Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
T |
5: 109,884,144 (GRCm39) |
H571Q |
probably damaging |
Het |
Abcf2 |
T |
A |
5: 24,773,774 (GRCm39) |
M372L |
probably benign |
Het |
Acaca |
A |
C |
11: 84,206,795 (GRCm39) |
T1552P |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,229,219 (GRCm39) |
D1682G |
probably damaging |
Het |
Acvr1b |
T |
C |
15: 101,091,906 (GRCm39) |
V62A |
probably benign |
Het |
Aimp1 |
C |
T |
3: 132,379,825 (GRCm39) |
V97M |
probably benign |
Het |
Aldh1l1 |
C |
T |
6: 90,554,813 (GRCm39) |
T557I |
possibly damaging |
Het |
Alpk1 |
T |
C |
3: 127,471,447 (GRCm39) |
T1012A |
probably damaging |
Het |
Amot |
G |
A |
X: 144,233,585 (GRCm39) |
|
probably benign |
Het |
Arap1 |
T |
A |
7: 101,037,829 (GRCm39) |
H477Q |
probably benign |
Het |
Arhgap18 |
T |
A |
10: 26,736,732 (GRCm39) |
|
probably benign |
Het |
Arhgef10l |
C |
T |
4: 140,242,684 (GRCm39) |
V862M |
probably damaging |
Het |
Arl4d |
A |
G |
11: 101,557,554 (GRCm39) |
I27V |
probably benign |
Het |
Asb18 |
G |
A |
1: 89,942,277 (GRCm39) |
P8L |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,977,616 (GRCm39) |
H2682R |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,385,079 (GRCm39) |
V241E |
probably benign |
Het |
Atf7ip |
G |
T |
6: 136,586,217 (GRCm39) |
|
probably benign |
Het |
AY358078 |
T |
G |
14: 52,042,051 (GRCm39) |
M142R |
unknown |
Het |
C3 |
T |
A |
17: 57,526,592 (GRCm39) |
K796N |
possibly damaging |
Het |
Ceacam16 |
T |
C |
7: 19,590,041 (GRCm39) |
T301A |
probably damaging |
Het |
Ceacam5 |
T |
G |
7: 17,481,320 (GRCm39) |
Y356D |
probably benign |
Het |
Cep192 |
C |
T |
18: 67,984,838 (GRCm39) |
A1616V |
possibly damaging |
Het |
Cfap91 |
T |
A |
16: 38,141,781 (GRCm39) |
N384Y |
possibly damaging |
Het |
Cherp |
A |
T |
8: 73,216,994 (GRCm39) |
H645Q |
probably benign |
Het |
CK137956 |
T |
C |
4: 127,845,242 (GRCm39) |
D167G |
probably benign |
Het |
Clcn1 |
T |
A |
6: 42,275,860 (GRCm39) |
|
probably null |
Het |
Cntn1 |
C |
T |
15: 92,189,552 (GRCm39) |
T625I |
possibly damaging |
Het |
Cpn2 |
T |
A |
16: 30,078,142 (GRCm39) |
N520Y |
probably damaging |
Het |
Crocc |
G |
A |
4: 140,746,620 (GRCm39) |
R1762W |
probably damaging |
Het |
Cts3 |
C |
A |
13: 61,715,967 (GRCm39) |
V100F |
probably benign |
Het |
Ddx56 |
A |
T |
11: 6,216,934 (GRCm39) |
V87D |
probably damaging |
Het |
Dnah9 |
C |
T |
11: 66,010,420 (GRCm39) |
|
probably null |
Het |
Dock1 |
T |
A |
7: 134,700,456 (GRCm39) |
|
probably null |
Het |
Dst |
T |
A |
1: 34,191,552 (GRCm39) |
Y291* |
probably null |
Het |
Eif4g3 |
T |
C |
4: 137,898,442 (GRCm39) |
I1071T |
probably damaging |
Het |
Fblim1 |
T |
C |
4: 141,322,549 (GRCm39) |
Q78R |
probably damaging |
Het |
Fcamr |
C |
T |
1: 130,739,284 (GRCm39) |
P195S |
probably benign |
Het |
Fcho1 |
G |
A |
8: 72,161,666 (GRCm39) |
Q835* |
probably null |
Het |
Frem3 |
A |
G |
8: 81,339,741 (GRCm39) |
N678S |
probably benign |
Het |
Frk |
G |
A |
10: 34,483,878 (GRCm39) |
R413H |
probably benign |
Het |
Gm10619 |
C |
A |
7: 73,459,758 (GRCm39) |
|
noncoding transcript |
Het |
Gm12185 |
G |
A |
11: 48,806,583 (GRCm39) |
R203* |
probably null |
Het |
Gm12886 |
A |
G |
4: 121,280,174 (GRCm39) |
V34A |
probably benign |
Het |
Gna12 |
A |
T |
5: 140,746,707 (GRCm39) |
I246N |
probably damaging |
Het |
Gpm6a |
T |
C |
8: 55,507,867 (GRCm39) |
M201T |
probably benign |
Het |
Gpsm2 |
T |
