Other mutations in this stock |
Total: 130 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,214,257 (GRCm39) |
Y191H |
probably damaging |
Het |
Aco1 |
T |
C |
4: 40,167,193 (GRCm39) |
|
probably null |
Het |
Adap1 |
A |
G |
5: 139,259,096 (GRCm39) |
Y364H |
probably benign |
Het |
Add2 |
T |
C |
6: 86,073,738 (GRCm39) |
F209S |
probably damaging |
Het |
Adgb |
A |
T |
10: 10,270,993 (GRCm39) |
D883E |
probably benign |
Het |
Anapc1 |
C |
A |
2: 128,475,335 (GRCm39) |
R1381S |
probably benign |
Het |
Aoah |
A |
G |
13: 20,978,564 (GRCm39) |
M1V |
probably null |
Het |
Arap1 |
C |
A |
7: 101,022,222 (GRCm39) |
A8E |
probably damaging |
Het |
Arhgap10 |
A |
G |
8: 78,136,255 (GRCm39) |
F319S |
possibly damaging |
Het |
Btrc |
T |
G |
19: 45,515,782 (GRCm39) |
I480S |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,570,924 (GRCm39) |
V784E |
possibly damaging |
Het |
Card9 |
T |
A |
2: 26,244,885 (GRCm39) |
|
probably null |
Het |
Cdk18 |
A |
G |
1: 132,045,559 (GRCm39) |
I238T |
possibly damaging |
Het |
Clec12a |
A |
C |
6: 129,327,444 (GRCm39) |
T21P |
possibly damaging |
Het |
Commd3 |
A |
T |
2: 18,678,774 (GRCm39) |
I70F |
probably benign |
Het |
Cspg5 |
G |
A |
9: 110,080,094 (GRCm39) |
V340M |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 86,937,902 (GRCm39) |
S307N |
possibly damaging |
Het |
Cyp26c1 |
T |
A |
19: 37,675,825 (GRCm39) |
F230I |
probably damaging |
Het |
Ddx11 |
A |
G |
17: 66,437,723 (GRCm39) |
M150V |
probably benign |
Het |
Dennd4b |
A |
G |
3: 90,176,080 (GRCm39) |
Y190C |
probably damaging |
Het |
Det1 |
A |
G |
7: 78,493,191 (GRCm39) |
V271A |
probably benign |
Het |
Dgkd |
C |
A |
1: 87,857,549 (GRCm39) |
P754T |
possibly damaging |
Het |
Dhx36 |
T |
C |
3: 62,386,806 (GRCm39) |
S649G |
probably benign |
Het |
Dlgap5 |
A |
G |
14: 47,653,843 (GRCm39) |
I62T |
possibly damaging |
Het |
Dmgdh |
A |
G |
13: 93,857,067 (GRCm39) |
M724V |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,724,142 (GRCm39) |
S108P |
probably benign |
Het |
Dock4 |
A |
T |
12: 40,760,797 (GRCm39) |
K495M |
probably damaging |
Het |
Dse |
A |
G |
10: 34,036,202 (GRCm39) |
Y225H |
probably damaging |
Het |
Emx1 |
G |
A |
6: 85,180,916 (GRCm39) |
R211K |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,100,852 (GRCm39) |
|
probably null |
Het |
Fbxo27 |
G |
A |
7: 28,397,797 (GRCm39) |
C277Y |
possibly damaging |
Het |
Fcrl1 |
T |
C |
3: 87,283,827 (GRCm39) |
I9T |
possibly damaging |
Het |
Fjx1 |
T |
C |
2: 102,281,152 (GRCm39) |
E261G |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,698,437 (GRCm39) |
V327D |
possibly damaging |
Het |
Flnb |
C |
T |
14: 7,884,735 (GRCm38) |
Q445* |
probably null |
Het |
Flrt2 |
G |
A |
12: 95,747,074 (GRCm39) |
V471I |
probably benign |
Het |
Frmd4a |
G |
A |
2: 4,539,997 (GRCm39) |
V210M |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,821,894 (GRCm39) |
K5876E |
probably benign |
Het |
Galnt10 |
T |
C |
11: 57,656,443 (GRCm39) |
L209P |
probably damaging |
Het |
Gata5 |
A |
T |
2: 179,968,729 (GRCm39) |
S382T |
possibly damaging |
Het |
Glt6d1 |
C |
A |
2: 25,684,425 (GRCm39) |
V194L |
probably damaging |
Het |
Gm10803 |
T |
G |
2: 93,394,288 (GRCm39) |
V20G |
unknown |
Het |
Gm44511 |
T |
G |
6: 128,797,234 (GRCm39) |
T52P |
probably damaging |
Het |
Gpat4 |
A |
T |
8: 23,672,952 (GRCm39) |
L88Q |
possibly damaging |
Het |
Gpr15 |
T |
A |
16: 58,538,370 (GRCm39) |
I240L |
