Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5330417H12Rik |
T |
C |
7: 107,223,897 (GRCm39) |
|
probably benign |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Adgrf2 |
T |
C |
17: 43,022,084 (GRCm39) |
I247V |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,418,857 (GRCm39) |
|
probably null |
Het |
Ankrd22 |
T |
A |
19: 34,126,752 (GRCm39) |
K26I |
possibly damaging |
Het |
Arhgap32 |
T |
A |
9: 32,156,552 (GRCm39) |
|
probably null |
Het |
Armc10 |
A |
G |
5: 21,866,522 (GRCm39) |
Y262C |
probably damaging |
Het |
Arrb2 |
A |
G |
11: 70,330,725 (GRCm39) |
D374G |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,625,227 (GRCm39) |
R1675C |
probably damaging |
Het |
Atg5 |
T |
C |
10: 44,239,046 (GRCm39) |
*276R |
probably null |
Het |
Bcl11b |
G |
A |
12: 107,882,968 (GRCm39) |
T377M |
probably damaging |
Het |
C1s2 |
C |
A |
6: 124,612,073 (GRCm39) |
E104* |
probably null |
Het |
Carf |
A |
T |
1: 60,180,526 (GRCm39) |
H316L |
probably damaging |
Het |
Ccdc77 |
A |
T |
6: 120,311,796 (GRCm39) |
I234N |
probably damaging |
Het |
Cd300c2 |
A |
T |
11: 114,887,826 (GRCm39) |
V192E |
possibly damaging |
Het |
Cep72 |
G |
A |
13: 74,207,584 (GRCm39) |
R62C |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,436,640 (GRCm39) |
L308* |
probably null |
Het |
Clec2g |
A |
G |
6: 128,956,411 (GRCm39) |
S25G |
probably benign |
Het |
Cngb1 |
T |
C |
8: 95,978,601 (GRCm39) |
M1046V |
probably damaging |
Het |
Cobll1 |
A |
T |
2: 64,928,037 (GRCm39) |
D1095E |
probably benign |
Het |
Cpeb2 |
A |
G |
5: 43,402,005 (GRCm39) |
H662R |
possibly damaging |
Het |
Cps1 |
A |
T |
1: 67,178,922 (GRCm39) |
T45S |
probably benign |
Het |
Cspp1 |
A |
G |
1: 10,152,553 (GRCm39) |
Q368R |
possibly damaging |
Het |
Dcaf6 |
C |
A |
1: 165,239,032 (GRCm39) |
|
probably null |
Het |
Dcst1 |
T |
C |
3: 89,257,814 (GRCm39) |
Y652C |
possibly damaging |
Het |
Elf5 |
T |
G |
2: 103,279,918 (GRCm39) |
Y225* |
probably null |
Het |
Ermap |
A |
C |
4: 119,046,015 (GRCm39) |
|
probably benign |
Het |
Fam186b |
A |
T |
15: 99,169,202 (GRCm39) |
V915D |
probably damaging |
Het |
Fbxo34 |
C |
A |
14: 47,766,911 (GRCm39) |
N90K |
probably benign |
Het |
Flnc |
A |
G |
6: 29,447,524 (GRCm39) |
E1109G |
probably damaging |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Gabpb2 |
A |
G |
3: 95,097,947 (GRCm39) |
V242A |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm21798 |
A |
T |
15: 64,689,732 (GRCm39) |
|
probably benign |
Het |
Gpr179 |
A |
T |
11: 97,237,487 (GRCm39) |
S345T |
possibly damaging |
Het |
Gusb |
A |
T |
5: 130,026,959 (GRCm39) |
F377L |
probably damaging |
Het |
Hnrnpu |
T |
C |
1: 178,156,938 (GRCm39) |
|
probably benign |
Het |
Htr3b |
C |
T |
9: 48,848,348 (GRCm39) |
|
probably null |
Het |
Iqub |
A |
T |
6: 24,501,368 (GRCm39) |
V194D |
probably damaging |
Het |
Itga2b |
A |
G |
