Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
A |
8: 25,204,287 (GRCm39) |
|
probably benign |
Het |
Aoc2 |
A |
G |
11: 101,217,321 (GRCm39) |
Y468C |
probably damaging |
Het |
Cdyl2 |
A |
G |
8: 117,306,056 (GRCm39) |
|
probably benign |
Het |
Cyp2j9 |
G |
T |
4: 96,472,201 (GRCm39) |
|
probably benign |
Het |
Dapk1 |
T |
G |
13: 60,901,957 (GRCm39) |
F929V |
probably benign |
Het |
Dhx9 |
A |
T |
1: 153,359,493 (GRCm39) |
M35K |
probably benign |
Het |
Dnah5 |
G |
A |
15: 28,346,003 (GRCm39) |
E2448K |
probably benign |
Het |
Doc2b |
A |
T |
11: 75,670,981 (GRCm39) |
C217S |
possibly damaging |
Het |
Dock11 |
A |
G |
X: 35,333,565 (GRCm39) |
I2010V |
probably benign |
Het |
Dram1 |
T |
C |
10: 88,160,641 (GRCm39) |
T227A |
possibly damaging |
Het |
Eppin |
G |
A |
2: 164,431,323 (GRCm39) |
T101M |
probably damaging |
Het |
F13a1 |
T |
C |
13: 37,082,105 (GRCm39) |
D533G |
probably damaging |
Het |
Fmo1 |
C |
A |
1: 162,667,293 (GRCm39) |
R174L |
probably damaging |
Het |
Fsip2 |
C |
A |
2: 82,828,407 (GRCm39) |
L6735I |
possibly damaging |
Het |
Gab1 |
G |
T |
8: 81,515,241 (GRCm39) |
T359K |
probably benign |
Het |
Ggta1 |
T |
C |
2: 35,298,029 (GRCm39) |
D118G |
possibly damaging |
Het |
Gramd1a |
A |
G |
7: 30,832,211 (GRCm39) |
S609P |
probably damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,089,150 (GRCm39) |
Y1607C |
possibly damaging |
Het |
Lrrc24 |
G |
T |
15: 76,607,992 (GRCm39) |
|
probably null |
Het |
Mak |
C |
A |
13: 41,223,760 (GRCm39) |
|
probably benign |
Het |
Megf8 |
G |
A |
7: 25,063,768 (GRCm39) |
R2708Q |
possibly damaging |
Het |
Mettl24 |
T |
C |
10: 40,613,791 (GRCm39) |
C177R |
probably damaging |
Het |
Mgam |
G |
C |
6: 40,733,305 (GRCm39) |
E812D |
probably benign |
Het |
Mroh8 |
T |
C |
2: 157,111,445 (GRCm39) |
R170G |
possibly damaging |
Het |
Msn |
G |
A |
X: 95,196,325 (GRCm39) |
V130I |
probably benign |
Het |
Ncoa4 |
G |
A |
14: 31,898,679 (GRCm39) |
V500I |
probably benign |
Het |
Or2aj5 |
A |
G |
16: 19,424,752 (GRCm39) |
L222P |
probably damaging |
Het |
Or2y1b |
A |
G |
11: 49,208,928 (GRCm39) |
|
probably null |
Het |
Or5an6 |
C |
T |
19: 12,371,801 (GRCm39) |
T58I |
probably benign |
Het |
Or8k3b |
T |
C |
2: 86,520,866 (GRCm39) |
Y151C |
possibly damaging |
Het |
Ppm1h |
T |
C |
10: 122,693,004 (GRCm39) |
S302P |
probably damaging |
Het |
Prkce |
T |
A |
17: 86,866,565 (GRCm39) |
|
probably benign |
Het |
Psenen |
T |
C |
7: 30,261,815 (GRCm39) |
I34V |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,011,826 (GRCm39) |
T710A |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Slc1a5 |
A |
G |
7: 16,516,328 (GRCm39) |
D168G |
probably benign |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Syce1 |
A |
T |
7: 140,359,351 (GRCm39) |
|
probably benign |
Het |
Tbc1d23 |
G |
T |
16: 57,034,573 (GRCm39) |
D75E |
probably damaging |
Het |
Tbk1 |
A |
G |
10: 121,395,839 (GRCm39) |
V418A |
probably benign |
Het |
Tmem132e |
T |
C |
11: 82,329,122 (GRCm39) |
V467A |
probably damaging |
Het |
Tmem241 |
T |
C |
18: 12,126,651 (GRCm39) |
D144G |
probably benign |
Het |
Tsc2 |
A |
G |
17: 24,817,997 (GRCm39) |
|
probably null |
Het |
Ubxn4 |
T |
A |
1: 128,202,617 (GRCm39) |
F420I |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,409,151 (GRCm39) |
T2645A |
probably damaging |
Het |
Utp14b |
A |
G |
1: 78,644,111 (GRCm39) |
K670E |
probably benign |
Het |
Zfp407 |
C |
T |
18: 84,227,580 (GRCm39) |
V2010M |
probably benign |
Het |
Zfp879 |
A |
G |
11: 50,724,784 (GRCm39) |
F91L |
probably benign |
Het |
Zfyve26 |
A |
G |
12: 79,329,591 (GRCm39) |
S532P |
probably benign |
Het |
|
Other mutations in Cfh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00969:Cfh
|
APN |
1 |
140,016,420 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01124:Cfh
|
APN |
1 |
140,110,999 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01389:Cfh
|
APN |
1 |
140,082,377 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01455:Cfh
|
APN |
1 |
140,033,277 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01877:Cfh
|
