Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
C |
T |
10: 28,862,242 (GRCm39) |
C16Y |
probably benign |
Het |
Abca13 |
C |
T |
11: 9,240,626 (GRCm39) |
L830F |
probably benign |
Het |
Apcdd1 |
T |
C |
18: 63,083,259 (GRCm39) |
V363A |
probably damaging |
Het |
Atosb |
T |
A |
4: 43,036,468 (GRCm39) |
R88* |
probably null |
Het |
Cachd1 |
A |
G |
4: 100,809,294 (GRCm39) |
I260V |
possibly damaging |
Het |
Cass4 |
T |
A |
2: 172,268,962 (GRCm39) |
M350K |
possibly damaging |
Het |
Ccnjl |
A |
G |
11: 43,470,615 (GRCm39) |
T128A |
probably benign |
Het |
Cd6 |
C |
T |
19: 10,773,752 (GRCm39) |
G361D |
probably benign |
Het |
Cdh22 |
T |
C |
2: 164,965,639 (GRCm39) |
|
probably benign |
Het |
Ces2h |
T |
A |
8: 105,746,572 (GRCm39) |
F475Y |
probably benign |
Het |
Col15a1 |
A |
T |
4: 47,245,380 (GRCm39) |
T44S |
probably damaging |
Het |
Cplx3 |
C |
T |
9: 57,509,741 (GRCm39) |
E86K |
possibly damaging |
Het |
Crbn |
A |
G |
6: 106,772,004 (GRCm39) |
V100A |
possibly damaging |
Het |
D430041D05Rik |
C |
A |
2: 104,071,500 (GRCm39) |
V1267L |
possibly damaging |
Het |
Ecrg4 |
T |
A |
1: 43,770,111 (GRCm39) |
C23S |
probably damaging |
Het |
Elapor1 |
C |
A |
3: 108,375,113 (GRCm39) |
A585S |
probably benign |
Het |
F930017D23Rik |
A |
G |
10: 43,480,405 (GRCm39) |
|
noncoding transcript |
Het |
Fastkd3 |
A |
G |
13: 68,731,796 (GRCm39) |
D39G |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,733,490 (GRCm39) |
S912R |
probably benign |
Het |
H2-T24 |
T |
C |
17: 36,328,264 (GRCm39) |
Y73C |
probably damaging |
Het |
Ifna9 |
A |
T |
4: 88,510,591 (GRCm39) |
L11* |
probably null |
Het |
Igsf10 |
A |
T |
3: 59,238,573 (GRCm39) |
L536* |
probably null |
Het |
Itprid1 |
A |
T |
6: 55,861,673 (GRCm39) |
|
probably benign |
Het |
Kcnma1 |
A |
T |
14: 23,593,144 (GRCm39) |
I215K |
probably damaging |
Het |
Kdm4c |
A |
C |
4: 74,291,953 (GRCm39) |
I857L |
possibly damaging |
Het |
Kptn |
A |
T |
7: 15,857,786 (GRCm39) |
H229L |
probably benign |
Het |
Krt32 |
A |
T |
11: 99,978,967 (GRCm39) |
M29K |
probably benign |
Het |
Lama2 |
A |
G |
10: 26,877,112 (GRCm39) |
|
probably benign |
Het |
Lpcat2b |
A |
C |
5: 107,581,982 (GRCm39) |
D437A |
probably damaging |
Het |
Lrrc8c |
T |
C |
5: 105,755,764 (GRCm39) |
L513P |
probably damaging |
Het |
Mon1a |
T |
C |
9: 107,778,997 (GRCm39) |
V407A |
possibly damaging |
Het |
Myo5c |
C |
T |
9: 75,153,519 (GRCm39) |
P135L |
probably damaging |
Het |
Myof |
C |
T |
19: 37,942,877 (GRCm39) |
V218M |
possibly damaging |
Het |
Myof |
T |
A |
19: 37,963,311 (GRCm39) |
I429F |
possibly damaging |
Het |
Nckap1 |
G |
A |
2: 80,358,962 (GRCm39) |
P560S |
probably benign |
Het |
Notch2 |
G |
A |
3: 98,044,713 (GRCm39) |
G1545D |
probably damaging |
Het |
Ntrk1 |
G |
A |
3: 87,688,838 (GRCm39) |
H572Y |
probably damaging |
Het |
Or2t44 |
T |
C |
11: 58,677,551 (GRCm39) |
F164L |
probably benign |
Het |
Or7e177 |
T |
C |
9: 20,211,588 (GRCm39) |
S31P |
probably damaging |
Het |
Pate8 |
T |
C |
9: 36,493,166 (GRCm39) |
Y52C |
possibly damaging |
Het |
Pcdh15 |
A |
T |
10: 74,178,504 (GRCm39) |
D587V |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,928,609 (GRCm39) |
Y882C |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,606,704 (GRCm39) |
*1074C |
probably null |
Het |
Plcxd1 |
T |
C |
5: 110,248,140 (GRCm39) |
|
probably benign |
Het |
Ppp2r2d |
A |
G |
7: 138,474,700 (GRCm39) |
N27S |
probably null |
Het |
Prkar2a |
A |
G |
9: 108,624,152 (GRCm39) |
M390V |
probably benign |
Het |
Rab3gap1 |
A |
G |
1: 127,796,695 (GRCm39) |
T18A |
probably damaging |
Het |
Ranbp2 |
T |
C |
10: 58,329,475 (GRCm39) |
|
probably benign |
Het |
Rasl12 |
T |
C |
9: 65,305,946 (GRCm39) |
S34P |
probably damaging |
Het |
Rpusd3 |
A |
T |
