Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3300002I08Rik |
T |
C |
2: 150,153,122 (GRCm39) |
N88D |
possibly damaging |
Het |
4933430I17Rik |
A |
G |
4: 62,460,916 (GRCm39) |
I264V |
probably benign |
Het |
Abcc8 |
A |
G |
7: 45,787,429 (GRCm39) |
F591L |
probably benign |
Het |
Abr |
G |
T |
11: 76,310,658 (GRCm39) |
T810K |
probably damaging |
Het |
Abracl |
T |
C |
10: 17,894,631 (GRCm39) |
E6G |
unknown |
Het |
Adamts3 |
A |
T |
5: 89,834,750 (GRCm39) |
Y871N |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,354,275 (GRCm39) |
Y80H |
probably benign |
Het |
Alas1 |
A |
G |
9: 106,115,840 (GRCm39) |
|
probably null |
Het |
Anapc1 |
A |
C |
2: 128,517,633 (GRCm39) |
L337R |
possibly damaging |
Het |
Apaf1 |
T |
C |
10: 90,915,816 (GRCm39) |
Y24C |
probably damaging |
Het |
Arhgef16 |
A |
G |
4: 154,365,432 (GRCm39) |
V561A |
possibly damaging |
Het |
Atp10b |
T |
A |
11: 43,121,224 (GRCm39) |
H962Q |
probably benign |
Het |
Brsk2 |
A |
G |
7: 141,546,852 (GRCm39) |
T432A |
probably benign |
Het |
C1rl |
T |
A |
6: 124,485,802 (GRCm39) |
V391E |
probably damaging |
Het |
Caps2 |
A |
T |
10: 112,036,637 (GRCm39) |
H399L |
probably benign |
Het |
Ccdc43 |
C |
A |
11: 102,577,207 (GRCm39) |
K199N |
probably benign |
Het |
Ccdc7a |
G |
T |
8: 129,555,774 (GRCm39) |
P1198T |
unknown |
Het |
Cct7 |
A |
G |
6: 85,444,625 (GRCm39) |
Y423C |
possibly damaging |
Het |
Cep112 |
A |
G |
11: 108,648,514 (GRCm39) |
T783A |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,833,459 (GRCm39) |
T1795A |
probably benign |
Het |
Clasp1 |
T |
G |
1: 118,431,560 (GRCm39) |
S397A |
possibly damaging |
Het |
Clock |
A |
C |
5: 76,377,227 (GRCm39) |
F691V |
possibly damaging |
Het |
Cmklr1 |
A |
G |
5: 113,752,341 (GRCm39) |
V220A |
probably benign |
Het |
Coro2b |
A |
T |
9: 62,335,291 (GRCm39) |
Y298* |
probably null |
Het |
Cspg4b |
A |
T |
13: 113,455,649 (GRCm39) |
N565I |
|
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Dlk2 |
G |
A |
17: 46,613,432 (GRCm39) |
G186D |
probably damaging |
Het |
Dok1 |
T |
C |
6: 83,009,972 (GRCm39) |
K46E |
probably damaging |
Het |
Dok3 |
A |
G |
13: 55,672,186 (GRCm39) |
I164T |
probably benign |
Het |
Ercc5 |
T |
A |
1: 44,207,041 (GRCm39) |
D651E |
probably damaging |
Het |
Erp27 |
T |
C |
6: 136,885,066 (GRCm39) |
K244R |
probably benign |
Het |
Fhip1a |
G |
A |
3: 85,580,559 (GRCm39) |
Q549* |
probably null |
Het |
Flvcr2 |
T |
C |
12: 85,793,954 (GRCm39) |
V110A |
possibly damaging |
Het |
Gsta3 |
T |
C |
1: 21,320,060 (GRCm39) |
L22P |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,093,522 (GRCm39) |
T493A |
probably benign |
Het |
Hivep2 |
T |
A |
10: 14,005,523 (GRCm39) |
I707N |
probably benign |
Het |
Hmox1 |
A |
G |
8: 75,823,544 (GRCm39) |
N71D |
probably benign |
Het |
Hnrnpr |
G |
T |
4: 136,063,615 (GRCm39) |
V342F |
probably damaging |
Het |
Ifi44 |
T |
C |
3: 151,438,108 (GRCm39) |
D393G |
probably damaging |
Het |
Ighv1-82 |
A |
T |
12: 115,916,566 (GRCm39) |
F9I |
probably damaging |
Het |
Kalrn |
A |
G |
16: 33,854,864 (GRCm39) |
S1999P |
probably damaging |
Het |
Kcnq2 |
A |
G |
2: 180,776,753 (GRCm39) |
S45P |
probably benign |
Het |
Krt77 |
A |
T |
15: 101,769,779 (GRCm39) |
Y364N |
probably damaging |
Het |
Kti12 |
T |
C |
4: 108,705,476 (GRCm39) |
V130A |
probably benign |
Het |
Lama2 |
T |
C |
10: 27,100,015 (GRCm39) |
E830G |
probably benign |
Het |
Lrrn1 |
T |
A |
6: 107,545,505 (GRCm39) |
H434Q |
probably benign |
Het |
Med13 |
A |
T |
11: 86,179,801 (GRCm39) |
N1382K |
probably benign |
Het |
Mrpl42 |
A |
G |
10: 95,332,684 (GRCm39) |
|
