Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
C |
A |
11: 109,960,635 (GRCm39) |
A628S |
probably damaging |
Het |
Abca9 |
T |
C |
11: 110,036,405 (GRCm39) |
N568S |
probably damaging |
Het |
Ada |
C |
T |
2: 163,574,814 (GRCm39) |
A108T |
possibly damaging |
Het |
Adam6a |
T |
A |
12: 113,508,069 (GRCm39) |
D147E |
possibly damaging |
Het |
Ampd1 |
A |
T |
3: 103,006,154 (GRCm39) |
T655S |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,327,139 (GRCm39) |
F680S |
probably damaging |
Het |
Asap1 |
G |
A |
15: 63,991,869 (GRCm39) |
T783I |
probably benign |
Het |
Astn1 |
T |
A |
1: 158,329,923 (GRCm39) |
N259K |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,886,673 (GRCm39) |
V667A |
probably damaging |
Het |
Brat1 |
G |
A |
5: 140,698,382 (GRCm39) |
V185I |
probably benign |
Het |
Btnl6 |
T |
C |
17: 34,732,620 (GRCm39) |
Y318C |
probably damaging |
Het |
Caskin2 |
G |
A |
11: 115,694,522 (GRCm39) |
P360S |
probably benign |
Het |
Ccdc121rt3 |
T |
C |
5: 112,503,642 (GRCm39) |
T21A |
probably benign |
Het |
Cd68 |
T |
A |
11: 69,555,754 (GRCm39) |
|
probably benign |
Het |
Cdca2 |
T |
C |
14: 67,952,355 (GRCm39) |
|
probably benign |
Het |
Cdk6 |
G |
A |
5: 3,523,217 (GRCm39) |
M212I |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,481,159 (GRCm39) |
F302Y |
probably damaging |
Het |
Celsr2 |
T |
C |
3: 108,301,055 (GRCm39) |
E2746G |
possibly damaging |
Het |
Clec4a4 |
G |
A |
6: 122,989,703 (GRCm39) |
V115I |
probably benign |
Het |
Clip3 |
C |
A |
7: 29,998,307 (GRCm39) |
A251E |
possibly damaging |
Het |
Cmah |
T |
C |
13: 24,623,180 (GRCm39) |
L350P |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,370,103 (GRCm39) |
R907* |
probably null |
Het |
Cntnap5b |
T |
C |
1: 99,999,814 (GRCm39) |
Y191H |
probably benign |
Het |
Col4a4 |
A |
T |
1: 82,458,207 (GRCm39) |
C1122* |
probably null |
Het |
Coq5 |
A |
G |
5: 115,433,842 (GRCm39) |
|
probably benign |
Het |
Cpxcr1 |
A |
G |
X: 115,387,136 (GRCm39) |
K16E |
possibly damaging |
Het |
Dclk3 |
T |
C |
9: 111,298,304 (GRCm39) |
I616T |
probably benign |
Het |
Dhrs3 |
A |
T |
4: 144,646,057 (GRCm39) |
T122S |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,210,596 (GRCm39) |
I502V |
probably benign |
Het |
Dscaml1 |
G |
T |
9: 45,596,519 (GRCm39) |
G788W |
probably damaging |
Het |
Dusp10 |
C |
T |
1: 183,769,645 (GRCm39) |
|
probably null |
Het |
Ehbp1l1 |
C |
A |
19: 5,769,112 (GRCm39) |
L730F |
possibly damaging |
Het |
Eif2ak1 |
C |
T |
5: 143,808,785 (GRCm39) |
H75Y |
probably damaging |
Het |
Evi2a |
T |
C |
11: 79,418,398 (GRCm39) |
T71A |
probably benign |
Het |
Fam184a |
A |
T |
10: 53,511,461 (GRCm39) |
S1073T |
probably damaging |
Het |
Fam227a |
T |
C |
15: 79,499,582 (GRCm39) |
Y591C |
probably damaging |
Het |
Fam83a |
C |
T |
15: 57,873,272 (GRCm39) |
T367M |
probably benign |
Het |
Fam83g |
A |
G |
11: 61,593,819 (GRCm39) |
D451G |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,203,185 (GRCm39) |
F1213L |
possibly damaging |
Het |
Fcgbp |
G |
A |
7: 27,791,273 (GRCm39) |
V845I |
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,766,942 (GRCm39) |
E342K |
probably benign |
Het |
Foxn1 |
T |
A |
11: 78,251,933 (GRCm39) |
M433L |
probably benign |
Het |
Gm6632 |
T |
G |
5: 59,211,679 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
A |
T |
14: 30,738,418 (GRCm39) |
|
probably benign |
Het |
Hhipl1 |
C |
T |
12: 108,277,996 (GRCm39) |
T108I |
probably damaging |
Het |
Hs2st1 |
A |
T |
3: 144,141,256 (GRCm39) |
F271I |
possibly damaging |
Het |
Ido1 |
T |
C |
8: 25,074,462 (GRCm39) |
S303G |
probably damaging |
Het |
Ints2 |
C |
T |
11: 86,117,607 (GRCm39) |
R705H |
probably damaging |
Het |
Kcnc2 |
A |
G |
10: 112,292,305 (GRCm39) |
K49E |
probably damaging |
Het |
Kif3b |
T |
A |
2: 153,162,235 (GRCm39) |
V482E |
probably damaging |
Het |
Ldlrad2 |
G |
A |
4: 137,299,525 (GRCm39) |
P100S |
probably benign |
Het |
Lrba |
G |
T |
3: 86,687,573 (GRCm39) |
|
probably benign |
Het |
Lsm11 |
A |
T |
11: 45,824,730 (GRCm39) |
W266R |
probably benign |
Het |
Mob3a |
A |
T |
10: 80,522,988 (GRCm39) |
M215K |