6: 113,395,818 (GRCm39) |
L65Q |
possibly damaging |
Het |
Rtf2 |
A |
G |
2: 172,310,639 (GRCm39) |
K290R |
probably damaging |
Het |
Rwdd4a |
T |
A |
8: 48,003,731 (GRCm39) |
L179* |
probably null |
Het |
Scgb1b24 |
A |
G |
7: 33,444,388 (GRCm39) |
E87G |
possibly damaging |
Het |
Sgo2a |
A |
G |
1: 58,056,881 (GRCm39) |
I1022V |
probably benign |
Het |
Smg1 |
A |
C |
7: 117,781,764 (GRCm39) |
I1174M |
probably benign |
Het |
Spata17 |
A |
T |
1: 186,872,595 (GRCm39) |
M72K |
probably damaging |
Het |
Synpo2 |
G |
A |
3: 122,910,632 (GRCm39) |
P338S |
probably damaging |
Het |
Tpi1 |
G |
A |
6: 124,791,087 (GRCm39) |
T50I |
probably benign |
Het |
Trpm1 |
A |
G |
7: 63,867,362 (GRCm39) |
E354G |
probably damaging |
Het |
Uba2 |
A |
G |
7: 33,842,161 (GRCm39) |
|
probably null |
Het |
Wnk1 |
G |
A |
6: 119,914,334 (GRCm39) |
R1823* |
probably null |
Het |
Zfp248 |
A |
C |
6: 118,430,801 (GRCm39) |
|
probably benign |
Het |
Zfp51 |
A |
T |
17: 21,683,681 (GRCm39) |
K99* |
probably null |
Het |
|
Other mutations in Nbas |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00486:Nbas
|
APN |
12 |
13,503,076 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00712:Nbas
|
APN |
12 |
13,412,626 (GRCm39) |
splice site |
probably benign |
|
IGL00808:Nbas
|
APN |
12 |
13,616,121 (GRCm39) |
splice site |
probably benign |
|
IGL00915:Nbas
|
APN |
12 |
13,424,753 (GRCm39) |
nonsense |
probably null |
|
IGL00923:Nbas
|
APN |
12 |
13,386,285 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01152:Nbas
|
APN |
12 |
13,410,959 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Nbas
|
APN |
12 |
13,533,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01672:Nbas
|
APN |
12 |
13,429,650 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01799:Nbas
|
APN |
12 |
13,374,401 (GRCm39) |
splice site |
probably benign |
|
IGL01812:Nbas
|
APN |
12 |
13,503,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Nbas
|
APN |
12 |
13,339,880 (GRCm39) |
splice site |
probably benign |
|
IGL02093:Nbas
|
APN |
12 |
13,610,963 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02115:Nbas
|
APN |
12 |
13,367,693 (GRCm39) |
splice site |
probably benign |
|
IGL02175:Nbas
|
APN |
12 |
13,616,260 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02483:Nbas
|
APN |
12 |
13,374,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02539:Nbas
|
APN |
12 |
13,322,704 (GRCm39) |
splice site |
probably benign |
|
IGL02557:Nbas
|
APN |
12 |
13,411,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02815:Nbas
|
APN |
12 |
13,360,267 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Nbas
|
APN |
12 |
13,412,542 (GRCm39) |
missense |
probably benign |
|
IGL03131:Nbas
|
APN |
12 |
13,329,417 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03214:Nbas
|
APN |
12 |
13,381,111 (GRCm39) |
splice site |
probably benign |
|
IGL03308:Nbas
|
APN |
12 |
13,374,349 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03368:Nbas
|
APN |
12 |
13,378,452 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03372:Nbas
|
APN |
12 |
13,584,473 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Nbas
|
APN |
12 |
13,533,750 (GRCm39) |
missense |
probably benign |
0.28 |
medvedev
|
UTSW |
12 |
13,584,578 (GRCm39) |
critical splice donor site |
probably null |
|
oligarchs
|
UTSW |
12 |
13,570,751 (GRCm39) |
missense |
possibly damaging |
0.75 |
putin
|
UTSW |
12 |
13,371,756 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Nbas
|
UTSW |
12 |
13,338,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Nbas
|
UTSW |
12 |
13,440,958 (GRCm39) |
missense |
probably benign |
0.00 |
R0076:Nbas
|
UTSW |
12 |
13,374,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Nbas
|
UTSW |
12 |
13,323,877 (GRCm39) |
splice site |
