Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,266,082 (GRCm39) |
|
probably benign |
Het |
Adnp |
A |
T |
2: 168,025,647 (GRCm39) |
F549L |
possibly damaging |
Het |
Agl |
A |
G |
3: 116,546,935 (GRCm39) |
I1305T |
probably benign |
Het |
Aldh8a1 |
T |
A |
10: 21,267,593 (GRCm39) |
M326K |
probably benign |
Het |
Amdhd1 |
A |
T |
10: 93,363,513 (GRCm39) |
M295K |
probably damaging |
Het |
Arhgef4 |
T |
A |
1: 34,846,191 (GRCm39) |
C324S |
probably damaging |
Het |
Car8 |
A |
T |
4: 8,238,119 (GRCm39) |
|
probably null |
Het |
Cc2d1a |
T |
C |
8: 84,867,468 (GRCm39) |
|
probably benign |
Het |
Cd81 |
G |
A |
7: 142,616,242 (GRCm39) |
V27M |
possibly damaging |
Het |
Ces1b |
A |
T |
8: 93,806,056 (GRCm39) |
S62T |
probably benign |
Het |
Cfb |
A |
G |
17: 35,077,031 (GRCm39) |
S30P |
probably damaging |
Het |
Cmtm3 |
A |
G |
8: 105,070,543 (GRCm39) |
M101V |
possibly damaging |
Het |
Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
Ddb1 |
C |
T |
19: 10,590,280 (GRCm39) |
S269L |
probably benign |
Het |
Ddx25 |
G |
A |
9: 35,465,686 (GRCm39) |
Q143* |
probably null |
Het |
Dis3l2 |
T |
A |
1: 86,971,928 (GRCm39) |
|
probably null |
Het |
Dlgap4 |
G |
T |
2: 156,587,898 (GRCm39) |
E598* |
probably null |
Het |
Dus1l |
C |
T |
11: 120,680,262 (GRCm39) |
G471D |
possibly damaging |
Het |
Elp4 |
C |
A |
2: 105,727,290 (GRCm39) |
|
probably benign |
Het |
Eya3 |
A |
G |
4: 132,417,097 (GRCm39) |
N194S |
probably benign |
Het |
Golgb1 |
G |
T |
16: 36,732,639 (GRCm39) |
V629L |
possibly damaging |
Het |
Hars2 |
G |
A |
18: 36,920,648 (GRCm39) |
A164T |
possibly damaging |
Het |
Hexb |
T |
A |
13: 97,322,135 (GRCm39) |
I217L |
probably benign |
Het |
Hgh1 |
A |
G |
15: 76,253,848 (GRCm39) |
|
probably null |
Het |
Hsd3b3 |
A |
T |
3: 98,649,757 (GRCm39) |
|
probably null |
Het |
Ighg2c |
T |
A |
12: 113,251,053 (GRCm39) |
N321Y |
unknown |
Het |
Il5 |
A |
G |
11: 53,611,763 (GRCm39) |
T34A |
probably benign |
Het |
Jph1 |
C |
A |
1: 17,074,507 (GRCm39) |
E504* |
probably null |
Het |
Kif2b |
G |
T |
11: 91,466,420 (GRCm39) |
T621K |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,556,268 (GRCm39) |
|
probably benign |
Het |
Leprotl1 |
A |
G |
8: 34,606,006 (GRCm39) |
|
probably null |
Het |
Lpar3 |
C |
T |
3: 145,946,348 (GRCm39) |
R9C |
possibly damaging |
Het |
Map1a |
A |
G |
2: 121,131,014 (GRCm39) |
E372G |
probably damaging |
Het |
Map2 |
C |
A |
1: 66,419,927 (GRCm39) |
T86K |
probably damaging |
Het |
Map7 |
A |
G |
10: 20,149,629 (GRCm39) |
|
probably null |
Het |
Mdn1 |
T |
C |
4: 32,701,713 (GRCm39) |
V1482A |
probably benign |
Het |
Mks1 |
G |
A |
11: 87,747,777 (GRCm39) |
|
probably benign |
Het |
Morf4l1 |
T |
G |
9: 89,984,403 (GRCm39) |
K102N |
probably damaging |
Het |
Mroh1 |
T |
A |
15: 76,293,138 (GRCm39) |
V304D |
possibly damaging |
Het |
Mtg1 |
G |
A |
7: 139,729,665 (GRCm39) |
V252M |
probably damaging |
Het |
Myh13 |
A |
T |
11: 67,225,427 (GRCm39) |
D264V |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,077,334 (GRCm39) |
Y823C |
possibly damaging |
Het |
Myoz1 |
A |
T |
14: 20,701,252 (GRCm39) |
S112R |
probably benign |
Het |
