Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.11880974C= | CA2284983244 | GNAL | c.1231-15C= (n.1231-15C=) c.1000-15C= (n.1000-15C=) c.379-15C= (n.379-15C=) | |
18 | g.11880974C>T | CA8894251 | GNAL | c.1231-15C>T (n.1231-15C>T) c.1000-15C>T (n.1000-15C>T) c.379-15C>T (n.379-15C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11880975_11880976del | CA2576457632 | GNAL | c.1231-14_1231-13del (n.1231-14_1231-13del) c.1000-14_1000-13del (n.1000-14_1000-13del) c.379-14_379-13del (n.379-14_379-13del) | gnomAD v4 |
18 | g.11880975G>A | CA8894252 | GNAL | c.1231-14G>A (n.1231-14G>A) c.1000-14G>A (n.1000-14G>A) c.379-14G>A (n.379-14G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11880975G= | CA2284983245 | GNAL | c.1231-14G= (n.1231-14G=) c.1000-14G= (n.1000-14G=) c.379-14G= (n.379-14G=) | |
18 | g.11880975G>T | CA296058586 | GNAL | c.1231-14G>T (n.1231-14G>T) c.1000-14G>T (n.1000-14G>T) c.379-14G>T (n.379-14G>T) | dbSNP gnomAD v2 gnomAD v4 |
18 | g.11880975_11880977delinsGCT | CA2284983246 | GNAL | c.1231-14_1231-12delinsGCT (n.1231-14_1231-12delinsGCT) c.1000-14_1000-12delinsGCT (n.1000-14_1000-12delinsGCT) c.379-14_379-12delinsGCT (n.379-14_379-12delinsGCT) | |
18 | g.11880976C= | CA2284983247 | GNAL | c.1231-13C= (n.1231-13C=) c.1000-13C= (n.1000-13C=) c.379-13C= (n.379-13C=) | |
18 | g.11880976C>G | CA8894254 | GNAL | c.1231-13C>G (n.1231-13C>G) c.1000-13C>G (n.1000-13C>G) c.379-13C>G (n.379-13C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11880982_11880983del | CA8894253 | GNAL | c.1231-7_1231-6del (n.1231-7_1231-6del) c.1000-7_1000-6del (n.1000-7_1000-6del) c.379-7_379-6del (n.379-7_379-6del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11880977T>A | CA2576457633 | GNAL | c.1231-12T>A (n.1231-12T>A) c.1000-12T>A (n.1000-12T>A) c.379-12T>A (n.379-12T>A) | |
18 | g.11880977T>C | CA8894255 | GNAL | c.1231-12T>C (n.1231-12T>C) c.1000-12T>C (n.1000-12T>C) c.379-12T>C (n.379-12T>C) | dbSNP ExAC gnomAD v4 |
18 | g.11880977T= | CA2284983248 | GNAL | c.1231-12T= (n.1231-12T=) c.1000-12T= (n.1000-12T=) c.379-12T= (n.379-12T=) | |
18 | g.11880978C= | CA2284983249 | GNAL | c.1231-11C= (n.1231-11C=) c.1000-11C= (n.1000-11C=) c.379-11C= (n.379-11C=) | |
18 | g.11880978C>G | CA8894256 | GNAL | c.1231-11C>G (n.1231-11C>G) c.1000-11C>G (n.1000-11C>G) c.379-11C>G (n.379-11C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11880978C>T | CA776156668 | GNAL | c.1231-11C>T (n.1231-11C>T) c.1000-11C>T (n.1000-11C>T) c.379-11C>T (n.379-11C>T) | dbSNP gnomAD v4 |
18 | g.11880980C>G | CA2641033639 | GNAL | c.1231-9C>G (n.1231-9C>G) c.1000-9C>G (n.1000-9C>G) c.379-9C>G (n.379-9C>G) | gnomAD v4 |
18 | g.11880980C>T | CA2641033640 | GNAL | c.1231-9C>T (n.1231-9C>T) c.1000-9C>T (n.1000-9C>T) c.379-9C>T (n.379-9C>T) | gnomAD v4 |
18 | g.11880982C= | CA2284983250 | GNAL | c.1231-7C= (n.1231-7C=) c.1000-7C= (n.1000-7C=) c.379-7C= (n.379-7C=) | |
18 | g.11880982C>T | CA8894257 | GNAL | c.1231-7C>T (n.1231-7C>T) c.1000-7C>T (n.1000-7C>T) c.379-7C>T (n.379-7C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11880983T>C | CA2641033641 | GNAL | c.1231-6T>C (n.1231-6T>C) c.1000-6T>C (n.1000-6T>C) c.379-6T>C (n.379-6T>C) | gnomAD v4 |
18 | g.11880985G>C | CA2641033642 | GNAL | c.1231-4G>C (n.1231-4G>C) c.1000-4G>C (n.1000-4G>C) c.379-4G>C (n.379-4G>C) | gnomAD v4 |
18 | g.11880987A>C | CA401928129 | GNAL | c.1231-2A>C (n.1231-2A>C) c.1000-2A>C (n.1000-2A>C) c.379-2A>C (n.379-2A>C) | |
18 | g.11880987A>G | CA401928127 | GNAL | c.1231-2A>G (n.1231-2A>G) c.1000-2A>G (n.1000-2A>G) c.379-2A>G (n.379-2A>G) | |
18 | g.11880987A>T | CA401928128 | GNAL | c.1231-2A>T (n.1231-2A>T) c.1000-2A>T (n.1000-2A>T) c.379-2A>T (n.379-2A>T) | |
18 | g.11880988G>A | CA401928130 | GNAL | c.1231-1G>A (n.1231-1G>A) c.1000-1G>A (n.1000-1G>A) c.379-1G>A (n.379-1G>A) | |
18 | g.11880988G>C | CA401928131 | GNAL | c.1231-1G>C (n.1231-1G>C) c.1000-1G>C (n.1000-1G>C) c.379-1G>C (n.379-1G>C) | |
18 | g.11880988G>T | CA401928132 | GNAL | c.1231-1G>T (n.1231-1G>T) c.1000-1G>T (n.1000-1G>T) c.379-1G>T (n.379-1G>T) | |
18 | g.11880989A>C | CA502927768 | GNAL | c.1231A>C (p.Arg411=) c.1000A>C (p.Arg334=) c.379A>C (p.Arg127=) | |
18 | g.11880989A>G | CA401928133 | GNAL | c.1231A>G (p.Arg411Gly) c.1000A>G (p.Arg334Gly) c.379A>G (p.Arg127Gly) | |
18 | g.11880989A>T | CA401928134 | GNAL | c.1231A>T (p.Arg411Trp) c.1000A>T (p.Arg334Trp) c.379A>T (p.Arg127Trp) | |
18 | g.11880990G>A | CA401928136 | GNAL | c.1232G>A (p.Arg411Lys) c.1001G>A (p.Arg334Lys) c.380G>A (p.Arg127Lys) | |
18 | g.11880990G>C | CA8894258 | GNAL | c.1232G>C (p.Arg411Thr) c.1001G>C (p.Arg334Thr) c.380G>C (p.Arg127Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11880990G= | CA2284983251 | GNAL | c.1232G= (p.Arg411=) c.1001G= (p.Arg334=) c.380G= (p.Arg127=) | |
18 | g.11880990G>T | CA401928135 | GNAL | c.1232G>T (p.Arg411Met) c.1001G>T (p.Arg334Met) c.380G>T (p.Arg127Met) | |
