Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
C |
A |
2: 68,494,693 (GRCm39) |
S77R |
unknown |
Het |
Adamts1 |
T |
C |
16: 85,595,002 (GRCm39) |
Y582C |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,745,398 (GRCm39) |
V683E |
|
Het |
Allc |
T |
G |
12: 28,603,971 (GRCm39) |
T371P |
probably damaging |
Het |
Ankrd12 |
A |
G |
17: 66,291,191 (GRCm39) |
I1414T |
probably benign |
Het |
Bahcc1 |
A |
G |
11: 120,163,717 (GRCm39) |
K672E |
probably damaging |
Het |
C3ar1 |
A |
T |
6: 122,826,964 (GRCm39) |
S418T |
probably damaging |
Het |
Calca |
A |
G |
7: 114,234,413 (GRCm39) |
V12A |
possibly damaging |
Het |
Carmil3 |
A |
G |
14: 55,734,409 (GRCm39) |
E410G |
probably benign |
Het |
Cracd |
T |
C |
5: 76,805,897 (GRCm39) |
V123A |
unknown |
Het |
Csf3 |
G |
A |
11: 98,593,273 (GRCm39) |
G130D |
probably damaging |
Het |
Cuedc1 |
A |
T |
11: 88,073,342 (GRCm39) |
Q169L |
probably benign |
Het |
Cyp2c66 |
T |
A |
19: 39,102,430 (GRCm39) |
W20R |
probably null |
Het |
Dguok |
C |
T |
6: 83,457,914 (GRCm39) |
E240K |
probably damaging |
Het |
Dlg1 |
T |
G |
16: 31,606,923 (GRCm39) |
Y220* |
probably null |
Het |
Dnah7a |
T |
C |
1: 53,557,886 (GRCm39) |
Y2176C |
probably damaging |
Het |
Dnai1 |
T |
C |
4: 41,630,055 (GRCm39) |
I488T |
probably benign |
Het |
Dock1 |
G |
T |
7: 134,348,683 (GRCm39) |
C299F |
possibly damaging |
Het |
Ebi3 |
C |
T |
17: 56,260,997 (GRCm39) |
T59M |
probably benign |
Het |
Esrp1 |
G |
A |
4: 11,367,153 (GRCm39) |
S160F |
probably benign |
Het |
Evi5l |
A |
G |
8: 4,253,536 (GRCm39) |
D471G |
probably benign |
Het |
Farp2 |
T |
C |
1: 93,504,246 (GRCm39) |
F341S |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,143,798 (GRCm39) |
V2777A |
probably benign |
Het |
Glcci1 |
T |
C |
6: 8,573,186 (GRCm39) |
I225T |
probably damaging |
Het |
Gm3336 |
A |
G |
8: 71,173,176 (GRCm39) |
T63A |
unknown |
Het |
Gm9767 |
A |
G |
10: 25,954,681 (GRCm39) |
T78A |
unknown |
Het |
H2-T5 |
T |
G |
17: 36,478,445 (GRCm39) |
T168P |
probably damaging |
Het |
Habp4 |
T |
A |
13: 64,323,860 (GRCm39) |
M261K |
probably benign |
Het |
Herc2 |
A |
G |
7: 55,814,992 (GRCm39) |
T2744A |
probably benign |
Het |
Hlx |
A |
G |
1: 184,464,223 (GRCm39) |
V39A |
probably benign |
Het |
Ifi204 |
G |
A |
1: 173,587,772 (GRCm39) |
T129I |
possibly damaging |
Het |
Itfg1 |
A |
G |
8: 86,452,197 (GRCm39) |
I534T |
probably damaging |
Het |
Klhl33 |
A |
T |
14: 51,128,962 (GRCm39) |
C496S |
probably benign |
Het |
Lamb1 |
T |
A |
12: 31,350,214 (GRCm39) |
V713D |
possibly damaging |
Het |
Mon2 |
G |
T |
10: 122,852,213 (GRCm39) |
H1052Q |
probably damaging |
Het |
Ndst2 |
T |
C |
14: 20,778,478 (GRCm39) |
|
probably null |
Het |
Nphp1 |
A |
T |
2: 127,587,829 (GRCm39) |
M582K |
probably damaging |
Het |
Nt5el |
C |
T |
13: 105,256,482 (GRCm39) |
T517I |
probably benign |
Het |
Ogfr |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,850 (GRCm39) |
|
probably benign |
Het |
Or2w3b |
A |
G |
11: 58,623,532 (GRCm39) |
V153A |
possibly damaging |
Het |
Or8b47 |
T |
A |
9: 38,435,239 (GRCm39) |
D70E |
probably damaging |
Het |
Padi2 |
A |
T |
4: 140,659,403 (GRCm39) |
H236L |
probably benign |
Het |
Pira2 |
A |
T |
7: 3,844,696 (GRCm39) |
F445Y |
probably benign |
Het |
Psenen |
T |
C |
7: 30,261,503 (GRCm39) |
I75V |
probably benign |
Het |
Pycr1 |
A |
T |
11: 120,533,746 (GRCm39) |
M37K |
probably benign |
Het |
Rpl4 |
T |
A |
9: 64,085,212 (GRCm39) |
N317K |
probably damaging |
Het |
Scart2 |
T |
A |
7: 139,876,806 (GRCm39) |
D732E |
probably damaging |
Het |
Scn8a |
T |
A |
15: 100,914,843 (GRCm39) |
|
probably null |
Het |
Sdk1 |
A |
G |
5: 142,113,602 (GRCm39) |
T1550A |
probably damaging |
Het |
Shisa6 |
G |
T |
11: 66,265,990 (GRCm39) |
T246K |
|
Het |
Sis |
A |
T |
3: 72,844,294 (GRCm39) |
|
probably null |
Het |
Slc22a14 |
A |
C |
9: 118,999,704 (GRCm39) |
S496A |
probably benign |
Het |
Slc8a3 |
G |
A |
12: 81,361,767 (GRCm39) |
R351C |
probably damaging |
Het |
Surf2 |
A |
G |
2: 26,809,288 (GRCm39) |
K202R |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,935,984 (GRCm39) |
|
probably null |
Het |
Ugt2b36 |
T |
A |
5: 87,239,983 (GRCm39) |
N134I |
probably damaging |
Het |
Wdr97 |
T |
C |
15: 76,245,687 (GRCm39) |
V1308A |
|
Het |
Xpr1 |
G |
A |
1: 155,188,641 (GRCm39) |
A333V |
possibly damaging |
Het |
Zfp408 |
A |
T |
2: 91,476,776 (GRCm39) |
M126K |
probably benign |
Het |
Zfy2 |
T |
C |
Y: 2,116,263 (GRCm39) |
Q259R |
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 |
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 |
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 |
|