Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
T |
A |
5: 88,120,649 (GRCm39) |
Y469N |
probably benign |
Het |
Actl11 |
T |
C |
9: 107,805,964 (GRCm39) |
S96P |
possibly damaging |
Het |
Ankrd13b |
T |
A |
11: 77,363,198 (GRCm39) |
|
probably null |
Het |
Apobec4 |
T |
A |
1: 152,632,017 (GRCm39) |
I15K |
probably damaging |
Het |
Arhgef28 |
G |
T |
13: 98,090,401 (GRCm39) |
D1039E |
probably damaging |
Het |
Atp1a1 |
C |
T |
3: 101,498,769 (GRCm39) |
G175R |
probably damaging |
Het |
AU040320 |
T |
A |
4: 126,763,171 (GRCm39) |
|
probably benign |
Het |
Bcl9l |
G |
A |
9: 44,418,121 (GRCm39) |
R653H |
probably damaging |
Het |
Ccdc141 |
T |
A |
2: 76,958,669 (GRCm39) |
I144L |
possibly damaging |
Het |
Cdh20 |
C |
T |
1: 104,875,154 (GRCm39) |
T312I |
possibly damaging |
Het |
Cdh23 |
C |
T |
10: 60,220,848 (GRCm39) |
V1297I |
possibly damaging |
Het |
Cfap57 |
T |
C |
4: 118,467,792 (GRCm39) |
Y315C |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,442,044 (GRCm39) |
|
probably benign |
Het |
Cog5 |
A |
G |
12: 31,944,095 (GRCm39) |
D660G |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,196,945 (GRCm39) |
I332T |
probably damaging |
Het |
Csgalnact2 |
T |
C |
6: 118,103,288 (GRCm39) |
T225A |
probably damaging |
Het |
Dchs1 |
A |
G |
7: 105,421,490 (GRCm39) |
L310P |
probably damaging |
Het |
Dgki |
T |
C |
6: 36,977,025 (GRCm39) |
N695S |
probably damaging |
Het |
Gas7 |
T |
A |
11: 67,543,740 (GRCm39) |
|
probably null |
Het |
Gm21286 |
T |
C |
4: 60,794,323 (GRCm39) |
|
noncoding transcript |
Het |
Gm4799 |
C |
T |
10: 82,790,518 (GRCm39) |
|
noncoding transcript |
Het |
Hdac4 |
T |
C |
1: 91,887,196 (GRCm39) |
|
probably benign |
Het |
Hif1a |
T |
A |
12: 73,987,307 (GRCm39) |
S467T |
probably benign |
Het |
Ier5 |
A |
G |
1: 154,974,296 (GRCm39) |
V294A |
probably damaging |
Het |
Ifna11 |
T |
C |
4: 88,738,314 (GRCm39) |
V40A |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,436,191 (GRCm39) |
|
probably benign |
Het |
Lbx1 |
G |
T |
19: 45,222,670 (GRCm39) |
Q118K |
probably benign |
Het |
Lta |
A |
T |
17: 35,423,061 (GRCm39) |
|
probably null |
Het |
Matr3 |
A |
G |
18: 35,721,442 (GRCm39) |
Y471C |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,178,905 (GRCm39) |
|
probably benign |
Het |
Or4c103 |
C |
T |
2: 88,513,575 (GRCm39) |
C167Y |
probably damaging |
Het |
Or4k51 |
T |
C |
2: 111,584,848 (GRCm39) |
F85L |
probably benign |
Het |
Or4k51 |
T |
A |
2: 111,584,948 (GRCm39) |
M118K |
probably damaging |
Het |
Or5l13 |
G |
T |
2: 87,780,207 (GRCm39) |
F123L |
probably damaging |
Het |
Patl1 |
A |
G |
19: 11,901,247 (GRCm39) |
K299R |
probably damaging |
Het |
Pdgfrb |
A |
G |
18: 61,205,736 (GRCm39) |
E574G |
probably damaging |
Het |
Phf3 |
G |
A |
1: 30,843,386 (GRCm39) |
Q1858* |
probably null |
Het |
Prkca |
T |
C |
11: 107,905,148 (GRCm39) |
K197E |
possibly damaging |
Het |
Psmc6 |
C |
A |
14: 45,581,124 (GRCm39) |
Q307K |
probably benign |
Het |
Scel |
A |
G |
14: 103,845,530 (GRCm39) |
|
probably benign |
Het |
Scn5a |
A |
T |
9: 119,363,770 (GRCm39) |
S457T |
probably damaging |
Het |
Sesn3 |
A |
G |
9: 14,232,374 (GRCm39) |
T216A |
probably benign |
Het |
Slc25a21 |
A |
G |
12: 57,205,974 (GRCm39) |
V19A |
probably benign |
Het |
Slc34a1 |
A |
G |
13: 55,550,546 (GRCm39) |
T81A |
probably damaging |
Het |
Slc35a5 |
A |
G |
16: 44,971,866 (GRCm39) |