18 | g.11880991G>A | CA502927769 | GNAL | c.1233G>A (p.Arg411=) c.1002G>A (p.Arg334=) c.381G>A (p.Arg127=) | |
18 | g.11880991G>C | CA401928137 | GNAL | c.1233G>C (p.Arg411Ser) c.1002G>C (p.Arg334Ser) c.381G>C (p.Arg127Ser) | gnomAD v4 |
18 | g.11880991G>T | CA401928138 | GNAL | c.1233G>T (p.Arg411Ser) c.1002G>T (p.Arg334Ser) c.381G>T (p.Arg127Ser) | |
18 | g.11880992A>C | CA401928139 | GNAL | c.1234A>C (p.Ile412Leu) c.1003A>C (p.Ile335Leu) c.382A>C (p.Ile128Leu) | |
18 | g.11880992A>G | CA401928140 | GNAL | c.1234A>G (p.Ile412Val) c.1003A>G (p.Ile335Val) c.382A>G (p.Ile128Val) | |
18 | g.11880992A>T | CA401928141 | GNAL | c.1234A>T (p.Ile412Phe) c.1003A>T (p.Ile335Phe) c.382A>T (p.Ile128Phe) | |
18 | g.11880993T>A | CA401928142 | GNAL | c.1235T>A (p.Ile412Asn) c.1004T>A (p.Ile335Asn) c.383T>A (p.Ile128Asn) | |
18 | g.11880993T>C | CA401928143 | GNAL | c.1235T>C (p.Ile412Thr) c.1004T>C (p.Ile335Thr) c.383T>C (p.Ile128Thr) | |
18 | g.11880993T>G | CA401928144 | GNAL | c.1235T>G (p.Ile412Ser) c.1004T>G (p.Ile335Ser) c.383T>G (p.Ile128Ser) | |
18 | g.11880994C>A | CA502927770 | GNAL | c.1236C>A (p.Ile412=) c.1005C>A (p.Ile335=) c.384C>A (p.Ile128=) | |
18 | g.11880994C= | CA2284983252 | GNAL | c.1236C= (p.Ile412=) c.1005C= (p.Ile335=) c.384C= (p.Ile128=) | |
18 | g.11880994C>G | CA401928145 | GNAL | c.1236C>G (p.Ile412Met) c.1005C>G (p.Ile335Met) c.384C>G (p.Ile128Met) | |
18 | g.11880994C>T | CA8894259 | GNAL | c.1236C>T (p.Ile412=) c.1005C>T (p.Ile335=) c.384C>T (p.Ile128=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11880995A>C | CA401928146 | GNAL | c.1237A>C (p.Ser413Arg) c.1006A>C (p.Ser336Arg) c.385A>C (p.Ser129Arg) | |
18 | g.11880995A>G | CA401928147 | GNAL | c.1237A>G (p.Ser413Gly) c.1006A>G (p.Ser336Gly) c.385A>G (p.Ser129Gly) | |
18 | g.11880995A>T | CA401928148 | GNAL | c.1237A>T (p.Ser413Cys) c.1006A>T (p.Ser336Cys) c.385A>T (p.Ser129Cys) | |
18 | g.11880996G>A | CA401928151 | GNAL | c.1238G>A (p.Ser413Asn) c.1007G>A (p.Ser336Asn) c.386G>A (p.Ser129Asn) | |
18 | g.11880996G>C | CA401928149 | GNAL | c.1238G>C (p.Ser413Thr) c.1007G>C (p.Ser336Thr) c.386G>C (p.Ser129Thr) | gnomAD v4 COSMIC |
18 | g.11880996G= | CA2284983253 | GNAL | c.1238G= (p.Ser413=) c.1007G= (p.Ser336=) c.386G= (p.Ser129=) | |
18 | g.11880996G>T | CA401928150 | GNAL | c.1238G>T (p.Ser413Ile) c.1007G>T (p.Ser336Ile) c.386G>T (p.Ser129Ile) | dbSNP |
18 | g.11880997C>A | CA401928152 | GNAL | c.1239C>A (p.Ser413Arg) c.1008C>A (p.Ser336Arg) c.387C>A (p.Ser129Arg) | gnomAD v4 |
18 | g.11880997C>G | CA401928153 | GNAL | c.1239C>G (p.Ser413Arg) c.1008C>G (p.Ser336Arg) c.387C>G (p.Ser129Arg) | |
18 | g.11880997C>T | CA502927771 | GNAL | c.1239C>T (p.Ser413=) c.1008C>T (p.Ser336=) c.387C>T (p.Ser129=) | gnomAD v4 |
18 | g.11880998A>C | CA401928154 | GNAL | c.1240A>C (p.Thr414Pro) c.1009A>C (p.Thr337Pro) c.388A>C (p.Thr130Pro) | |
18 | g.11880998A>G | CA401928155 | GNAL | c.1240A>G (p.Thr414Ala) c.1009A>G (p.Thr337Ala) c.388A>G (p.Thr130Ala) | gnomAD v4 |
18 | g.11880998A>T | CA401928156 | GNAL | c.1240A>T (p.Thr414Ser) c.1009A>T (p.Thr337Ser) c.388A>T (p.Thr130Ser) | |
18 | g.11880999del | CA502927772 | GNAL | c.1241del (p.Thr414ArgfsTer?) c.1010del (p.Thr337ArgfsTer?) c.389del (p.Thr130ArgfsTer?) | COSMIC COSMIC |
18 | g.11880999C>A | CA401928157 | GNAL | c.1241C>A (p.Thr414Lys) c.1010C>A (p.Thr337Lys) c.389C>A (p.Thr130Lys) | |
18 | g.11880999C= | CA2284983254 | GNAL | c.1241C= (p.Thr414=) c.1010C= (p.Thr337=) c.389C= (p.Thr130=) | |
18 | g.11880999C>G | CA401928158 | GNAL | c.1241C>G (p.Thr414Arg) c.1010C>G (p.Thr337Arg) c.389C>G (p.Thr130Arg) | |
18 | g.11880999C>T | CA401928159 | GNAL | c.1241C>T (p.Thr414Met) c.1010C>T (p.Thr337Met) c.389C>T (p.Thr130Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881000G>A | CA8894260 | GNAL | c.1242G>A (p.Thr414=) c.1011G>A (p.Thr337=) c.390G>A (p.Thr130=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
18 | g.11881000G>C | CA502927773 | GNAL | c.1242G>C (p.Thr414=) c.1011G>C (p.Thr337=) c.390G>C (p.Thr130=) | |
18 | g.11881000G= | CA2284983255 | GNAL | c.1242G= (p.Thr414=) c.1011G= (p.Thr337=) c.390G= (p.Thr130=) | |
18 | g.11881000G>T | CA502927774 | GNAL | c.1242G>T (p.Thr414=) c.1011G>T (p.Thr337=) c.390G>T (p.Thr130=) | |
18 | g.11881001G>A | CA401928160 | GNAL | c.1243G>A (p.Ala415Thr) c.1012G>A (p.Ala338Thr) c.391G>A (p.Ala131Thr) | |
18 | g.11881001G>C | CA401928161 | GNAL | c.1243G>C (p.Ala415Pro) c.1012G>C (p.Ala338Pro) c.391G>C (p.Ala131Pro) | |
18 | g.11881001G>T | CA401928162 | GNAL | c.1243G>T (p.Ala415Ser) c.1012G>T (p.Ala338Ser) c.391G>T (p.Ala131Ser) | |
18 | g.11881002C>A | CA401928163 | GNAL | c.1244C>A (p.Ala415Asp) c.1013C>A (p.Ala338Asp) c.392C>A (p.Ala131Asp) | gnomAD v4 |
18 | g.11881002C>G | CA401928164 | GNAL | c.1244C>G (p.Ala415Gly) c.1013C>G (p.Ala338Gly) c.392C>G (p.Ala131Gly) | |
