Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AB124611 |
C |
A |
9: 21,447,276 (GRCm39) |
T146K |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,599,958 (GRCm39) |
S1595T |
possibly damaging |
Het |
Ankrd44 |
A |
T |
1: 54,831,635 (GRCm39) |
I56N |
probably damaging |
Het |
Anln |
C |
A |
9: 22,272,176 (GRCm39) |
V648F |
probably damaging |
Het |
Arhgap29 |
A |
G |
3: 121,807,981 (GRCm39) |
D1053G |
probably benign |
Het |
Baalc |
T |
C |
15: 38,797,412 (GRCm39) |
S68P |
probably benign |
Het |
Begain |
T |
C |
12: 109,004,856 (GRCm39) |
D52G |
probably damaging |
Het |
Blmh |
A |
G |
11: 76,837,040 (GRCm39) |
I41V |
probably benign |
Het |
Bpifc |
T |
A |
10: 85,812,114 (GRCm39) |
I365F |
possibly damaging |
Het |
C2 |
G |
T |
17: 35,095,347 (GRCm39) |
S199R |
possibly damaging |
Het |
Ccbe1 |
T |
A |
18: 66,199,828 (GRCm39) |
H298L |
probably damaging |
Het |
Ccdc112 |
T |
A |
18: 46,423,826 (GRCm39) |
K304I |
probably damaging |
Het |
Ccdc15 |
T |
C |
9: 37,226,678 (GRCm39) |
E432G |
probably benign |
Het |
Cdh13 |
T |
A |
8: 119,010,594 (GRCm39) |
M1K |
probably null |
Het |
Cipc |
T |
C |
12: 87,008,899 (GRCm39) |
S253P |
possibly damaging |
Het |
Clcn1 |
A |
G |
6: 42,287,282 (GRCm39) |
|
probably null |
Het |
Clock |
A |
T |
5: 76,390,982 (GRCm39) |
N273K |
probably benign |
Het |
Cyp19a1 |
T |
C |
9: 54,074,126 (GRCm39) |
D476G |
probably benign |
Het |
Dnaaf9 |
T |
C |
2: 130,552,785 (GRCm39) |
K1092E |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,253,527 (GRCm39) |
I1811V |
probably benign |
Het |
Fat1 |
C |
A |
8: 45,495,010 (GRCm39) |
T4091K |
probably damaging |
Het |
Gm10340 |
T |
A |
14: 14,826,724 (GRCm39) |
N64K |
probably damaging |
Het |
Hectd1 |
G |
A |
12: 51,792,171 (GRCm39) |
R2523C |
probably damaging |
Het |
Hgf |
A |
G |
5: 16,782,009 (GRCm39) |
H244R |
probably damaging |
Het |
Hgs |
G |
T |
11: 120,370,760 (GRCm39) |
A567S |
probably damaging |
Het |
Igdcc4 |
T |
C |
9: 65,041,077 (GRCm39) |
V1036A |
probably benign |
Het |
Keg1 |
G |
A |
19: 12,691,998 (GRCm39) |
|
probably null |
Het |
Klhl8 |
A |
T |
5: 104,023,932 (GRCm39) |
L156Q |
probably damaging |
Het |
Lmln |
T |
C |
16: 32,927,501 (GRCm39) |
Y521H |
probably benign |
Het |
Lrrc7 |
A |
G |
3: 157,866,124 (GRCm39) |
S1206P |
probably damaging |
Het |
Mad1l1 |
T |
A |
5: 140,074,541 (GRCm39) |
I550F |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,971,753 (GRCm39) |
W28* |
probably null |
Het |
Mfsd11 |
T |
G |
11: 116,754,733 (GRCm39) |
S215A |
probably benign |
Het |
Mpped2 |
C |
A |
2: 106,575,085 (GRCm39) |
H57N |
possibly damaging |
Het |
Mslnl |
A |
G |
17: 25,965,751 (GRCm39) |
M542V |
probably benign |
Het |
Myh6 |
G |
T |
14: 55,179,897 (GRCm39) |
H1903Q |
probably damaging |
Het |
Neo1 |
T |
C |
9: 58,897,777 (GRCm39) |
T60A |
probably benign |
Het |
Npm2 |
T |
A |
14: 70,889,947 (GRCm39) |
|
probably null |
Het |
Or5b123 |
C |
A |
19: 13,597,285 (GRCm39) |
T210K |
probably damaging |
Het |
Or5d20-ps1 |
T |
C |
2: 87,931,909 (GRCm39) |
S141G |
probably benign |
Het |
Or7a39 |
T |
A |
10: 78,715,043 (GRCm39) |
S12R |
probably benign |
Het |
Pax9 |
A |
T |
12: 56,743,850 (GRCm39) |
I166F |
possibly damaging |
Het |
Pcsk9 |
A |
G |
4: 106,321,092 (GRCm39) |
S6P |
possibly damaging |
Het |
Pikfyve |
A |
G |
1: 65,309,101 (GRCm39) |
Y1893C |
probably damaging |
Het |
Pirb |
T |
C |
7: 3,722,864 (GRCm39) |
T43A |
possibly damaging |
Het |
Pou3f1 |
A |
G |
4: 124,552,074 (GRCm39) |
D192G |
