Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.99583415A>C | CA440328601 | MTTP | c.291A>C (p.Gly97=) c.42A>C (p.Gly14=) c.*381A>C (n.*381A>C) c.321A>C (p.Gly107=) c.372A>C (p.Gly124=) c.*354A>C (n.*354A>C) | ClinVar dbSNP gnomAD v4 |
4 | g.99583415A>G | CA440328602 | MTTP | c.291A>G (p.Gly97=) c.42A>G (p.Gly14=) c.*381A>G (n.*381A>G) c.321A>G (p.Gly107=) c.372A>G (p.Gly124=) c.*354A>G (n.*354A>G) | |
4 | g.99583415A>T | CA440328603 | MTTP | c.291A>T (p.Gly97=) c.42A>T (p.Gly14=) c.*381A>T (n.*381A>T) c.321A>T (p.Gly107=) c.372A>T (p.Gly124=) c.*354A>T (n.*354A>T) | |
4 | g.99583416G>A | CA357502104 | MTTP | c.292G>A (p.Glu98Lys) c.43G>A (p.Glu15Lys) c.*382G>A (n.*382G>A) c.322G>A (p.Glu108Lys) c.373G>A (p.Glu125Lys) c.*355G>A (n.*355G>A) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.99583416G>C | CA3021798 | MTTP | c.292G>C (p.Glu98Gln) c.43G>C (p.Glu15Gln) c.*382G>C (n.*382G>C) c.322G>C (p.Glu108Gln) c.373G>C (p.Glu125Gln) c.*355G>C (n.*355G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.99583416G= | CA1480066693 | MTTP | c.292G= (p.Glu98=) c.43G= (p.Glu15=) c.*382G= (n.*382G=) c.322G= (p.Glu108=) c.373G= (p.Glu125=) c.*355G= (n.*355G=) | |
4 | g.99583416G>T | CA357502107 | MTTP | c.292G>T (p.Glu98Ter) c.43G>T (p.Glu15Ter) c.*382G>T (n.*382G>T) c.322G>T (p.Glu108Ter) c.373G>T (p.Glu125Ter) c.*355G>T (n.*355G>T) | |
4 | g.99583417A= | CA1480066696 | MTTP | c.293A= (p.Glu98=) c.44A= (p.Glu15=) c.*383A= (n.*383A=) c.323A= (p.Glu108=) c.374A= (p.Glu125=) c.*356A= (n.*356A=) | |
4 | g.99583417A>C | CA357502110 | MTTP | c.293A>C (p.Glu98Ala) c.44A>C (p.Glu15Ala) c.*383A>C (n.*383A>C) c.323A>C (p.Glu108Ala) c.374A>C (p.Glu125Ala) c.*356A>C (n.*356A>C) | dbSNP |
4 | g.99583417A>G | CA357502112 | MTTP | c.293A>G (p.Glu98Gly) c.44A>G (p.Glu15Gly) c.*383A>G (n.*383A>G) c.323A>G (p.Glu108Gly) c.374A>G (p.Glu125Gly) c.*356A>G (n.*356A>G) | dbSNP gnomAD v4 |
4 | g.99583417A>T | CA357502114 | MTTP | c.293A>T (p.Glu98Val) c.44A>T (p.Glu15Val) c.*383A>T (n.*383A>T) c.323A>T (p.Glu108Val) c.374A>T (p.Glu125Val) c.*356A>T (n.*356A>T) | |
4 | g.99583418G>A | CA440328604 | MTTP | c.294G>A (p.Glu98=) c.45G>A (p.Glu15=) c.*384G>A (n.*384G>A) c.324G>A (p.Glu108=) c.375G>A (p.Glu125=) c.*357G>A (n.*357G>A) | dbSNP |
4 | g.99583418G>C | CA3021799 | MTTP | c.294G>C (p.Glu98Asp) c.45G>C (p.Glu15Asp) c.*384G>C (n.*384G>C) c.324G>C (p.Glu108Asp) c.375G>C (p.Glu125Asp) c.*357G>C (n.*357G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.99583418G= | CA1480066702 | MTTP | c.294G= (p.Glu98=) c.45G= (p.Glu15=) c.*384G= (n.*384G=) c.324G= (p.Glu108=) c.375G= (p.Glu125=) c.*357G= (n.*357G=) | |
4 | g.99583418G>T | CA102617498 | MTTP | c.294G>T (p.Glu98Asp) c.45G>T (p.Glu15Asp) c.*384G>T (n.*384G>T) c.324G>T (p.Glu108Asp) c.375G>T (p.Glu125Asp) c.*357G>T (n.*357G>T) | dbSNP |
4 | g.99583419A>C | CA357502116 | MTTP | c.295A>C (p.Lys99Gln) c.46A>C (p.Lys16Gln) c.*385A>C (n.*385A>C) c.325A>C (p.Lys109Gln) c.376A>C (p.Lys126Gln) c.*358A>C (n.*358A>C) | |