18 | g.11881002C>T | CA401928165 | GNAL | c.1244C>T (p.Ala415Val) c.1013C>T (p.Ala338Val) c.392C>T (p.Ala131Val) | |
18 | g.11881003C>A | CA502927775 | GNAL | c.1245C>A (p.Ala415=) c.1014C>A (p.Ala338=) c.393C>A (p.Ala131=) | |
18 | g.11881003C= | CA2284983256 | GNAL | c.1245C= (p.Ala415=) c.1014C= (p.Ala338=) c.393C= (p.Ala131=) | |
18 | g.11881003C>G | CA502927776 | GNAL | c.1245C>G (p.Ala415=) c.1014C>G (p.Ala338=) c.393C>G (p.Ala131=) | |
18 | g.11881003C>T | CA8894261 | GNAL | c.1245C>T (p.Ala415=) c.1014C>T (p.Ala338=) c.393C>T (p.Ala131=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881004A>C | CA401928166 | GNAL | c.1246A>C (p.Thr416Pro) c.1015A>C (p.Thr339Pro) c.394A>C (p.Thr132Pro) | |
18 | g.11881004A>G | CA401928167 | GNAL | c.1246A>G (p.Thr416Ala) c.1015A>G (p.Thr339Ala) c.394A>G (p.Thr132Ala) | |
18 | g.11881004A>T | CA401928168 | GNAL | c.1246A>T (p.Thr416Ser) c.1015A>T (p.Thr339Ser) c.394A>T (p.Thr132Ser) | |
18 | g.11881005C>A | CA401928169 | GNAL | c.1247C>A (p.Thr416Asn) c.1016C>A (p.Thr339Asn) c.395C>A (p.Thr132Asn) | |
18 | g.11881005C>G | CA401928170 | GNAL | c.1247C>G (p.Thr416Ser) c.1016C>G (p.Thr339Ser) c.395C>G (p.Thr132Ser) | |
18 | g.11881005C>T | CA401928171 | GNAL | c.1247C>T (p.Thr416Ile) c.1016C>T (p.Thr339Ile) c.395C>T (p.Thr132Ile) | |
18 | g.11881006C>A | CA502927777 | GNAL | c.1248C>A (p.Thr416=) c.1017C>A (p.Thr339=) c.396C>A (p.Thr132=) | dbSNP |
18 | g.11881006C= | CA2284983257 | GNAL | c.1248C= (p.Thr416=) c.1017C= (p.Thr339=) c.396C= (p.Thr132=) | |
18 | g.11881006C>G | CA502927778 | GNAL | c.1248C>G (p.Thr416=) c.1017C>G (p.Thr339=) c.396C>G (p.Thr132=) | dbSNP gnomAD v2 gnomAD v4 |
18 | g.11881006C>T | CA8894262 | GNAL | c.1248C>T (p.Thr416=) c.1017C>T (p.Thr339=) c.396C>T (p.Thr132=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881007G>A | CA8894263 | GNAL | c.1249G>A (p.Gly417Ser) c.1018G>A (p.Gly340Ser) c.397G>A (p.Gly133Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881007G>C | CA401928172 | GNAL | c.1249G>C (p.Gly417Arg) c.1018G>C (p.Gly340Arg) c.397G>C (p.Gly133Arg) | |
18 | g.11881007G= | CA2284983258 | GNAL | c.1249G= (p.Gly417=) c.1018G= (p.Gly340=) c.397G= (p.Gly133=) | |
18 | g.11881007G>T | CA401928173 | GNAL | c.1249G>T (p.Gly417Cys) c.1018G>T (p.Gly340Cys) c.397G>T (p.Gly133Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
18 | g.11881008G>A | CA401928174 | GNAL | c.1250G>A (p.Gly417Asp) c.1019G>A (p.Gly340Asp) c.398G>A (p.Gly133Asp) | |
18 | g.11881008G>C | CA401928175 | GNAL | c.1250G>C (p.Gly417Ala) c.1019G>C (p.Gly340Ala) c.398G>C (p.Gly133Ala) | |
18 | g.11881008G>T | CA401928176 | GNAL | c.1250G>T (p.Gly417Val) c.1019G>T (p.Gly340Val) c.398G>T (p.Gly133Val) | |
18 | g.11881009T>A | CA502927779 | GNAL | c.1251T>A (p.Gly417=) c.1020T>A (p.Gly340=) c.399T>A (p.Gly133=) | |
18 | g.11881009T>C | CA502927780 | GNAL | c.1251T>C (p.Gly417=) c.1020T>C (p.Gly340=) c.399T>C (p.Gly133=) | |
18 | g.11881009T>G | CA502927781 | GNAL | c.1251T>G (p.Gly417=) c.1020T>G (p.Gly340=) c.399T>G (p.Gly133=) | |
18 | g.11881010G>A | CA401928177 | GNAL | c.1252G>A (p.Asp418Asn) c.1021G>A (p.Asp341Asn) c.400G>A (p.Asp134Asn) | |
18 | g.11881010G>C | CA401928179 | GNAL | c.1252G>C (p.Asp418His) c.1021G>C (p.Asp341His) c.400G>C (p.Asp134His) | |
18 | g.11881010G>T | CA401928178 | GNAL | c.1252G>T (p.Asp418Tyr) c.1021G>T (p.Asp341Tyr) c.400G>T (p.Asp134Tyr) | |
18 | g.11881011A>C | CA401928180 | GNAL | c.1253A>C (p.Asp418Ala) c.1022A>C (p.Asp341Ala) c.401A>C (p.Asp134Ala) | |
18 | g.11881011A>G | CA401928182 | GNAL | c.1253A>G (p.Asp418Gly) c.1022A>G (p.Asp341Gly) c.401A>G (p.Asp134Gly) | |
18 | g.11881011A>T | CA401928181 | GNAL | c.1253A>T (p.Asp418Val) c.1022A>T (p.Asp341Val) c.401A>T (p.Asp134Val) | gnomAD v4 |
18 | g.11881012C>A | CA401928183 | GNAL | c.1254C>A (p.Asp418Glu) c.1023C>A (p.Asp341Glu) c.402C>A (p.Asp134Glu) | |
18 | g.11881012C= | CA2284983259 | GNAL | c.1254C= (p.Asp418=) c.1023C= (p.Asp341=) c.402C= (p.Asp134=) | |
18 | g.11881012C>G | CA8894265 | GNAL | c.1254C>G (p.Asp418Glu) c.1023C>G (p.Asp341Glu) c.402C>G (p.Asp134Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11881012C>T | CA8894264 | GNAL | c.1254C>T (p.Asp418=) c.1023C>T (p.Asp341=) c.402C>T (p.Asp134=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881013G>A | CA8894266 | GNAL | c.1255G>A (p.Gly419Ser) c.1024G>A (p.Gly342Ser) c.403G>A (p.Gly135Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11881013G>C | CA401928184 | GNAL | c.1255G>C (p.Gly419Arg) c.1024G>C (p.Gly342Arg) c.403G>C (p.Gly135Arg) | |
18 | g.11881013G= | CA2284983260 | GNAL | c.1255G= (p.Gly419=) c.1024G= (p.Gly342=) c.403G= (p.Gly135=) | |
18 | g.11881013G>T | CA401928185 | GNAL | c.1255G>T (p.Gly419Cys) c.1024G>T (p.Gly342Cys) c.403G>T (p.Gly135Cys) | |
