Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anks1 |
T |
C |
17: 28,204,095 (GRCm39) |
V181A |
probably damaging |
Het |
Aqp4 |
T |
C |
18: 15,526,608 (GRCm39) |
D291G |
probably damaging |
Het |
Atad1 |
G |
T |
19: 32,673,210 (GRCm39) |
D224E |
probably benign |
Het |
Atp1a3 |
T |
G |
7: 24,700,400 (GRCm39) |
E33A |
probably benign |
Het |
Baz2b |
A |
G |
2: 59,754,024 (GRCm39) |
F1100L |
possibly damaging |
Het |
Car7 |
C |
T |
8: 105,275,009 (GRCm39) |
|
probably benign |
Het |
Casp8 |
C |
A |
1: 58,868,121 (GRCm39) |
|
probably null |
Het |
Cdh23 |
A |
T |
10: 60,214,530 (GRCm39) |
L1495H |
probably damaging |
Het |
Ceacam9 |
T |
G |
7: 16,459,232 (GRCm39) |
L177R |
probably benign |
Het |
Col16a1 |
C |
G |
4: 129,959,236 (GRCm39) |
P346A |
unknown |
Het |
Cyp2c29 |
A |
G |
19: 39,296,216 (GRCm39) |
|
probably null |
Het |
Cyp3a13 |
T |
C |
5: 137,910,118 (GRCm39) |
S139G |
probably damaging |
Het |
Dapk2 |
A |
G |
9: 66,176,180 (GRCm39) |
H327R |
probably benign |
Het |
Ddx19b |
T |
C |
8: 111,735,975 (GRCm39) |
T357A |
possibly damaging |
Het |
Dnah2 |
A |
G |
11: 69,365,151 (GRCm39) |
Y1944H |
probably damaging |
Het |
Dnai2 |
T |
A |
11: 114,623,755 (GRCm39) |
V6E |
probably damaging |
Het |
Eipr1 |
T |
C |
12: 28,913,024 (GRCm39) |
Y242H |
probably damaging |
Het |
Fam149a |
T |
G |
8: 45,834,778 (GRCm39) |
D7A |
probably damaging |
Het |
Fam217a |
T |
A |
13: 35,100,737 (GRCm39) |
D140V |
probably benign |
Het |
Fat4 |
G |
A |
3: 39,045,813 (GRCm39) |
C3944Y |
probably damaging |
Het |
Fezf2 |
G |
T |
14: 12,344,405 (GRCm38) |
P261T |
probably benign |
Het |
Gcsam |
A |
T |
16: 45,440,337 (GRCm39) |
T127S |
probably damaging |
Het |
Git2 |
C |
T |
5: 114,887,620 (GRCm39) |
|
probably benign |
Het |
Gm1527 |
T |
C |
3: 28,969,984 (GRCm39) |
|
probably null |
Het |
Gtf3c1 |
A |
G |
7: 125,243,444 (GRCm39) |
L1720P |
possibly damaging |
Het |
H2-T9 |
T |
A |
17: 36,439,614 (GRCm39) |
D122V |
probably damaging |
Het |
Hat1 |
A |
G |
2: 71,220,321 (GRCm39) |
T28A |
probably benign |
Het |
Igf2r |
G |
A |
17: 12,952,790 (GRCm39) |
Q219* |
probably null |
Het |
Impdh1 |
T |
A |
6: 29,206,450 (GRCm39) |
D129V |
possibly damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Ltbp3 |
A |
G |
19: 5,808,107 (GRCm39) |
Q1250R |
probably benign |
Het |
Mansc4 |
T |
A |
6: 146,977,173 (GRCm39) |
I148F |
probably benign |
Het |
Mast2 |
T |
C |
4: 116,172,037 (GRCm39) |
Y569C |
probably damaging |
Het |
Mcoln3 |
A |
T |
3: 145,846,345 (GRCm39) |
K552* |
probably null |
Het |
Mctp2 |
T |
C |
7: 71,814,446 (GRCm39) |
Q601R |
probably benign |
Het |
Mei1 |
A |
G |
15: 81,987,513 (GRCm39) |
N859S |
probably benign |
Het |
Myo19 |
A |
T |
11: 84,782,996 (GRCm39) |
Q170L |
possibly damaging |
Het |
Myo1h |
T |
C |
5: 114,491,898 (GRCm39) |
F676S |
probably damaging |
Het |
Myo9a |
A |
G |
9: 59,801,429 (GRCm39) |
T1876A |
probably benign |
Het |
Nav3 |
G |
T |
10: 109,554,951 (GRCm39) |
|
probably benign |
Het |
Ndor1 |
T |
C |
2: 25,145,236 (GRCm39) |
Y43C |
probably damaging |
Het |
Nmnat3 |
T |
C |
9: 98,292,352 (GRCm39) |
I199T |
possibly damaging |
Het |
Nsun7 |
T |
C |
5: 66,418,557 (GRCm39) |
S96P |
probably damaging |
Het |
Ntng1 |
A |
G |
3: 109,842,326 (GRCm39) |
V149A |
possibly damaging |
Het |
Oas3 |
T |
C |
5: 120,899,900 (GRCm39) |
|
probably benign |
Het |
Or10v9 |
T |
G |
19: 11,832,371 (GRCm39) |
Q315H |
possibly damaging |
Het |
Or4k47 |
T |
A |
2: 111,451,586 (GRCm39) |
I278F |
probably benign |
Het |
Or5bw2 |
A |
G |
7: 6,573,557 (GRCm39) |
D189G |
probably benign |
Het |
Or6z7 |
T |
C |
7: 6,483,931 (GRCm39) |
M75V |
probably benign |
Het |
Or8b3 |
