Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
C |
A |
3: 121,847,843 (GRCm39) |
H55N |
probably damaging |
Het |
Acan |
G |
T |
7: 78,742,066 (GRCm39) |
V488L |
probably damaging |
Het |
Adam12 |
T |
C |
7: 133,521,240 (GRCm39) |
E638G |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,220,772 (GRCm39) |
Q1387L |
possibly damaging |
Het |
Adamts3 |
G |
T |
5: 89,825,601 (GRCm39) |
D1079E |
probably benign |
Het |
Barx1 |
G |
T |
13: 48,818,555 (GRCm39) |
G93C |
probably damaging |
Het |
Carmil2 |
C |
T |
8: 106,419,677 (GRCm39) |
R828C |
probably damaging |
Het |
Catsper4 |
TTCTC |
TTC |
4: 133,954,423 (GRCm39) |
|
probably null |
Het |
Ccdc159 |
T |
C |
9: 21,843,007 (GRCm39) |
M148T |
probably benign |
Het |
Cdk5rap1 |
T |
A |
2: 154,202,652 (GRCm39) |
N193Y |
probably benign |
Het |
Csnk1g2 |
G |
A |
10: 80,470,332 (GRCm39) |
G15D |
probably damaging |
Het |
Dach1 |
T |
C |
14: 98,406,295 (GRCm39) |
S151G |
probably benign |
Het |
Elf5 |
C |
A |
2: 103,269,645 (GRCm39) |
N75K |
probably benign |
Het |
Elp3 |
T |
C |
14: 65,802,782 (GRCm39) |
D272G |
probably damaging |
Het |
Epb41l1 |
T |
A |
2: 156,337,043 (GRCm39) |
|
probably null |
Het |
Epha6 |
A |
G |
16: 59,596,028 (GRCm39) |
Y888H |
probably damaging |
Het |
Fibcd1 |
T |
C |
2: 31,707,222 (GRCm39) |
Y345C |
probably damaging |
Het |
Gjd3 |
C |
T |
11: 102,690,963 (GRCm39) |
E347K |
possibly damaging |
Het |
Gse1 |
A |
G |
8: 121,300,910 (GRCm39) |
D892G |
unknown |
Het |
Gtpbp6 |
A |
T |
5: 110,251,915 (GRCm39) |
I506N |
probably benign |
Het |
Hivep1 |
T |
A |
13: 42,311,668 (GRCm39) |
F1303I |
possibly damaging |
Het |
Il21r |
A |
G |
7: 125,232,077 (GRCm39) |
T502A |
probably benign |
Het |
Ints1 |
T |
C |
5: 139,749,834 (GRCm39) |
T997A |
possibly damaging |
Het |
Invs |
C |
A |
4: 48,396,381 (GRCm39) |
N351K |
probably damaging |
Het |
Iqcm |
A |
G |
8: 76,489,701 (GRCm39) |
T390A |
probably benign |
Het |
Iqcn |
A |
G |
8: 71,163,425 (GRCm39) |
N873D |
possibly damaging |
Het |
Kcnh4 |
C |
T |
11: 100,632,643 (GRCm39) |
G948D |
probably benign |
Het |
Kcnh7 |
T |
A |
2: 62,566,314 (GRCm39) |
|
probably null |
Het |
Lrrc72 |
A |
G |
12: 36,258,611 (GRCm39) |
V82A |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,271,943 (GRCm39) |
L6535Q |
probably damaging |
Het |
Ncor2 |
G |
C |
5: 125,109,196 (GRCm39) |
L585V |
|
Het |
Nipal2 |
G |
C |
15: 34,578,904 (GRCm39) |
Y298* |
probably null |
Het |
Nipsnap1 |
C |
T |
11: 4,832,960 (GRCm39) |
|
probably benign |
Het |
Or12e1 |
T |
A |
2: 87,022,476 (GRCm39) |
C148* |
probably null |
Het |
Or4x12-ps1 |
T |
C |
2: 89,916,332 (GRCm39) |
I158V |
not run |
