Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,771,237 (GRCm39) |
L142P |
probably benign |
Het |
Abca13 |
A |
T |
11: 9,241,126 (GRCm39) |
R996S |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,151,017 (GRCm39) |
F558L |
possibly damaging |
Het |
Acp7 |
T |
A |
7: 28,330,307 (GRCm39) |
D2V |
unknown |
Het |
Acvr1c |
T |
C |
2: 58,174,948 (GRCm39) |
D280G |
probably damaging |
Het |
Atp8a1 |
A |
G |
5: 67,781,380 (GRCm39) |
S1124P |
|
Het |
B4galnt1 |
A |
T |
10: 127,003,657 (GRCm39) |
T207S |
probably benign |
Het |
C2cd4d |
C |
A |
3: 94,271,445 (GRCm39) |
T237N |
probably benign |
Het |
C8b |
T |
C |
4: 104,637,824 (GRCm39) |
C99R |
probably damaging |
Het |
Ccnk |
C |
A |
12: 108,159,964 (GRCm39) |
Q149K |
possibly damaging |
Het |
Chfr |
A |
G |
5: 110,288,226 (GRCm39) |
D47G |
probably benign |
Het |
Chid1 |
A |
T |
7: 141,109,401 (GRCm39) |
|
probably null |
Het |
Cibar2 |
T |
A |
8: 120,895,342 (GRCm39) |
T187S |
possibly damaging |
Het |
Cmya5 |
T |
A |
13: 93,232,208 (GRCm39) |
E960V |
probably damaging |
Het |
Col18a1 |
A |
G |
10: 76,932,118 (GRCm39) |
S112P |
unknown |
Het |
Crispld1 |
A |
G |
1: 17,823,102 (GRCm39) |
T390A |
probably benign |
Het |
Cyp2c54 |
A |
T |
19: 40,058,697 (GRCm39) |
L245* |
probably null |
Het |
Ddr2 |
G |
T |
1: 169,812,530 (GRCm39) |
T654K |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,868,855 (GRCm39) |
|
probably null |
Het |
Elavl4 |
C |
T |
4: 110,068,622 (GRCm39) |
|
probably null |
Het |
Emilin1 |
T |
C |
5: 31,078,004 (GRCm39) |
V921A |
probably benign |
Het |
Evpl |
T |
A |
11: 116,113,939 (GRCm39) |
E1250D |
probably damaging |
Het |
Fam228a |
C |
T |
12: 4,782,790 (GRCm39) |
G101E |
probably benign |
Het |
Gemin4 |
T |
C |
11: 76,102,932 (GRCm39) |
T610A |
probably damaging |
Het |
Glis1 |
T |
C |
4: 107,292,880 (GRCm39) |
M1T |
probably null |
Het |
Gm14399 |
C |
T |
2: 174,972,252 (GRCm39) |
|
probably benign |
Het |
Gorasp2 |
C |
T |
2: 70,509,849 (GRCm39) |
T170I |
probably damaging |
Het |
Gpr37 |
A |
G |
6: 25,669,341 (GRCm39) |
V501A |
possibly damaging |
Het |
Grik4 |
T |
A |
9: 42,533,356 (GRCm39) |
Q388L |
probably benign |
Het |
Hspg2 |
T |
A |
4: 137,278,436 (GRCm39) |
D3035E |
probably damaging |
Het |
Htr4 |
A |
T |
18: 62,545,247 (GRCm39) |
N11Y |
probably benign |
Het |
Itgb2l |
A |
G |
16: 96,230,243 (GRCm39) |
S356P |
probably damaging |
Het |
Klk1b22 |
A |
G |
7: 43,764,173 (GRCm39) |
N34D |
probably benign |
Het |
Lmcd1 |
A |
G |
6: 112,287,500 (GRCm39) |
D62G |
possibly damaging |
Het |
Lrp2 |
C |
T |
2: 69,316,696 (GRCm39) |
G2095E |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,334,536 (GRCm39) |
E4407V |
possibly damaging |
Het |
Mcm5 |
T |
C |
8: 75,851,487 (GRCm39) |
F631L |
probably benign |
Het |
Mov10l1 |
A |
G |
15: 88,878,071 (GRCm39) |
S170G |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,411,239 (GRCm39) |
D1395V |
unknown |
Het |
Muc6 |
G |
A |
7: 141,226,842 (GRCm39) |
T1395M |
probably benign |
Het |
Myh15 |
A |
G |
16: 48,911,468 (GRCm39) |
