Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
C |
16: 90,852,551 (GRCm39) |
Y195C |
probably damaging |
Het |
Abcb1a |
T |
A |
5: 8,735,371 (GRCm39) |
F159L |
probably damaging |
Het |
Adam6b |
A |
G |
12: 113,454,371 (GRCm39) |
N396S |
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,823,055 (GRCm39) |
M338V |
possibly damaging |
Het |
Adamts7 |
T |
A |
9: 90,077,321 (GRCm39) |
H1329Q |
probably damaging |
Het |
Aim2 |
C |
T |
1: 173,289,786 (GRCm39) |
P243L |
probably damaging |
Het |
Ankdd1a |
T |
C |
9: 65,412,418 (GRCm39) |
D311G |
probably damaging |
Het |
Apon |
A |
T |
10: 128,090,428 (GRCm39) |
E35D |
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,078,566 (GRCm39) |
D224G |
probably damaging |
Het |
Atp6v0a1 |
T |
A |
11: 100,953,229 (GRCm39) |
*839R |
probably null |
Het |
Bco2 |
A |
G |
9: 50,461,878 (GRCm39) |
L42P |
probably damaging |
Het |
Bicral |
T |
A |
17: 47,141,873 (GRCm39) |
|
probably benign |
Het |
Ccna1 |
T |
C |
3: 54,955,878 (GRCm39) |
Q306R |
probably benign |
Het |
Cep152 |
G |
T |
2: 125,406,131 (GRCm39) |
S1467* |
probably null |
Het |
Cfap44 |
T |
A |
16: 44,225,085 (GRCm39) |
V110E |
probably damaging |
Het |
Clip2 |
G |
A |
5: 134,531,462 (GRCm39) |
A781V |
probably benign |
Het |
Cux1 |
A |
G |
5: 136,336,710 (GRCm39) |
V934A |
possibly damaging |
Het |
Depdc5 |
T |
C |
5: 33,101,382 (GRCm39) |
F891L |
possibly damaging |
Het |
Dnai7 |
T |
A |
6: 145,127,542 (GRCm39) |
I456F |
probably benign |
Het |
Dnajc13 |
A |
G |
9: 104,057,338 (GRCm39) |
V1554A |
probably benign |
Het |
Echs1 |
A |
T |
7: 139,690,499 (GRCm39) |
M191K |
probably damaging |
Het |
Eif6 |
T |
A |
2: 155,664,772 (GRCm39) |
D238V |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,144,692 (GRCm39) |
L4061F |
probably benign |
Het |
Fat3 |
T |
C |
9: 15,908,703 (GRCm39) |
D2433G |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,320,265 (GRCm39) |
V33A |
probably benign |
Het |
Garin2 |
TGATGTCACAGATGTCAC |
TGATGTCAC |
12: 78,762,057 (GRCm39) |
|
probably benign |
Het |
Gpr155 |
T |
C |
2: 73,174,039 (GRCm39) |
E790G |
probably damaging |
Het |
Ighv1-67 |
A |
T |
12: 115,567,861 (GRCm39) |
V17E |
probably damaging |
Het |
Klra9 |
T |
A |
6: 130,165,639 (GRCm39) |
R125S |
probably damaging |
Het |
Leo1 |
T |
C |
9: 75,353,277 (GRCm39) |
|
probably null |
Het |
Map2 |
G |
T |
1: 66,460,872 (GRCm39) |
R1556L |
probably damaging |
Het |
Megf8 |
A |
G |
7: 25,059,166 (GRCm39) |
|
probably null |
Het |
Meikin |
T |
C |
11: 54,317,477 (GRCm39) |
I426T |
possibly damaging |
Het |
Muc16 |
A |
T |
9: 18,556,015 (GRCm39) |
V3426E |
unknown |
Het |
Or4a15 |
T |
A |
2: 89,193,065 (GRCm39) |
Y236F |
probably benign |
Het |
Or51af1 |
G |
A |
7: 103,142,029 (GRCm39) |
L19F |
probably damaging |
Het |
Or52n2c |
A |
G |
7: 104,574,620 (GRCm39) |
L117P |
probably damaging |
Het |
Or7e168 |
T |
G |
9: 19,720,105 (GRCm39) |
S164A |
possibly damaging |
Het |
Or8k25 |
T |
C |
2: 86,243,935 (GRCm39) |
I154V |
probably benign |
Het |
Or9s13 |
T |
C |
1: 92,547,643 (GRCm39) |
V5A |
probably benign |
Het |
Otogl |
A |
G |
10: 107,747,936 (GRCm39) |
|
probably null |
Het |
Palm3 |
T |
C |
8: 84,756,504 (GRCm39) |
L672P |
probably damaging |
Het |
Perm1 |
A |
G |
4: 156,302,091 (GRCm39) |