probably benign |
|
R0371:Nbas
|
UTSW |
12 |
13,381,096 (GRCm39) |
missense |
probably damaging |
0.97 |
R0449:Nbas
|
UTSW |
12 |
13,569,109 (GRCm39) |
missense |
probably benign |
0.18 |
R0791:Nbas
|
UTSW |
12 |
13,532,634 (GRCm39) |
missense |
probably benign |
0.28 |
R0931:Nbas
|
UTSW |
12 |
13,381,115 (GRCm39) |
splice site |
probably benign |
|
R1236:Nbas
|
UTSW |
12 |
13,319,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R1371:Nbas
|
UTSW |
12 |
13,532,379 (GRCm39) |
splice site |
probably benign |
|
R1567:Nbas
|
UTSW |
12 |
13,335,279 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1587:Nbas
|
UTSW |
12 |
13,608,686 (GRCm39) |
missense |
probably benign |
|
R1719:Nbas
|
UTSW |
12 |
13,610,978 (GRCm39) |
critical splice donor site |
probably null |
|
R1747:Nbas
|
UTSW |
12 |
13,385,899 (GRCm39) |
missense |
probably benign |
0.00 |
R1777:Nbas
|
UTSW |
12 |
13,563,563 (GRCm39) |
missense |
probably benign |
0.16 |
R1848:Nbas
|
UTSW |
12 |
13,463,598 (GRCm39) |
missense |
probably damaging |
0.97 |
R1856:Nbas
|
UTSW |
12 |
13,524,230 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1891:Nbas
|
UTSW |
12 |
13,440,973 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1911:Nbas
|
UTSW |
12 |
13,616,145 (GRCm39) |
missense |
probably benign |
|
R1912:Nbas
|
UTSW |
12 |
13,616,145 (GRCm39) |
missense |
probably benign |
|
R2006:Nbas
|
UTSW |
12 |
13,464,742 (GRCm39) |
splice site |
probably null |
|
R2054:Nbas
|
UTSW |
12 |
13,524,207 (GRCm39) |
missense |
probably benign |
0.36 |
R2065:Nbas
|
UTSW |
12 |
13,616,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2089:Nbas
|
UTSW |
12 |
13,411,046 (GRCm39) |
missense |
probably benign |
0.03 |
R2091:Nbas
|
UTSW |
12 |
13,411,046 (GRCm39) |
missense |
probably benign |
0.03 |
R2091:Nbas
|
UTSW |
12 |
13,411,046 (GRCm39) |
missense |
probably benign |
0.03 |
R2156:Nbas
|
UTSW |
12 |
13,491,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2164:Nbas
|
UTSW |
12 |
13,380,647 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2339:Nbas
|
UTSW |
12 |
13,412,593 (GRCm39) |
missense |
probably benign |
0.12 |
R2398:Nbas
|
UTSW |
12 |
13,482,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R3806:Nbas
|
UTSW |
12 |
13,532,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Nbas
|
UTSW |
12 |
13,329,415 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4019:Nbas
|
UTSW |
12 |
13,532,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4083:Nbas
|
UTSW |
12 |
13,524,192 (GRCm39) |
missense |
probably damaging |
0.96 |
R4201:Nbas
|
UTSW |
12 |
13,424,827 (GRCm39) |
missense |
probably benign |
0.00 |
R4231:Nbas
|
UTSW |
12 |
13,443,344 (GRCm39) |
missense |
probably damaging |
0.98 |
R4552:Nbas
|
UTSW |
12 |
13,385,938 (GRCm39) |
critical splice donor site |
probably null |
|
R4560:Nbas
|
UTSW |
12 |
13,633,528 (GRCm39) |
missense |
probably benign |
0.00 |
R4728:Nbas
|
UTSW |
12 |
13,338,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R4752:Nbas
|
UTSW |
12 |
13,532,538 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4832:Nbas
|
UTSW |
12 |
13,533,740 (GRCm39) |
missense |
probably benign |
0.00 |
R4874:Nbas
|
UTSW |
12 |
13,371,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Nbas
|
UTSW |
12 |
13,458,266 (GRCm39) |
missense |
probably benign |
0.45 |
R5020:Nbas
|
UTSW |
12 |
13,424,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R5079:Nbas
|
UTSW |
12 |
13,424,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5129:Nbas
|
UTSW |
12 |
13,440,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Nbas
|
UTSW |
12 |
13,491,519 (GRCm39) |
missense |
probably benign |
0.31 |
R5299:Nbas
|
UTSW |
12 |
13,491,926 (GRCm39) |
nonsense |
probably null |
|
R5351:Nbas
|
UTSW |
12 |
