Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
C |
17: 9,219,989 (GRCm39) |
L357S |
probably benign |
Het |
1700129C05Rik |
C |
T |
14: 59,380,256 (GRCm39) |
R14H |
probably damaging |
Het |
Aatf |
A |
G |
11: 84,402,965 (GRCm39) |
|
probably null |
Het |
Abca13 |
T |
A |
11: 9,247,669 (GRCm39) |
M2472K |
possibly damaging |
Het |
Abcd3 |
C |
A |
3: 121,562,816 (GRCm39) |
Q540H |
probably null |
Het |
Adam17 |
C |
T |
12: 21,399,939 (GRCm39) |
V156I |
probably benign |
Het |
Adam26a |
A |
G |
8: 44,021,490 (GRCm39) |
S667P |
probably benign |
Het |
Adcy10 |
A |
G |
1: 165,391,818 (GRCm39) |
K1333E |
probably benign |
Het |
Apob |
G |
A |
12: 8,060,521 (GRCm39) |
R2968Q |
probably benign |
Het |
Arap3 |
G |
A |
18: 38,106,278 (GRCm39) |
P1522S |
possibly damaging |
Het |
Catsper1 |
A |
T |
19: 5,386,573 (GRCm39) |
S269C |
probably damaging |
Het |
Cd209d |
A |
T |
8: 3,928,258 (GRCm39) |
S42R |
probably benign |
Het |
Cntln |
T |
A |
4: 85,010,932 (GRCm39) |
V1049E |
probably damaging |
Het |
Cracr2b |
T |
C |
7: 141,043,659 (GRCm39) |
F87L |
probably damaging |
Het |
Crb3 |
T |
C |
17: 57,372,133 (GRCm39) |
L60P |
probably damaging |
Het |
Crispld1 |
T |
C |
1: 17,819,815 (GRCm39) |
V271A |
probably benign |
Het |
Cyp2c66 |
G |
T |
19: 39,165,135 (GRCm39) |
R372L |
probably benign |
Het |
Deup1 |
G |
A |
9: 15,493,829 (GRCm39) |
R438W |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,150,541 (GRCm39) |
E741K |
possibly damaging |
Het |
Epha4 |
T |
C |
1: 77,360,188 (GRCm39) |
E703G |
probably damaging |
Het |
Evc2 |
G |
A |
5: 37,550,443 (GRCm39) |
R819H |
probably damaging |
Het |
Fam217a |
A |
C |
13: 35,094,944 (GRCm39) |
C272G |
possibly damaging |
Het |
Fndc7 |
T |
C |
3: 108,784,015 (GRCm39) |
|
probably null |
Het |
Foxs1 |
C |
T |
2: 152,774,607 (GRCm39) |
G149S |
probably benign |
Het |
Galnt13 |
T |
C |
2: 54,744,628 (GRCm39) |
V109A |
probably benign |
Het |
Hmgxb4 |
G |
A |
8: 75,725,556 (GRCm39) |
M7I |
probably benign |
Het |
Klk1b1 |
T |
A |
7: 43,620,165 (GRCm39) |
C209* |
probably null |
Het |
Klra10 |
A |
G |
6: 130,249,613 (GRCm39) |
|
probably null |
Het |
Lpgat1 |
T |
A |
1: 191,481,754 (GRCm39) |
L114Q |
probably damaging |
Het |
Mecom |
T |
A |
3: 30,017,261 (GRCm39) |
Q468L |
probably damaging |
Het |
Med15 |
T |
C |
16: 17,515,476 (GRCm39) |
T70A |
probably damaging |
Het |
Msh6 |
T |
A |
17: 88,294,048 (GRCm39) |
Y934* |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,537,432 (GRCm39) |
T95A |
probably benign |
Het |
Mylk3 |
C |
A |
8: 86,079,535 (GRCm39) |
R444S |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,965,369 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
T |
C |
1: 60,332,032 (GRCm39) |
V2242A |
probably damaging |
Het |
Nhp2 |
A |
G |
11: 51,513,334 (GRCm39) |
T85A |
possibly damaging |
Het |
Nlk |
A |
G |
11: 78,463,257 (GRCm39) |
S413P |
possibly damaging |
Het |
Nmbr |
A |
G |
10: 14,636,192 (GRCm39) |
I54V |
possibly damaging |
Het |
Nmur2 |
A |
T |
11: 55,931,346 (GRCm39) |
C122S |
probably damaging |
Het |
Nudt13 |
G |
T |
14: 20,361,583 (GRCm39) |
V220L |
probably damaging |
Het |
Or5m13 |
G |
A |
2: 85,748,295 (GRCm39) |
V9M |
probably benign |
Het |
Pclo |
G |
A |
5: 14,719,447 (GRCm39) |
G1195R |
unknown |
Het |
Pcsk7 |
A |
G |
9: 45,824,309 (GRCm39) |
H276R |
possibly damaging |
Het |
Pdss2 |
