Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.47936933C>A | CA356825239 | CNGA1,NIPAL1 | c.1549G>T (p.Glu517Ter) c.1561G>T (p.Glu521Ter) c.1768G>T (p.Glu590Ter) n.479-22091C>A n.563+22229C>A c.1786G>T (p.Glu596Ter) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.47936933C= | CA1455551773 | CNGA1,NIPAL1 | c.1549G= (p.Glu517=) c.1561G= (p.Glu521=) c.1768G= (p.Glu590=) n.479-22091C= n.563+22229C= c.1786G= (p.Glu596=) | |
4 | g.47936933C>G | CA356825237 | CNGA1,NIPAL1 | c.1549G>C (p.Glu517Gln) c.1561G>C (p.Glu521Gln) c.1768G>C (p.Glu590Gln) n.479-22091C>G n.563+22229C>G c.1786G>C (p.Glu596Gln) | |
4 | g.47936933C>T | CA356825235 | CNGA1,NIPAL1 | c.1549G>A (p.Glu517Lys) c.1561G>A (p.Glu521Lys) c.1768G>A (p.Glu590Lys) n.479-22091C>T n.563+22229C>T c.1786G>A (p.Glu596Lys) | |
4 | g.47936934C>A | CA356825244 | CNGA1,NIPAL1 | c.1548G>T (p.Lys516Asn) c.1560G>T (p.Lys520Asn) c.1767G>T (p.Lys589Asn) n.479-22090C>A n.563+22230C>A c.1785G>T (p.Lys595Asn) | |
4 | g.47936934C= | CA1455551774 | CNGA1,NIPAL1 | c.1548G= (p.Lys516=) c.1560G= (p.Lys520=) c.1767G= (p.Lys589=) n.479-22090C= n.563+22230C= c.1785G= (p.Lys595=) | |
4 | g.47936934C>G | CA356825246 | CNGA1,NIPAL1 | c.1548G>C (p.Lys516Asn) c.1560G>C (p.Lys520Asn) c.1767G>C (p.Lys589Asn) n.479-22090C>G n.563+22230C>G c.1785G>C (p.Lys595Asn) | |
4 | g.47936934C>T | CA2911057 | CNGA1,NIPAL1 | c.1548G>A (p.Lys516=) c.1560G>A (p.Lys520=) c.1767G>A (p.Lys589=) n.479-22090C>T n.563+22230C>T c.1785G>A (p.Lys595=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936935T>A | CA356825252 | CNGA1,NIPAL1 | c.1547A>T (p.Lys516Met) c.1559A>T (p.Lys520Met) c.1766A>T (p.Lys589Met) n.479-22089T>A n.563+22231T>A c.1784A>T (p.Lys595Met) | gnomAD v4 |
4 | g.47936935T>C | CA356825254 | CNGA1,NIPAL1 | c.1547A>G (p.Lys516Arg) c.1559A>G (p.Lys520Arg) c.1766A>G (p.Lys589Arg) n.479-22089T>C n.563+22231T>C c.1784A>G (p.Lys595Arg) | |
4 | g.47936935T>G | CA356825257 | CNGA1,NIPAL1 | c.1547A>C (p.Lys516Thr) c.1559A>C (p.Lys520Thr) c.1766A>C (p.Lys589Thr) n.479-22089T>G n.563+22231T>G c.1784A>C (p.Lys595Thr) | |
4 | g.47936936T>A | CA356825262 | CNGA1,NIPAL1 | c.1546A>T (p.Lys516Ter) c.1558A>T (p.Lys520Ter) c.1765A>T (p.Lys589Ter) n.479-22088T>A n.563+22232T>A c.1783A>T (p.Lys595Ter) | |
4 | g.47936936T>C | CA356825263 | CNGA1,NIPAL1 | c.1546A>G (p.Lys516Glu) c.1558A>G (p.Lys520Glu) c.1765A>G (p.Lys589Glu) n.479-22088T>C n.563+22232T>C c.1783A>G (p.Lys595Glu) | gnomAD v4 |
4 | g.47936936T>G | CA356825266 | CNGA1,NIPAL1 | c.1546A>C (p.Lys516Gln) c.1558A>C (p.Lys520Gln) c.1765A>C (p.Lys589Gln) n.479-22088T>G n.563+22232T>G c.1783A>C (p.Lys595Gln) | |
4 | g.47936937G>A | CA439403816 | CNGA1,NIPAL1 | c.1545C>T (p.Ile515=) c.1557C>T (p.Ile519=) c.1764C>T (p.Ile588=) n.479-22087G>A n.563+22233G>A c.1782C>T (p.Ile594=) | |
4 | g.47936937G>C | CA356825269 | CNGA1,NIPAL1 | c.1545C>G (p.Ile515Met) c.1557C>G (p.Ile519Met) c.1764C>G (p.Ile588Met) n.479-22087G>C n.563+22233G>C c.1782C>G (p.Ile594Met) | |
4 | g.47936937G>T | CA439403817 | CNGA1,NIPAL1 | c.1545C>A (p.Ile515=) c.1557C>A (p.Ile519=) c.1764C>A (p.Ile588=) n.479-22087G>T n.563+22233G>T c.1782C>A (p.Ile594=) | |
4 | g.47936938A= | CA1455551775 | CNGA1,NIPAL1 | c.1544T= (p.Ile515=) c.1556T= (p.Ile519=) c.1763T= (p.Ile588=) n.479-22086A= n.563+22234A= c.1781T= (p.Ile594=) | |
4 | g.47936938A>C | CA356825272 | CNGA1,NIPAL1 | c.1544T>G (p.Ile515Ser) c.1556T>G (p.Ile519Ser) c.1763T>G (p.Ile588Ser) n.479-22086A>C n.563+22234A>C c.1781T>G (p.Ile594Ser) | |
4 | g.47936938A>G | CA2911058 | CNGA1,NIPAL1 | c.1544T>C (p.Ile515Thr) c.1556T>C (p.Ile519Thr) c.1763T>C (p.Ile588Thr) n.479-22086A>G n.563+22234A>G c.1781T>C (p.Ile594Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.47936938A>T | CA356825274 | CNGA1,NIPAL1 | c.1544T>A (p.Ile515Asn) c.1556T>A (p.Ile519Asn) c.1763T>A (p.Ile588Asn) n.479-22086A>T n.563+22234A>T c.1781T>A (p.Ile594Asn) | |
4 | g.47936939T>A | CA356825277 | CNGA1,NIPAL1 | c.1543A>T (p.Ile515Phe) c.1555A>T (p.Ile519Phe) c.1762A>T (p.Ile588Phe) n.479-22085T>A n.563+22235T>A c.1780A>T (p.Ile594Phe) | |
4 | g.47936939T>C | CA356825275 | CNGA1,NIPAL1 | c.1543A>G (p.Ile515Val) c.1555A>G (p.Ile519Val) c.1762A>G (p.Ile588Val) n.479-22085T>C n.563+22235T>C c.1780A>G (p.Ile594Val) | |
4 | g.47936939T>G | CA356825276 | CNGA1,NIPAL1 | c.1543A>C (p.Ile515Leu) c.1555A>C (p.Ile519Leu) c.1762A>C (p.Ile588Leu) n.479-22085T>G n.563+22235T>G c.1780A>C (p.Ile594Leu) | |
4 | g.47936940A= | CA1455551776 | CNGA1,NIPAL1 | c.1542T= (p.Ile514=) c.1554T= (p.Ile518=) c.1761T= (p.Ile587=) n.479-22084A= n.563+22236A= c.1779T= (p.Ile593=) | |
4 | g.47936940A>C | CA356825279 | CNGA1,NIPAL1 | c.1542T>G (p.Ile514Met) c.1554T>G (p.Ile518Met) c.1761T>G (p.Ile587Met) n.479-22084A>C n.563+22236A>C c.1779T>G (p.Ile593Met) | |
4 | g.47936940A>G | CA439403818 | CNGA1,NIPAL1 | c.1542T>C (p.Ile514=) c.1554T>C (p.Ile518=) c.1761T>C (p.Ile587=) n.479-22084A>G n.563+22236A>G c.1779T>C (p.Ile593=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.47936940A>T | CA439403819 | CNGA1,NIPAL1 | c.1542T>A (p.Ile514=) c.1554T>A (p.Ile518=) c.1761T>A (p.Ile587=) n.479-22084A>T n.563+22236A>T c.1779T>A (p.Ile593=) | |
4 | g.47936941A>C | CA356825281 | CNGA1,NIPAL1 | c.1541T>G (p.Ile514Ser) c.1553T>G (p.Ile518Ser) c.1760T>G (p.Ile587Ser) n.479-22083A>C n.563+22237A>C c.1778T>G (p.Ile593Ser) | gnomAD v4 |
4 | g.47936941A>G | CA356825282 | CNGA1,NIPAL1 | c.1541T>C (p.Ile514Thr) c.1553T>C (p.Ile518Thr) c.1760T>C (p.Ile587Thr) n.479-22083A>G n.563+22237A>G c.1778T>C (p.Ile593Thr) | |
4 | g.47936941A>T | CA356825284 | CNGA1,NIPAL1 | c.1541T>A (p.Ile514Asn) c.1553T>A (p.Ile518Asn) c.1760T>A (p.Ile587Asn) n.479-22083A>T n.563+22237A>T c.1778T>A (p.Ile593Asn) | |
4 | g.47936942T>A | CA356825287 | CNGA1,NIPAL1 | c.1540A>T (p.Ile514Phe) c.1552A>T (p.Ile518Phe) c.1759A>T (p.Ile587Phe) n.479-22082T>A n.563+22238T>A c.1777A>T (p.Ile593Phe) | |
4 | g.47936942T>C | CA356825288 | CNGA1,NIPAL1 | c.1540A>G (p.Ile514Val) c.1552A>G (p.Ile518Val) c.1759A>G (p.Ile587Val) n.479-22082T>C n.563+22238T>C c.1777A>G (p.Ile593Val) | |
4 | g.47936942T>G | CA356825290 | CNGA1,NIPAL1 | c.1540A>C (p.Ile514Leu) c.1552A>C (p.Ile518Leu) c.1759A>C (p.Ile587Leu) n.479-22082T>G n.563+22238T>G c.1777A>C (p.Ile593Leu) | |
4 | g.47936943G>A | CA439403822 | CNGA1,NIPAL1 | c.1539C>T (p.Tyr513=) c.1551C>T (p.Tyr517=) c.1758C>T (p.Tyr586=) n.479-22081G>A n.563+22239G>A c.1776C>T (p.Tyr592=) | |
4 | g.47936943G>C | CA356825292 | CNGA1,NIPAL1 | c.1539C>G (p.Tyr513Ter) c.1551C>G (p.Tyr517Ter) c.1758C>G (p.Tyr586Ter) n.479-22081G>C n.563+22239G>C c.1776C>G (p.Tyr592Ter) | |
4 | g.47936943G>T | CA356825294 | CNGA1,NIPAL1 | c.1539C>A (p.Tyr513Ter) c.1551C>A (p.Tyr517Ter) c.1758C>A (p.Tyr586Ter) n.479-22081G>T n.563+22239G>T c.1776C>A (p.Tyr592Ter) | |
4 | g.47936944T>A | CA356825297 | CNGA1,NIPAL1 | c.1538A>T (p.Tyr513Phe) c.1550A>T (p.Tyr517Phe) c.1757A>T (p.Tyr586Phe) n.479-22080T>A n.563+22240T>A c.1775A>T (p.Tyr592Phe) | |
4 | g.47936944T>C | CA356825298 | CNGA1,NIPAL1 | c.1538A>G (p.Tyr513Cys) c.1550A>G (p.Tyr517Cys) c.1757A>G (p.Tyr586Cys) n.479-22080T>C n.563+22240T>C c.1775A>G (p.Tyr592Cys) | gnomAD v4 |
4 | g.47936944T>G | CA356825300 | CNGA1,NIPAL1 | c.1538A>C (p.Tyr513Ser) c.1550A>C (p.Tyr517Ser) c.1757A>C (p.Tyr586Ser) n.479-22080T>G n.563+22240T>G c.1775A>C (p.Tyr592Ser) | |
4 | g.47936945A>C | CA356825306 | CNGA1,NIPAL1 | c.1537T>G (p.Tyr513Asp) c.1549T>G (p.Tyr517Asp) c.1756T>G (p.Tyr586Asp) n.479-22079A>C n.563+22241A>C c.1774T>G (p.Tyr592Asp) | |
4 | g.47936945A>G | CA356825304 | CNGA1,NIPAL1 | c.1537T>C (p.Tyr513His) c.1549T>C (p.Tyr517His) c.1756T>C (p.Tyr586His) n.479-22079A>G n.563+22241A>G c.1774T>C (p.Tyr592His) | |
4 | g.47936945A>T | CA356825303 | CNGA1,NIPAL1 | c.1537T>A (p.Tyr513Asn) c.1549T>A (p.Tyr517Asn) c.1756T>A (p.Tyr586Asn) n.479-22079A>T n.563+22241A>T c.1774T>A (p.Tyr592Asn) | |
4 | g.47936946C>A | CA356825309 | CNGA1,NIPAL1 | c.1536G>T (p.Met512Ile) c.1548G>T (p.Met516Ile) c.1755G>T (p.Met585Ile) n.479-22078C>A n.563+22242C>A c.1773G>T (p.Met591Ile) | |