Het |
Or51g1 |
A |
T |
7: 102,633,524 (GRCm39) |
Y282* |
probably null |
Het |
Pcdhga4 |
C |
T |
18: 37,819,873 (GRCm39) |
T474I |
probably benign |
Het |
Pdp1 |
G |
T |
4: 11,960,821 (GRCm39) |
Q516K |
possibly damaging |
Het |
Pik3c2b |
C |
T |
1: 133,017,940 (GRCm39) |
P934L |
probably damaging |
Het |
Pp2d1 |
A |
G |
17: 53,822,358 (GRCm39) |
I236T |
probably benign |
Het |
Pygm |
G |
A |
19: 6,438,357 (GRCm39) |
R278H |
probably damaging |
Het |
Rb1 |
A |
T |
14: 73,520,363 (GRCm39) |
C215* |
probably null |
Het |
Rgs22 |
A |
G |
15: 36,015,789 (GRCm39) |
S1156P |
possibly damaging |
Het |
Rgs9bp |
T |
C |
7: 35,284,126 (GRCm39) |
T174A |
probably damaging |
Het |
Rnf133 |
A |
T |
6: 23,649,667 (GRCm39) |
Y130* |
probably null |
Het |
Sctr |
G |
A |
1: 119,949,955 (GRCm39) |
R48Q |
probably benign |
Het |
Serpinb6e |
A |
T |
13: 34,022,923 (GRCm39) |
F153L |
probably benign |
Het |
Slc22a1 |
A |
T |
17: 12,885,587 (GRCm39) |
Y200N |
probably damaging |
Het |
Slc22a22 |
C |
A |
15: 57,113,107 (GRCm39) |
M377I |
probably benign |
Het |
Slc36a4 |
A |
G |
9: 15,633,452 (GRCm39) |
|
probably null |
Het |
Slc39a6 |
A |
G |
18: 24,734,260 (GRCm39) |
V143A |
probably benign |
Het |
Slf2 |
G |
A |
19: 44,926,863 (GRCm39) |
|
probably null |
Het |
Sowaha |
T |
C |
11: 53,370,485 (GRCm39) |
K84E |
probably benign |
Het |
Spef2 |
T |
G |
15: 9,653,098 (GRCm39) |
|
probably null |
Het |
Sphkap |
A |
T |
1: 83,254,399 (GRCm39) |
F1117I |
probably damaging |
Het |
Tas2r113 |
T |
C |
6: 132,870,539 (GRCm39) |
I189T |
possibly damaging |
Het |
Tescl |
T |
C |
7: 24,033,247 (GRCm39) |
E26G |
possibly damaging |
Het |
Uba1y |
T |
A |
Y: 822,200 (GRCm39) |
C178S |
possibly damaging |
Het |
Ush2a |
T |
A |
1: 188,175,526 (GRCm39) |
V1208D |
possibly damaging |
Het |
Usp13 |
G |
C |
3: 32,949,000 (GRCm39) |
A446P |
probably damaging |
Het |
Usp7 |
A |
T |
16: 8,514,588 (GRCm39) |
C722S |
possibly damaging |
Het |
Vmn1r52 |
A |
G |
6: 90,156,535 (GRCm39) |
S280G |
probably benign |
Het |
Vmn2r84 |
T |
C |
10: 130,225,077 (GRCm39) |
K478E |
probably damaging |
Het |
Zfp112 |
C |
A |
7: 23,824,952 (GRCm39) |
L311I |
probably benign |
Het |
Zfp180 |
G |
T |
7: 23,805,125 (GRCm39) |
E515* |
probably null |
Het |
Zfp518b |
A |
G |
5: 38,829,671 (GRCm39) |
I778T |
probably damaging |
Het |
Zfp800 |
A |
T |
6: 28,243,662 (GRCm39) |
H434Q |
probably benign |
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 |
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 |
|
R7807:Trpm6
|
UTSW |
19 |
18,807,220 (GRCm39) |
missense |
probably benign |
0.11 |
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 |
|