Other mutations in this stock |
Total: 139 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700031F05Rik |
G |
T |
X: 101,904,515 (GRCm39) |
N132K |
possibly damaging |
Het |
Aatf |
T |
C |
11: 84,362,023 (GRCm39) |
D313G |
possibly damaging |
Het |
Abcb11 |
T |
G |
2: 69,115,615 (GRCm39) |
D583A |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,676,914 (GRCm39) |
Y1252* |
probably null |
Het |
Aim2 |
T |
C |
1: 173,283,090 (GRCm39) |
|
silent |
Het |
Angpt1 |
T |
A |
15: 42,539,580 (GRCm39) |
Y93F |
probably benign |
Het |
Ankrd27 |
C |
T |
7: 35,337,659 (GRCm39) |
P991L |
probably benign |
Het |
Ap1s3 |
C |
T |
1: 79,591,920 (GRCm39) |
|
probably null |
Het |
Apbb1 |
A |
C |
7: 105,214,745 (GRCm39) |
S500A |
probably benign |
Het |
Arc |
G |
A |
15: 74,543,374 (GRCm39) |
A283V |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
C1galt1c1 |
A |
T |
X: 37,720,349 (GRCm39) |
S216T |
probably benign |
Het |
C1qtnf4 |
T |
A |
2: 90,719,996 (GRCm39) |
S90T |
probably damaging |
Het |
Cachd1 |
A |
T |
4: 100,810,327 (GRCm39) |
K310* |
probably null |
Het |
Calhm1 |
A |
G |
19: 47,132,240 (GRCm39) |
L125P |
probably damaging |
Het |
Carmil1 |
G |
A |
13: 24,321,162 (GRCm39) |
L278F |
probably damaging |
Het |
Ccar1 |
A |
T |
10: 62,583,196 (GRCm39) |
Y972* |
probably null |
Het |
Cd163 |
C |
T |
6: 124,297,580 (GRCm39) |
P909S |
probably damaging |
Het |
Cd44 |
T |
A |
2: 102,668,274 (GRCm39) |
H268L |
possibly damaging |
Het |
Cdkl2 |
A |
T |
5: 92,165,072 (GRCm39) |
L517Q |
probably damaging |
Het |
Cep68 |
G |
T |
11: 20,189,349 (GRCm39) |
N554K |
probably benign |
Het |
Ces1d |
A |
G |
8: 93,893,038 (GRCm39) |
W515R |
probably damaging |
Het |
Clca4b |
A |
C |
3: 144,634,286 (GRCm39) |
H102Q |
probably benign |
Het |
Cldn15 |
T |
A |
5: 137,003,337 (GRCm39) |
I142N |
probably damaging |
Het |
Cmklr1 |
T |
A |
5: 113,752,701 (GRCm39) |
D100V |
probably damaging |
Het |
Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly damaging |
Het |
D430041D05Rik |
G |
A |
2: 104,088,788 (GRCm39) |
P63S |
probably damaging |
Het |
Ddx39a |
A |
T |
8: 84,448,902 (GRCm39) |
H259L |
probably benign |
Het |
Dhx16 |
C |
G |
17: 36,196,527 (GRCm39) |
A565G |
probably benign |
Het |
Dimt1 |
A |
T |
13: 107,084,163 (GRCm39) |
D50V |
probably benign |
Het |
Dock9 |
A |
T |
14: 121,823,658 (GRCm39) |
L1428H |
probably damaging |
Het |
Dpp4 |
G |
T |
2: 62,164,949 (GRCm39) |
T700K |
probably damaging |
Het |
E030030I06Rik |
T |
A |
10: 22,024,744 (GRCm39) |
R56S |
unknown |
Het |
Eea1 |
A |
G |
10: 95,864,255 (GRCm39) |
T925A |
probably benign |
Het |
Ext1 |
A |
G |
15: 52,953,383 (GRCm39) |
S494P |
possibly damaging |
Het |
Fam171a1 |
G |
A |
2: 3,221,328 (GRCm39) |
E140K |
probably damaging |
Het |
Fgfr3 |
C |
T |
5: 33,892,330 (GRCm39) |
|
probably benign |
Het |
Gabra6 |
A |
G |
11: 42,198,199 (GRCm39) |
I407T |
probably damaging |
Het |
Gm16223 |
C |
A |
5: 42,371,954 (GRCm39) |
L115M |
unknown |
Het |
Gm4781 |
G |
T |
10: 100,232,862 (GRCm39) |
|
noncoding transcript |
Het |
Gm9772 |
T |
A |
17: 22,226,013 (GRCm39) |
I70F |
possibly damaging |
Het |
Gpr107 |
T |
A |
2: 31,100,513 (GRCm39) |
F497Y |
probably damaging |
Het |
Gtf2ird2 |
G |
A |
5: 134,245,034 (GRCm39) |
A431T |
probably damaging |
Het |
H2-K2 |
T |
A |
17: 34,194,989 (GRCm39) |
|
noncoding transcript |
Het |
H2-M11 |
T |
A |
17: 36,858,883 (GRCm39) |
V141D |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,551,262 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
