Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco2 |
G |
A |
15: 81,773,635 (GRCm39) |
R58Q |
probably null |
Het |
Actl11 |
A |
T |
9: 107,808,121 (GRCm39) |
T815S |
possibly damaging |
Het |
Actr5 |
A |
G |
2: 158,470,135 (GRCm39) |
D255G |
probably damaging |
Het |
Acvr1 |
T |
C |
2: 58,338,385 (GRCm39) |
K446E |
probably damaging |
Het |
Adam39 |
T |
C |
8: 41,277,755 (GRCm39) |
Y49H |
probably benign |
Het |
Adcy7 |
TGG |
TG |
8: 89,053,053 (GRCm39) |
|
probably null |
Het |
Amn1 |
C |
T |
6: 149,090,103 (GRCm39) |
|
probably benign |
Het |
Ankdd1a |
C |
T |
9: 65,411,452 (GRCm39) |
A352T |
possibly damaging |
Het |
Aoc1l2 |
T |
C |
6: 48,907,909 (GRCm39) |
M303T |
probably benign |
Het |
Arl4c |
A |
G |
1: 88,629,134 (GRCm39) |
C85R |
probably damaging |
Het |
Asgr2 |
T |
A |
11: 69,996,310 (GRCm39) |
|
probably null |
Het |
Bdkrb1 |
G |
A |
12: 105,571,078 (GRCm39) |
V215I |
probably benign |
Het |
Btn2a2 |
C |
A |
13: 23,662,848 (GRCm39) |
K367N |
possibly damaging |
Het |
Btnl10 |
T |
A |
11: 58,813,189 (GRCm39) |
F273I |
probably benign |
Het |
C7 |
T |
A |
15: 5,086,579 (GRCm39) |
|
probably null |
Het |
Cap1 |
A |
G |
4: 122,758,505 (GRCm39) |
V225A |
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Ccdc187 |
T |
C |
2: 26,183,698 (GRCm39) |
S101G |
possibly damaging |
Het |
Ccdc30 |
T |
C |
4: 119,250,821 (GRCm39) |
N141S |
possibly damaging |
Het |
Cdc42bpg |
T |
G |
19: 6,370,696 (GRCm39) |
L1263R |
probably damaging |
Het |
Cdc42ep1 |
A |
T |
15: 78,733,782 (GRCm39) |
H294L |
probably benign |
Het |
Cdk12 |
A |
G |
11: 98,140,628 (GRCm39) |
N1290D |
unknown |
Het |
Ces1g |
A |
G |
8: 94,061,792 (GRCm39) |
V38A |
probably benign |
Het |
Cntnap4 |
A |
C |
8: 113,582,982 (GRCm39) |
Y1020S |
probably benign |
Het |
Col7a1 |
T |
C |
9: 108,791,809 (GRCm39) |
V1232A |
unknown |
Het |
Ctdsp2 |
A |
G |
10: 126,832,040 (GRCm39) |
D216G |
probably damaging |
Het |
Cyp2j6 |
A |
G |
4: 96,414,245 (GRCm39) |
I340T |
probably damaging |
Het |
Cyp4f37 |
A |
G |
17: 32,844,205 (GRCm39) |
D103G |
possibly damaging |
Het |
Dlgap1 |
T |
G |
17: 70,964,458 (GRCm39) |
N400K |
probably benign |
Het |
Dnaaf9 |
G |
A |
2: 130,648,711 (GRCm39) |
T257M |
unknown |
Het |
Dnah1 |
C |
A |
14: 30,986,394 (GRCm39) |
A3698S |
probably damaging |
Het |
Dnah12 |
C |
A |
14: 26,597,281 (GRCm39) |
R3547S |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,610,114 (GRCm39) |
V1774A |
probably benign |
Het |
Drc7 |
A |
G |
8: 95,801,866 (GRCm39) |
E709G |
probably damaging |
Het |
Dsc1 |
T |
A |
18: 20,240,791 (GRCm39) |
D178V |
probably damaging |
Het |
Duox1 |
T |
C |
2: 122,151,203 (GRCm39) |
Y293H |
probably damaging |
Het |
Elp1 |
G |
T |
4: 56,772,521 (GRCm39) |
P867T |
probably benign |
Het |
Epas1 |
T |
A |
17: 87,112,667 (GRCm39) |
D88E |
probably damaging |
Het |
Epdr1 |
A |
G |
13: 19,778,821 (GRCm39) |
