Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
C |
6: 23,107,709 (GRCm39) |
D358G |
possibly damaging |
Het |
Adam26a |
A |
T |
8: 44,022,178 (GRCm39) |
C437* |
probably null |
Het |
Arhgap10 |
A |
T |
8: 78,037,468 (GRCm39) |
C587S |
probably benign |
Het |
Bank1 |
G |
A |
3: 135,948,721 (GRCm39) |
T285I |
probably benign |
Het |
Bhlha15 |
C |
T |
5: 144,128,257 (GRCm39) |
S123L |
probably damaging |
Het |
Cacul1 |
T |
C |
19: 60,517,475 (GRCm39) |
*305W |
probably null |
Het |
Cep112 |
A |
C |
11: 108,393,977 (GRCm39) |
K365T |
probably damaging |
Het |
Chrm1 |
T |
A |
19: 8,656,453 (GRCm39) |
L386Q |
probably damaging |
Het |
Cnbp |
C |
A |
6: 87,822,194 (GRCm39) |
R110L |
probably damaging |
Het |
Cntnap5a |
A |
T |
1: 116,116,140 (GRCm39) |
I541F |
possibly damaging |
Het |
Dscaml1 |
T |
G |
9: 45,658,438 (GRCm39) |
|
probably benign |
Het |
Enpp3 |
C |
T |
10: 24,653,824 (GRCm39) |
S711N |
probably damaging |
Het |
Eps8 |
G |
T |
6: 137,459,252 (GRCm39) |
N750K |
probably benign |
Het |
Fan1 |
G |
T |
7: 64,023,054 (GRCm39) |
N66K |
probably benign |
Het |
Fbf1 |
G |
A |
11: 116,044,845 (GRCm39) |
T323I |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,127,517 (GRCm39) |
N2143I |
unknown |
Het |
Fn3k |
A |
C |
11: 121,339,744 (GRCm39) |
T169P |
probably benign |
Het |
Fubp1 |
T |
G |
3: 151,926,356 (GRCm39) |
I320R |
probably damaging |
Het |
Gfpt2 |
A |
T |
11: 49,714,607 (GRCm39) |
E335D |
probably benign |
Het |
Gm17472 |
T |
C |
6: 42,957,968 (GRCm39) |
I79T |
probably benign |
Het |
Gpr151 |
C |
A |
18: 42,711,437 (GRCm39) |
E414* |
probably null |
Het |
Gpr179 |
G |
A |
11: 97,226,983 (GRCm39) |
S1724L |
probably benign |
Het |
Gtf2h3 |
C |
A |
5: 124,728,967 (GRCm39) |
Y175* |
probably null |
Het |
Hal |
T |
A |
10: 93,328,369 (GRCm39) |
I215N |
probably damaging |
Het |
Htt |
A |
G |
5: 35,053,304 (GRCm39) |
T2546A |
probably benign |
Het |
Ighv1-11 |
T |
C |
12: 114,576,077 (GRCm39) |
Y46C |
probably damaging |
Het |
Lcn4 |
T |
C |
2: 26,558,375 (GRCm39) |
D170G |
probably benign |
Het |
Lrch1 |
T |
A |
14: 75,055,935 (GRCm39) |
D306V |
probably damaging |
Het |
Mtcl1 |
A |
C |
17: 66,650,653 (GRCm39) |
V1604G |
probably damaging |
Het |
Or10g3b |
T |
C |
14: 52,586,625 (GRCm39) |
N293D |
probably damaging |
Het |
Or3a10 |
A |
G |
11: 73,935,926 (GRCm39) |
L58P |
probably damaging |
Het |
Or4c108 |
T |
G |
2: 88,803,552 (GRCm39) |
S228R |
probably damaging |
Het |
Or4k49 |
T |
G |
2: 111,494,587 (GRCm39) |
N5K |
possibly damaging |
Het |
Or9i1b |
G |
A |
19: 13,897,226 (GRCm39) |
V281I |
probably benign |
Het |
Ormdl2 |
A |
G |
10: 128,654,837 (GRCm39) |
L125P |
possibly damaging |
Het |
Pcnx3 |
C |
T |
19: 5,715,412 (GRCm39) |
G1946E |
probably damaging |
Het |
Pde3a |
T |
A |
6: 141,433,527 (GRCm39) |
F803Y |
possibly damaging |
Het |
Pnpla7 |
C |
T |
2: 24,873,635 (GRCm39) |
R214W |
probably damaging |
Het |
Prtg |
T |
C |
9: 72,813,520 (GRCm39) |
V960A |
probably benign |
Het |
Ptgdr |
T |
C |
14: 45,090,858 (GRCm39) |
E300G |
probably benign |
Het |
Ptpru |
G |
T |
4: 131,522,274 (GRCm39) |
Y710* |
probably null |
Het |
Pxdn |
T |
A |
12: 30,049,195 (GRCm39) |
Y620* |
probably null |
Het |
Pycard |
T |
C |
7: 127,592,797 (GRCm39) |
D10G |
possibly damaging |
Het |
Sh3d21 |
G |
T |
4: 126,055,775 (GRCm39) |
Q160K |
probably benign |
Het |
Slc26a7 |
G |
A |
4: 14,621,269 (GRCm39) |
P39L |
probably benign |
Het |
Sox8 |
T |
C |
17: 25,786,617 (GRCm39) |
D362G |
possibly damaging |
Het |
Tcp11 |
T |
G |
17: 28,286,001 (GRCm39) |
N538T |
probably damaging |
Het |
Tent2 |
T |
C |
13: 93,310,997 (GRCm39) |
|
probably benign |
Het |
Tmem132e |
A |
C |
11: 82,325,666 (GRCm39) |
E222A |
probably benign |
Het |
Trpc7 |
T |
C |
13: 56,937,602 (GRCm39) |
E618G |
probably benign |
Het |
Tsc2 |
G |
T |
17: 24,833,340 (GRCm39) |
Q695K |
probably benign |
Het |
Txlnb |
C |
A |
10: 17,718,752 (GRCm39) |
L528M |
possibly damaging |
Het |
Vmn1r176 |
A |
G |
7: 23,534,878 (GRCm39) |
Y92H |
probably benign |
Het |
Vmn2r85 |
T |
A |
10: 130,254,738 (GRCm39) |
I649F |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,171,272 (GRCm39) |
|
probably null |
Het |
Wrn |
A |
T |
8: 33,814,274 (GRCm39) |
I390N |
probably benign |
Het |
Zfp493 |
T |
A |
13: 67,934,976 (GRCm39) |
C310S |
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 |
IGL02437:Snrnp200
|
APN |
2 |
127,058,030 (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 |
|
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 |
|