4 | g.99583419A>G | CA357502118 | MTTP | c.295A>G (p.Lys99Glu) c.46A>G (p.Lys16Glu) c.*385A>G (n.*385A>G) c.325A>G (p.Lys109Glu) c.376A>G (p.Lys126Glu) c.*358A>G (n.*358A>G) | |
4 | g.99583419A>T | CA357502126 | MTTP | c.295A>T (p.Lys99Ter) c.46A>T (p.Lys16Ter) c.*385A>T (n.*385A>T) c.325A>T (p.Lys109Ter) c.376A>T (p.Lys126Ter) c.*358A>T (n.*358A>T) | |
4 | g.99583420A= | CA1480066703 | MTTP | c.296A= (p.Lys99=) c.47A= (p.Lys16=) c.*386A= (n.*386A=) c.326A= (p.Lys109=) c.377A= (p.Lys126=) c.*359A= (n.*359A=) | |
4 | g.99583420A>C | CA357502131 | MTTP | c.296A>C (p.Lys99Thr) c.47A>C (p.Lys16Thr) c.*386A>C (n.*386A>C) c.326A>C (p.Lys109Thr) c.377A>C (p.Lys126Thr) c.*359A>C (n.*359A>C) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.99583420A>G | CA357502129 | MTTP | c.296A>G (p.Lys99Arg) c.47A>G (p.Lys16Arg) c.*386A>G (n.*386A>G) c.326A>G (p.Lys109Arg) c.377A>G (p.Lys126Arg) c.*359A>G (n.*359A>G) | |
4 | g.99583420A>T | CA357502128 | MTTP | c.296A>T (p.Lys99Met) c.47A>T (p.Lys16Met) c.*386A>T (n.*386A>T) c.326A>T (p.Lys109Met) c.377A>T (p.Lys126Met) c.*359A>T (n.*359A>T) | |
4 | g.99583421G>A | CA440328605 | MTTP | c.297G>A (p.Lys99=) c.48G>A (p.Lys16=) c.*387G>A (n.*387G>A) c.327G>A (p.Lys109=) c.378G>A (p.Lys126=) c.*360G>A (n.*360G>A) | ClinVar dbSNP |
4 | g.99583421G>C | CA357502132 | MTTP | c.297G>C (p.Lys99Asn) c.48G>C (p.Lys16Asn) c.*387G>C (n.*387G>C) c.327G>C (p.Lys109Asn) c.378G>C (p.Lys126Asn) c.*360G>C (n.*360G>C) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.99583421G= | CA1480066708 | MTTP | c.297G= (p.Lys99=) c.48G= (p.Lys16=) c.*387G= (n.*387G=) c.327G= (p.Lys109=) c.378G= (p.Lys126=) c.*360G= (n.*360G=) | |
4 | g.99583421G>T | CA357502136 | MTTP | c.297G>T (p.Lys99Asn) c.48G>T (p.Lys16Asn) c.*387G>T (n.*387G>T) c.327G>T (p.Lys109Asn) c.378G>T (p.Lys126Asn) c.*360G>T (n.*360G>T) | COSMIC |
4 | g.99583422A>C | CA357502137 | MTTP | c.298A>C (p.Ser100Arg) c.49A>C c.49A>C (p.Ser17Arg) c.*388A>C (n.*388A>C) c.328A>C (p.Ser110Arg) c.379A>C (p.Ser127Arg) c.*361A>C (n.*361A>C) | |
4 | g.99583422A>G | CA357502138 | MTTP | c.298A>G (p.Ser100Gly) c.49A>G c.49A>G (p.Ser17Gly) c.*388A>G (n.*388A>G) c.328A>G (p.Ser110Gly) c.379A>G (p.Ser127Gly) c.*361A>G (n.*361A>G) | gnomAD v4 |
4 | g.99583422A>T | CA357502140 | MTTP | c.298A>T (p.Ser100Cys) c.49A>T c.49A>T (p.Ser17Cys) c.*388A>T (n.*388A>T) c.328A>T (p.Ser110Cys) c.379A>T (p.Ser127Cys) c.*361A>T (n.*361A>T) | |
4 | g.99583423G>A | CA357502142 | MTTP | c.299G>A (p.Ser100Asn) c.50G>A (p.Ser17Asn) c.329G>A (p.Ser110Asn) c.380G>A (p.Ser127Asn) c.*362G>A (n.*362G>A) | |
4 | g.99583423G>C | CA357502144 | MTTP | c.299G>C (p.Ser100Thr) c.50G>C (p.Ser17Thr) c.329G>C (p.Ser110Thr) c.380G>C (p.Ser127Thr) c.*362G>C (n.*362G>C) | |
4 | g.99583423G>T | CA357502146 | MTTP | c.299G>T (p.Ser100Ile) c.50G>T (p.Ser17Ile) c.329G>T (p.Ser110Ile) c.380G>T (p.Ser127Ile) c.*362G>T (n.*362G>T) | |