4 | g.47936946C>G | CA356825313 | CNGA1,NIPAL1 | c.1536G>C (p.Met512Ile) c.1548G>C (p.Met516Ile) c.1755G>C (p.Met585Ile) n.479-22078C>G n.563+22242C>G c.1773G>C (p.Met591Ile) | |
4 | g.47936946C>T | CA356825311 | CNGA1,NIPAL1 | c.1536G>A (p.Met512Ile) c.1548G>A (p.Met516Ile) c.1755G>A (p.Met585Ile) n.479-22078C>T n.563+22242C>T c.1773G>A (p.Met591Ile) | |
4 | g.47936947A= | CA1455551777 | CNGA1,NIPAL1 | c.1535T= (p.Met512=) c.1547T= (p.Met516=) c.1754T= (p.Met585=) n.479-22077A= n.563+22243A= c.1772T= (p.Met591=) | |
4 | g.47936947A>C | CA2911059 | CNGA1,NIPAL1 | c.1535T>G (p.Met512Arg) c.1547T>G (p.Met516Arg) c.1754T>G (p.Met585Arg) n.479-22077A>C n.563+22243A>C c.1772T>G (p.Met591Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936947A>G | CA356825316 | CNGA1,NIPAL1 | c.1535T>C (p.Met512Thr) c.1547T>C (p.Met516Thr) c.1754T>C (p.Met585Thr) n.479-22077A>G n.563+22243A>G c.1772T>C (p.Met591Thr) | |
4 | g.47936947A>T | CA356825318 | CNGA1,NIPAL1 | c.1535T>A (p.Met512Lys) c.1547T>A (p.Met516Lys) c.1754T>A (p.Met585Lys) n.479-22077A>T n.563+22243A>T c.1772T>A (p.Met591Lys) | |
4 | g.47936948T>A | CA356825320 | CNGA1,NIPAL1 | c.1534A>T (p.Met512Leu) c.1546A>T (p.Met516Leu) c.1753A>T (p.Met585Leu) n.479-22076T>A n.563+22244T>A c.1771A>T (p.Met591Leu) | |
4 | g.47936948T>C | CA356825322 | CNGA1,NIPAL1 | c.1534A>G (p.Met512Val) c.1546A>G (p.Met516Val) c.1753A>G (p.Met585Val) n.479-22076T>C n.563+22244T>C c.1771A>G (p.Met591Val) | |
4 | g.47936948T>G | CA356825324 | CNGA1,NIPAL1 | c.1534A>C (p.Met512Leu) c.1546A>C (p.Met516Leu) c.1753A>C (p.Met585Leu) n.479-22076T>G n.563+22244T>G c.1771A>C (p.Met591Leu) | |
4 | g.47936949C>A | CA356825326 | CNGA1,NIPAL1 | c.1533G>T (p.Glu511Asp) c.1545G>T (p.Glu515Asp) c.1752G>T (p.Glu584Asp) n.479-22075C>A n.563+22245C>A c.1770G>T (p.Glu590Asp) | |
4 | g.47936949C>G | CA356825328 | CNGA1,NIPAL1 | c.1533G>C (p.Glu511Asp) c.1545G>C (p.Glu515Asp) c.1752G>C (p.Glu584Asp) n.479-22075C>G n.563+22245C>G c.1770G>C (p.Glu590Asp) | |
4 | g.47936949C>T | CA439403825 | CNGA1,NIPAL1 | c.1533G>A (p.Glu511=) c.1545G>A (p.Glu515=) c.1752G>A (p.Glu584=) n.479-22075C>T n.563+22245C>T c.1770G>A (p.Glu590=) | |
4 | g.47936950T>A | CA356825330 | CNGA1,NIPAL1 | c.1532A>T (p.Glu511Val) c.1544A>T (p.Glu515Val) c.1751A>T (p.Glu584Val) n.479-22074T>A n.563+22246T>A c.1769A>T (p.Glu590Val) | |
4 | g.47936950T>C | CA356825332 | CNGA1,NIPAL1 | c.1532A>G (p.Glu511Gly) c.1544A>G (p.Glu515Gly) c.1751A>G (p.Glu584Gly) n.479-22074T>C n.563+22246T>C c.1769A>G (p.Glu590Gly) | |
4 | g.47936950T>G | CA356825334 | CNGA1,NIPAL1 | c.1532A>C (p.Glu511Ala) c.1544A>C (p.Glu515Ala) c.1751A>C (p.Glu584Ala) n.479-22074T>G n.563+22246T>G c.1769A>C (p.Glu590Ala) | |
4 | g.47936951C>A | CA356825341 | CNGA1,NIPAL1 | c.1531G>T (p.Glu511Ter) c.1543G>T (p.Glu515Ter) c.1750G>T (p.Glu584Ter) n.479-22073C>A n.563+22247C>A c.1768G>T (p.Glu590Ter) | |
4 | g.47936951C>G | CA356825339 | CNGA1,NIPAL1 | c.1531G>C (p.Glu511Gln) c.1543G>C (p.Glu515Gln) c.1750G>C (p.Glu584Gln) n.479-22073C>G n.563+22247C>G c.1768G>C (p.Glu590Gln) | |
4 | g.47936951C>T | CA356825338 | CNGA1,NIPAL1 | c.1531G>A (p.Glu511Lys) c.1543G>A (p.Glu515Lys) c.1750G>A (p.Glu584Lys) n.479-22073C>T n.563+22247C>T c.1768G>A (p.Glu590Lys) | |
4 | g.47936952T>A | CA439403827 | CNGA1,NIPAL1 | c.1530A>T (p.Arg510=) c.1542A>T (p.Arg514=) c.1749A>T (p.Arg583=) n.479-22072T>A n.563+22248T>A c.1767A>T (p.Arg589=) | |
4 | g.47936952T>C | CA439403828 | CNGA1,NIPAL1 | c.1530A>G (p.Arg510=) c.1542A>G (p.Arg514=) c.1749A>G (p.Arg583=) n.479-22072T>C n.563+22248T>C c.1767A>G (p.Arg589=) | |
4 | g.47936952T>G | CA439403829 | CNGA1,NIPAL1 | c.1530A>C (p.Arg510=) c.1542A>C (p.Arg514=) c.1749A>C (p.Arg583=) n.479-22072T>G n.563+22248T>G c.1767A>C (p.Arg589=) | |
4 | g.47936953C>A | CA356825343 | CNGA1,NIPAL1 | c.1529G>T (p.Arg510Leu) c.1541G>T (p.Arg514Leu) c.1748G>T (p.Arg583Leu) n.479-22071C>A n.563+22249C>A c.1766G>T (p.Arg589Leu) | |
4 | g.47936953C= | CA1455551778 | CNGA1,NIPAL1 | c.1529G= (p.Arg510=) c.1541G= (p.Arg514=) c.1748G= (p.Arg583=) n.479-22071C= n.563+22249C= c.1766G= (p.Arg589=) | |
4 | g.47936953C>G | CA356825346 | CNGA1,NIPAL1 | c.1529G>C (p.Arg510Pro) c.1541G>C (p.Arg514Pro) c.1748G>C (p.Arg583Pro) n.479-22071C>G n.563+22249C>G c.1766G>C (p.Arg589Pro) | |
4 | g.47936953C>T | CA2911060 | CNGA1,NIPAL1 | c.1529G>A (p.Arg510Gln) c.1541G>A (p.Arg514Gln) c.1748G>A (p.Arg583Gln) n.479-22071C>T n.563+22249C>T c.1766G>A (p.Arg589Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.47936954G>A | CA2911061 | CNGA1,NIPAL1 | c.1528C>T (p.Arg510Ter) c.1540C>T (p.Arg514Ter) c.1747C>T (p.Arg583Ter) n.479-22070G>A n.563+22250G>A c.1765C>T (p.Arg589Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936954G>C | CA356825350 | CNGA1,NIPAL1 | c.1528C>G (p.Arg510Gly) c.1540C>G (p.Arg514Gly) c.1747C>G (p.Arg583Gly) n.479-22070G>C n.563+22250G>C c.1765C>G (p.Arg589Gly) | |
4 | g.47936954G= | CA1455551779 | CNGA1,NIPAL1 | c.1528C= (p.Arg510=) c.1540C= (p.Arg514=) c.1747C= (p.Arg583=) n.479-22070G= n.563+22250G= c.1765C= (p.Arg589=) | |
4 | g.47936954G>T | CA439403830 | CNGA1,NIPAL1 | c.1528C>A (p.Arg510=) c.1540C>A (p.Arg514=) c.1747C>A (p.Arg583=) n.479-22070G>T n.563+22250G>T c.1765C>A (p.Arg589=) | gnomAD v4 |
4 | g.47936955T>A | CA439403834 | CNGA1,NIPAL1 | c.1527A>T (p.Gly509=) c.1539A>T (p.Gly513=) c.1746A>T (p.Gly582=) n.479-22069T>A n.563+22251T>A c.1764A>T (p.Gly588=) | |
4 | g.47936955T>C | CA439403831 | CNGA1,NIPAL1 | c.1527A>G (p.Gly509=) c.1539A>G (p.Gly513=) c.1746A>G (p.Gly582=) n.479-22069T>C n.563+22251T>C c.1764A>G (p.Gly588=) | |
4 | g.47936955T>G | CA439403832 | CNGA1,NIPAL1 | c.1527A>C (p.Gly509=) c.1539A>C (p.Gly513=) c.1746A>C (p.Gly582=) n.479-22069T>G n.563+22251T>G c.1764A>C (p.Gly588=) | |
4 | g.47936956C>A | CA356825353 | CNGA1,NIPAL1 | c.1526G>T (p.Gly509Val) c.1538G>T (p.Gly513Val) c.1745G>T (p.Gly582Val) n.479-22068C>A n.563+22252C>A c.1763G>T (p.Gly588Val) | |
4 | g.47936956C= | CA1455551780 | CNGA1,NIPAL1 | c.1526G= (p.Gly509=) c.1538G= (p.Gly513=) c.1745G= (p.Gly582=) n.479-22068C= n.563+22252C= c.1763G= (p.Gly588=) | |
4 | g.47936956C>G | CA356825354 | CNGA1,NIPAL1 | c.1526G>C (p.Gly509Ala) c.1538G>C (p.Gly513Ala) c.1745G>C (p.Gly582Ala) n.479-22068C>G n.563+22252C>G c.1763G>C (p.Gly588Ala) | |
4 | g.47936956C>T | CA96688521 | CNGA1,NIPAL1 | c.1526G>A (p.Gly509Glu) c.1538G>A (p.Gly513Glu) c.1745G>A (p.Gly582Glu) n.479-22068C>T n.563+22252C>T c.1763G>A (p.Gly588Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936957C>A | CA356825358 | CNGA1,NIPAL1 | c.1525G>T (p.Gly509Ter) c.1537G>T (p.Gly513Ter) c.1744G>T (p.Gly582Ter) n.479-22067C>A n.563+22253C>A c.1762G>T (p.Gly588Ter) | |
4 | g.47936957C= | CA1455551781 | CNGA1,NIPAL1 | c.1525G= (p.Gly509=) c.1537G= (p.Gly513=) c.1744G= (p.Gly582=) n.479-22067C= n.563+22253C= c.1762G= (p.Gly588=) | |
4 | g.47936957C>G | CA356825360 | CNGA1,NIPAL1 | c.1525G>C (p.Gly509Arg) c.1537G>C (p.Gly513Arg) c.1744G>C (p.Gly582Arg) n.479-22067C>G n.563+22253C>G c.1762G>C (p.Gly588Arg) | |
4 | g.47936957C>T | CA2911062 | CNGA1,NIPAL1 | c.1525G>A (p.Gly509Arg) c.1537G>A (p.Gly513Arg) c.1744G>A (p.Gly582Arg) n.479-22067C>T n.563+22253C>T c.1762G>A (p.Gly588Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936958G>A | CA2911063 | CNGA1,NIPAL1 | c.1524C>T (p.Ile508=) c.1536C>T (p.Ile512=) c.1743C>T (p.Ile581=) n.479-22066G>A n.563+22254G>A c.1761C>T (p.Ile587=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.47936958G>C | CA356825363 | CNGA1,NIPAL1 | c.1524C>G (p.Ile508Met) c.1536C>G (p.Ile512Met) c.1743C>G (p.Ile581Met) n.479-22066G>C n.563+22254G>C c.1761C>G (p.Ile587Met) | |
4 | g.47936958G= | CA1455551782 | CNGA1,NIPAL1 | c.1524C= (p.Ile508=) c.1536C= (p.Ile512=) c.1743C= (p.Ile581=) n.479-22066G= n.563+22254G= c.1761C= (p.Ile587=) | |
4 | g.47936958G>T | CA439403836 | CNGA1,NIPAL1 | c.1524C>A (p.Ile508=) c.1536C>A (p.Ile512=) c.1743C>A (p.Ile581=) n.479-22066G>T n.563+22254G>T c.1761C>A (p.Ile587=) | |
4 | g.47936959A>C | CA356825369 | CNGA1,NIPAL1 | c.1523T>G (p.Ile508Ser) c.1535T>G (p.Ile512Ser) c.1742T>G (p.Ile581Ser) n.479-22065A>C n.563+22255A>C c.1760T>G (p.Ile587Ser) | |
