Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
A |
2: 35,244,782 (GRCm39) |
N190I |
probably damaging |
Het |
Ablim1 |
G |
T |
19: 57,204,173 (GRCm39) |
L73I |
probably benign |
Het |
Adamts4 |
A |
T |
1: 171,086,608 (GRCm39) |
Q800L |
probably benign |
Het |
Atm |
A |
T |
9: 53,376,598 (GRCm39) |
I2014N |
probably damaging |
Het |
Atp2a1 |
A |
G |
7: 126,062,061 (GRCm39) |
C12R |
possibly damaging |
Het |
B3galnt1 |
A |
T |
3: 69,483,157 (GRCm39) |
Y35N |
probably damaging |
Het |
Bnc2 |
A |
T |
4: 84,210,308 (GRCm39) |
M687K |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,320,939 (GRCm39) |
Y917C |
probably damaging |
Het |
Cemip2 |
T |
C |
19: 21,833,575 (GRCm39) |
F1338L |
probably benign |
Het |
Ces2e |
A |
G |
8: 105,659,632 (GRCm39) |
|
probably null |
Het |
Cldn23 |
A |
G |
8: 36,292,659 (GRCm39) |
|
probably null |
Het |
Cntn5 |
G |
T |
9: 10,172,021 (GRCm39) |
S54R |
probably benign |
Het |
Cyria |
T |
A |
12: 12,390,665 (GRCm39) |
|
probably null |
Het |
Dido1 |
G |
T |
2: 180,304,310 (GRCm39) |
S1198* |
probably null |
Het |
Dnah12 |
A |
G |
14: 26,445,766 (GRCm39) |
M776V |
probably benign |
Het |
Dnah14 |
A |
G |
1: 181,518,089 (GRCm39) |
|
probably null |
Het |
Dnttip1 |
GGGCCGGC |
GGGC |
2: 164,599,605 (GRCm39) |
|
probably null |
Het |
Dusp28 |
A |
T |
1: 92,834,861 (GRCm39) |
T29S |
probably benign |
Het |
Erich1 |
A |
T |
8: 14,083,688 (GRCm39) |
S127R |
probably benign |
Het |
Fam151a |
T |
A |
4: 106,602,681 (GRCm39) |
L200H |
probably damaging |
Het |
Fbxw8 |
A |
T |
5: 118,263,057 (GRCm39) |
H207Q |
probably damaging |
Het |
Fgf22 |
A |
G |
10: 79,592,676 (GRCm39) |
E116G |
probably benign |
Het |
Gapvd1 |
C |
A |
2: 34,602,207 (GRCm39) |
V647F |
probably benign |
Het |
Garin4 |
A |
T |
1: 190,895,910 (GRCm39) |
S244R |
probably damaging |
Het |
Gja4 |
T |
A |
4: 127,206,487 (GRCm39) |
Y92F |
probably damaging |
Het |
Gtf3c2 |
G |
A |
5: 31,327,600 (GRCm39) |
R288W |
probably damaging |
Het |
Hira |
G |
T |
16: 18,716,532 (GRCm39) |
R99L |
possibly damaging |
Het |
Ighv16-1 |
C |
T |
12: 114,032,721 (GRCm39) |
G27D |
probably damaging |
Het |
Igkv1-133 |
C |
T |
6: 67,702,395 (GRCm39) |
P38S |
probably benign |
Het |
Igkv4-59 |
T |
C |
6: 69,415,396 (GRCm39) |
Y53C |
probably damaging |
Het |
Il23a |
T |
C |
10: 128,133,020 (GRCm39) |
E113G |
probably damaging |
Het |
Kcnip1 |
A |
G |
11: 33,584,589 (GRCm39) |
V188A |
probably benign |
Het |
L3mbtl3 |
T |
C |
10: 26,216,850 (GRCm39) |
K155E |
unknown |
Het |
Lancl2 |
T |
G |
6: 57,699,664 (GRCm39) |
C169G |
probably benign |
Het |
Lrrc26 |
A |
G |
2: 25,180,581 (GRCm39) |
D194G |
probably benign |
Het |
Lrrfip1 |
C |
T |
1: 91,050,842 (GRCm39) |
A545V |
probably benign |
Het |
Lrtm1 |
T |
C |
14: 28,743,850 (GRCm39) |
F106S |
probably damaging |
Het |
Lypd2 |
A |
T |
15: 74,604,848 (GRCm39) |
M49K |
probably damaging |
Het |
Mbd1 |
A |
C |
18: 74,406,357 (GRCm39) |
D63A |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,691,729 (GRCm39) |
F990L |
probably damaging |
Het |
Mtfr1l |
T |
C |
4: 134,256,577 (GRCm39) |
E196G |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,705,874 (GRCm39) |
T2007A |
probably benign |
Het |
Nckap1 |
G |
A |
2: 80,370,512 (GRCm39) |
R393C |
probably damaging |
Het |
Nup205 |
C |
T |
6: 35,209,508 (GRCm39) |
T1605M |
probably benign |
Het |
Or1e33 |
T |
C |