T |
C |
10: 43,269,924 (GRCm39) |
S256P |
probably damaging |
Het |
Pgf |
G |
T |
12: 85,218,198 (GRCm39) |
H116N |
probably benign |
Het |
Pglyrp2 |
T |
C |
17: 32,637,302 (GRCm39) |
D242G |
probably benign |
Het |
Plk2 |
G |
A |
13: 110,534,242 (GRCm39) |
R274K |
probably benign |
Het |
Ppp6r3 |
G |
T |
19: 3,514,693 (GRCm39) |
P141T |
probably benign |
Het |
Prss54 |
T |
C |
8: 96,292,295 (GRCm39) |
T95A |
probably benign |
Het |
Rab3il1 |
A |
G |
19: 10,005,653 (GRCm39) |
D149G |
probably damaging |
Het |
Rasgef1c |
T |
C |
11: 49,852,057 (GRCm39) |
|
probably null |
Het |
Rhpn1 |
T |
C |
15: 75,583,437 (GRCm39) |
M334T |
probably damaging |
Het |
Rigi |
T |
C |
4: 40,213,766 (GRCm39) |
T586A |
probably benign |
Het |
Robo2 |
C |
T |
16: 73,764,739 (GRCm39) |
V630M |
probably damaging |
Het |
Rptor |
C |
T |
11: 119,783,467 (GRCm39) |
R1154W |
probably damaging |
Het |
Scnn1g |
A |
G |
7: 121,339,778 (GRCm39) |
I192M |
possibly damaging |
Het |
Sit1 |
G |
A |
4: 43,482,815 (GRCm39) |
Q115* |
probably null |
Het |
Slc13a2 |
T |
C |
11: 78,295,350 (GRCm39) |
N141S |
probably damaging |
Het |
Slc19a2 |
C |
A |
1: 164,084,344 (GRCm39) |
T78K |
probably damaging |
Het |
Snx14 |
A |
G |
9: 88,287,291 (GRCm39) |
|
probably null |
Het |
Stil |
T |
A |
4: 114,896,346 (GRCm39) |
C944S |
probably benign |
Het |
Tex56 |
A |
G |
13: 35,108,596 (GRCm39) |
N26S |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,419,893 (GRCm39) |
N675S |
probably damaging |
Het |
Trim30c |
A |
G |
7: 104,032,516 (GRCm39) |
I270T |
possibly damaging |
Het |
Ugt2a3 |
C |
T |
5: 87,474,932 (GRCm39) |
|
probably null |
Het |
Vmn1r213 |
A |
T |
13: 23,195,588 (GRCm39) |
|
probably benign |
Het |
Vmn2r8 |
A |
C |
5: 108,945,807 (GRCm39) |
|
probably null |
Het |
Vps13c |
T |
C |
9: 67,871,591 (GRCm39) |
F3253L |
possibly damaging |
Het |
Zbtb16 |
G |
T |
9: 48,576,575 (GRCm39) |
Q502K |
possibly damaging |
Het |
Zfp143 |
A |
G |
7: 109,676,354 (GRCm39) |
K218E |
possibly damaging |
Het |
Zfp946 |
A |
G |
17: 22,673,417 (GRCm39) |
N57S |
probably benign |
Het |
Zfp985 |
T |
C |
4: 147,667,314 (GRCm39) |
Y61H |
probably benign |
Het |
Zkscan1 |
G |
A |
5: 138,095,785 (GRCm39) |
R246Q |
probably damaging |
Het |
Zpld1 |
A |
G |
16: 55,071,978 (GRCm39) |
F94L |
probably damaging |
Het |
Zswim5 |
G |
T |
4: 116,844,103 (GRCm39) |
W1047L |
probably damaging |
Het |
|
Other mutations in Kntc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Kntc1
|
APN |
5 |
123,928,222 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00514:Kntc1
|
APN |
5 |
123,929,590 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01103:Kntc1
|
APN |
5 |
123,902,283 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01106:Kntc1
|
APN |
5 |
123,900,666 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01357:Kntc1
|
APN |
5 |
123,895,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01367:Kntc1
|
APN |
5 |
123,896,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01538:Kntc1
|
APN |
5 |
123,919,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01546:Kntc1
|
APN |
5 |
123,903,068 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01595:Kntc1
|
APN |
5 |
123,941,758 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01725:Kntc1
|
APN |
5 |
123,902,253 (GRCm39) |
missense |
probably benign |
|
IGL01916:Kntc1
