Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130008F23Rik |
T |
C |
17: 41,190,962 (GRCm39) |
T156A |
probably benign |
Het |
9230106D20Rik |
A |
T |
10: 19,536,065 (GRCm39) |
|
noncoding transcript |
Het |
Abca3 |
A |
G |
17: 24,585,171 (GRCm39) |
D144G |
probably benign |
Het |
Anxa2 |
T |
A |
9: 69,390,260 (GRCm39) |
L121Q |
probably damaging |
Het |
Anxa7 |
A |
T |
14: 20,512,732 (GRCm39) |
I267N |
probably damaging |
Het |
Asb14 |
A |
T |
14: 26,633,797 (GRCm39) |
D334V |
possibly damaging |
Het |
Batf3 |
A |
G |
1: 190,830,714 (GRCm39) |
N20S |
probably benign |
Het |
Bub1b |
A |
G |
2: 118,468,920 (GRCm39) |
H895R |
probably benign |
Het |
C1qtnf12 |
G |
A |
4: 156,050,160 (GRCm39) |
|
probably null |
Het |
Cars1 |
T |
C |
7: 143,130,385 (GRCm39) |
I294V |
probably damaging |
Het |
Ccdc142 |
G |
A |
6: 83,084,462 (GRCm39) |
A527T |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,096,234 (GRCm39) |
N1621K |
possibly damaging |
Het |
Ccdc92 |
T |
C |
5: 124,913,242 (GRCm39) |
N96D |
probably benign |
Het |
Ceacam18 |
T |
A |
7: 43,288,880 (GRCm39) |
D210E |
probably benign |
Het |
Cenpe |
A |
G |
3: 134,952,257 (GRCm39) |
T1373A |
probably damaging |
Het |
Cfap161 |
T |
G |
7: 83,440,932 (GRCm39) |
|
probably null |
Het |
Cimip4 |
T |
C |
15: 78,270,588 (GRCm39) |
Y60C |
possibly damaging |
Het |
Cldn19 |
A |
G |
4: 119,112,990 (GRCm39) |
D74G |
probably benign |
Het |
Clec12a |
A |
G |
6: 129,330,762 (GRCm39) |
T115A |
probably damaging |
Het |
Cox7a2l |
T |
A |
17: 83,811,397 (GRCm39) |
Q78L |
probably benign |
Het |
Crot |
T |
C |
5: 9,019,080 (GRCm39) |
N491S |
probably benign |
Het |
Cspg4b |
T |
A |
13: 113,505,342 (GRCm39) |
L2157Q |
probably damaging |
Het |
Ctr9 |
A |
G |
7: 110,643,165 (GRCm39) |
|
probably null |
Het |
Cyp4f14 |
T |
G |
17: 33,130,209 (GRCm39) |
D190A |
probably damaging |
Het |
D630039A03Rik |
C |
T |
4: 57,910,240 (GRCm39) |
V191I |
probably benign |
Het |
Dnah10 |
A |
T |
5: 124,838,343 (GRCm39) |
N1124I |
probably benign |
Het |
Duox1 |
T |
A |
2: 122,177,861 (GRCm39) |
Y1548* |
probably null |
Het |
Epdr1 |
G |
A |
13: 19,778,773 (GRCm39) |
Q6* |
probably null |
Het |
Erbin |
A |
G |
13: 103,996,577 (GRCm39) |
|
probably null |
Het |
Ero1a |
A |
T |
14: 45,525,217 (GRCm39) |
I436K |
probably damaging |
Het |
Exph5 |
A |
T |
9: 53,287,941 (GRCm39) |
Q1674L |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,037,607 (GRCm39) |
Y3753F |
probably damaging |
Het |
Gaa |
T |
C |
11: 119,174,098 (GRCm39) |
V763A |
probably damaging |
Het |
Golim4 |
G |
A |
3: 75,809,745 (GRCm39) |
T216I |
probably damaging |
Het |
Gpr83 |
G |
T |
9: 14,779,629 (GRCm39) |
C269F |
possibly damaging |
Het |
Gtf2f2 |
A |
G |
14: 76,245,143 (GRCm39) |
|
probably null |
Het |
Gtf3c5 |
T |
C |
2: 28,469,694 (GRCm39) |
Y70C |
probably damaging |
Het |
Hao1 |
T |
A |
2: 134,372,584 (GRCm39) |
R141S |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,965,182 (GRCm39) |
D548G |
probably benign |
Het |
Hr |
G |
A |
14: 70,809,477 (GRCm39) |
|
probably null |
Het |
Hrg |
A |
C |
16: 22,774,853 (GRCm39) |
E161A |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,237,526 (GRCm39) |
N1933I |
