Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
G |
A |
3: 137,889,470 (GRCm39) |
P49L |
probably benign |
Het |
Adam34l |
T |
A |
8: 44,079,970 (GRCm39) |
R85* |
probably null |
Het |
Anapc2 |
C |
T |
2: 25,163,303 (GRCm39) |
T180I |
probably benign |
Het |
Ankib1 |
A |
T |
5: 3,756,276 (GRCm39) |
H556Q |
probably damaging |
Het |
Aox1 |
A |
T |
1: 58,378,777 (GRCm39) |
K1009* |
probably null |
Het |
Apob |
C |
T |
12: 8,047,925 (GRCm39) |
P968L |
probably damaging |
Het |
Bpi |
T |
A |
2: 158,116,608 (GRCm39) |
F335Y |
probably benign |
Het |
Cabcoco1 |
T |
C |
10: 68,272,719 (GRCm39) |
Y222C |
probably damaging |
Het |
Camk2b |
G |
T |
11: 5,939,332 (GRCm39) |
C273* |
probably null |
Het |
Catsperd |
G |
A |
17: 56,968,252 (GRCm39) |
D546N |
probably benign |
Het |
Cenpb |
C |
T |
2: 131,021,463 (GRCm39) |
G112S |
probably damaging |
Het |
Col6a5 |
A |
G |
9: 105,739,178 (GRCm39) |
L2585P |
probably damaging |
Het |
Cop1 |
A |
G |
1: 159,147,339 (GRCm39) |
E555G |
probably damaging |
Het |
Cyfip2 |
G |
A |
11: 46,176,920 (GRCm39) |
R87C |
probably damaging |
Het |
Dthd1 |
A |
C |
5: 63,045,410 (GRCm39) |
I725L |
probably benign |
Het |
Dydc1 |
A |
C |
14: 40,800,054 (GRCm39) |
E20A |
probably damaging |
Het |
Ermp1 |
T |
C |
19: 29,609,845 (GRCm39) |
I317V |
probably benign |
Het |
Fat4 |
A |
G |
3: 38,942,556 (GRCm39) |
N483S |
possibly damaging |
Het |
Fbxo33 |
A |
G |
12: 59,251,095 (GRCm39) |
|
probably null |
Het |
Fcgbp |
G |
T |
7: 27,803,198 (GRCm39) |
E1601* |
probably null |
Het |
Fer1l5 |
A |
T |
1: 36,449,999 (GRCm39) |
S1118C |
probably null |
Het |
Fer1l6 |
T |
C |
15: 58,494,230 (GRCm39) |
V1141A |
probably benign |
Het |
Flnb |
C |
T |
14: 7,818,219 (GRCm38) |
T23M |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,815,574 (GRCm39) |
L3769P |
possibly damaging |
Het |
Gna11 |
T |
C |
10: 81,370,942 (GRCm39) |
K98R |
|
Het |
Gpat3 |
A |
T |
5: 101,032,230 (GRCm39) |
T176S |
probably benign |
Het |
Gprc5b |
A |
G |
7: 118,583,542 (GRCm39) |
L109P |
probably damaging |
Het |
Hadha |
A |
T |
5: 30,340,038 (GRCm39) |
N246K |
probably benign |
Het |
Haus3 |
G |
A |
5: 34,324,835 (GRCm39) |
Q275* |
probably null |
Het |
Higd1b |
A |
G |
11: 102,728,090 (GRCm39) |
Y44C |
possibly damaging |
Het |
Igkv1-131 |
T |
C |
6: 67,743,218 (GRCm39) |
K55R |
probably benign |
Het |
Igtp |
G |
T |
11: 58,098,091 (GRCm39) |
E421* |
probably null |
Het |
Kcnk3 |
G |
T |
5: 30,745,532 (GRCm39) |
|
probably benign |
Het |
Krtap4-13 |
A |
T |
11: 99,700,165 (GRCm39) |
C165S |
unknown |
Het |
Lrfn4 |
T |
C |
19: 4,663,353 (GRCm39) |
R394G |
probably benign |
Het |
Lrrc7 |
A |
C |
3: 157,867,011 (GRCm39) |
L910R |
possibly damaging |
Het |
Mbtd1 |
A |
G |
11: 93,823,218 (GRCm39) |
D568G |
probably damaging |
Het |
Mettl16 |
T |
A |
11: 74,693,826 (GRCm39) |
I279N |
probably benign |
Het |
Mmrn2 |
A |
G |
14: 34,121,158 (GRCm39) |
H676R |
probably benign |
Het |
Mrgprg |
T |
C |
7: 143,318,350 (GRCm39) |
K254R |
probably benign |
Het |
Muc16 |
A |
C |
9: 18,554,038 (GRCm39) |
V4085G |
unknown |
Het |
Mvp |
T |
C |
7: 126,591,822 (GRCm39) |
Q456R |
probably benign |
Het |
Myf6 |
T |
C |
10: 107,329,318 (GRCm39) |
D209G |
probably benign |
Het |
Ociad1 |
A |
G |
5: 73,467,725 (GRCm39) |
D167G |
probably benign |
Het |
Or11l3 |
A |
G |
11: 58,516,062 (GRCm39) |
L270P |
probably benign |
Het |
Or1l4 |
A |
G |
2: 37,091,292 (GRCm39) |
D13G |
probably benign |
Het |
Or51f23b |
T |
A |
7: 102,402,734 (GRCm39) |
Y134F |
probably damaging |
Het |
Or5m3 |
T |
G |
2: 85,838,325 (GRCm39) |
D68E |
probably damaging |
Het |
Or6c1b |
T |
C |
10: 129,272,858 (GRCm39) |
F59S |
probably damaging |
Het |
Phf20 |
A |
G |
2: 156,114,537 (GRCm39) |
D295G |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Ppp1r13b |
A |
T |
12: 111,811,416 (GRCm39) |
H157Q |
probably benign |
Het |
Prss3b |
A |
G |
6: 41,008,681 (GRCm39) |
L211P |
