Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
Abca16 |
T |
G |
7: 120,132,952 (GRCm39) |
C1294G |
probably benign |
Het |
Abca7 |
T |
A |
10: 79,844,223 (GRCm39) |
S1410T |
probably damaging |
Het |
Abhd12 |
T |
C |
2: 150,676,289 (GRCm39) |
D356G |
probably benign |
Het |
BC004004 |
T |
C |
17: 29,517,671 (GRCm39) |
L295P |
probably damaging |
Het |
Bpifc |
T |
C |
10: 85,824,595 (GRCm39) |
S215G |
probably damaging |
Het |
Bptf |
C |
T |
11: 106,965,521 (GRCm39) |
M1109I |
probably benign |
Het |
Brat1 |
C |
T |
5: 140,698,563 (GRCm39) |
A245V |
possibly damaging |
Het |
Cask |
G |
A |
X: 13,403,860 (GRCm39) |
T16I |
probably damaging |
Het |
Cemip2 |
T |
C |
19: 21,789,342 (GRCm39) |
|
probably null |
Het |
Cibar2 |
T |
C |
8: 120,901,525 (GRCm39) |
E60G |
probably damaging |
Het |
Clic6 |
A |
T |
16: 92,327,817 (GRCm39) |
I541F |
probably damaging |
Het |
Clnk |
C |
T |
5: 38,931,909 (GRCm39) |
|
probably null |
Het |
Cntnap1 |
T |
A |
11: 101,077,677 (GRCm39) |
I1113N |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyp26a1 |
T |
C |
19: 37,686,943 (GRCm39) |
S132P |
probably benign |
Het |
Cyp4f13 |
G |
T |
17: 33,149,582 (GRCm39) |
H85N |
probably benign |
Het |
Dcaf15 |
C |
T |
8: 84,828,445 (GRCm39) |
G215D |
probably damaging |
Het |
Dip2a |
T |
C |
10: 76,134,101 (GRCm39) |
T500A |
probably benign |
Het |
Gbe1 |
T |
A |
16: 70,231,546 (GRCm39) |
|
probably benign |
Het |
Gli2 |
T |
A |
1: 118,763,733 (GRCm39) |
I1473F |
probably damaging |
Het |
Gm5129 |
A |
T |
5: 29,940,861 (GRCm39) |
|
probably benign |
Het |
Hdgf |
C |
T |
3: 87,821,792 (GRCm39) |
R168C |
probably damaging |
Het |
Heph |
A |
G |
X: 95,516,633 (GRCm39) |
T342A |
probably benign |
Het |
Kdelr3 |
T |
C |
15: 79,409,988 (GRCm39) |
Y158H |
probably damaging |
Het |
Lamb3 |
C |
T |
1: 193,010,253 (GRCm39) |
R289C |
probably damaging |
Het |
Leng8 |
C |
T |
7: 4,145,092 (GRCm39) |
A164V |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,194,889 (GRCm39) |
T1337A |
probably benign |
Het |
Mast3 |
C |
A |
8: 71,233,202 (GRCm39) |
R316L |
possibly damaging |
Het |
Nampt |
A |
G |
12: 32,880,215 (GRCm39) |
Y36C |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,975,264 (GRCm39) |
|
probably benign |
Het |
Nipbl |
T |
C |
15: 8,388,558 (GRCm39) |
D354G |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,461,254 (GRCm39) |
R2494W |
probably damaging |
Het |
Nt5c1a |
A |
G |
4: 123,108,034 (GRCm39) |
N239S |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,231,329 (GRCm39) |
E19G |
possibly damaging |
Het |
Or11h4b |
A |
T |
14: 50,918,657 (GRCm39) |
S145T |
probably benign |
Het |
Or4c58 |
A |
G |
2: 89,675,128 (GRCm39) |
L63P |
probably damaging |
Het |
Pcna |
A |
T |
2: 132,093,155 (GRCm39) |
|
probably benign |
Het |
Pdia3 |
T |
A |
2: 121,264,129 (GRCm39) |
V326E |
probably damaging |
Het |
Phf8 |
T |
A |
X: 150,414,356 (GRCm39) |
L1002Q |
possibly damaging |
Het |
Rhobtb2 |
T |
C |
14: 70,033,365 (GRCm39) |
E535G |
probably damaging |
Het |
Rusc2 |
G |
T |
4: 43,415,545 (GRCm39) |
D284Y |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,825,491 (GRCm39) |
Y212C |
probably benign |
Het |
Sash3 |
C |
A |
X: 47,247,672 (GRCm39) |
Q169K |
probably benign |
Het |
Scyl1 |
C |
T |
19: 5,816,224 (GRCm39) |
G324S |
probably damaging |
Het |
Sec62 |
G |
A |
3: 30,872,996 (GRCm39) |
G360R |
unknown |
Het |
Sis |
T |
C |
3: 72,826,947 (GRCm39) |
|
probably null |
Het |
Slc6a1 |
T |
A |
6: 114,285,578 (GRCm39) |
I338N |
probably damaging |
Het |
Tgm3 |
G |
T |
2: 129,871,961 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
T |
G |
15: 80,764,658 (GRCm39) |
L720R |
probably damaging |
Het |
Tspyl4 |
A |
T |
10: 34,174,228 (GRCm39) |
Q240L |
probably damaging |
Het |
Tube1 |
G |
A |
10: 39,016,846 (GRCm39) |
V80I |
probably damaging |
Het |
Uap1l1 |
C |
T |
2: 25,253,945 (GRCm39) |
V304M |
probably damaging |
Het |
Wtap |
T |
C |
17: 13,186,620 (GRCm39) |
N309S |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,315,621 (GRCm39) |
D1285G |
probably benign |
Het |
Zscan20 |
G |
A |
4: 128,482,210 (GRCm39) |
T484I |
probably damaging |
Het |
|
Other mutations in Snrnp200 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00482:Snrnp200
|
APN |
2 |