11: 102,351,985 (GRCm39) |
V504A |
probably benign |
Het |
Itga4 |
T |
A |
2: 79,118,592 (GRCm39) |
F430L |
probably damaging |
Het |
Jcad |
C |
A |
18: 4,673,762 (GRCm39) |
P508H |
probably damaging |
Het |
Jph1 |
T |
C |
1: 17,161,835 (GRCm39) |
T276A |
probably damaging |
Het |
Kansl2 |
A |
G |
15: 98,429,771 (GRCm39) |
F87S |
possibly damaging |
Het |
Kdm1b |
T |
C |
13: 47,216,620 (GRCm39) |
|
probably null |
Het |
Kif5b |
C |
T |
18: 6,220,930 (GRCm39) |
D393N |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,747,420 (GRCm39) |
|
probably benign |
Het |
Krt75 |
A |
G |
15: 101,478,674 (GRCm39) |
I320T |
probably damaging |
Het |
Lhfpl7 |
T |
A |
5: 113,386,036 (GRCm39) |
M161K |
probably benign |
Het |
Lipo5 |
T |
C |
19: 33,443,348 (GRCm39) |
N156S |
unknown |
Het |
Mblac2 |
A |
C |
13: 81,859,706 (GRCm39) |
Q19P |
probably null |
Het |
Mdfic2 |
A |
T |
6: 98,215,080 (GRCm39) |
M181K |
probably damaging |
Het |
Mfsd4b3-ps |
T |
C |
10: 39,824,056 (GRCm39) |
H68R |
probably damaging |
Het |
Mzb1 |
A |
T |
18: 35,781,006 (GRCm39) |
|
probably null |
Het |
Nup210l |
T |
A |
3: 90,077,337 (GRCm39) |
I891N |
probably benign |
Het |
Nwd1 |
G |
A |
8: 73,398,841 (GRCm39) |
R667Q |
probably damaging |
Het |
Oas1h |
C |
T |
5: 121,005,172 (GRCm39) |
Q207* |
probably null |
Het |
Or13c7d |
A |
T |
4: 43,770,476 (GRCm39) |
F178L |
possibly damaging |
Het |
Pcdh15 |
C |
T |
10: 74,340,625 (GRCm39) |
R1120* |
probably null |
Het |
Pfkl |
A |
G |
10: 77,824,144 (GRCm39) |
L748P |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,571,758 (GRCm39) |
K473N |
probably damaging |
Het |
Rapgef6 |
G |
A |
11: 54,443,662 (GRCm39) |
V82I |
probably damaging |
Het |
Rfc3 |
A |
T |
5: 151,570,960 (GRCm39) |
L112Q |
probably damaging |
Het |
Rsph6a |
T |
A |
7: 18,801,997 (GRCm39) |
C349S |
possibly damaging |
Het |
Sec16a |
A |
T |
2: 26,331,979 (GRCm39) |
|
probably benign |
Het |
Septin14 |
T |
A |
5: 129,770,030 (GRCm39) |
Y222F |
probably benign |
Het |
Skor2 |
T |
C |
18: 76,947,990 (GRCm39) |
S571P |
possibly damaging |
Het |
Slc13a5 |
T |
A |
11: 72,148,244 (GRCm39) |
M264L |
probably damaging |
Het |
Slc45a3 |
T |
A |
1: 131,909,315 (GRCm39) |
V504E |
probably damaging |
Het |
Smim20 |
A |
G |
5: 53,434,503 (GRCm39) |
N45S |
probably null |
Het |
Spp2 |
A |
T |
1: 88,339,991 (GRCm39) |
S111C |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,442,664 (GRCm39) |
|
probably null |
Het |
Sycp2 |
C |
T |
2: 178,045,450 (GRCm39) |
|
probably null |
Het |
Tas2r113 |
A |
G |
6: 132,870,521 (GRCm39) |
N183S |
possibly damaging |
Het |
Tcaf2 |
A |
T |
6: 42,606,679 (GRCm39) |
M425K |
probably benign |
Het |
Tdrp |
A |
G |
8: 14,003,845 (GRCm39) |
V164A |
possibly damaging |
Het |
Tmbim1 |
A |
G |
1: 74,328,568 (GRCm39) |
F298S |
probably damaging |
Het |
Tmem89 |
A |
G |
9: 108,743,829 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