probably benign |
Het |
Kcnma1 |
C |
A |
14: 23,380,997 (GRCm39) |
D903Y |
probably damaging |
Het |
Kif5c |
T |
C |
2: 49,570,252 (GRCm39) |
|
probably null |
Het |
Mgat5b |
C |
A |
11: 116,868,614 (GRCm39) |
H512Q |
probably damaging |
Het |
Mtmr4 |
T |
C |
11: 87,502,943 (GRCm39) |
V999A |
probably benign |
Het |
Mttp |
G |
T |
3: 137,813,041 (GRCm39) |
Q545K |
probably damaging |
Het |
Ncstn |
CAGCTCCACGAAG |
CAG |
1: 171,899,038 (GRCm39) |
|
probably null |
Het |
Nexn |
A |
G |
3: 151,948,405 (GRCm39) |
I386T |
probably damaging |
Het |
Nrip3 |
A |
G |
7: 109,365,763 (GRCm39) |
S85P |
probably benign |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Olr1 |
T |
C |
6: 129,465,895 (GRCm39) |
N37S |
possibly damaging |
Het |
Or14j5 |
C |
T |
17: 38,161,966 (GRCm39) |
A161V |
probably benign |
Het |
Or4b1d |
A |
G |
2: 89,968,931 (GRCm39) |
L184S |
probably damaging |
Het |
Or4c105 |
A |
T |
2: 88,648,402 (GRCm39) |
I296F |
probably benign |
Het |
Or55b3 |
A |
G |
7: 102,126,720 (GRCm39) |
L119P |
probably damaging |
Het |
Or5p80 |
G |
T |
7: 108,229,855 (GRCm39) |
V219F |
possibly damaging |
Het |
Pax4 |
T |
C |
6: 28,443,446 (GRCm39) |
Y290C |
probably benign |
Het |
Pcdhb2 |
T |
A |
18: 37,429,038 (GRCm39) |
V337D |
probably damaging |
Het |
Pglyrp4 |
T |
C |
3: 90,640,310 (GRCm39) |
Y187H |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,098,614 (GRCm39) |
M2017T |
probably benign |
Het |
Pkdrej |
T |
C |
15: 85,703,483 (GRCm39) |
T818A |
possibly damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Pygm |
T |
C |
19: 6,447,637 (GRCm39) |
I648T |
possibly damaging |
Het |
Rab4a |
A |
T |
8: 124,550,565 (GRCm39) |
K15I |
probably damaging |
Het |
Rasa3 |
T |
C |
8: 13,635,035 (GRCm39) |
E428G |
probably benign |
Het |
Rnf182 |
G |
A |
13: 43,822,010 (GRCm39) |
W187* |
probably null |
Het |
Rpl3 |
C |
T |
15: 79,964,591 (GRCm39) |
V222M |
possibly damaging |
Het |
Rtl9 |
C |
T |
X: 141,886,011 (GRCm39) |
S1141F |
possibly damaging |
Het |
S100a11 |
A |
T |
3: 93,433,428 (GRCm39) |
I91F |
probably benign |
Het |
Sfswap |
C |
T |
5: 129,590,148 (GRCm39) |
T215I |
probably damaging |
Het |
Slit2 |
A |
G |
5: 48,461,372 (GRCm39) |
D1456G |
probably damaging |
Het |
Tex19.2 |
C |
T |
11: 121,008,317 (GRCm39) |
V44I |
probably benign |
Het |
Tmem127 |
G |
A |
2: 127,098,094 (GRCm39) |
|
probably null |
Het |
Tpd52 |
G |
T |
3: 9,012,579 (GRCm39) |
N59K |
probably damaging |
Het |
Trpc3 |
G |
A |
3: 36,692,695 (GRCm39) |
P766S |
possibly damaging |
Het |
Usp17la |
T |
A |
7: 104,510,331 (GRCm39) |
V312D |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,345,582 (GRCm39) |
N2608D |
possibly damaging |
Het |
Zfp764l1 |
T |
A |
7: 126,991,081 (GRCm39) |
H302L |
probably damaging |
Het |
Zscan25 |
C |
A |
5: 145,227,858 (GRCm39) |
H507Q |
possibly 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 |
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 |
146,131,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R3960:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
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 |
R6603:Itpr2
|
UTSW |
6 |
146,248,669 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|