127,072,055 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01013:Snrnp200
|
APN |
2 |
127,074,392 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01073:Snrnp200
|
APN |
2 |
127,056,832 (GRCm39) |
splice site |
probably benign |
|
IGL01319:Snrnp200
|
APN |
2 |
127,072,047 (GRCm39) |
splice site |
probably benign |
|
IGL01597:Snrnp200
|
APN |
2 |
127,080,652 (GRCm39) |
unclassified |
probably benign |
|
IGL01631:Snrnp200
|
APN |
2 |
127,080,744 (GRCm39) |
unclassified |
probably benign |
|
IGL01646:Snrnp200
|
APN |
2 |
127,064,148 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02019:Snrnp200
|
APN |
2 |
127,074,825 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02158:Snrnp200
|
APN |
2 |
127,079,403 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02269:Snrnp200
|
APN |
2 |
127,071,911 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02288:Snrnp200
|
APN |
2 |
127,071,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02476:Snrnp200
|
APN |
2 |
127,059,408 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02613:Snrnp200
|
APN |
2 |
127,060,346 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02898:Snrnp200
|
APN |
2 |
127,058,676 (GRCm39) |
splice site |
probably benign |
|
IGL03108:Snrnp200
|
APN |
2 |
127,080,087 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03143:Snrnp200
|
APN |
2 |
127,071,962 (GRCm39) |
critical splice donor site |
probably benign |
|
IGL03237:Snrnp200
|
APN |
2 |
127,075,233 (GRCm39) |
missense |
probably damaging |
0.99 |
R0012:Snrnp200
|
UTSW |
2 |
127,070,469 (GRCm39) |
missense |
probably benign |
0.35 |
R0012:Snrnp200
|
UTSW |
2 |
127,070,469 (GRCm39) |
missense |
probably benign |
0.35 |
R0033:Snrnp200
|
UTSW |
2 |
127,079,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R0033:Snrnp200
|
UTSW |
2 |
127,079,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R0047:Snrnp200
|
UTSW |
2 |
127,076,874 (GRCm39) |
splice site |
probably benign |
|
R0047:Snrnp200
|
UTSW |
2 |
127,076,874 (GRCm39) |
splice site |
probably benign |
|
R0057:Snrnp200
|
UTSW |
2 |
127,079,827 (GRCm39) |
missense |
probably damaging |
0.96 |
R0270:Snrnp200
|
UTSW |
2 |
127,074,902 (GRCm39) |
missense |
probably damaging |
0.97 |
R0626:Snrnp200
|
UTSW |
2 |
127,063,734 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0731:Snrnp200
|
UTSW |
2 |
127,068,065 (GRCm39) |
splice site |
probably benign |
|
R1175:Snrnp200
|
UTSW |
2 |
127,070,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Snrnp200
|
UTSW |
2 |
127,078,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:Snrnp200
|
UTSW |
2 |
127,060,331 (GRCm39) |
missense |
probably benign |
0.10 |
R1444:Snrnp200
|
UTSW |
2 |
127,070,158 (GRCm39) |
splice site |
probably benign |
|
R1757:Snrnp200
|
UTSW |
2 |
127,074,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1794:Snrnp200
|
UTSW |
2 |
127,058,656 (GRCm39) |
missense |
probably benign |
|
R1808:Snrnp200
|
UTSW |
2 |
127,060,948 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1808:Snrnp200
|
UTSW |
2 |
127,060,947 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1957:Snrnp200
|
UTSW |
2 |
127,058,095 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2007:Snrnp200
|
UTSW |
2 |
127,068,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R2039:Snrnp200
|
UTSW |
2 |
127,076,904 (GRCm39) |
missense |
probably benign |
0.19 |
R2070:Snrnp200
|
UTSW |
2 |
127,079,803 (GRCm39) |
missense |
probably benign |
0.00 |
R2070:Snrnp200
|
UTSW |
2 |
127,054,323 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2892:Snrnp200
|
UTSW |
2 |
127,073,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R3236:Snrnp200
|
UTSW |
2 |
127,063,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R3862:Snrnp200
|
UTSW |
2 |
127,075,019 (GRCm39) |
splice site |
probably benign |
|
R4028:Snrnp200
|
UTSW |
2 |
127,079,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R4105:Snrnp200
|
UTSW |
2 |
127,069,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R4328:Snrnp200
|
UTSW |
2 |
127,064,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R4471:Snrnp200
|
UTSW |
2 |
127,080,673 (GRCm39) |
missense |
probably benign |
0.03 |
R4526:Snrnp200
|
UTSW |
2 |
127,071,022 (GRCm39) |
missense |
probably benign |
|
R4575:Snrnp200
|
UTSW |
2 |
127,076,986 (GRCm39) |