A |
T |
2: 31,289,031 (GRCm39) |
Q2280L |
possibly damaging |
Het |
Hmg20b |
T |
A |
10: 81,184,416 (GRCm39) |
Q129L |
probably damaging |
Het |
Igfbp7 |
T |
A |
5: 77,499,143 (GRCm39) |
Q285L |
possibly damaging |
Het |
Igkv13-85 |
T |
A |
6: 68,907,720 (GRCm39) |
|
probably benign |
Het |
Inpp5e |
A |
T |
2: 26,297,926 (GRCm39) |
L225H |
probably benign |
Het |
Inpp5f |
T |
A |
7: 128,260,833 (GRCm39) |
V91E |
possibly damaging |
Het |
Khdc3 |
A |
G |
9: 73,009,868 (GRCm39) |
E26G |
possibly damaging |
Het |
Klra5 |
T |
A |
6: 129,876,339 (GRCm39) |
D156V |
probably damaging |
Het |
Kmo |
C |
A |
1: 175,487,340 (GRCm39) |
Y430* |
probably null |
Het |
Lbx2 |
A |
G |
6: 83,065,027 (GRCm39) |
D188G |
probably damaging |
Het |
Lcorl |
A |
T |
5: 45,890,931 (GRCm39) |
L474* |
probably null |
Het |
Lnx1 |
C |
T |
5: 74,771,457 (GRCm39) |
V350I |
probably benign |
Het |
Lrrc45 |
T |
A |
11: 120,609,947 (GRCm39) |
S464T |
probably benign |
Het |
Ltc4s |
T |
A |
11: 50,128,052 (GRCm39) |
T61S |
probably benign |
Het |
Luc7l3 |
A |
C |
11: 94,200,467 (GRCm39) |
N50K |
probably damaging |
Het |
Ly75 |
G |
A |
2: 60,138,622 (GRCm39) |
T1415M |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,367,420 (GRCm39) |
E2447G |
probably benign |
Het |
Map3k21 |
A |
G |
8: 126,668,850 (GRCm39) |
D812G |
probably benign |
Het |
Mbtd1 |
C |
T |
11: 93,815,437 (GRCm39) |
H342Y |
probably damaging |
Het |
Mest |
C |
T |
6: 30,745,109 (GRCm39) |
R226* |
probably null |
Het |
Mindy1 |
A |
T |
3: 95,190,054 (GRCm39) |
|
probably benign |
Het |
Mmp13 |
A |
T |
9: 7,274,233 (GRCm39) |
D180V |
probably damaging |
Het |
Mn1 |
A |
G |
5: 111,567,949 (GRCm39) |
T640A |
probably benign |
Het |
Msi2 |
T |
C |
11: 88,608,864 (GRCm39) |
H18R |
possibly damaging |
Het |
Myo18a |
T |
A |
11: 77,708,776 (GRCm39) |
V61E |
probably damaging |
Het |
Myo19 |
T |
G |
11: 84,785,468 (GRCm39) |
I237S |
probably damaging |
Het |
Ncaph2 |
T |
A |
15: 89,254,635 (GRCm39) |
L416Q |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 70,987,952 (GRCm39) |
|
probably null |
Het |
Or1n1b |
A |
G |
2: 36,780,663 (GRCm39) |
F66L |
probably benign |
Het |
Or2d4 |
A |
T |
7: 106,543,547 (GRCm39) |
N220K |
probably benign |
Het |
Or51a25 |
A |
G |
7: 102,373,299 (GRCm39) |
S133P |
probably damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,441 (GRCm39) |
I163V |
probably benign |
Het |
Or8s10 |
G |
T |
15: 98,335,457 (GRCm39) |
V36F |
probably benign |
Het |
Padi2 |
T |
C |
4: 140,671,757 (GRCm39) |
F495S |
probably damaging |
Het |
Pan3 |
G |
T |
5: 147,464,013 (GRCm39) |
D535Y |
probably damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,069 (GRCm39) |
R102* |
probably null |
Het |
Patl1 |
T |
A |
19: 11,891,798 (GRCm39) |
D34E |
probably damaging |
Het |
Pcdha6 |
A |
T |
18: 37,102,189 (GRCm39) |
T461S |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,190,047 (GRCm39) |
S2830G |
probably benign |
Het |
Pdgfa |
G |
A |
5: 138,964,939 (GRCm39) |
T181I |
probably benign |
Het |
Pds5a |
C |
A |
5: 65,813,661 (GRCm39) |
D275Y |
probably damaging |
Het |
Plod2 |
T |
A |
9: 92,487,503 (GRCm39) |
Y607* |
probably null |
Het |
Pomt2 |
G |
T |
12: 87,164,857 (GRCm39) |
T517K |
possibly damaging |
Het |
Pramel23 |
T |
C |
4: 143,425,914 (GRCm39) |
M10V |
probably benign |
Het |
Prdm1 |
T |
C |
10: 44,315,686 (GRCm39) |
T817A |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,859,525 (GRCm39) |
D1255G |
possibly damaging |
Het |