18 | g.11881014G>A | CA401928186 | GNAL | c.1256G>A (p.Gly419Asp) c.1025G>A (p.Gly342Asp) c.404G>A (p.Gly135Asp) | dbSNP gnomAD v3 gnomAD v4 |
18 | g.11881014G>C | CA401928187 | GNAL | c.1256G>C (p.Gly419Ala) c.1025G>C (p.Gly342Ala) c.404G>C (p.Gly135Ala) | |
18 | g.11881014G= | CA2284983261 | GNAL | c.1256G= (p.Gly419=) c.1025G= (p.Gly342=) c.404G= (p.Gly135=) | |
18 | g.11881014G>T | CA401928188 | GNAL | c.1256G>T (p.Gly419Val) c.1025G>T (p.Gly342Val) c.404G>T (p.Gly135Val) | |
18 | g.11881015C>A | CA502927782 | GNAL | c.1257C>A (p.Gly419=) c.1026C>A (p.Gly342=) c.405C>A (p.Gly135=) | |
18 | g.11881015C>G | CA502927783 | GNAL | c.1257C>G (p.Gly419=) c.1026C>G (p.Gly342=) c.405C>G (p.Gly135=) | |
18 | g.11881015C>T | CA502927784 | GNAL | c.1257C>T (p.Gly419=) c.1026C>T (p.Gly342=) c.405C>T (p.Gly135=) | |
18 | g.11881016A>C | CA401928189 | GNAL | c.1258A>C (p.Lys420Gln) c.1027A>C (p.Lys343Gln) c.406A>C (p.Lys136Gln) | |
18 | g.11881016A>G | CA401928190 | GNAL | c.1258A>G (p.Lys420Glu) c.1027A>G (p.Lys343Glu) c.406A>G (p.Lys136Glu) | |
18 | g.11881016A>T | CA401928191 | GNAL | c.1258A>T (p.Lys420Ter) c.1027A>T (p.Lys343Ter) c.406A>T (p.Lys136Ter) | |
18 | g.11881017A>C | CA401928192 | GNAL | c.1259A>C (p.Lys420Thr) c.1028A>C (p.Lys343Thr) c.407A>C (p.Lys136Thr) | |
18 | g.11881017A>G | CA401928194 | GNAL | c.1259A>G (p.Lys420Arg) c.1028A>G (p.Lys343Arg) c.407A>G (p.Lys136Arg) | |
18 | g.11881017A>T | CA401928193 | GNAL | c.1259A>T (p.Lys420Ile) c.1028A>T (p.Lys343Ile) c.407A>T (p.Lys136Ile) | |
18 | g.11881018A>C | CA401928195 | GNAL | c.1260A>C (p.Lys420Asn) c.1029A>C (p.Lys343Asn) c.408A>C (p.Lys136Asn) | |
18 | g.11881018A>G | CA502927785 | GNAL | c.1260A>G (p.Lys420=) c.1029A>G (p.Lys343=) c.408A>G (p.Lys136=) | |
18 | g.11881018A>T | CA401928196 | GNAL | c.1260A>T (p.Lys420Asn) c.1029A>T (p.Lys343Asn) c.408A>T (p.Lys136Asn) | |
18 | g.11881019C>A | CA401928197 | GNAL | c.1261C>A (p.His421Asn) c.1030C>A (p.His344Asn) c.409C>A (p.His137Asn) | |
18 | g.11881019C= | CA2284983262 | GNAL | c.1261C= (p.His421=) c.1030C= (p.His344=) c.409C= (p.His137=) | |
18 | g.11881019C>G | CA8894267 | GNAL | c.1261C>G (p.His421Asp) c.1030C>G (p.His344Asp) c.409C>G (p.His137Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11881019C>T | CA401928198 | GNAL | c.1261C>T (p.His421Tyr) c.1030C>T (p.His344Tyr) c.409C>T (p.His137Tyr) | |
18 | g.11881020A>C | CA401928199 | GNAL | c.1262A>C (p.His421Pro) c.1031A>C (p.His344Pro) c.410A>C (p.His137Pro) | |
18 | g.11881020A>G | CA401928200 | GNAL | c.1262A>G (p.His421Arg) c.1031A>G (p.His344Arg) c.410A>G (p.His137Arg) | |
18 | g.11881020A>T | CA401928201 | GNAL | c.1262A>T (p.His421Leu) c.1031A>T (p.His344Leu) c.410A>T (p.His137Leu) | |
18 | g.11881021T>A | CA401928202 | GNAL | c.1263T>A (p.His421Gln) c.1032T>A (p.His344Gln) c.411T>A (p.His137Gln) | |
18 | g.11881021T>C | CA502927786 | GNAL | c.1263T>C (p.His421=) c.1032T>C (p.His344=) c.411T>C (p.His137=) | |
18 | g.11881021T>G | CA401928203 | GNAL | c.1263T>G (p.His421Gln) c.1032T>G (p.His344Gln) c.411T>G (p.His137Gln) | |
18 | g.11881022T>A | CA401928205 | GNAL | c.1264T>A (p.Tyr422Asn) c.1033T>A (p.Tyr345Asn) c.412T>A (p.Tyr138Asn) | |
18 | g.11881022T>C | CA401928206 | GNAL | c.1264T>C (p.Tyr422His) c.1033T>C (p.Tyr345His) c.412T>C (p.Tyr138His) | |
18 | g.11881022T>G | CA401928204 | GNAL | c.1264T>G (p.Tyr422Asp) c.1033T>G (p.Tyr345Asp) c.412T>G (p.Tyr138Asp) | |
18 | g.11881023A>C | CA401928207 | GNAL | c.1265A>C (p.Tyr422Ser) c.1034A>C (p.Tyr345Ser) c.413A>C (p.Tyr138Ser) | |
18 | g.11881023A>G | CA401928208 | GNAL | c.1265A>G (p.Tyr422Cys) c.1034A>G (p.Tyr345Cys) c.413A>G (p.Tyr138Cys) | |
18 | g.11881023A>T | CA401928209 | GNAL | c.1265A>T (p.Tyr422Phe) c.1034A>T (p.Tyr345Phe) c.413A>T (p.Tyr138Phe) | |
18 | g.11881024C>A | CA401928210 | GNAL | c.1266C>A (p.Tyr422Ter) c.1035C>A (p.Tyr345Ter) c.414C>A (p.Tyr138Ter) | |
18 | g.11881024C>G | CA401928211 | GNAL | c.1266C>G (p.Tyr422Ter) c.1035C>G (p.Tyr345Ter) c.414C>G (p.Tyr138Ter) | |
18 | g.11881024C>T | CA502927787 | GNAL | c.1266C>T (p.Tyr422=) c.1035C>T (p.Tyr345=) c.414C>T (p.Tyr138=) | gnomAD v4 |
18 | g.11881025T>A | CA401928212 | GNAL | c.1267T>A (p.Cys423Ser) c.1036T>A (p.Cys346Ser) c.415T>A (p.Cys139Ser) | |
18 | g.11881025T>C | CA401928213 | GNAL | c.1267T>C (p.Cys423Arg) c.1036T>C (p.Cys346Arg) c.415T>C (p.Cys139Arg) | |
18 | g.11881025T>G | CA401928214 | GNAL | c.1267T>G (p.Cys423Gly) c.1036T>G (p.Cys346Gly) c.415T>G (p.Cys139Gly) | |
18 | g.11881026G>A | CA401928215 | GNAL | c.1268G>A (p.Cys423Tyr) c.1037G>A (p.Cys346Tyr) c.416G>A (p.Cys139Tyr) | |
18 | g.11881026G>C | CA401928216 | GNAL | c.1268G>C (p.Cys423Ser) c.1037G>C (p.Cys346Ser) c.416G>C (p.Cys139Ser) | |
18 | g.11881026G>T | CA401928217 | GNAL | c.1268G>T (p.Cys423Phe) c.1037G>T (p.Cys346Phe) c.416G>T (p.Cys139Phe) | |
18 | g.11881027C>A | CA401928218 | GNAL | c.1269C>A (p.Cys423Ter) c.1038C>A (p.Cys346Ter) c.417C>A (p.Cys139Ter) | |
