Other mutations in this stock |
Total: 133 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,262,897 (GRCm39) |
I1410N |
possibly damaging |
Het |
9230106D20Rik |
T |
C |
10: 19,536,001 (GRCm39) |
|
noncoding transcript |
Het |
Acsf3 |
T |
A |
8: 123,508,218 (GRCm39) |
I238N |
probably damaging |
Het |
Ahctf1 |
T |
C |
1: 179,580,964 (GRCm39) |
N1746S |
probably benign |
Het |
Akap3 |
T |
C |
6: 126,842,601 (GRCm39) |
S407P |
probably damaging |
Het |
Ankfy1 |
T |
A |
11: 72,621,437 (GRCm39) |
M241K |
probably benign |
Het |
Ano7 |
C |
A |
1: 93,328,216 (GRCm39) |
T622K |
probably benign |
Het |
App |
T |
C |
16: 84,900,202 (GRCm39) |
T83A |
probably damaging |
Het |
Asb2 |
C |
A |
12: 103,291,317 (GRCm39) |
V489L |
probably benign |
Het |
Atrn |
T |
C |
2: 130,862,910 (GRCm39) |
V1330A |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,059,116 (GRCm39) |
N3267K |
possibly damaging |
Het |
Brca1 |
A |
G |
11: 101,383,001 (GRCm39) |
|
probably null |
Het |
Bspry |
G |
A |
4: 62,404,762 (GRCm39) |
R186Q |
probably damaging |
Het |
Ccdc168 |
A |
G |
1: 44,100,861 (GRCm39) |
I79T |
probably benign |
Het |
Cdkn2d |
C |
G |
9: 21,202,185 (GRCm39) |
V21L |
probably benign |
Het |
Celsr1 |
T |
A |
15: 85,790,230 (GRCm39) |
|
probably null |
Het |
Ckap4 |
A |
G |
10: 84,369,384 (GRCm39) |
V116A |
possibly damaging |
Het |
Crb3 |
A |
G |
17: 57,372,207 (GRCm39) |
T85A |
probably damaging |
Het |
Cyld |
T |
C |
8: 89,456,278 (GRCm39) |
S443P |
probably damaging |
Het |
Cyp27a1 |
T |
G |
1: 74,776,366 (GRCm39) |
V434G |
possibly damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,787,720 (GRCm39) |
T339A |
probably benign |
Het |
Dars1 |
A |
T |
1: 128,303,971 (GRCm39) |
L252* |
probably null |
Het |
Dcaf10 |
G |
A |
4: 45,372,769 (GRCm39) |
R394Q |
possibly damaging |
Het |
Ddx55 |
T |
C |
5: 124,704,539 (GRCm39) |
F382S |
probably damaging |
Het |
Dmtf1l |
T |
A |
X: 125,722,217 (GRCm39) |
K296M |
probably damaging |
Het |
Dnah7b |
G |
A |
1: 46,106,115 (GRCm39) |
R33Q |
unknown |
Het |
Dnm2 |
G |
T |
9: 21,385,883 (GRCm39) |
S302I |
probably damaging |
Het |
Dock4 |
T |
A |
12: 40,681,525 (GRCm39) |
F75I |
probably benign |
Het |
Dpp10 |
T |
C |
1: 123,326,356 (GRCm39) |
N365S |
probably benign |
Het |
Dpy19l3 |
G |
T |
7: 35,422,146 (GRCm39) |
Q236K |
probably benign |
Het |
Dsp |
T |
C |
13: 38,380,016 (GRCm39) |
S1655P |
probably damaging |
Het |
Ebpl |
A |
T |
14: 61,579,567 (GRCm39) |
I117N |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,613,818 (GRCm39) |
V386E |
probably damaging |
Het |
Eif2s2 |
T |
A |
2: 154,720,467 (GRCm39) |
|
probably null |
Het |
Elob |
A |
T |
17: 24,046,562 (GRCm39) |
|
probably null |
Het |
Enox2 |
T |
C |
X: 48,158,554 (GRCm39) |
I71V |
probably damaging |
Het |
Fez1 |
A |
T |
9: 36,772,141 (GRCm39) |
K149* |
probably null |
Het |
Fhip2a |
A |
G |
19: 57,359,661 (GRCm39) |
E67G |
probably damaging |
Het |
Fign |
A |
G |
2: 63,810,782 (GRCm39) |
Y163H |
probably damaging |
Het |
Flnc |
G |
A |
6: 29,455,812 (GRCm39) |
G2048S |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,736,022 (GRCm39) |
D539G |
probably benign |
Het |
Frmd4b |
T |
C |
6: 97,436,220 (GRCm39) |
|
probably benign |
Het |
Gan |