G |
T |
10: 77,768,023 (GRCm39) |
C825* |
probably null |
Het |
Tsc1 |
A |
G |
2: 28,565,201 (GRCm39) |
E421G |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,245,834 (GRCm39) |
I1364T |
probably benign |
Het |
Vmn1r52 |
G |
A |
6: 90,155,930 (GRCm39) |
G78E |
possibly damaging |
Het |
Vmn2r73 |
T |
G |
7: 85,506,829 (GRCm39) |
I828L |
probably damaging |
Het |
Vwa5b1 |
A |
T |
4: 138,338,058 (GRCm39) |
D87E |
probably benign |
Het |
Zfp1010 |
T |
C |
2: 176,957,223 (GRCm39) |
T92A |
possibly damaging |
Het |
Zfp451 |
A |
T |
1: 33,844,465 (GRCm39) |
D47E |
probably damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,841 (GRCm39) |
E278G |
probably damaging |
Het |
Zfp930 |
A |
T |
8: 69,681,597 (GRCm39) |
T430S |
probably benign |
Het |
Zfp994 |
G |
T |
17: 22,419,448 (GRCm39) |
Y500* |
probably null |
Het |
Zmat3 |
A |
T |
3: 32,397,836 (GRCm39) |
I142N |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,792,214 (GRCm39) |
I2266N |
probably damaging |
Het |
|
Other mutations in Smg1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Smg1
|
APN |
7 |
117,797,494 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00481:Smg1
|
APN |
7 |
117,810,017 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL00503:Smg1
|
APN |
7 |
117,784,706 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00927:Smg1
|
APN |
7 |
117,739,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01333:Smg1
|
APN |
7 |
117,762,601 (GRCm39) |
splice site |
probably benign |
|
IGL01344:Smg1
|
APN |
7 |
117,790,059 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01397:Smg1
|
APN |
7 |
117,762,444 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01403:Smg1
|
APN |
7 |
117,757,355 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01573:Smg1
|
APN |
7 |
117,767,185 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01872:Smg1
|
APN |
7 |
117,748,167 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02010:Smg1
|
APN |
7 |
117,785,369 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02158:Smg1
|
APN |
7 |
117,812,169 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02268:Smg1
|
APN |
7 |
117,781,764 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02314:Smg1
|
APN |
7 |
117,753,932 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02552:Smg1
|
APN |
7 |
117,795,117 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02577:Smg1
|
APN |
7 |
117,802,345 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02859:Smg1
|
APN |
7 |
117,748,156 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02890:Smg1
|
APN |
7 |
117,784,724 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02892:Smg1
|
APN |
7 |
117,767,178 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03119:Smg1
|
APN |
7 |
117,794,336 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03123:Smg1
|
APN |
7 |