4 | g.47936959A>G | CA356825367 | CNGA1,NIPAL1 | c.1523T>C (p.Ile508Thr) c.1535T>C (p.Ile512Thr) c.1742T>C (p.Ile581Thr) n.479-22065A>G n.563+22255A>G c.1760T>C (p.Ile587Thr) | gnomAD v4 |
4 | g.47936959A>T | CA356825365 | CNGA1,NIPAL1 | c.1523T>A (p.Ile508Asn) c.1535T>A (p.Ile512Asn) c.1742T>A (p.Ile581Asn) n.479-22065A>T n.563+22255A>T c.1760T>A (p.Ile587Asn) | |
4 | g.47936960T>A | CA356825375 | CNGA1,NIPAL1 | c.1522A>T (p.Ile508Phe) c.1534A>T (p.Ile512Phe) c.1741A>T (p.Ile581Phe) n.479-22064T>A n.563+22256T>A c.1759A>T (p.Ile587Phe) | |
4 | g.47936960T>C | CA356825371 | CNGA1,NIPAL1 | c.1522A>G (p.Ile508Val) c.1534A>G (p.Ile512Val) c.1741A>G (p.Ile581Val) n.479-22064T>C n.563+22256T>C c.1759A>G (p.Ile587Val) | ClinVar dbSNP gnomAD v4 |
4 | g.47936960T>G | CA356825373 | CNGA1,NIPAL1 | c.1522A>C (p.Ile508Leu) c.1534A>C (p.Ile512Leu) c.1741A>C (p.Ile581Leu) n.479-22064T>G n.563+22256T>G c.1759A>C (p.Ile587Leu) | |
4 | g.47936960T= | CA1455551783 | CNGA1,NIPAL1 | c.1522A= (p.Ile508=) c.1534A= (p.Ile512=) c.1741A= (p.Ile581=) n.479-22064T= n.563+22256T= c.1759A= (p.Ile587=) | |
4 | g.47936961A>C | CA356825377 | CNGA1,NIPAL1 | c.1521T>G (p.Asp507Glu) c.1533T>G (p.Asp511Glu) c.1740T>G (p.Asp580Glu) n.479-22063A>C n.563+22257A>C c.1758T>G (p.Asp586Glu) | |
4 | g.47936961A>G | CA439403840 | CNGA1,NIPAL1 | c.1521T>C (p.Asp507=) c.1533T>C (p.Asp511=) c.1740T>C (p.Asp580=) n.479-22063A>G n.563+22257A>G c.1758T>C (p.Asp586=) | |
4 | g.47936961A>T | CA356825379 | CNGA1,NIPAL1 | c.1521T>A (p.Asp507Glu) c.1533T>A (p.Asp511Glu) c.1740T>A (p.Asp580Glu) n.479-22063A>T n.563+22257A>T c.1758T>A (p.Asp586Glu) | |
4 | g.47936962T>A | CA356825381 | CNGA1,NIPAL1 | c.1520A>T (p.Asp507Val) c.1532A>T (p.Asp511Val) c.1739A>T (p.Asp580Val) n.479-22062T>A n.563+22258T>A c.1757A>T (p.Asp586Val) | |
4 | g.47936962T>C | CA356825383 | CNGA1,NIPAL1 | c.1520A>G (p.Asp507Gly) c.1532A>G (p.Asp511Gly) c.1739A>G (p.Asp580Gly) n.479-22062T>C n.563+22258T>C c.1757A>G (p.Asp586Gly) | |
4 | g.47936962T>G | CA356825385 | CNGA1,NIPAL1 | c.1520A>C (p.Asp507Ala) c.1532A>C (p.Asp511Ala) c.1739A>C (p.Asp580Ala) n.479-22062T>G n.563+22258T>G c.1757A>C (p.Asp586Ala) | |
4 | g.47936963C>A | CA356825387 | CNGA1,NIPAL1 | c.1519G>T (p.Asp507Tyr) c.1531G>T (p.Asp511Tyr) c.1738G>T (p.Asp580Tyr) n.479-22061C>A n.563+22259C>A c.1756G>T (p.Asp586Tyr) | |
4 | g.47936963C= | CA1455551784 | CNGA1,NIPAL1 | c.1519G= (p.Asp507=) c.1531G= (p.Asp511=) c.1738G= (p.Asp580=) n.479-22061C= n.563+22259C= c.1756G= (p.Asp586=) | |
4 | g.47936963C>G | CA356825389 | CNGA1,NIPAL1 | c.1519G>C (p.Asp507His) c.1531G>C (p.Asp511His) c.1738G>C (p.Asp580His) n.479-22061C>G n.563+22259C>G c.1756G>C (p.Asp586His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
4 | g.47936963C>T | CA356825390 | CNGA1,NIPAL1 | c.1519G>A (p.Asp507Asn) c.1531G>A (p.Asp511Asn) c.1738G>A (p.Asp580Asn) n.479-22061C>T n.563+22259C>T c.1756G>A (p.Asp586Asn) | |
4 | g.47936964C>A | CA439403845 | CNGA1,NIPAL1 | c.1518G>T (p.Gly506=) c.1530G>T (p.Gly510=) c.1737G>T (p.Gly579=) n.479-22060C>A n.563+22260C>A c.1755G>T (p.Gly585=) | |
4 | g.47936964C= | CA1455551785 | CNGA1,NIPAL1 | c.1518G= (p.Gly506=) c.1530G= (p.Gly510=) c.1737G= (p.Gly579=) n.479-22060C= n.563+22260C= c.1755G= (p.Gly585=) | |
4 | g.47936964C>G | CA439403846 | CNGA1,NIPAL1 | c.1518G>C (p.Gly506=) c.1530G>C (p.Gly510=) c.1737G>C (p.Gly579=) n.479-22060C>G n.563+22260C>G c.1755G>C (p.Gly585=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.47936964C>T | CA439403847 | CNGA1,NIPAL1 | c.1518G>A (p.Gly506=) c.1530G>A (p.Gly510=) c.1737G>A (p.Gly579=) n.479-22060C>T n.563+22260C>T c.1755G>A (p.Gly585=) | gnomAD v4 |
4 | g.47936965C>A | CA356825392 | CNGA1,NIPAL1 | c.1517G>T (p.Gly506Val) c.1529G>T (p.Gly510Val) c.1736G>T (p.Gly579Val) n.479-22059C>A n.563+22261C>A c.1754G>T (p.Gly585Val) | |
4 | g.47936965C>G | CA356825393 | CNGA1,NIPAL1 | c.1517G>C (p.Gly506Ala) c.1529G>C (p.Gly510Ala) c.1736G>C (p.Gly579Ala) n.479-22059C>G n.563+22261C>G c.1754G>C (p.Gly585Ala) | |
4 | g.47936965C>T | CA356825395 | CNGA1,NIPAL1 | c.1517G>A (p.Gly506Glu) c.1529G>A (p.Gly510Glu) c.1736G>A (p.Gly579Glu) n.479-22059C>T n.563+22261C>T c.1754G>A (p.Gly585Glu) | |
4 | g.47936966C>A | CA356825400 | CNGA1,NIPAL1 | c.1516G>T (p.Gly506Trp) c.1528G>T (p.Gly510Trp) c.1735G>T (p.Gly579Trp) n.479-22058C>A n.563+22262C>A c.1753G>T (p.Gly585Trp) | |
4 | g.47936966C= | CA1455551786 | CNGA1,NIPAL1 | c.1516G= (p.Gly506=) c.1528G= (p.Gly510=) c.1735G= (p.Gly579=) n.479-22058C= n.563+22262C= c.1753G= (p.Gly585=) | |
4 | g.47936966C>G | CA356825396 | CNGA1,NIPAL1 | c.1516G>C (p.Gly506Arg) c.1528G>C (p.Gly510Arg) c.1735G>C (p.Gly579Arg) n.479-22058C>G n.563+22262C>G c.1753G>C (p.Gly585Arg) | |
4 | g.47936966C>T | CA356825398 | CNGA1,NIPAL1 | c.1516G>A (p.Gly506Arg) c.1528G>A (p.Gly510Arg) c.1735G>A (p.Gly579Arg) n.479-22058C>T n.563+22262C>T c.1753G>A (p.Gly585Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.47936966_47936967delinsCT | CA1455551787 | CNGA1,NIPAL1 | c.1515_1516delinsAG (p.Lys505=) c.1527_1528delinsAG (p.Lys509=) c.1734_1735delinsAG (p.Lys578=) n.479-22058_479-22057delinsCT n.563+22262_563+22263delinsCT c.1752_1753delinsAG (p.Lys584=) | |
4 | g.47936967T>A | CA356825402 | CNGA1,NIPAL1 | c.1515A>T (p.Lys505Asn) c.1527A>T (p.Lys509Asn) c.1734A>T (p.Lys578Asn) n.479-22057T>A n.563+22263T>A c.1752A>T (p.Lys584Asn) | |
4 | g.47936967T>C | CA439403851 | CNGA1,NIPAL1 | c.1515A>G (p.Lys505=) c.1527A>G (p.Lys509=) c.1734A>G (p.Lys578=) n.479-22057T>C n.563+22263T>C c.1752A>G (p.Lys584=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.47936967T>G | CA356825404 | CNGA1,NIPAL1 | c.1515A>C (p.Lys505Asn) c.1527A>C (p.Lys509Asn) c.1734A>C (p.Lys578Asn) n.479-22057T>G n.563+22263T>G c.1752A>C (p.Lys584Asn) | |
4 | g.47936967T= | CA1455551788 | CNGA1,NIPAL1 | c.1515A= (p.Lys505=) c.1527A= (p.Lys509=) c.1734A= (p.Lys578=) n.479-22057T= n.563+22263T= c.1752A= (p.Lys584=) | |
4 | g.47936969del | CA795526791 | CNGA1,NIPAL1 | c.1515del (p.Asp507IlefsTer28) c.1527del (p.Asp511IlefsTer28) c.1734del (p.Asp580IlefsTer28) n.479-22055del n.563+22265del c.1752del (p.Asp586IlefsTer28) | dbSNP gnomAD v4 |
4 | g.47936968T>A | CA356825406 | CNGA1,NIPAL1 | c.1514A>T (p.Lys505Ile) c.1526A>T (p.Lys509Ile) c.1733A>T (p.Lys578Ile) n.479-22056T>A n.563+22264T>A c.1751A>T (p.Lys584Ile) | |
4 | g.47936968T>C | CA356825408 | CNGA1,NIPAL1 | c.1514A>G (p.Lys505Arg) c.1526A>G (p.Lys509Arg) c.1733A>G (p.Lys578Arg) n.479-22056T>C n.563+22264T>C c.1751A>G (p.Lys584Arg) | |
4 | g.47936968T>G | CA356825410 | CNGA1,NIPAL1 | c.1514A>C (p.Lys505Thr) c.1526A>C (p.Lys509Thr) c.1733A>C (p.Lys578Thr) n.479-22056T>G n.563+22264T>G c.1751A>C (p.Lys584Thr) | |
4 | g.47936969T>A | CA356825412 | CNGA1,NIPAL1 | c.1513A>T (p.Lys505Ter) c.1525A>T (p.Lys509Ter) c.1732A>T (p.Lys578Ter) n.479-22055T>A n.563+22265T>A c.1750A>T (p.Lys584Ter) | |
4 | g.47936969T>C | CA356825414 | CNGA1,NIPAL1 | c.1513A>G (p.Lys505Glu) c.1525A>G (p.Lys509Glu) c.1732A>G (p.Lys578Glu) n.479-22055T>C n.563+22265T>C c.1750A>G (p.Lys584Glu) | |
4 | g.47936969T>G | CA356825416 | CNGA1,NIPAL1 | c.1513A>C (p.Lys505Gln) c.1525A>C (p.Lys509Gln) c.1732A>C (p.Lys578Gln) n.479-22055T>G n.563+22265T>G c.1750A>C (p.Lys584Gln) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.47936969T= | CA1455551789 | CNGA1,NIPAL1 | c.1513A= (p.Lys505=) c.1525A= (p.Lys509=) c.1732A= (p.Lys578=) n.479-22055T= n.563+22265T= c.1750A= (p.Lys584=) | |
4 | g.47936970C>A | CA356825418 | CNGA1,NIPAL1 | c.1512G>T (p.Lys504Asn) c.1524G>T (p.Lys508Asn) c.1731G>T (p.Lys577Asn) n.479-22054C>A n.563+22266C>A c.1749G>T (p.Lys583Asn) | |
4 | g.47936970C>G | CA356825420 | CNGA1,NIPAL1 | c.1512G>C (p.Lys504Asn) c.1524G>C (p.Lys508Asn) c.1731G>C (p.Lys577Asn) n.479-22054C>G n.563+22266C>G c.1749G>C (p.Lys583Asn) | |
4 | g.47936970C>T | CA439403861 | CNGA1,NIPAL1 | c.1512G>A (p.Lys504=) c.1524G>A (p.Lys508=) c.1731G>A (p.Lys577=) n.479-22054C>T n.563+22266C>T c.1749G>A (p.Lys583=) | |