C |
T |
8: 117,920,970 (GRCm39) |
T402M |
probably damaging |
Het |
Ganc |
T |
A |
2: 120,267,104 (GRCm39) |
|
silent |
Het |
Ggt6 |
C |
A |
11: 72,327,425 (GRCm39) |
R103S |
probably benign |
Het |
Gli2 |
T |
C |
1: 118,768,052 (GRCm39) |
D725G |
probably damaging |
Het |
Gm15446 |
T |
A |
5: 110,090,818 (GRCm39) |
C357S |
probably damaging |
Het |
Gm44501 |
A |
G |
17: 40,889,810 (GRCm39) |
N108S |
probably benign |
Het |
Gm6309 |
A |
T |
5: 146,105,054 (GRCm39) |
D286E |
probably damaging |
Het |
Gm6358 |
G |
A |
16: 88,937,848 (GRCm39) |
G29E |
unknown |
Het |
Grik5 |
A |
G |
7: 24,757,713 (GRCm39) |
I422T |
probably damaging |
Het |
Grin2c |
A |
G |
11: 115,140,422 (GRCm39) |
I1232T |
possibly damaging |
Het |
Gsg1 |
C |
T |
6: 135,214,405 (GRCm39) |
R365H |
possibly damaging |
Het |
H2-M2 |
A |
G |
17: 37,794,135 (GRCm39) |
S30P |
possibly damaging |
Het |
Hcfc2 |
A |
G |
10: 82,547,914 (GRCm39) |
D302G |
probably damaging |
Het |
Hk2 |
T |
C |
6: 82,721,955 (GRCm39) |
D128G |
probably benign |
Het |
Hmcn2 |
C |
A |
2: 31,273,787 (GRCm39) |
Q1380K |
probably benign |
Het |
Hsp90b1 |
G |
T |
10: 86,529,819 (GRCm39) |
P617T |
probably damaging |
Het |
Htr1d |
A |
G |
4: 136,170,197 (GRCm39) |
E142G |
probably benign |
Het |
Hydin |
G |
A |
8: 111,282,264 (GRCm39) |
|
probably null |
Het |
Il1r1 |
T |
A |
1: 40,332,455 (GRCm39) |
N81K |
probably benign |
Het |
Inpp5b |
T |
C |
4: 124,677,760 (GRCm39) |
S407P |
probably damaging |
Het |
Itpkb |
T |
C |
1: 180,245,780 (GRCm39) |
Y766H |
probably damaging |
Het |
Lyrm2 |
T |
A |
4: 32,801,150 (GRCm39) |
I65N |
probably damaging |
Het |
Mink1 |
T |
A |
11: 70,500,086 (GRCm39) |
|
probably null |
Het |
Mkrn3 |
C |
T |
7: 62,069,452 (GRCm39) |
R113H |
probably damaging |
Het |
Msx3 |
G |
A |
7: 139,627,798 (GRCm39) |
A157V |
probably damaging |
Het |
Nrxn2 |
T |
G |
19: 6,548,484 (GRCm39) |
V59G |
possibly damaging |
Het |
Nt5c3b |
T |
C |
11: 100,331,732 (GRCm39) |
T12A |
probably benign |
Het |
Nwd2 |
G |
A |
5: 63,965,594 (GRCm39) |
R1726Q |
probably benign |
Het |
Nynrin |
A |
G |
14: 56,107,625 (GRCm39) |
T911A |
probably benign |
Het |
Or11i1 |
T |
A |
3: 106,728,996 (GRCm39) |
Y293F |
probably damaging |
Het |
Or4p18 |
T |
C |
2: 88,233,267 (GRCm39) |
T4A |
probably benign |
Het |
Or51aa5 |
A |
G |
7: 103,167,030 (GRCm39) |
I187T |
possibly damaging |
Het |
Or51af1 |
C |
T |
7: 103,141,267 (GRCm39) |
V273M |
possibly damaging |
Het |
Or52n20 |
C |
T |
7: 104,320,200 (GRCm39) |
T97I |
probably benign |
Het |
Or5p66 |
A |
G |
7: 107,885,520 (GRCm39) |
M271T |
probably benign |
Het |
Or6c212 |
A |
G |
10: 129,558,792 (GRCm39) |
I207T |
probably benign |
Het |
Patl1 |
G |
T |
19: 11,899,869 (GRCm39) |
M220I |
probably benign |
Het |
Pcnx2 |
A |
T |
8: 126,554,780 (GRCm39) |
|
probably null |
Het |
Pigr |
A |
T |
1: 130,774,291 (GRCm39) |
T424S |
probably damaging |
Het |
Pik3c2b |
T |
A |
1: 132,994,787 (GRCm39) |
D250E |
probably benign |
Het |
Ppa2 |
G |
A |
3: 133,076,186 (GRCm39) |
E272K |
probably benign |
Het |
Pramel7 |
G |
A |
2: 87,321,187 (GRCm39) |
Q283* |
probably null |
Het |
Prelid3b |
A |
G |
2: 174,307,683 (GRCm39) |
I81T |
probably benign |
Het |
Prpf38a |
T |
C |
4: 108,436,242 (GRCm39) |