117,756,404 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03128:Smg1
|
APN |
7 |
117,802,282 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03184:Smg1
|
APN |
7 |
117,779,603 (GRCm39) |
missense |
possibly damaging |
0.86 |
PIT4508001:Smg1
|
UTSW |
7 |
117,784,764 (GRCm39) |
missense |
unknown |
|
R0010:Smg1
|
UTSW |
7 |
117,771,082 (GRCm39) |
utr 3 prime |
probably benign |
|
R0010:Smg1
|
UTSW |
7 |
117,771,082 (GRCm39) |
utr 3 prime |
probably benign |
|
R0025:Smg1
|
UTSW |
7 |
117,811,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0025:Smg1
|
UTSW |
7 |
117,811,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0098:Smg1
|
UTSW |
7 |
117,744,690 (GRCm39) |
missense |
probably benign |
0.02 |
R0139:Smg1
|
UTSW |
7 |
117,751,898 (GRCm39) |
critical splice donor site |
probably null |
|
R0371:Smg1
|
UTSW |
7 |
117,767,523 (GRCm39) |
utr 3 prime |
probably benign |
|
R0415:Smg1
|
UTSW |
7 |
117,781,691 (GRCm39) |
missense |
probably benign |
0.34 |
R0416:Smg1
|
UTSW |
7 |
117,783,684 (GRCm39) |
splice site |
probably benign |
|
R0423:Smg1
|
UTSW |
7 |
117,776,103 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0600:Smg1
|
UTSW |
7 |
117,759,606 (GRCm39) |
utr 3 prime |
probably benign |
|
R0626:Smg1
|
UTSW |
7 |
117,781,606 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0627:Smg1
|
UTSW |
7 |
117,767,084 (GRCm39) |
utr 3 prime |
probably benign |
|
R0727:Smg1
|
UTSW |
7 |
117,765,645 (GRCm39) |
utr 3 prime |
probably benign |
|
R0729:Smg1
|
UTSW |
7 |
117,745,512 (GRCm39) |
utr 3 prime |
probably benign |
|
R0841:Smg1
|
UTSW |
7 |
117,742,524 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1114:Smg1
|
UTSW |
7 |
117,759,013 (GRCm39) |
utr 3 prime |
probably benign |
|
R1256:Smg1
|
UTSW |
7 |
117,802,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1298:Smg1
|
UTSW |
7 |
117,767,434 (GRCm39) |
utr 3 prime |
probably benign |
|
R1370:Smg1
|
UTSW |
7 |
117,758,975 (GRCm39) |
utr 3 prime |
probably benign |
|
R1591:Smg1
|
UTSW |
7 |
117,756,142 (GRCm39) |
utr 3 prime |
probably benign |
|
R1736:Smg1
|
UTSW |
7 |
117,765,190 (GRCm39) |
splice site |
probably null |
|
R1755:Smg1
|
UTSW |
7 |
117,802,287 (GRCm39) |
nonsense |
probably null |
|
R1765:Smg1
|
UTSW |
7 |
117,738,938 (GRCm39) |
missense |
probably benign |
0.03 |
R1789:Smg1
|
UTSW |
7 |
117,745,021 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1845:Smg1
|
UTSW |
7 |
117,753,845 (GRCm39) |
utr 3 prime |
probably benign |
|
R1908:Smg1
|
UTSW |
7 |
117,753,422 (GRCm39) |
utr 3 prime |
probably benign |
|
R1909:Smg1
|
UTSW |
7 |
117,753,422 (GRCm39) |
utr 3 prime |
probably benign |
|
R1942:Smg1
|
UTSW |
7 |
117,757,326 (GRCm39) |
utr 3 prime |
probably benign |
|
R2064:Smg1
|
UTSW |
7 |
117,756,090 (GRCm39) |
utr 3 prime |
probably benign |
|
R2072:Smg1
|
UTSW |
7 |
117,762,389 (GRCm39) |
utr 3 prime |
probably benign |