F92L |
possibly damaging |
Het |
Eri3 |
T |
A |
4: 117,422,013 (GRCm39) |
V136E |
probably benign |
Het |
Espl1 |
T |
A |
15: 102,228,233 (GRCm39) |
I1669N |
possibly damaging |
Het |
Etv6 |
A |
G |
6: 134,225,672 (GRCm39) |
N212S |
probably benign |
Het |
Fam186b |
A |
T |
15: 99,176,685 (GRCm39) |
L735Q |
probably damaging |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fan1 |
A |
G |
7: 63,999,240 (GRCm39) |
L874P |
possibly damaging |
Het |
Fancm |
A |
G |
12: 65,168,494 (GRCm39) |
N1619S |
probably damaging |
Het |
Fbln5 |
A |
T |
12: 101,734,722 (GRCm39) |
N183K |
probably damaging |
Het |
Fbn2 |
T |
C |
18: 58,228,298 (GRCm39) |
H746R |
probably benign |
Het |
Fbxw17 |
T |
C |
13: 50,579,605 (GRCm39) |
W141R |
probably damaging |
Het |
Fbxw25 |
T |
A |
9: 109,483,676 (GRCm39) |
N179Y |
|
Het |
Gbe1 |
A |
T |
16: 70,198,664 (GRCm39) |
Y119F |
probably benign |
Het |
Gcnt7 |
T |
A |
2: 172,293,180 (GRCm39) |
Y369F |
probably damaging |
Het |
Gdf9 |
T |
A |
11: 53,327,511 (GRCm39) |
S156T |
probably damaging |
Het |
Gm14295 |
T |
C |
2: 176,499,162 (GRCm39) |
V4A |
probably benign |
Het |
Gm8369 |
A |
C |
19: 11,489,015 (GRCm39) |
T101P |
probably benign |
Het |
Herc3 |
A |
G |
6: 58,835,999 (GRCm39) |
N280S |
probably null |
Het |
Hipk2 |
T |
A |
6: 38,724,390 (GRCm39) |
R447W |
probably damaging |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Hltf |
G |
A |
3: 20,136,996 (GRCm39) |
|
probably null |
Het |
Ik |
C |
A |
18: 36,886,959 (GRCm39) |
D397E |
probably benign |
Het |
Inka1 |
T |
A |
9: 107,861,488 (GRCm39) |
Y276F |
probably benign |
Het |
Kcnc1 |
G |
A |
7: 46,077,010 (GRCm39) |
V271M |
probably benign |
Het |
Kif21b |
A |
T |
1: 136,077,090 (GRCm39) |
I371F |
probably damaging |
Het |
Klrc1 |
A |
G |
6: 129,655,746 (GRCm39) |
F43S |
probably damaging |
Het |
Krt8 |
A |
G |
15: 101,912,460 (GRCm39) |
V72A |
probably benign |
Het |
Krtap6-2 |
A |
G |
16: 89,216,722 (GRCm39) |
S82P |
unknown |
Het |
Lrrc15 |
G |
A |
16: 30,093,016 (GRCm39) |
L108F |
probably damaging |
Het |
Lvrn |
T |
G |
18: 47,017,506 (GRCm39) |
I612S |
probably damaging |
Het |
Map3k3 |
T |
A |
11: 106,041,860 (GRCm39) |
I413N |
probably damaging |
Het |
Mark3 |
A |
G |
12: 111,570,960 (GRCm39) |
I87V |
probably damaging |
Het |
Mki67 |
GTT |
GTTT |
7: 135,309,233 (GRCm39) |
|
probably null |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mrgprb2 |
G |
A |
7: 48,202,674 (GRCm39) |
T17M |
possibly damaging |
Het |
Msantd5f4 |
G |
T |
4: 73,557,190 (GRCm39) |
V8F |
probably damaging |
Het |
Myh3 |
C |
T |
11: 66,983,187 (GRCm39) |
R905* |
probably null |
Het |
Myh8 |
T |
C |
11: 67,177,215 (GRCm39) |
V427A |
probably benign |
Het |
Myocd |
T |
C |
11: 65,078,209 (GRCm39) |
K529E |
probably damaging |
Het |
Myom2 |
A |
T |
8: 15,158,399 (GRCm39) |
K784* |
probably null |
Het |
Or1l4 |