probably benign |
Het |
Hivep2 |
A |
T |
10: 14,008,453 (GRCm39) |
I1684F |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,525,427 (GRCm39) |
T3366A |
probably benign |
Het |
Hnmt |
A |
G |
2: 23,893,894 (GRCm39) |
V200A |
possibly damaging |
Het |
Hps6 |
A |
T |
19: 45,992,774 (GRCm39) |
H237L |
probably benign |
Het |
Hspg2 |
C |
T |
4: 137,292,206 (GRCm39) |
P4033S |
probably damaging |
Het |
Ift70b |
C |
T |
2: 75,767,443 (GRCm39) |
E437K |
probably benign |
Het |
Irf9 |
T |
A |
14: 55,845,174 (GRCm39) |
S297T |
possibly damaging |
Het |
Kdm3b |
T |
C |
18: 34,945,448 (GRCm39) |
V753A |
possibly damaging |
Het |
Kif21a |
G |
A |
15: 90,855,051 (GRCm39) |
A703V |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,440,937 (GRCm39) |
R1159S |
probably benign |
Het |
Krtap4-16 |
A |
G |
11: 99,742,373 (GRCm39) |
V9A |
unknown |
Het |
Lama2 |
G |
T |
10: 27,298,614 (GRCm39) |
P161T |
probably damaging |
Het |
Ltbp4 |
G |
A |
7: 27,028,443 (GRCm39) |
P273L |
unknown |
Het |
Lvrn |
T |
A |
18: 47,027,784 (GRCm39) |
S866R |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,189,805 (GRCm39) |
Y1035H |
probably damaging |
Het |
Mertk |
T |
A |
2: 128,601,010 (GRCm39) |
N331K |
probably damaging |
Het |
Mios |
T |
A |
6: 8,215,437 (GRCm39) |
F211Y |
probably benign |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Mphosph9 |
A |
T |
5: 124,453,764 (GRCm39) |
S183T |
possibly damaging |
Het |
Mrto4 |
A |
T |
4: 139,076,949 (GRCm39) |
I56N |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,416,374 (GRCm39) |
C3107R |
possibly damaging |
Het |
Ncoa2 |
A |
G |
1: 13,230,476 (GRCm39) |
Y1023H |
probably damaging |
Het |
Nlrp6 |
GAGAAGAAGAAGAAGAAGAAGA |
GAGAAGAAGAAGAAGAAGA |
7: 140,504,026 (GRCm39) |
|
probably benign |
Het |
Nr2f1 |
T |
C |
13: 78,337,935 (GRCm39) |
T237A |
probably damaging |
Het |
Nup205 |
C |
A |
6: 35,210,301 (GRCm39) |
Q1621K |
probably benign |
Het |
Nup50l |
A |
G |
6: 96,142,250 (GRCm39) |
S265P |
possibly damaging |
Het |
Nxpe2 |
T |
A |
9: 48,231,026 (GRCm39) |
S448C |
probably benign |
Het |
Ogdh |
T |
A |
11: 6,296,638 (GRCm39) |
C498S |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or14a256 |
A |
T |
7: 86,265,639 (GRCm39) |
F71L |
probably benign |
Het |
Or2ag15 |
T |
C |
7: 106,340,601 (GRCm39) |
E180G |
probably damaging |
Het |
Or2d2 |
A |
T |
7: 106,727,717 (GRCm39) |
D294E |
possibly damaging |
Het |
Or5ak24 |
T |
C |
2: 85,260,963 (GRCm39) |
D70G |
probably damaging |
Het |
Or5d46 |
T |
C |
2: 88,170,545 (GRCm39) |
L212P |
probably damaging |
Het |
Or6p1 |
A |
T |
1: 174,258,471 (GRCm39) |
K159M |
probably damaging |
Het |
Or8s8 |
T |
C |
15: 98,354,634 (GRCm39) |
S148P |
probably damaging |
Het |
Pcdhb9 |
T |
A |
18: 37,536,369 (GRCm39) |
Y788N |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,410,782 (GRCm39) |
D1870G |
unknown |
Het |
Pde6g |
A |
G |
11: 120,338,962 (GRCm39) |
L76P |
probably damaging |
Het |
Peak1 |
A |
T |
9: 56,114,073 (GRCm39) |
Y593N |
probably damaging |
Het |
Pfas |
C |
T |
11: 68,885,110 (GRCm39) |
G16R |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,769,970 (GRCm39) |
|
probably null |
Het |
Pla2g3 |
C |
T |
11: 3,440,983 (GRCm39) |
T316I |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,530,788 (GRCm39) |
I489F |
probably damaging |
Het |
Rere |
T |
G |
4: 150,553,247 (GRCm39) |
H146Q |
probably benign |
Het |
Rundc1 |
A |
T |
11: 101,322,322 (GRCm39) |