4 | g.47936971T>A | CA356825422 | CNGA1,NIPAL1 | c.1511A>T (p.Lys504Met) c.1523A>T (p.Lys508Met) c.1730A>T (p.Lys577Met) n.479-22053T>A n.563+22267T>A c.1748A>T (p.Lys583Met) | |
4 | g.47936971T>C | CA2911064 | CNGA1,NIPAL1 | c.1511A>G (p.Lys504Arg) c.1523A>G (p.Lys508Arg) c.1730A>G (p.Lys577Arg) n.479-22053T>C n.563+22267T>C c.1748A>G (p.Lys583Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.47936971T>G | CA356825425 | CNGA1,NIPAL1 | c.1511A>C (p.Lys504Thr) c.1523A>C (p.Lys508Thr) c.1730A>C (p.Lys577Thr) n.479-22053T>G n.563+22267T>G c.1748A>C (p.Lys583Thr) | |
4 | g.47936971T= | CA1455551790 | CNGA1,NIPAL1 | c.1511A= (p.Lys504=) c.1523A= (p.Lys508=) c.1730A= (p.Lys577=) n.479-22053T= n.563+22267T= c.1748A= (p.Lys583=) | |
4 | g.47936972T>A | CA356825429 | CNGA1,NIPAL1 | c.1510A>T (p.Lys504Ter) c.1522A>T (p.Lys508Ter) c.1729A>T (p.Lys577Ter) n.479-22052T>A n.563+22268T>A c.1747A>T (p.Lys583Ter) | |
4 | g.47936972T>C | CA356825431 | CNGA1,NIPAL1 | c.1510A>G (p.Lys504Glu) c.1522A>G (p.Lys508Glu) c.1729A>G (p.Lys577Glu) n.479-22052T>C n.563+22268T>C c.1747A>G (p.Lys583Glu) | |
4 | g.47936972T>G | CA356825427 | CNGA1,NIPAL1 | c.1510A>C (p.Lys504Gln) c.1522A>C (p.Lys508Gln) c.1729A>C (p.Lys577Gln) n.479-22052T>G n.563+22268T>G c.1747A>C (p.Lys583Gln) | |
4 | g.47936973G>A | CA439403863 | CNGA1,NIPAL1 | c.1509C>T (p.Cys503=) c.1521C>T (p.Cys507=) c.1728C>T (p.Cys576=) n.479-22051G>A n.563+22269G>A c.1746C>T (p.Cys582=) | dbSNP |
4 | g.47936973G>C | CA356825433 | CNGA1,NIPAL1 | c.1509C>G (p.Cys503Trp) c.1521C>G (p.Cys507Trp) c.1728C>G (p.Cys576Trp) n.479-22051G>C n.563+22269G>C c.1746C>G (p.Cys582Trp) | |
4 | g.47936973G>T | CA356825435 | CNGA1,NIPAL1 | c.1509C>A (p.Cys503Ter) c.1521C>A (p.Cys507Ter) c.1728C>A (p.Cys576Ter) n.479-22051G>T n.563+22269G>T c.1746C>A (p.Cys582Ter) | |
4 | g.47936974C>A | CA356825437 | CNGA1,NIPAL1 | c.1508G>T (p.Cys503Phe) c.1520G>T (p.Cys507Phe) c.1727G>T (p.Cys576Phe) n.479-22050C>A n.563+22270C>A c.1745G>T (p.Cys582Phe) | |
4 | g.47936974C>G | CA356825439 | CNGA1,NIPAL1 | c.1508G>C (p.Cys503Ser) c.1520G>C (p.Cys507Ser) c.1727G>C (p.Cys576Ser) n.479-22050C>G n.563+22270C>G c.1745G>C (p.Cys582Ser) | |
4 | g.47936974C>T | CA356825441 | CNGA1,NIPAL1 | c.1508G>A (p.Cys503Tyr) c.1520G>A (p.Cys507Tyr) c.1727G>A (p.Cys576Tyr) n.479-22050C>T n.563+22270C>T c.1745G>A (p.Cys582Tyr) | |
4 | g.47936975A>C | CA356825443 | CNGA1,NIPAL1 | c.1507T>G (p.Cys503Gly) c.1519T>G (p.Cys507Gly) c.1726T>G (p.Cys576Gly) n.479-22049A>C n.563+22271A>C c.1744T>G (p.Cys582Gly) | |
4 | g.47936975A>G | CA356825444 | CNGA1,NIPAL1 | c.1507T>C (p.Cys503Arg) c.1519T>C (p.Cys507Arg) c.1726T>C (p.Cys576Arg) n.479-22049A>G n.563+22271A>G c.1744T>C (p.Cys582Arg) | |
4 | g.47936975A>T | CA356825446 | CNGA1,NIPAL1 | c.1507T>A (p.Cys503Ser) c.1519T>A (p.Cys507Ser) c.1726T>A (p.Cys576Ser) n.479-22049A>T n.563+22271A>T c.1744T>A (p.Cys582Ser) | |
4 | g.47936976A= | CA1455551791 | CNGA1,NIPAL1 | c.1506T= (p.Ile502=) c.1518T= (p.Ile506=) c.1725T= (p.Ile575=) n.479-22048A= n.563+22272A= c.1743T= (p.Ile581=) | |
4 | g.47936976A>C | CA356825449 | CNGA1,NIPAL1 | c.1506T>G (p.Ile502Met) c.1518T>G (p.Ile506Met) c.1725T>G (p.Ile575Met) n.479-22048A>C n.563+22272A>C c.1743T>G (p.Ile581Met) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.47936976A>G | CA439403867 | CNGA1,NIPAL1 | c.1506T>C (p.Ile502=) c.1518T>C (p.Ile506=) c.1725T>C (p.Ile575=) n.479-22048A>G n.563+22272A>G c.1743T>C (p.Ile581=) | |
4 | g.47936976A>T | CA439403868 | CNGA1,NIPAL1 | c.1506T>A (p.Ile502=) c.1518T>A (p.Ile506=) c.1725T>A (p.Ile575=) n.479-22048A>T n.563+22272A>T c.1743T>A (p.Ile581=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.47936977A>C | CA356825451 | CNGA1,NIPAL1 | c.1505T>G (p.Ile502Ser) c.1517T>G (p.Ile506Ser) c.1724T>G (p.Ile575Ser) n.479-22047A>C n.563+22273A>C c.1742T>G (p.Ile581Ser) | |
4 | g.47936977A>G | CA356825453 | CNGA1,NIPAL1 | c.1505T>C (p.Ile502Thr) c.1517T>C (p.Ile506Thr) c.1724T>C (p.Ile575Thr) n.479-22047A>G n.563+22273A>G c.1742T>C (p.Ile581Thr) | |
4 | g.47936977A>T | CA356825455 | CNGA1,NIPAL1 | c.1505T>A (p.Ile502Asn) c.1517T>A (p.Ile506Asn) c.1724T>A (p.Ile575Asn) n.479-22047A>T n.563+22273A>T c.1742T>A (p.Ile581Asn) | |
4 | g.47936978T>A | CA356825458 | CNGA1,NIPAL1 | c.1504A>T (p.Ile502Phe) c.1516A>T (p.Ile506Phe) c.1723A>T (p.Ile575Phe) n.479-22046T>A n.563+22274T>A c.1741A>T (p.Ile581Phe) | COSMIC |
4 | g.47936978T>C | CA356825459 | CNGA1,NIPAL1 | c.1504A>G (p.Ile502Val) c.1516A>G (p.Ile506Val) c.1723A>G (p.Ile575Val) n.479-22046T>C n.563+22274T>C c.1741A>G (p.Ile581Val) | |
4 | g.47936978T>G | CA356825461 | CNGA1,NIPAL1 | c.1504A>C (p.Ile502Leu) c.1516A>C (p.Ile506Leu) c.1723A>C (p.Ile575Leu) n.479-22046T>G n.563+22274T>G c.1741A>C (p.Ile581Leu) | |
4 | g.47936979A>C | CA356825464 | CNGA1,NIPAL1 | c.1503T>G (p.Tyr501Ter) c.1515T>G (p.Tyr505Ter) c.1722T>G (p.Tyr574Ter) n.479-22045A>C n.563+22275A>C c.1740T>G (p.Tyr580Ter) | |
4 | g.47936979A>G | CA439403872 | CNGA1,NIPAL1 | c.1503T>C (p.Tyr501=) c.1515T>C (p.Tyr505=) c.1722T>C (p.Tyr574=) n.479-22045A>G n.563+22275A>G c.1740T>C (p.Tyr580=) | |
4 | g.47936979A>T | CA356825465 | CNGA1,NIPAL1 | c.1503T>A (p.Tyr501Ter) c.1515T>A (p.Tyr505Ter) c.1722T>A (p.Tyr574Ter) n.479-22045A>T n.563+22275A>T c.1740T>A (p.Tyr580Ter) | |
4 | g.47936980T>A | CA356825469 | CNGA1,NIPAL1 | c.1502A>T (p.Tyr501Phe) c.1514A>T (p.Tyr505Phe) c.1721A>T (p.Tyr574Phe) n.479-22044T>A n.563+22276T>A c.1739A>T (p.Tyr580Phe) | |
4 | g.47936980T>C | CA356825470 | CNGA1,NIPAL1 | c.1502A>G (p.Tyr501Cys) c.1514A>G (p.Tyr505Cys) c.1721A>G (p.Tyr574Cys) n.479-22044T>C n.563+22276T>C c.1739A>G (p.Tyr580Cys) | gnomAD v4 |
4 | g.47936980T>G | CA356825471 | CNGA1,NIPAL1 | c.1502A>C (p.Tyr501Ser) c.1514A>C (p.Tyr505Ser) c.1721A>C (p.Tyr574Ser) n.479-22044T>G n.563+22276T>G c.1739A>C (p.Tyr580Ser) | |
4 | g.47936981A>C | CA356825474 | CNGA1,NIPAL1 | c.1501T>G (p.Tyr501Asp) c.1513T>G (p.Tyr505Asp) c.1720T>G (p.Tyr574Asp) n.479-22043A>C n.563+22277A>C c.1738T>G (p.Tyr580Asp) | |
4 | g.47936981A>G | CA356825475 | CNGA1,NIPAL1 | c.1501T>C (p.Tyr501His) c.1513T>C (p.Tyr505His) c.1720T>C (p.Tyr574His) n.479-22043A>G n.563+22277A>G c.1738T>C (p.Tyr580His) | gnomAD v4 |
4 | g.47936981A>T | CA356825477 | CNGA1,NIPAL1 | c.1501T>A (p.Tyr501Asn) c.1513T>A (p.Tyr505Asn) c.1720T>A (p.Tyr574Asn) n.479-22043A>T n.563+22277A>T c.1738T>A (p.Tyr580Asn) | |
4 | g.47936982A>C | CA356825480 | CNGA1,NIPAL1 | c.1500T>G (p.Asp500Glu) c.1512T>G (p.Asp504Glu) c.1719T>G (p.Asp573Glu) n.479-22042A>C n.563+22278A>C c.1737T>G (p.Asp579Glu) | |
4 | g.47936982A>G | CA439403874 | CNGA1,NIPAL1 | c.1500T>C (p.Asp500=) c.1512T>C (p.Asp504=) c.1719T>C (p.Asp573=) n.479-22042A>G n.563+22278A>G c.1737T>C (p.Asp579=) | gnomAD v4 |
4 | g.47936982A>T | CA356825481 | CNGA1,NIPAL1 | c.1500T>A (p.Asp500Glu) c.1512T>A (p.Asp504Glu) c.1719T>A (p.Asp573Glu) n.479-22042A>T n.563+22278A>T c.1737T>A (p.Asp579Glu) | |
4 | g.47936983T>A | CA356825484 | CNGA1,NIPAL1 | c.1499A>T (p.Asp500Val) c.1511A>T (p.Asp504Val) c.1718A>T (p.Asp573Val) n.479-22041T>A n.563+22279T>A c.1736A>T (p.Asp579Val) | |
4 | g.47936983T>C | CA2911065 | CNGA1,NIPAL1 | c.1499A>G (p.Asp500Gly) c.1511A>G (p.Asp504Gly) c.1718A>G (p.Asp573Gly) n.479-22041T>C n.563+22279T>C c.1736A>G (p.Asp579Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936983T>G | CA356825486 | CNGA1,NIPAL1 | c.1499A>C (p.Asp500Ala) c.1511A>C (p.Asp504Ala) c.1718A>C (p.Asp573Ala) n.479-22041T>G n.563+22279T>G c.1736A>C (p.Asp579Ala) | |
4 | g.47936983T= | CA1455551792 | CNGA1,NIPAL1 | c.1499A= (p.Asp500=) c.1511A= (p.Asp504=) c.1718A= (p.Asp573=) n.479-22041T= n.563+22279T= c.1736A= (p.Asp579=) | |
4 | g.47936984C>A | CA356825491 | CNGA1,NIPAL1 | c.1498G>T (p.Asp500Tyr) c.1510G>T (p.Asp504Tyr) c.1717G>T (p.Asp573Tyr) n.479-22040C>A n.563+22280C>A c.1735G>T (p.Asp579Tyr) | |
4 | g.47936984C>G | CA356825493 | CNGA1,NIPAL1 | c.1498G>C (p.Asp500His) c.1510G>C (p.Asp504His) c.1717G>C (p.Asp573His) n.479-22040C>G n.563+22280C>G c.1735G>C (p.Asp579His) | |
4 | g.47936984C>T | CA356825489 | CNGA1,NIPAL1 | c.1498G>A (p.Asp500Asn) c.1510G>A (p.Asp504Asn) c.1717G>A (p.Asp573Asn) n.479-22040C>T n.563+22280C>T c.1735G>A (p.Asp579Asn) | |