11: 73,738,741 (GRCm39) |
D70G |
probably damaging |
Het |
Or5j3 |
GTACTTTTT |
GT |
2: 86,128,338 (GRCm39) |
|
probably null |
Het |
Pgap2 |
T |
A |
7: 101,875,467 (GRCm39) |
|
probably null |
Het |
Pitrm1 |
A |
G |
13: 6,619,387 (GRCm39) |
S741G |
probably benign |
Het |
Plcd4 |
A |
T |
1: 74,590,231 (GRCm39) |
S155C |
probably null |
Het |
Poc5 |
A |
T |
13: 96,540,925 (GRCm39) |
T365S |
possibly damaging |
Het |
Ppp2r5c |
G |
A |
12: 110,489,041 (GRCm39) |
A71T |
probably benign |
Het |
Prdm6 |
T |
A |
18: 53,598,199 (GRCm39) |
I187N |
possibly damaging |
Het |
Pxk |
A |
G |
14: 8,152,118 (GRCm38) |
Q478R |
probably benign |
Het |
Rgl1 |
T |
C |
1: 152,394,914 (GRCm39) |
Y718C |
probably damaging |
Het |
Ring1 |
G |
T |
17: 34,243,336 (GRCm39) |
T2K |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 142,173,897 (GRCm39) |
S2022G |
probably benign |
Het |
Sec61a1 |
C |
A |
6: 88,492,533 (GRCm39) |
V32F |
probably benign |
Het |
Sv2b |
G |
A |
7: 74,797,402 (GRCm39) |
P331S |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,090,970 (GRCm39) |
S795G |
possibly damaging |
Het |
Tmod2 |
T |
C |
9: 75,484,023 (GRCm39) |
E309G |
probably damaging |
Het |
Tpp2 |
T |
G |
1: 44,024,582 (GRCm39) |
S987A |
probably benign |
Het |
Trim75 |
G |
C |
8: 65,435,539 (GRCm39) |
H304D |
probably damaging |
Het |
Ube3a |
A |
G |
7: 58,936,751 (GRCm39) |
K697E |
probably benign |
Het |
Vmn2r13 |
T |
A |
5: 109,339,909 (GRCm39) |
H22L |
probably benign |
Het |
Vmn2r4 |
G |
A |
3: 64,314,432 (GRCm39) |
S183F |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,256,147 (GRCm39) |
Y721H |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,569 (GRCm39) |
P190L |
possibly damaging |
Het |
Zcchc4 |
A |
T |
5: 52,942,510 (GRCm39) |
Q105L |
possibly damaging |
Het |
Zfp236 |
T |
C |
18: 82,639,456 (GRCm39) |
R1264G |
probably damaging |
Het |
Zfpm2 |
T |
A |
15: 40,616,413 (GRCm39) |
N54K |
probably damaging |
Het |
Zkscan3 |
C |
T |
13: 21,571,992 (GRCm39) |
G547S |
probably damaging |
Het |
|
Other mutations in Trp53bp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Trp53bp2
|
APN |
1 |
182,268,541 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00920:Trp53bp2
|
APN |
1 |
182,272,219 (GRCm39) |
unclassified |
probably benign |
|
IGL01336:Trp53bp2
|
APN |
1 |
182,259,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01760:Trp53bp2
|
APN |
1 |
182,275,993 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02539:Trp53bp2
|
APN |
1 |
182,276,256 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02609:Trp53bp2
|
APN |
1 |
182,281,289 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02720:Trp53bp2
|
APN |
1 |
182,281,289 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02962:Trp53bp2
|
APN |
1 |
182,259,160 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03348:Trp53bp2
|
APN |
1 |
182,281,313 (GRCm39) |
missense |
probably damaging |
1.00 |
ganglion
|
UTSW |
1 |
182,256,475 (GRCm39) |
missense |
probably damaging |
1.00 |
Nosa
|
UTSW |
1 |
182,283,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Trp53bp2
|
UTSW |
1 |
182,272,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R0012:Trp53bp2
|
UTSW |
1 |
182,272,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R0347:Trp53bp2
|
UTSW |
1 |
182,269,213 (GRCm39) |
missense |
probably benign |
0.08 |
R1422:Trp53bp2
|
UTSW |
1 |