T212A |
probably benign |
Het |
Poc1a |
T |
C |
9: 106,226,960 (GRCm39) |
M400T |
probably benign |
Het |
Pou6f2 |
T |
A |
13: 18,414,196 (GRCm39) |
Q193L |
unknown |
Het |
Ppl |
C |
T |
16: 4,905,300 (GRCm39) |
R1665H |
probably benign |
Het |
Ppp4r3b |
T |
C |
11: 29,123,449 (GRCm39) |
|
probably null |
Het |
Ptger1 |
T |
C |
8: 84,394,654 (GRCm39) |
S44P |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,473,009 (GRCm39) |
T787A |
probably benign |
Het |
Rab44 |
A |
T |
17: 29,358,642 (GRCm39) |
R277* |
probably null |
Het |
Rasgef1a |
T |
A |
6: 118,064,088 (GRCm39) |
I334K |
probably damaging |
Het |
Rfx1 |
T |
C |
8: 84,818,084 (GRCm39) |
V554A |
possibly damaging |
Het |
Ripk1 |
T |
A |
13: 34,214,032 (GRCm39) |
I518K |
possibly damaging |
Het |
Rpl22 |
A |
G |
4: 152,416,763 (GRCm39) |
Y90C |
probably damaging |
Het |
Rps27a |
C |
A |
11: 29,495,998 (GRCm39) |
R118L |
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,319,331 (GRCm39) |
S19T |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,520,509 (GRCm39) |
|
probably null |
Het |
Sema4c |
A |
T |
1: 36,589,867 (GRCm39) |
S496T |
probably benign |
Het |
Serpina3i |
T |
C |
12: 104,231,387 (GRCm39) |
V8A |
possibly damaging |
Het |
Sis |
G |
A |
3: 72,867,628 (GRCm39) |
T139M |
probably damaging |
Het |
Skic3 |
A |
T |
13: 76,303,587 (GRCm39) |
H1227L |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,000,972 (GRCm39) |
S24T |
probably benign |
Het |
Slc5a11 |
A |
G |
7: 122,866,975 (GRCm39) |
I423M |
probably benign |
Het |
Slc7a10 |
G |
A |
7: 34,885,997 (GRCm39) |
G31S |
probably benign |
Het |
Sowahc |
A |
G |
10: 59,059,001 (GRCm39) |
N379S |
probably benign |
Het |
Stat5a |
T |
C |
11: 100,774,714 (GRCm39) |
M741T |
unknown |
Het |
Tcf15 |
T |
C |
2: 151,986,020 (GRCm39) |
S159P |
probably benign |
Het |
Tdrd5 |
C |
A |
1: 156,098,788 (GRCm39) |
R669L |
possibly damaging |
Het |
Tln1 |
T |
C |
4: 43,553,041 (GRCm39) |
E350G |
possibly damaging |
Het |
Trim12c |
T |
G |
7: 103,997,271 (GRCm39) |
N95T |
|
Het |
Urb1 |
T |
C |
16: 90,571,513 (GRCm39) |
T1099A |
probably benign |
Het |
Vmn1r44 |
T |
A |
6: 89,870,578 (GRCm39) |
V108D |
probably damaging |
Het |
Vmn2r65 |
A |
G |
7: 84,589,388 (GRCm39) |
Y843H |
probably benign |
Het |
Vmn2r68 |
A |
G |
7: 84,871,321 (GRCm39) |
I654T |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,623,270 (GRCm39) |
N2797S |
possibly damaging |
Het |
Wscd2 |
T |
C |
5: 113,712,235 (GRCm39) |
Y385H |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,229,500 (GRCm39) |
I318V |
probably benign |
Het |
Xrcc3 |
T |
A |
12: 111,774,313 (GRCm39) |
K172M |
probably damaging |
Het |
|
Other mutations in Cps1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00757:Cps1
|
APN |
1 |
67,191,539 (GRCm39) |
splice site |
probably benign |
|
IGL00897:Cps1
|
APN |
1 |
67,254,723 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00928:Cps1
|
APN |
1 |
67,162,393 (GRCm39) |
missense |
probably benign |
|
IGL01063:Cps1
|
APN |
1 |
67,234,325 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01081:Cps1
|
APN |
1 |
67,245,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01361:Cps1
|
APN |
1 |
67,234,304 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01396:Cps1