Prex2 |
T |
A |
1: 11,232,509 (GRCm39) |
C859S |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,229,549 (GRCm39) |
M1077K |
possibly damaging |
Het |
Ralgds |
T |
C |
2: 28,435,532 (GRCm39) |
|
probably null |
Het |
Rasa3 |
T |
C |
8: 13,638,865 (GRCm39) |
E314G |
probably null |
Het |
Rasa4 |
T |
A |
5: 136,130,217 (GRCm39) |
D324E |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,765 (GRCm39) |
D283E |
probably benign |
Het |
Rnf139 |
A |
T |
15: 58,771,836 (GRCm39) |
L620F |
probably benign |
Het |
Rptor |
T |
A |
11: 119,781,989 (GRCm39) |
N1105K |
probably benign |
Het |
Scaf11 |
A |
T |
15: 96,317,981 (GRCm39) |
|
probably null |
Het |
Sectm1b |
A |
T |
11: 120,946,760 (GRCm39) |
V45E |
probably damaging |
Het |
Selenon |
A |
G |
4: 134,272,968 (GRCm39) |
W157R |
probably damaging |
Het |
Sema3b |
C |
A |
9: 107,476,250 (GRCm39) |
R657L |
possibly damaging |
Het |
Setd1b |
C |
T |
5: 123,286,175 (GRCm39) |
A407V |
unknown |
Het |
Sh3tc1 |
C |
T |
5: 35,863,662 (GRCm39) |
A842T |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,965,566 (GRCm39) |
E1268G |
probably damaging |
Het |
Shmt1 |
G |
A |
11: 60,692,291 (GRCm39) |
S155F |
probably damaging |
Het |
Sim2 |
A |
G |
16: 93,924,385 (GRCm39) |
E510G |
possibly damaging |
Het |
Slc25a46 |
A |
T |
18: 31,733,245 (GRCm39) |
I168N |
probably damaging |
Het |
Slc26a4 |
T |
G |
12: 31,590,525 (GRCm39) |
D376A |
possibly damaging |
Het |
Slfn14 |
G |
T |
11: 83,167,484 (GRCm39) |
A677E |
probably benign |
Het |
Slk |
G |
T |
19: 47,608,713 (GRCm39) |
Q555H |
possibly damaging |
Het |
Synj1 |
A |
T |
16: 90,770,877 (GRCm39) |
D517E |
probably damaging |
Het |
Syvn1 |
G |
A |
19: 6,101,504 (GRCm39) |
R440Q |
probably benign |
Het |
Tafa5 |
T |
G |
15: 87,604,783 (GRCm39) |
S115A |
probably damaging |
Het |
Tas2r118 |
A |
T |
6: 23,969,467 (GRCm39) |
I198N |
probably damaging |
Het |
Tdh |
A |
G |
14: 63,731,205 (GRCm39) |
L323P |
possibly damaging |
Het |
Tet2 |
A |
T |
3: 133,193,843 (GRCm39) |
M197K |
probably benign |
Het |
Timeless |
A |
G |
10: 128,075,825 (GRCm39) |
Y19C |
possibly damaging |
Het |
Tnn |
T |
C |
1: 159,973,612 (GRCm39) |
M252V |
probably benign |
Het |
Trdn |
G |
T |
10: 33,071,977 (GRCm39) |
E215* |
probably null |
Het |
Trmt1l |
G |
T |
1: 151,333,632 (GRCm39) |
V712F |
possibly damaging |
Het |
Tti1 |
T |
C |
2: 157,848,940 (GRCm39) |
|
probably benign |
Het |
Ulk4 |
T |
C |
9: 120,970,918 (GRCm39) |
H1018R |
probably benign |
Het |
Vim |
A |
T |
2: 13,587,306 (GRCm39) |
H461L |
probably benign |
Het |
Vmn2r118 |
T |
A |
17: 55,917,665 (GRCm39) |
E282D |
probably damaging |
Het |
Vmn2r31 |
T |
A |
7: 7,387,367 (GRCm39) |
I735F |
probably damaging |
Het |
Vmn2r88 |
A |
G |
14: 51,656,250 (GRCm39) |
M829V |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,410,407 (GRCm39) |
M665K |
possibly damaging |
Het |
Wbp2 |
T |
A |
11: 115,973,207 (GRCm39) |
M67L |
probably benign |
Het |
Wdr81 |
T |
A |
11: 75,336,814 (GRCm39) |
E1525V |
probably damaging |
Het |
Xbp1 |
A |
G |
11: 5,472,006 (GRCm39) |
D44G |
probably damaging |
Het |
Zfhx4 |
T |
G |
3: 5,464,341 (GRCm39) |
F1500V |
probably damaging |
Het |
Zfp286 |
A |
C |
11: 62,674,559 (GRCm39) |
Y95* |
probably null |
Het |
Zfp872 |
A |
G |
9: 22,111,057 (GRCm39) |
T178A |
possibly damaging |
Het |
Zkscan5 |
A |
G |
5: 145,155,640 (GRCm39) |
H364R |
possibly damaging |
Het |
Zp3r |
A |
T |
1: 130,505,697 (GRCm39) |
Y422N |
probably damaging |
Het |
Zscan10 |
C |
T |