probably damaging |
Het |
Rbm26 |
C |
T |
14: 105,391,039 (GRCm39) |
R149H |
unknown |
Het |
Reg3d |
C |
T |
6: 78,355,443 (GRCm39) |
C16Y |
possibly damaging |
Het |
Rrp36 |
A |
G |
17: 46,978,980 (GRCm39) |
F193L |
possibly damaging |
Het |
Rtca |
A |
T |
3: 116,282,905 (GRCm39) |
M361K |
probably benign |
Het |
Ryr3 |
T |
G |
2: 112,491,981 (GRCm39) |
D3790A |
probably damaging |
Het |
Serpina3n |
C |
A |
12: 104,377,440 (GRCm39) |
A231E |
probably benign |
Het |
Sh2d2a |
A |
G |
3: 87,759,070 (GRCm39) |
D224G |
possibly damaging |
Het |
Sh3bp2 |
A |
T |
5: 34,718,377 (GRCm39) |
K526* |
probably null |
Het |
Slc12a2 |
A |
G |
18: 58,069,469 (GRCm39) |
T1017A |
possibly damaging |
Het |
Slc12a8 |
T |
C |
16: 33,361,397 (GRCm39) |
L93P |
probably damaging |
Het |
Slc5a6 |
A |
G |
5: 31,195,190 (GRCm39) |
I469T |
probably damaging |
Het |
Smarcc1 |
T |
A |
9: 109,964,728 (GRCm39) |
V95D |
probably damaging |
Het |
Snap29 |
T |
A |
16: 17,224,163 (GRCm39) |
S59R |
probably damaging |
Het |
Tmem121b |
T |
A |
6: 120,469,784 (GRCm39) |
Y311F |
probably damaging |
Het |
Tpcn1 |
C |
A |
5: 120,694,000 (GRCm39) |
V199L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,618,721 (GRCm39) |
I16188V |
probably benign |
Het |
Usp24 |
T |
C |
4: 106,216,247 (GRCm39) |
I366T |
possibly damaging |
Het |
Utrn |
T |
A |
10: 12,545,463 (GRCm39) |
E1727D |
probably damaging |
Het |
Vav2 |
T |
C |
2: 27,182,701 (GRCm39) |
D301G |
probably damaging |
Het |
Vmn2r104 |
T |
C |
17: 20,263,087 (GRCm39) |
T125A |
probably benign |
Het |
Vmn2r73 |
T |
G |
7: 85,507,123 (GRCm39) |
I730L |
probably benign |
Het |
Zfp352 |
A |
T |
4: 90,113,118 (GRCm39) |
K419N |
probably benign |
Het |
Zfp84 |
C |
A |
7: 29,474,873 (GRCm39) |
S48R |
probably damaging |
Het |
Zfp947 |
A |
T |
17: 22,364,386 (GRCm39) |
H429Q |
probably damaging |
Het |
|
Other mutations in Coro1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02986:Coro1b
|
APN |
19 |
4,199,470 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03411:Coro1b
|
APN |
19 |
4,200,225 (GRCm39) |
splice site |
probably benign |
|
R0189:Coro1b
|
UTSW |
19 |
4,203,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R0410:Coro1b
|
UTSW |
19 |
4,199,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R1165:Coro1b
|
UTSW |
19 |
4,199,901 (GRCm39) |
missense |
probably damaging |
0.99 |
R1302:Coro1b
|
UTSW |
19 |
4,199,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:Coro1b
|
UTSW |
19 |
4,200,583 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4085:Coro1b
|
UTSW |
19 |
4,203,618 (GRCm39) |
missense |
probably benign |
0.02 |
R4528:Coro1b
|
UTSW |
19 |
4,199,980 (GRCm39) |
missense |
probably benign |
0.23 |
R4692:Coro1b
|
UTSW |
19 |
4,199,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R4919:Coro1b
|
UTSW |
19 |
4,200,709 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5433:Coro1b
|
UTSW |
19 |
4,203,449 (GRCm39) |
missense |
probably benign |
|
R5650:Coro1b
|
UTSW |
19 |
4,200,610 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5870:Coro1b
|
UTSW |
19 |
4,199,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Coro1b
|
UTSW |
19 |
4,200,770 (GRCm39) |
missense |
probably benign |
0.32 |
R7332:Coro1b
|
UTSW |
19 |
4,199,356 (GRCm39) |
missense |
probably benign |
0.00 |
R7511:Coro1b
|
UTSW |
19 |
4,202,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R7559:Coro1b
|
UTSW |
19 |
4,200,220 (GRCm39) |
critical splice donor site |
probably null |
|
R8684:Coro1b
|
UTSW |
19 |
4,199,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Coro1b
|
UTSW |
19 |
4,200,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R9086:Coro1b
|
UTSW |
19 |
4,202,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R9416:Coro1b
|
UTSW |
19 |
4,201,473 (GRCm39) |
missense |
probably damaging |
0.97 |
R9593:Coro1b
|
UTSW |
19 |
4,199,497 (GRCm39) |
missense |
probably damaging |
1.00 |
|