probably null |
Het |
Mtor |
A |
G |
4: 148,569,103 (GRCm39) |
D1140G |
probably benign |
Het |
Mtrr |
A |
G |
13: 68,720,755 (GRCm39) |
I280T |
probably benign |
Het |
Myh4 |
A |
T |
11: 67,139,290 (GRCm39) |
I536F |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,141,129 (GRCm39) |
N730K |
probably damaging |
Het |
Nat10 |
A |
C |
2: 103,563,364 (GRCm39) |
L545R |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,520,015 (GRCm39) |
D2356V |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,937,366 (GRCm39) |
S748R |
probably damaging |
Het |
Nlrp1a |
T |
C |
11: 70,998,488 (GRCm39) |
T904A |
probably benign |
Het |
Nod2 |
A |
T |
8: 89,397,050 (GRCm39) |
N820I |
probably damaging |
Het |
Nptx1 |
A |
G |
11: 119,433,381 (GRCm39) |
V406A |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,901,863 (GRCm39) |
I644K |
probably benign |
Het |
Or4e1 |
T |
C |
14: 52,700,873 (GRCm39) |
I198V |
probably benign |
Het |
Ostf1 |
T |
A |
19: 18,573,735 (GRCm39) |
I38F |
probably benign |
Het |
Pacc1 |
G |
A |
1: 191,082,004 (GRCm39) |
R337Q |
probably damaging |
Het |
Pde4b |
G |
T |
4: 102,462,183 (GRCm39) |
D605Y |
probably damaging |
Het |
Pde4d |
A |
G |
13: 109,397,196 (GRCm39) |
T3A |
|
Het |
Pknox1 |
A |
G |
17: 31,822,183 (GRCm39) |
I317V |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,918,240 (GRCm39) |
N1283S |
probably benign |
Het |
Ppp3cb |
G |
A |
14: 20,573,868 (GRCm39) |
A289V |
probably damaging |
Het |
Prag1 |
A |
G |
8: 36,607,208 (GRCm39) |
D983G |
probably damaging |
Het |
Psmd13 |
C |
T |
7: 140,478,455 (GRCm39) |
T62M |
|
Het |
Rab42 |
C |
T |
4: 132,029,890 (GRCm39) |
V111I |
|
Het |
Rabl2 |
T |
A |
15: 89,474,631 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
T |
A |
11: 54,582,169 (GRCm39) |
S1365R |
probably damaging |
Het |
Rassf4 |
G |
T |
6: 116,617,265 (GRCm39) |
H247N |
possibly damaging |
Het |
Rbfox1 |
A |
G |
16: 7,227,573 (GRCm39) |
T363A |
probably benign |
Het |
Rbmyf9 |
T |
A |
Y: 3,774,888 (GRCm39) |
F28L |
probably damaging |
Het |
Sbf1 |
T |
C |
15: 89,184,742 (GRCm39) |
D1091G |
probably damaging |
Het |
Selenbp2 |
G |
A |
3: 94,607,352 (GRCm39) |
D258N |
probably benign |
Het |
Sirpa |
A |
T |
2: 129,457,555 (GRCm39) |
I210F |
probably damaging |
Het |
Skint4 |
T |
C |
4: 112,015,236 (GRCm39) |
S434P |
probably benign |
Het |
Slc26a5 |
G |
A |
5: 22,016,337 (GRCm39) |
Q682* |
probably null |
Het |
Slco4a1 |
C |
T |
2: 180,115,943 (GRCm39) |
S693F |
possibly damaging |
Het |
Smpd3 |
A |
G |
8: 106,992,119 (GRCm39) |
F145L |
probably benign |
Het |
Son |
CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC |
CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC |
16: 91,453,579 (GRCm39) |
|
probably benign |
Het |
Spata31d1c |
A |
T |
13: 65,184,040 (GRCm39) |
L527F |
probably damaging |
Het |
Srd5a3 |
A |
G |
5: 76,297,794 (GRCm39) |
N199D |
probably benign |
Het |
Stard9 |
C |
G |
2: 120,534,564 (GRCm39) |
P3607R |
probably damaging |
Het |
Sytl1 |
A |
G |
4: 132,986,291 (GRCm39) |
|
probably null |
Het |
Tas2r126 |
A |
G |
6: 42,412,307 (GRCm39) |
H280R |
probably null |
Het |
Tcf4 |
C |
T |
18: 69,652,944 (GRCm39) |
|
probably benign |
Het |
Tlcd2 |
A |
G |
11: 75,359,112 (GRCm39) |
T28A |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem119 |
A |
G |
5: 113,933,267 (GRCm39) |
L178P |
probably damaging |
Het |
Tmprss7 |
T |
C |
16: 45,484,564 (GRCm39) |
D532G |
probably benign |
Het |
Tnfaip8l3 |
A |
G |
9: 53,934,777 (GRCm39) |
I66T |
probably benign |
Het |
Tor1b |
A |
G |
2: 30,843,185 (GRCm39) |
Y50C |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,017,648 (GRCm39) |
