C>A | CA412822398 | SYN1 | c.1841G>T (p.Gly614Val) c.70+545G>T (n.70+545G>T) | gnomAD v4 |
X | g.47574143C>G | CA412822399 | SYN1 | c.1841G>C (p.Gly614Ala) c.70+545G>C (n.70+545G>C) | gnomAD v4 |
X | g.47574143C>T | CA412822400 | SYN1 | c.1841G>A (p.Gly614Glu) c.70+545G>A (n.70+545G>A) | |
X | g.47574144C>A | CA412822402 | SYN1 | c.1840G>T (p.Gly614Trp) c.70+544G>T (n.70+544G>T) | gnomAD v4 |
X | g.47574144C>G | CA412822404 | SYN1 | c.1840G>C (p.Gly614Arg) c.70+544G>C (n.70+544G>C) | |
X | g.47574144C>T | CA412822405 | SYN1 | c.1840G>A (p.Gly614Arg) c.70+544G>A (n.70+544G>A) | gnomAD v4 |
X | g.47574145A>C | CA516353391 | SYN1 | c.1839T>G (p.Thr613=) c.70+543T>G (n.70+543T>G) | |
X | g.47574145A>G | CA516353392 | SYN1 | c.1839T>C (p.Thr613=) c.70+543T>C (n.70+543T>C) | gnomAD v4 |
X | g.47574145A>T | CA516353393 | SYN1 | c.1839T>A (p.Thr613=) c.70+543T>A (n.70+543T>A) | |
X | g.47574146G>A | CA412822410 | SYN1 | c.1838C>T (p.Thr613Ile) c.70+542C>T (n.70+542C>T) | gnomAD v4 |
X | g.47574146G>C | CA412822409 | SYN1 | c.1838C>G (p.Thr613Ser) c.70+542C>G (n.70+542C>G) | |
X | g.47574146G>T | CA412822407 | SYN1 | c.1838C>A (p.Thr613Asn) c.70+542C>A (n.70+542C>A) | gnomAD v4 |
X | g.47574147T>A | CA412822412 | SYN1 | c.1837A>T (p.Thr613Ser) c.70+541A>T (n.70+541A>T) | gnomAD v4 |
X | g.47574147T>C | CA412822413 | SYN1 | c.1837A>G (p.Thr613Ala) c.70+541A>G (n.70+541A>G) | |
X | g.47574147T>G | CA412822415 | SYN1 | c.1837A>C (p.Thr613Pro) c.70+541A>C (n.70+541A>C) | ClinVar dbSNP gnomAD v4 |
X | g.47574147T= | CA2427971194 | SYN1 | c.1837A= (p.Thr613=) c.70+541A= (n.70+541A=) | |
X | g.47574148G>A | CA516353395 | SYN1 | c.1836C>T (p.Arg612=) c.70+540C>T (n.70+540C>T) | |
X | g.47574148G>C | CA516353396 | SYN1 | c.1836C>G (p.Arg612=) c.70+540C>G (n.70+540C>G) | |
X | g.47574148G>T | CA516353397 | SYN1 | c.1836C>A (p.Arg612=) c.70+540C>A (n.70+540C>A) | gnomAD v4 |
X | g.47574149del | CA2693584756 | SYN1 | c.1835del (p.Arg612ProfsTer?) c.70+539del (n.70+539del) | gnomAD v4 |
X | g.47574149C>A | CA412822417 | SYN1 | c.1835G>T (p.Arg612Leu) c.70+539G>T (n.70+539G>T) | gnomAD v4 |
X | g.47574149C= | CA2427971195 | SYN1 | c.1835G= (p.Arg612=) c.70+539G= (n.70+539G=) | |
X | g.47574149C>G | CA412822418 | SYN1 | c.1835G>C (p.Arg612Pro) c.70+539G>C (n.70+539G>C) | |
X | g.47574149C>T | CA412822419 | SYN1 | c.1835G>A (p.Arg612His) c.70+539G>A (n.70+539G>A) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47574150G>A | CA412822420 | SYN1 | c.1834C>T (p.Arg612Cys) c.70+538C>T (n.70+538C>T) | gnomAD v4 |
X | g.47574150G>C | CA412822424 | SYN1 | c.1834C>G (p.Arg612Gly) c.70+538C>G (n.70+538C>G) | |