G |
T |
2: 37,091,575 (GRCm39) |
M107I |
probably benign |
Het |
Or2w25 |
T |
G |
11: 59,504,339 (GRCm39) |
I183S |
probably damaging |
Het |
Or6c33 |
T |
C |
10: 129,853,287 (GRCm39) |
I19T |
probably benign |
Het |
Pabpc4 |
T |
C |
4: 123,180,653 (GRCm39) |
I125T |
probably damaging |
Het |
Parp14 |
A |
G |
16: 35,677,775 (GRCm39) |
I731T |
probably benign |
Het |
Pde6c |
T |
A |
19: 38,147,008 (GRCm39) |
|
probably null |
Het |
Pias3 |
T |
A |
3: 96,610,867 (GRCm39) |
C391S |
possibly damaging |
Het |
Pknox2 |
A |
T |
9: 36,835,067 (GRCm39) |
M134K |
probably damaging |
Het |
Pot1b |
A |
G |
17: 55,969,465 (GRCm39) |
S568P |
possibly damaging |
Het |
Ppp1r3a |
T |
A |
6: 14,719,466 (GRCm39) |
T483S |
probably benign |
Het |
Rag1 |
A |
T |
2: 101,473,327 (GRCm39) |
V605E |
probably damaging |
Het |
Relch |
T |
C |
1: 105,591,876 (GRCm39) |
V15A |
probably damaging |
Het |
Ros1 |
T |
C |
10: 51,943,170 (GRCm39) |
D2048G |
probably damaging |
Het |
Rp2 |
A |
G |
X: 20,243,781 (GRCm39) |
D252G |
probably benign |
Het |
Rpgrip1l |
A |
C |
8: 92,031,516 (GRCm39) |
H120Q |
probably benign |
Het |
Rpl24 |
T |
A |
16: 55,790,509 (GRCm39) |
S122T |
probably benign |
Het |
Sec61b |
A |
G |
4: 47,483,049 (GRCm39) |
Y93C |
probably damaging |
Het |
Sema6a |
A |
T |
18: 47,382,594 (GRCm39) |
L651Q |
probably null |
Het |
Serpinb6a |
T |
A |
13: 34,102,400 (GRCm39) |
K275I |
probably damaging |
Het |
Skic2 |
C |
T |
17: 35,063,758 (GRCm39) |
A562T |
probably benign |
Het |
Skor2 |
C |
T |
18: 76,946,376 (GRCm39) |
H33Y |
unknown |
Het |
Slc26a7 |
T |
C |
4: 14,519,496 (GRCm39) |
N508S |
probably benign |
Het |
Slc2a4 |
A |
G |
11: 69,837,173 (GRCm39) |
F88L |
probably damaging |
Het |
Slc8b1 |
A |
G |
5: 120,665,865 (GRCm39) |
T399A |
probably benign |
Het |
Slfn5 |
A |
T |
11: 82,847,699 (GRCm39) |
M195L |
possibly damaging |
Het |
Snx17 |
C |
A |
5: 31,355,088 (GRCm39) |
Q368K |
probably damaging |
Het |
Tasor |
T |
C |
14: 27,201,766 (GRCm39) |
|
probably null |
Het |
Tbcb |
A |
T |
7: 29,930,549 (GRCm39) |
|
probably null |
Het |
Telo2 |
A |
G |
17: 25,334,199 (GRCm39) |
I16T |
probably benign |
Het |
Timm50 |
A |
G |
7: 28,007,069 (GRCm39) |
F202S |
possibly damaging |
Het |
Tle2 |
A |
G |
10: 81,417,567 (GRCm39) |
D244G |
probably benign |
Het |
Tlr4 |
G |
A |
4: 66,759,522 (GRCm39) |
V772I |
possibly damaging |
Het |
Tmem214 |
G |
A |
5: 31,027,043 (GRCm39) |
W11* |
probably null |
Het |
Top2b |
A |
C |
14: 16,365,718 (GRCm38) |
T14P |
probably benign |
Het |
Trim44 |
T |
C |
2: 102,187,827 (GRCm39) |
T309A |
probably benign |
Het |
Tuba8 |
A |
G |
6: 121,200,063 (GRCm39) |
N249S |
probably benign |
Het |
Tubb4a |
A |
G |
17: 57,388,027 (GRCm39) |
V333A |
probably benign |
Het |
Ugdh |
C |
A |
5: 65,575,876 (GRCm39) |
D328Y |
possibly damaging |
Het |
Vmn1r189 |
A |
G |
13: 22,286,426 (GRCm39) |