182,274,029 (GRCm39) |
missense |
probably benign |
|
R1833:Trp53bp2
|
UTSW |
1 |
182,256,581 (GRCm39) |
missense |
probably damaging |
0.98 |
R1845:Trp53bp2
|
UTSW |
1 |
182,286,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Trp53bp2
|
UTSW |
1 |
182,259,193 (GRCm39) |
missense |
probably benign |
0.01 |
R1927:Trp53bp2
|
UTSW |
1 |
182,280,229 (GRCm39) |
missense |
probably damaging |
0.98 |
R2017:Trp53bp2
|
UTSW |
1 |
182,276,580 (GRCm39) |
missense |
probably benign |
|
R2020:Trp53bp2
|
UTSW |
1 |
182,270,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Trp53bp2
|
UTSW |
1 |
182,286,432 (GRCm39) |
missense |
probably benign |
0.00 |
R2120:Trp53bp2
|
UTSW |
1 |
182,269,204 (GRCm39) |
missense |
probably benign |
0.06 |
R2504:Trp53bp2
|
UTSW |
1 |
182,269,204 (GRCm39) |
missense |
probably benign |
0.26 |
R2970:Trp53bp2
|
UTSW |
1 |
182,259,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R3051:Trp53bp2
|
UTSW |
1 |
182,281,347 (GRCm39) |
missense |
probably damaging |
0.96 |
R3052:Trp53bp2
|
UTSW |
1 |
182,281,347 (GRCm39) |
missense |
probably damaging |
0.96 |
R3053:Trp53bp2
|
UTSW |
1 |
182,281,347 (GRCm39) |
missense |
probably damaging |
0.96 |
R3151:Trp53bp2
|
UTSW |
1 |
182,256,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Trp53bp2
|
UTSW |
1 |
182,276,626 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4757:Trp53bp2
|
UTSW |
1 |
182,286,339 (GRCm39) |
missense |
probably benign |
0.04 |
R4785:Trp53bp2
|
UTSW |
1 |
182,276,562 (GRCm39) |
missense |
probably benign |
|
R4817:Trp53bp2
|
UTSW |
1 |
182,269,370 (GRCm39) |
critical splice donor site |
probably null |
|
R4836:Trp53bp2
|
UTSW |
1 |
182,259,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5040:Trp53bp2
|
UTSW |
1 |
182,272,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R5882:Trp53bp2
|
UTSW |
1 |
182,269,777 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6007:Trp53bp2
|
UTSW |
1 |
182,283,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R6356:Trp53bp2
|
UTSW |
1 |
182,276,562 (GRCm39) |
missense |
probably benign |
|
R6886:Trp53bp2
|
UTSW |
1 |
182,256,608 (GRCm39) |
critical splice donor site |
probably null |
|
R6987:Trp53bp2
|
UTSW |
1 |
182,274,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R7026:Trp53bp2
|
UTSW |
1 |
182,270,300 (GRCm39) |
missense |
probably benign |
|
R7141:Trp53bp2
|
UTSW |
1 |
182,276,073 (GRCm39) |
missense |
|
|
R7452:Trp53bp2
|
UTSW |
1 |
182,274,133 (GRCm39) |
nonsense |
probably null |
|
R7816:Trp53bp2
|
UTSW |
1 |
182,276,260 (GRCm39) |
missense |
probably damaging |
0.99 |
R7838:Trp53bp2
|
UTSW |
1 |
182,283,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R8729:Trp53bp2
|
UTSW |
1 |
182,276,587 (GRCm39) |
missense |
probably benign |
|
R8850:Trp53bp2
|
UTSW |
1 |
182,256,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8921:Trp53bp2
|
UTSW |
1 |
182,273,971 (GRCm39) |
missense |
|
|
R8982:Trp53bp2
|
UTSW |
1 |
182,263,001 (GRCm39) |
critical splice donor site |
probably null |
|
R8988:Trp53bp2
|
UTSW |
1 |
182,268,433 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9135:Trp53bp2
|
UTSW |
1 |
182,286,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R9424:Trp53bp2
|
UTSW |
1 |
182,273,864 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9563:Trp53bp2
|
UTSW |
1 |
182,276,378 (GRCm39) |
missense |
probably benign |
|
|