I24V |
possibly damaging |
Het |
Ptger2 |
A |
G |
14: 45,239,295 (GRCm39) |
D311G |
possibly damaging |
Het |
Rab4b |
A |
T |
7: 26,872,191 (GRCm39) |
|
probably benign |
Het |
Rad17 |
A |
C |
13: 100,755,637 (GRCm39) |
D581E |
probably damaging |
Het |
Samd11 |
T |
C |
4: 156,333,230 (GRCm39) |
T333A |
probably benign |
Het |
Scaf4 |
C |
T |
16: 90,049,320 (GRCm39) |
D256N |
unknown |
Het |
Serinc2 |
A |
G |
4: 130,157,438 (GRCm39) |
F82L |
probably benign |
Het |
Serpina3g |
T |
A |
12: 104,205,372 (GRCm39) |
V37E |
probably damaging |
Het |
Serpinb9c |
T |
A |
13: 33,334,254 (GRCm39) |
M263L |
probably benign |
Het |
Shbg |
A |
G |
11: 69,508,326 (GRCm39) |
I67T |
possibly damaging |
Het |
Slc25a48 |
G |
A |
13: 56,596,887 (GRCm39) |
|
probably null |
Het |
Slc25a54 |
T |
C |
3: 109,005,923 (GRCm39) |
W144R |
probably damaging |
Het |
Slc34a1 |
A |
T |
13: 55,561,397 (GRCm39) |
T621S |
probably benign |
Het |
Slc6a18 |
A |
T |
13: 73,814,554 (GRCm39) |
C419S |
probably benign |
Het |
Smc5 |
A |
T |
19: 23,220,069 (GRCm39) |
D389E |
probably benign |
Het |
Smco3 |
T |
A |
6: 136,808,636 (GRCm39) |
E79D |
probably damaging |
Het |
Sox5 |
A |
G |
6: 143,906,561 (GRCm39) |
F298S |
probably damaging |
Het |
Sphkap |
A |
G |
1: 83,256,838 (GRCm39) |
S304P |
probably benign |
Het |
Tcea2 |
C |
T |
2: 181,328,514 (GRCm39) |
T211I |
probably damaging |
Het |
Tcf4 |
G |
T |
18: 69,697,226 (GRCm39) |
S34I |
possibly damaging |
Het |
Tlr4 |
C |
T |
4: 66,759,435 (GRCm39) |
R743C |
probably damaging |
Het |
Tmem183a |
T |
C |
1: 134,288,620 (GRCm39) |
E67G |
probably damaging |
Het |
Tpr |
C |
T |
1: 150,317,947 (GRCm39) |
R2152C |
possibly damaging |
Het |
Trbv15 |
T |
C |
6: 41,118,358 (GRCm39) |
I38T |
probably benign |
Het |
Treh |
G |
A |
9: 44,592,849 (GRCm39) |
A125T |
probably damaging |
Het |
Trio |
A |
T |
15: 27,752,875 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,782,293 (GRCm39) |
V981A |
probably damaging |
Het |
Uap1l1 |
A |
G |
2: 25,252,732 (GRCm39) |
L436P |
probably damaging |
Het |
Uba7 |
A |
T |
9: 107,854,115 (GRCm39) |
I182F |
possibly damaging |
Het |
Unc13c |
A |
T |
9: 73,600,620 (GRCm39) |
S1375T |
probably benign |
Het |
Usp48 |
C |
CT |
4: 137,360,680 (GRCm39) |
|
probably null |
Het |
Utp20 |
A |
C |
10: 88,652,780 (GRCm39) |
V378G |
possibly damaging |
Het |
Vmn1r69 |
A |
T |
7: 10,314,926 (GRCm39) |
|
probably benign |
Het |
Vmn1r86 |
A |
T |
7: 12,836,221 (GRCm39) |
H218Q |
probably damaging |
Het |
Vmn2r121 |
T |
A |
X: 123,038,335 (GRCm39) |
I562L |
probably benign |
Het |
Vmn2r45 |
A |
T |
7: 8,486,472 (GRCm39) |
I272N |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,078,424 (GRCm39) |
V320A |
probably benign |
Het |
Wfikkn1 |
A |
G |
17: 26,097,367 (GRCm39) |
V319A |
possibly damaging |
Het |
Whamm |
A |
G |
7: 81,221,122 (GRCm39) |
D18G |
probably benign |
Het |
Wrn |
T |
A |
8: 33,775,250 (GRCm39) |
I605F |
probably damaging |
Het |
Zdhhc18 |
A |
G |
4: 133,341,178 (GRCm39) |
F232L |
probably damaging |
Het |
Zfp41 |
T |
C |
15: 75,490,609 (GRCm39) |
I187T |
probably benign |
Het |
Zfp418 |
A |
G |
7: 7,185,561 (GRCm39) |
Y508C |
probably damaging |
Het |
Zfp560 |
T |
G |
9: 20,260,347 (GRCm39) |
