Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.55276321T>G | CA826030889 | HCRTR2 | c.763-1059T>G (n.763-1059T>G) c.568-1059T>G (n.568-1059T>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276322A>G | CA1089240356 | HCRTR2 | c.763-1058A>G (n.763-1058A>G) c.568-1058A>G (n.568-1058A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276326G>A | CA2711803654 | HCRTR2 | c.763-1054G>A (n.763-1054G>A) c.568-1054G>A (n.568-1054G>A) | dbSNP |
6 | g.55276328A>G | CA826030891 | HCRTR2 | c.763-1052A>G (n.763-1052A>G) c.568-1052A>G (n.568-1052A>G) | dbSNP |
6 | g.55276336G>A | CA2711609677 | HCRTR2 | c.763-1044G>A (n.763-1044G>A) c.568-1044G>A (n.568-1044G>A) | dbSNP |
6 | g.55276337T>C | CA2711803697 | HCRTR2 | c.763-1043T>C (n.763-1043T>C) c.568-1043T>C (n.568-1043T>C) | dbSNP |
6 | g.55276342A>C | CA139610900 | HCRTR2 | c.763-1038A>C (n.763-1038A>C) c.568-1038A>C (n.568-1038A>C) | dbSNP |
6 | g.55276345_55276349del | CA2497154673 | HCRTR2 | c.763-1035_763-1031del (n.763-1035_763-1031del) c.568-1035_568-1031del (n.568-1035_568-1031del) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276343A>T | CA139610901 | HCRTR2 | c.763-1037A>T (n.763-1037A>T) c.568-1037A>T (n.568-1037A>T) | dbSNP |
6 | g.55276344A>G | CA139610902 | HCRTR2 | c.763-1036A>G (n.763-1036A>G) c.568-1036A>G (n.568-1036A>G) | dbSNP |
6 | g.55276346T>A | CA1089240357 | HCRTR2 | c.763-1034T>A (n.763-1034T>A) c.568-1034T>A (n.568-1034T>A) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276347A>G | CA2711803880 | HCRTR2 | c.763-1033A>G (n.763-1033A>G) c.568-1033A>G (n.568-1033A>G) | dbSNP |
6 | g.55276348A>G | CA139610903 | HCRTR2 | c.763-1032A>G (n.763-1032A>G) c.568-1032A>G (n.568-1032A>G) | dbSNP |
6 | g.55276349_55276351del | CA567488246 | HCRTR2 | c.763-1031_763-1029del (n.763-1031_763-1029del) c.568-1031_568-1029del (n.568-1031_568-1029del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276349A>G | CA1089240364 | HCRTR2 | c.763-1031A>G (n.763-1031A>G) c.568-1031A>G (n.568-1031A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276351A>T | CA2597583422 | HCRTR2 | c.763-1029A>T (n.763-1029A>T) c.568-1029A>T (n.568-1029A>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276355T>C | CA2711609715 | HCRTR2 | c.763-1025T>C (n.763-1025T>C) c.568-1025T>C (n.568-1025T>C) | dbSNP |
6 | g.55276356C>T | CA139610904 | HCRTR2 | c.763-1024C>T (n.763-1024C>T) c.568-1024C>T (n.568-1024C>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276357G>A | CA826030898 | HCRTR2 | c.763-1023G>A (n.763-1023G>A) c.568-1023G>A (n.568-1023G>A) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276358A>G | CA826030900 | HCRTR2 | c.763-1022A>G (n.763-1022A>G) c.568-1022A>G (n.568-1022A>G) | dbSNP |
6 | g.55276360C>A | CA2571401976 | HCRTR2 | c.763-1020C>A (n.763-1020C>A) c.568-1020C>A (n.568-1020C>A) | |
6 | g.55276361A>T | CA2711609716 | HCRTR2 | c.763-1019A>T (n.763-1019A>T) c.568-1019A>T (n.568-1019A>T) | dbSNP |
6 | g.55276362G>A | CA2711609719 | HCRTR2 | c.763-1018G>A (n.763-1018G>A) c.568-1018G>A (n.568-1018G>A) | dbSNP |
6 | g.55276363A>C | CA139610905 | HCRTR2 | c.763-1017A>C (n.763-1017A>C) c.568-1017A>C (n.568-1017A>C) | dbSNP |
