Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
A |
T |
8: 25,155,518 (GRCm39) |
F167Y |
possibly damaging |
Het |
Ap3d1 |
A |
G |
10: 80,549,881 (GRCm39) |
S755P |
probably benign |
Het |
Aph1a |
A |
T |
3: 95,802,808 (GRCm39) |
N136I |
probably damaging |
Het |
AU040320 |
T |
A |
4: 126,686,046 (GRCm39) |
N207K |
probably benign |
Het |
Caprin1 |
A |
T |
2: 103,605,856 (GRCm39) |
D377E |
probably benign |
Het |
Col18a1 |
A |
G |
10: 76,899,811 (GRCm39) |
|
probably null |
Het |
Ddi2 |
T |
C |
4: 141,411,181 (GRCm39) |
N577S |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,704,624 (GRCm39) |
|
probably null |
Het |
Dmbt1 |
A |
T |
7: 130,648,240 (GRCm39) |
|
probably null |
Het |
Fam13a |
T |
C |
6: 58,964,174 (GRCm39) |
K86R |
probably benign |
Het |
Fam168b |
C |
A |
1: 34,875,822 (GRCm39) |
G21V |
probably damaging |
Het |
Fbxl8 |
A |
T |
8: 105,994,842 (GRCm39) |
D118V |
probably damaging |
Het |
Garin5b |
G |
A |
7: 4,761,431 (GRCm39) |
P427L |
possibly damaging |
Het |
Git2 |
C |
A |
5: 114,869,052 (GRCm39) |
|
probably null |
Het |
Gm17190 |
T |
G |
13: 96,218,770 (GRCm39) |
D35E |
possibly damaging |
Het |
Gnb4 |
C |
T |
3: 32,639,295 (GRCm39) |
D333N |
probably damaging |
Het |
Has2 |
T |
A |
15: 56,531,968 (GRCm39) |
D249V |
probably damaging |
Het |
Ighv1-23 |
A |
G |
12: 114,728,141 (GRCm39) |
S94P |
probably damaging |
Het |
Kctd16 |
T |
C |
18: 40,391,544 (GRCm39) |
I44T |
probably benign |
Het |
Kpna1 |
A |
G |
16: 35,849,890 (GRCm39) |
|
probably null |
Het |
Lonrf1 |
T |
A |
8: 36,690,095 (GRCm39) |
R654S |
probably damaging |
Het |
Lrrc49 |
A |
C |
9: 60,501,052 (GRCm39) |
|
probably null |
Het |
Miip |
T |
G |
4: 147,950,380 (GRCm39) |
K72T |
possibly damaging |
Het |
Mink1 |
C |
T |
11: 70,500,419 (GRCm39) |
P782S |
probably damaging |
Het |
Mpped2 |
A |
G |
2: 106,697,322 (GRCm39) |
T266A |
probably benign |
Het |
Naip1 |
G |
A |
13: 100,559,578 (GRCm39) |
S1142F |
probably benign |
Het |
Naip1 |
C |
T |
13: 100,559,666 (GRCm39) |
G1113S |
probably benign |
Het |
Nbr1 |
A |
G |
11: 101,446,931 (GRCm39) |
|
probably benign |
Het |
Necab3 |
A |
T |
2: 154,396,842 (GRCm39) |
N46K |
probably damaging |
Het |
Or51a8 |
A |
T |
7: 102,549,621 (GRCm39) |
I16F |
probably benign |
Het |
Phtf1 |
C |
T |
3: 103,901,189 (GRCm39) |
R360C |
probably damaging |
Het |
Plcl2 |
A |
G |
17: 50,914,145 (GRCm39) |
I385V |
probably benign |
Het |
Prmt8 |
A |
T |
6: 127,706,376 (GRCm39) |
F138L |
probably benign |
Het |
Prpf40a |
T |
G |
2: 53,042,975 (GRCm39) |
R436S |
probably damaging |
Het |
Rab27b |
T |
A |
18: 70,118,375 (GRCm39) |
I181F |
probably damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,792,310 (GRCm39) |
E87G |
probably damaging |
Het |
Scrib |
T |
A |
15: 75,934,572 (GRCm39) |
T674S |
probably benign |
Het |
Slc9a4 |
A |
G |
1: 40,662,664 (GRCm39) |
S644G |
probably benign |
Het |
Slc9a9 |
G |
A |
9: 94,821,599 (GRCm39) |
A329T |
probably damaging |
Het |
Smc4 |
T |
C |
3: 68,929,794 (GRCm39) |
|
probably null |
Het |
Sox7 |
T |
A |
14: 64,185,637 (GRCm39) |
H224Q |
probably benign |
Het |
Spata31 |
T |
C |
13: 65,070,479 (GRCm39) |
S876P |
probably damaging |
Het |
Syndig1 |
G |
A |
2: 149,845,208 (GRCm39) |
V244M |
probably damaging |
Het |
Tas2r113 |
A |
T |
6: 132,870,421 (GRCm39) |
I150L |
probably benign |
Het |
Tasor |
A |
G |
14: 27,168,343 (GRCm39) |
Y295C |
probably damaging |
Het |
Tmem59l |
G |
A |
8: 70,939,006 (GRCm39) |
P56L |
probably benign |
Het |
Tnfrsf8 |
A |
T |
4: 145,019,168 (GRCm39) |
D222E |
possibly damaging |
Het |
Trim52 |
T |
C |
14: 106,344,483 (GRCm39) |
L47P |
probably damaging |
Het |
Ttc34 |
T |
A |
4: 154,923,762 (GRCm39) |
I157K |
probably benign |
Het |
Txndc16 |
A |
G |
14: 45,389,224 (GRCm39) |
F492S |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,182,897 (GRCm39) |
I428V |