Y117H |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,114,196 (GRCm39) |
V569A |
probably benign |
Het |
Sqle |
A |
G |
15: 59,195,723 (GRCm39) |
Y333C |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,068,552 (GRCm39) |
E3078G |
possibly damaging |
Het |
Tacc2 |
T |
A |
7: 130,360,919 (GRCm39) |
I2737N |
probably damaging |
Het |
Tet3 |
A |
T |
6: 83,346,620 (GRCm39) |
Y1272* |
probably null |
Het |
Tnr |
G |
T |
1: 159,724,594 (GRCm39) |
R1095L |
possibly damaging |
Het |
Vmn1r184 |
T |
C |
7: 25,966,862 (GRCm39) |
S203P |
probably damaging |
Het |
Vmn2r94 |
A |
G |
17: 18,477,301 (GRCm39) |
L370P |
probably damaging |
Het |
Xrcc5 |
A |
G |
1: 72,393,404 (GRCm39) |
H559R |
probably benign |
Het |
|
Other mutations in Rasa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00863:Rasa1
|
APN |
13 |
85,436,548 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01670:Rasa1
|
APN |
13 |
85,373,609 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02095:Rasa1
|
APN |
13 |
85,364,274 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02822:Rasa1
|
APN |
13 |
85,400,633 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03126:Rasa1
|
APN |
13 |
85,404,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
F5770:Rasa1
|
UTSW |
13 |
85,375,064 (GRCm39) |
splice site |
probably null |
|
PIT4458001:Rasa1
|
UTSW |
13 |
85,375,237 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1393:Rasa1
|
UTSW |
13 |
85,371,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R1441:Rasa1
|
UTSW |
13 |
85,400,540 (GRCm39) |
splice site |
probably null |
|
R1907:Rasa1
|
UTSW |
13 |
85,374,691 (GRCm39) |
nonsense |
probably null |
|
R4243:Rasa1
|
UTSW |
13 |
85,392,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R4593:Rasa1
|
UTSW |
13 |
85,386,340 (GRCm39) |
splice site |
probably null |
|
R4687:Rasa1
|
UTSW |
13 |
85,374,754 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4689:Rasa1
|
UTSW |
13 |
85,386,282 (GRCm39) |
nonsense |
probably null |
|
R4753:Rasa1
|
UTSW |
13 |
85,436,509 (GRCm39) |
splice site |
probably null |
|
R4758:Rasa1
|
UTSW |
13 |
85,382,567 (GRCm39) |
missense |
probably benign |
|
R4774:Rasa1
|
UTSW |
13 |
85,398,621 (GRCm39) |
intron |
probably benign |
|
R5363:Rasa1
|
UTSW |
13 |
85,436,674 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5375:Rasa1
|
UTSW |
13 |
85,437,022 (GRCm39) |
intron |
probably benign |
|
R6134:Rasa1
|
UTSW |
13 |
85,374,745 (GRCm39) |
missense |
probably benign |
0.01 |
R6190:Rasa1
|
UTSW |
13 |
85,381,814 (GRCm39) |
missense |
probably benign |
0.02 |
R6755:Rasa1
|
UTSW |
13 |
85,374,717 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7564:Rasa1
|
UTSW |
13 |
85,376,827 (GRCm39) |
missense |
probably benign |
0.09 |
R7862:Rasa1
|
UTSW |
13 |
85,403,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R9138:Rasa1
|
UTSW |
13 |
85,369,635 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9280:Rasa1
|
UTSW |
13 |
85,436,732 (GRCm39) |
missense |
unknown |
|
R9328:Rasa1
|
UTSW |
13 |
85,403,575 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9340:Rasa1
|
UTSW |
13 |
85,369,649 (GRCm39) |
missense |
probably damaging |
0.98 |
R9648:Rasa1
|
UTSW |
13 |
85,436,690 (GRCm39) |
missense |
possibly damaging |
0.73 |
RF016:Rasa1
|
UTSW |
13 |
85,371,607 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0023:Rasa1
|
UTSW |
13 |
85,381,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|