|
R2154:Smg1
|
UTSW |
7 |
117,757,299 (GRCm39) |
utr 3 prime |
probably benign |
|
R2895:Smg1
|
UTSW |
7 |
117,788,366 (GRCm39) |
utr 3 prime |
probably benign |
|
R2915:Smg1
|
UTSW |
7 |
117,810,102 (GRCm39) |
splice site |
probably benign |
|
R3416:Smg1
|
UTSW |
7 |
117,748,076 (GRCm39) |
utr 3 prime |
probably benign |
|
R3417:Smg1
|
UTSW |
7 |
117,748,076 (GRCm39) |
utr 3 prime |
probably benign |
|
R3873:Smg1
|
UTSW |
7 |
117,753,885 (GRCm39) |
utr 3 prime |
probably benign |
|
R4082:Smg1
|
UTSW |
7 |
117,759,469 (GRCm39) |
utr 3 prime |
probably benign |
|
R4230:Smg1
|
UTSW |
7 |
117,747,956 (GRCm39) |
critical splice donor site |
probably null |
|
R4304:Smg1
|
UTSW |
7 |
117,738,741 (GRCm39) |
missense |
probably benign |
0.03 |
R4549:Smg1
|
UTSW |
7 |
117,758,906 (GRCm39) |
utr 3 prime |
probably benign |
|
R4571:Smg1
|
UTSW |
7 |
117,738,688 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4638:Smg1
|
UTSW |
7 |
117,795,149 (GRCm39) |
utr 3 prime |
probably benign |
|
R4642:Smg1
|
UTSW |
7 |
117,753,487 (GRCm39) |
utr 3 prime |
probably benign |
|
R4656:Smg1
|
UTSW |
7 |
117,812,174 (GRCm39) |
missense |
probably benign |
0.00 |
R4754:Smg1
|
UTSW |
7 |
117,755,954 (GRCm39) |
utr 3 prime |
probably benign |
|
R4798:Smg1
|
UTSW |
7 |
117,779,697 (GRCm39) |
missense |
probably benign |
0.32 |
R4978:Smg1
|
UTSW |
7 |
117,753,470 (GRCm39) |
utr 3 prime |
probably benign |
|
R4989:Smg1
|
UTSW |
7 |
117,807,274 (GRCm39) |
missense |
probably benign |
|
R4989:Smg1
|
UTSW |
7 |
117,757,323 (GRCm39) |
utr 3 prime |
probably benign |
|
R5026:Smg1
|
UTSW |
7 |
117,792,768 (GRCm39) |
utr 3 prime |
probably benign |
|
R5124:Smg1
|
UTSW |
7 |
117,812,235 (GRCm39) |
missense |
probably benign |
0.00 |
R5318:Smg1
|
UTSW |
7 |
117,759,427 (GRCm39) |
utr 3 prime |
probably benign |
|
R5356:Smg1
|
UTSW |
7 |
117,794,356 (GRCm39) |
utr 3 prime |
probably benign |
|
R5404:Smg1
|
UTSW |
7 |
117,806,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Smg1
|
UTSW |
7 |
117,745,294 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5441:Smg1
|
UTSW |
7 |
117,794,304 (GRCm39) |
utr 3 prime |
probably benign |
|
R5490:Smg1
|
UTSW |
7 |
117,738,659 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5541:Smg1
|
UTSW |
7 |
117,756,386 (GRCm39) |
utr 3 prime |
probably benign |
|
R5564:Smg1
|
UTSW |
7 |
117,789,042 (GRCm39) |
utr 3 prime |
probably benign |
|
R5580:Smg1
|
UTSW |
7 |
117,748,125 (GRCm39) |
utr 3 prime |
probably benign |
|
R5600:Smg1
|
UTSW |
7 |
117,767,107 (GRCm39) |
utr 3 prime |
probably benign |
|
R5628:Smg1
|
UTSW |
7 |
117,753,924 (GRCm39) |
utr 3 prime |
probably benign |
|
R5646:Smg1
|
UTSW |
7 |
117,811,782 (GRCm39) |
missense |
probably benign |
0.42 |
R5656:Smg1
|
UTSW |
7 |
117,753,887 (GRCm39) |
utr 3 prime |
probably benign |
|
R5660:Smg1
|
UTSW |
7 |
117,742,570 (GRCm39) |
missense |
