Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
G |
T |
14: 35,818,536 (GRCm39) |
R178L |
possibly damaging |
Het |
Acot4 |
T |
C |
12: 84,089,948 (GRCm39) |
|
probably benign |
Het |
Add3 |
C |
A |
19: 53,230,955 (GRCm39) |
D543E |
probably benign |
Het |
Angpt4 |
A |
C |
2: 151,785,238 (GRCm39) |
D418A |
probably benign |
Het |
Ano8 |
A |
T |
8: 71,935,936 (GRCm39) |
V260D |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,710,667 (GRCm39) |
D1536G |
probably damaging |
Het |
Dnajb9 |
A |
T |
12: 44,253,860 (GRCm39) |
D182E |
probably benign |
Het |
Epb42 |
G |
T |
2: 120,860,570 (GRCm39) |
|
probably null |
Het |
Fam185a |
T |
A |
5: 21,630,122 (GRCm39) |
|
probably benign |
Het |
Fer1l6 |
A |
G |
15: 58,518,998 (GRCm39) |
D1710G |
probably damaging |
Het |
Gabra2 |
G |
A |
5: 71,165,341 (GRCm39) |
P210S |
probably benign |
Het |
Gm8369 |
C |
T |
19: 11,479,596 (GRCm39) |
P9S |
probably damaging |
Het |
Il17ra |
A |
G |
6: 120,458,472 (GRCm39) |
D541G |
probably damaging |
Het |
Ints4 |
T |
G |
7: 97,156,940 (GRCm39) |
H337Q |
probably damaging |
Het |
Itgam |
A |
G |
7: 127,663,904 (GRCm39) |
T44A |
probably benign |
Het |
Lyst |
C |
A |
13: 13,915,098 (GRCm39) |
T3264N |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,366,835 (GRCm39) |
F1077S |
possibly damaging |
Het |
Myo3a |
T |
A |
2: 22,412,188 (GRCm39) |
F728I |
probably damaging |
Het |
Nacad |
T |
C |
11: 6,555,534 (GRCm39) |
E72G |
probably benign |
Het |
Nkain3 |
G |
A |
4: 20,485,003 (GRCm39) |
Q25* |
probably null |
Het |
Oca2 |
T |
C |
7: 55,946,997 (GRCm39) |
F342S |
probably damaging |
Het |
Or10d1c |
T |
A |
9: 38,894,313 (GRCm39) |
Q9L |
probably benign |
Het |
Osbpl6 |
T |
A |
2: 76,415,573 (GRCm39) |
L499Q |
probably damaging |
Het |
Pcdhgb8 |
G |
C |
18: 37,896,594 (GRCm39) |
D555H |
probably damaging |
Het |
Peak1 |
A |
T |
9: 56,166,025 (GRCm39) |
N634K |
probably damaging |
Het |
Pitpnm3 |
T |
C |
11: 71,942,785 (GRCm39) |
K818R |
possibly damaging |
Het |
Rab3gap1 |
T |
A |
1: 127,853,207 (GRCm39) |
|
probably benign |
Het |
Rcc1l |
T |
C |
5: 134,184,648 (GRCm39) |
T385A |
probably benign |
Het |
Rrm2 |
T |
C |
12: 24,758,377 (GRCm39) |
I11T |
probably benign |
Het |
Scnn1b |
A |
G |
7: 121,501,962 (GRCm39) |
T207A |
possibly damaging |
Het |
Spata31f3 |
A |
T |
4: 42,874,185 (GRCm39) |
|
probably benign |
Het |
Syt12 |
T |
A |
19: 4,497,709 (GRCm39) |
|
probably benign |
Het |
Tmprss6 |
A |
T |
15: 78,330,857 (GRCm39) |
|
probably null |
Het |
Ttbk1 |
A |
T |
17: 46,790,173 (GRCm39) |
C91S |
probably damaging |
Het |
Ube2q2l |
T |
C |
6: 136,378,435 (GRCm39) |
T132A |
probably benign |
Het |
Vit |
A |
G |
17: 78,894,255 (GRCm39) |
H219R |
probably benign |
Het |
Vmn1r27 |
A |
C |
6: 58,192,812 (GRCm39) |
I14R |
probably damaging |
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 |
R1430:Cfh
|
UTSW |
1 |
140,030,436 (GRCm39) |
splice site |
probably benign |
|
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 |
140,064,526 (GRCm39) |
missense |
probably benign |
0.02 |
R1729:Cfh
|
UTSW |
1 |
140,075,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
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 |
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 |
|