Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Acot6 |
A |
G |
12: 84,155,789 (GRCm39) |
K246E |
probably benign |
Het |
Actl11 |
T |
A |
9: 107,808,615 (GRCm39) |
H979Q |
probably damaging |
Het |
Adal |
T |
A |
2: 120,986,030 (GRCm39) |
|
probably benign |
Het |
Add2 |
G |
A |
6: 86,087,840 (GRCm39) |
V596I |
probably benign |
Het |
Adrb3 |
A |
C |
8: 27,717,798 (GRCm39) |
M217R |
probably damaging |
Het |
Ank1 |
T |
C |
8: 23,631,134 (GRCm39) |
|
probably benign |
Het |
Ank2 |
A |
T |
3: 126,757,094 (GRCm39) |
N1054K |
possibly damaging |
Het |
Ankib1 |
T |
C |
5: 3,763,217 (GRCm39) |
Y504C |
probably damaging |
Het |
Ankrd29 |
T |
C |
18: 12,395,242 (GRCm39) |
K217R |
probably damaging |
Het |
Ankrd45 |
T |
C |
1: 160,982,876 (GRCm39) |
V129A |
probably damaging |
Het |
Aox4 |
A |
T |
1: 58,275,835 (GRCm39) |
D389V |
probably benign |
Het |
Aph1a |
G |
T |
3: 95,802,843 (GRCm39) |
G148W |
probably damaging |
Het |
Arhgef26 |
G |
A |
3: 62,247,806 (GRCm39) |
D297N |
possibly damaging |
Het |
Atxn7l3b |
C |
A |
10: 112,764,649 (GRCm39) |
|
probably benign |
Het |
Auh |
A |
G |
13: 52,995,065 (GRCm39) |
S167P |
probably damaging |
Het |
Bach1 |
A |
T |
16: 87,515,888 (GRCm39) |
K143I |
possibly damaging |
Het |
Bbx |
T |
A |
16: 50,045,101 (GRCm39) |
T487S |
probably damaging |
Het |
Bche |
T |
G |
3: 73,609,177 (GRCm39) |
D83A |
probably benign |
Het |
Bri3bp |
G |
T |
5: 125,518,760 (GRCm39) |
|
probably benign |
Het |
Cd3d |
A |
T |
9: 44,896,296 (GRCm39) |
E28D |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,965,366 (GRCm39) |
T1028A |
probably damaging |
Het |
Ceacam23 |
A |
G |
7: 17,639,143 (GRCm39) |
|
probably null |
Het |
Celsr2 |
T |
C |
3: 108,319,945 (GRCm39) |
I956V |
possibly damaging |
Het |
Cep95 |
A |
T |
11: 106,707,480 (GRCm39) |
|
probably null |
Het |
Cic |
G |
T |
7: 24,986,535 (GRCm39) |
G1289C |
probably damaging |
Het |
Cndp1 |
A |
G |
18: 84,650,025 (GRCm39) |
Y223H |
probably damaging |
Het |
Cops8 |
A |
G |
1: 90,538,724 (GRCm39) |
D51G |
probably damaging |
Het |
Csgalnact1 |
T |
C |
8: 68,913,623 (GRCm39) |
E194G |
probably benign |
Het |
Ctsm |
A |
G |
13: 61,686,776 (GRCm39) |
Y39H |
probably damaging |
Het |
Dhrs2 |
T |
C |
14: 55,474,722 (GRCm39) |
V119A |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,935,093 (GRCm39) |
M1336K |
probably benign |
Het |
Dsp |
G |
A |
13: 38,381,678 (GRCm39) |
D2808N |
possibly damaging |
Het |
Ehmt1 |
G |
T |
2: 24,767,509 (GRCm39) |
P135T |
probably damaging |
Het |
Epas1 |
A |
G |
17: 87,116,882 (GRCm39) |
N184S |
probably damaging |
Het |
Erich3 |
C |
T |
3: 154,454,025 (GRCm39) |
T597I |
possibly damaging |
Het |
F10 |
T |
C |
8: 13,105,698 (GRCm39) |
V421A |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fcgrt |
C |
T |