probably benign |
0.33 |
R5706:Smg1
|
UTSW |
7 |
117,744,813 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5786:Smg1
|
UTSW |
7 |
117,812,120 (GRCm39) |
missense |
probably benign |
0.12 |
R5890:Smg1
|
UTSW |
7 |
117,789,809 (GRCm39) |
utr 3 prime |
probably benign |
|
R5912:Smg1
|
UTSW |
7 |
117,753,809 (GRCm39) |
utr 3 prime |
probably benign |
|
R5977:Smg1
|
UTSW |
7 |
117,740,580 (GRCm39) |
utr 3 prime |
probably benign |
|
R5993:Smg1
|
UTSW |
7 |
117,739,732 (GRCm39) |
missense |
probably benign |
0.33 |
R6161:Smg1
|
UTSW |
7 |
117,762,553 (GRCm39) |
utr 3 prime |
probably benign |
|
R6187:Smg1
|
UTSW |
7 |
117,788,386 (GRCm39) |
utr 3 prime |
probably benign |
|
R6264:Smg1
|
UTSW |
7 |
117,765,310 (GRCm39) |
utr 3 prime |
probably benign |
|
R6331:Smg1
|
UTSW |
7 |
117,753,500 (GRCm39) |
utr 3 prime |
probably benign |
|
R6561:Smg1
|
UTSW |
7 |
117,765,300 (GRCm39) |
utr 3 prime |
probably benign |
|
R6571:Smg1
|
UTSW |
7 |
117,783,737 (GRCm39) |
utr 3 prime |
probably benign |
|
R6736:Smg1
|
UTSW |
7 |
117,756,389 (GRCm39) |
utr 3 prime |
probably benign |
|
R6752:Smg1
|
UTSW |
7 |
117,762,539 (GRCm39) |
utr 3 prime |
probably benign |
|
R6777:Smg1
|
UTSW |
7 |
117,788,340 (GRCm39) |
utr 3 prime |
probably benign |
|
R6788:Smg1
|
UTSW |
7 |
117,783,794 (GRCm39) |
utr 3 prime |
probably benign |
|
R6883:Smg1
|
UTSW |
7 |
117,767,403 (GRCm39) |
utr 3 prime |
probably benign |
|
R6991:Smg1
|
UTSW |
7 |
117,767,091 (GRCm39) |
utr 3 prime |
probably benign |
|
R7056:Smg1
|
UTSW |
7 |
117,745,623 (GRCm39) |
splice site |
probably benign |
|
R7058:Smg1
|
UTSW |
7 |
117,797,502 (GRCm39) |
utr 3 prime |
probably benign |
|
R7100:Smg1
|
UTSW |
7 |
117,783,743 (GRCm39) |
missense |
unknown |
|
R7133:Smg1
|
UTSW |
7 |
117,752,131 (GRCm39) |
missense |
unknown |
|
R7221:Smg1
|
UTSW |
7 |
117,782,020 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7229:Smg1
|
UTSW |
7 |
117,776,178 (GRCm39) |
missense |
probably benign |
0.03 |
R7293:Smg1
|
UTSW |
7 |
117,765,322 (GRCm39) |
missense |
unknown |
|
R7361:Smg1
|
UTSW |
7 |
117,784,200 (GRCm39) |
missense |
unknown |
|
R7438:Smg1
|
UTSW |
7 |
117,795,116 (GRCm39) |
missense |
unknown |
|
R7686:Smg1
|
UTSW |
7 |
117,767,081 (GRCm39) |
missense |
unknown |
|
R7798:Smg1
|
UTSW |
7 |
117,771,162 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7908:Smg1
|
UTSW |
7 |
117,785,357 (GRCm39) |
missense |
unknown |
|
R7923:Smg1
|
UTSW |
7 |
117,742,545 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7978:Smg1
|
UTSW |
7 |
117,792,878 (GRCm39) |
missense |
unknown |
|
R7997:Smg1
|
UTSW |
7 |
117,772,365 (GRCm39) |
missense |
unknown |
|
R7997:Smg1
|
UTSW |
7 |
117,772,364 (GRCm39) |
missense |
unknown |
|
R8025:Smg1
|
UTSW |
7 |
117,806,212 (GRCm39) |
nonsense |
probably null |
|
R8056:Smg1
|
UTSW |
7 |
117,759,589 (GRCm39) |
missense |
unknown |
|