|
APN |
5 |
123,939,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01936:Kntc1
|
APN |
5 |
123,949,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01942:Kntc1
|
APN |
5 |
123,916,330 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01973:Kntc1
|
APN |
5 |
123,904,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Kntc1
|
APN |
5 |
123,947,159 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02145:Kntc1
|
APN |
5 |
123,900,661 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02510:Kntc1
|
APN |
5 |
123,957,125 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02611:Kntc1
|
APN |
5 |
123,950,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Kntc1
|
APN |
5 |
123,893,727 (GRCm39) |
splice site |
probably benign |
|
IGL02737:Kntc1
|
APN |
5 |
123,957,183 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02793:Kntc1
|
APN |
5 |
123,916,340 (GRCm39) |
splice site |
probably null |
|
IGL02809:Kntc1
|
APN |
5 |
123,914,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02860:Kntc1
|
APN |
5 |
123,907,936 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02875:Kntc1
|
APN |
5 |
123,916,340 (GRCm39) |
splice site |
probably null |
|
IGL02931:Kntc1
|
APN |
5 |
123,937,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03169:Kntc1
|
APN |
5 |
123,913,884 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03267:Kntc1
|
APN |
5 |
123,896,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Kntc1
|
UTSW |
5 |
123,927,201 (GRCm39) |
missense |
probably benign |
0.19 |
R0006:Kntc1
|
UTSW |
5 |
123,927,201 (GRCm39) |
missense |
probably benign |
0.19 |
R0017:Kntc1
|
UTSW |
5 |
123,919,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Kntc1
|
UTSW |
5 |
123,903,120 (GRCm39) |
splice site |
probably benign |
|
R0580:Kntc1
|
UTSW |
5 |
123,941,732 (GRCm39) |
missense |
probably benign |
0.00 |
R0608:Kntc1
|
UTSW |
5 |
123,924,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R0725:Kntc1
|
UTSW |
5 |
123,907,767 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0733:Kntc1
|
UTSW |
5 |
123,928,979 (GRCm39) |
missense |
probably null |
|
R0781:Kntc1
|
UTSW |
5 |
123,937,965 (GRCm39) |
splice site |
probably benign |
|
R0787:Kntc1
|
UTSW |
5 |
123,934,167 (GRCm39) |
missense |
probably benign |
|
R1250:Kntc1
|
UTSW |
5 |
123,922,262 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1253:Kntc1
|
UTSW |
5 |
123,948,925 (GRCm39) |
frame shift |
probably null |
|
R1467:Kntc1
|
UTSW |
5 |
123,925,047 (GRCm39) |
missense |
probably benign |
0.04 |
R1467:Kntc1
|
UTSW |
5 |
123,925,047 (GRCm39) |
missense |
probably benign |
0.04 |
R1481:Kntc1
|
UTSW |
5 |
123,916,338 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Kntc1
|
UTSW |
5 |
123,910,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R1624:Kntc1
|
UTSW |
5 |
123,896,540 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1749:Kntc1
|
UTSW |
5 |
123,927,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1993:Kntc1
|
UTSW |
5 |
123,948,874 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1993:Kntc1
|
UTSW |
5 |
123,897,162 (GRCm39) |
critical splice donor site |
probably null |
|
R2071:Kntc1
|
UTSW |
5 |
123,932,340 (GRCm39) |
splice site |
probably null |
|
R2237:Kntc1
|
UTSW |
5 |
123,941,733 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2239:Kntc1
|
UTSW |
5 |