D300G |
probably damaging |
Het |
Naa80 |
T |
C |
9: 107,460,498 (GRCm39) |
L131P |
probably damaging |
Het |
Ndst4 |
A |
G |
3: 125,231,952 (GRCm39) |
T174A |
probably benign |
Het |
Nek5 |
T |
A |
8: 22,580,500 (GRCm39) |
N406I |
probably benign |
Het |
Nr2c2 |
G |
A |
6: 92,136,359 (GRCm39) |
V400I |
probably damaging |
Het |
Or1l4 |
T |
C |
2: 37,092,092 (GRCm39) |
Y280H |
probably damaging |
Het |
Or1l4b |
G |
T |
2: 37,037,021 (GRCm39) |
V266L |
probably benign |
Het |
Or51aa2 |
A |
T |
7: 103,187,935 (GRCm39) |
Y169N |
probably benign |
Het |
Or52m1 |
T |
C |
7: 102,290,190 (GRCm39) |
S246P |
probably damaging |
Het |
Or6b1 |
G |
A |
6: 42,811,330 (GRCm39) |
|
probably null |
Het |
Or6c5c |
T |
A |
10: 129,298,620 (GRCm39) |
I25N |
probably damaging |
Het |
Parn |
T |
C |
16: 13,443,927 (GRCm39) |
|
probably null |
Het |
Pfkl |
T |
C |
10: 77,827,857 (GRCm39) |
T468A |
probably damaging |
Het |
Pi16 |
C |
A |
17: 29,538,208 (GRCm39) |
P7Q |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,768,340 (GRCm39) |
I2205T |
possibly damaging |
Het |
Prss16 |
A |
T |
13: 22,187,317 (GRCm39) |
N442K |
probably damaging |
Het |
Pus7 |
A |
G |
5: 23,957,342 (GRCm39) |
S370P |
probably damaging |
Het |
Ripk3 |
G |
T |
14: 56,024,741 (GRCm39) |
Y210* |
probably null |
Het |
Rps6ka2 |
C |
A |
17: 7,539,034 (GRCm39) |
F317L |
probably damaging |
Het |
Slc13a3 |
G |
A |
2: 165,287,448 (GRCm39) |
R169W |
possibly damaging |
Het |
Slc6a21 |
T |
A |
7: 44,931,904 (GRCm39) |
I256N |
possibly damaging |
Het |
Slc6a9 |
G |
A |
4: 117,725,303 (GRCm39) |
R589Q |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 15,875,077 (GRCm39) |
S442P |
probably damaging |
Het |
Snupn |
T |
A |
9: 56,890,028 (GRCm39) |
M283K |
probably damaging |
Het |
Steap3 |
A |
T |
1: 120,162,087 (GRCm39) |
M395K |
probably damaging |
Het |
Sv2b |
G |
A |
7: 74,797,402 (GRCm39) |
P331S |
probably damaging |
Het |
Tlr1 |
A |
G |
5: 65,084,115 (GRCm39) |
V154A |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,835,382 (GRCm39) |
S1580P |
probably damaging |
Het |
Tmem51 |
TCCCC |
TCCC |
4: 141,764,996 (GRCm39) |
|
probably null |
Het |
Trav14d-3-dv8 |
G |
A |
14: 53,316,218 (GRCm39) |
R26H |
probably benign |
Het |
Trp53 |
C |
T |
11: 69,482,081 (GRCm39) |
L365F |
probably benign |
Het |
Trp53bp1 |
A |
T |
2: 121,029,516 (GRCm39) |
I1838N |
probably damaging |
Het |
Ugt1a5 |
A |
T |
1: 88,094,608 (GRCm39) |
K279* |
probably null |
Het |
Unc80 |
A |
G |
1: 66,591,368 (GRCm39) |
E1141G |
possibly damaging |
Het |
Vti1b |
T |
C |
12: 79,213,153 (GRCm39) |
D49G |
probably benign |
Het |
Wnt10a |
A |
T |
1: 74,832,641 (GRCm39) |
H78L |
possibly damaging |
Het |
Zfp869 |
G |
A |
8: 70,159,128 (GRCm39) |
H482Y |
probably damaging |
Het |
Zfyve1 |
A |
G |
12: 83,598,314 (GRCm39) |
V638A |
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 |
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 |
R8680:Cps1
|
UTSW |
1 |
67,243,772 (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 |
|