X | g.47574150G>T | CA412822422 | SYN1 | c.1834C>A (p.Arg612Ser) c.70+538C>A (n.70+538C>A) | gnomAD v4 |
X | g.47574153del | CA2693584768 | SYN1 | c.1834del (p.Arg612AlafsTer?) c.70+538del (n.70+538del) | gnomAD v4 |
X | g.47574151G>A | CA516353398 | SYN1 | c.1833C>T (p.Pro611=) c.70+537C>T (n.70+537C>T) | gnomAD v4 |
X | g.47574151G>C | CA516353401 | SYN1 | c.1833C>G (p.Pro611=) c.70+537C>G (n.70+537C>G) | |
X | g.47574151G>T | CA516353399 | SYN1 | c.1833C>A (p.Pro611=) c.70+537C>A (n.70+537C>A) | gnomAD v4 |
X | g.47574152G>A | CA412822426 | SYN1 | c.1832C>T (p.Pro611Leu) c.70+536C>T (n.70+536C>T) | gnomAD v4 |
X | g.47574152G>C | CA412822427 | SYN1 | c.1832C>G (p.Pro611Arg) c.70+536C>G (n.70+536C>G) | |
X | g.47574152G>T | CA412822428 | SYN1 | c.1832C>A (p.Pro611His) c.70+536C>A (n.70+536C>A) | |
X | g.47574153G>A | CA412822430 | SYN1 | c.1831C>T (p.Pro611Ser) c.70+535C>T (n.70+535C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.47574153G>C | CA412822432 | SYN1 | c.1831C>G (p.Pro611Ala) c.70+535C>G (n.70+535C>G) | |
X | g.47574153G= | CA2427971196 | SYN1 | c.1831C= (p.Pro611=) c.70+535C= (n.70+535C=) | |
X | g.47574153G>T | CA412822433 | SYN1 | c.1831C>A (p.Pro611Thr) c.70+535C>A (n.70+535C>A) | gnomAD v4 |
X | g.47574154C>A | CA516353404 | SYN1 | c.1830G>T (p.Val610=) c.70+534G>T (n.70+534G>T) | gnomAD v4 |
X | g.47574154C>G | CA516353405 | SYN1 | c.1830G>C (p.Val610=) c.70+534G>C (n.70+534G>C) | |
X | g.47574154C>T | CA516353406 | SYN1 | c.1830G>A (p.Val610=) c.70+534G>A (n.70+534G>A) | gnomAD v4 |
X | g.47574155A>C | CA412822434 | SYN1 | c.1829T>G (p.Val610Gly) c.70+533T>G (n.70+533T>G) | |
X | g.47574155A>G | CA412822435 | SYN1 | c.1829T>C (p.Val610Ala) c.70+533T>C (n.70+533T>C) | |
X | g.47574155A>T | CA412822436 | SYN1 | c.1829T>A (p.Val610Glu) c.70+533T>A (n.70+533T>A) | |
X | g.47574156C>A | CA412822437 | SYN1 | c.1828G>T (p.Val610Leu) c.70+532G>T (n.70+532G>T) | gnomAD v4 |
X | g.47574156C>G | CA412822439 | SYN1 | c.1828G>C (p.Val610Leu) c.70+532G>C (n.70+532G>C) | |
X | g.47574156C>T | CA412822441 | SYN1 | c.1828G>A (p.Val610Met) c.70+532G>A (n.70+532G>A) | gnomAD v4 |
X | g.47574157G>A | CA516353408 | SYN1 | c.1827C>T (p.Pro609=) c.70+531C>T (n.70+531C>T) | gnomAD v4 |
X | g.47574157G>C | CA516353409 | SYN1 | c.1827C>G (p.Pro609=) c.70+531C>G (n.70+531C>G) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47574157G= | CA2427971197 | SYN1 | c.1827C= (p.Pro609=) c.70+531C= (n.70+531C=) | |
X | g.47574157G>T | CA516353410 | SYN1 | c.1827C>A (p.Pro609=) c.70+531C>A (n.70+531C>A) | gnomAD v4 |