T |
C |
9: 38,315,031 (GRCm39) |
L287P |
probably damaging |
Het |
Or8k53 |
A |
T |
2: 86,177,486 (GRCm39) |
I208N |
possibly damaging |
Het |
Pax2 |
G |
A |
19: 44,806,904 (GRCm39) |
D301N |
probably damaging |
Het |
Pcsk4 |
T |
A |
10: 80,161,613 (GRCm39) |
E176V |
probably damaging |
Het |
Pkhd1 |
G |
A |
1: 20,187,284 (GRCm39) |
P3675S |
probably benign |
Het |
Plekho2 |
A |
T |
9: 65,465,974 (GRCm39) |
L138Q |
probably damaging |
Het |
Ppp4r3c1 |
A |
T |
X: 88,975,051 (GRCm39) |
V382E |
probably damaging |
Het |
Prkcsh |
A |
G |
9: 21,924,164 (GRCm39) |
D458G |
probably damaging |
Het |
Prr11 |
T |
A |
11: 86,994,116 (GRCm39) |
D100V |
probably damaging |
Het |
Qars1 |
A |
G |
9: 108,392,227 (GRCm39) |
N136D |
probably damaging |
Het |
Rbm15b |
A |
G |
9: 106,758,822 (GRCm39) |
|
probably benign |
Het |
Rel |
C |
T |
11: 23,692,761 (GRCm39) |
G424D |
probably benign |
Het |
Rsrc1 |
A |
G |
3: 67,257,338 (GRCm39) |
D250G |
probably benign |
Het |
Samt3 |
A |
C |
X: 85,090,740 (GRCm39) |
M211L |
probably benign |
Het |
Scn2a |
C |
A |
2: 65,520,514 (GRCm39) |
N503K |
probably damaging |
Het |
Sh2d6 |
G |
A |
6: 72,494,527 (GRCm39) |
|
probably benign |
Het |
Smg8 |
T |
C |
11: 86,976,157 (GRCm39) |
T475A |
probably benign |
Het |
Ssxb10 |
A |
G |
X: 8,197,258 (GRCm39) |
D77G |
probably benign |
Het |
Tbx20 |
T |
A |
9: 24,682,209 (GRCm39) |
K48N |
possibly damaging |
Het |
Tead1 |
C |
A |
7: 112,490,952 (GRCm39) |
D231E |
probably benign |
Het |
Ticam1 |
C |
T |
17: 56,578,555 (GRCm39) |
R180H |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,962,603 (GRCm39) |
F1111L |
probably damaging |
Het |
Tlr11 |
T |
A |
14: 50,599,445 (GRCm39) |
I477K |
possibly damaging |
Het |
Ttc13 |
A |
G |
8: 125,440,926 (GRCm39) |
|
probably null |
Het |
Ttc17 |
T |
C |
2: 94,157,049 (GRCm39) |
N411S |
probably benign |
Het |
Usp15 |
T |
A |
10: 122,960,946 (GRCm39) |
|
probably benign |
Het |
Usp18 |
A |
G |
6: 121,229,476 (GRCm39) |
K32E |
probably benign |
Het |
Vmn1r12 |
A |
T |
6: 57,136,646 (GRCm39) |
M248L |
probably benign |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp930 |
T |
A |
8: 69,680,824 (GRCm39) |
L172H |
probably damaging |
Het |
Zfp976 |
G |
A |
7: 42,263,046 (GRCm39) |
H264Y |
probably damaging |
Het |
|
Other mutations in Nlrp1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00648:Nlrp1a
|
APN |
11 |
70,983,783 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00771:Nlrp1a
|
APN |
11 |
71,013,567 (GRCm39) |
nonsense |
probably null |
|
IGL01408:Nlrp1a
|
APN |
11 |
71,013,742 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01886:Nlrp1a
|
APN |
11 |
71,014,327 (GRCm39) |
missense |
probably benign |
|
IGL02221:Nlrp1a
|
APN |
11 |
71,013,944 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02291:Nlrp1a
|
APN |
11 |
71,013,415 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02375:Nlrp1a
|
APN |
11 |
71,004,339 (GRCm39) |
nonsense |
probably null |
|
IGL02408:Nlrp1a
|
APN |
11 |
71,013,456 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02516:Nlrp1a
|
APN |
11 |
71,005,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02583:Nlrp1a
|
APN |
11 |
71,014,227 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02622:Nlrp1a
|
APN |
11 |
71,013,826 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02642:Nlrp1a
|
APN |
11 |
71,014,358 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02823:Nlrp1a
|
APN |
11 |
70,983,249 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02859:Nlrp1a
|
APN |
11 |
70,996,912 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02997:Nlrp1a
|
APN |
11 |