probably benign |
Het |
Vmn2r41 |
T |
A |
7: 8,141,359 (GRCm39) |
I702F |
probably damaging |
Het |
Wdr12 |
T |
A |
1: 60,121,783 (GRCm39) |
H256L |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,346,888 (GRCm39) |
H3043R |
probably benign |
Het |
Xrcc1 |
C |
T |
7: 24,270,459 (GRCm39) |
Q500* |
probably null |
Het |
Zfp583 |
T |
C |
7: 6,328,475 (GRCm39) |
N38S |
probably damaging |
Het |
|
Other mutations in Itpr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Itpr2
|
APN |
6 |
146,298,510 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00163:Itpr2
|
APN |
6 |
146,292,334 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00229:Itpr2
|
APN |
6 |
146,045,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00712:Itpr2
|
APN |
6 |
146,133,934 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL00952:Itpr2
|
APN |
6 |
146,060,459 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00983:Itpr2
|
APN |
6 |
146,212,479 (GRCm39) |
splice site |
probably benign |
|
IGL01012:Itpr2
|
APN |
6 |
146,246,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Itpr2
|
APN |
6 |
146,014,033 (GRCm39) |
nonsense |
probably null |
|
IGL01411:Itpr2
|
APN |
6 |
146,277,560 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01557:Itpr2
|
APN |
6 |
146,060,474 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01669:Itpr2
|
APN |
6 |
146,081,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01809:Itpr2
|
APN |
6 |
146,129,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01814:Itpr2
|
APN |
6 |
146,134,044 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02198:Itpr2
|
APN |
6 |
146,224,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Itpr2
|
APN |
6 |
146,141,760 (GRCm39) |
splice site |
probably benign |
|
IGL02332:Itpr2
|
APN |
6 |
146,328,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Itpr2
|
APN |
6 |
146,292,819 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02432:Itpr2
|
APN |
6 |
146,226,671 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02726:Itpr2
|
APN |
6 |
146,277,419 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02851:Itpr2
|
APN |
6 |
146,287,477 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02933:Itpr2
|
APN |
6 |
146,214,402 (GRCm39) |
missense |
probably benign |
|
IGL03015:Itpr2
|
APN |
6 |
146,277,435 (GRCm39) |
missense |
probably benign |
|
IGL03067:Itpr2
|
APN |
6 |
146,226,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03093:Itpr2
|
APN |
6 |
146,281,008 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03214:Itpr2
|
APN |
6 |
146,081,742 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03275:Itpr2
|
APN |
6 |
146,060,375 (GRCm39) |
splice site |
probably benign |
|
IGL03332:Itpr2
|
APN |
6 |
146,045,647 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03352:Itpr2
|
APN |
6 |
146,058,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03377:Itpr2
|
APN |
6 |
146,231,256 (GRCm39) |
missense |
probably benign |
|
IGL03377:Itpr2
|
APN |
6 |
146,231,213 (GRCm39) |
missense |
probably damaging |
0.96 |
dollar_short
|
UTSW |
6 |
146,298,517 (GRCm39) |
nonsense |
probably null |
|
enfermos
|
UTSW |
6 |
146,135,504 (GRCm39) |
missense |
probably damaging |
0.98 |
Hopla
|
UTSW |
6 |
146,096,096 (GRCm39) |
missense |
probably damaging |
0.98 |
P0029:Itpr2
|
UTSW |
6 |
146,280,987 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:Itpr2
|
UTSW |
6 |
146,256,218 (GRCm39) |
missense |
probably benign |
|
PIT4453001:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4504001:Itpr2
|
UTSW |
6 |
146,131,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R0040:Itpr2
|
UTSW |
6 |
146,246,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Itpr2
|
UTSW |
6 |
146,246,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Itpr2
|
UTSW |
6 |
146,133,789 (GRCm39) |
splice site |
probably null |
|