L137P |
probably damaging |
Het |
Vmn1r208 |
A |
G |
13: 22,956,789 (GRCm39) |
V236A |
probably damaging |
Het |
Vmn2r29 |
A |
T |
7: 7,244,855 (GRCm39) |
W340R |
probably benign |
Het |
Vmn2r52 |
A |
C |
7: 9,893,476 (GRCm39) |
D554E |
probably benign |
Het |
Wdr36 |
C |
T |
18: 32,994,168 (GRCm39) |
Q669* |
probably null |
Het |
Wiz |
G |
T |
17: 32,575,939 (GRCm39) |
D812E |
probably benign |
Het |
Zfp777 |
A |
T |
6: 48,021,580 (GRCm39) |
V14D |
possibly damaging |
Het |
|
Other mutations in Ccdc18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00836:Ccdc18
|
APN |
5 |
108,328,391 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01380:Ccdc18
|
APN |
5 |
108,328,753 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01405:Ccdc18
|
APN |
5 |
108,350,052 (GRCm39) |
splice site |
probably benign |
|
IGL01718:Ccdc18
|
APN |
5 |
108,349,214 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02098:Ccdc18
|
APN |
5 |
108,349,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02227:Ccdc18
|
APN |
5 |
108,296,788 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02391:Ccdc18
|
APN |
5 |
108,283,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Ccdc18
|
APN |
5 |
108,319,614 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02808:Ccdc18
|
APN |
5 |
108,283,835 (GRCm39) |
splice site |
probably benign |
|
IGL02880:Ccdc18
|
APN |
5 |
108,283,310 (GRCm39) |
missense |
probably benign |
0.31 |
IGL03069:Ccdc18
|
APN |
5 |
108,376,767 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03390:Ccdc18
|
APN |
5 |
108,359,997 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Ccdc18
|
UTSW |
5 |
108,306,485 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0004:Ccdc18
|
UTSW |
5 |
108,309,566 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0112:Ccdc18
|
UTSW |
5 |
108,321,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Ccdc18
|
UTSW |
5 |
108,321,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Ccdc18
|
UTSW |
5 |
108,322,830 (GRCm39) |
missense |
probably benign |
0.06 |
R0619:Ccdc18
|
UTSW |
5 |
108,328,282 (GRCm39) |
missense |
probably benign |
0.04 |
R0648:Ccdc18
|
UTSW |
5 |
108,322,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Ccdc18
|
UTSW |
5 |
108,283,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R0666:Ccdc18
|
UTSW |
5 |
108,311,530 (GRCm39) |
missense |
probably benign |
0.19 |
R1271:Ccdc18
|
UTSW |
5 |
108,349,982 (GRCm39) |
nonsense |
probably null |
|
R1509:Ccdc18
|
UTSW |
5 |
108,336,844 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1539:Ccdc18
|
UTSW |
5 |
108,339,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Ccdc18
|
UTSW |
5 |
108,360,054 (GRCm39) |
missense |
probably benign |
|
R1663:Ccdc18
|
UTSW |
5 |
108,363,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Ccdc18
|
UTSW |
5 |
108,341,668 (GRCm39) |
missense |