18 | g.11881027C>G | CA401928219 | GNAL | c.1269C>G (p.Cys423Trp) c.1038C>G (p.Cys346Trp) c.417C>G (p.Cys139Trp) | |
18 | g.11881027C>T | CA502927788 | GNAL | c.1269C>T (p.Cys423=) c.1038C>T (p.Cys346=) c.417C>T (p.Cys139=) | |
18 | g.11881028T>A | CA401928222 | GNAL | c.1270T>A (p.Tyr424Asn) c.1039T>A (p.Tyr347Asn) c.418T>A (p.Tyr140Asn) | |
18 | g.11881028T>C | CA401928221 | GNAL | c.1270T>C (p.Tyr424His) c.1039T>C (p.Tyr347His) c.418T>C (p.Tyr140His) | |
18 | g.11881028T>G | CA401928220 | GNAL | c.1270T>G (p.Tyr424Asp) c.1039T>G (p.Tyr347Asp) c.418T>G (p.Tyr140Asp) | |
18 | g.11881029A= | CA2284983263 | GNAL | c.1271A= (p.Tyr424=) c.1040A= (p.Tyr347=) c.419A= (p.Tyr140=) | |
18 | g.11881029A>C | CA401928223 | GNAL | c.1271A>C (p.Tyr424Ser) c.1040A>C (p.Tyr347Ser) c.419A>C (p.Tyr140Ser) | dbSNP |
18 | g.11881029A>G | CA401928224 | GNAL | c.1271A>G (p.Tyr424Cys) c.1040A>G (p.Tyr347Cys) c.419A>G (p.Tyr140Cys) | |
18 | g.11881029A>T | CA401928225 | GNAL | c.1271A>T (p.Tyr424Phe) c.1040A>T (p.Tyr347Phe) c.419A>T (p.Tyr140Phe) | |
18 | g.11881030C>A | CA401928226 | GNAL | c.1272C>A (p.Tyr424Ter) c.1041C>A (p.Tyr347Ter) c.420C>A (p.Tyr140Ter) | |
18 | g.11881030C>G | CA401928227 | GNAL | c.1272C>G (p.Tyr424Ter) c.1041C>G (p.Tyr347Ter) c.420C>G (p.Tyr140Ter) | |
18 | g.11881030C>T | CA502927789 | GNAL | c.1272C>T (p.Tyr424=) c.1041C>T (p.Tyr347=) c.420C>T (p.Tyr140=) | |
18 | g.11881031C>A | CA401928228 | GNAL | c.1273C>A (p.Pro425Thr) c.1042C>A (p.Pro348Thr) c.421C>A (p.Pro141Thr) | |
18 | g.11881031C= | CA2284983264 | GNAL | c.1273C= (p.Pro425=) c.1042C= (p.Pro348=) c.421C= (p.Pro141=) | |
18 | g.11881031C>G | CA401928229 | GNAL | c.1273C>G (p.Pro425Ala) c.1042C>G (p.Pro348Ala) c.421C>G (p.Pro141Ala) | dbSNP |
18 | g.11881031C>T | CA401928230 | GNAL | c.1273C>T (p.Pro425Ser) c.1042C>T (p.Pro348Ser) c.421C>T (p.Pro141Ser) | |
18 | g.11881032C>A | CA401928231 | GNAL | c.1274C>A (p.Pro425Gln) c.1043C>A (p.Pro348Gln) c.422C>A (p.Pro141Gln) | ClinVar dbSNP gnomAD v4 |
18 | g.11881032C= | CA2284983265 | GNAL | c.1274C= (p.Pro425=) c.1043C= (p.Pro348=) c.422C= (p.Pro141=) | |
18 | g.11881032C>G | CA401928232 | GNAL | c.1274C>G (p.Pro425Arg) c.1043C>G (p.Pro348Arg) c.422C>G (p.Pro141Arg) | |
18 | g.11881032C>T | CA8894268 | GNAL | c.1274C>T (p.Pro425Leu) c.1043C>T (p.Pro348Leu) c.422C>T (p.Pro141Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11881033G>A | CA8894269 | GNAL | c.1275G>A (p.Pro425=) c.1044G>A (p.Pro348=) c.423G>A (p.Pro141=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881033G>C | CA502927790 | GNAL | c.1275G>C (p.Pro425=) c.1044G>C (p.Pro348=) c.423G>C (p.Pro141=) | dbSNP gnomAD v2 |
18 | g.11881033G= | CA2284983266 | GNAL | c.1275G= (p.Pro425=) c.1044G= (p.Pro348=) c.423G= (p.Pro141=) | |
18 | g.11881033G>T | CA502927791 | GNAL | c.1275G>T (p.Pro425=) c.1044G>T (p.Pro348=) c.423G>T (p.Pro141=) | |
18 | g.11881034C>A | CA401928235 | GNAL | c.1276C>A (p.His426Asn) c.1045C>A (p.His349Asn) c.424C>A (p.His142Asn) | |
18 | g.11881034C>G | CA401928234 | GNAL | c.1276C>G (p.His426Asp) c.1045C>G (p.His349Asp) c.424C>G (p.His142Asp) | |
18 | g.11881034C>T | CA401928233 | GNAL | c.1276C>T (p.His426Tyr) c.1045C>T (p.His349Tyr) c.424C>T (p.His142Tyr) | |
18 | g.11881035A>C | CA401928236 | GNAL | c.1277A>C (p.His426Pro) c.1046A>C (p.His349Pro) c.425A>C (p.His142Pro) | |
18 | g.11881035A>G | CA401928238 | GNAL | c.1277A>G (p.His426Arg) c.1046A>G (p.His349Arg) c.425A>G (p.His142Arg) | dbSNP |
18 | g.11881035A>T | CA401928237 | GNAL | c.1277A>T (p.His426Leu) c.1046A>T (p.His349Leu) c.425A>T (p.His142Leu) | |
18 | g.11881036C>A | CA401928239 | GNAL | c.1278C>A (p.His426Gln) c.1047C>A (p.His349Gln) c.426C>A (p.His142Gln) | |
18 | g.11881036C>G | CA401928240 | GNAL | c.1278C>G (p.His426Gln) c.1047C>G (p.His349Gln) c.426C>G (p.His142Gln) | |
18 | g.11881036C>T | CA502927792 | GNAL | c.1278C>T (p.His426=) c.1047C>T (p.His349=) c.426C>T (p.His142=) | gnomAD v4 |
18 | g.11881037T>A | CA401928241 | GNAL | c.1279T>A (p.Phe427Ile) c.1048T>A (p.Phe350Ile) c.427T>A (p.Phe143Ile) | |
18 | g.11881037T>C | CA401928242 | GNAL | c.1279T>C (p.Phe427Leu) c.1048T>C (p.Phe350Leu) c.427T>C (p.Phe143Leu) | |
18 | g.11881037T>G | CA401928243 | GNAL | c.1279T>G (p.Phe427Val) c.1048T>G (p.Phe350Val) c.427T>G (p.Phe143Val) | |
18 | g.11881038T>A | CA401928246 | GNAL | c.1280T>A (p.Phe427Tyr) c.1049T>A (p.Phe350Tyr) c.428T>A (p.Phe143Tyr) | |
18 | g.11881038T>C | CA401928245 | GNAL | c.1280T>C (p.Phe427Ser) c.1049T>C (p.Phe350Ser) c.428T>C (p.Phe143Ser) | |
18 | g.11881038T>G | CA401928244 | GNAL | c.1280T>G (p.Phe427Cys) c.1049T>G (p.Phe350Cys) c.428T>G (p.Phe143Cys) | |
18 | g.11881039C>A | CA401928247 | GNAL | c.1281C>A (p.Phe427Leu) c.1050C>A (p.Phe350Leu) c.429C>A (p.Phe143Leu) | |
18 | g.11881039C= | CA2284983267 | GNAL | c.1281C= (p.Phe427=) c.1050C= (p.Phe350=) c.429C= (p.Phe143=) | |