7: 44,751,372 (GRCm39) |
G192D |
probably benign |
Het |
Fras1 |
A |
G |
5: 96,798,541 (GRCm39) |
E1184G |
possibly damaging |
Het |
Garre1 |
A |
C |
7: 33,945,225 (GRCm39) |
Y552D |
probably damaging |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Gvin-ps5 |
A |
T |
7: 105,928,664 (GRCm39) |
|
noncoding transcript |
Het |
Hadh |
A |
T |
3: 131,029,197 (GRCm39) |
L274* |
probably null |
Het |
Hus1 |
T |
C |
11: 8,956,027 (GRCm39) |
S169G |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,290,554 (GRCm39) |
I3338F |
possibly damaging |
Het |
Ighv11-1 |
T |
G |
12: 113,945,768 (GRCm39) |
E28D |
probably benign |
Het |
Kctd9 |
C |
T |
14: 67,966,805 (GRCm39) |
T106I |
probably damaging |
Het |
Krit1 |
A |
T |
5: 3,872,238 (GRCm39) |
N421I |
probably damaging |
Het |
Lamb1 |
A |
G |
12: 31,376,677 (GRCm39) |
D1619G |
probably damaging |
Het |
Lpar6 |
G |
A |
14: 73,476,147 (GRCm39) |
C36Y |
probably damaging |
Het |
Lrrc37a |
G |
C |
11: 103,347,565 (GRCm39) |
F3043L |
unknown |
Het |
Lrrc46 |
A |
T |
11: 96,931,765 (GRCm39) |
V19D |
probably damaging |
Het |
Mapkap1 |
G |
T |
2: 34,471,303 (GRCm39) |
S197I |
probably damaging |
Het |
Mrps35 |
A |
C |
6: 146,961,645 (GRCm39) |
K173N |
possibly damaging |
Het |
Mtf2 |
A |
G |
5: 108,220,894 (GRCm39) |
|
probably benign |
Het |
Ncf1 |
A |
C |
5: 134,252,267 (GRCm39) |
D261E |
probably damaging |
Het |
Notch1 |
C |
T |
2: 26,371,193 (GRCm39) |
E298K |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 90,928,274 (GRCm39) |
|
probably benign |
Het |
Or13a18 |
C |
A |
7: 140,190,304 (GRCm39) |
A75E |
possibly damaging |
Het |
Or4x13 |
T |
A |
2: 90,231,107 (GRCm39) |
M34K |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,289,308 (GRCm39) |
F13S |
probably damaging |
Het |
Or5k3 |
T |
C |
16: 58,969,981 (GRCm39) |
L256P |
probably damaging |
Het |
Or5v1 |
G |
T |
17: 37,810,017 (GRCm39) |
L158F |
probably benign |
Het |
Otud4 |
G |
A |
8: 80,382,318 (GRCm39) |
V176I |
probably damaging |
Het |
Pakap |
T |
A |
4: 57,856,552 (GRCm39) |
V668E |
probably benign |
Het |
Papolg |
T |
C |
11: 23,823,919 (GRCm39) |
|
probably null |
Het |
Pgk2 |
A |
G |
17: 40,518,402 (GRCm39) |
V342A |
probably damaging |
Het |
Phf2 |
G |
A |
13: 48,961,320 (GRCm39) |
A790V |
unknown |
Het |
Prkdc |
T |
C |
16: 15,491,861 (GRCm39) |
I602T |
possibly damaging |
Het |
Prl3d3 |
T |
C |
13: 27,343,072 (GRCm39) |
I86T |
possibly damaging |
Het |
Prss8 |
G |
T |
7: 127,525,635 (GRCm39) |
Q295K |
probably benign |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pwwp3a |
T |
C |
10: 80,068,702 (GRCm39) |
L282P |
probably benign |
Het |
Qrfpr |
A |
G |
3: 36,276,285 (GRCm39) |
V35A |
probably damaging |
Het |
Rpf1 |
A |
G |
3: 146,212,293 (GRCm39) |
L349S |
probably damaging |
Het |
Rpl41 |
G |