4 | g.47936985T>A | CA439403879 | CNGA1,NIPAL1 | c.1497A>T (p.Gly499=) c.1509A>T (p.Gly503=) c.1716A>T (p.Gly572=) n.479-22039T>A n.563+22281T>A c.1734A>T (p.Gly578=) | |
4 | g.47936985T>C | CA439403880 | CNGA1,NIPAL1 | c.1497A>G (p.Gly499=) c.1509A>G (p.Gly503=) c.1716A>G (p.Gly572=) n.479-22039T>C n.563+22281T>C c.1734A>G (p.Gly578=) | |
4 | g.47936985T>G | CA439403882 | CNGA1,NIPAL1 | c.1497A>C (p.Gly499=) c.1509A>C (p.Gly503=) c.1716A>C (p.Gly572=) n.479-22039T>G n.563+22281T>G c.1734A>C (p.Gly578=) | |
4 | g.47936986C>A | CA356825495 | CNGA1,NIPAL1 | c.1496G>T (p.Gly499Val) c.1508G>T (p.Gly503Val) c.1715G>T (p.Gly572Val) n.479-22038C>A n.563+22282C>A c.1733G>T (p.Gly578Val) | |
4 | g.47936986C= | CA1455551793 | CNGA1,NIPAL1 | c.1496G= (p.Gly499=) c.1508G= (p.Gly503=) c.1715G= (p.Gly572=) n.479-22038C= n.563+22282C= c.1733G= (p.Gly578=) | |
4 | g.47936986C>G | CA2911066 | CNGA1,NIPAL1 | c.1496G>C (p.Gly499Ala) c.1508G>C (p.Gly503Ala) c.1715G>C (p.Gly572Ala) n.479-22038C>G n.563+22282C>G c.1733G>C (p.Gly578Ala) | dbSNP ExAC gnomAD v2 |
4 | g.47936986C>T | CA356825498 | CNGA1,NIPAL1 | c.1496G>A (p.Gly499Glu) c.1508G>A (p.Gly503Glu) c.1715G>A (p.Gly572Glu) n.479-22038C>T n.563+22282C>T c.1733G>A (p.Gly578Glu) | gnomAD v4 |
4 | g.47936987C>A | CA356825500 | CNGA1,NIPAL1 | c.1495G>T (p.Gly499Ter) c.1507G>T (p.Gly503Ter) c.1714G>T (p.Gly572Ter) n.479-22037C>A n.563+22283C>A c.1732G>T (p.Gly578Ter) | |
4 | g.47936987C= | CA1455551794 | CNGA1,NIPAL1 | c.1495G= (p.Gly499=) c.1507G= (p.Gly503=) c.1714G= (p.Gly572=) n.479-22037C= n.563+22283C= c.1732G= (p.Gly578=) | |
4 | g.47936987C>G | CA356825502 | CNGA1,NIPAL1 | c.1495G>C (p.Gly499Arg) c.1507G>C (p.Gly503Arg) c.1714G>C (p.Gly572Arg) n.479-22037C>G n.563+22283C>G c.1732G>C (p.Gly578Arg) | dbSNP |
4 | g.47936987C>T | CA356825504 | CNGA1,NIPAL1 | c.1495G>A (p.Gly499Arg) c.1507G>A (p.Gly503Arg) c.1714G>A (p.Gly572Arg) n.479-22037C>T n.563+22283C>T c.1732G>A (p.Gly578Arg) | |
4 | g.47936988A>C | CA439403885 | CNGA1,NIPAL1 | c.1494T>G (p.Pro498=) c.1506T>G (p.Pro502=) c.1713T>G (p.Pro571=) n.479-22036A>C n.563+22284A>C c.1731T>G (p.Pro577=) | |
4 | g.47936988A>G | CA439403888 | CNGA1,NIPAL1 | c.1494T>C (p.Pro498=) c.1506T>C (p.Pro502=) c.1713T>C (p.Pro571=) n.479-22036A>G n.563+22284A>G c.1731T>C (p.Pro577=) | gnomAD v4 |
4 | g.47936988A>T | CA439403890 | CNGA1,NIPAL1 | c.1494T>A (p.Pro498=) c.1506T>A (p.Pro502=) c.1713T>A (p.Pro571=) n.479-22036A>T n.563+22284A>T c.1731T>A (p.Pro577=) | |
4 | g.47936989G>A | CA356825510 | CNGA1,NIPAL1 | c.1493C>T (p.Pro498Leu) c.1505C>T (p.Pro502Leu) c.1712C>T (p.Pro571Leu) n.479-22035G>A n.563+22285G>A c.1730C>T (p.Pro577Leu) | |
4 | g.47936989G>C | CA356825506 | CNGA1,NIPAL1 | c.1493C>G (p.Pro498Arg) c.1505C>G (p.Pro502Arg) c.1712C>G (p.Pro571Arg) n.479-22035G>C n.563+22285G>C c.1730C>G (p.Pro577Arg) | |
4 | g.47936989G>T | CA356825508 | CNGA1,NIPAL1 | c.1493C>A (p.Pro498His) c.1505C>A (p.Pro502His) c.1712C>A (p.Pro571His) n.479-22035G>T n.563+22285G>T c.1730C>A (p.Pro577His) | |
4 | g.47936990G>A | CA356825512 | CNGA1,NIPAL1 | c.1492C>T (p.Pro498Ser) c.1504C>T (p.Pro502Ser) c.1711C>T (p.Pro571Ser) n.479-22034G>A n.563+22286G>A c.1729C>T (p.Pro577Ser) | |
4 | g.47936990G>C | CA356825515 | CNGA1,NIPAL1 | c.1492C>G (p.Pro498Ala) c.1504C>G (p.Pro502Ala) c.1711C>G (p.Pro571Ala) n.479-22034G>C n.563+22286G>C c.1729C>G (p.Pro577Ala) | |
4 | g.47936990G>T | CA356825517 | CNGA1,NIPAL1 | c.1492C>A (p.Pro498Thr) c.1504C>A (p.Pro502Thr) c.1711C>A (p.Pro571Thr) n.479-22034G>T n.563+22286G>T c.1729C>A (p.Pro577Thr) | |
4 | g.47936991A>C | CA356825518 | CNGA1,NIPAL1 | c.1491T>G (p.Ser497Arg) c.1503T>G (p.Ser501Arg) c.1710T>G (p.Ser570Arg) n.479-22033A>C n.563+22287A>C c.1728T>G (p.Ser576Arg) | |
4 | g.47936991A>G | CA439403896 | CNGA1,NIPAL1 | c.1491T>C (p.Ser497=) c.1503T>C (p.Ser501=) c.1710T>C (p.Ser570=) n.479-22033A>G n.563+22287A>G c.1728T>C (p.Ser576=) | |
4 | g.47936991A>T | CA356825520 | CNGA1,NIPAL1 | c.1491T>A (p.Ser497Arg) c.1503T>A (p.Ser501Arg) c.1710T>A (p.Ser570Arg) n.479-22033A>T n.563+22287A>T c.1728T>A (p.Ser576Arg) | |
4 | g.47936992C>A | CA356825522 | CNGA1,NIPAL1 | c.1490G>T (p.Ser497Ile) c.1502G>T (p.Ser501Ile) c.1709G>T (p.Ser570Ile) n.479-22032C>A n.563+22288C>A c.1727G>T (p.Ser576Ile) | |
4 | g.47936992C>G | CA356825526 | CNGA1,NIPAL1 | c.1490G>C (p.Ser497Thr) c.1502G>C (p.Ser501Thr) c.1709G>C (p.Ser570Thr) n.479-22032C>G n.563+22288C>G c.1727G>C (p.Ser576Thr) | |
4 | g.47936992C>T | CA356825524 | CNGA1,NIPAL1 | c.1490G>A (p.Ser497Asn) c.1502G>A (p.Ser501Asn) c.1709G>A (p.Ser570Asn) n.479-22032C>T n.563+22288C>T c.1727G>A (p.Ser576Asn) | |
4 | g.47936993del | CA2670552348 | CNGA1,NIPAL1 | c.1489del (p.Ser497ValfsTer?) c.1501del (p.Ser501ValfsTer?) c.1708del (p.Ser570ValfsTer?) n.479-22031del n.563+22289del c.1726del (p.Ser576ValfsTer?) | gnomAD v4 |
4 | g.47936993T>A | CA356825528 | CNGA1,NIPAL1 | c.1489A>T (p.Ser497Cys) c.1501A>T (p.Ser501Cys) c.1708A>T (p.Ser570Cys) n.479-22031T>A n.563+22289T>A c.1726A>T (p.Ser576Cys) | |
4 | g.47936993T>C | CA356825530 | CNGA1,NIPAL1 | c.1489A>G (p.Ser497Gly) c.1501A>G (p.Ser501Gly) c.1708A>G (p.Ser570Gly) n.479-22031T>C n.563+22289T>C c.1726A>G (p.Ser576Gly) | |
4 | g.47936993T>G | CA356825532 | CNGA1,NIPAL1 | c.1489A>C (p.Ser497Arg) c.1501A>C (p.Ser501Arg) c.1708A>C (p.Ser570Arg) n.479-22031T>G n.563+22289T>G c.1726A>C (p.Ser576Arg) | |
4 | g.47936994G>A | CA2911067 | CNGA1,NIPAL1 | c.1488C>T (p.Tyr496=) c.1500C>T (p.Tyr500=) c.1707C>T (p.Tyr569=) n.479-22030G>A n.563+22290G>A c.1725C>T (p.Tyr575=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47936994G>C | CA356825534 | CNGA1,NIPAL1 | c.1488C>G (p.Tyr496Ter) c.1500C>G (p.Tyr500Ter) c.1707C>G (p.Tyr569Ter) n.479-22030G>C n.563+22290G>C c.1725C>G (p.Tyr575Ter) | |
4 | g.47936994G= | CA1455551795 | CNGA1,NIPAL1 | c.1488C= (p.Tyr496=) c.1500C= (p.Tyr500=) c.1707C= (p.Tyr569=) n.479-22030G= n.563+22290G= c.1725C= (p.Tyr575=) | |
4 | g.47936994G>T | CA356825535 | CNGA1,NIPAL1 | c.1488C>A (p.Tyr496Ter) c.1500C>A (p.Tyr500Ter) c.1707C>A (p.Tyr569Ter) n.479-22030G>T n.563+22290G>T c.1725C>A (p.Tyr575Ter) | |
4 | g.47936995T>A | CA356825538 | CNGA1,NIPAL1 | c.1487A>T (p.Tyr496Phe) c.1499A>T (p.Tyr500Phe) c.1706A>T (p.Tyr569Phe) n.479-22029T>A n.563+22291T>A c.1724A>T (p.Tyr575Phe) | |
4 | g.47936995T>C | CA356825540 | CNGA1,NIPAL1 | c.1487A>G (p.Tyr496Cys) c.1499A>G (p.Tyr500Cys) c.1706A>G (p.Tyr569Cys) n.479-22029T>C n.563+22291T>C c.1724A>G (p.Tyr575Cys) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.47936995T>G | CA356825541 | CNGA1,NIPAL1 | c.1487A>C (p.Tyr496Ser) c.1499A>C (p.Tyr500Ser) c.1706A>C (p.Tyr569Ser) n.479-22029T>G n.563+22291T>G c.1724A>C (p.Tyr575Ser) | |
4 | g.47936995T= | CA1455551796 | CNGA1,NIPAL1 | c.1487A= (p.Tyr496=) c.1499A= (p.Tyr500=) c.1706A= (p.Tyr569=) n.479-22029T= n.563+22291T= c.1724A= (p.Tyr575=) | |
4 | g.47936996A>C | CA356825544 | CNGA1,NIPAL1 | c.1486T>G (p.Tyr496Asp) c.1498T>G (p.Tyr500Asp) c.1705T>G (p.Tyr569Asp) n.479-22028A>C n.563+22292A>C c.1723T>G (p.Tyr575Asp) | |
4 | g.47936996A>G | CA356825546 | CNGA1,NIPAL1 | c.1486T>C (p.Tyr496His) c.1498T>C (p.Tyr500His) c.1705T>C (p.Tyr569His) n.479-22028A>G n.563+22292A>G c.1723T>C (p.Tyr575His) | |
4 | g.47936996A>T | CA356825547 | CNGA1,NIPAL1 | c.1486T>A (p.Tyr496Asn) c.1498T>A (p.Tyr500Asn) c.1705T>A (p.Tyr569Asn) n.479-22028A>T n.563+22292A>T c.1723T>A (p.Tyr575Asn) | |
4 | g.47936997G>A | CA439403905 | CNGA1,NIPAL1 | c.1485C>T (p.Val495=) c.1497C>T (p.Val499=) c.1704C>T (p.Val568=) n.479-22027G>A n.563+22293G>A c.1722C>T (p.Val574=) | gnomAD v4 |
4 | g.47936997G>C | CA439403903 | CNGA1,NIPAL1 | c.1485C>G (p.Val495=) c.1497C>G (p.Val499=) c.1704C>G (p.Val568=) n.479-22027G>C n.563+22293G>C c.1722C>G (p.Val574=) | |
4 | g.47936997G>T | CA439403904 | CNGA1,NIPAL1 | c.1485C>A (p.Val495=) c.1497C>A (p.Val499=) c.1704C>A (p.Val568=) n.479-22027G>T n.563+22293G>T c.1722C>A (p.Val574=) | |
4 | g.47936998A= | CA1455551797 | CNGA1,NIPAL1 | c.1484T= (p.Val495=) c.1496T= (p.Val499=) c.1703T= (p.Val568=) n.479-22026A= n.563+22294A= c.1721T= (p.Val574=) | |