|
APN |
1 |
67,196,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Cps1
|
APN |
1 |
67,269,443 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01695:Cps1
|
APN |
1 |
67,236,194 (GRCm39) |
missense |
probably benign |
|
IGL02022:Cps1
|
APN |
1 |
67,212,031 (GRCm39) |
splice site |
probably benign |
|
IGL02032:Cps1
|
APN |
1 |
67,269,474 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02049:Cps1
|
APN |
1 |
67,183,113 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02197:Cps1
|
APN |
1 |
67,196,923 (GRCm39) |
missense |
probably benign |
|
IGL02217:Cps1
|
APN |
1 |
67,213,541 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02555:Cps1
|
APN |
1 |
67,253,180 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02570:Cps1
|
APN |
1 |
67,187,862 (GRCm39) |
splice site |
probably benign |
|
IGL02633:Cps1
|
APN |
1 |
67,162,396 (GRCm39) |
missense |
probably benign |
|
IGL02711:Cps1
|
APN |
1 |
67,251,676 (GRCm39) |
splice site |
probably benign |
|
IGL02737:Cps1
|
APN |
1 |
67,187,933 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03030:Cps1
|
APN |
1 |
67,182,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Cps1
|
APN |
1 |
67,184,960 (GRCm39) |
nonsense |
probably null |
|
Madman
|
UTSW |
1 |
67,200,030 (GRCm39) |
missense |
probably damaging |
0.96 |
maniac
|
UTSW |
1 |
67,197,037 (GRCm39) |
critical splice donor site |
probably null |
|
R0109:Cps1
|
UTSW |
1 |
67,268,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0109:Cps1
|
UTSW |
1 |
67,268,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0140:Cps1
|
UTSW |
1 |
67,219,275 (GRCm39) |
missense |
probably benign |
|
R0318:Cps1
|
UTSW |
1 |
67,216,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R0486:Cps1
|
UTSW |
1 |
67,204,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0488:Cps1
|
UTSW |
1 |
67,187,967 (GRCm39) |
splice site |
probably benign |
|
R0492:Cps1
|
UTSW |
1 |
67,196,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Cps1
|
UTSW |
1 |
67,254,723 (GRCm39) |
missense |
probably benign |
0.02 |
R0534:Cps1
|
UTSW |
1 |
67,183,059 (GRCm39) |
missense |
probably benign |
0.06 |
R0565:Cps1
|
UTSW |
1 |
67,205,608 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0609:Cps1
|
UTSW |
1 |
67,211,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Cps1
|
UTSW |
1 |
67,178,929 (GRCm39) |
missense |
probably benign |
0.01 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1220:Cps1
|
UTSW |
1 |
67,243,862 (GRCm39) |
critical splice donor site |
probably null |
|
R1321:Cps1
|
UTSW |
1 |
67,182,178 (GRCm39) |
splice site |
probably benign |
|
R1343:Cps1
|
UTSW |
1 |
67,248,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Cps1
|
UTSW |
1 |
67,268,583 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1374:Cps1
|
UTSW |
1 |
67,269,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1481:Cps1
|
UTSW |
1 |
67,183,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R1711:Cps1
|
UTSW |
1 |
67,207,533 (GRCm39) |
splice site |
probably null |
|
R1712:Cps1
|
UTSW |
1 |
67,269,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1774:Cps1
|
UTSW |
1 |
67,210,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1799:Cps1
|
UTSW |
1 |
67,248,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Cps1