possibly damaging |
Het |
Pus3 |
C |
G |
9: 35,478,021 (GRCm39) |
R418G |
probably damaging |
Het |
Rexo1 |
C |
T |
10: 80,385,970 (GRCm39) |
V363I |
probably benign |
Het |
Sdcbp |
A |
G |
4: 6,393,688 (GRCm39) |
T269A |
probably damaging |
Het |
Sele |
T |
C |
1: 163,881,462 (GRCm39) |
V523A |
probably benign |
Het |
Serpinb8 |
T |
A |
1: 107,532,457 (GRCm39) |
M183K |
probably damaging |
Het |
Sh2d4a |
T |
G |
8: 68,735,033 (GRCm39) |
S51A |
probably benign |
Het |
Siglec15 |
A |
G |
18: 78,090,696 (GRCm39) |
S201P |
probably damaging |
Het |
Slc10a5 |
C |
T |
3: 10,400,529 (GRCm39) |
V44I |
probably benign |
Het |
Slc16a13 |
A |
G |
11: 70,111,388 (GRCm39) |
V39A |
probably damaging |
Het |
Slc25a13 |
G |
A |
6: 6,117,164 (GRCm39) |
R184W |
probably damaging |
Het |
Slc35f5 |
T |
A |
1: 125,512,278 (GRCm39) |
D359E |
probably damaging |
Het |
Slc3a1 |
A |
G |
17: 85,371,371 (GRCm39) |
E641G |
probably benign |
Het |
Slf1 |
T |
C |
13: 77,194,823 (GRCm39) |
D834G |
probably damaging |
Het |
Spata31f1e |
A |
C |
4: 42,793,885 (GRCm39) |
H82Q |
probably benign |
Het |
Stim1 |
T |
C |
7: 102,076,348 (GRCm39) |
I433T |
probably damaging |
Het |
Stra6 |
T |
A |
9: 58,057,444 (GRCm39) |
I418K |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,758,480 (GRCm39) |
N747S |
probably benign |
Het |
Tet2 |
T |
C |
3: 133,192,302 (GRCm39) |
T711A |
possibly damaging |
Het |
Ttc41 |
T |
A |
10: 86,612,495 (GRCm39) |
I1256N |
probably benign |
Het |
Uba2 |
T |
C |
7: 33,862,638 (GRCm39) |
D100G |
possibly damaging |
Het |
Vmn1r43 |
A |
G |
6: 89,847,219 (GRCm39) |
I89T |
probably benign |
Het |
Vmn2r58 |
T |
A |
7: 41,521,910 (GRCm39) |
Y62F |
probably benign |
Het |
Ylpm1 |
C |
T |
12: 85,060,855 (GRCm39) |
Q428* |
probably null |
Het |
Zcrb1 |
T |
C |
15: 93,289,002 (GRCm39) |
D88G |
probably damaging |
Het |
Zmym1 |
A |
C |
4: 126,941,667 (GRCm39) |
I907S |
probably damaging |
Het |
|
Other mutations in Trpm6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00540:Trpm6
|
APN |
19 |
18,761,272 (GRCm39) |
splice site |
probably benign |
|
IGL00862:Trpm6
|
APN |
19 |
18,804,892 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01348:Trpm6
|
APN |
19 |
18,855,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01400:Trpm6
|
APN |
19 |
18,803,158 (GRCm39) |
nonsense |
probably null |
|
IGL01451:Trpm6
|
APN |
19 |
18,786,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01508:Trpm6
|
APN |
19 |
18,773,894 (GRCm39) |
nonsense |
probably null |
|
IGL01995:Trpm6
|
APN |
19 |
18,807,691 (GRCm39) |
splice site |
probably benign |
|
IGL02092:Trpm6
|
APN |
19 |
18,749,695 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02152:Trpm6
|
APN |
19 |
18,809,903 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02294:Trpm6
|
APN |
19 |
18,831,427 (GRCm39) |
missense |
probably benign |
|
IGL02329:Trpm6
|
APN |
19 |
18,831,581 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02366:Trpm6
|
APN |
19 |
18,755,874 (GRCm39) |
splice site |
probably benign |
|
IGL02402:Trpm6
|
APN |
19 |
18,764,120 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02457:Trpm6
|
APN |
19 |
18,804,762 (GRCm39) |
nonsense |
probably null |
|
IGL02457:Trpm6
|
APN |
19 |
18,803,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02684:Trpm6
|
APN |
19 |
18,779,571 (GRCm39) |
splice site |
probably benign |
|
IGL02705:Trpm6
|
APN |
19 |
18,754,097 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02728:Trpm6
|
APN |
19 |