17: 23,829,314 (GRCm39) |
R542C |
probably benign |
Het |
|
Other mutations in Grm7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01729:Grm7
|
APN |
6 |
111,223,145 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02058:Grm7
|
APN |
6 |
111,335,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Grm7
|
APN |
6 |
111,335,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Grm7
|
APN |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03074:Grm7
|
APN |
6 |
111,472,604 (GRCm39) |
splice site |
probably null |
|
IGL03185:Grm7
|
APN |
6 |
110,623,183 (GRCm39) |
missense |
possibly damaging |
0.84 |
Appropriated
|
UTSW |
6 |
111,472,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
Consumed
|
UTSW |
6 |
111,335,836 (GRCm39) |
missense |
probably damaging |
1.00 |
Devoured
|
UTSW |
6 |
111,335,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Ravaged
|
UTSW |
6 |
111,335,874 (GRCm39) |
missense |
probably damaging |
1.00 |
shaky
|
UTSW |
6 |
111,472,752 (GRCm39) |
nonsense |
probably null |
|
PIT4651001:Grm7
|
UTSW |
6 |
110,623,050 (GRCm39) |
missense |
probably benign |
|
R0539:Grm7
|
UTSW |
6 |
111,336,055 (GRCm39) |
splice site |
probably benign |
|
R0622:Grm7
|
UTSW |
6 |
111,335,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Grm7
|
UTSW |
6 |
111,335,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Grm7
|
UTSW |
6 |
111,335,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Grm7
|
UTSW |
6 |
111,472,752 (GRCm39) |
nonsense |
probably null |
|
R1823:Grm7
|
UTSW |
6 |
111,184,730 (GRCm39) |
missense |
probably benign |
0.17 |
R1864:Grm7
|
UTSW |
6 |
111,057,384 (GRCm39) |
missense |
probably benign |
0.03 |
R1894:Grm7
|
UTSW |
6 |
111,335,568 (GRCm39) |
missense |
probably benign |
|
R1987:Grm7
|
UTSW |
6 |
110,891,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Grm7
|
UTSW |
6 |
111,184,769 (GRCm39) |
missense |
probably benign |
0.13 |
R2138:Grm7
|
UTSW |
6 |
110,623,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Grm7
|
UTSW |
6 |
111,335,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2289:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2296:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2339:Grm7
|
UTSW |
6 |
111,472,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2847:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2879:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2921:Grm7
|
UTSW |
6 |
111,472,866 (GRCm39) |
splice site |
probably null |
|
R2923:Grm7
|
UTSW |
6 |
111,472,866 (GRCm39) |
splice site |
probably null |
|
R3014:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3015:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3703:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4009:Grm7
|
UTSW |
6 |
111,472,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Grm7
|
UTSW |
6 |
110,891,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4132:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Grm7
|
UTSW |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R4329:Grm7
|
UTSW |
6 |
110,891,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4357:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4359:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Grm7
|
UTSW |
6 |
111,223,335 (GRCm39) |
missense |
probably benign |
0.05 |
R4379:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4380:Grm7
|
UTSW |
6 |
110,623,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Grm7
|
UTSW |
6 |