|
UTSW |
1 |
67,234,355 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2074:Cps1
|
UTSW |
1 |
67,243,797 (GRCm39) |
missense |
probably benign |
0.21 |
R2078:Cps1
|
UTSW |
1 |
67,234,424 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2078:Cps1
|
UTSW |
1 |
67,196,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Cps1
|
UTSW |
1 |
67,216,139 (GRCm39) |
missense |
probably benign |
0.01 |
R2112:Cps1
|
UTSW |
1 |
67,216,139 (GRCm39) |
missense |
probably benign |
0.01 |
R2146:Cps1
|
UTSW |
1 |
67,191,538 (GRCm39) |
splice site |
probably benign |
|
R2355:Cps1
|
UTSW |
1 |
67,195,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2375:Cps1
|
UTSW |
1 |
67,257,019 (GRCm39) |
missense |
probably benign |
0.00 |
R2860:Cps1
|
UTSW |
1 |
67,205,534 (GRCm39) |
missense |
probably benign |
0.44 |
R2861:Cps1
|
UTSW |
1 |
67,205,534 (GRCm39) |
missense |
probably benign |
0.44 |
R2979:Cps1
|
UTSW |
1 |
67,243,863 (GRCm39) |
critical splice donor site |
probably null |
|
R3427:Cps1
|
UTSW |
1 |
67,213,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3833:Cps1
|
UTSW |
1 |
67,178,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3858:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3859:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3887:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3888:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3889:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4386:Cps1
|
UTSW |
1 |
67,210,154 (GRCm39) |
critical splice donor site |
probably null |
|
R4497:Cps1
|
UTSW |
1 |
67,244,358 (GRCm39) |
missense |
probably null |
1.00 |
R4671:Cps1
|
UTSW |
1 |
67,235,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Cps1
|
UTSW |
1 |
67,259,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R4799:Cps1
|
UTSW |
1 |
67,182,145 (GRCm39) |
missense |
probably damaging |
0.96 |
R4853:Cps1
|
UTSW |
1 |
67,195,361 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4884:Cps1
|
UTSW |
1 |
67,216,183 (GRCm39) |
missense |
probably benign |
0.11 |
R4900:Cps1
|
UTSW |
1 |
67,200,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Cps1
|
UTSW |
1 |
67,178,922 (GRCm39) |
missense |
probably benign |
0.10 |
R5091:Cps1
|
UTSW |
1 |
67,268,679 (GRCm39) |
critical splice donor site |
probably null |
|
R5102:Cps1
|
UTSW |
1 |
67,245,952 (GRCm39) |
missense |
probably benign |
0.00 |
R5215:Cps1
|
UTSW |
1 |
67,205,539 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5290:Cps1
|
UTSW |
1 |
67,211,868 (GRCm39) |
missense |
probably benign |
0.21 |
R5732:Cps1
|
UTSW |
1 |
67,196,923 (GRCm39) |
missense |
probably benign |
0.22 |
R5818:Cps1
|
UTSW |
1 |
67,205,647 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5878:Cps1
|
UTSW |
1 |
67,197,037 (GRCm39) |
critical splice donor site |
probably null |
|
R6002:Cps1
|
UTSW |
1 |
67,211,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6034:Cps1
|
UTSW |
1 |
67,196,872 (GRCm39) |
splice site |
probably null |
|
R6034:Cps1
|
UTSW |
1 |
67,196,872 (GRCm39) |
splice site |
probably null |
|
R6199:Cps1
|
UTSW |
1 |
67,201,774 (GRCm39) |
frame shift |
probably null |
|
R6310:Cps1
|
UTSW |
1 |
67,182,140 (GRCm39) |
missense |
probably benign |
0.00 |
R6554:Cps1
|