X | g.47574158G>A | CA412822445 | SYN1 | c.1826C>T (p.Pro609Leu) c.70+530C>T (n.70+530C>T) | |
X | g.47574158G>C | CA412822443 | SYN1 | c.1826C>G (p.Pro609Arg) c.70+530C>G (n.70+530C>G) | |
X | g.47574158G>T | CA412822444 | SYN1 | c.1826C>A (p.Pro609His) c.70+530C>A (n.70+530C>A) | |
X | g.47574159G>A | CA412822447 | SYN1 | c.1825C>T (p.Pro609Ser) c.70+529C>T (n.70+529C>T) | gnomAD v4 |
X | g.47574159G>C | CA412822449 | SYN1 | c.1825C>G (p.Pro609Ala) c.70+529C>G (n.70+529C>G) | |
X | g.47574159G>T | CA412822450 | SYN1 | c.1825C>A (p.Pro609Thr) c.70+529C>A (n.70+529C>A) | gnomAD v4 |
X | g.47574160A>C | CA516353412 | SYN1 | c.1824T>G (p.Gly608=) c.70+528T>G (n.70+528T>G) | |
X | g.47574160A>G | CA516353413 | SYN1 | c.1824T>C (p.Gly608=) c.70+528T>C (n.70+528T>C) | gnomAD v4 |
X | g.47574160A>T | CA516353414 | SYN1 | c.1824T>A (p.Gly608=) c.70+528T>A (n.70+528T>A) | |
X | g.47574161C>A | CA412822452 | SYN1 | c.1823G>T (p.Gly608Val) c.70+527G>T (n.70+527G>T) | |
X | g.47574161C>G | CA412822453 | SYN1 | c.1823G>C (p.Gly608Ala) c.70+527G>C (n.70+527G>C) | gnomAD v4 |
X | g.47574161C>T | CA412822455 | SYN1 | c.1823G>A (p.Gly608Asp) c.70+527G>A (n.70+527G>A) | gnomAD v4 |
X | g.47574162C>A | CA329057198 | SYN1 | c.1822G>T (p.Gly608Cys) c.70+526G>T (n.70+526G>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.47574162C= | CA2427971198 | SYN1 | c.1822G= (p.Gly608=) c.70+526G= (n.70+526G=) | |
X | g.47574162C>G | CA412822458 | SYN1 | c.1822G>C (p.Gly608Arg) c.70+526G>C (n.70+526G>C) | |
X | g.47574162C>T | CA412822459 | SYN1 | c.1822G>A (p.Gly608Ser) c.70+526G>A (n.70+526G>A) | gnomAD v4 |
X | g.47574163C>A | CA516353415 | SYN1 | c.1821G>T (p.Ala607=) c.70+525G>T (n.70+525G>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47574163C= | CA2427971199 | SYN1 | c.1821G= (p.Ala607=) c.70+525G= (n.70+525G=) | |
X | g.47574163C>G | CA516353416 | SYN1 | c.1821G>C (p.Ala607=) c.70+525G>C (n.70+525G>C) | |
X | g.47574163C>T | CA516353417 | SYN1 | c.1821G>A (p.Ala607=) c.70+525G>A (n.70+525G>A) | ClinVar gnomAD v4 |
X | g.47574164G>A | CA412822461 | SYN1 | c.1820C>T (p.Ala607Val) c.70+524C>T (n.70+524C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.47574164G>C | CA412822463 | SYN1 | c.1820C>G (p.Ala607Gly) c.70+524C>G (n.70+524C>G) | ClinVar gnomAD v4 |
X | g.47574164G= | CA2427971200 | SYN1 | c.1820C= (p.Ala607=) c.70+524C= (n.70+524C=) | |
X | g.47574164G>T | CA412822464 | SYN1 | c.1820C>A (p.Ala607Glu) c.70+524C>A (n.70+524C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47574165C>A | CA412822470 | SYN1 | c.1819G>T (p.Ala607Ser) c.70+523G>T (n.70+523G>T) | |