Ncapd2 |
A |
G |
6: 125,150,445 (GRCm39) |
V860A |
probably benign |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Npffr1 |
T |
C |
10: 61,450,010 (GRCm39) |
F95L |
possibly damaging |
Het |
Or51f1e |
G |
T |
7: 102,747,641 (GRCm39) |
R231L |
probably benign |
Het |
Or8b9 |
T |
C |
9: 37,766,492 (GRCm39) |
I126T |
probably damaging |
Het |
Orc4 |
A |
C |
2: 48,822,622 (GRCm39) |
|
probably benign |
Het |
Pak4 |
T |
C |
7: 28,259,202 (GRCm39) |
D552G |
probably benign |
Het |
Pcdhb4 |
G |
T |
18: 37,442,423 (GRCm39) |
|
probably null |
Het |
Pdcd4 |
G |
T |
19: 53,917,525 (GRCm39) |
R454L |
probably damaging |
Het |
Phf8-ps |
T |
C |
17: 33,284,263 (GRCm39) |
I846M |
probably benign |
Het |
Pkd1l2 |
A |
G |
8: 117,771,231 (GRCm39) |
I1116T |
probably damaging |
Het |
Plcb2 |
A |
G |
2: 118,555,586 (GRCm39) |
|
probably benign |
Het |
Pmpca |
T |
C |
2: 26,283,230 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
T |
A |
2: 24,887,252 (GRCm39) |
I32N |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,384,775 (GRCm39) |
K718E |
probably damaging |
Het |
Racgap1 |
C |
T |
15: 99,524,411 (GRCm39) |
A359T |
probably benign |
Het |
Rgs3 |
G |
A |
4: 62,523,798 (GRCm39) |
|
probably null |
Het |
Rhpn1 |
A |
G |
15: 75,583,503 (GRCm39) |
E356G |
probably damaging |
Het |
Rps6ka5 |
T |
C |
12: 100,540,697 (GRCm39) |
H488R |
possibly damaging |
Het |
Scn11a |
A |
G |
9: 119,632,396 (GRCm39) |
|
probably null |
Het |
Sema4f |
A |
T |
6: 82,912,948 (GRCm39) |
|
probably benign |
Het |
Serpina1f |
A |
G |
12: 103,660,094 (GRCm39) |
S63P |
probably damaging |
Het |
Slc9a3 |
T |
C |
13: 74,307,365 (GRCm39) |
W386R |
probably damaging |
Het |
Slc9b1 |
A |
C |
3: 135,100,651 (GRCm39) |
L465F |
probably benign |
Het |
Smc5 |
A |
G |
19: 23,241,017 (GRCm39) |
V165A |
possibly damaging |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm39) |
R637Q |
probably benign |
Het |
Tinagl1 |
G |
T |
4: 130,067,816 (GRCm39) |
D59E |
probably damaging |
Het |
Tns3 |
A |
G |
11: 8,443,302 (GRCm39) |
Y354H |
probably damaging |
Het |
Trappc9 |
C |
T |
15: 72,461,956 (GRCm39) |
G1103D |
probably damaging |
Het |
Unc79 |
A |
T |
12: 102,957,687 (GRCm39) |
D34V |
probably damaging |
Het |
Unc80 |
T |
C |
1: 66,560,645 (GRCm39) |
L791P |
probably damaging |
Het |
Unc93a2 |
A |
G |
17: 7,641,926 (GRCm39) |
L174P |
probably damaging |
Het |
Xpo7 |
G |
T |
14: 70,903,537 (GRCm39) |
|
probably benign |
Het |
Zbtb1 |
T |
A |
12: 76,432,113 (GRCm39) |
I33N |
probably damaging |
Het |
|
Other mutations in P3h3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00985:P3h3
|
APN |
6 |
124,822,552 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02158:P3h3
|
APN |
6 |
124,830,055 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02654:P3h3
|
APN |
6 |
124,822,228 (GRCm39) |
missense |
possibly damaging |
0.95 |
P0040:P3h3
|
UTSW |
6 |
124,830,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R0024:P3h3
|
UTSW |
6 |
124,834,421 (GRCm39) |
missense |
probably benign |
|
R0196:P3h3
|
UTSW |
6 |
124,822,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R0328:P3h3
|
UTSW |
6 |