missense |
probably benign |
0.00 |
R4710:Snrnp200
|
UTSW |
2 |
127,068,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Snrnp200
|
UTSW |
2 |
127,069,798 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4728:Snrnp200
|
UTSW |
2 |
127,059,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Snrnp200
|
UTSW |
2 |
127,074,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R4828:Snrnp200
|
UTSW |
2 |
127,053,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R5082:Snrnp200
|
UTSW |
2 |
127,068,290 (GRCm39) |
nonsense |
probably null |
|
R5213:Snrnp200
|
UTSW |
2 |
127,073,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R5287:Snrnp200
|
UTSW |
2 |
127,073,607 (GRCm39) |
missense |
probably benign |
0.13 |
R5486:Snrnp200
|
UTSW |
2 |
127,074,986 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5595:Snrnp200
|
UTSW |
2 |
127,067,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R5598:Snrnp200
|
UTSW |
2 |
127,068,007 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5681:Snrnp200
|
UTSW |
2 |
127,067,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R6207:Snrnp200
|
UTSW |
2 |
127,052,655 (GRCm39) |
missense |
probably benign |
0.00 |
R6258:Snrnp200
|
UTSW |
2 |
127,060,343 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6259:Snrnp200
|
UTSW |
2 |
127,060,343 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6299:Snrnp200
|
UTSW |
2 |
127,064,081 (GRCm39) |
nonsense |
probably null |
|
R6434:Snrnp200
|
UTSW |
2 |
127,080,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Snrnp200
|
UTSW |
2 |
127,063,747 (GRCm39) |
missense |
probably benign |
0.12 |
R6647:Snrnp200
|
UTSW |
2 |
127,068,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Snrnp200
|
UTSW |
2 |
127,071,085 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7027:Snrnp200
|
UTSW |
2 |
127,059,192 (GRCm39) |
missense |
probably benign |
0.09 |
R7358:Snrnp200
|
UTSW |
2 |
127,063,746 (GRCm39) |
missense |
probably benign |
0.03 |
R7436:Snrnp200
|
UTSW |
2 |
127,068,404 (GRCm39) |
critical splice donor site |
probably null |
|
R7587:Snrnp200
|
UTSW |
2 |
127,069,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7672:Snrnp200
|
UTSW |
2 |
127,063,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7731:Snrnp200
|
UTSW |
2 |
127,071,022 (GRCm39) |
missense |
probably benign |
|
R7841:Snrnp200
|
UTSW |
2 |
127,078,754 (GRCm39) |
missense |
probably benign |
0.23 |
R7863:Snrnp200
|
UTSW |
2 |
127,073,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Snrnp200
|
UTSW |
2 |
127,074,979 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8117:Snrnp200
|
UTSW |
2 |
127,071,051 (GRCm39) |
missense |
probably benign |
|
R8262:Snrnp200
|
UTSW |
2 |
127,068,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R8551:Snrnp200
|
UTSW |
2 |
127,068,971 (GRCm39) |
missense |
probably benign |
0.03 |
R8675:Snrnp200
|
UTSW |
2 |
127,074,443 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8754:Snrnp200
|
UTSW |
2 |
127,068,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8852:Snrnp200
|
UTSW |
2 |
127,060,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R8899:Snrnp200
|
UTSW |
2 |
127,078,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Snrnp200
|
UTSW |
2 |
127,068,902 (GRCm39) |
missense |
probably benign |
0.04 |
R9030:Snrnp200
|
UTSW |
2 |
127,053,466 (GRCm39) |
intron |
probably benign |
|
R9260:Snrnp200
|
UTSW |
2 |
127,078,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R9366:Snrnp200
|
UTSW |
2 |
127,058,010 (GRCm39) |
missense |
probably benign |
0.01 |
R9385:Snrnp200
|
UTSW |
2 |
127,079,978 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9478:Snrnp200
|
UTSW |
2 |
127,076,993 (GRCm39) |
critical splice donor site |
probably null |
|
R9652:Snrnp200
|
UTSW |
2 |
127,067,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R9653:Snrnp200
|
UTSW |
2 |
127,067,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R9733:Snrnp200
|
UTSW |
2 |
127,068,240 (GRCm39) |
missense |
probably damaging |
1.00 |
RF016:Snrnp200
|
UTSW |
2 |
127,072,476 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Snrnp200
|
UTSW |
2 |
127,076,895 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Snrnp200
|
UTSW |
2 |
127,077,951 (GRCm39) |
missense |
probably benign |
0.04 |
|