Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
A |
T |
19: 43,801,629 (GRCm39) |
D632V |
probably damaging |
Het |
Acbd6 |
C |
T |
1: 155,463,205 (GRCm39) |
A135V |
probably benign |
Het |
Adam26a |
A |
T |
8: 44,022,889 (GRCm39) |
F200L |
probably benign |
Het |
Ago3 |
A |
T |
4: 126,248,843 (GRCm39) |
N569K |
probably damaging |
Het |
Ak9 |
A |
T |
10: 41,234,560 (GRCm39) |
L640F |
probably damaging |
Het |
Ampd2 |
A |
G |
3: 107,987,088 (GRCm39) |
V178A |
probably damaging |
Het |
Anapc4 |
C |
G |
5: 53,023,288 (GRCm39) |
H710D |
probably benign |
Het |
Atad2 |
T |
C |
15: 57,969,055 (GRCm39) |
I495V |
probably benign |
Het |
Bhmt2 |
T |
C |
13: 93,799,705 (GRCm39) |
T244A |
probably benign |
Het |
Capg |
T |
C |
6: 72,532,483 (GRCm39) |
V16A |
probably benign |
Het |
Capn13 |
A |
G |
17: 73,637,997 (GRCm39) |
F469L |
possibly damaging |
Het |
Ccdc149 |
C |
T |
5: 52,533,877 (GRCm39) |
V430I |
probably benign |
Het |
Cma1 |
A |
C |
14: 56,181,226 (GRCm39) |
Y47D |
probably benign |
Het |
Col6a3 |
A |
T |
1: 90,739,163 (GRCm39) |
L355Q |
probably damaging |
Het |
Cripto |
C |
A |
9: 110,773,281 (GRCm39) |
R18L |
unknown |
Het |
Crocc |
G |
T |
4: 140,745,229 (GRCm39) |
T1796K |
possibly damaging |
Het |
Cyp2c50 |
A |
T |
19: 40,079,387 (GRCm39) |
|
probably null |
Het |
Dsp |
T |
C |
13: 38,378,934 (GRCm39) |
I1294T |
possibly damaging |
Het |
Erbin |
A |
T |
13: 103,966,700 (GRCm39) |
F1250Y |
probably benign |
Het |
Fbn1 |
A |
C |
2: 125,200,802 (GRCm39) |
C1298W |
probably damaging |
Het |
Fbn2 |
A |
C |
18: 58,177,328 (GRCm39) |
F1990V |
probably damaging |
Het |
Fez2 |
A |
T |
17: 78,694,472 (GRCm39) |
V306D |
probably damaging |
Het |
Gigyf1 |
G |
A |
5: 137,521,769 (GRCm39) |
|
probably null |
Het |
Gjb4 |
A |
T |
4: 127,245,745 (GRCm39) |
Y65* |
probably null |
Het |
Gm26661 |
G |
A |
14: 7,791,776 (GRCm38) |
A64T |
unknown |
Het |
Igkv1-135 |
T |
C |
6: 67,587,263 (GRCm39) |
S45P |
possibly damaging |
Het |
Il27 |
T |
C |
7: 126,194,070 (GRCm39) |
T5A |
probably benign |
Het |
Il27ra |
T |
C |
8: 84,767,451 (GRCm39) |
D124G |
probably benign |
Het |
Itgad |
A |
G |
7: 127,788,653 (GRCm39) |
H424R |
probably benign |
Het |
Itgal |
T |
C |
7: 126,904,161 (GRCm39) |
V258A |
possibly damaging |
Het |
Kpna4 |
A |
G |
3: 68,997,134 (GRCm39) |
V351A |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,839,267 (GRCm39) |
Q747R |
probably damaging |
Het |
Map4k5 |
A |
G |
12: 69,891,164 (GRCm39) |
F168L |
probably damaging |
Het |
Mecom |
A |
G |
3: 30,015,195 (GRCm39) |
Y843H |
probably damaging |
Het |
Mical3 |
T |
C |
6: 121,010,711 (GRCm39) |
M424V |
probably damaging |
Het |
Mtrfr |
G |
T |
5: 124,478,837 (GRCm39) |
E153* |
probably null |
Het |
Myb |
A |
G |
10: 21,028,398 (GRCm39) |
I155T |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,588,404 (GRCm39) |
V2445E |
probably benign |
Het |
Nlrp1b |
A |
T |
11: 71,108,691 (GRCm39) |
I270N |
probably damaging |
Het |
Nlrp4f |
A |
T |
13: 65,342,895 (GRCm39) |
M250K |
probably benign |
Het |
Or13c7 |
T |
A |
4: 43,854,898 (GRCm39) |
N196K |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or52w1 |
C |
T |
7: 105,017,776 (GRCm39) |
A72V |
probably damaging |
Het |
P4ha1 |
A |
G |
10: 59,178,618 (GRCm39) |
S96G |
probably benign |
Het |
Pcnt |
G |
T |
10: 76,247,456 (GRCm39) |
N1025K |
possibly damaging |
Het |
Pgap4 |
T |
C |
4: 49,586,613 (GRCm39) |
E185G |
probably damaging |
Het |
Phactr4 |
A |
G |
4: 132,114,220 (GRCm39) |
F58S |
probably damaging |
Het |
Phlpp1 |
T |
A |
1: 106,291,960 (GRCm39) |
|
probably null |
Het |
Rab40c |
A |
C |
17: 26,103,631 (GRCm39) |
V144G |
probably damaging |
Het |
Rnasel |
A |
G |
1: 153,630,146 (GRCm39) |
I221V |
probably benign |
Het |
Rps6kb1 |
T |
C |
11: 86,404,431 (GRCm39) |
K241E |
probably damaging |
Het |
Rrbp1 |
C |
G |
2: 143,791,597 (GRCm39) |
E1370Q |
probably benign |
Het |
Rttn |
T |
C |
18: 89,139,133 (GRCm39) |
Y2111H |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,843,152 (GRCm39) |
H364R |
probably damaging |
Het |
Scnm1 |
T |
C |
3: 95,037,596 (GRCm39) |
I157V |
probably benign |
Het |
Setdb1 |
A |
G |
3: 95,246,153 (GRCm39) |
Y590H |
probably damaging |
Het |
Shkbp1 |
T |
C |
7: 27,041,949 (GRCm39) |
N635S |
probably benign |
Het |
Usp48 |
A |
G |
4: 137,343,129 (GRCm39) |
N426S |
probably benign |
Het |
Vmn2r16 |
G |
A |
5: 109,511,613 (GRCm39) |
V607M |
possibly damaging |
Het |
Xdh |
A |
T |
17: 74,205,315 (GRCm39) |
V1050D |
probably damaging |
Het |
Zfp110 |
C |
T |
7: 12,582,672 (GRCm39) |
T440I |
possibly 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 |
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 |
|
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 |
|