4 | g.99583424C>A | CA357502148 | MTTP | c.300C>A (p.Ser100Arg) c.51C>A (p.Ser17Arg) c.330C>A (p.Ser110Arg) c.381C>A (p.Ser127Arg) c.*363C>A (n.*363C>A) | |
4 | g.99583424C>G | CA357502150 | MTTP | c.300C>G (p.Ser100Arg) c.51C>G (p.Ser17Arg) c.330C>G (p.Ser110Arg) c.381C>G (p.Ser127Arg) c.*363C>G (n.*363C>G) | |
4 | g.99583424C>T | CA440328606 | MTTP | c.300C>T (p.Ser100=) c.51C>T (p.Ser17=) c.330C>T (p.Ser110=) c.381C>T (p.Ser127=) c.*363C>T (n.*363C>T) | |
4 | g.99583425A>C | CA357502151 | MTTP | c.301A>C (p.Ile101Leu) c.52A>C (p.Ile18Leu) c.331A>C (p.Ile111Leu) c.382A>C (p.Ile128Leu) c.*364A>C (n.*364A>C) | |
4 | g.99583425A>G | CA357502153 | MTTP | c.301A>G (p.Ile101Val) c.52A>G (p.Ile18Val) c.331A>G (p.Ile111Val) c.382A>G (p.Ile128Val) c.*364A>G (n.*364A>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.99583425A>T | CA357502154 | MTTP | c.301A>T (p.Ile101Phe) c.52A>T (p.Ile18Phe) c.331A>T (p.Ile111Phe) c.382A>T (p.Ile128Phe) c.*364A>T (n.*364A>T) | |
4 | g.99583426T>A | CA357502161 | MTTP | c.302T>A (p.Ile101Asn) c.53T>A (p.Ile18Asn) c.332T>A (p.Ile111Asn) c.383T>A (p.Ile128Asn) c.*365T>A (n.*365T>A) | |
4 | g.99583426T>C | CA357502157 | MTTP | c.302T>C (p.Ile101Thr) c.53T>C (p.Ile18Thr) c.332T>C (p.Ile111Thr) c.383T>C (p.Ile128Thr) c.*365T>C (n.*365T>C) | |
4 | g.99583426T>G | CA357502159 | MTTP | c.302T>G (p.Ile101Ser) c.53T>G (p.Ile18Ser) c.332T>G (p.Ile111Ser) c.383T>G (p.Ile128Ser) c.*365T>G (n.*365T>G) | |
4 | g.99583427C>A | CA440328607 | MTTP | c.303C>A (p.Ile101=) c.54C>A (p.Ile18=) c.333C>A (p.Ile111=) c.384C>A (p.Ile128=) c.*366C>A (n.*366C>A) | COSMIC |
4 | g.99583427C= | CA1480066711 | MTTP | c.303C= (p.Ile101=) c.54C= (p.Ile18=) c.333C= (p.Ile111=) c.384C= (p.Ile128=) c.*366C= (n.*366C=) | |
4 | g.99583427C>G | CA357502163 | MTTP | c.303C>G (p.Ile101Met) c.54C>G (p.Ile18Met) c.333C>G (p.Ile111Met) c.384C>G (p.Ile128Met) c.*366C>G (n.*366C>G) | |
4 | g.99583427C>T | CA3021800 | MTTP | c.303C>T (p.Ile101=) c.54C>T (p.Ile18=) c.333C>T (p.Ile111=) c.384C>T (p.Ile128=) c.*366C>T (n.*366C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.99583428T>A | CA357502165 | MTTP | c.304T>A (p.Phe102Ile) c.55T>A (p.Phe19Ile) c.334T>A (p.Phe112Ile) c.385T>A (p.Phe129Ile) c.*367T>A (n.*367T>A) | |
4 | g.99583428T>C | CA357502167 | MTTP | c.304T>C (p.Phe102Leu) c.55T>C (p.Phe19Leu) c.334T>C (p.Phe112Leu) c.385T>C (p.Phe129Leu) c.*367T>C (n.*367T>C) | |
4 | g.99583428T>G | CA357502169 | MTTP | c.304T>G (p.Phe102Val) c.55T>G (p.Phe19Val) c.334T>G (p.Phe112Val) c.385T>G (p.Phe129Val) c.*367T>G (n.*367T>G) | COSMIC |
4 | g.99583429T>A | CA357502171 | MTTP | c.305T>A (p.Phe102Tyr) c.56T>A (p.Phe19Tyr) c.335T>A (p.Phe112Tyr) c.386T>A (p.Phe129Tyr) c.*368T>A (n.*368T>A) | |
4 | g.99583429T>C | CA357502173 | MTTP | c.305T>C (p.Phe102Ser) c.56T>C (p.Phe19Ser) c.335T>C (p.Phe112Ser) c.386T>C (p.Phe129Ser) c.*368T>C (n.*368T>C) |