APN |
1 |
140,028,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Cfh
|
APN |
1 |
140,030,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02937:Cfh
|
APN |
1 |
140,033,180 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03039:Cfh
|
APN |
1 |
140,063,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03069:Cfh
|
APN |
1 |
140,026,793 (GRCm39) |
intron |
probably benign |
|
IGL03192:Cfh
|
APN |
1 |
140,026,759 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03201:Cfh
|
APN |
1 |
140,030,557 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Cfh
|
UTSW |
1 |
140,090,863 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4449001:Cfh
|
UTSW |
1 |
140,040,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R0257:Cfh
|
UTSW |
1 |
140,071,773 (GRCm39) |
missense |
probably benign |
0.01 |
R0294:Cfh
|
UTSW |
1 |
140,110,999 (GRCm39) |
missense |
probably benign |
0.01 |
R0571:Cfh
|
UTSW |
1 |
140,030,071 (GRCm39) |
splice site |
probably null |
|
R0576:Cfh
|
UTSW |
1 |
140,064,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R0586:Cfh
|
UTSW |
1 |
140,110,920 (GRCm39) |
missense |
probably damaging |
0.98 |
R0605:Cfh
|
UTSW |
1 |
140,030,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Cfh
|
UTSW |
1 |
140,028,621 (GRCm39) |
missense |
probably benign |
0.01 |
R0725:Cfh
|
UTSW |
1 |
140,085,081 (GRCm39) |
splice site |
probably benign |
|
R0853:Cfh
|
UTSW |
1 |
140,033,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1500:Cfh
|
UTSW |
1 |
140,028,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Cfh
|
UTSW |
1 |
140,028,716 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1667:Cfh
|
UTSW |
1 |
140,033,261 (GRCm39) |
missense |
probably benign |
0.01 |
R1695:Cfh
|
UTSW |
1 |
140,030,575 (GRCm39) |
missense |
probably damaging |
0.98 |
R1728:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1729:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1729:Cfh
|
UTSW |
1 |
140,064,526 (GRCm39) |
missense |
probably benign |
0.02 |
R1730:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1739:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1739:Cfh
|
UTSW |
1 |
140,064,526 (GRCm39) |
missense |
probably benign |
0.02 |
R1756:Cfh
|
UTSW |
1 |
140,028,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1762:Cfh
|
UTSW |
1 |
140,064,526 (GRCm39) |
missense |
probably benign |
0.02 |
R1783:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1784:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1785:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1785:Cfh
|
UTSW |
1 |
140,064,526 (GRCm39) |
missense |
probably benign |
0.02 |
R1912:Cfh
|
UTSW |
1 |
140,063,879 (GRCm39) |
splice site |
probably null |
|
R2273:Cfh
|
UTSW |
1 |
140,030,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R2288:Cfh
|
UTSW |
1 |
140,026,639 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3725:Cfh
|
UTSW |
1 |
140,014,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R3731:Cfh
|
UTSW |
1 |
140,047,708 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4060:Cfh
|
UTSW |
1 |
140,047,664 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4192:Cfh
|
UTSW |
1 |
140,030,454 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4226:Cfh
|
UTSW |
1 |
140,036,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Cfh
|
UTSW |
1 |
140,028,613 (GRCm39) |
nonsense |
probably null |
|
R4431:Cfh
|
UTSW |
1 |
140,064,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R4712:Cfh
|
UTSW |
1 |
140,036,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Cfh
|
UTSW |
1 |
140,016,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Cfh
|
UTSW |
1 |
140,028,561 (GRCm39) |
nonsense |
probably null |
|
R4831:Cfh
|
UTSW |
1 |
140,014,125 (GRCm39) |
missense |
probably benign |
|
R5052:Cfh
|
UTSW |
1 |
140,071,782 (GRCm39) |
missense |
probably damaging |
0.96 |
R5181:Cfh
|
UTSW |
1 |
140,075,384 (GRCm39) |
splice site |
probably benign |
|
R5205:Cfh
|
UTSW |
1 |
140,071,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Cfh
|
UTSW |
1 |
140,028,636 (GRCm39) |