18,787,016 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02742:Trpm6
|
APN |
19 |
18,807,376 (GRCm39) |
splice site |
probably benign |
|
IGL02818:Trpm6
|
APN |
19 |
18,843,621 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02836:Trpm6
|
APN |
19 |
18,790,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03119:Trpm6
|
APN |
19 |
18,815,381 (GRCm39) |
nonsense |
probably null |
|
IGL03193:Trpm6
|
APN |
19 |
18,803,236 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03227:Trpm6
|
APN |
19 |
18,764,143 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03227:Trpm6
|
APN |
19 |
18,796,483 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03231:Trpm6
|
APN |
19 |
18,796,545 (GRCm39) |
missense |
probably benign |
|
IGL03245:Trpm6
|
APN |
19 |
18,855,065 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Trpm6
|
APN |
19 |
18,815,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03341:Trpm6
|
APN |
19 |
18,790,850 (GRCm39) |
missense |
probably benign |
|
P0043:Trpm6
|
UTSW |
19 |
18,855,129 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4260001:Trpm6
|
UTSW |
19 |
18,803,166 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0057:Trpm6
|
UTSW |
19 |
18,764,119 (GRCm39) |
missense |
probably benign |
0.05 |
R0115:Trpm6
|
UTSW |
19 |
18,807,316 (GRCm39) |
missense |
probably damaging |
0.98 |
R0119:Trpm6
|
UTSW |
19 |
18,809,957 (GRCm39) |
missense |
probably benign |
0.05 |
R0140:Trpm6
|
UTSW |
19 |
18,796,558 (GRCm39) |
splice site |
probably null |
|
R0267:Trpm6
|
UTSW |
19 |
18,800,742 (GRCm39) |
missense |
probably benign |
|
R0350:Trpm6
|
UTSW |
19 |
18,861,321 (GRCm39) |
splice site |
probably null |
|
R0373:Trpm6
|
UTSW |
19 |
18,830,951 (GRCm39) |
missense |
probably benign |
0.15 |
R0393:Trpm6
|
UTSW |
19 |
18,756,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R0416:Trpm6
|
UTSW |
19 |
18,760,389 (GRCm39) |
splice site |
probably benign |
|
R0505:Trpm6
|
UTSW |
19 |
18,851,266 (GRCm39) |
splice site |
probably benign |
|
R0526:Trpm6
|
UTSW |
19 |
18,770,240 (GRCm39) |
missense |
probably damaging |
0.97 |
R0607:Trpm6
|
UTSW |
19 |
18,849,585 (GRCm39) |
missense |
probably benign |
0.00 |
R0609:Trpm6
|
UTSW |
19 |
18,803,226 (GRCm39) |
missense |
probably damaging |
0.97 |
R0714:Trpm6
|
UTSW |
19 |
18,815,451 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1215:Trpm6
|
UTSW |
19 |
18,773,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Trpm6
|
UTSW |
19 |
18,773,859 (GRCm39) |
missense |
probably benign |
0.28 |
R1512:Trpm6
|
UTSW |
19 |
18,853,295 (GRCm39) |
missense |
probably benign |
|
R1558:Trpm6
|
UTSW |
19 |
18,764,192 (GRCm39) |
missense |
probably benign |
0.04 |
R1597:Trpm6
|
UTSW |
19 |
18,804,888 (GRCm39) |
missense |
probably damaging |
0.98 |
R1618:Trpm6
|
UTSW |
19 |
18,854,995 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1779:Trpm6
|
UTSW |
19 |
18,833,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Trpm6
|
UTSW |
19 |
18,804,931 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1799:Trpm6
|
UTSW |
19 |
18,869,363 (GRCm39) |
splice site |
probably null |
|
R1840:Trpm6
|
UTSW |
19 |
18,843,631 (GRCm39) |
missense |
probably benign |
0.21 |
R1991:Trpm6
|
UTSW |
19 |
18,773,648 (GRCm39) |
missense |
probably benign |
0.00 |
R2030:Trpm6
|
UTSW |
19 |
18,831,629 (GRCm39) |
missense |
probably benign |
|
R2073:Trpm6
|
UTSW |
19 |
18,853,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Trpm6
|
UTSW |
19 |
18,855,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R2096:Trpm6