71,014,491 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03342:Nlrp1a
|
APN |
11 |
71,013,617 (GRCm39) |
missense |
probably benign |
0.19 |
Ants
|
UTSW |
11 |
71,033,164 (GRCm39) |
missense |
probably benign |
0.01 |
dreary
|
UTSW |
11 |
71,004,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
picnic
|
UTSW |
11 |
71,013,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
seedless
|
UTSW |
11 |
71,014,378 (GRCm39) |
missense |
probably benign |
0.44 |
watermelon
|
UTSW |
11 |
71,013,531 (GRCm39) |
missense |
probably benign |
0.08 |
R0022:Nlrp1a
|
UTSW |
11 |
71,014,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R0345:Nlrp1a
|
UTSW |
11 |
71,014,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Nlrp1a
|
UTSW |
11 |
71,004,830 (GRCm39) |
intron |
probably benign |
|
R0364:Nlrp1a
|
UTSW |
11 |
71,004,830 (GRCm39) |
intron |
probably benign |
|
R0566:Nlrp1a
|
UTSW |
11 |
71,013,768 (GRCm39) |
missense |
probably benign |
0.00 |
R1177:Nlrp1a
|
UTSW |
11 |
70,998,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Nlrp1a
|
UTSW |
11 |
71,004,292 (GRCm39) |
critical splice donor site |
probably null |
|
R1263:Nlrp1a
|
UTSW |
11 |
70,987,948 (GRCm39) |
missense |
probably benign |
0.01 |
R1681:Nlrp1a
|
UTSW |
11 |
71,033,184 (GRCm39) |
missense |
unknown |
|
R1743:Nlrp1a
|
UTSW |
11 |
71,015,032 (GRCm39) |
missense |
probably benign |
0.04 |
R1826:Nlrp1a
|
UTSW |
11 |
71,013,573 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1826:Nlrp1a
|
UTSW |
11 |
70,998,806 (GRCm39) |
intron |
probably benign |
|
R2083:Nlrp1a
|
UTSW |
11 |
71,015,046 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2116:Nlrp1a
|
UTSW |
11 |
71,005,326 (GRCm39) |
nonsense |
probably null |
|
R2134:Nlrp1a
|
UTSW |
11 |
71,015,014 (GRCm39) |
missense |
probably benign |
0.00 |
R2148:Nlrp1a
|
UTSW |
11 |
71,013,733 (GRCm39) |
nonsense |
probably null |
|
R2301:Nlrp1a
|
UTSW |
11 |
70,996,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3029:Nlrp1a
|
UTSW |
11 |
71,014,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3113:Nlrp1a
|
UTSW |
11 |
71,014,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Nlrp1a
|
UTSW |
11 |
71,013,529 (GRCm39) |
missense |
probably benign |
0.08 |
R3898:Nlrp1a
|
UTSW |
11 |
71,013,700 (GRCm39) |
missense |
probably benign |
0.00 |
R4254:Nlrp1a
|
UTSW |
11 |
71,013,854 (GRCm39) |
nonsense |
probably null |
|
R4397:Nlrp1a
|
UTSW |
11 |
70,988,030 (GRCm39) |
missense |
probably benign |
0.00 |
R4647:Nlrp1a
|
UTSW |
11 |
70,987,952 (GRCm39) |
splice site |
probably null |
|
R4740:Nlrp1a
|
UTSW |
11 |
71,004,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4965:Nlrp1a
|
UTSW |
11 |
70,983,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5009:Nlrp1a
|
UTSW |
11 |
71,013,531 (GRCm39) |
missense |
probably benign |
0.08 |
R5103:Nlrp1a
|
UTSW |
11 |
70,990,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R5355:Nlrp1a
|
UTSW |
11 |
71,015,077 (GRCm39) |
missense |
probably benign |
0.00 |
R5577:Nlrp1a
|
UTSW |
11 |
70,990,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Nlrp1a
|
UTSW |
11 |
70,990,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Nlrp1a
|
UTSW |
11 |
70,989,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Nlrp1a
|
UTSW |
11 |
71,013,846 (GRCm39) |
missense |
probably benign |
0.00 |
R6220:Nlrp1a
|
UTSW |
11 |
71,033,164 (GRCm39) |
missense |
probably benign |
0.01 |
R6564:Nlrp1a
|
UTSW |
11 |
71,014,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6586:Nlrp1a
|
UTSW |
11 |
70,996,899 (GRCm39) |
missense |
probably benign |
0.00 |
R6925:Nlrp1a
|
UTSW |
11 |
70,983,339 (GRCm39) |
missense |
probably null |
0.99 |
R7013:Nlrp1a
|
UTSW |
