Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd6 |
A |
G |
1: 155,434,454 (GRCm39) |
D24G |
probably damaging |
Het |
Adarb1 |
A |
G |
10: 77,153,183 (GRCm39) |
V322A |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,557,777 (GRCm39) |
G37R |
probably damaging |
Het |
Capzb |
T |
A |
4: 138,989,334 (GRCm39) |
D85E |
possibly damaging |
Het |
Cd81 |
T |
A |
7: 142,620,056 (GRCm39) |
N71K |
probably benign |
Het |
Cemip |
G |
T |
7: 83,647,770 (GRCm39) |
D103E |
probably benign |
Het |
Chfr |
A |
G |
5: 110,318,729 (GRCm39) |
K580E |
probably damaging |
Het |
Chrnb1 |
A |
T |
11: 69,686,428 (GRCm39) |
I64N |
probably damaging |
Het |
Clca3a1 |
G |
T |
3: 144,714,829 (GRCm39) |
P596Q |
possibly damaging |
Het |
Cpb1 |
A |
T |
3: 20,329,629 (GRCm39) |
D32E |
probably benign |
Het |
Crh |
A |
T |
3: 19,748,096 (GRCm39) |
M182K |
probably damaging |
Het |
Csta1 |
C |
T |
16: 35,945,445 (GRCm39) |
V23I |
probably damaging |
Het |
Dazap1 |
A |
G |
10: 80,113,433 (GRCm39) |
K110E |
possibly damaging |
Het |
Dhx16 |
T |
C |
17: 36,198,778 (GRCm39) |
C737R |
probably damaging |
Het |
Dync1i2 |
C |
T |
2: 71,079,764 (GRCm39) |
Q419* |
probably null |
Het |
Eml5 |
A |
C |
12: 98,807,840 (GRCm39) |
D984E |
probably damaging |
Het |
Fat3 |
G |
A |
9: 15,909,567 (GRCm39) |
S2145F |
probably damaging |
Het |
Gm12695 |
C |
T |
4: 96,612,266 (GRCm39) |
R499Q |
probably damaging |
Het |
Hid1 |
A |
G |
11: 115,241,945 (GRCm39) |
I555T |
probably damaging |
Het |
Hspa2 |
A |
G |
12: 76,451,419 (GRCm39) |
T38A |
possibly damaging |
Het |
Igf1r |
T |
A |
7: 67,861,828 (GRCm39) |
N1129K |
probably damaging |
Het |
Iglon5 |
T |
C |
7: 43,130,062 (GRCm39) |
E34G |
probably damaging |
Het |
Itprid1 |
A |
T |
6: 55,874,797 (GRCm39) |
H249L |
possibly damaging |
Het |
Kalrn |
C |
A |
16: 33,996,632 (GRCm39) |
|
probably null |
Het |
Kmt2d |
T |
C |
15: 98,763,129 (GRCm39) |
D240G |
probably damaging |
Het |
Lrrc56 |
T |
A |
7: 140,778,207 (GRCm39) |
D66E |
probably damaging |
Het |
Myot |
A |
G |
18: 44,487,339 (GRCm39) |
D392G |
probably damaging |
Het |
Nphp3 |
G |
A |
9: 103,914,575 (GRCm39) |
R1052H |
probably benign |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Or2d4 |
C |
A |
7: 106,543,827 (GRCm39) |
C127F |
probably damaging |
Het |
Or4c114 |
A |
G |
2: 88,904,592 (GRCm39) |
L281P |
probably damaging |
Het |
Or6z5 |
T |
C |
7: 6,477,441 (GRCm39) |
S111P |
possibly damaging |
Het |
Or7g19 |
A |
T |
9: 18,856,112 (GRCm39) |
H56L |
probably damaging |
Het |
Or8k39 |
A |
G |
2: 86,563,921 (GRCm39) |
F12L |
possibly damaging |
Het |
Pax8 |
A |
G |
2: 24,333,114 (GRCm39) |
I77T |
probably damaging |
Het |
Paxbp1 |
T |
C |
16: 90,831,822 (GRCm39) |
I355M |
probably benign |
Het |
Pds5a |
A |
T |
5: 65,811,441 (GRCm39) |
F331I |
probably damaging |
Het |
Plec |
A |
T |
15: 76,061,147 (GRCm39) |
I2952N |
probably damaging |
Het |
Ppp1r12a |
A |
G |
10: 108,034,780 (GRCm39) |
I108M |
possibly damaging |
Het |
Rabepk |
A |
T |
2: 34,685,246 (GRCm39) |
I58N |
possibly damaging |
Het |
Rnf216 |
G |
A |
5: 143,076,681 (GRCm39) |
H68Y |
probably benign |
Het |
Scap |
T |
C |
9: 110,210,661 (GRCm39) |
C998R |