4 | g.47936998A>C | CA356825552 | CNGA1,NIPAL1 | c.1484T>G (p.Val495Gly) c.1496T>G (p.Val499Gly) c.1703T>G (p.Val568Gly) n.479-22026A>C n.563+22294A>C c.1721T>G (p.Val574Gly) | |
4 | g.47936998A>G | CA356825549 | CNGA1,NIPAL1 | c.1484T>C (p.Val495Ala) c.1496T>C (p.Val499Ala) c.1703T>C (p.Val568Ala) n.479-22026A>G n.563+22294A>G c.1721T>C (p.Val574Ala) | dbSNP gnomAD v4 |
4 | g.47936998A>T | CA356825550 | CNGA1,NIPAL1 | c.1484T>A (p.Val495Asp) c.1496T>A (p.Val499Asp) c.1703T>A (p.Val568Asp) n.479-22026A>T n.563+22294A>T c.1721T>A (p.Val574Asp) | |
4 | g.47936999C>A | CA356825555 | CNGA1,NIPAL1 | c.1483G>T (p.Val495Phe) c.1495G>T (p.Val499Phe) c.1702G>T (p.Val568Phe) n.479-22025C>A n.563+22295C>A c.1720G>T (p.Val574Phe) | |
4 | g.47936999C>G | CA356825559 | CNGA1,NIPAL1 | c.1483G>C (p.Val495Leu) c.1495G>C (p.Val499Leu) c.1702G>C (p.Val568Leu) n.479-22025C>G n.563+22295C>G c.1720G>C (p.Val574Leu) | |
4 | g.47936999C>T | CA356825557 | CNGA1,NIPAL1 | c.1483G>A (p.Val495Ile) c.1495G>A (p.Val499Ile) c.1702G>A (p.Val568Ile) n.479-22025C>T n.563+22295C>T c.1720G>A (p.Val574Ile) | |
4 | g.47937000T>A | CA356825561 | CNGA1,NIPAL1 | c.1482A>T (p.Gln494His) c.1494A>T (p.Gln498His) c.1701A>T (p.Gln567His) n.479-22024T>A n.563+22296T>A c.1719A>T (p.Gln573His) | |
4 | g.47937000T>C | CA439403907 | CNGA1,NIPAL1 | c.1482A>G (p.Gln494=) c.1494A>G (p.Gln498=) c.1701A>G (p.Gln567=) n.479-22024T>C n.563+22296T>C c.1719A>G (p.Gln573=) | |
4 | g.47937000T>G | CA356825563 | CNGA1,NIPAL1 | c.1482A>C (p.Gln494His) c.1494A>C (p.Gln498His) c.1701A>C (p.Gln567His) n.479-22024T>G n.563+22296T>G c.1719A>C (p.Gln573His) | |
4 | g.47937001del | CA2586973852 | CNGA1,NIPAL1 | c.1482del (p.Val495SerfsTer?) c.1494del (p.Val499SerfsTer?) c.1701del (p.Val568SerfsTer?) n.479-22023del n.563+22297del c.1719del (p.Val574SerfsTer?) | |
4 | g.47937001T>A | CA356825564 | CNGA1,NIPAL1 | c.1481A>T (p.Gln494Leu) c.1493A>T (p.Gln498Leu) c.1700A>T (p.Gln567Leu) n.479-22023T>A n.563+22297T>A c.1718A>T (p.Gln573Leu) | |
4 | g.47937001T>C | CA356825565 | CNGA1,NIPAL1 | c.1481A>G (p.Gln494Arg) c.1493A>G (p.Gln498Arg) c.1700A>G (p.Gln567Arg) n.479-22023T>C n.563+22297T>C c.1718A>G (p.Gln573Arg) | gnomAD v4 |
4 | g.47937001T>G | CA356825567 | CNGA1,NIPAL1 | c.1481A>C (p.Gln494Pro) c.1493A>C (p.Gln498Pro) c.1700A>C (p.Gln567Pro) n.479-22023T>G n.563+22297T>G c.1718A>C (p.Gln573Pro) | |
4 | g.47937002G>A | CA356825570 | CNGA1,NIPAL1 | c.1480C>T (p.Gln494Ter) c.1492C>T (p.Gln498Ter) c.1699C>T (p.Gln567Ter) n.479-22022G>A n.563+22298G>A c.1717C>T (p.Gln573Ter) | |
4 | g.47937002G>C | CA356825571 | CNGA1,NIPAL1 | c.1480C>G (p.Gln494Glu) c.1492C>G (p.Gln498Glu) c.1699C>G (p.Gln567Glu) n.479-22022G>C n.563+22298G>C c.1717C>G (p.Gln573Glu) | gnomAD v4 |
4 | g.47937002G>T | CA356825573 | CNGA1,NIPAL1 | c.1480C>A (p.Gln494Lys) c.1492C>A (p.Gln498Lys) c.1699C>A (p.Gln567Lys) n.479-22022G>T n.563+22298G>T c.1717C>A (p.Gln573Lys) | |
4 | g.47937003G>A | CA2911068 | CNGA1,NIPAL1 | c.1479C>T (p.Pro493=) c.1491C>T (p.Pro497=) c.1698C>T (p.Pro566=) n.479-22021G>A n.563+22299G>A c.1716C>T (p.Pro572=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47937003G>C | CA439403909 | CNGA1,NIPAL1 | c.1479C>G (p.Pro493=) c.1491C>G (p.Pro497=) c.1698C>G (p.Pro566=) n.479-22021G>C n.563+22299G>C c.1716C>G (p.Pro572=) | |
4 | g.47937003G= | CA1455551798 | CNGA1,NIPAL1 | c.1479C= (p.Pro493=) c.1491C= (p.Pro497=) c.1698C= (p.Pro566=) n.479-22021G= n.563+22299G= c.1716C= (p.Pro572=) | |
4 | g.47937003G>T | CA439403910 | CNGA1,NIPAL1 | c.1479C>A (p.Pro493=) c.1491C>A (p.Pro497=) c.1698C>A (p.Pro566=) n.479-22021G>T n.563+22299G>T c.1716C>A (p.Pro572=) | |
4 | g.47937004G>A | CA96688544 | CNGA1,NIPAL1 | c.1478C>T (p.Pro493Leu) c.1490C>T (p.Pro497Leu) c.1697C>T (p.Pro566Leu) n.479-22020G>A n.563+22300G>A c.1715C>T (p.Pro572Leu) | dbSNP gnomAD v4 |
4 | g.47937004G>C | CA356825578 | CNGA1,NIPAL1 | c.1478C>G (p.Pro493Arg) c.1490C>G (p.Pro497Arg) c.1697C>G (p.Pro566Arg) n.479-22020G>C n.563+22300G>C c.1715C>G (p.Pro572Arg) | |
4 | g.47937004G= | CA1455551799 | CNGA1,NIPAL1 | c.1478C= (p.Pro493=) c.1490C= (p.Pro497=) c.1697C= (p.Pro566=) n.479-22020G= n.563+22300G= c.1715C= (p.Pro572=) | |
4 | g.47937004G>T | CA356825580 | CNGA1,NIPAL1 | c.1478C>A (p.Pro493His) c.1490C>A (p.Pro497His) c.1697C>A (p.Pro566His) n.479-22020G>T n.563+22300G>T c.1715C>A (p.Pro572His) | dbSNP |
4 | g.47937005G>A | CA356825586 | CNGA1,NIPAL1 | c.1477C>T (p.Pro493Ser) c.1489C>T (p.Pro497Ser) c.1696C>T (p.Pro566Ser) n.479-22019G>A n.563+22301G>A c.1714C>T (p.Pro572Ser) | gnomAD v4 |
4 | g.47937005G>C | CA356825584 | CNGA1,NIPAL1 | c.1477C>G (p.Pro493Ala) c.1489C>G (p.Pro497Ala) c.1696C>G (p.Pro566Ala) n.479-22019G>C n.563+22301G>C c.1714C>G (p.Pro572Ala) | |
4 | g.47937005G>T | CA356825583 | CNGA1,NIPAL1 | c.1477C>A (p.Pro493Thr) c.1489C>A (p.Pro497Thr) c.1696C>A (p.Pro566Thr) n.479-22019G>T n.563+22301G>T c.1714C>A (p.Pro572Thr) | dbSNP |
4 | g.47937005_47937021del | CA2670552349 | CNGA1,NIPAL1 | c.1461_1477del (p.Leu487PhefsTer?) c.1473_1489del (p.Leu491PhefsTer?) c.1680_1696del (p.Leu560PhefsTer?) n.479-22019_479-22003del n.563+22301_563+22317del c.1698_1714del (p.Leu566PhefsTer?) | gnomAD v4 |
4 | g.47937006T>A | CA356825587 | CNGA1,NIPAL1 | c.1476A>T (p.Gln492His) c.1488A>T (p.Gln496His) c.1695A>T (p.Gln565His) n.479-22018T>A n.563+22302T>A c.1713A>T (p.Gln571His) | |
4 | g.47937006T>C | CA2911069 | CNGA1,NIPAL1 | c.1476A>G (p.Gln492=) c.1488A>G (p.Gln496=) c.1695A>G (p.Gln565=) n.479-22018T>C n.563+22302T>C c.1713A>G (p.Gln571=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47937006T>G | CA356825589 | CNGA1,NIPAL1 | c.1476A>C (p.Gln492His) c.1488A>C (p.Gln496His) c.1695A>C (p.Gln565His) n.479-22018T>G n.563+22302T>G c.1713A>C (p.Gln571His) | |
4 | g.47937006T= | CA1455551800 | CNGA1,NIPAL1 | c.1476A= (p.Gln492=) c.1488A= (p.Gln496=) c.1695A= (p.Gln565=) n.479-22018T= n.563+22302T= c.1713A= (p.Gln571=) | |
4 | g.47937007T>A | CA356825590 | CNGA1,NIPAL1 | c.1475A>T (p.Gln492Leu) c.1487A>T (p.Gln496Leu) c.1694A>T (p.Gln565Leu) n.479-22017T>A n.563+22303T>A c.1712A>T (p.Gln571Leu) | |
4 | g.47937007T>C | CA356825592 | CNGA1,NIPAL1 | c.1475A>G (p.Gln492Arg) c.1487A>G (p.Gln496Arg) c.1694A>G (p.Gln565Arg) n.479-22017T>C n.563+22303T>C c.1712A>G (p.Gln571Arg) | gnomAD v4 |
4 | g.47937007T>G | CA356825594 | CNGA1,NIPAL1 | c.1475A>C (p.Gln492Pro) c.1487A>C (p.Gln496Pro) c.1694A>C (p.Gln565Pro) n.479-22017T>G n.563+22303T>G c.1712A>C (p.Gln571Pro) | ClinVar dbSNP gnomAD v4 |
4 | g.47937007T= | CA1455551801 | CNGA1,NIPAL1 | c.1475A= (p.Gln492=) c.1487A= (p.Gln496=) c.1694A= (p.Gln565=) n.479-22017T= n.563+22303T= c.1712A= (p.Gln571=) | |
4 | g.47937008G>A | CA356825596 | CNGA1,NIPAL1 | c.1474C>T (p.Gln492Ter) c.1486C>T (p.Gln496Ter) c.1693C>T (p.Gln565Ter) n.479-22016G>A n.563+22304G>A c.1711C>T (p.Gln571Ter) | dbSNP |
4 | g.47937008G>C | CA356825598 | CNGA1,NIPAL1 | c.1474C>G (p.Gln492Glu) c.1486C>G (p.Gln496Glu) c.1693C>G (p.Gln565Glu) n.479-22016G>C n.563+22304G>C c.1711C>G (p.Gln571Glu) | |
4 | g.47937008G= | CA1455551802 | CNGA1,NIPAL1 | c.1474C= (p.Gln492=) c.1486C= (p.Gln496=) c.1693C= (p.Gln565=) n.479-22016G= n.563+22304G= c.1711C= (p.Gln571=) | |
4 | g.47937008G>T | CA356825600 | CNGA1,NIPAL1 | c.1474C>A (p.Gln492Lys) c.1486C>A (p.Gln496Lys) c.1693C>A (p.Gln565Lys) n.479-22016G>T n.563+22304G>T c.1711C>A (p.Gln571Lys) | |
4 | g.47937009C>A | CA356825601 | CNGA1,NIPAL1 | c.1473G>T (p.Leu491Phe) c.1485G>T (p.Leu495Phe) c.1692G>T (p.Leu564Phe) n.479-22015C>A n.563+22305C>A c.1710G>T (p.Leu570Phe) | |
4 | g.47937009C= | CA1455551803 | CNGA1,NIPAL1 | c.1473G= (p.Leu491=) c.1485G= (p.Leu495=) c.1692G= (p.Leu564=) n.479-22015C= n.563+22305C= c.1710G= (p.Leu570=) | |
4 | g.47937009C>G | CA356825602 | CNGA1,NIPAL1 | c.1473G>C (p.Leu491Phe) c.1485G>C (p.Leu495Phe) c.1692G>C (p.Leu564Phe) n.479-22015C>G n.563+22305C>G c.1710G>C (p.Leu570Phe) | ClinVar |