124,831,269 (GRCm39) |
unclassified |
probably benign |
|
R0589:P3h3
|
UTSW |
6 |
124,818,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:P3h3
|
UTSW |
6 |
124,832,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R0793:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0794:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0795:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0796:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0853:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0854:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0856:P3h3
|
UTSW |
6 |
124,831,896 (GRCm39) |
missense |
probably benign |
0.00 |
R1819:P3h3
|
UTSW |
6 |
124,831,895 (GRCm39) |
missense |
probably benign |
0.05 |
R2100:P3h3
|
UTSW |
6 |
124,822,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R4332:P3h3
|
UTSW |
6 |
124,819,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4461:P3h3
|
UTSW |
6 |
124,822,531 (GRCm39) |
missense |
probably benign |
0.08 |
R4533:P3h3
|
UTSW |
6 |
124,831,371 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4829:P3h3
|
UTSW |
6 |
124,818,601 (GRCm39) |
utr 3 prime |
probably benign |
|
R4840:P3h3
|
UTSW |
6 |
124,827,600 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4962:P3h3
|
UTSW |
6 |
124,818,736 (GRCm39) |
missense |
probably benign |
0.09 |
R5014:P3h3
|
UTSW |
6 |
124,832,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R5591:P3h3
|
UTSW |
6 |
124,831,658 (GRCm39) |
unclassified |
probably benign |
|
R5691:P3h3
|
UTSW |
6 |
124,832,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R5777:P3h3
|
UTSW |
6 |
124,832,921 (GRCm39) |
missense |
probably benign |
0.24 |
R5846:P3h3
|
UTSW |
6 |
124,834,157 (GRCm39) |
critical splice donor site |
probably null |
|
R6212:P3h3
|
UTSW |
6 |
124,822,606 (GRCm39) |
missense |
probably benign |
0.19 |
R6254:P3h3
|
UTSW |
6 |
124,822,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R6320:P3h3
|
UTSW |
6 |
124,831,835 (GRCm39) |
missense |
probably benign |
0.02 |
R6860:P3h3
|
UTSW |
6 |
124,834,331 (GRCm39) |
missense |
probably benign |
0.01 |
R7385:P3h3
|
UTSW |
6 |
124,832,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:P3h3
|
UTSW |
6 |
124,827,594 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7617:P3h3
|
UTSW |
6 |
124,832,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:P3h3
|
UTSW |
6 |
124,831,395 (GRCm39) |
missense |
probably benign |
0.00 |
R7831:P3h3
|
UTSW |
6 |
124,832,118 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8317:P3h3
|
UTSW |
6 |
124,832,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R8436:P3h3
|
UTSW |
6 |
124,828,041 (GRCm39) |
critical splice donor site |
probably null |
|
R8749:P3h3
|
UTSW |
6 |
124,822,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R8944:P3h3
|
UTSW |
6 |
124,832,196 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8988:P3h3
|
UTSW |
6 |
124,834,564 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9508:P3h3
|
UTSW |
6 |
124,830,012 (GRCm39) |
critical splice donor site |
probably null |
|
X0021:P3h3
|
UTSW |
6 |
124,832,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|