S751T |
probably benign |
Het |
Tpra1 |
T |
C |
6: 88,887,221 (GRCm39) |
V193A |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,735,215 (GRCm39) |
V932E |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,777,104 (GRCm39) |
T1479S |
unknown |
Het |
Unc13c |
A |
T |
9: 73,392,220 (GRCm39) |
V2044D |
probably damaging |
Het |
Usp25 |
T |
G |
16: 76,852,076 (GRCm39) |
V197G |
probably damaging |
Het |
Vmn2r34 |
A |
G |
7: 7,675,366 (GRCm39) |
V674A |
probably benign |
Het |
Zfp7 |
T |
C |
15: 76,775,484 (GRCm39) |
S509P |
probably damaging |
Het |
Zfp821 |
A |
G |
8: 110,447,856 (GRCm39) |
T66A |
probably damaging |
Het |
Zfp97 |
T |
A |
17: 17,365,930 (GRCm39) |
N476K |
possibly damaging |
Het |
|
Other mutations in Scaper |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00653:Scaper
|
APN |
9 |
55,767,143 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00912:Scaper
|
APN |
9 |
55,593,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01469:Scaper
|
APN |
9 |
55,767,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01626:Scaper
|
APN |
9 |
55,819,335 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01779:Scaper
|
APN |
9 |
55,799,524 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02011:Scaper
|
APN |
9 |
55,487,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02997:Scaper
|
APN |
9 |
55,722,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03107:Scaper
|
APN |
9 |
55,765,686 (GRCm39) |
splice site |
probably benign |
|
IGL03167:Scaper
|
APN |
9 |
55,767,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03293:Scaper
|
APN |
9 |
55,782,107 (GRCm39) |
missense |
probably benign |
|
IGL03340:Scaper
|
APN |
9 |
55,510,116 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03368:Scaper
|
APN |
9 |
55,563,311 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0111:Scaper
|
UTSW |
9 |
55,510,074 (GRCm39) |
missense |
probably benign |
0.01 |
R0510:Scaper
|
UTSW |
9 |
55,665,346 (GRCm39) |
splice site |
probably benign |
|
R0531:Scaper
|
UTSW |
9 |
55,517,158 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0558:Scaper
|
UTSW |
9 |
55,593,207 (GRCm39) |
missense |
probably benign |
0.08 |
R0605:Scaper
|
UTSW |
9 |
55,722,802 (GRCm39) |
splice site |
probably benign |
|
R0646:Scaper
|
UTSW |
9 |
55,665,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R0837:Scaper
|
UTSW |
9 |
55,766,326 (GRCm39) |
nonsense |
probably null |
|
R1440:Scaper
|
UTSW |
9 |
55,510,202 (GRCm39) |
nonsense |
probably null |
|
R1548:Scaper
|
UTSW |
9 |
55,723,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Scaper
|
UTSW |
9 |
55,771,830 (GRCm39) |
missense |
probably benign |
0.33 |
R1822:Scaper
|
UTSW |
9 |
55,767,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R1834:Scaper
|
UTSW |
9 |
55,724,018 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1870:Scaper
|
UTSW |
9 |
55,593,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Scaper
|
UTSW |
9 |
55,819,334 (GRCm39) |
missense |
probably benign |
0.43 |
R2168:Scaper
|
UTSW |
9 |
55,650,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Scaper
|
UTSW |
9 |
55,766,321 (GRCm39) |
missense |
probably null |
0.01 |
R3690:Scaper
|
UTSW |
9 |
55,791,205 (GRCm39) |
missense |
probably benign |
0.00 |
R4392:Scaper
|
UTSW |
9 |
55,765,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R4418:Scaper
|
UTSW |
9 |
55,745,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4606:Scaper
|
UTSW |
9 |
55,563,187 (GRCm39) |
critical splice donor site |
probably null |
|
R4643:Scaper
|
UTSW |
9 |