18 | g.11881039C>G | CA401928248 | GNAL | c.1281C>G (p.Phe427Leu) c.1050C>G (p.Phe350Leu) c.429C>G (p.Phe143Leu) | |
18 | g.11881039C>T | CA8894270 | GNAL | c.1281C>T (p.Phe427=) c.1050C>T (p.Phe350=) c.429C>T (p.Phe143=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11881040A= | CA2284983268 | GNAL | c.1282A= (p.Thr428=) c.1051A= (p.Thr351=) c.430A= (p.Thr144=) | |
18 | g.11881040A>C | CA401928249 | GNAL | c.1282A>C (p.Thr428Pro) c.1051A>C (p.Thr351Pro) c.430A>C (p.Thr144Pro) | dbSNP |
18 | g.11881040A>G | CA401928250 | GNAL | c.1282A>G (p.Thr428Ala) c.1051A>G (p.Thr351Ala) c.430A>G (p.Thr144Ala) | |
18 | g.11881040A>T | CA401928251 | GNAL | c.1282A>T (p.Thr428Ser) c.1051A>T (p.Thr351Ser) c.430A>T (p.Thr144Ser) | |
18 | g.11881041C>A | CA401928254 | GNAL | c.1283C>A (p.Thr428Asn) c.1052C>A (p.Thr351Asn) c.431C>A (p.Thr144Asn) | |
18 | g.11881041C>G | CA401928252 | GNAL | c.1283C>G (p.Thr428Ser) c.1052C>G (p.Thr351Ser) c.431C>G (p.Thr144Ser) | |
18 | g.11881041C>T | CA401928253 | GNAL | c.1283C>T (p.Thr428Ile) c.1052C>T (p.Thr351Ile) c.431C>T (p.Thr144Ile) | |
18 | g.11881042C>A | CA502927793 | GNAL | c.1284C>A (p.Thr428=) c.1053C>A (p.Thr351=) c.432C>A (p.Thr144=) | |
18 | g.11881042C>G | CA502927794 | GNAL | c.1284C>G (p.Thr428=) c.1053C>G (p.Thr351=) c.432C>G (p.Thr144=) | |
18 | g.11881042C>T | CA502927795 | GNAL | c.1284C>T (p.Thr428=) c.1053C>T (p.Thr351=) c.432C>T (p.Thr144=) | |
18 | g.11881043T>A | CA401928255 | GNAL | c.1285T>A (p.Cys429Ser) c.1054T>A (p.Cys352Ser) c.433T>A (p.Cys145Ser) | |
18 | g.11881043T>C | CA401928256 | GNAL | c.1285T>C (p.Cys429Arg) c.1054T>C (p.Cys352Arg) c.433T>C (p.Cys145Arg) | |
18 | g.11881043T>G | CA401928257 | GNAL | c.1285T>G (p.Cys429Gly) c.1054T>G (p.Cys352Gly) c.433T>G (p.Cys145Gly) | |
18 | g.11881044G>A | CA401928258 | GNAL | c.1286G>A (p.Cys429Tyr) c.1055G>A (p.Cys352Tyr) c.434G>A (p.Cys145Tyr) | |
18 | g.11881044G>C | CA401928259 | GNAL | c.1286G>C (p.Cys429Ser) c.1055G>C (p.Cys352Ser) c.434G>C (p.Cys145Ser) | |
18 | g.11881044G>T | CA401928260 | GNAL | c.1286G>T (p.Cys429Phe) c.1055G>T (p.Cys352Phe) c.434G>T (p.Cys145Phe) | |
18 | g.11881045C>A | CA401928261 | GNAL | c.1287C>A (p.Cys429Ter) c.1056C>A (p.Cys352Ter) c.435C>A (p.Cys145Ter) | |
18 | g.11881045C= | CA2284983269 | GNAL | c.1287C= (p.Cys429=) c.1056C= (p.Cys352=) c.435C= (p.Cys145=) | |
18 | g.11881045C>G | CA401928262 | GNAL | c.1287C>G (p.Cys429Trp) c.1056C>G (p.Cys352Trp) c.435C>G (p.Cys145Trp) | |
18 | g.11881045C>T | CA8894271 | GNAL | c.1287C>T (p.Cys429=) c.1056C>T (p.Cys352=) c.435C>T (p.Cys145=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881046G>A | CA401928263 | GNAL | c.1288G>A (p.Ala430Thr) c.1057G>A (p.Ala353Thr) c.436G>A (p.Ala146Thr) | ClinVar dbSNP gnomAD v4 |
18 | g.11881046G>C | CA401928264 | GNAL | c.1288G>C (p.Ala430Pro) c.1057G>C (p.Ala353Pro) c.436G>C (p.Ala146Pro) | |
18 | g.11881046G= | CA2284983270 | GNAL | c.1288G= (p.Ala430=) c.1057G= (p.Ala353=) c.436G= (p.Ala146=) | |
18 | g.11881046G>T | CA401928265 | GNAL | c.1288G>T (p.Ala430Ser) c.1057G>T (p.Ala353Ser) c.436G>T (p.Ala146Ser) | |
18 | g.11881047C>A | CA401928266 | GNAL | c.1289C>A (p.Ala430Asp) c.1058C>A (p.Ala353Asp) c.437C>A (p.Ala146Asp) | |
18 | g.11881047C>G | CA401928268 | GNAL | c.1289C>G (p.Ala430Gly) c.1058C>G (p.Ala353Gly) c.437C>G (p.Ala146Gly) | |
18 | g.11881047C>T | CA401928267 | GNAL | c.1289C>T (p.Ala430Val) c.1058C>T (p.Ala353Val) c.437C>T (p.Ala146Val) | |
18 | g.11881048C>A | CA502927796 | GNAL | c.1290C>A (p.Ala430=) c.1059C>A (p.Ala353=) c.438C>A (p.Ala146=) | |
18 | g.11881048C= | CA2284983271 | GNAL | c.1290C= (p.Ala430=) c.1059C= (p.Ala353=) c.438C= (p.Ala146=) | |
18 | g.11881048C>G | CA502927797 | GNAL | c.1290C>G (p.Ala430=) c.1059C>G (p.Ala353=) c.438C>G (p.Ala146=) | |
18 | g.11881048C>T | CA8894272 | GNAL | c.1290C>T (p.Ala430=) c.1059C>T (p.Ala353=) c.438C>T (p.Ala146=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
18 | g.11881049G>A | CA16620660 | GNAL | c.1291G>A (p.Val431Met) c.1060G>A (p.Val354Met) c.439G>A (p.Val147Met) | ClinVar dbSNP COSMIC |
18 | g.11881049G>C | CA401928269 | GNAL | c.1291G>C (p.Val431Leu) c.1060G>C (p.Val354Leu) c.439G>C (p.Val147Leu) | |
18 | g.11881049G= | CA2284983272 | GNAL | c.1291G= (p.Val431=) c.1060G= (p.Val354=) c.439G= (p.Val147=) | |
18 | g.11881049G>T | CA401928270 | GNAL | c.1291G>T (p.Val431Leu) c.1060G>T (p.Val354Leu) c.439G>T (p.Val147Leu) | |
18 | g.11881050T>A | CA401928271 | GNAL | c.1292T>A (p.Val431Glu) c.1061T>A (p.Val354Glu) c.440T>A (p.Val147Glu) | |
18 | g.11881050T>C | CA401928272 | GNAL | c.1292T>C (p.Val431Ala) c.1061T>C (p.Val354Ala) c.440T>C (p.Val147Ala) | ClinVar |
18 | g.11881050T>G | CA401928273 | GNAL | c.1292T>G (p.Val431Gly) c.1061T>G (p.Val354Gly) c.440T>G (p.Val147Gly) | |