G |
3: 108,608,225 (GRCm39) |
D220A |
probably benign |
Het |
Grip2 |
C |
G |
6: 91,760,623 (GRCm39) |
V325L |
probably benign |
Het |
Grk5 |
C |
A |
19: 61,065,200 (GRCm39) |
A288D |
probably damaging |
Het |
Herpud2 |
G |
A |
9: 25,021,953 (GRCm39) |
A231V |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,624,834 (GRCm39) |
S1024G |
probably benign |
Het |
Hp1bp3 |
A |
G |
4: 137,957,820 (GRCm39) |
D295G |
probably damaging |
Het |
Igsf21 |
T |
C |
4: 139,761,703 (GRCm39) |
H325R |
probably damaging |
Het |
Ing2 |
T |
A |
8: 48,122,364 (GRCm39) |
L61F |
probably damaging |
Het |
Jak3 |
T |
C |
8: 72,138,590 (GRCm39) |
|
probably benign |
Het |
Kcnn3 |
T |
A |
3: 89,516,712 (GRCm39) |
C374S |
probably benign |
Het |
Klk1b22 |
A |
G |
7: 43,765,775 (GRCm39) |
|
probably benign |
Het |
Larp1 |
T |
C |
11: 57,940,764 (GRCm39) |
M630T |
possibly damaging |
Het |
Lhx5 |
T |
A |
5: 120,572,725 (GRCm39) |
C115S |
probably damaging |
Het |
Lmcd1 |
C |
A |
6: 112,305,712 (GRCm39) |
T271K |
probably benign |
Het |
Lpar1 |
G |
A |
4: 58,486,798 (GRCm39) |
R158* |
probably null |
Het |
Lyst |
T |
A |
13: 13,821,668 (GRCm39) |
C1347* |
probably null |
Het |
Map3k8 |
G |
A |
18: 4,332,389 (GRCm39) |
Q441* |
probably null |
Het |
Mboat1 |
T |
C |
13: 30,403,633 (GRCm39) |
V144A |
probably damaging |
Het |
Mcur1 |
C |
T |
13: 43,713,491 (GRCm39) |
G38S |
unknown |
Het |
Mefv |
A |
G |
16: 3,526,528 (GRCm39) |
S699P |
possibly damaging |
Het |
Mfsd4a |
C |
A |
1: 131,987,077 (GRCm39) |
A62S |
probably damaging |
Het |
Mmp27 |
A |
G |
9: 7,571,459 (GRCm39) |
M1V |
probably null |
Het |
Myo1c |
C |
T |
11: 75,548,415 (GRCm39) |
T58I |
probably damaging |
Het |
Myom3 |
A |
T |
4: 135,538,066 (GRCm39) |
D1316V |
probably benign |
Het |
Naa25 |
T |
A |
5: 121,555,478 (GRCm39) |
C235S |
possibly damaging |
Het |
Naa25 |
C |
A |
5: 121,558,656 (GRCm39) |
R333S |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,539,233 (GRCm39) |
T2056I |
probably benign |
Het |
Nol4 |
A |
G |
18: 22,902,878 (GRCm39) |
Y378H |
probably damaging |
Het |
Npat |
G |
A |
9: 53,463,589 (GRCm39) |
R124Q |
probably damaging |
Het |
Npr3 |
T |
A |
15: 11,848,665 (GRCm39) |
E434V |
probably benign |
Het |
Nptx2 |
A |
G |
5: 144,485,130 (GRCm39) |
T208A |
probably benign |
Het |
Obscn |
C |
T |
11: 58,968,606 (GRCm39) |
V2798M |
probably damaging |
Het |
Odad4 |
C |
A |
11: 100,460,679 (GRCm39) |
|
probably null |
Het |
Or10j7 |
A |
T |
1: 173,011,976 (GRCm39) |
H8Q |
probably benign |
Het |
Or52r1 |
A |
G |
7: 102,537,250 (GRCm39) |
Y37H |
probably benign |
Het |
Or5b122 |
C |
T |
19: 13,562,779 (GRCm39) |
T37I |
probably benign |
Het |
Padi1 |
G |
A |
4: 140,541,967 (GRCm39) |
P652S |
probably damaging |
Het |
Pcdh1 |
G |
T |
18: 38,331,938 (GRCm39) |
P355Q |
probably damaging |
Het |
Pck2 |
G |
A |
14: 55,781,422 (GRCm39) |
R189H |
possibly damaging |
Het |
Pcsk5 |
T |
A |
19: 17,432,114 (GRCm39) |
K1500N |
possibly damaging |
Het |
Phc3 |
A |
T |
3: 31,002,865 (GRCm39) |
S218T |
probably damaging |
Het |
Piezo2 |
T |
A |
18: 63,239,355 (GRCm39) |
M510L |
possibly damaging |
Het |
Polr1g |
T |
C |
7: 19,091,904 (GRCm39) |
T68A |
possibly damaging |
Het |
Ppp1r3a |
A |
T |
6: 14,754,717 (GRCm39) |
Y177N |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,836,361 (GRCm39) |
D195E |
probably damaging |
Het |
Ptprr |
T |
C |
10: 116,088,827 (GRCm39) |
V463A |