Q272L |
probably damaging |
Het |
Scml4 |
T |
C |
10: 42,832,017 (GRCm39) |
L305P |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,320,144 (GRCm39) |
H1431Q |
probably benign |
Het |
Serpina1a |
G |
A |
12: 103,820,059 (GRCm39) |
Q373* |
probably null |
Het |
Shank1 |
A |
T |
7: 43,974,801 (GRCm39) |
N377I |
unknown |
Het |
Shc2 |
T |
C |
10: 79,462,625 (GRCm39) |
|
probably null |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,368,002 (GRCm39) |
I589F |
probably damaging |
Het |
Smim8 |
C |
T |
4: 34,771,316 (GRCm39) |
R26Q |
probably damaging |
Het |
Smox |
C |
A |
2: 131,362,384 (GRCm39) |
A221D |
probably damaging |
Het |
Sox5 |
A |
G |
6: 143,819,831 (GRCm39) |
S62P |
possibly damaging |
Het |
Spg21 |
A |
C |
9: 65,391,774 (GRCm39) |
K240N |
probably damaging |
Het |
Sv2c |
C |
T |
13: 96,113,153 (GRCm39) |
V599M |
probably damaging |
Het |
Tanc2 |
T |
A |
11: 105,801,121 (GRCm39) |
H1112Q |
probably damaging |
Het |
Tbata |
T |
C |
10: 61,011,623 (GRCm39) |
I58T |
possibly damaging |
Het |
Tbc1d2 |
T |
G |
4: 46,606,419 (GRCm39) |
Y842S |
probably benign |
Het |
Tctn1 |
A |
T |
5: 122,379,903 (GRCm39) |
|
probably null |
Het |
Tenm1 |
T |
C |
X: 41,916,078 (GRCm39) |
D402G |
probably benign |
Het |
Tfcp2l1 |
T |
C |
1: 118,597,119 (GRCm39) |
V400A |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,363,576 (GRCm39) |
L99I |
probably benign |
Het |
Top2a |
T |
C |
11: 98,886,803 (GRCm39) |
|
probably null |
Het |
Traf7 |
C |
A |
17: 24,732,255 (GRCm39) |
G191C |
probably damaging |
Het |
Trpm1 |
T |
A |
7: 63,879,978 (GRCm39) |
L661Q |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,580,967 (GRCm39) |
I23309V |
probably benign |
Het |
Usp50 |
T |
C |
2: 126,619,881 (GRCm39) |
K199E |
possibly damaging |
Het |
Vmn1r218 |
T |
C |
13: 23,320,683 (GRCm39) |
F10S |
probably damaging |
Het |
Vmn2r89 |
C |
A |
14: 51,694,897 (GRCm39) |
T459K |
probably benign |
Het |
Vps13a |
T |
G |
19: 16,655,302 (GRCm39) |
S1909R |
possibly damaging |
Het |
Vwa5b2 |
T |
C |
16: 20,420,941 (GRCm39) |
|
probably null |
Het |
Vwa8 |
A |
G |
14: 79,219,800 (GRCm39) |
H516R |
possibly damaging |
Het |
Wnk1 |
T |
C |
6: 119,946,208 (GRCm39) |
I648M |
probably damaging |
Het |
Zfat |
G |
C |
15: 68,018,392 (GRCm39) |
P974R |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,259,158 (GRCm39) |
I1601K |
probably benign |
Het |
Zfp239 |
A |
G |
6: 117,848,778 (GRCm39) |
K172R |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,736,722 (GRCm39) |
G971D |
probably damaging |
Het |
Zfp532 |
A |
T |
18: 65,757,563 (GRCm39) |
I499F |
probably damaging |
Het |
Zfp647 |
T |
C |
15: 76,795,314 (GRCm39) |
T449A |
possibly damaging |
Het |
Zfp938 |
C |
T |
10: 82,061,465 (GRCm39) |
G385D |
probably damaging |
Het |
Zfp959 |
T |
G |
17: 56,204,404 (GRCm39) |
V147G |
probably damaging |
Het |
Znfx1 |
A |
T |
2: 166,892,270 (GRCm39) |
C649S |
probably damaging |
Het |
|
Other mutations in Nlrp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00485:Nlrp2
|
APN |
7 |
5,340,547 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00545:Nlrp2
|
APN |
7 |
5,331,251 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01311:Nlrp2
|
APN |
7 |
5,322,238 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01345:Nlrp2
|
APN |
7 |
5,320,491 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01583:Nlrp2
|
APN |
7 |
5,340,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01659:Nlrp2