T |
10: 128,384,652 (GRCm39) |
|
probably null |
Het |
Rprd2 |
G |
C |
3: 95,672,632 (GRCm39) |
R924G |
probably benign |
Het |
Serpini1 |
T |
A |
3: 75,521,795 (GRCm39) |
N95K |
probably benign |
Het |
Sfxn1 |
A |
T |
13: 54,242,933 (GRCm39) |
T64S |
probably benign |
Het |
Siae |
T |
G |
9: 37,557,816 (GRCm39) |
I541S |
possibly damaging |
Het |
Slc25a4 |
T |
A |
8: 46,660,509 (GRCm39) |
K296N |
probably benign |
Het |
Slc37a1 |
A |
G |
17: 31,541,120 (GRCm39) |
N204S |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,413,800 (GRCm39) |
N976S |
probably benign |
Het |
Smarcal1 |
T |
C |
1: 72,672,019 (GRCm39) |
S847P |
possibly damaging |
Het |
Sptlc1 |
A |
G |
13: 53,505,692 (GRCm39) |
I242T |
probably damaging |
Het |
St8sia2 |
T |
C |
7: 73,616,709 (GRCm39) |
I89V |
possibly damaging |
Het |
Supt20 |
A |
T |
3: 54,602,555 (GRCm39) |
|
probably benign |
Het |
Tep1 |
T |
C |
14: 51,076,457 (GRCm39) |
D1659G |
probably benign |
Het |
Tex10 |
C |
A |
4: 48,458,525 (GRCm39) |
|
probably benign |
Het |
Thbs3 |
CAGAAG |
CAG |
3: 89,130,409 (GRCm39) |
|
probably benign |
Het |
Tmbim6 |
C |
A |
15: 99,299,950 (GRCm39) |
S22* |
probably null |
Het |
Tmc2 |
A |
T |
2: 130,043,961 (GRCm39) |
K65M |
possibly damaging |
Het |
Tmod1 |
A |
G |
4: 46,090,872 (GRCm39) |
S142G |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt6 |
T |
C |
2: 132,650,191 (GRCm39) |
R349G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,537,586 (GRCm39) |
T26454S |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,605,122 (GRCm39) |
V16555I |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,384,042 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,850,790 (GRCm39) |
|
probably benign |
Het |
Vmn1r17 |
A |
C |
6: 57,337,460 (GRCm39) |
F253V |
possibly damaging |
Het |
Vmn1r201 |
G |
T |
13: 22,659,622 (GRCm39) |
A279S |
possibly damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,575,739 (GRCm39) |
R203S |
probably benign |
Het |
Vwa5a |
A |
G |
9: 38,633,926 (GRCm39) |
E43G |
probably benign |
Het |
Wdr86 |
C |
T |
5: 24,917,843 (GRCm39) |
|
probably null |
Het |
Wdsub1 |
A |
T |
2: 59,700,758 (GRCm39) |
|
probably benign |
Het |
Zcchc7 |
T |
C |
4: 44,931,039 (GRCm39) |
L76P |
probably damaging |
Het |
Zfp108 |
G |
T |
7: 23,960,163 (GRCm39) |
K251N |
probably benign |
Het |
Zfp263 |
T |
C |
16: 3,566,992 (GRCm39) |
C148R |
probably damaging |
Het |
Zfp687 |
A |
C |
3: 94,917,697 (GRCm39) |
F692V |
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 |
R4906:Smg1
|
UTSW |
7 |
117,751,631 (GRCm39) |
utr 3 prime |
probably benign |
|
R4978:Smg1
|
UTSW |
7 |
117,753,470 (GRCm39) |
utr 3 prime |
probably benign |
|
R4989:Smg1
|
UTSW |
7 |
117,807,274 (GRCm39) |
missense |
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 |
|
|