probably damaging |
Het |
Pwwp2b |
G |
A |
7: 138,836,281 (GRCm39) |
R574Q |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,756,314 (GRCm39) |
T14S |
possibly damaging |
Het |
Rbm11 |
A |
T |
16: 75,397,685 (GRCm39) |
K205M |
probably damaging |
Het |
Rfx1 |
T |
A |
8: 84,793,050 (GRCm39) |
|
probably benign |
Het |
Rnasel |
C |
A |
1: 153,630,169 (GRCm39) |
H228Q |
probably damaging |
Het |
Sap130 |
T |
A |
18: 31,831,640 (GRCm39) |
I710K |
probably benign |
Het |
Slc27a4 |
C |
A |
2: 29,695,733 (GRCm39) |
D89E |
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,863,779 (GRCm39) |
V309A |
probably benign |
Het |
Syt7 |
T |
G |
19: 10,421,354 (GRCm39) |
Y420D |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,515,859 (GRCm39) |
|
probably null |
Het |
Tbc1d10b |
A |
G |
7: 126,802,930 (GRCm39) |
S333P |
possibly damaging |
Het |
Tenm2 |
G |
A |
11: 35,914,209 (GRCm39) |
P2442S |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 49,127,579 (GRCm39) |
C33Y |
probably damaging |
Het |
Timmdc1 |
A |
G |
16: 38,319,419 (GRCm39) |
L245P |
possibly damaging |
Het |
Tlr5 |
T |
C |
1: 182,800,012 (GRCm39) |
F5L |
probably benign |
Het |
Ttll4 |
T |
A |
1: 74,726,999 (GRCm39) |
F784L |
possibly damaging |
Het |
Tulp4 |
A |
G |
17: 6,189,387 (GRCm39) |
T70A |
possibly damaging |
Het |
Txndc17 |
T |
A |
11: 72,099,571 (GRCm39) |
N81K |
probably benign |
Het |
Ubr3 |
C |
T |
2: 69,830,895 (GRCm39) |
|
probably benign |
Het |
Uri1 |
A |
C |
7: 37,681,116 (GRCm39) |
V96G |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,150,246 (GRCm39) |
I482N |
probably damaging |
Het |
Vmn1r229 |
A |
G |
17: 21,034,974 (GRCm39) |
N73S |
possibly damaging |
Het |
Vwa7 |
G |
T |
17: 35,243,388 (GRCm39) |
G689* |
probably null |
Het |
Zfp114 |
T |
A |
7: 23,877,164 (GRCm39) |
|
probably null |
Het |
Zfp618 |
A |
G |
4: 63,051,474 (GRCm39) |
S659G |
probably damaging |
Het |
Zfp872 |
A |
G |
9: 22,111,349 (GRCm39) |
K275R |
probably damaging |
Het |
Zzef1 |
C |
T |
11: 72,777,535 (GRCm39) |
P1789S |
probably damaging |
Het |
|
Other mutations in Med13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00960:Med13
|
APN |
11 |
86,181,866 (GRCm39) |
splice site |
probably benign |
|
IGL01391:Med13
|
APN |
11 |
86,219,323 (GRCm39) |
missense |
probably benign |
|
IGL01767:Med13
|
APN |
11 |
86,210,609 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01830:Med13
|
APN |
11 |
86,179,754 (GRCm39) |
splice site |
probably benign |
|
IGL01859:Med13
|
APN |
11 |
86,174,577 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01924:Med13
|
APN |
11 |
86,199,522 (GRCm39) |
splice site |
probably benign |
|
IGL02080:Med13
|
APN |
11 |
86,174,638 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02138:Med13
|
APN |
11 |
86,177,591 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02259:Med13
|
APN |
11 |
86,248,327 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02339:Med13
|
APN |
11 |
86,179,765 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02399:Med13
|
APN |
11 |
86,174,771 (GRCm39) |
splice site |
probably benign |
|
IGL02646:Med13
|
APN |
11 |
86,174,212 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03227:Med13
|
APN |
11 |
86,218,618 (GRCm39) |
splice site |
probably benign |
|
R0197_Med13_854
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R0360_Med13_060
|
UTSW |
11 |
86,219,987 (GRCm39) |
splice site |