R0048:Itpr2
|
UTSW |
6 |
146,133,789 (GRCm39) |
splice site |
probably null |
|
R0055:Itpr2
|
UTSW |
6 |
146,224,631 (GRCm39) |
missense |
probably benign |
0.42 |
R0055:Itpr2
|
UTSW |
6 |
146,224,631 (GRCm39) |
missense |
probably benign |
0.42 |
R0088:Itpr2
|
UTSW |
6 |
146,142,683 (GRCm39) |
missense |
probably benign |
|
R0089:Itpr2
|
UTSW |
6 |
146,251,520 (GRCm39) |
critical splice donor site |
probably null |
|
R0114:Itpr2
|
UTSW |
6 |
146,214,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Itpr2
|
UTSW |
6 |
146,141,951 (GRCm39) |
missense |
probably benign |
0.00 |
R0144:Itpr2
|
UTSW |
6 |
146,228,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R0180:Itpr2
|
UTSW |
6 |
146,403,407 (GRCm39) |
start gained |
probably benign |
|
R0211:Itpr2
|
UTSW |
6 |
146,096,111 (GRCm39) |
missense |
probably benign |
0.17 |
R0305:Itpr2
|
UTSW |
6 |
146,212,601 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0367:Itpr2
|
UTSW |
6 |
146,135,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Itpr2
|
UTSW |
6 |
146,260,890 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Itpr2
|
UTSW |
6 |
146,131,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R0450:Itpr2
|
UTSW |
6 |
146,319,477 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0464:Itpr2
|
UTSW |
6 |
146,277,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Itpr2
|
UTSW |
6 |
146,319,477 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0532:Itpr2
|
UTSW |
6 |
146,013,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R0625:Itpr2
|
UTSW |
6 |
146,068,149 (GRCm39) |
missense |
probably benign |
|
R0633:Itpr2
|
UTSW |
6 |
146,275,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Itpr2
|
UTSW |
6 |
146,072,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1086:Itpr2
|
UTSW |
6 |
146,251,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1352:Itpr2
|
UTSW |
6 |
146,013,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Itpr2
|
UTSW |
6 |
146,081,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Itpr2
|
UTSW |
6 |
146,277,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1767:Itpr2
|
UTSW |
6 |
146,251,566 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1779:Itpr2
|
UTSW |
6 |
146,060,399 (GRCm39) |
nonsense |
probably null |
|
R1796:Itpr2
|
UTSW |
6 |
146,198,171 (GRCm39) |
missense |
probably benign |
|
R1815:Itpr2
|
UTSW |
6 |
146,260,914 (GRCm39) |
missense |
probably benign |
0.08 |
R1827:Itpr2
|
UTSW |
6 |
146,229,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1828:Itpr2
|
UTSW |
6 |
146,229,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Itpr2
|
UTSW |
6 |
146,287,469 (GRCm39) |
missense |
probably benign |
0.16 |
R1902:Itpr2
|
UTSW |
6 |
146,131,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Itpr2
|
UTSW |
6 |
146,141,852 (GRCm39) |
missense |
probably benign |
0.41 |
R1964:Itpr2
|
UTSW |
6 |
146,013,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Itpr2
|
UTSW |
6 |
146,129,022 (GRCm39) |
splice site |
probably null |
|
R2168:Itpr2
|
UTSW |
6 |
146,013,176 (GRCm39) |
missense |
probably benign |
0.05 |
R2179:Itpr2
|
UTSW |
6 |
146,277,464 (GRCm39) |
missense |
probably benign |
|
R2290:Itpr2
|
UTSW |
6 |
146,324,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R2874:Itpr2
|
UTSW |
6 |
146,327,996 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2888:Itpr2
|
UTSW |
6 |
146,072,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Itpr2
|
UTSW |
6 |
146,224,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Itpr2
|
UTSW |
6 |
146,074,839 (GRCm39) |
missense |
probably benign |
0.03 |
R2898:Itpr2
|
UTSW |
6 |
146,224,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Itpr2
|
UTSW |
6 |
146,074,839 (GRCm39) |
missense |
probably benign |
0.03 |
R3024:Itpr2
|
UTSW |
6 |
146,081,808 (GRCm39) |
missense |
probably benign |
0.35 |
R3104:Itpr2