123,941,733 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2366:Kntc1
|
UTSW |
5 |
123,919,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Kntc1
|
UTSW |
5 |
123,919,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2382:Kntc1
|
UTSW |
5 |
123,898,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R2389:Kntc1
|
UTSW |
5 |
123,919,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2413:Kntc1
|
UTSW |
5 |
123,902,212 (GRCm39) |
missense |
probably benign |
0.01 |
R2442:Kntc1
|
UTSW |
5 |
123,948,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Kntc1
|
UTSW |
5 |
123,916,410 (GRCm39) |
nonsense |
probably null |
|
R2943:Kntc1
|
UTSW |
5 |
123,935,847 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3116:Kntc1
|
UTSW |
5 |
123,940,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4107:Kntc1
|
UTSW |
5 |
123,900,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R4176:Kntc1
|
UTSW |
5 |
123,914,680 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4275:Kntc1
|
UTSW |
5 |
123,905,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4440:Kntc1
|
UTSW |
5 |
123,932,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Kntc1
|
UTSW |
5 |
123,904,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Kntc1
|
UTSW |
5 |
123,904,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Kntc1
|
UTSW |
5 |
123,904,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Kntc1
|
UTSW |
5 |
123,950,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Kntc1
|
UTSW |
5 |
123,949,496 (GRCm39) |
missense |
probably damaging |
0.96 |
R4720:Kntc1
|
UTSW |
5 |
123,903,086 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4784:Kntc1
|
UTSW |
5 |
123,954,825 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4785:Kntc1
|
UTSW |
5 |
123,954,825 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4824:Kntc1
|
UTSW |
5 |
123,928,196 (GRCm39) |
nonsense |
probably null |
|
R4847:Kntc1
|
UTSW |
5 |
123,940,337 (GRCm39) |
missense |
probably benign |
0.18 |
R4849:Kntc1
|
UTSW |
5 |
123,897,128 (GRCm39) |
missense |
probably benign |
0.02 |
R4904:Kntc1
|
UTSW |
5 |
123,916,396 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4922:Kntc1
|
UTSW |
5 |
123,940,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R5080:Kntc1
|
UTSW |
5 |
123,900,649 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5114:Kntc1
|
UTSW |
5 |
123,919,118 (GRCm39) |
critical splice donor site |
probably null |
|
R5171:Kntc1
|
UTSW |
5 |
123,937,907 (GRCm39) |
missense |
probably benign |
0.01 |
R5220:Kntc1
|
UTSW |
5 |
123,950,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R5226:Kntc1
|
UTSW |
5 |
123,932,235 (GRCm39) |
missense |
probably benign |
0.09 |
R5278:Kntc1
|
UTSW |
5 |
123,919,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5329:Kntc1
|
UTSW |
5 |
123,902,254 (GRCm39) |
missense |
probably benign |
0.02 |
R5496:Kntc1
|
UTSW |
5 |
123,922,245 (GRCm39) |
missense |
probably benign |
0.00 |
R5503:Kntc1
|
UTSW |
5 |
123,957,939 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5633:Kntc1
|
UTSW |
5 |
123,957,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R5638:Kntc1
|
UTSW |
5 |
123,956,538 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5697:Kntc1
|
UTSW |
5 |
123,903,070 (GRCm39) |
missense |
probably benign |
0.00 |
R5757:Kntc1
|
UTSW |
5 |
123,945,372 (GRCm39) |