probably benign |
|
R2359_Med13_079
|
UTSW |
11 |
86,181,861 (GRCm39) |
splice site |
probably benign |
|
R3735_Med13_085
|
UTSW |
11 |
86,170,484 (GRCm39) |
missense |
probably benign |
0.00 |
R4974_Med13_508
|
UTSW |
11 |
86,189,673 (GRCm39) |
missense |
probably damaging |
0.98 |
R0116:Med13
|
UTSW |
11 |
86,210,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R0189:Med13
|
UTSW |
11 |
86,210,702 (GRCm39) |
missense |
probably benign |
|
R0197:Med13
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R0206:Med13
|
UTSW |
11 |
86,191,682 (GRCm39) |
splice site |
probably benign |
|
R0208:Med13
|
UTSW |
11 |
86,191,682 (GRCm39) |
splice site |
probably benign |
|
R0310:Med13
|
UTSW |
11 |
86,236,829 (GRCm39) |
missense |
probably benign |
0.11 |
R0360:Med13
|
UTSW |
11 |
86,219,987 (GRCm39) |
splice site |
probably benign |
|
R0413:Med13
|
UTSW |
11 |
86,190,033 (GRCm39) |
splice site |
probably benign |
|
R0482:Med13
|
UTSW |
11 |
86,175,977 (GRCm39) |
missense |
probably benign |
0.41 |
R0497:Med13
|
UTSW |
11 |
86,167,809 (GRCm39) |
splice site |
probably benign |
|
R0589:Med13
|
UTSW |
11 |
86,174,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Med13
|
UTSW |
11 |
86,236,788 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0646:Med13
|
UTSW |
11 |
86,221,915 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0701:Med13
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R0709:Med13
|
UTSW |
11 |
86,210,422 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0711:Med13
|
UTSW |
11 |
86,192,179 (GRCm39) |
splice site |
probably benign |
|
R0734:Med13
|
UTSW |
11 |
86,192,063 (GRCm39) |
missense |
probably benign |
|
R0883:Med13
|
UTSW |
11 |
86,197,864 (GRCm39) |
missense |
probably benign |
0.13 |
R1926:Med13
|
UTSW |
11 |
86,179,899 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1959:Med13
|
UTSW |
11 |
86,189,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R2286:Med13
|
UTSW |
11 |
86,210,515 (GRCm39) |
missense |
probably benign |
0.05 |
R2359:Med13
|
UTSW |
11 |
86,181,861 (GRCm39) |
splice site |
probably benign |
|
R2444:Med13
|
UTSW |
11 |
86,222,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Med13
|
UTSW |
11 |
86,189,403 (GRCm39) |
missense |
probably benign |
0.00 |
R2879:Med13
|
UTSW |
11 |
86,189,988 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3439:Med13
|
UTSW |
11 |
86,176,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R3735:Med13
|
UTSW |
11 |
86,170,484 (GRCm39) |
missense |
probably benign |
0.00 |
R4333:Med13
|
UTSW |
11 |
86,179,009 (GRCm39) |
missense |
probably benign |
|
R4558:Med13
|
UTSW |
11 |
86,189,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R4598:Med13
|
UTSW |
11 |
86,169,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R4773:Med13
|
UTSW |
11 |
86,167,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R4801:Med13
|
UTSW |
11 |
86,169,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Med13
|
UTSW |
11 |
86,169,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Med13
|
UTSW |
11 |
86,189,403 (GRCm39) |
missense |
probably benign |
0.00 |
R4940:Med13
|
UTSW |
11 |
86,178,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Med13
|
UTSW |
11 |
86,189,673 (GRCm39) |
missense |
probably damaging |
0.98 |
R5056:Med13
|
UTSW |
11 |
86,219,391 (GRCm39) |
missense |
probably benign |
0.00 |
R5133:Med13
|
UTSW |
11 |
86,210,675 (GRCm39) |