X | g.47574165C= | CA2427971201 | SYN1 | c.1819G= (p.Ala607=) c.70+523G= (n.70+523G=) | |
X | g.47574165C>G | CA412822468 | SYN1 | c.1819G>C (p.Ala607Pro) c.70+523G>C (n.70+523G>C) | |
X | g.47574165C>T | CA412822466 | SYN1 | c.1819G>A (p.Ala607Thr) c.70+523G>A (n.70+523G>A) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47574166C>A | CA412822471 | SYN1 | c.1818G>T (p.Gln606His) c.70+522G>T (n.70+522G>T) | |
X | g.47574166C= | CA2427971202 | SYN1 | c.1818G= (p.Gln606=) c.70+522G= (n.70+522G=) | |
X | g.47574166C>G | CA412822473 | SYN1 | c.1818G>C (p.Gln606His) c.70+522G>C (n.70+522G>C) | gnomAD v4 |
X | g.47574166C>T | CA329057201 | SYN1 | c.1818G>A (p.Gln606=) c.70+522G>A (n.70+522G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47574167T>A | CA412822475 | SYN1 | c.1817A>T (p.Gln606Leu) c.70+521A>T (n.70+521A>T) | |
X | g.47574167T>C | CA412822477 | SYN1 | c.1817A>G (p.Gln606Arg) c.70+521A>G (n.70+521A>G) | gnomAD v4 |
X | g.47574167T>G | CA412822478 | SYN1 | c.1817A>C (p.Gln606Pro) c.70+521A>C (n.70+521A>C) | |
X | g.47574168G>A | CA412822480 | SYN1 | c.1816C>T (p.Gln606Ter) c.70+520C>T (n.70+520C>T) | gnomAD v4 |
X | g.47574168G>C | CA412822482 | SYN1 | c.1816C>G (p.Gln606Glu) c.70+520C>G (n.70+520C>G) | |
X | g.47574168G>T | CA412822483 | SYN1 | c.1816C>A (p.Gln606Lys) c.70+520C>A (n.70+520C>A) | gnomAD v4 |
X | g.47574169G>A | CA516353422 | SYN1 | c.1815C>T (p.Ser605=) c.70+519C>T (n.70+519C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.47574169G>C | CA412822485 | SYN1 | c.1815C>G (p.Ser605Arg) c.70+519C>G (n.70+519C>G) | |
X | g.47574169G= | CA2427971203 | SYN1 | c.1815C= (p.Ser605=) c.70+519C= (n.70+519C=) | |
X | g.47574169G>T | CA412822486 | SYN1 | c.1815C>A (p.Ser605Arg) c.70+519C>A (n.70+519C>A) | gnomAD v4 |
X | g.47574170C>A | CA412822487 | SYN1 | c.1814G>T (p.Ser605Ile) c.70+518G>T (n.70+518G>T) | gnomAD v4 |
X | g.47574170C>G | CA412822489 | SYN1 | c.1814G>C (p.Ser605Thr) c.70+518G>C (n.70+518G>C) | |
X | g.47574170C>T | CA412822491 | SYN1 | c.1814G>A (p.Ser605Asn) c.70+518G>A (n.70+518G>A) | gnomAD v4 |
X | g.47574171T>A | CA412822494 | SYN1 | c.1813A>T (p.Ser605Cys) c.70+517A>T (n.70+517A>T) | |
X | g.47574171T>C | CA412822496 | SYN1 | c.1813A>G (p.Ser605Gly) c.70+517A>G (n.70+517A>G) | gnomAD v4 |
X | g.47574171T>G | CA412822493 | SYN1 | c.1813A>C (p.Ser605Arg) c.70+517A>C (n.70+517A>C) | ClinVar gnomAD v4 |
X | g.47574172G>A | CA516353426 | SYN1 | c.1812C>T (p.Ala604=) c.70+516C>T (n.70+516C>T) | gnomAD v4 |
X | g.47574172G>C | CA516353428 | SYN1 | c.1812C>G (p.Ala604=) c.70+516C>G (n.70+516C>G) | |
X | g.47574172G>T | CA516353430 | SYN1 | c.1812C>A (p.Ala604=) c.70+516C>A (n.70+516C>A) | |