I172L |
probably benign |
Het |
Zfp943 |
A |
T |
17: 22,211,391 (GRCm39) |
D159V |
probably benign |
Het |
Zfp955a |
T |
C |
17: 33,460,696 (GRCm39) |
I479V |
probably benign |
Het |
Zfpm1 |
T |
A |
8: 123,062,219 (GRCm39) |
V426D |
probably benign |
Het |
Zic1 |
C |
T |
9: 91,246,558 (GRCm39) |
M171I |
possibly damaging |
Het |
|
Other mutations in Arhgef28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00426:Arhgef28
|
APN |
13 |
98,124,785 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00945:Arhgef28
|
APN |
13 |
98,103,907 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01099:Arhgef28
|
APN |
13 |
98,090,480 (GRCm39) |
splice site |
probably benign |
|
IGL01328:Arhgef28
|
APN |
13 |
98,106,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01396:Arhgef28
|
APN |
13 |
98,090,401 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02067:Arhgef28
|
APN |
13 |
98,213,825 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02147:Arhgef28
|
APN |
13 |
98,097,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02285:Arhgef28
|
APN |
13 |
98,187,536 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02439:Arhgef28
|
APN |
13 |
98,067,647 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02499:Arhgef28
|
APN |
13 |
98,090,291 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02532:Arhgef28
|
APN |
13 |
98,166,391 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02634:Arhgef28
|
APN |
13 |
98,187,566 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02902:Arhgef28
|
APN |
13 |
98,083,383 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03067:Arhgef28
|
APN |
13 |
98,124,794 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03081:Arhgef28
|
APN |
13 |
98,165,881 (GRCm39) |
splice site |
probably benign |
|
IGL03106:Arhgef28
|
APN |
13 |
98,094,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03195:Arhgef28
|
APN |
13 |
98,088,071 (GRCm39) |
splice site |
probably null |
|
IGL03325:Arhgef28
|
APN |
13 |
98,036,324 (GRCm39) |
missense |
probably benign |
0.03 |
H8786:Arhgef28
|
UTSW |
13 |
98,083,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Arhgef28
|
UTSW |
13 |
98,082,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0027:Arhgef28
|
UTSW |
13 |
98,082,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0062:Arhgef28
|
UTSW |
13 |
98,093,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0062:Arhgef28
|
UTSW |
13 |
98,093,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0090:Arhgef28
|
UTSW |
13 |
98,211,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R0096:Arhgef28
|
UTSW |
13 |
98,067,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Arhgef28
|
UTSW |
13 |
98,067,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Arhgef28
|
UTSW |
13 |
98,094,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Arhgef28
|
UTSW |
13 |
98,106,863 (GRCm39) |
missense |
probably benign |
0.21 |
R0711:Arhgef28
|
UTSW |
13 |
98,067,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Arhgef28
|
UTSW |
13 |
98,075,987 (GRCm39) |
missense |
probably benign |
0.16 |
R0790:Arhgef28
|
UTSW |
13 |
98,117,914 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1240:Arhgef28
|
UTSW |
13 |
98,066,000 (GRCm39) |
