Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
A |
T |
16: 88,555,992 (GRCm39) |
T69S |
probably benign |
Het |
5730455P16Rik |
A |
G |
11: 80,268,798 (GRCm39) |
S4P |
possibly damaging |
Het |
Abca13 |
T |
A |
11: 9,241,867 (GRCm39) |
N1243K |
probably damaging |
Het |
Adgrg6 |
A |
T |
10: 14,303,943 (GRCm39) |
S824T |
probably benign |
Het |
Armh4 |
G |
T |
14: 50,010,993 (GRCm39) |
A238E |
probably damaging |
Het |
C3ar1 |
T |
A |
6: 122,827,059 (GRCm39) |
Y386F |
probably damaging |
Het |
Cdc14a |
T |
C |
3: 116,087,577 (GRCm39) |
N527S |
probably benign |
Het |
Cfap69 |
A |
T |
5: 5,669,085 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,804,631 (GRCm39) |
P2279S |
unknown |
Het |
Crb2 |
G |
A |
2: 37,683,252 (GRCm39) |
G918D |
probably benign |
Het |
Dcn |
C |
A |
10: 97,349,479 (GRCm39) |
N250K |
probably damaging |
Het |
Dctn5 |
G |
A |
7: 121,732,466 (GRCm39) |
|
probably benign |
Het |
Ddx55 |
T |
C |
5: 124,694,821 (GRCm39) |
V83A |
probably damaging |
Het |
Dnaja2 |
T |
A |
8: 86,265,876 (GRCm39) |
H403L |
possibly damaging |
Het |
Dpy19l4 |
T |
C |
4: 11,303,982 (GRCm39) |
I143V |
probably benign |
Het |
Efna5 |
G |
T |
17: 62,957,977 (GRCm39) |
T93K |
probably benign |
Het |
Eml6 |
A |
G |
11: 29,843,201 (GRCm39) |
V171A |
possibly damaging |
Het |
Esyt1 |
C |
G |
10: 128,347,955 (GRCm39) |
V942L |
probably benign |
Het |
Fam184a |
C |
A |
10: 53,509,802 (GRCm39) |
E126* |
probably null |
Het |
Fam78a |
C |
A |
2: 31,973,035 (GRCm39) |
|
probably benign |
Het |
Fat2 |
A |
G |
11: 55,202,892 (GRCm39) |
Y61H |
probably benign |
Het |
Fbxw14 |
A |
T |
9: 109,105,211 (GRCm39) |
M318K |
probably damaging |
Het |
Gm14295 |
A |
G |
2: 176,500,871 (GRCm39) |
I120M |
probably benign |
Het |
Gm14403 |
T |
A |
2: 177,200,311 (GRCm39) |
Y86N |
probably benign |
Het |
Gmcl1 |
G |
T |
6: 86,698,408 (GRCm39) |
A163E |
probably damaging |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Gpr55 |
T |
C |
1: 85,869,419 (GRCm39) |
D54G |
probably benign |
Het |
Gtf2b |
T |
G |
3: 142,483,975 (GRCm39) |
S50A |
probably damaging |
Het |
Ifit3 |
A |
T |
19: 34,565,480 (GRCm39) |
E342V |
possibly damaging |
Het |
Iqgap3 |
T |
A |
3: 88,011,609 (GRCm39) |
I798N |
probably damaging |
Het |
Kplce |
A |
T |
3: 92,776,202 (GRCm39) |
Y160* |
probably null |
Het |
Lpin1 |
T |
C |
12: 16,613,685 (GRCm39) |
D494G |
|
Het |
Lsm12 |
T |
C |
11: 102,056,235 (GRCm39) |
E149G |
possibly damaging |
Het |
Mtfr2 |
T |
C |
10: 20,228,603 (GRCm39) |
S50P |
possibly damaging |
Het |
Ndnf |
T |
C |
6: 65,680,414 (GRCm39) |
M231T |
probably benign |
Het |
Noc3l |
A |
T |
19: 38,800,873 (GRCm39) |
V203E |
probably benign |
Het |
Or1e27-ps1 |
G |
T |
11: 73,555,988 (GRCm39) |
K184N |
possibly damaging |
Het |
Or52h2 |
C |
A |
7: 103,839,017 (GRCm39) |