missense |
probably benign |
0.21 |
R5366:Cfh
|
UTSW |
1 |
140,063,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R5776:Cfh
|
UTSW |
1 |
140,071,761 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5914:Cfh
|
UTSW |
1 |
140,063,967 (GRCm39) |
missense |
probably benign |
0.39 |
R5948:Cfh
|
UTSW |
1 |
140,036,546 (GRCm39) |
missense |
probably damaging |
0.96 |
R5979:Cfh
|
UTSW |
1 |
140,046,409 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6034:Cfh
|
UTSW |
1 |
140,090,869 (GRCm39) |
missense |
probably damaging |
0.98 |
R6034:Cfh
|
UTSW |
1 |
140,090,869 (GRCm39) |
missense |
probably damaging |
0.98 |
R6059:Cfh
|
UTSW |
1 |
140,046,428 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6198:Cfh
|
UTSW |
1 |
140,033,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Cfh
|
UTSW |
1 |
140,030,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6523:Cfh
|
UTSW |
1 |
140,029,445 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6610:Cfh
|
UTSW |
1 |
140,029,486 (GRCm39) |
nonsense |
probably null |
|
R6652:Cfh
|
UTSW |
1 |
140,071,806 (GRCm39) |
missense |
probably benign |
0.39 |
R6852:Cfh
|
UTSW |
1 |
140,075,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Cfh
|
UTSW |
1 |
140,028,621 (GRCm39) |
missense |
probably benign |
0.07 |
R6862:Cfh
|
UTSW |
1 |
140,030,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Cfh
|
UTSW |
1 |
140,014,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R7191:Cfh
|
UTSW |
1 |
140,040,305 (GRCm39) |
missense |
probably benign |
0.04 |
R7197:Cfh
|
UTSW |
1 |
140,016,505 (GRCm39) |
nonsense |
probably null |
|
R7355:Cfh
|
UTSW |
1 |
140,064,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:Cfh
|
UTSW |
1 |
140,014,259 (GRCm39) |
missense |
probably damaging |
0.97 |
R7419:Cfh
|
UTSW |
1 |
140,033,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R7579:Cfh
|
UTSW |
1 |
140,036,328 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7586:Cfh
|
UTSW |
1 |
140,075,459 (GRCm39) |
missense |
probably damaging |
0.99 |
R7985:Cfh
|
UTSW |
1 |
140,036,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R8119:Cfh
|
UTSW |
1 |
140,047,753 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8277:Cfh
|
UTSW |
1 |
140,029,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R8742:Cfh
|
UTSW |
1 |
140,029,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R8742:Cfh
|
UTSW |
1 |
140,064,469 (GRCm39) |
missense |
probably damaging |
0.97 |
R8743:Cfh
|
UTSW |
1 |
140,046,323 (GRCm39) |
critical splice donor site |
probably null |
|
R8874:Cfh
|
UTSW |
1 |
140,014,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R8909:Cfh
|
UTSW |
1 |
140,014,086 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8949:Cfh
|
UTSW |
1 |
140,026,705 (GRCm39) |
missense |
probably damaging |
0.98 |
R9126:Cfh
|
UTSW |
1 |
140,014,111 (GRCm39) |
missense |
probably damaging |
0.98 |
R9309:Cfh
|
UTSW |
1 |
140,082,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R9441:Cfh
|
UTSW |
1 |
140,030,149 (GRCm39) |
missense |
probably benign |
0.08 |
R9502:Cfh
|
UTSW |
1 |
140,040,320 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9544:Cfh
|
UTSW |
1 |
140,036,266 (GRCm39) |
missense |
probably benign |
0.14 |
R9559:Cfh
|
UTSW |
1 |
140,030,275 (GRCm39) |
missense |
probably benign |
0.32 |
R9616:Cfh
|
UTSW |
1 |
140,030,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R9617:Cfh
|
UTSW |
1 |
140,090,718 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9733:Cfh
|
UTSW |
1 |
140,016,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Cfh
|
UTSW |
1 |
140,090,687 (GRCm39) |
critical splice donor site |
probably null |
|
R9788:Cfh
|
UTSW |
1 |
140,036,499 (GRCm39) |
missense |
probably benign |
0.01 |
T0975:Cfh
|
UTSW |
1 |
140,082,336 (GRCm39) |
missense |
probably benign |
0.05 |
Z1088:Cfh
|
UTSW |
1 |
140,075,456 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1088:Cfh
|
UTSW |
1 |
140,036,642 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Cfh
|
UTSW |
1 |
140,071,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|