missense |
probably benign |
0.00 |
R1365:Arhgef28
|
UTSW |
13 |
98,211,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Arhgef28
|
UTSW |
13 |
98,211,510 (GRCm39) |
missense |
probably benign |
0.01 |
R1490:Arhgef28
|
UTSW |
13 |
98,114,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Arhgef28
|
UTSW |
13 |
98,102,054 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1660:Arhgef28
|
UTSW |
13 |
98,117,884 (GRCm39) |
missense |
probably benign |
0.05 |
R1671:Arhgef28
|
UTSW |
13 |
98,067,542 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1747:Arhgef28
|
UTSW |
13 |
98,073,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Arhgef28
|
UTSW |
13 |
98,067,694 (GRCm39) |
missense |
probably benign |
0.03 |
R1864:Arhgef28
|
UTSW |
13 |
98,130,640 (GRCm39) |
missense |
probably benign |
0.00 |
R1887:Arhgef28
|
UTSW |
13 |
98,282,081 (GRCm39) |
missense |
probably damaging |
0.97 |
R1924:Arhgef28
|
UTSW |
13 |
98,073,324 (GRCm39) |
splice site |
probably benign |
|
R1987:Arhgef28
|
UTSW |
13 |
98,103,604 (GRCm39) |
missense |
probably benign |
|
R2215:Arhgef28
|
UTSW |
13 |
98,187,529 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2342:Arhgef28
|
UTSW |
13 |
98,130,537 (GRCm39) |
missense |
probably benign |
0.00 |
R2495:Arhgef28
|
UTSW |
13 |
98,165,881 (GRCm39) |
splice site |
probably benign |
|
R3897:Arhgef28
|
UTSW |
13 |
98,093,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R3922:Arhgef28
|
UTSW |
13 |
98,130,452 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4063:Arhgef28
|
UTSW |
13 |
98,130,575 (GRCm39) |
missense |
probably benign |
0.16 |
R4086:Arhgef28
|
UTSW |
13 |
98,103,712 (GRCm39) |
missense |
probably damaging |
0.98 |
R4543:Arhgef28
|
UTSW |
13 |
98,211,508 (GRCm39) |
missense |
probably benign |
0.00 |
R4730:Arhgef28
|
UTSW |
13 |
98,114,650 (GRCm39) |
missense |
probably benign |
0.00 |
R4953:Arhgef28
|
UTSW |
13 |
98,066,062 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5069:Arhgef28
|
UTSW |
13 |
98,211,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R5558:Arhgef28
|
UTSW |
13 |
98,097,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Arhgef28
|
UTSW |
13 |
98,065,999 (GRCm39) |
missense |
probably benign |
0.01 |
R5594:Arhgef28
|
UTSW |
13 |
98,076,000 (GRCm39) |
missense |
probably benign |
0.00 |
R5937:Arhgef28
|
UTSW |
13 |
98,076,051 (GRCm39) |
missense |
probably benign |
0.00 |
R5987:Arhgef28
|
UTSW |
13 |
98,073,368 (GRCm39) |
nonsense |
probably null |
|
R6015:Arhgef28
|
UTSW |
13 |
98,211,530 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6193:Arhgef28
|
UTSW |
13 |
98,121,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Arhgef28
|
UTSW |
13 |
98,065,917 (GRCm39) |
critical splice donor site |
probably null |
|
R6306:Arhgef28
|
UTSW |
13 |
98,121,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Arhgef28
|
UTSW |
13 |
98,130,527 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6562:Arhgef28
|
UTSW |
13 |
98,124,647 (GRCm39) |
critical splice donor site |
probably null |
|
R6646:Arhgef28
|
UTSW |
13 |
98,076,002 (GRCm39) |
missense |
probably benign |
0.09 |
R6655:Arhgef28
|
UTSW |
13 |
98,036,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R6707:Arhgef28