critical splice donor site |
probably null |
|
R5773:Kntc1
|
UTSW |
5 |
123,932,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:Kntc1
|
UTSW |
5 |
123,924,258 (GRCm39) |
missense |
probably benign |
0.05 |
R6019:Kntc1
|
UTSW |
5 |
123,900,579 (GRCm39) |
missense |
probably benign |
0.03 |
R6230:Kntc1
|
UTSW |
5 |
123,927,072 (GRCm39) |
splice site |
probably null |
|
R6437:Kntc1
|
UTSW |
5 |
123,907,754 (GRCm39) |
missense |
probably damaging |
0.98 |
R6888:Kntc1
|
UTSW |
5 |
123,949,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Kntc1
|
UTSW |
5 |
123,939,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R7123:Kntc1
|
UTSW |
5 |
123,919,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7262:Kntc1
|
UTSW |
5 |
123,925,036 (GRCm39) |
missense |
probably benign |
0.18 |
R7381:Kntc1
|
UTSW |
5 |
123,948,971 (GRCm39) |
missense |
probably benign |
0.12 |
R7485:Kntc1
|
UTSW |
5 |
123,925,019 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7512:Kntc1
|
UTSW |
5 |
123,929,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R7581:Kntc1
|
UTSW |
5 |
123,954,818 (GRCm39) |
missense |
probably benign |
0.05 |
R7687:Kntc1
|
UTSW |
5 |
123,897,152 (GRCm39) |
missense |
probably benign |
0.01 |
R7798:Kntc1
|
UTSW |
5 |
123,957,180 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7798:Kntc1
|
UTSW |
5 |
123,924,357 (GRCm39) |
missense |
probably benign |
|
R7871:Kntc1
|
UTSW |
5 |
123,922,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7876:Kntc1
|
UTSW |
5 |
123,913,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7947:Kntc1
|
UTSW |
5 |
123,919,951 (GRCm39) |
missense |
unknown |
|
R7997:Kntc1
|
UTSW |
5 |
123,916,117 (GRCm39) |
missense |
probably damaging |
0.96 |
R8231:Kntc1
|
UTSW |
5 |
123,920,959 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8257:Kntc1
|
UTSW |
5 |
123,896,586 (GRCm39) |
critical splice donor site |
probably null |
|
R8345:Kntc1
|
UTSW |
5 |
123,924,993 (GRCm39) |
missense |
probably benign |
0.37 |
R8354:Kntc1
|
UTSW |
5 |
123,916,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R8732:Kntc1
|
UTSW |
5 |
123,928,180 (GRCm39) |
missense |
probably benign |
0.00 |
R8754:Kntc1
|
UTSW |
5 |
123,897,115 (GRCm39) |
missense |
probably benign |
0.01 |
R8947:Kntc1
|
UTSW |
5 |
123,925,041 (GRCm39) |
missense |
probably benign |
0.01 |
R9041:Kntc1
|
UTSW |
5 |
123,927,093 (GRCm39) |
missense |
probably benign |
0.00 |
R9182:Kntc1
|
UTSW |
5 |
123,940,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Kntc1
|
UTSW |
5 |
123,925,112 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9460:Kntc1
|
UTSW |
5 |
123,941,378 (GRCm39) |
nonsense |
probably null |
|
R9468:Kntc1
|
UTSW |
5 |
123,954,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9643:Kntc1
|
UTSW |
5 |
123,949,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Kntc1
|
UTSW |
5 |
123,897,119 (GRCm39) |
missense |
probably benign |
0.01 |
R9721:Kntc1
|
UTSW |
5 |
123,939,948 (GRCm39) |
missense |
probably benign |
0.01 |
R9789:Kntc1
|
UTSW |
5 |
123,898,706 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0027:Kntc1
|
UTSW |
5 |
123,948,992 (GRCm39) |
missense |
probably benign |
0.00 |
X0065:Kntc1
|
UTSW |
5 |
123,916,100 (GRCm39) |
nonsense |
probably null |
|
X0067:Kntc1
|
UTSW |
5 |
123,916,137 (GRCm39) |
unclassified |
probably benign |
|
|