R8061:Smg1
|
UTSW |
7 |
117,751,610 (GRCm39) |
missense |
unknown |
|
R8095:Smg1
|
UTSW |
7 |
117,772,285 (GRCm39) |
missense |
unknown |
|
R8198:Smg1
|
UTSW |
7 |
117,744,829 (GRCm39) |
missense |
probably benign |
0.03 |
R8399:Smg1
|
UTSW |
7 |
117,789,794 (GRCm39) |
missense |
unknown |
|
R8445:Smg1
|
UTSW |
7 |
117,736,200 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8519:Smg1
|
UTSW |
7 |
117,770,982 (GRCm39) |
utr 3 prime |
probably benign |
|
R8817:Smg1
|
UTSW |
7 |
117,758,887 (GRCm39) |
missense |
unknown |
|
R8832:Smg1
|
UTSW |
7 |
117,739,006 (GRCm39) |
missense |
probably benign |
0.33 |
R8855:Smg1
|
UTSW |
7 |
117,806,122 (GRCm39) |
missense |
unknown |
|
R8866:Smg1
|
UTSW |
7 |
117,806,122 (GRCm39) |
missense |
unknown |
|
R8946:Smg1
|
UTSW |
7 |
117,751,900 (GRCm39) |
missense |
probably null |
|
R8954:Smg1
|
UTSW |
7 |
117,806,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8967:Smg1
|
UTSW |
7 |
117,765,739 (GRCm39) |
missense |
unknown |
|
R9072:Smg1
|
UTSW |
7 |
117,783,032 (GRCm39) |
missense |
unknown |
|
R9090:Smg1
|
UTSW |
7 |
117,811,786 (GRCm39) |
missense |
unknown |
|
R9156:Smg1
|
UTSW |
7 |
117,753,884 (GRCm39) |
missense |
unknown |
|
R9198:Smg1
|
UTSW |
7 |
117,795,179 (GRCm39) |
missense |
unknown |
|
R9240:Smg1
|
UTSW |
7 |
117,739,031 (GRCm39) |
missense |
probably benign |
0.18 |
R9271:Smg1
|
UTSW |
7 |
117,811,786 (GRCm39) |
missense |
unknown |
|
R9289:Smg1
|
UTSW |
7 |
117,744,639 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9378:Smg1
|
UTSW |
7 |
117,777,998 (GRCm39) |
nonsense |
probably null |
|
R9396:Smg1
|
UTSW |
7 |
117,807,303 (GRCm39) |
missense |
unknown |
|
R9469:Smg1
|
UTSW |
7 |
117,739,774 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9539:Smg1
|
UTSW |
7 |
117,744,976 (GRCm39) |
missense |
probably benign |
0.03 |
R9549:Smg1
|
UTSW |
7 |
117,795,254 (GRCm39) |
missense |
unknown |
|
R9563:Smg1
|
UTSW |
7 |
117,812,208 (GRCm39) |
missense |
unknown |
|
R9564:Smg1
|
UTSW |
7 |
117,812,208 (GRCm39) |
missense |
unknown |
|
R9597:Smg1
|
UTSW |
7 |
117,812,270 (GRCm39) |
missense |
unknown |
|
R9643:Smg1
|
UTSW |
7 |
117,755,933 (GRCm39) |
missense |
unknown |
|
R9703:Smg1
|
UTSW |
7 |
117,739,744 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9730:Smg1
|
UTSW |
7 |
117,783,004 (GRCm39) |
missense |
unknown |
|
Z1088:Smg1
|
UTSW |
7 |
117,777,622 (GRCm39) |
missense |
possibly damaging |
0.96 |
Z1088:Smg1
|
UTSW |
7 |
117,767,884 (GRCm39) |
nonsense |
probably null |
|
Z1088:Smg1
|
UTSW |
7 |
117,753,858 (GRCm39) |
utr 3 prime |
probably benign |
|
Z1176:Smg1
|
UTSW |
7 |
117,806,130 (GRCm39) |
missense |
unknown |
|
Z1176:Smg1
|
UTSW |
7 |
117,806,110 (GRCm39) |
missense |
unknown |
|
Z1177:Smg1
|
UTSW |
7 |
117,812,256 (GRCm39) |
missense |
unknown |
|
Z1177:Smg1
|
UTSW |
7 |
117,767,831 (GRCm39) |
missense |
probably null |
|
|