6 | g.55276364C>T | CA826030903 | HCRTR2 | c.763-1016C>T (n.763-1016C>T) c.568-1016C>T (n.568-1016C>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276367T>C | CA567488248 | HCRTR2 | c.763-1013T>C (n.763-1013T>C) c.568-1013T>C (n.568-1013T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276369_55276373del | CA2497154674 | HCRTR2 | c.763-1011_763-1007del (n.763-1011_763-1007del) c.568-1011_568-1007del (n.568-1011_568-1007del) | dbSNP |
6 | g.55276369A>G | CA2711609720 | HCRTR2 | c.763-1011A>G (n.763-1011A>G) c.568-1011A>G (n.568-1011A>G) | dbSNP |
6 | g.55276371C>A | CA826030907 | HCRTR2 | c.763-1009C>A (n.763-1009C>A) c.568-1009C>A (n.568-1009C>A) | dbSNP |
6 | g.55276372T>A | CA2711803883 | HCRTR2 | c.763-1008T>A (n.763-1008T>A) c.568-1008T>A (n.568-1008T>A) | dbSNP |
6 | g.55276373G>A | CA139610906 | HCRTR2 | c.763-1007G>A (n.763-1007G>A) c.568-1007G>A (n.568-1007G>A) | dbSNP |
6 | g.55276373G>C | CA139610907 | HCRTR2 | c.763-1007G>C (n.763-1007G>C) c.568-1007G>C (n.568-1007G>C) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276374del | CA1089240371 | HCRTR2 | c.763-1006del (n.763-1006del) c.568-1006del (n.568-1006del) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276374G>A | CA1089240375 | HCRTR2 | c.763-1006G>A (n.763-1006G>A) c.568-1006G>A (n.568-1006G>A) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276376G>T | CA1089240385 | HCRTR2 | c.763-1004G>T (n.763-1004G>T) c.568-1004G>T (n.568-1004G>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276382A>G | CA1089240386 | HCRTR2 | c.763-998A>G (n.763-998A>G) c.568-998A>G (n.568-998A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276385A>C | CA139610908 | HCRTR2 | c.763-995A>C (n.763-995A>C) c.568-995A>C (n.568-995A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276386G>T | CA139610909 | HCRTR2 | c.763-994G>T (n.763-994G>T) c.568-994G>T (n.568-994G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276389A>C | CA1089240392 | HCRTR2 | c.763-991A>C (n.763-991A>C) c.568-991A>C (n.568-991A>C) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276389A>G | CA567488251 | HCRTR2 | c.763-991A>G (n.763-991A>G) c.568-991A>G (n.568-991A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276390C>A | CA139610910 | HCRTR2 | c.763-990C>A (n.763-990C>A) c.568-990C>A (n.568-990C>A) | dbSNP |
6 | g.55276390C>G | CA2597583423 | HCRTR2 | c.763-990C>G (n.763-990C>G) c.568-990C>G (n.568-990C>G) | gnomAD v3 gnomAD v4 |
6 | g.55276394dup | CA2597583424 | HCRTR2 | c.763-986dup (n.763-986dup) c.568-986dup (n.568-986dup) | gnomAD v3 gnomAD v4 |
6 | g.55276394A>G | CA826030913 | HCRTR2 | c.763-986A>G (n.763-986A>G) c.568-986A>G (n.568-986A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276398A>G | CA139610911 | HCRTR2 | c.763-982A>G (n.763-982A>G) c.568-982A>G (n.568-982A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276400C>A | CA2711540673 | HCRTR2 | c.763-980C>A (n.763-980C>A) c.568-980C>A (n.568-980C>A) | dbSNP |
6 | g.55276401G>A | CA139610912 | HCRTR2 | c.763-979G>A (n.763-979G>A) c.568-979G>A (n.568-979G>A) | dbSNP |
6 | g.55276401G>T | CA826030918 | HCRTR2 | c.763-979G>T (n.763-979G>T) c.568-979G>T (n.568-979G>T) | dbSNP |
6 | g.55276403del | CA2497154675 | HCRTR2 | c.763-977del (n.763-977del) c.568-977del (n.568-977del) | dbSNP |
6 | g.55276403A>G | CA1089240395 | HCRTR2 | c.763-977A>G (n.763-977A>G) c.568-977A>G (n.568-977A>G) | dbSNP gnomAD v3 gnomAD v4 |