18 | g.11881051G>A | CA502927798 | GNAL | c.1293G>A (p.Val431=) c.1062G>A (p.Val354=) c.441G>A (p.Val147=) | |
18 | g.11881051G>C | CA502927799 | GNAL | c.1293G>C (p.Val431=) c.1062G>C (p.Val354=) c.441G>C (p.Val147=) | |
18 | g.11881051G>T | CA502927800 | GNAL | c.1293G>T (p.Val431=) c.1062G>T (p.Val354=) c.441G>T (p.Val147=) | |
18 | g.11881052G>A | CA401928274 | GNAL | c.1294G>A (p.Asp432Asn) c.1063G>A (p.Asp355Asn) c.442G>A (p.Asp148Asn) | |
18 | g.11881052G>C | CA401928275 | GNAL | c.1294G>C (p.Asp432His) c.1063G>C (p.Asp355His) c.442G>C (p.Asp148His) | |
18 | g.11881052G>T | CA401928276 | GNAL | c.1294G>T (p.Asp432Tyr) c.1063G>T (p.Asp355Tyr) c.442G>T (p.Asp148Tyr) | |
18 | g.11881053A>C | CA401928277 | GNAL | c.1295A>C (p.Asp432Ala) c.1064A>C (p.Asp355Ala) c.443A>C (p.Asp148Ala) | |
18 | g.11881053A>G | CA401928278 | GNAL | c.1295A>G (p.Asp432Gly) c.1064A>G (p.Asp355Gly) c.443A>G (p.Asp148Gly) | |
18 | g.11881053A>T | CA401928279 | GNAL | c.1295A>T (p.Asp432Val) c.1064A>T (p.Asp355Val) c.443A>T (p.Asp148Val) | |
18 | g.11881054C>A | CA401928280 | GNAL | c.1296C>A (p.Asp432Glu) c.1065C>A (p.Asp355Glu) c.444C>A (p.Asp148Glu) | |
18 | g.11881054C>G | CA401928281 | GNAL | c.1296C>G (p.Asp432Glu) c.1065C>G (p.Asp355Glu) c.444C>G (p.Asp148Glu) | |
18 | g.11881054C>T | CA502927801 | GNAL | c.1296C>T (p.Asp432=) c.1065C>T (p.Asp355=) c.444C>T (p.Asp148=) | gnomAD v4 |
18 | g.11881055A>C | CA401928282 | GNAL | c.1297A>C (p.Thr433Pro) c.1066A>C (p.Thr356Pro) c.445A>C (p.Thr149Pro) | |
18 | g.11881055A>G | CA401928283 | GNAL | c.1297A>G (p.Thr433Ala) c.1066A>G (p.Thr356Ala) c.445A>G (p.Thr149Ala) | |
18 | g.11881055A>T | CA401928284 | GNAL | c.1297A>T (p.Thr433Ser) c.1066A>T (p.Thr356Ser) c.445A>T (p.Thr149Ser) | |
18 | g.11881056C>A | CA401928285 | GNAL | c.1298C>A (p.Thr433Lys) c.1067C>A (p.Thr356Lys) c.446C>A (p.Thr149Lys) | |
18 | g.11881056C>G | CA401928286 | GNAL | c.1298C>G (p.Thr433Arg) c.1067C>G (p.Thr356Arg) c.446C>G (p.Thr149Arg) | |
18 | g.11881056C>T | CA401928287 | GNAL | c.1298C>T (p.Thr433Ile) c.1067C>T (p.Thr356Ile) c.446C>T (p.Thr149Ile) | |
18 | g.11881057A>C | CA502927802 | GNAL | c.1299A>C (p.Thr433=) c.1068A>C (p.Thr356=) c.447A>C (p.Thr149=) | |
18 | g.11881057A>G | CA502927803 | GNAL | c.1299A>G (p.Thr433=) c.1068A>G (p.Thr356=) c.447A>G (p.Thr149=) | |
18 | g.11881057A>T | CA502927804 | GNAL | c.1299A>T (p.Thr433=) c.1068A>T (p.Thr356=) c.447A>T (p.Thr149=) | |
18 | g.11881058G>A | CA401928288 | GNAL | c.1300G>A (p.Glu434Lys) c.1069G>A (p.Glu357Lys) c.448G>A (p.Glu150Lys) | |
18 | g.11881058G>C | CA401928289 | GNAL | c.1300G>C (p.Glu434Gln) c.1069G>C (p.Glu357Gln) c.448G>C (p.Glu150Gln) | gnomAD v4 COSMIC COSMIC |
18 | g.11881058G>T | CA401928290 | GNAL | c.1300G>T (p.Glu434Ter) c.1069G>T (p.Glu357Ter) c.448G>T (p.Glu150Ter) | |
18 | g.11881059A= | CA2284983273 | GNAL | c.1301A= (p.Glu434=) c.1070A= (p.Glu357=) c.449A= (p.Glu150=) | |
18 | g.11881059A>C | CA8894273 | GNAL | c.1301A>C (p.Glu434Ala) c.1070A>C (p.Glu357Ala) c.449A>C (p.Glu150Ala) | dbSNP ExAC gnomAD v2 |
18 | g.11881059A>G | CA401928291 | GNAL | c.1301A>G (p.Glu434Gly) c.1070A>G (p.Glu357Gly) c.449A>G (p.Glu150Gly) | |
18 | g.11881059A>T | CA401928292 | GNAL | c.1301A>T (p.Glu434Val) c.1070A>T (p.Glu357Val) c.449A>T (p.Glu150Val) | |
18 | g.11881060G>A | CA502927805 | GNAL | c.1302G>A (p.Glu434=) c.1071G>A (p.Glu357=) c.450G>A (p.Glu150=) | dbSNP gnomAD v3 gnomAD v4 |
18 | g.11881060G>C | CA401928293 | GNAL | c.1302G>C (p.Glu434Asp) c.1071G>C (p.Glu357Asp) c.450G>C (p.Glu150Asp) | |
18 | g.11881060G= | CA2284983274 | GNAL | c.1302G= (p.Glu434=) c.1071G= (p.Glu357=) c.450G= (p.Glu150=) | |
18 | g.11881060G>T | CA401928294 | GNAL | c.1302G>T (p.Glu434Asp) c.1071G>T (p.Glu357Asp) c.450G>T (p.Glu150Asp) | |
18 | g.11881061A>C | CA401928295 | GNAL | c.1303A>C (p.Asn435His) c.1072A>C (p.Asn358His) c.451A>C (p.Asn151His) | |
18 | g.11881061A>G | CA401928297 | GNAL | c.1303A>G (p.Asn435Asp) c.1072A>G (p.Asn358Asp) c.451A>G (p.Asn151Asp) | |
18 | g.11881061A>T | CA401928296 | GNAL | c.1303A>T (p.Asn435Tyr) c.1072A>T (p.Asn358Tyr) c.451A>T (p.Asn151Tyr) | |
18 | g.11881062A>C | CA401928298 | GNAL | c.1304A>C (p.Asn435Thr) c.1073A>C (p.Asn358Thr) c.452A>C (p.Asn151Thr) | |
18 | g.11881062A>G | CA401928299 | GNAL | c.1304A>G (p.Asn435Ser) c.1073A>G (p.Asn358Ser) c.452A>G (p.Asn151Ser) | |
18 | g.11881062A>T | CA401928300 | GNAL | c.1304A>T (p.Asn435Ile) c.1073A>T (p.Asn358Ile) c.452A>T (p.Asn151Ile) | |
18 | g.11881063C>A | CA401928301 | GNAL | c.1305C>A (p.Asn435Lys) c.1074C>A (p.Asn358Lys) c.453C>A (p.Asn151Lys) | |
18 | g.11881063C= | CA2284983275 | GNAL | c.1305C= (p.Asn435=) c.1074C= (p.Asn358=) c.453C= (p.Asn151=) | |
18 | g.11881063C>G | CA401928302 | GNAL | c.1305C>G (p.Asn435Lys) c.1074C>G (p.Asn358Lys) c.453C>G (p.Asn151Lys) | |
