Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,087,930 (GRCm39) |
I1066V |
probably benign |
Het |
Abcd2 |
T |
C |
15: 91,033,197 (GRCm39) |
T740A |
probably benign |
Het |
Amigo1 |
T |
C |
3: 108,094,852 (GRCm39) |
L117P |
probably damaging |
Het |
Ankar |
A |
T |
1: 72,686,160 (GRCm39) |
S1347T |
probably damaging |
Het |
Apol7e |
T |
C |
15: 77,601,956 (GRCm39) |
S185P |
probably damaging |
Het |
Ash1l |
G |
A |
3: 88,942,734 (GRCm39) |
C2088Y |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,630,895 (GRCm39) |
T221A |
probably benign |
Het |
Caln1 |
A |
G |
5: 130,851,825 (GRCm39) |
S205G |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,704,672 (GRCm39) |
I2803V |
unknown |
Het |
Cldn23 |
A |
G |
8: 36,293,056 (GRCm39) |
V144A |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 17,077,310 (GRCm39) |
S116P |
probably damaging |
Het |
Dgkd |
A |
T |
1: 87,845,689 (GRCm39) |
T299S |
possibly damaging |
Het |
Fam20b |
T |
G |
1: 156,518,072 (GRCm39) |
T241P |
probably damaging |
Het |
Fndc3b |
A |
T |
3: 27,505,493 (GRCm39) |
M925K |
probably benign |
Het |
Ftdc1 |
C |
A |
16: 58,437,211 (GRCm39) |
M32I |
probably benign |
Het |
Ints3 |
C |
T |
3: 90,299,607 (GRCm39) |
R987Q |
probably damaging |
Het |
Kctd10 |
A |
G |
5: 114,505,316 (GRCm39) |
V226A |
probably damaging |
Het |
Lypd2 |
A |
G |
15: 74,604,881 (GRCm39) |
V38A |
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,909,156 (GRCm39) |
R265G |
possibly damaging |
Het |
Mcc |
C |
T |
18: 44,601,500 (GRCm39) |
V610M |
possibly damaging |
Het |
Mocs1 |
C |
T |
17: 49,756,547 (GRCm39) |
R244C |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,103,232 (GRCm39) |
T677A |
probably damaging |
Het |
Ngp |
A |
G |
9: 110,251,421 (GRCm39) |
N150D |
probably benign |
Het |
Nipbl |
C |
T |
15: 8,388,696 (GRCm39) |
R308Q |
probably benign |
Het |
Nsrp1 |
A |
G |
11: 76,939,177 (GRCm39) |
|
probably null |
Het |
Or2y16 |
A |
T |
11: 49,334,953 (GRCm39) |
I92F |
probably damaging |
Het |
Or4f47 |
T |
A |
2: 111,972,908 (GRCm39) |
I206N |
probably damaging |
Het |
Or52n20 |
A |
T |
7: 104,320,061 (GRCm39) |
I51F |
probably damaging |
Het |
Pbld2 |
A |
T |
10: 62,889,656 (GRCm39) |
D146V |
probably benign |
Het |
Prss22 |
T |
A |
17: 24,213,701 (GRCm39) |
K197* |
probably null |
Het |
Ptprd |
G |
T |
4: 76,047,263 (GRCm39) |
S87R |
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Slc25a35 |
T |
C |
11: 68,862,798 (GRCm39) |
L251S |
probably benign |
Het |
Slx4 |
A |
T |
16: 3,803,136 (GRCm39) |
L1226* |
probably null |
Het |
Smarca4 |
T |
C |
9: 21,558,922 (GRCm39) |
V651A |
possibly damaging |
Het |
Smarcad1 |
T |
C |
6: 65,071,303 (GRCm39) |
F583L |
probably benign |
Het |
Taf2 |
T |
C |
15: 54,894,526 (GRCm39) |
K932E |
probably benign |
Het |
Trav8d-1 |
A |
T |
14: 53,016,425 (GRCm39) |
T104S |
probably benign |
Het |
Trmt9b |
G |
A |
8: 36,965,576 (GRCm39) |
W32* |
probably null |
Het |
Trpm4 |
A |
T |
7: 44,976,552 (GRCm39) |
V155D |
probably damaging |
Het |
Ttc6 |
A |
T |
12: 57,752,429 (GRCm39) |
Y1445F |
possibly damaging |
Het |
Ttll5 |
C |
A |
12: 86,067,322 (GRCm39) |
N1270K |
probably damaging |
Het |
Usp40 |
G |
T |
1: 87,895,400 (GRCm39) |
|
probably null |
Het |
Vmn2r74 |
T |
C |
7: 85,610,690 (GRCm39) |
M1V |
probably null |
Het |
Wwox |
T |
C |
8: 115,433,108 (GRCm39) |
V258A |
probably damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp770 |
G |
A |
2: 114,027,508 (GRCm39) |
T187I |
probably damaging |
Het |
Zranb2 |
A |
G |
3: 157,241,969 (GRCm39) |
|
probably null |
Het |
Zscan4-ps3 |
A |
G |
7: 11,344,267 (GRCm39) |
Q75R |
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 |
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 |
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 |
|