|
UTSW |
19 |
18,803,116 (GRCm39) |
missense |
probably damaging |
0.97 |
R2103:Trpm6
|
UTSW |
19 |
18,773,648 (GRCm39) |
missense |
probably benign |
0.00 |
R2106:Trpm6
|
UTSW |
19 |
18,790,714 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2117:Trpm6
|
UTSW |
19 |
18,807,316 (GRCm39) |
missense |
probably damaging |
0.98 |
R2850:Trpm6
|
UTSW |
19 |
18,769,454 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3125:Trpm6
|
UTSW |
19 |
18,831,795 (GRCm39) |
missense |
probably benign |
0.05 |
R3719:Trpm6
|
UTSW |
19 |
18,749,757 (GRCm39) |
nonsense |
probably null |
|
R3779:Trpm6
|
UTSW |
19 |
18,853,403 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4115:Trpm6
|
UTSW |
19 |
18,809,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4367:Trpm6
|
UTSW |
19 |
18,804,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R4523:Trpm6
|
UTSW |
19 |
18,773,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Trpm6
|
UTSW |
19 |
18,809,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4564:Trpm6
|
UTSW |
19 |
18,809,961 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4565:Trpm6
|
UTSW |
19 |
18,803,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Trpm6
|
UTSW |
19 |
18,831,155 (GRCm39) |
missense |
probably benign |
0.01 |
R4714:Trpm6
|
UTSW |
19 |
18,831,564 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4750:Trpm6
|
UTSW |
19 |
18,853,428 (GRCm39) |
missense |
probably damaging |
0.99 |
R4771:Trpm6
|
UTSW |
19 |
18,790,857 (GRCm39) |
missense |
probably damaging |
0.97 |
R4791:Trpm6
|
UTSW |
19 |
18,845,345 (GRCm39) |
missense |
probably benign |
0.00 |
R4814:Trpm6
|
UTSW |
19 |
18,839,576 (GRCm39) |
missense |
probably benign |
0.11 |
R5028:Trpm6
|
UTSW |
19 |
18,764,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Trpm6
|
UTSW |
19 |
18,790,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Trpm6
|
UTSW |
19 |
18,807,297 (GRCm39) |
missense |
probably damaging |
0.96 |
R5642:Trpm6
|
UTSW |
19 |
18,807,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Trpm6
|
UTSW |
19 |
18,830,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Trpm6
|
UTSW |
19 |
18,830,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R5832:Trpm6
|
UTSW |
19 |
18,764,183 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5843:Trpm6
|
UTSW |
19 |
18,833,539 (GRCm39) |
missense |
probably benign |
0.04 |
R5955:Trpm6
|
UTSW |
19 |
18,869,383 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6101:Trpm6
|
UTSW |
19 |
18,831,112 (GRCm39) |
nonsense |
probably null |
|
R6105:Trpm6
|
UTSW |
19 |
18,831,112 (GRCm39) |
nonsense |
probably null |
|
R6211:Trpm6
|
UTSW |
19 |
18,760,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6228:Trpm6
|
UTSW |
19 |
18,831,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Trpm6
|
UTSW |
19 |
18,831,472 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6453:Trpm6
|
UTSW |
19 |
18,807,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R6562:Trpm6
|
UTSW |
19 |
18,815,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6624:Trpm6
|
UTSW |
19 |
18,866,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6624:Trpm6
|
UTSW |
19 |
18,773,803 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6729:Trpm6
|
UTSW |
19 |
18,807,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R6765:Trpm6
|
UTSW |
19 |
18,855,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R6976:Trpm6
|
UTSW |
19 |
18,760,527 (GRCm39) |
missense |
probably benign |
|