|
UTSW |
6 |
146,214,335 (GRCm39) |
critical splice donor site |
probably null |
|
R3607:Itpr2
|
UTSW |
6 |
146,129,099 (GRCm39) |
missense |
probably damaging |
0.98 |
R3732:Itpr2
|
UTSW |
6 |
146,284,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Itpr2
|
UTSW |
6 |
146,284,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3733:Itpr2
|
UTSW |
6 |
146,284,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Itpr2
|
UTSW |
6 |
146,316,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Itpr2
|
UTSW |
6 |
146,133,789 (GRCm39) |
splice site |
probably null |
|
R3821:Itpr2
|
UTSW |
6 |
146,319,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R3929:Itpr2
|
UTSW |
6 |
146,275,857 (GRCm39) |
splice site |
probably null |
|
R3958:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R3959:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R3960:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R3960:Itpr2
|
UTSW |
6 |
146,131,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Itpr2
|
UTSW |
6 |
146,274,742 (GRCm39) |
splice site |
probably null |
|
R4085:Itpr2
|
UTSW |
6 |
146,045,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R4115:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R4588:Itpr2
|
UTSW |
6 |
146,142,694 (GRCm39) |
missense |
probably benign |
0.33 |
R4663:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4686:Itpr2
|
UTSW |
6 |
146,131,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Itpr2
|
UTSW |
6 |
146,298,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Itpr2
|
UTSW |
6 |
146,272,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Itpr2
|
UTSW |
6 |
146,272,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Itpr2
|
UTSW |
6 |
146,226,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Itpr2
|
UTSW |
6 |
146,135,489 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4986:Itpr2
|
UTSW |
6 |
146,141,840 (GRCm39) |
missense |
probably damaging |
0.96 |
R5112:Itpr2
|
UTSW |
6 |
146,135,489 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5200:Itpr2
|
UTSW |
6 |
146,045,605 (GRCm39) |
critical splice donor site |
probably null |
|
R5224:Itpr2
|
UTSW |
6 |
146,068,149 (GRCm39) |
missense |
probably benign |
|
R5243:Itpr2
|
UTSW |
6 |
146,089,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Itpr2
|
UTSW |
6 |
146,378,191 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5393:Itpr2
|
UTSW |
6 |
146,277,653 (GRCm39) |
nonsense |
probably null |
|
R5552:Itpr2
|
UTSW |
6 |
146,195,578 (GRCm39) |
missense |
probably benign |
|
R5579:Itpr2
|
UTSW |
6 |
146,074,864 (GRCm39) |
nonsense |
probably null |
|
R5744:Itpr2
|
UTSW |
6 |
146,277,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Itpr2
|
UTSW |
6 |
146,045,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R5910:Itpr2
|
UTSW |
6 |
146,231,069 (GRCm39) |
missense |
probably benign |
0.10 |
R5911:Itpr2
|
UTSW |
6 |
146,214,441 (GRCm39) |
missense |
probably benign |
0.42 |
R6044:Itpr2
|
UTSW |
6 |
146,298,449 (GRCm39) |
missense |
probably null |
0.98 |
R6072:Itpr2
|
UTSW |
6 |
146,248,609 (GRCm39) |
missense |
probably damaging |
0.98 |
R6191:Itpr2
|
UTSW |
6 |
146,229,833 (GRCm39) |
missense |
probably benign |
0.01 |
R6483:Itpr2
|
UTSW |
6 |
146,013,975 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6511:Itpr2
|
UTSW |
6 |
146,231,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Itpr2
|
UTSW |
6 |
146,246,709 (GRCm39) |
missense |
probably benign |
0.01 |
R6561:Itpr2
|
UTSW |
6 |
146,135,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R6594:Itpr2
|
UTSW |
6 |
146,091,978 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6736:Itpr2
|
UTSW |
6 |
146,226,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Itpr2
|
UTSW |
6 |
146,287,371 (GRCm39) |
critical splice donor site |
probably null |
|
R6831:Itpr2
|
UTSW |
6 |