55,745,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R4665:Scaper
|
UTSW |
9 |
55,819,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Scaper
|
UTSW |
9 |
55,650,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Scaper
|
UTSW |
9 |
55,799,519 (GRCm39) |
missense |
probably benign |
0.02 |
R4934:Scaper
|
UTSW |
9 |
55,716,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R4956:Scaper
|
UTSW |
9 |
55,745,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Scaper
|
UTSW |
9 |
55,767,003 (GRCm39) |
splice site |
probably null |
|
R5107:Scaper
|
UTSW |
9 |
55,487,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Scaper
|
UTSW |
9 |
55,463,370 (GRCm39) |
missense |
probably null |
1.00 |
R5265:Scaper
|
UTSW |
9 |
55,771,830 (GRCm39) |
missense |
probably benign |
|
R5408:Scaper
|
UTSW |
9 |
55,493,508 (GRCm39) |
missense |
probably damaging |
0.99 |
R5623:Scaper
|
UTSW |
9 |
55,771,791 (GRCm39) |
missense |
probably benign |
0.02 |
R5665:Scaper
|
UTSW |
9 |
55,714,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5748:Scaper
|
UTSW |
9 |
55,766,360 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5771:Scaper
|
UTSW |
9 |
55,724,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6534:Scaper
|
UTSW |
9 |
55,791,260 (GRCm39) |
missense |
probably benign |
0.00 |
R6557:Scaper
|
UTSW |
9 |
55,458,134 (GRCm39) |
missense |
probably benign |
0.02 |
R6651:Scaper
|
UTSW |
9 |
55,765,788 (GRCm39) |
missense |
probably benign |
0.05 |
R6796:Scaper
|
UTSW |
9 |
55,771,711 (GRCm39) |
missense |
probably benign |
0.00 |
R6962:Scaper
|
UTSW |
9 |
55,767,055 (GRCm39) |
missense |
probably benign |
0.01 |
R7145:Scaper
|
UTSW |
9 |
55,819,395 (GRCm39) |
missense |
unknown |
|
R7199:Scaper
|
UTSW |
9 |
55,745,460 (GRCm39) |
nonsense |
probably null |
|
R7356:Scaper
|
UTSW |
9 |
55,799,495 (GRCm39) |
missense |
unknown |
|
R7426:Scaper
|
UTSW |
9 |
55,669,561 (GRCm39) |
nonsense |
probably null |
|
R7503:Scaper
|
UTSW |
9 |
55,715,038 (GRCm39) |
missense |
probably damaging |
0.98 |
R7844:Scaper
|
UTSW |
9 |
55,722,732 (GRCm39) |
missense |
probably benign |
0.04 |
R7966:Scaper
|
UTSW |
9 |
55,669,611 (GRCm39) |
missense |
probably damaging |
0.98 |
R7992:Scaper
|
UTSW |
9 |
55,765,438 (GRCm39) |
missense |
probably benign |
0.02 |
R8081:Scaper
|
UTSW |
9 |
55,823,330 (GRCm39) |
missense |
unknown |
|
R8189:Scaper
|
UTSW |
9 |
55,819,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R8294:Scaper
|
UTSW |
9 |
55,517,280 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8351:Scaper
|
UTSW |
9 |
55,724,088 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8451:Scaper
|
UTSW |
9 |
55,724,088 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8473:Scaper
|
UTSW |
9 |
55,458,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R8476:Scaper
|
UTSW |
9 |
55,669,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Scaper
|
UTSW |
9 |
55,771,722 (GRCm39) |
missense |
probably benign |
|
R9058:Scaper
|
UTSW |
9 |
55,722,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9071:Scaper
|
UTSW |
9 |
55,771,803 (GRCm39) |
missense |
probably benign |
|
R9099:Scaper
|
UTSW |
9 |
55,669,616 (GRCm39) |
missense |
probably damaging |
0.98 |
R9104:Scaper
|
UTSW |
9 |
55,819,400 (GRCm39) |
missense |
unknown |
|
R9685:Scaper
|
UTSW |
9 |
55,771,835 (GRCm39) |
missense |
probably benign |
0.10 |
X0012:Scaper
|
UTSW |
9 |
55,563,214 (GRCm39) |
missense |
probably damaging |
0.98 |
X0052:Scaper
|
UTSW |
9 |
55,723,948 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Scaper
|
UTSW |
9 |
55,463,532 (GRCm39) |
missense |
probably damaging |
1.00 |
|