4 | g.47937009C>T | CA439403921 | CNGA1,NIPAL1 | c.1473G>A (p.Leu491=) c.1485G>A (p.Leu495=) c.1692G>A (p.Leu564=) n.479-22015C>T n.563+22305C>T c.1710G>A (p.Leu570=) | dbSNP gnomAD v2 |
4 | g.47937010A>C | CA356825607 | CNGA1,NIPAL1 | c.1472T>G (p.Leu491Trp) c.1484T>G (p.Leu495Trp) c.1691T>G (p.Leu564Trp) n.479-22014A>C n.563+22306A>C c.1709T>G (p.Leu570Trp) | |
4 | g.47937010A>G | CA356825609 | CNGA1,NIPAL1 | c.1472T>C (p.Leu491Ser) c.1484T>C (p.Leu495Ser) c.1691T>C (p.Leu564Ser) n.479-22014A>G n.563+22306A>G c.1709T>C (p.Leu570Ser) | |
4 | g.47937010A>T | CA356825606 | CNGA1,NIPAL1 | c.1472T>A (p.Leu491Ter) c.1484T>A (p.Leu495Ter) c.1691T>A (p.Leu564Ter) n.479-22014A>T n.563+22306A>T c.1709T>A (p.Leu570Ter) | |
4 | g.47937010_47937013del | CA2586973853 | CNGA1,NIPAL1 | c.1469_1472del (p.Lys490SerfsTer?) c.1481_1484del (p.Lys494SerfsTer?) c.1688_1691del (p.Lys563SerfsTer?) n.479-22014_479-22011del n.563+22306_563+22309del c.1706_1709del (p.Lys569SerfsTer?) | |
4 | g.47937011A= | CA1455551804 | CNGA1,NIPAL1 | c.1471T= (p.Leu491=) c.1483T= (p.Leu495=) c.1690T= (p.Leu564=) n.479-22013A= n.563+22307A= c.1708T= (p.Leu570=) | |
4 | g.47937011A>C | CA356825612 | CNGA1,NIPAL1 | c.1471T>G (p.Leu491Val) c.1483T>G (p.Leu495Val) c.1690T>G (p.Leu564Val) n.479-22013A>C n.563+22307A>C c.1708T>G (p.Leu570Val) | |
4 | g.47937011A>G | CA2911070 | CNGA1,NIPAL1 | c.1471T>C (p.Leu491=) c.1483T>C (p.Leu495=) c.1690T>C (p.Leu564=) n.479-22013A>G n.563+22307A>G c.1708T>C (p.Leu570=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47937011A>T | CA356825614 | CNGA1,NIPAL1 | c.1471T>A (p.Leu491Met) c.1483T>A (p.Leu495Met) c.1690T>A (p.Leu564Met) n.479-22013A>T n.563+22307A>T c.1708T>A (p.Leu570Met) | |
4 | g.47937012T>A | CA356825616 | CNGA1,NIPAL1 | c.1470A>T (p.Lys490Asn) c.1482A>T (p.Lys494Asn) c.1689A>T (p.Lys563Asn) n.479-22012T>A n.563+22308T>A c.1707A>T (p.Lys569Asn) | |
4 | g.47937012T>C | CA439403922 | CNGA1,NIPAL1 | c.1470A>G (p.Lys490=) c.1482A>G (p.Lys494=) c.1689A>G (p.Lys563=) n.479-22012T>C n.563+22308T>C c.1707A>G (p.Lys569=) | |
4 | g.47937012T>G | CA356825618 | CNGA1,NIPAL1 | c.1470A>C (p.Lys490Asn) c.1482A>C (p.Lys494Asn) c.1689A>C (p.Lys563Asn) n.479-22012T>G n.563+22308T>G c.1707A>C (p.Lys569Asn) | |
4 | g.47937013_47937014del | CA2578081538 | CNGA1,NIPAL1 | c.1469_1470del (p.Lys490IlefsTer?) c.1481_1482del (p.Lys494IlefsTer?) c.1688_1689del (p.Lys563IlefsTer?) n.479-22011_479-22010del n.563+22309_563+22310del c.1706_1707del (p.Lys569IlefsTer?) | |
4 | g.47937013T>A | CA356825624 | CNGA1,NIPAL1 | c.1469A>T (p.Lys490Ile) c.1481A>T (p.Lys494Ile) c.1688A>T (p.Lys563Ile) n.479-22011T>A n.563+22309T>A c.1706A>T (p.Lys569Ile) | |
4 | g.47937013T>C | CA356825621 | CNGA1,NIPAL1 | c.1469A>G (p.Lys490Arg) c.1481A>G (p.Lys494Arg) c.1688A>G (p.Lys563Arg) n.479-22011T>C n.563+22309T>C c.1706A>G (p.Lys569Arg) | |
4 | g.47937013T>G | CA356825622 | CNGA1,NIPAL1 | c.1469A>C (p.Lys490Thr) c.1481A>C (p.Lys494Thr) c.1688A>C (p.Lys563Thr) n.479-22011T>G n.563+22309T>G c.1706A>C (p.Lys569Thr) | |
4 | g.47937014T>A | CA356825627 | CNGA1,NIPAL1 | c.1468A>T (p.Lys490Ter) c.1480A>T (p.Lys494Ter) c.1687A>T (p.Lys563Ter) n.479-22010T>A n.563+22310T>A c.1705A>T (p.Lys569Ter) | |
4 | g.47937014T>C | CA356825629 | CNGA1,NIPAL1 | c.1468A>G (p.Lys490Glu) c.1480A>G (p.Lys494Glu) c.1687A>G (p.Lys563Glu) n.479-22010T>C n.563+22310T>C c.1705A>G (p.Lys569Glu) | |
4 | g.47937014T>G | CA356825630 | CNGA1,NIPAL1 | c.1468A>C (p.Lys490Gln) c.1480A>C (p.Lys494Gln) c.1687A>C (p.Lys563Gln) n.479-22010T>G n.563+22310T>G c.1705A>C (p.Lys569Gln) | |
4 | g.47937015C>A | CA356825632 | CNGA1,NIPAL1 | c.1467G>T (p.Leu489Phe) c.1479G>T (p.Leu493Phe) c.1686G>T (p.Leu562Phe) n.479-22009C>A n.563+22311C>A c.1704G>T (p.Leu568Phe) | |
4 | g.47937015C>G | CA356825633 | CNGA1,NIPAL1 | c.1467G>C (p.Leu489Phe) c.1479G>C (p.Leu493Phe) c.1686G>C (p.Leu562Phe) n.479-22009C>G n.563+22311C>G c.1704G>C (p.Leu568Phe) | |
4 | g.47937015C>T | CA439403928 | CNGA1,NIPAL1 | c.1467G>A (p.Leu489=) c.1479G>A (p.Leu493=) c.1686G>A (p.Leu562=) n.479-22009C>T n.563+22311C>T c.1704G>A (p.Leu568=) | ClinVar |
4 | g.47937016A>C | CA356825636 | CNGA1,NIPAL1 | c.1466T>G (p.Leu489Trp) c.1478T>G (p.Leu493Trp) c.1685T>G (p.Leu562Trp) n.479-22008A>C n.563+22312A>C c.1703T>G (p.Leu568Trp) | |
4 | g.47937016A>G | CA356825639 | CNGA1,NIPAL1 | c.1466T>C (p.Leu489Ser) c.1478T>C (p.Leu493Ser) c.1685T>C (p.Leu562Ser) n.479-22008A>G n.563+22312A>G c.1703T>C (p.Leu568Ser) | |
4 | g.47937016A>T | CA356825637 | CNGA1,NIPAL1 | c.1466T>A (p.Leu489Ter) c.1478T>A (p.Leu493Ter) c.1685T>A (p.Leu562Ter) n.479-22008A>T n.563+22312A>T c.1703T>A (p.Leu568Ter) | |
4 | g.47937017A= | CA1455551805 | CNGA1,NIPAL1 | c.1465T= (p.Leu489=) c.1477T= (p.Leu493=) c.1684T= (p.Leu562=) n.479-22007A= n.563+22313A= c.1702T= (p.Leu568=) | |
4 | g.47937017A>C | CA356825641 | CNGA1,NIPAL1 | c.1465T>G (p.Leu489Val) c.1477T>G (p.Leu493Val) c.1684T>G (p.Leu562Val) n.479-22007A>C n.563+22313A>C c.1702T>G (p.Leu568Val) | |
4 | g.47937017A>G | CA2911071 | CNGA1,NIPAL1 | c.1465T>C (p.Leu489=) c.1477T>C (p.Leu493=) c.1684T>C (p.Leu562=) n.479-22007A>G n.563+22313A>G c.1702T>C (p.Leu568=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47937017A>T | CA356825644 | CNGA1,NIPAL1 | c.1465T>A (p.Leu489Met) c.1477T>A (p.Leu493Met) c.1684T>A (p.Leu562Met) n.479-22007A>T n.563+22313A>T c.1702T>A (p.Leu568Met) | |
4 | g.47937018G>A | CA439404036 | CNGA1,NIPAL1 | c.1464C>T (p.Val488=) c.1476C>T (p.Val492=) c.1683C>T (p.Val561=) n.479-22006G>A n.563+22314G>A c.1701C>T (p.Val567=) | |
4 | g.47937018G>C | CA439404039 | CNGA1,NIPAL1 | c.1464C>G (p.Val488=) c.1476C>G (p.Val492=) c.1683C>G (p.Val561=) n.479-22006G>C n.563+22314G>C c.1701C>G (p.Val567=) | |
4 | g.47937018G>T | CA439404041 | CNGA1,NIPAL1 | c.1464C>A (p.Val488=) c.1476C>A (p.Val492=) c.1683C>A (p.Val561=) n.479-22006G>T n.563+22314G>T c.1701C>A (p.Val567=) | |
4 | g.47937018_47937021del | CA2761332294 | CNGA1,NIPAL1 | c.1461_1464del (p.Leu487PhefsTer2) c.1473_1476del (p.Leu491PhefsTer2) c.1680_1683del (p.Leu560PhefsTer2) n.479-22006_479-22003del n.563+22314_563+22317del c.1698_1701del (p.Leu566PhefsTer2) | |
4 | g.47937019A= | CA1455551806 | CNGA1,NIPAL1 | c.1463T= (p.Val488=) c.1475T= (p.Val492=) c.1682T= (p.Val561=) n.479-22005A= n.563+22315A= c.1700T= (p.Val567=) | |
4 | g.47937019A>C | CA356825646 | CNGA1,NIPAL1 | c.1463T>G (p.Val488Gly) c.1475T>G (p.Val492Gly) c.1682T>G (p.Val561Gly) n.479-22005A>C n.563+22315A>C c.1700T>G (p.Val567Gly) | |
4 | g.47937019A>G | CA2911072 | CNGA1,NIPAL1 | c.1463T>C (p.Val488Ala) c.1475T>C (p.Val492Ala) c.1682T>C (p.Val561Ala) n.479-22005A>G n.563+22315A>G c.1700T>C (p.Val567Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.47937019A>T | CA356825649 | CNGA1,NIPAL1 | c.1463T>A (p.Val488Asp) c.1475T>A (p.Val492Asp) c.1682T>A (p.Val561Asp) n.479-22005A>T n.563+22315A>T c.1700T>A (p.Val567Asp) | |
4 | g.47937020C>A | CA356825651 | CNGA1,NIPAL1 | c.1462G>T (p.Val488Phe) c.1474G>T (p.Val492Phe) c.1681G>T (p.Val561Phe) n.479-22004C>A n.563+22316C>A c.1699G>T (p.Val567Phe) | gnomAD v4 |
4 | g.47937020C>G | CA356825653 | CNGA1,NIPAL1 | c.1462G>C (p.Val488Leu) c.1474G>C (p.Val492Leu) c.1681G>C (p.Val561Leu) n.479-22004C>G n.563+22316C>G c.1699G>C (p.Val567Leu) | gnomAD v4 |
4 | g.47937020C>T | CA356825654 | CNGA1,NIPAL1 | c.1462G>A (p.Val488Ile) c.1474G>A (p.Val492Ile) c.1681G>A (p.Val561Ile) n.479-22004C>T n.563+22316C>T c.1699G>A (p.Val567Ile) | |
4 | g.47937021C>A | CA356825655 | CNGA1,NIPAL1 | c.1461G>T (p.Leu487Phe) c.1473G>T (p.Leu491Phe) c.1680G>T (p.Leu560Phe) n.479-22003C>A n.563+22317C>A c.1698G>T (p.Leu566Phe) | |
4 | g.47937021C= | CA1455551807 | CNGA1,NIPAL1 | c.1461G= (p.Leu487=) c.1473G= (p.Leu491=) c.1680G= (p.Leu560=) n.479-22003C= n.563+22317C= c.1698G= (p.Leu566=) | |
4 | g.47937021C>G | CA356825657 | CNGA1,NIPAL1 | c.1461G>C (p.Leu487Phe) c.1473G>C (p.Leu491Phe) c.1680G>C (p.Leu560Phe) n.479-22003C>G n.563+22317C>G c.1698G>C (p.Leu566Phe) | |