111,335,265 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4518:Grm7
|
UTSW |
6 |
110,891,507 (GRCm39) |
splice site |
probably null |
|
R4714:Grm7
|
UTSW |
6 |
111,057,383 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4775:Grm7
|
UTSW |
6 |
110,891,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Grm7
|
UTSW |
6 |
111,335,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Grm7
|
UTSW |
6 |
111,057,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R5062:Grm7
|
UTSW |
6 |
110,623,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Grm7
|
UTSW |
6 |
111,335,182 (GRCm39) |
missense |
probably benign |
0.01 |
R5431:Grm7
|
UTSW |
6 |
111,335,387 (GRCm39) |
missense |
probably benign |
|
R6026:Grm7
|
UTSW |
6 |
111,478,500 (GRCm39) |
nonsense |
probably null |
|
R6174:Grm7
|
UTSW |
6 |
111,223,258 (GRCm39) |
missense |
probably benign |
|
R6305:Grm7
|
UTSW |
6 |
111,335,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Grm7
|
UTSW |
6 |
111,335,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6440:Grm7
|
UTSW |
6 |
111,230,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:Grm7
|
UTSW |
6 |
111,184,713 (GRCm39) |
missense |
probably benign |
0.00 |
R6531:Grm7
|
UTSW |
6 |
111,335,386 (GRCm39) |
missense |
probably benign |
0.29 |
R6888:Grm7
|
UTSW |
6 |
111,335,314 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6949:Grm7
|
UTSW |
6 |
111,472,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Grm7
|
UTSW |
6 |
110,623,265 (GRCm39) |
missense |
probably benign |
0.03 |
R6989:Grm7
|
UTSW |
6 |
111,184,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Grm7
|
UTSW |
6 |
111,335,113 (GRCm39) |
missense |
probably benign |
0.04 |
R7203:Grm7
|
UTSW |
6 |
111,335,530 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7208:Grm7
|
UTSW |
6 |
111,335,530 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7217:Grm7
|
UTSW |
6 |
111,335,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Grm7
|
UTSW |
6 |
110,623,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R7297:Grm7
|
UTSW |
6 |
110,622,974 (GRCm39) |
missense |
probably benign |
0.16 |
R7470:Grm7
|
UTSW |
6 |
111,478,476 (GRCm39) |
missense |
|
|
R7567:Grm7
|
UTSW |
6 |
111,335,722 (GRCm39) |
missense |
probably damaging |
0.96 |
R7806:Grm7
|
UTSW |
6 |
111,223,314 (GRCm39) |
nonsense |
probably null |
|
R8018:Grm7
|
UTSW |
6 |
111,184,737 (GRCm39) |
missense |
probably benign |
0.01 |
R8076:Grm7
|
UTSW |
6 |
111,543,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R8409:Grm7
|
UTSW |
6 |
110,891,297 (GRCm39) |
missense |
probably benign |
0.02 |
R8420:Grm7
|
UTSW |
6 |
111,057,315 (GRCm39) |
missense |
probably benign |
|
R8523:Grm7
|
UTSW |
6 |
111,223,280 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8816:Grm7
|
UTSW |
6 |
111,230,966 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8958:Grm7
|
UTSW |
6 |
111,472,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R9135:Grm7
|
UTSW |
6 |
111,472,729 (GRCm39) |
missense |
probably benign |
0.39 |
R9207:Grm7
|
UTSW |
6 |
111,335,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Grm7
|
UTSW |
6 |
110,622,869 (GRCm39) |
missense |
probably benign |
0.01 |
R9438:Grm7
|
UTSW |
6 |
111,231,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9448:Grm7
|
UTSW |
6 |
111,335,193 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Grm7
|
UTSW |
6 |
111,335,451 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Grm7
|
UTSW |
6 |
111,335,110 (GRCm39) |
missense |
probably benign |
0.01 |
|