13,610,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Nbas
|
UTSW |
12 |
13,584,578 (GRCm39) |
critical splice donor site |
probably null |
|
R5436:Nbas
|
UTSW |
12 |
13,424,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Nbas
|
UTSW |
12 |
13,633,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5690:Nbas
|
UTSW |
12 |
13,386,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Nbas
|
UTSW |
12 |
13,319,267 (GRCm39) |
critical splice donor site |
probably null |
|
R5959:Nbas
|
UTSW |
12 |
13,338,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R5982:Nbas
|
UTSW |
12 |
13,443,431 (GRCm39) |
missense |
probably benign |
0.00 |
R6238:Nbas
|
UTSW |
12 |
13,532,596 (GRCm39) |
missense |
probably benign |
|
R6270:Nbas
|
UTSW |
12 |
13,374,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R6363:Nbas
|
UTSW |
12 |
13,532,577 (GRCm39) |
missense |
probably benign |
|
R6424:Nbas
|
UTSW |
12 |
13,465,734 (GRCm39) |
critical splice donor site |
probably null |
|
R6458:Nbas
|
UTSW |
12 |
13,338,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6526:Nbas
|
UTSW |
12 |
13,455,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Nbas
|
UTSW |
12 |
13,533,875 (GRCm39) |
nonsense |
probably null |
|
R7085:Nbas
|
UTSW |
12 |
13,335,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Nbas
|
UTSW |
12 |
13,455,398 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7197:Nbas
|
UTSW |
12 |
13,570,751 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7378:Nbas
|
UTSW |
12 |
13,324,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Nbas
|
UTSW |
12 |
13,443,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:Nbas
|
UTSW |
12 |
13,519,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R7446:Nbas
|
UTSW |
12 |
13,443,499 (GRCm39) |
missense |
probably benign |
0.02 |
R7481:Nbas
|
UTSW |
12 |
13,406,960 (GRCm39) |
missense |
probably damaging |
0.97 |
R7535:Nbas
|
UTSW |
12 |
13,329,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R7626:Nbas
|
UTSW |
12 |
13,608,661 (GRCm39) |
missense |
probably benign |
0.00 |
R7678:Nbas
|
UTSW |
12 |
13,465,662 (GRCm39) |
missense |
probably damaging |
0.97 |
R7912:Nbas
|
UTSW |
12 |
13,455,458 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7964:Nbas
|
UTSW |
12 |
13,406,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R8193:Nbas
|
UTSW |
12 |
13,483,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R8325:Nbas
|
UTSW |
12 |
13,338,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8405:Nbas
|
UTSW |
12 |
13,329,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Nbas
|
UTSW |
12 |
13,616,251 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8559:Nbas
|
UTSW |
12 |
13,402,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8684:Nbas
|
UTSW |
12 |
13,386,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R8826:Nbas
|
UTSW |
12 |
13,402,875 (GRCm39) |
splice site |
probably benign |
|
R8921:Nbas
|
UTSW |
12 |
13,463,590 (GRCm39) |
missense |
probably benign |
|
R8956:Nbas
|
UTSW |
12 |
13,482,923 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9083:Nbas
|
UTSW |
12 |
13,385,856 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9172:Nbas
|
UTSW |
12 |
13,424,751 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9430:Nbas
|
UTSW |
12 |
13,371,654 (GRCm39) |
missense |
probably benign |
0.35 |
R9627:Nbas
|
UTSW |
12 |
13,350,203 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9649:Nbas
|
UTSW |
12 |
13,633,417 (GRCm39) |
missense |
probably damaging |
1.00 |
RF013:Nbas
|
UTSW |
12 |
13,329,409 (GRCm39) |
missense |
possibly damaging |
0.54 |
T0722:Nbas
|
UTSW |
12 |
13,402,809 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Nbas
|
UTSW |
12 |
13,533,877 (GRCm39) |
missense |
probably benign |
0.06 |
|