146,013,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Itpr2
|
UTSW |
6 |
146,298,517 (GRCm39) |
nonsense |
probably null |
|
R7103:Itpr2
|
UTSW |
6 |
146,226,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Itpr2
|
UTSW |
6 |
146,226,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Itpr2
|
UTSW |
6 |
146,259,294 (GRCm39) |
nonsense |
probably null |
|
R7165:Itpr2
|
UTSW |
6 |
146,195,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Itpr2
|
UTSW |
6 |
146,212,585 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7249:Itpr2
|
UTSW |
6 |
146,212,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Itpr2
|
UTSW |
6 |
146,060,447 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7342:Itpr2
|
UTSW |
6 |
146,228,685 (GRCm39) |
missense |
probably damaging |
0.98 |
R7392:Itpr2
|
UTSW |
6 |
146,260,838 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7414:Itpr2
|
UTSW |
6 |
146,274,706 (GRCm39) |
missense |
probably benign |
0.06 |
R7448:Itpr2
|
UTSW |
6 |
146,231,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R7492:Itpr2
|
UTSW |
6 |
146,292,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R7515:Itpr2
|
UTSW |
6 |
146,228,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Itpr2
|
UTSW |
6 |
146,096,096 (GRCm39) |
missense |
probably damaging |
0.98 |
R7558:Itpr2
|
UTSW |
6 |
146,292,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Itpr2
|
UTSW |
6 |
146,135,492 (GRCm39) |
missense |
probably benign |
0.36 |
R7678:Itpr2
|
UTSW |
6 |
146,089,048 (GRCm39) |
missense |
probably benign |
0.00 |
R7790:Itpr2
|
UTSW |
6 |
146,126,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Itpr2
|
UTSW |
6 |
146,287,513 (GRCm39) |
missense |
probably benign |
0.06 |
R7831:Itpr2
|
UTSW |
6 |
146,193,082 (GRCm39) |
missense |
probably benign |
0.04 |
R8023:Itpr2
|
UTSW |
6 |
146,088,988 (GRCm39) |
missense |
probably damaging |
0.97 |
R8046:Itpr2
|
UTSW |
6 |
146,327,957 (GRCm39) |
missense |
probably damaging |
0.96 |
R8236:Itpr2
|
UTSW |
6 |
146,292,281 (GRCm39) |
critical splice donor site |
probably null |
|
R8241:Itpr2
|
UTSW |
6 |
146,320,013 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8245:Itpr2
|
UTSW |
6 |
146,274,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R8324:Itpr2
|
UTSW |
6 |
146,229,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R8339:Itpr2
|
UTSW |
6 |
146,214,396 (GRCm39) |
missense |
probably benign |
0.19 |
R8458:Itpr2
|
UTSW |
6 |
146,135,464 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8506:Itpr2
|
UTSW |
6 |
146,319,914 (GRCm39) |
critical splice donor site |
probably null |
|
R8529:Itpr2
|
UTSW |
6 |
146,231,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Itpr2
|
UTSW |
6 |
146,276,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Itpr2
|
UTSW |
6 |
146,133,926 (GRCm39) |
missense |
probably benign |
|
R8816:Itpr2
|
UTSW |
6 |
146,142,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R9160:Itpr2
|
UTSW |
6 |
146,276,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Itpr2
|
UTSW |
6 |
146,226,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R9284:Itpr2
|
UTSW |
6 |
146,256,174 (GRCm39) |
missense |
probably benign |
0.01 |
R9322:Itpr2
|
UTSW |
6 |
146,226,587 (GRCm39) |
missense |
probably benign |
0.19 |
R9357:Itpr2
|
UTSW |
6 |
146,260,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Itpr2
|
UTSW |
6 |
146,212,505 (GRCm39) |
missense |
probably damaging |
0.98 |
R9438:Itpr2
|
UTSW |
6 |
146,068,166 (GRCm39) |
missense |
probably benign |
|
R9576:Itpr2
|
UTSW |
6 |
146,212,505 (GRCm39) |
missense |
probably damaging |
0.98 |
V8831:Itpr2
|
UTSW |
6 |
146,287,380 (GRCm39) |
missense |
probably damaging |
1.00 |
X0054:Itpr2
|
UTSW |
6 |
146,224,734 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Itpr2
|
UTSW |
6 |
146,081,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|