L132F |
probably damaging |
Het |
Or5c1 |
A |
T |
2: 37,222,346 (GRCm39) |
T196S |
probably damaging |
Het |
Or9r7 |
A |
T |
10: 129,962,469 (GRCm39) |
Y152* |
probably null |
Het |
Pcnx1 |
C |
T |
12: 81,965,593 (GRCm39) |
R59* |
probably null |
Het |
Pde6b |
C |
T |
5: 108,573,118 (GRCm39) |
P496L |
probably benign |
Het |
Plppr1 |
A |
T |
4: 49,300,942 (GRCm39) |
M92L |
probably benign |
Het |
Pphln1-ps1 |
C |
T |
16: 13,495,623 (GRCm39) |
R241C |
probably damaging |
Het |
Ptprk |
C |
G |
10: 28,259,565 (GRCm39) |
S335C |
possibly damaging |
Het |
Rars2 |
T |
A |
4: 34,650,217 (GRCm39) |
M334K |
probably benign |
Het |
Rgs12 |
T |
A |
5: 35,183,374 (GRCm39) |
V1007E |
possibly damaging |
Het |
Rnf122 |
T |
A |
8: 31,618,608 (GRCm39) |
C119S |
probably damaging |
Het |
Scn11a |
T |
A |
9: 119,584,149 (GRCm39) |
I1489F |
probably damaging |
Het |
Setd6 |
C |
A |
8: 96,443,316 (GRCm39) |
S186R |
probably benign |
Het |
Tex19.1 |
A |
G |
11: 121,038,148 (GRCm39) |
T169A |
probably benign |
Het |
Th |
G |
A |
7: 142,447,860 (GRCm39) |
P408S |
probably damaging |
Het |
Trappc13 |
T |
C |
13: 104,281,052 (GRCm39) |
M337V |
probably benign |
Het |
Treml2 |
A |
T |
17: 48,609,762 (GRCm39) |
K65* |
probably null |
Het |
Ubxn4 |
T |
C |
1: 128,183,933 (GRCm39) |
S98P |
probably damaging |
Het |
Wrnip1 |
A |
G |
13: 33,005,960 (GRCm39) |
S601G |
probably benign |
Het |
Zfp1006 |
A |
T |
8: 129,946,555 (GRCm39) |
L90H |
probably damaging |
Het |
|
Other mutations in Rasl10a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02233:Rasl10a
|
APN |
11 |
5,008,333 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03149:Rasl10a
|
APN |
11 |
5,008,429 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1630:Rasl10a
|
UTSW |
11 |
5,009,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R1678:Rasl10a
|
UTSW |
11 |
5,009,815 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1925:Rasl10a
|
UTSW |
11 |
5,009,473 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2086:Rasl10a
|
UTSW |
11 |
5,009,431 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3792:Rasl10a
|
UTSW |
11 |
5,009,461 (GRCm39) |
missense |
probably damaging |
0.99 |
R4482:Rasl10a
|
UTSW |
11 |
5,008,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Rasl10a
|
UTSW |
11 |
5,008,517 (GRCm39) |
missense |
probably benign |
0.03 |
R5743:Rasl10a
|
UTSW |
11 |
5,009,519 (GRCm39) |
missense |
probably benign |
0.02 |
R6168:Rasl10a
|
UTSW |
11 |
5,008,442 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6530:Rasl10a
|
UTSW |
11 |
5,008,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R6684:Rasl10a
|
UTSW |
11 |
5,008,396 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9144:Rasl10a
|
UTSW |
11 |
5,008,473 (GRCm39) |
missense |
probably benign |
0.31 |
|