Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
G |
A |
17: 24,499,452 (GRCm39) |
T1359M |
probably benign |
Het |
Acacb |
T |
A |
5: 114,384,085 (GRCm39) |
C2205S |
possibly damaging |
Het |
Akap3 |
A |
G |
6: 126,841,591 (GRCm39) |
E70G |
probably benign |
Het |
Aldh1a3 |
C |
A |
7: 66,068,992 (GRCm39) |
|
probably null |
Het |
Asb4 |
A |
G |
6: 5,429,817 (GRCm39) |
I352M |
probably benign |
Het |
Bach1 |
C |
G |
16: 87,516,603 (GRCm39) |
S381R |
probably benign |
Het |
BC034090 |
A |
G |
1: 155,101,961 (GRCm39) |
L101P |
probably benign |
Het |
Bms1 |
A |
T |
6: 118,382,217 (GRCm39) |
D440E |
probably benign |
Het |
Bpifb6 |
A |
T |
2: 153,747,914 (GRCm39) |
D191V |
probably benign |
Het |
Cfap298 |
A |
T |
16: 90,726,832 (GRCm39) |
V116E |
probably benign |
Het |
Cfd |
T |
C |
10: 79,726,816 (GRCm39) |
|
probably null |
Het |
Cnot3 |
G |
A |
7: 3,656,560 (GRCm39) |
E252K |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,707,068 (GRCm39) |
D2622G |
unknown |
Het |
Crybg2 |
T |
C |
4: 133,801,602 (GRCm39) |
S612P |
probably benign |
Het |
Cyp4b1 |
T |
C |
4: 115,493,581 (GRCm39) |
K167R |
probably damaging |
Het |
Gbp3 |
T |
C |
3: 142,272,335 (GRCm39) |
V279A |
possibly damaging |
Het |
Gipc2 |
T |
C |
3: 151,833,706 (GRCm39) |
T192A |
possibly damaging |
Het |
Gm3285 |
T |
C |
10: 77,697,911 (GRCm39) |
V20A |
|
Het |
Gorasp2 |
T |
C |
2: 70,541,469 (GRCm39) |
|
probably null |
Het |
Gpr179 |
A |
G |
11: 97,229,315 (GRCm39) |
S947P |
probably benign |
Het |
Klra5 |
C |
A |
6: 129,883,686 (GRCm39) |
W147L |
possibly damaging |
Het |
Lrch4 |
G |
A |
5: 137,636,051 (GRCm39) |
R368Q |
probably damaging |
Het |
Mamdc4 |
A |
G |
2: 25,455,600 (GRCm39) |
V876A |
probably benign |
Het |
Marf1 |
A |
C |
16: 13,938,196 (GRCm39) |
D1433E |
probably benign |
Het |
Mcm4 |
A |
T |
16: 15,453,175 (GRCm39) |
C171* |
probably null |
Het |
Micall1 |
C |
T |
15: 79,011,159 (GRCm39) |
P510S |
|
Het |
Morc3 |
A |
G |
16: 93,649,975 (GRCm39) |
|
probably null |
Het |
Mrpl28 |
G |
T |
17: 26,345,266 (GRCm39) |
V229F |
possibly damaging |
Het |
Mrps33 |
A |
T |
6: 39,782,364 (GRCm39) |
Y52* |
probably null |
Het |
Mybphl |
T |
C |
3: 108,282,202 (GRCm39) |
I144T |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,433,329 (GRCm39) |
M1657V |
probably benign |
Het |
Ogfr |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,850 (GRCm39) |
|
probably benign |
Het |
Or5p67 |
A |
G |
7: 107,922,037 (GRCm39) |
I282T |
probably benign |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Plxna1 |
T |
C |
6: 89,318,912 (GRCm39) |
K637R |
probably benign |
Het |
Prob1 |
G |
T |
18: 35,786,218 (GRCm39) |
L679I |
possibly damaging |
Het |
Sgms2 |
C |
A |
3: 131,118,718 (GRCm39) |
C255F |
probably damaging |
Het |
Slc17a9 |
T |
C |
2: 180,383,090 (GRCm39) |
C399R |
probably benign |
Het |
Smc4 |
T |
A |
3: 68,915,455 (GRCm39) |
|
probably null |
Het |
St14 |
A |
G |
9: 31,007,845 (GRCm39) |
L578P |
probably damaging |
Het |
Tcaf3 |
A |
T |
6: 42,573,906 (GRCm39) |
L102* |
probably null |
Het |
Tex15 |
A |
G |
8: 34,072,273 (GRCm39) |
T2607A |
possibly damaging |
Het |
Trip4 |
T |
C |
9: 65,760,234 (GRCm39) |
|
probably null |
Het |
Ttf1 |
A |
G |
2: 28,955,709 (GRCm39) |
I358V |
probably benign |
Het |
Uroc1 |
C |
A |
6: 90,322,353 (GRCm39) |
S292R |
possibly damaging |
Het |
Vmn1r5 |
T |
C |
6: 56,962,415 (GRCm39) |
I30T |
possibly damaging |
Het |
Vps33a |
A |
T |
5: 123,703,047 (GRCm39) |
I192N |
probably damaging |
Het |
Vps50 |
A |
G |
6: 3,516,724 (GRCm39) |
I69V |
probably benign |
Het |
Wdr97 |
T |
C |
15: 76,245,064 (GRCm39) |
S1176P |
|
Het |
Xirp1 |
G |
A |
9: 119,847,203 (GRCm39) |
T560M |
probably damaging |
Het |
Zfp512 |
A |
T |
5: 31,628,359 (GRCm39) |
T266S |
possibly damaging |
Het |
|
Other mutations in Trav15-2-dv6-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4304:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,207 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,214 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,214 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,213 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,214 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,211 (GRCm39) |
nonsense |
probably null |
|
R5966:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6113:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,182 (GRCm39) |
missense |
probably benign |
0.00 |
R6270:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,323 (GRCm39) |
missense |
probably benign |
0.00 |
R7298:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,242 (GRCm39) |
missense |
probably benign |
0.41 |
R7528:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,308 (GRCm39) |
missense |
probably benign |
0.09 |
R8996:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,247 (GRCm39) |
missense |
probably benign |
0.00 |
RF004:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,212 (GRCm39) |
small insertion |
probably benign |
|
RF004:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,211 (GRCm39) |
nonsense |
probably null |
|
RF004:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,207 (GRCm39) |
small insertion |
probably benign |
|
RF005:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,211 (GRCm39) |
small insertion |
probably benign |
|
RF005:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,208 (GRCm39) |
small insertion |
probably benign |
|
RF005:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,207 (GRCm39) |
small insertion |
probably benign |
|
RF007:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,212 (GRCm39) |
small insertion |
probably benign |
|
RF007:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,208 (GRCm39) |
small insertion |
probably benign |
|
RF007:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,207 (GRCm39) |
small insertion |
probably benign |
|
RF026:Trav15-2-dv6-2
|
UTSW |
14 |
53,887,214 (GRCm39) |
small insertion |
probably benign |
|
|