|
APN |
7 |
5,331,034 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02240:Nlrp2
|
APN |
7 |
5,330,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02353:Nlrp2
|
APN |
7 |
5,340,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02360:Nlrp2
|
APN |
7 |
5,340,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02399:Nlrp2
|
APN |
7 |
5,331,809 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02441:Nlrp2
|
APN |
7 |
5,338,566 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02588:Nlrp2
|
APN |
7 |
5,330,551 (GRCm39) |
nonsense |
probably null |
|
IGL02803:Nlrp2
|
APN |
7 |
5,331,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02968:Nlrp2
|
APN |
7 |
5,304,024 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03342:Nlrp2
|
APN |
7 |
5,320,482 (GRCm39) |
missense |
probably damaging |
1.00 |
BB006:Nlrp2
|
UTSW |
7 |
5,330,498 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Nlrp2
|
UTSW |
7 |
5,330,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Nlrp2
|
UTSW |
7 |
5,325,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Nlrp2
|
UTSW |
7 |
5,325,333 (GRCm39) |
unclassified |
probably benign |
|
R0079:Nlrp2
|
UTSW |
7 |
5,330,729 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0130:Nlrp2
|
UTSW |
7 |
5,325,417 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0157:Nlrp2
|
UTSW |
7 |
5,311,769 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0201:Nlrp2
|
UTSW |
7 |
5,331,328 (GRCm39) |
missense |
probably benign |
0.00 |
R0276:Nlrp2
|
UTSW |
7 |
5,331,108 (GRCm39) |
missense |
probably benign |
0.00 |
R0288:Nlrp2
|
UTSW |
7 |
5,331,544 (GRCm39) |
missense |
probably benign |
0.19 |
R0332:Nlrp2
|
UTSW |
7 |
5,320,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Nlrp2
|
UTSW |
7 |
5,322,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1241:Nlrp2
|
UTSW |
7 |
5,331,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Nlrp2
|
UTSW |
7 |
5,330,490 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1392:Nlrp2
|
UTSW |
7 |
5,332,014 (GRCm39) |
splice site |
probably benign |
|
R1470:Nlrp2
|
UTSW |
7 |
5,303,950 (GRCm39) |
missense |
probably benign |
0.18 |
R1470:Nlrp2
|
UTSW |
7 |
5,303,950 (GRCm39) |
missense |
probably benign |
0.18 |
R1563:Nlrp2
|
UTSW |
7 |
5,311,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Nlrp2
|
UTSW |
7 |
5,330,715 (GRCm39) |
nonsense |
probably null |
|
R1942:Nlrp2
|
UTSW |
7 |
5,325,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1960:Nlrp2
|
UTSW |
7 |
5,330,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1961:Nlrp2
|
UTSW |
7 |
5,330,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Nlrp2
|
UTSW |
7 |
5,328,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Nlrp2
|
UTSW |
7 |
5,328,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R2190:Nlrp2
|
UTSW |
7 |
5,322,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2243:Nlrp2
|
UTSW |
7 |
5,338,597 (GRCm39) |
missense |
probably benign |
0.03 |
R2277:Nlrp2
|
UTSW |
7 |
5,331,128 (GRCm39) |
missense |
probably benign |
|
R2334:Nlrp2
|
UTSW |
7 |
5,340,534 (GRCm39) |
missense |
probably benign |
0.39 |
R3030:Nlrp2
|
UTSW |
7 |
5,330,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Nlrp2
|
UTSW |
7 |
5,322,286 (GRCm39) |
missense |
probably benign |
0.01 |
R3941:Nlrp2
|
UTSW |
7 |
5,330,551 (GRCm39) |
nonsense |
probably null |
|
R4021:Nlrp2
|
UTSW |
7 |
5,328,011 (GRCm39) |