probably benign |
Het |
Mterf1b |
T |
G |
5: 4,247,163 (GRCm39) |
L268R |
probably damaging |
Het |
Mvk |
T |
C |
5: 114,598,157 (GRCm39) |
F365L |
probably damaging |
Het |
Myo16 |
T |
A |
8: 10,552,796 (GRCm39) |
F945I |
probably damaging |
Het |
Myo1f |
G |
T |
17: 33,813,001 (GRCm39) |
K602N |
possibly damaging |
Het |
Nr2c2ap |
A |
T |
8: 70,585,765 (GRCm39) |
M108L |
probably benign |
Het |
Ofcc1 |
C |
T |
13: 40,362,305 (GRCm39) |
G206R |
probably benign |
Het |
Ogfrl1 |
A |
G |
1: 23,414,890 (GRCm39) |
F206L |
probably damaging |
Het |
Ola1 |
A |
T |
2: 72,987,188 (GRCm39) |
I148N |
probably damaging |
Het |
Or14c46 |
G |
T |
7: 85,918,270 (GRCm39) |
H242Q |
probably damaging |
Het |
Or4d10b |
T |
A |
19: 12,036,844 (GRCm39) |
T91S |
probably benign |
Het |
Or51f1d |
A |
G |
7: 102,701,288 (GRCm39) |
Y261C |
probably damaging |
Het |
Or6c2 |
A |
T |
10: 129,362,824 (GRCm39) |
M243L |
probably benign |
Het |
Or9m2 |
A |
G |
2: 87,821,334 (GRCm39) |
N293S |
probably damaging |
Het |
Otof |
A |
G |
5: 30,536,876 (GRCm39) |
|
probably null |
Het |
Pah |
G |
T |
10: 87,414,175 (GRCm39) |
K341N |
probably damaging |
Het |
Pfdn5 |
T |
A |
15: 102,236,946 (GRCm39) |
|
probably null |
Het |
Piezo2 |
A |
G |
18: 63,216,202 (GRCm39) |
C960R |
probably damaging |
Het |
Pitx2 |
T |
C |
3: 129,012,488 (GRCm39) |
V306A |
probably damaging |
Het |
Pkd1l2 |
C |
A |
8: 117,792,236 (GRCm39) |
|
probably benign |
Het |
Plekho1 |
T |
C |
3: 95,896,878 (GRCm39) |
E197G |
probably damaging |
Het |
Polr2i |
A |
G |
7: 29,932,227 (GRCm39) |
N34S |
probably damaging |
Het |
Psph |
A |
T |
5: 129,848,614 (GRCm39) |
D22E |
probably damaging |
Het |
Ptprs |
C |
A |
17: 56,731,128 (GRCm39) |
A687S |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,788,265 (GRCm39) |
K606R |
probably benign |
Het |
Rigi |
A |
G |
4: 40,208,868 (GRCm39) |
V703A |
possibly damaging |
Het |
Rims1 |
A |
G |
1: 22,577,362 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
C |
T |
11: 119,328,576 (GRCm39) |
P2002L |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,740,307 (GRCm39) |
C555S |
probably damaging |
Het |
Sftpd |
C |
A |
14: 40,894,384 (GRCm39) |
G345V |
probably damaging |
Het |
Slc41a1 |
T |
A |
1: 131,774,319 (GRCm39) |
M462K |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,264,990 (GRCm39) |
E676G |
probably damaging |
Het |
Sox6 |
T |
A |
7: 115,300,926 (GRCm39) |
|
probably benign |
Het |
Spdye4b |
G |
A |
5: 143,181,472 (GRCm39) |
R109Q |
probably damaging |
Het |
Spef1l |
C |
A |
7: 139,556,555 (GRCm39) |
R144L |
probably benign |
Het |
Spink8 |
A |
T |
9: 109,649,706 (GRCm39) |
I63L |
probably damaging |
Het |
St3gal3 |
A |
G |
4: 117,871,983 (GRCm39) |
L73P |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,871,818 (GRCm39) |
L1247P |
probably benign |
Het |
Tat |
A |
G |
8: 110,718,195 (GRCm39) |
R27G |
probably benign |
Het |
Tcerg1l |
C |
T |
7: 137,881,804 (GRCm39) |
R295H |
probably damaging |
Het |
Tfrc |
T |
C |
16: 32,445,467 (GRCm39) |
V596A |
probably damaging |
Het |
Tgfb3 |
C |
T |
12: 86,116,120 (GRCm39) |
|
probably null |
Het |
Tmed5 |
A |
T |
5: 108,280,248 (GRCm39) |
S15T |
probably benign |
Het |
Tph1 |
A |
T |
7: 46,303,286 (GRCm39) |
S231T |
probably benign |
Het |
Trim30d |
G |
A |
7: 104,121,701 (GRCm39) |
S198L |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,612,589 (GRCm39) |
D15417E |
probably benign |
Het |
U2surp |
A |
G |
9: 95,375,251 (GRCm39) |
I157T |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,156,890 (GRCm39) |
D2305G |
probably damaging |
Het |
Uvssa |
A |
G |
5: 33,546,165 (GRCm39) |
K179E |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,359,436 (GRCm39) |
F230S |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,355,411 (GRCm39) |
K3391E |
probably benign |
Het |
Xpo7 |
T |
A |
14: 70,936,473 (GRCm39) |
H170L |
probably benign |
Het |
Zrsr2-ps1 |
T |
C |
11: 22,924,404 (GRCm39) |
W393R |
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 |
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 |
|
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 |
|