18 | g.11881063C>T | CA8894274 | GNAL | c.1305C>T (p.Asn435=) c.1074C>T (p.Asn358=) c.453C>T (p.Asn151=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.11881064A>C | CA401928303 | GNAL | c.1306A>C (p.Ile436Leu) c.1075A>C (p.Ile359Leu) c.454A>C (p.Ile152Leu) | |
18 | g.11881064A>G | CA401928304 | GNAL | c.1306A>G (p.Ile436Val) c.1075A>G (p.Ile359Val) c.454A>G (p.Ile152Val) | gnomAD v4 |
18 | g.11881064A>T | CA401928305 | GNAL | c.1306A>T (p.Ile436Phe) c.1075A>T (p.Ile359Phe) c.454A>T (p.Ile152Phe) | |
18 | g.11881065T>A | CA401928306 | GNAL | c.1307T>A (p.Ile436Asn) c.1076T>A (p.Ile359Asn) c.455T>A (p.Ile152Asn) | |
18 | g.11881065T>C | CA401928307 | GNAL | c.1307T>C (p.Ile436Thr) c.1076T>C (p.Ile359Thr) c.455T>C (p.Ile152Thr) | dbSNP gnomAD v2 |
18 | g.11881065T>G | CA401928308 | GNAL | c.1307T>G (p.Ile436Ser) c.1076T>G (p.Ile359Ser) c.455T>G (p.Ile152Ser) | |
18 | g.11881065T= | CA2284983276 | GNAL | c.1307T= (p.Ile436=) c.1076T= (p.Ile359=) c.455T= (p.Ile152=) | |
18 | g.11881066C>A | CA296058690 | GNAL | c.1308C>A (p.Ile436=) c.1077C>A (p.Ile359=) c.456C>A (p.Ile152=) | dbSNP |
18 | g.11881066C= | CA2284983277 | GNAL | c.1308C= (p.Ile436=) c.1077C= (p.Ile359=) c.456C= (p.Ile152=) | |
18 | g.11881066C>G | CA401928309 | GNAL | c.1308C>G (p.Ile436Met) c.1077C>G (p.Ile359Met) c.456C>G (p.Ile152Met) | |
18 | g.11881066C>T | CA502927806 | GNAL | c.1308C>T (p.Ile436=) c.1077C>T (p.Ile359=) c.456C>T (p.Ile152=) | |
18 | g.11881067C>A | CA401928310 | GNAL | c.1309C>A (p.Arg437Ser) c.1078C>A (p.Arg360Ser) c.457C>A (p.Arg153Ser) | COSMIC COSMIC |
18 | g.11881067C= | CA2284983278 | GNAL | c.1309C= (p.Arg437=) c.1078C= (p.Arg360=) c.457C= (p.Arg153=) | |
18 | g.11881067C>G | CA401928312 | GNAL | c.1309C>G (p.Arg437Gly) c.1078C>G (p.Arg360Gly) c.457C>G (p.Arg153Gly) | |
18 | g.11881067C>T | CA401928311 | GNAL | c.1309C>T (p.Arg437Cys) c.1078C>T (p.Arg360Cys) c.457C>T (p.Arg153Cys) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
18 | g.11881068G>A | CA401928313 | GNAL | c.1310G>A (p.Arg437His) c.1079G>A (p.Arg360His) c.458G>A (p.Arg153His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
18 | g.11881068G>C | CA401928314 | GNAL | c.1310G>C (p.Arg437Pro) c.1079G>C (p.Arg360Pro) c.458G>C (p.Arg153Pro) | |
18 | g.11881068G= | CA2284983279 | GNAL | c.1310G= (p.Arg437=) c.1079G= (p.Arg360=) c.458G= (p.Arg153=) | |
18 | g.11881068G>T | CA8894275 | GNAL | c.1310G>T (p.Arg437Leu) c.1079G>T (p.Arg360Leu) c.458G>T (p.Arg153Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.11881069C>A | CA502927808 | GNAL | c.1311C>A (p.Arg437=) c.1080C>A (p.Arg360=) c.459C>A (p.Arg153=) | |
18 | g.11881069C= | CA2284983280 | GNAL | c.1311C= (p.Arg437=) c.1080C= (p.Arg360=) c.459C= (p.Arg153=) | |
18 | g.11881069C>G | CA502927809 | GNAL | c.1311C>G (p.Arg437=) c.1080C>G (p.Arg360=) c.459C>G (p.Arg153=) | |
18 | g.11881069C>T | CA502927810 | GNAL | c.1311C>T (p.Arg437=) c.1080C>T (p.Arg360=) c.459C>T (p.Arg153=) | dbSNP gnomAD v4 |
18 | g.11881070A>C | CA502927811 | GNAL | c.1312A>C (p.Arg438=) c.1081A>C (p.Arg361=) c.460A>C (p.Arg154=) | |
18 | g.11881070A>G | CA401928315 | GNAL | c.1312A>G (p.Arg438Gly) c.1081A>G (p.Arg361Gly) c.460A>G (p.Arg154Gly) | |
18 | g.11881070A>T | CA401928316 | GNAL | c.1312A>T (p.Arg438Trp) c.1081A>T (p.Arg361Trp) c.460A>T (p.Arg154Trp) | |
18 | g.11881071G>A | CA401928317 | GNAL | c.1313G>A (p.Arg438Lys) c.1082G>A (p.Arg361Lys) c.461G>A (p.Arg154Lys) | dbSNP |
18 | g.11881071G>C | CA401928318 | GNAL | c.1313G>C (p.Arg438Thr) c.1082G>C (p.Arg361Thr) c.461G>C (p.Arg154Thr) | |
18 | g.11881071G= | CA2284983281 | GNAL | c.1313G= (p.Arg438=) c.1082G= (p.Arg361=) c.461G= (p.Arg154=) | |
18 | g.11881071G>T | CA401928319 | GNAL | c.1313G>T (p.Arg438Met) c.1082G>T (p.Arg361Met) c.461G>T (p.Arg154Met) | |
18 | g.11881072G>A | CA296058700 | GNAL | c.1314G>A (p.Arg438=) c.1083G>A (p.Arg361=) c.462G>A (p.Arg154=) | dbSNP |
18 | g.11881072G>C | CA401928320 | GNAL | c.1314G>C (p.Arg438Ser) c.1083G>C (p.Arg361Ser) c.462G>C (p.Arg154Ser) | |
18 | g.11881072G= | CA2284983282 | GNAL | c.1314G= (p.Arg438=) c.1083G= (p.Arg361=) c.462G= (p.Arg154=) | |
18 | g.11881072G>T | CA401928321 | GNAL | c.1314G>T (p.Arg438Ser) c.1083G>T (p.Arg361Ser) c.462G>T (p.Arg154Ser) | |
18 | g.11881073G>A | CA401928324 | GNAL | c.1315G>A (p.Val439Met) c.1084G>A (p.Val362Met) c.463G>A (p.Val155Met) | |
18 | g.11881073G>C | CA401928323 | GNAL | c.1315G>C (p.Val439Leu) c.1084G>C (p.Val362Leu) c.463G>C (p.Val155Leu) | |
18 | g.11881073G>T | CA401928322 | GNAL | c.1315G>T (p.Val439Leu) c.1084G>T (p.Val362Leu) c.463G>T (p.Val155Leu) | |
18 | g.11881074T>A | CA401928325 | GNAL | c.1316T>A (p.Val439Glu) c.1085T>A (p.Val362Glu) c.464T>A (p.Val155Glu) | |
18 | g.11881074T>C | CA401928326 | GNAL | c.1316T>C (p.Val439Ala) c.1085T>C (p.Val362Ala) c.464T>C (p.Val155Ala) | |
18 | g.11881074T>G | CA401928327 | GNAL | c.1316T>G (p.Val439Gly) c.1085T>G (p.Val362Gly) c.464T>G (p.Val155Gly) |