missense |
probably benign |
0.32 |
R5206:Med13
|
UTSW |
11 |
86,210,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Med13
|
UTSW |
11 |
86,192,294 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5534:Med13
|
UTSW |
11 |
86,210,191 (GRCm39) |
missense |
probably benign |
0.09 |
R5556:Med13
|
UTSW |
11 |
86,218,664 (GRCm39) |
missense |
probably benign |
0.25 |
R5633:Med13
|
UTSW |
11 |
86,169,757 (GRCm39) |
splice site |
probably benign |
|
R5769:Med13
|
UTSW |
11 |
86,236,829 (GRCm39) |
missense |
probably benign |
0.11 |
R6236:Med13
|
UTSW |
11 |
86,219,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R6479:Med13
|
UTSW |
11 |
86,248,353 (GRCm39) |
start gained |
probably benign |
|
R6487:Med13
|
UTSW |
11 |
86,221,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Med13
|
UTSW |
11 |
86,192,293 (GRCm39) |
missense |
probably damaging |
0.98 |
R6528:Med13
|
UTSW |
11 |
86,189,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Med13
|
UTSW |
11 |
86,169,622 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6913:Med13
|
UTSW |
11 |
86,210,702 (GRCm39) |
missense |
probably benign |
|
R7221:Med13
|
UTSW |
11 |
86,178,921 (GRCm39) |
missense |
probably benign |
0.00 |
R7254:Med13
|
UTSW |
11 |
86,210,661 (GRCm39) |
missense |
probably benign |
|
R7267:Med13
|
UTSW |
11 |
86,199,652 (GRCm39) |
missense |
probably benign |
0.01 |
R7309:Med13
|
UTSW |
11 |
86,181,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7404:Med13
|
UTSW |
11 |
86,177,272 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7586:Med13
|
UTSW |
11 |
86,161,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R7704:Med13
|
UTSW |
11 |
86,236,744 (GRCm39) |
nonsense |
probably null |
|
R7922:Med13
|
UTSW |
11 |
86,161,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R7943:Med13
|
UTSW |
11 |
86,169,352 (GRCm39) |
missense |
probably damaging |
0.97 |
R8062:Med13
|
UTSW |
11 |
86,210,264 (GRCm39) |
missense |
probably benign |
|
R8075:Med13
|
UTSW |
11 |
86,163,296 (GRCm39) |
missense |
probably damaging |
0.98 |
R8207:Med13
|
UTSW |
11 |
86,194,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R8671:Med13
|
UTSW |
11 |
86,161,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R9056:Med13
|
UTSW |
11 |
86,189,660 (GRCm39) |
nonsense |
probably null |
|
R9084:Med13
|
UTSW |
11 |
86,191,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Med13
|
UTSW |
11 |
86,192,297 (GRCm39) |
missense |
probably benign |
0.27 |
R9329:Med13
|
UTSW |
11 |
86,189,283 (GRCm39) |
missense |
probably benign |
0.10 |
R9380:Med13
|
UTSW |
11 |
86,177,598 (GRCm39) |
missense |
probably benign |
0.42 |
R9515:Med13
|
UTSW |
11 |
86,199,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9516:Med13
|
UTSW |
11 |
86,179,801 (GRCm39) |
missense |
probably benign |
0.01 |
R9690:Med13
|
UTSW |
11 |
86,169,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R9751:Med13
|
UTSW |
11 |
86,189,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9752:Med13
|
UTSW |
11 |
86,174,147 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9764:Med13
|
UTSW |
11 |
86,177,345 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Med13
|
UTSW |
11 |
86,246,249 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Med13
|
UTSW |
11 |
86,236,688 (GRCm39) |
missense |
probably benign |
0.45 |
Z1176:Med13
|
UTSW |
11 |
86,219,370 (GRCm39) |
missense |
possibly damaging |
0.91 |
|