Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,262,870 (GRCm39) |
L1401P |
possibly damaging |
Het |
4930503B20Rik |
C |
T |
3: 146,356,251 (GRCm39) |
R219H |
probably benign |
Het |
Abcc9 |
T |
A |
6: 142,634,710 (GRCm39) |
I185F |
probably benign |
Het |
Adgrf1 |
T |
C |
17: 43,607,581 (GRCm39) |
L100P |
probably damaging |
Het |
Akt1 |
T |
C |
12: 112,621,576 (GRCm39) |
T407A |
probably damaging |
Het |
Alk |
C |
T |
17: 72,910,511 (GRCm39) |
R65H |
probably damaging |
Het |
Aplp2 |
T |
C |
9: 31,069,086 (GRCm39) |
E525G |
probably damaging |
Het |
Arhgef12 |
G |
A |
9: 42,883,300 (GRCm39) |
R1411C |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,383,460 (GRCm39) |
M242K |
probably damaging |
Het |
Atad5 |
T |
G |
11: 79,986,473 (GRCm39) |
V520G |
probably benign |
Het |
Avpr1a |
T |
A |
10: 122,285,374 (GRCm39) |
M222K |
possibly damaging |
Het |
Cbr2 |
T |
A |
11: 120,621,614 (GRCm39) |
I88L |
probably benign |
Het |
Cc2d2a |
T |
A |
5: 43,845,608 (GRCm39) |
|
probably null |
Het |
Ccdc51 |
T |
C |
9: 108,918,441 (GRCm39) |
M10T |
probably benign |
Het |
Cntnap5b |
T |
A |
1: 100,406,099 (GRCm39) |
D1136E |
possibly damaging |
Het |
Coil |
T |
A |
11: 88,872,979 (GRCm39) |
S447T |
probably damaging |
Het |
Cryba1 |
T |
A |
11: 77,609,693 (GRCm39) |
Y179F |
probably damaging |
Het |
Dcaf4 |
T |
A |
12: 83,582,735 (GRCm39) |
F277I |
probably damaging |
Het |
Ddost |
G |
A |
4: 138,036,913 (GRCm39) |
V159M |
probably damaging |
Het |
Dnaaf4 |
A |
T |
9: 72,868,649 (GRCm39) |
R127S |
possibly damaging |
Het |
Dnajb6 |
T |
C |
5: 29,990,077 (GRCm39) |
|
probably benign |
Het |
Dnase2a |
A |
G |
8: 85,635,417 (GRCm39) |
|
probably benign |
Het |
Dscam |
T |
C |
16: 96,517,279 (GRCm39) |
I877V |
possibly damaging |
Het |
Efcc1 |
A |
T |
6: 87,726,136 (GRCm39) |
T312S |
probably benign |
Het |
Elp1 |
T |
A |
4: 56,795,545 (GRCm39) |
I143F |
probably damaging |
Het |
Ermard |
A |
T |
17: 15,242,205 (GRCm39) |
Q127L |
probably damaging |
Het |
F2 |
T |
C |
2: 91,460,503 (GRCm39) |
E329G |
probably damaging |
Het |
Foxc2 |
T |
A |
8: 121,843,355 (GRCm39) |
M1K |
probably null |
Het |
Fuz |
T |
A |
7: 44,548,446 (GRCm39) |
|
probably null |
Het |
Ggnbp2 |
G |
A |
11: 84,731,139 (GRCm39) |
T325M |
probably damaging |
Het |
Gm6408 |
T |
A |
5: 146,419,870 (GRCm39) |
F115I |
probably benign |
Het |
Gp6 |
C |
T |
7: 4,376,208 (GRCm39) |
|
probably null |
Het |
Grin2a |
A |
G |
16: 9,397,037 (GRCm39) |
S1017P |
possibly damaging |
Het |
H2-T5 |
T |
C |
17: 36,478,899 (GRCm39) |
T117A |
probably damaging |
Het |
Hmmr |
A |
T |
11: 40,605,635 (GRCm39) |
M318K |
probably damaging |
Het |
Ifi205 |
T |
C |
1: 173,855,994 (GRCm39) |
E12G |
probably benign |
Het |
Ift74 |
C |
T |
4: 94,567,492 (GRCm39) |
T395I |
probably benign |
Het |
Irf8 |
A |
T |
8: 121,466,714 (GRCm39) |
D53V |
probably damaging |
Het |
Itgad |
A |
G |
7: 127,803,813 (GRCm39) |
Y69C |
probably damaging |
Het |
Krt4 |
C |
A |
15: 101,831,217 (GRCm39) |
S228I |
possibly damaging |
Het |
Lpin3 |
A |
T |
2: 160,740,601 (GRCm39) |
D382V |
probably damaging |
Het |
Ltbp3 |
T |
C |
19: 5,802,171 (GRCm39) |
|
probably null |
Het |
Map4k3 |
C |
T |
17: 80,952,270 (GRCm39) |
A179T |
probably damaging |
Het |
Nck1 |
A |
T |
9: 100,379,820 (GRCm39) |
W144R |
probably damaging |
Het |
Ndufb9 |
A |
T |
15: 58,811,131 (GRCm39) |
Q139L |
possibly damaging |