R7103:Trpm6
|
UTSW |
19 |
18,790,911 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7126:Trpm6
|
UTSW |
19 |
18,831,397 (GRCm39) |
nonsense |
probably null |
|
R7128:Trpm6
|
UTSW |
19 |
18,789,137 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7157:Trpm6
|
UTSW |
19 |
18,815,462 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7212:Trpm6
|
UTSW |
19 |
18,831,155 (GRCm39) |
missense |
probably benign |
0.01 |
R7263:Trpm6
|
UTSW |
19 |
18,854,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Trpm6
|
UTSW |
19 |
18,755,949 (GRCm39) |
missense |
probably benign |
0.13 |
R7305:Trpm6
|
UTSW |
19 |
18,853,455 (GRCm39) |
missense |
probably benign |
0.30 |
R7498:Trpm6
|
UTSW |
19 |
18,853,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Trpm6
|
UTSW |
19 |
18,756,029 (GRCm39) |
missense |
probably damaging |
0.96 |
R7590:Trpm6
|
UTSW |
19 |
18,809,945 (GRCm39) |
missense |
probably benign |
0.31 |
R7646:Trpm6
|
UTSW |
19 |
18,845,325 (GRCm39) |
missense |
probably benign |
0.10 |
R7650:Trpm6
|
UTSW |
19 |
18,853,377 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7727:Trpm6
|
UTSW |
19 |
18,831,613 (GRCm39) |
missense |
probably damaging |
0.97 |
R7743:Trpm6
|
UTSW |
19 |
18,804,772 (GRCm39) |
missense |
probably benign |
0.03 |
R7747:Trpm6
|
UTSW |
19 |
18,727,409 (GRCm39) |
splice site |
probably null |
|
R7870:Trpm6
|
UTSW |
19 |
18,792,605 (GRCm39) |
missense |
probably benign |
0.01 |
R7891:Trpm6
|
UTSW |
19 |
18,754,074 (GRCm39) |
missense |
probably benign |
0.01 |
R7955:Trpm6
|
UTSW |
19 |
18,831,654 (GRCm39) |
missense |
probably benign |
0.01 |
R7965:Trpm6
|
UTSW |
19 |
18,853,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7967:Trpm6
|
UTSW |
19 |
18,756,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R7992:Trpm6
|
UTSW |
19 |
18,792,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8035:Trpm6
|
UTSW |
19 |
18,770,226 (GRCm39) |
missense |
probably damaging |
0.97 |
R8108:Trpm6
|
UTSW |
19 |
18,789,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R8268:Trpm6
|
UTSW |
19 |
18,851,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8411:Trpm6
|
UTSW |
19 |
18,831,332 (GRCm39) |
missense |
probably benign |
0.39 |
R8413:Trpm6
|
UTSW |
19 |
18,809,849 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Trpm6
|
UTSW |
19 |
18,869,459 (GRCm39) |
missense |
probably benign |
0.00 |
R8932:Trpm6
|
UTSW |
19 |
18,815,366 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8990:Trpm6
|
UTSW |
19 |
18,792,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R9403:Trpm6
|
UTSW |
19 |
18,810,016 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9446:Trpm6
|
UTSW |
19 |
18,815,462 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9463:Trpm6
|
UTSW |
19 |
18,761,264 (GRCm39) |
critical splice donor site |
probably null |
|
R9485:Trpm6
|
UTSW |
19 |
18,755,978 (GRCm39) |
missense |
probably benign |
0.06 |
R9536:Trpm6
|
UTSW |
19 |
18,764,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R9549:Trpm6
|
UTSW |
19 |
18,853,394 (GRCm39) |
nonsense |
probably null |
|
R9564:Trpm6
|
UTSW |
19 |
18,851,240 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9626:Trpm6
|
UTSW |
19 |
18,790,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Trpm6
|
UTSW |
19 |
18,869,466 (GRCm39) |
missense |
probably benign |
|
R9721:Trpm6
|
UTSW |
19 |
18,807,336 (GRCm39) |
missense |
probably benign |
0.12 |
R9742:Trpm6
|
UTSW |
19 |
18,800,766 (GRCm39) |
missense |
probably benign |
0.09 |
|