4 | g.47937021C>T | CA2911073 | CNGA1,NIPAL1 | c.1461G>A (p.Leu487=) c.1473G>A (p.Leu491=) c.1680G>A (p.Leu560=) n.479-22003C>T n.563+22317C>T c.1698G>A (p.Leu566=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.47937022A>C | CA356825664 | CNGA1,NIPAL1 | c.1460T>G (p.Leu487Trp) c.1472T>G (p.Leu491Trp) c.1679T>G (p.Leu560Trp) n.479-22002A>C n.563+22318A>C c.1697T>G (p.Leu566Trp) | |
4 | g.47937022A>G | CA356825662 | CNGA1,NIPAL1 | c.1460T>C (p.Leu487Ser) c.1472T>C (p.Leu491Ser) c.1679T>C (p.Leu560Ser) n.479-22002A>G n.563+22318A>G c.1697T>C (p.Leu566Ser) | gnomAD v4 |
4 | g.47937022A>T | CA356825660 | CNGA1,NIPAL1 | c.1460T>A (p.Leu487Ter) c.1472T>A (p.Leu491Ter) c.1679T>A (p.Leu560Ter) n.479-22002A>T n.563+22318A>T c.1697T>A (p.Leu566Ter) | |
4 | g.47937023A= | CA1455551808 | CNGA1,NIPAL1 | c.1459T= (p.Leu487=) c.1471T= (p.Leu491=) c.1678T= (p.Leu560=) n.479-22001A= n.563+22319A= c.1696T= (p.Leu566=) | |
4 | g.47937023A>C | CA356825668 | CNGA1,NIPAL1 | c.1459T>G (p.Leu487Val) c.1471T>G (p.Leu491Val) c.1678T>G (p.Leu560Val) n.479-22001A>C n.563+22319A>C c.1696T>G (p.Leu566Val) | |
4 | g.47937023A>G | CA96688586 | CNGA1,NIPAL1 | c.1459T>C (p.Leu487=) c.1471T>C (p.Leu491=) c.1678T>C (p.Leu560=) n.479-22001A>G n.563+22319A>G c.1696T>C (p.Leu566=) | ClinVar dbSNP gnomAD v4 |
4 | g.47937023A>T | CA356825666 | CNGA1,NIPAL1 | c.1459T>A (p.Leu487Met) c.1471T>A (p.Leu491Met) c.1678T>A (p.Leu560Met) n.479-22001A>T n.563+22319A>T c.1696T>A (p.Leu566Met) | |
4 | g.47937024C>A | CA356825670 | CNGA1,NIPAL1 | c.1458G>T (p.Glu486Asp) c.1470G>T (p.Glu490Asp) c.1677G>T (p.Glu559Asp) n.479-22000C>A n.563+22320C>A c.1695G>T (p.Glu565Asp) | |
4 | g.47937024C>G | CA356825672 | CNGA1,NIPAL1 | c.1458G>C (p.Glu486Asp) c.1470G>C (p.Glu490Asp) c.1677G>C (p.Glu559Asp) n.479-22000C>G n.563+22320C>G c.1695G>C (p.Glu565Asp) | |
4 | g.47937024C>T | CA439404050 | CNGA1,NIPAL1 | c.1458G>A (p.Glu486=) c.1470G>A (p.Glu490=) c.1677G>A (p.Glu559=) n.479-22000C>T n.563+22320C>T c.1695G>A (p.Glu565=) | gnomAD v4 |
4 | g.47937024_47937025insAAGT | CA2761332295 | CNGA1,NIPAL1 | c.1457_1458insACTT (p.Leu489GlyfsTer?) c.1469_1470insACTT (p.Leu493GlyfsTer?) c.1676_1677insACTT (p.Leu562GlyfsTer?) n.479-22000_479-21999insAAGT n.563+22320_563+22321insAAGT c.1694_1695insACTT (p.Leu568GlyfsTer?) | |
4 | g.47937025T>A | CA356825675 | CNGA1,NIPAL1 | c.1457A>T (p.Glu486Val) c.1469A>T (p.Glu490Val) c.1676A>T (p.Glu559Val) n.479-21999T>A n.563+22321T>A c.1694A>T (p.Glu565Val) | |
4 | g.47937025T>C | CA356825677 | CNGA1,NIPAL1 | c.1457A>G (p.Glu486Gly) c.1469A>G (p.Glu490Gly) c.1676A>G (p.Glu559Gly) n.479-21999T>C n.563+22321T>C c.1694A>G (p.Glu565Gly) | |
4 | g.47937025T>G | CA356825679 | CNGA1,NIPAL1 | c.1457A>C (p.Glu486Ala) c.1469A>C (p.Glu490Ala) c.1676A>C (p.Glu559Ala) n.479-21999T>G n.563+22321T>G c.1694A>C (p.Glu565Ala) | |
4 | g.47937025_47937028delinsTCCA | CA1455551809 | CNGA1,NIPAL1 | c.1454_1457delinsTGGA (p.Val485=) c.1466_1469delinsTGGA (p.Val489=) c.1673_1676delinsTGGA (p.Val558=) n.479-21999_479-21996delinsTCCA n.563+22321_563+22324delinsTCCA c.1691_1694delinsTGGA (p.Val564=) | |
4 | g.47937026C>A | CA356825682 | CNGA1,NIPAL1 | c.1456G>T (p.Glu486Ter) c.1468G>T (p.Glu490Ter) c.1675G>T (p.Glu559Ter) n.479-21998C>A n.563+22322C>A c.1693G>T (p.Glu565Ter) | |
4 | g.47937026C= | CA1455551810 | CNGA1,NIPAL1 | c.1456G= (p.Glu486=) c.1468G= (p.Glu490=) c.1675G= (p.Glu559=) n.479-21998C= n.563+22322C= c.1693G= (p.Glu565=) | |
4 | g.47937026C>G | CA356825684 | CNGA1,NIPAL1 | c.1456G>C (p.Glu486Gln) c.1468G>C (p.Glu490Gln) c.1675G>C (p.Glu559Gln) n.479-21998C>G n.563+22322C>G c.1693G>C (p.Glu565Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.47937026C>T | CA356825685 | CNGA1,NIPAL1 | c.1456G>A (p.Glu486Lys) c.1468G>A (p.Glu490Lys) c.1675G>A (p.Glu559Lys) n.479-21998C>T n.563+22322C>T c.1693G>A (p.Glu565Lys) | |
4 | g.47937029_47937031del | CA2911074 | CNGA1,NIPAL1 | c.1454_1456del (p.Val485del) c.1466_1468del (p.Val489del) c.1673_1675del (p.Val558del) n.479-21995_479-21993del n.563+22325_563+22327del c.1691_1693del (p.Val564del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.47937027C>A | CA439404057 | CNGA1,NIPAL1 | c.1455G>T (p.Val485=) c.1467G>T (p.Val489=) c.1674G>T (p.Val558=) n.479-21997C>A n.563+22323C>A c.1692G>T (p.Val564=) | |
4 | g.47937027C>G | CA439404055 | CNGA1,NIPAL1 | c.1455G>C (p.Val485=) c.1467G>C (p.Val489=) c.1674G>C (p.Val558=) n.479-21997C>G n.563+22323C>G c.1692G>C (p.Val564=) | |
4 | g.47937027C>T | CA439404056 | CNGA1,NIPAL1 | c.1455G>A (p.Val485=) c.1467G>A (p.Val489=) c.1674G>A (p.Val558=) n.479-21997C>T n.563+22323C>T c.1692G>A (p.Val564=) | dbSNP |
4 | g.47937028A>C | CA356825688 | CNGA1,NIPAL1 | c.1454T>G (p.Val485Gly) c.1466T>G (p.Val489Gly) c.1673T>G (p.Val558Gly) n.479-21996A>C n.563+22324A>C c.1691T>G (p.Val564Gly) | |
4 | g.47937028A>G | CA356825689 | CNGA1,NIPAL1 | c.1454T>C (p.Val485Ala) c.1466T>C (p.Val489Ala) c.1673T>C (p.Val558Ala) n.479-21996A>G n.563+22324A>G c.1691T>C (p.Val564Ala) | |
4 | g.47937028A>T | CA356825691 | CNGA1,NIPAL1 | c.1454T>A (p.Val485Glu) c.1466T>A (p.Val489Glu) c.1673T>A (p.Val558Glu) n.479-21996A>T n.563+22324A>T c.1691T>A (p.Val564Glu) | |
4 | g.47937029C>A | CA356825695 | CNGA1,NIPAL1 | c.1453G>T (p.Val485Leu) c.1465G>T (p.Val489Leu) c.1672G>T (p.Val558Leu) n.479-21995C>A n.563+22325C>A c.1690G>T (p.Val564Leu) | |
4 | g.47937029C= | CA1455551811 | CNGA1,NIPAL1 | c.1453G= (p.Val485=) c.1465G= (p.Val489=) c.1672G= (p.Val558=) n.479-21995C= n.563+22325C= c.1690G= (p.Val564=) | |
4 | g.47937029C>G | CA356825693 | CNGA1,NIPAL1 | c.1453G>C (p.Val485Leu) c.1465G>C (p.Val489Leu) c.1672G>C (p.Val558Leu) n.479-21995C>G n.563+22325C>G c.1690G>C (p.Val564Leu) | |
4 | g.47937029C>T | CA2911075 | CNGA1,NIPAL1 | c.1453G>A (p.Val485Met) c.1465G>A (p.Val489Met) c.1672G>A (p.Val558Met) n.479-21995C>T n.563+22325C>T c.1690G>A (p.Val564Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.47937030C>A | CA356825698 | CNGA1,NIPAL1 | c.1452G>T (p.Leu484Phe) c.1464G>T (p.Leu488Phe) c.1671G>T (p.Leu557Phe) n.479-21994C>A n.563+22326C>A c.1689G>T (p.Leu563Phe) | gnomAD v4 |
4 | g.47937030C>G | CA356825699 | CNGA1,NIPAL1 | c.1452G>C (p.Leu484Phe) c.1464G>C (p.Leu488Phe) c.1671G>C (p.Leu557Phe) n.479-21994C>G n.563+22326C>G c.1689G>C (p.Leu563Phe) | |
4 | g.47937030C>T | CA439404059 | CNGA1,NIPAL1 | c.1452G>A (p.Leu484=) c.1464G>A (p.Leu488=) c.1671G>A (p.Leu557=) n.479-21994C>T n.563+22326C>T c.1689G>A (p.Leu563=) | |
4 | g.47937031A>C | CA356825702 | CNGA1,NIPAL1 | c.1451T>G (p.Leu484Trp) c.1463T>G (p.Leu488Trp) c.1670T>G (p.Leu557Trp) n.479-21993A>C n.563+22327A>C c.1688T>G (p.Leu563Trp) | |
4 | g.47937031A>G | CA356825704 | CNGA1,NIPAL1 | c.1451T>C (p.Leu484Ser) c.1463T>C (p.Leu488Ser) c.1670T>C (p.Leu557Ser) n.479-21993A>G n.563+22327A>G c.1688T>C (p.Leu563Ser) | |
4 | g.47937031A>T | CA356825705 | CNGA1,NIPAL1 | c.1451T>A (p.Leu484Ter) c.1463T>A (p.Leu488Ter) c.1670T>A (p.Leu557Ter) n.479-21993A>T n.563+22327A>T c.1688T>A (p.Leu563Ter) | |
4 | g.47937032A>C | CA356825708 | CNGA1,NIPAL1 | c.1450T>G (p.Leu484Val) c.1462T>G (p.Leu488Val) c.1669T>G (p.Leu557Val) n.479-21992A>C n.563+22328A>C c.1687T>G (p.Leu563Val) | |
4 | g.47937032A>G | CA439404063 | CNGA1,NIPAL1 | c.1450T>C (p.Leu484=) c.1462T>C (p.Leu488=) c.1669T>C (p.Leu557=) n.479-21992A>G n.563+22328A>G c.1687T>C (p.Leu563=) | |
4 | g.47937032A>T | CA356825709 | CNGA1,NIPAL1 | c.1450T>A (p.Leu484Met) c.1462T>A (p.Leu488Met) c.1669T>A (p.Leu557Met) n.479-21992A>T n.563+22328A>T c.1687T>A (p.Leu563Met) | |
4 | g.47937033C>A | CA439404065 | CNGA1,NIPAL1 | c.1449G>T (p.Leu483=) c.1461G>T (p.Leu487=) c.1668G>T (p.Leu556=) n.479-21991C>A n.563+22329C>A c.1686G>T (p.Leu562=) | gnomAD v4 |
4 | g.47937033C= | CA1455551812 | CNGA1,NIPAL1 | c.1449G= (p.Leu483=) c.1461G= (p.Leu487=) c.1668G= (p.Leu556=) n.479-21991C= n.563+22329C= c.1686G= (p.Leu562=) | |
4 | g.47937033C>G | CA439404067 | CNGA1,NIPAL1 | c.1449G>C (p.Leu483=) c.1461G>C (p.Leu487=) c.1668G>C (p.Leu556=) n.479-21991C>G n.563+22329C>G c.1686G>C (p.Leu562=) | |
4 | g.47937033C>T | CA439404069 | CNGA1,NIPAL1 | c.1449G>A (p.Leu483=) c.1461G>A (p.Leu487=) c.1668G>A (p.Leu556=) n.479-21991C>T n.563+22329C>T c.1686G>A (p.Leu562=) | dbSNP gnomAD v2 gnomAD v4 |