probably damaging |
Het |
Scgb1b27 |
T |
C |
7: 33,721,249 (GRCm39) |
Y46H |
probably damaging |
Het |
Sf3a2 |
G |
T |
10: 80,638,663 (GRCm39) |
A95S |
probably benign |
Het |
Smg7 |
A |
T |
1: 152,744,064 (GRCm39) |
Y40N |
probably damaging |
Het |
Ssc5d |
A |
G |
7: 4,946,849 (GRCm39) |
T1068A |
probably benign |
Het |
Stambp |
A |
G |
6: 83,528,960 (GRCm39) |
S362P |
probably damaging |
Het |
Tbx18 |
G |
T |
9: 87,606,403 (GRCm39) |
S247R |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,729,204 (GRCm39) |
I1601V |
probably benign |
Het |
Thap4 |
G |
T |
1: 93,652,934 (GRCm39) |
Q441K |
probably benign |
Het |
Tmprss11c |
G |
T |
5: 86,429,945 (GRCm39) |
T40K |
probably benign |
Het |
Tnk1 |
C |
T |
11: 69,746,017 (GRCm39) |
|
probably null |
Het |
Trim65 |
G |
T |
11: 116,021,503 (GRCm39) |
T110K |
possibly damaging |
Het |
Uck1 |
T |
C |
2: 32,148,315 (GRCm39) |
D167G |
probably damaging |
Het |
Vmn2r124 |
A |
T |
17: 18,269,927 (GRCm39) |
H61L |
possibly damaging |
Het |
Xpnpep1 |
T |
G |
19: 53,001,892 (GRCm39) |
D118A |
probably damaging |
Het |
Xylt2 |
C |
T |
11: 94,560,822 (GRCm39) |
V239M |
possibly damaging |
Het |
|
Other mutations in BC035947 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1853:BC035947
|
UTSW |
1 |
78,475,653 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2079:BC035947
|
UTSW |
1 |
78,488,561 (GRCm39) |
utr 5 prime |
probably benign |
|
R2235:BC035947
|
UTSW |
1 |
78,474,599 (GRCm39) |
missense |
probably damaging |
0.98 |
R3840:BC035947
|
UTSW |
1 |
78,474,482 (GRCm39) |
missense |
probably benign |
0.00 |
R3841:BC035947
|
UTSW |
1 |
78,474,482 (GRCm39) |
missense |
probably benign |
0.00 |
R4804:BC035947
|
UTSW |
1 |
78,474,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R4909:BC035947
|
UTSW |
1 |
78,474,666 (GRCm39) |
missense |
probably damaging |
0.99 |
R5139:BC035947
|
UTSW |
1 |
78,475,884 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5302:BC035947
|
UTSW |
1 |
78,488,599 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R5669:BC035947
|
UTSW |
1 |
78,474,550 (GRCm39) |
missense |
probably damaging |
0.98 |
R5686:BC035947
|
UTSW |
1 |
78,474,567 (GRCm39) |
missense |
probably benign |
0.03 |
R5868:BC035947
|
UTSW |
1 |
78,474,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:BC035947
|
UTSW |
1 |
78,475,843 (GRCm39) |
nonsense |
probably null |
|
R6787:BC035947
|
UTSW |
1 |
78,475,527 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6854:BC035947
|
UTSW |
1 |
78,475,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R7079:BC035947
|
UTSW |
1 |
78,474,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7168:BC035947
|
UTSW |
1 |
78,476,230 (GRCm39) |
missense |
probably benign |
0.04 |
R7387:BC035947
|
UTSW |
1 |
78,475,098 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8468:BC035947
|
UTSW |
1 |
78,474,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R8990:BC035947
|
UTSW |
1 |
78,475,486 (GRCm39) |
missense |
probably damaging |
0.98 |
R9192:BC035947
|
UTSW |
1 |
78,475,877 (GRCm39) |
nonsense |
probably null |
|
R9786:BC035947
|
UTSW |
1 |
78,488,561 (GRCm39) |
utr 5 prime |
probably benign |
|
|