X | g.47574173G>A | CA329057203 | SYN1 | c.1811C>T (p.Ala604Val) c.70+515C>T (n.70+515C>T) | dbSNP gnomAD v3 gnomAD v4 |
X | g.47574173G>C | CA412822498 | SYN1 | c.1811C>G (p.Ala604Gly) c.70+515C>G (n.70+515C>G) | |
X | g.47574173G= | CA2427971204 | SYN1 | c.1811C= (p.Ala604=) c.70+515C= (n.70+515C=) | |
X | g.47574173G>T | CA412822500 | SYN1 | c.1811C>A (p.Ala604Asp) c.70+515C>A (n.70+515C>A) | gnomAD v4 |
X | g.47574174C>A | CA412822501 | SYN1 | c.1810G>T (p.Ala604Ser) c.70+514G>T (n.70+514G>T) | |
X | g.47574174C>G | CA412822503 | SYN1 | c.1810G>C (p.Ala604Pro) c.70+514G>C (n.70+514G>C) | |
X | g.47574174C>T | CA412822505 | SYN1 | c.1810G>A (p.Ala604Thr) c.70+514G>A (n.70+514G>A) | gnomAD v4 |
X | g.47574175C>A | CA412822508 | SYN1 | c.1809G>T (p.Gln603His) c.70+513G>T (n.70+513G>T) | gnomAD v4 |
X | g.47574175C>G | CA412822507 | SYN1 | c.1809G>C (p.Gln603His) c.70+513G>C (n.70+513G>C) | |
X | g.47574175C>T | CA516353431 | SYN1 | c.1809G>A (p.Gln603=) c.70+513G>A (n.70+513G>A) | gnomAD v4 |
X | g.47574176T>A | CA412822511 | SYN1 | c.1808A>T (p.Gln603Leu) c.70+512A>T (n.70+512A>T) | |
X | g.47574176T>C | CA412822512 | SYN1 | c.1808A>G (p.Gln603Arg) c.70+512A>G (n.70+512A>G) | gnomAD v4 |
X | g.47574176T>G | CA412822514 | SYN1 | c.1808A>C (p.Gln603Pro) c.70+512A>C (n.70+512A>C) | |
X | g.47574177G>A | CA412822515 | SYN1 | c.1807C>T (p.Gln603Ter) c.70+511C>T (n.70+511C>T) | |
X | g.47574177G>C | CA412822517 | SYN1 | c.1807C>G (p.Gln603Glu) c.70+511C>G (n.70+511C>G) | |
X | g.47574177G>T | CA412822519 | SYN1 | c.1807C>A (p.Gln603Lys) c.70+511C>A (n.70+511C>A) | gnomAD v4 |
X | g.47574178G>A | CA516353432 | SYN1 | c.1806C>T (p.Arg602=) c.70+510C>T (n.70+510C>T) | gnomAD v4 |
X | g.47574178G>C | CA516353434 | SYN1 | c.1806C>G (p.Arg602=) c.70+510C>G (n.70+510C>G) | |
X | g.47574178G>T | CA516353435 | SYN1 | c.1806C>A (p.Arg602=) c.70+510C>A (n.70+510C>A) | gnomAD v4 |
X | g.47574179C>A | CA412822523 | SYN1 | c.1805G>T (p.Arg602Leu) c.70+509G>T (n.70+509G>T) | gnomAD v4 |
X | g.47574179C>G | CA412822521 | SYN1 | c.1805G>C (p.Arg602Pro) c.70+509G>C (n.70+509G>C) | |
X | g.47574179C>T | CA412822522 | SYN1 | c.1805G>A (p.Arg602His) c.70+509G>A (n.70+509G>A) | gnomAD v4 |
X | g.47574180G>A | CA412822525 | SYN1 | c.1804C>T (p.Arg602Cys) c.70+508C>T (n.70+508C>T) | gnomAD v4 |
X | g.47574180G>C | CA412822527 | SYN1 | c.1804C>G (p.Arg602Gly) c.70+508C>G (n.70+508C>G) | |
X | g.47574180G>T | CA412822528 | SYN1 | c.1804C>A (p.Arg602Ser) c.70+508C>A (n.70+508C>A) | gnomAD v4 |