11 |
71,014,378 (GRCm39) |
missense |
probably benign |
0.44 |
R7155:Nlrp1a
|
UTSW |
11 |
71,014,905 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7214:Nlrp1a
|
UTSW |
11 |
71,014,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Nlrp1a
|
UTSW |
11 |
71,015,068 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Nlrp1a
|
UTSW |
11 |
71,014,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7404:Nlrp1a
|
UTSW |
11 |
70,987,919 (GRCm39) |
nonsense |
probably null |
|
R7409:Nlrp1a
|
UTSW |
11 |
71,013,634 (GRCm39) |
missense |
probably benign |
0.03 |
R7410:Nlrp1a
|
UTSW |
11 |
71,014,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7440:Nlrp1a
|
UTSW |
11 |
70,983,150 (GRCm39) |
missense |
probably damaging |
0.99 |
R7447:Nlrp1a
|
UTSW |
11 |
70,983,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Nlrp1a
|
UTSW |
11 |
70,998,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7569:Nlrp1a
|
UTSW |
11 |
70,999,869 (GRCm39) |
missense |
probably benign |
0.00 |
R7600:Nlrp1a
|
UTSW |
11 |
70,989,740 (GRCm39) |
missense |
probably damaging |
0.96 |
R7634:Nlrp1a
|
UTSW |
11 |
70,990,354 (GRCm39) |
missense |
probably benign |
0.19 |
R7734:Nlrp1a
|
UTSW |
11 |
70,998,826 (GRCm39) |
missense |
unknown |
|
R7747:Nlrp1a
|
UTSW |
11 |
71,014,234 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8471:Nlrp1a
|
UTSW |
11 |
71,013,885 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8482:Nlrp1a
|
UTSW |
11 |
70,999,901 (GRCm39) |
splice site |
probably null |
|
R9008:Nlrp1a
|
UTSW |
11 |
71,014,735 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9028:Nlrp1a
|
UTSW |
11 |
71,013,819 (GRCm39) |
missense |
probably benign |
0.27 |
R9441:Nlrp1a
|
UTSW |
11 |
71,013,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Nlrp1a
|
UTSW |
11 |
70,998,488 (GRCm39) |
missense |
probably benign |
0.05 |
R9701:Nlrp1a
|
UTSW |
11 |
70,987,946 (GRCm39) |
missense |
probably benign |
0.08 |
X0026:Nlrp1a
|
UTSW |
11 |
71,033,142 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Nlrp1a
|
UTSW |
11 |
71,013,995 (GRCm39) |
missense |
probably benign |
0.27 |
Z1186:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1186:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1186:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1186:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1186:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1187:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1187:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1187:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1188:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1188:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1188:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1189:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1189:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1189:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1190:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1190:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1190:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1191:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1191:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1191:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
70,990,442 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
70,988,077 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1192:Nlrp1a
|
UTSW |
11 |
70,983,069 (GRCm39) |
missense |
probably benign |
|
Z1192:Nlrp1a
|
UTSW |
11 |
71,033,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1192:Nlrp1a
|
UTSW |
11 |
71,014,914 (GRCm39) |
missense |
probably benign |
|
|