Het |
Ngfr |
T |
G |
11: 95,462,738 (GRCm39) |
E300A |
probably damaging |
Het |
Nin |
T |
G |
12: 70,061,649 (GRCm39) |
T2072P |
probably damaging |
Het |
Nop2 |
T |
G |
6: 125,118,307 (GRCm39) |
L529R |
probably damaging |
Het |
Nrm |
T |
A |
17: 36,175,503 (GRCm39) |
L203Q |
probably damaging |
Het |
Nynrin |
T |
C |
14: 56,109,255 (GRCm39) |
F1454S |
probably benign |
Het |
Or10ak7 |
T |
A |
4: 118,791,467 (GRCm39) |
M191L |
probably benign |
Het |
Or5b101 |
T |
C |
19: 13,005,646 (GRCm39) |
T16A |
possibly damaging |
Het |
Or8j3c |
A |
C |
2: 86,253,451 (GRCm39) |
S190A |
probably damaging |
Het |
Os9 |
A |
G |
10: 126,956,905 (GRCm39) |
V27A |
probably damaging |
Het |
Osbpl9 |
T |
G |
4: 108,930,321 (GRCm39) |
T332P |
probably damaging |
Het |
Pcdhb10 |
A |
T |
18: 37,547,059 (GRCm39) |
M712L |
probably benign |
Het |
Pcx |
C |
T |
19: 4,670,227 (GRCm39) |
A935V |
probably damaging |
Het |
Pdzd7 |
A |
G |
19: 45,022,106 (GRCm39) |
V514A |
possibly damaging |
Het |
Plin4 |
C |
T |
17: 56,409,242 (GRCm39) |
G1326D |
probably damaging |
Het |
Plxnb1 |
T |
A |
9: 108,932,731 (GRCm39) |
Y568* |
probably null |
Het |
Pmfbp1 |
T |
A |
8: 110,268,372 (GRCm39) |
V973D |
probably benign |
Het |
Ppp2r1b |
T |
C |
9: 50,772,925 (GRCm39) |
V70A |
probably benign |
Het |
Prkar2b |
C |
A |
12: 32,022,183 (GRCm39) |
V201L |
probably benign |
Het |
Rgr |
T |
G |
14: 36,768,925 (GRCm39) |
T37P |
probably damaging |
Het |
Ripk3 |
A |
T |
14: 56,025,375 (GRCm39) |
L63Q |
probably damaging |
Het |
Rpusd2 |
A |
G |
2: 118,868,893 (GRCm39) |
S439G |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,100,335 (GRCm39) |
R438S |
possibly damaging |
Het |
Slc19a1 |
T |
A |
10: 76,874,300 (GRCm39) |
S24T |
possibly damaging |
Het |
Slc6a21 |
A |
C |
7: 44,937,667 (GRCm39) |
T653P |
possibly damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Spdef |
C |
T |
17: 27,933,894 (GRCm39) |
R309H |
probably damaging |
Het |
Srp68 |
A |
T |
11: 116,156,377 (GRCm39) |
Y84N |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,144,731 (GRCm39) |
Q6299L |
probably damaging |
Het |
Tmem63b |
T |
A |
17: 45,972,839 (GRCm39) |
M652L |
probably benign |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Tnk1 |
A |
G |
11: 69,746,007 (GRCm39) |
V306A |
probably damaging |
Het |
Tnnc2 |
T |
A |
2: 164,619,404 (GRCm39) |
I147F |
probably damaging |
Het |
Tnni3k |
C |
T |
3: 154,760,981 (GRCm39) |
|
probably benign |
Het |
Togaram2 |
T |
A |
17: 72,036,243 (GRCm39) |
V911D |
probably damaging |
Het |
Tyw3 |
T |
C |
3: 154,293,132 (GRCm39) |
N181S |
probably damaging |
Het |
Unc79 |
T |
A |
12: 103,039,051 (GRCm39) |
S682T |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,841,348 (GRCm39) |
L2634S |
probably benign |
Het |
Wasl |
G |
T |
6: 24,633,892 (GRCm39) |
A124E |
probably damaging |
Het |
Zfp287 |
T |
C |
11: 62,605,743 (GRCm39) |
H388R |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,749,612 (GRCm39) |
T262A |
probably damaging |
Het |
Zfp457 |
C |
G |
13: 67,441,211 (GRCm39) |
G359R |
probably benign |
Het |
Zfp536 |
T |
A |
7: 37,267,874 (GRCm39) |
E514V |
probably damaging |
Het |
Zfp872 |
T |
A |
9: 22,111,469 (GRCm39) |
I316N |
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 |
|
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 |
146,131,262 (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 |
|