X | g.47574180_47574181delinsGT | CA2427971205 | SYN1 | c.1803_1804delinsAC (p.Thr601=) c.70+507_70+508delinsAC (n.70+507_70+508delinsAC) | |
X | g.47574181del | CA641900863 | SYN1 | c.1803del (p.Arg602AlafsTer?) c.70+507del (n.70+507del) | dbSNP gnomAD v2 |
X | g.47574181T>A | CA516353437 | SYN1 | c.1803A>T (p.Thr601=) c.70+507A>T (n.70+507A>T) | |
X | g.47574181T>C | CA516353438 | SYN1 | c.1803A>G (p.Thr601=) c.70+507A>G (n.70+507A>G) | gnomAD v4 |
X | g.47574181T>G | CA516353436 | SYN1 | c.1803A>C (p.Thr601=) c.70+507A>C (n.70+507A>C) | |
X | g.47574182G>A | CA412822529 | SYN1 | c.1802C>T (p.Thr601Ile) c.70+506C>T (n.70+506C>T) | gnomAD v4 |
X | g.47574182G>C | CA412822530 | SYN1 | c.1802C>G (p.Thr601Arg) c.70+506C>G (n.70+506C>G) | dbSNP gnomAD v2 |
X | g.47574182G= | CA2427971206 | SYN1 | c.1802C= (p.Thr601=) c.70+506C= (n.70+506C=) | |
X | g.47574182G>T | CA412822531 | SYN1 | c.1802C>A (p.Thr601Lys) c.70+506C>A (n.70+506C>A) | |
X | g.47574183T>A | CA412822532 | SYN1 | c.1801A>T (p.Thr601Ser) c.70+505A>T (n.70+505A>T) | |
X | g.47574183T>C | CA412822534 | SYN1 | c.1801A>G (p.Thr601Ala) c.70+505A>G (n.70+505A>G) | |
X | g.47574183T>G | CA412822536 | SYN1 | c.1801A>C (p.Thr601Pro) c.70+505A>C (n.70+505A>C) | |
X | g.47574183_47574184delinsTG | CA2427971207 | SYN1 | c.1800_1801delinsCA (p.Pro600=) c.70+504_70+505delinsCA (n.70+504_70+505delinsCA) | |
X | g.47574184G>A | CA516353439 | SYN1 | c.1800C>T (p.Pro600=) c.70+504C>T (n.70+504C>T) | |
X | g.47574184G>C | CA516353440 | SYN1 | c.1800C>G (p.Pro600=) c.70+504C>G (n.70+504C>G) | |
X | g.47574184G>T | CA516353442 | SYN1 | c.1800C>A (p.Pro600=) c.70+504C>A (n.70+504C>A) | |
X | g.47574187del | CA2427971208 | SYN1 | c.1800del (p.Thr601HisfsTer?) c.70+504del (n.70+504del) | dbSNP gnomAD v4 |
X | g.47574185G>A | CA412822537 | SYN1 | c.1799C>T (p.Pro600Leu) c.70+503C>T (n.70+503C>T) | gnomAD v4 |
X | g.47574185G>C | CA412822538 | SYN1 | c.1799C>G (p.Pro600Arg) c.70+503C>G (n.70+503C>G) | gnomAD v4 |
X | g.47574185G>T | CA412822540 | SYN1 | c.1799C>A (p.Pro600His) c.70+503C>A (n.70+503C>A) | gnomAD v4 COSMIC COSMIC |
X | g.47574185_47574188delinsGGGC | CA2427971209 | SYN1 | c.1796_1799delinsGCCC (p.Gly599=) c.70+500_70+503delinsGCCC (n.70+500_70+503delinsGCCC) | |
X | g.47574186G>A | CA412822542 | SYN1 | c.1798C>T (p.Pro600Ser) c.70+502C>T (n.70+502C>T) | gnomAD v4 |
X | g.47574186G>C | CA412822545 | SYN1 | c.1798C>G (p.Pro600Ala) c.70+502C>G (n.70+502C>G) | |
X | g.47574186G>T | CA412822544 | SYN1 | c.1798C>A (p.Pro600Thr) c.70+502C>A (n.70+502C>A) | gnomAD v4 |
X | g.47574186_47574188del | CA516353444 | SYN1 | c.1796_1798del (p.Gly599_Pro600delinsAla) c.70+500_70+502del (n.70+500_70+502del) | dbSNP |