missense |
probably benign |
0.40 |
R4518:Nlrp2
|
UTSW |
7 |
5,328,055 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4666:Nlrp2
|
UTSW |
7 |
5,322,188 (GRCm39) |
missense |
probably benign |
0.18 |
R4767:Nlrp2
|
UTSW |
7 |
5,331,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Nlrp2
|
UTSW |
7 |
5,331,950 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4873:Nlrp2
|
UTSW |
7 |
5,301,858 (GRCm39) |
missense |
probably benign |
0.09 |
R4875:Nlrp2
|
UTSW |
7 |
5,301,858 (GRCm39) |
missense |
probably benign |
0.09 |
R5020:Nlrp2
|
UTSW |
7 |
5,331,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R5293:Nlrp2
|
UTSW |
7 |
5,330,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Nlrp2
|
UTSW |
7 |
5,328,007 (GRCm39) |
missense |
probably benign |
0.00 |
R5336:Nlrp2
|
UTSW |
7 |
5,331,118 (GRCm39) |
missense |
probably benign |
|
R5390:Nlrp2
|
UTSW |
7 |
5,303,908 (GRCm39) |
missense |
probably benign |
0.00 |
R5864:Nlrp2
|
UTSW |
7 |
5,325,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R5913:Nlrp2
|
UTSW |
7 |
5,327,902 (GRCm39) |
splice site |
probably null |
|
R6173:Nlrp2
|
UTSW |
7 |
5,340,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R6274:Nlrp2
|
UTSW |
7 |
5,320,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Nlrp2
|
UTSW |
7 |
5,340,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6343:Nlrp2
|
UTSW |
7 |
5,303,925 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6704:Nlrp2
|
UTSW |
7 |
5,328,040 (GRCm39) |
nonsense |
probably null |
|
R6814:Nlrp2
|
UTSW |
7 |
5,311,709 (GRCm39) |
missense |
probably benign |
0.01 |
R6872:Nlrp2
|
UTSW |
7 |
5,311,709 (GRCm39) |
missense |
probably benign |
0.01 |
R7023:Nlrp2
|
UTSW |
7 |
5,331,228 (GRCm39) |
nonsense |
probably null |
|
R7028:Nlrp2
|
UTSW |
7 |
5,331,571 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7109:Nlrp2
|
UTSW |
7 |
5,331,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Nlrp2
|
UTSW |
7 |
5,320,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Nlrp2
|
UTSW |
7 |
5,311,644 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7339:Nlrp2
|
UTSW |
7 |
5,330,627 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7573:Nlrp2
|
UTSW |
7 |
5,320,468 (GRCm39) |
critical splice donor site |
probably null |
|
R7657:Nlrp2
|
UTSW |
7 |
5,322,167 (GRCm39) |
missense |
probably benign |
0.01 |
R7929:Nlrp2
|
UTSW |
7 |
5,330,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Nlrp2
|
UTSW |
7 |
5,331,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8097:Nlrp2
|
UTSW |
7 |
5,330,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Nlrp2
|
UTSW |
7 |
5,320,494 (GRCm39) |
missense |
probably benign |
0.40 |
R8785:Nlrp2
|
UTSW |
7 |
5,330,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Nlrp2
|
UTSW |
7 |
5,330,887 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8982:Nlrp2
|
UTSW |
7 |
5,327,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Nlrp2
|
UTSW |
7 |
5,325,457 (GRCm39) |
missense |
probably null |
0.00 |
R9038:Nlrp2
|
UTSW |
7 |
5,330,478 (GRCm39) |
missense |
probably benign |
0.14 |
R9149:Nlrp2
|
UTSW |
7 |
5,330,572 (GRCm39) |
missense |
probably benign |
0.01 |
R9229:Nlrp2
|
UTSW |
7 |
5,304,052 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9584:Nlrp2
|
UTSW |
7 |
5,322,215 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Nlrp2
|
UTSW |
7 |
5,330,641 (GRCm39) |
missense |
probably benign |
0.03 |
|