|
UTSW |
13 |
98,211,624 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6707:Arhgef28
|
UTSW |
13 |
98,073,224 (GRCm39) |
missense |
probably damaging |
0.96 |
R6751:Arhgef28
|
UTSW |
13 |
98,211,755 (GRCm39) |
missense |
probably damaging |
0.97 |
R6940:Arhgef28
|
UTSW |
13 |
98,102,038 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7018:Arhgef28
|
UTSW |
13 |
98,101,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:Arhgef28
|
UTSW |
13 |
98,124,769 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7120:Arhgef28
|
UTSW |
13 |
98,081,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R7266:Arhgef28
|
UTSW |
13 |
98,101,960 (GRCm39) |
missense |
probably benign |
|
R7353:Arhgef28
|
UTSW |
13 |
98,211,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Arhgef28
|
UTSW |
13 |
98,133,370 (GRCm39) |
missense |
probably benign |
0.34 |
R7491:Arhgef28
|
UTSW |
13 |
98,081,194 (GRCm39) |
missense |
probably benign |
0.03 |
R7500:Arhgef28
|
UTSW |
13 |
98,115,003 (GRCm39) |
missense |
probably benign |
0.00 |
R7653:Arhgef28
|
UTSW |
13 |
98,105,821 (GRCm39) |
missense |
probably benign |
0.04 |
R7813:Arhgef28
|
UTSW |
13 |
98,082,189 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7989:Arhgef28
|
UTSW |
13 |
98,036,243 (GRCm39) |
missense |
probably benign |
|
R8064:Arhgef28
|
UTSW |
13 |
98,115,002 (GRCm39) |
missense |
probably benign |
0.13 |
R8221:Arhgef28
|
UTSW |
13 |
98,282,064 (GRCm39) |
missense |
probably benign |
0.00 |
R8293:Arhgef28
|
UTSW |
13 |
98,079,029 (GRCm39) |
missense |
probably benign |
0.00 |
R8328:Arhgef28
|
UTSW |
13 |
98,187,517 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8348:Arhgef28
|
UTSW |
13 |
98,190,375 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8432:Arhgef28
|
UTSW |
13 |
98,088,091 (GRCm39) |
missense |
probably benign |
0.29 |
R8843:Arhgef28
|
UTSW |
13 |
98,130,557 (GRCm39) |
missense |
probably benign |
|
R8859:Arhgef28
|
UTSW |
13 |
98,082,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Arhgef28
|
UTSW |
13 |
98,066,141 (GRCm39) |
missense |
probably benign |
0.03 |
R8987:Arhgef28
|
UTSW |
13 |
98,190,472 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9253:Arhgef28
|
UTSW |
13 |
98,124,779 (GRCm39) |
missense |
probably benign |
0.09 |
R9351:Arhgef28
|
UTSW |
13 |
98,130,576 (GRCm39) |
missense |
probably benign |
0.11 |
R9381:Arhgef28
|
UTSW |
13 |
98,036,269 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9395:Arhgef28
|
UTSW |
13 |
98,103,692 (GRCm39) |
frame shift |
probably null |
|
R9466:Arhgef28
|
UTSW |
13 |
98,124,825 (GRCm39) |
missense |
|
|
R9529:Arhgef28
|
UTSW |
13 |
98,213,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Arhgef28
|
UTSW |
13 |
98,078,983 (GRCm39) |
missense |
probably benign |
0.00 |
R9662:Arhgef28
|
UTSW |
13 |
98,065,969 (GRCm39) |
missense |
probably benign |
0.20 |
R9744:Arhgef28
|
UTSW |
13 |
98,094,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9776:Arhgef28
|
UTSW |
13 |
98,133,415 (GRCm39) |
missense |
probably benign |
0.19 |
Z1088:Arhgef28
|
UTSW |
13 |
98,082,199 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arhgef28
|
UTSW |
13 |
98,036,264 (GRCm39) |
missense |
probably benign |
0.43 |
|