X | g.47574187G>A | CA516353446 | SYN1 | c.1797C>T (p.Gly599=) c.70+501C>T (n.70+501C>T) | gnomAD v4 |
X | g.47574187G>C | CA516353449 | SYN1 | c.1797C>G (p.Gly599=) c.70+501C>G (n.70+501C>G) | gnomAD v4 |
X | g.47574187G>T | CA516353448 | SYN1 | c.1797C>A (p.Gly599=) c.70+501C>A (n.70+501C>A) | gnomAD v4 |
X | g.47574188_47574190del | CA412822546 | SYN1 | c.1795_1797del (p.Gly599del) c.70+499_70+501del (n.70+499_70+501del) | |
X | g.47574188C>A | CA412822548 | SYN1 | c.1796G>T (p.Gly599Val) c.70+500G>T (n.70+500G>T) | dbSNP gnomAD v2 gnomAD v4 |
X | g.47574188C= | CA2427971210 | SYN1 | c.1796G= (p.Gly599=) c.70+500G= (n.70+500G=) | |
X | g.47574188C>G | CA412822549 | SYN1 | c.1796G>C (p.Gly599Ala) c.70+500G>C (n.70+500G>C) | gnomAD v4 |
X | g.47574188C>T | CA412822550 | SYN1 | c.1796G>A (p.Gly599Asp) c.70+500G>A (n.70+500G>A) | dbSNP gnomAD v4 |
X | g.47574189C>A | CA412822551 | SYN1 | c.1795G>T (p.Gly599Cys) c.70+499G>T (n.70+499G>T) | gnomAD v4 |
X | g.47574189C>G | CA412822553 | SYN1 | c.1795G>C (p.Gly599Arg) c.70+499G>C (n.70+499G>C) | |
X | g.47574189C>T | CA412822554 | SYN1 | c.1795G>A (p.Gly599Ser) c.70+499G>A (n.70+499G>A) | gnomAD v4 |
X | g.47574190G>A | CA516353451 | SYN1 | c.1794C>T (p.Ala598=) c.70+498C>T (n.70+498C>T) | dbSNP gnomAD v4 |
X | g.47574190G>C | CA516353452 | SYN1 | c.1794C>G (p.Ala598=) c.70+498C>G (n.70+498C>G) | ClinVar dbSNP gnomAD v4 |
X | g.47574190G= | CA2427971211 | SYN1 | c.1794C= (p.Ala598=) c.70+498C= (n.70+498C=) | |
X | g.47574190G>T | CA516353453 | SYN1 | c.1794C>A (p.Ala598=) c.70+498C>A (n.70+498C>A) | |
X | g.47574191G>A | CA412822555 | SYN1 | c.1793C>T (p.Ala598Val) c.70+497C>T (n.70+497C>T) | dbSNP gnomAD v4 |
X | g.47574191G>C | CA412822556 | SYN1 | c.1793C>G (p.Ala598Gly) c.70+497C>G (n.70+497C>G) | |
X | g.47574191G= | CA2427971212 | SYN1 | c.1793C= (p.Ala598=) c.70+497C= (n.70+497C=) | |
X | g.47574191G>T | CA412822558 | SYN1 | c.1793C>A (p.Ala598Asp) c.70+497C>A (n.70+497C>A) | gnomAD v4 |
X | g.47574192C>A | CA412822559 | SYN1 | c.1792G>T (p.Ala598Ser) c.70+496G>T (n.70+496G>T) | gnomAD v4 |
X | g.47574192C>G | CA412822560 | SYN1 | c.1792G>C (p.Ala598Pro) c.70+496G>C (n.70+496G>C) | |
X | g.47574192C>T | CA412822562 | SYN1 | c.1792G>A (p.Ala598Thr) c.70+496G>A (n.70+496G>A) | gnomAD v4 |
X | g.47574193T>A | CA516353454 | SYN1 | c.1791A>T (p.Pro597=) c.70+495A>T (n.70+495A>T) | |
X | g.47574193T>C | CA516353455 | SYN1 | c.1791A>G (p.Pro597=) c.70+495A>G (n.70+495A>G) | ClinVar gnomAD v4 |
X | g.47574193T>G | CA516353456 | SYN1 | c.1791A>C (p.Pro597=) c.70+495A>C (n.70+495A>C) |