UTSW |
1 |
67,213,628 (GRCm39) |
nonsense |
probably null |
|
R6700:Cps1
|
UTSW |
1 |
67,268,682 (GRCm39) |
splice site |
probably null |
|
R6731:Cps1
|
UTSW |
1 |
67,200,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R7052:Cps1
|
UTSW |
1 |
67,237,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Cps1
|
UTSW |
1 |
67,210,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Cps1
|
UTSW |
1 |
67,237,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R7323:Cps1
|
UTSW |
1 |
67,197,028 (GRCm39) |
missense |
probably benign |
0.03 |
R7339:Cps1
|
UTSW |
1 |
67,236,174 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7485:Cps1
|
UTSW |
1 |
67,179,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Cps1
|
UTSW |
1 |
67,219,240 (GRCm39) |
missense |
probably benign |
|
R7748:Cps1
|
UTSW |
1 |
67,178,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Cps1
|
UTSW |
1 |
67,213,640 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8097:Cps1
|
UTSW |
1 |
67,267,429 (GRCm39) |
missense |
probably benign |
0.08 |
R8357:Cps1
|
UTSW |
1 |
67,196,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R8435:Cps1
|
UTSW |
1 |
67,251,589 (GRCm39) |
missense |
probably benign |
0.07 |
R8457:Cps1
|
UTSW |
1 |
67,196,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R8805:Cps1
|
UTSW |
1 |
67,216,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8811:Cps1
|
UTSW |
1 |
67,253,246 (GRCm39) |
missense |
probably benign |
0.03 |
R8819:Cps1
|
UTSW |
1 |
67,267,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8820:Cps1
|
UTSW |
1 |
67,267,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8854:Cps1
|
UTSW |
1 |
67,200,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Cps1
|
UTSW |
1 |
67,254,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Cps1
|
UTSW |
1 |
67,248,831 (GRCm39) |
missense |
probably benign |
0.08 |
R9273:Cps1
|
UTSW |
1 |
67,191,445 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9286:Cps1
|
UTSW |
1 |
67,198,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9308:Cps1
|
UTSW |
1 |
67,200,118 (GRCm39) |
critical splice donor site |
probably null |
|
R9326:Cps1
|
UTSW |
1 |
67,248,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Cps1
|
UTSW |
1 |
67,259,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R9454:Cps1
|
UTSW |
1 |
67,219,311 (GRCm39) |
missense |
probably damaging |
0.97 |
R9518:Cps1
|
UTSW |
1 |
67,259,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Cps1
|
UTSW |
1 |
67,198,048 (GRCm39) |
missense |
probably benign |
0.26 |
R9585:Cps1
|
UTSW |
1 |
67,195,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R9618:Cps1
|
UTSW |
1 |
67,196,975 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9641:Cps1
|
UTSW |
1 |
67,234,342 (GRCm39) |
missense |
probably benign |
0.03 |
R9650:Cps1
|
UTSW |
1 |
67,254,636 (GRCm39) |
missense |
|
|
R9668:Cps1
|
UTSW |
1 |
67,213,649 (GRCm39) |
missense |
probably benign |
0.24 |
R9726:Cps1
|
UTSW |
1 |
67,195,395 (GRCm39) |
missense |
probably benign |
0.39 |
X0024:Cps1
|
UTSW |
1 |
67,162,406 (GRCm39) |
missense |
probably benign |
|
Z1176:Cps1
|
UTSW |
1 |
67,187,878 (GRCm39) |
frame shift |
probably null |
|
Z1176:Cps1
|
UTSW |
1 |
67,162,427 (GRCm39) |
missense |
possibly damaging |
0.54 |
|