probably benign |
0.00 |
R1870:Ccdc18
|
UTSW |
5 |
108,368,703 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1897:Ccdc18
|
UTSW |
5 |
108,343,908 (GRCm39) |
missense |
probably benign |
0.00 |
R1946:Ccdc18
|
UTSW |
5 |
108,376,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R2420:Ccdc18
|
UTSW |
5 |
108,376,454 (GRCm39) |
missense |
probably damaging |
0.96 |
R2421:Ccdc18
|
UTSW |
5 |
108,376,454 (GRCm39) |
missense |
probably damaging |
0.96 |
R2422:Ccdc18
|
UTSW |
5 |
108,376,454 (GRCm39) |
missense |
probably damaging |
0.96 |
R4078:Ccdc18
|
UTSW |
5 |
108,306,394 (GRCm39) |
nonsense |
probably null |
|
R4079:Ccdc18
|
UTSW |
5 |
108,306,394 (GRCm39) |
nonsense |
probably null |
|
R4244:Ccdc18
|
UTSW |
5 |
108,296,838 (GRCm39) |
nonsense |
probably null |
|
R4409:Ccdc18
|
UTSW |
5 |
108,368,708 (GRCm39) |
nonsense |
probably null |
|
R4428:Ccdc18
|
UTSW |
5 |
108,283,943 (GRCm39) |
missense |
probably benign |
0.01 |
R4455:Ccdc18
|
UTSW |
5 |
108,309,395 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4499:Ccdc18
|
UTSW |
5 |
108,376,826 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4612:Ccdc18
|
UTSW |
5 |
108,283,307 (GRCm39) |
missense |
probably benign |
0.01 |
R4907:Ccdc18
|
UTSW |
5 |
108,284,007 (GRCm39) |
missense |
probably benign |
0.01 |
R4972:Ccdc18
|
UTSW |
5 |
108,339,869 (GRCm39) |
missense |
probably benign |
|
R5039:Ccdc18
|
UTSW |
5 |
108,306,514 (GRCm39) |
critical splice donor site |
probably null |
|
R5835:Ccdc18
|
UTSW |
5 |
108,288,740 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5854:Ccdc18
|
UTSW |
5 |
108,354,594 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6128:Ccdc18
|
UTSW |
5 |
108,311,625 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6229:Ccdc18
|
UTSW |
5 |
108,319,484 (GRCm39) |
missense |
probably benign |
0.00 |
R6271:Ccdc18
|
UTSW |
5 |
108,322,753 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6315:Ccdc18
|
UTSW |
5 |
108,309,448 (GRCm39) |
missense |
probably benign |
|
R6359:Ccdc18
|
UTSW |
5 |
108,283,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6375:Ccdc18
|
UTSW |
5 |
108,322,820 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6388:Ccdc18
|
UTSW |
5 |
108,349,214 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6415:Ccdc18
|
UTSW |
5 |
108,309,612 (GRCm39) |
missense |
probably benign |
0.03 |
R6560:Ccdc18
|
UTSW |
5 |
108,339,790 (GRCm39) |
missense |
probably benign |
0.09 |
R6645:Ccdc18
|
UTSW |
5 |
108,286,796 (GRCm39) |
missense |
probably benign |
|
R6664:Ccdc18
|
UTSW |
5 |
108,315,966 (GRCm39) |
nonsense |
probably null |
|
R6836:Ccdc18
|
UTSW |
5 |
108,345,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Ccdc18
|
UTSW |
5 |
108,309,401 (GRCm39) |
missense |
probably benign |
0.26 |
R7009:Ccdc18
|
UTSW |
5 |
108,321,728 (GRCm39) |
critical splice donor site |
probably null |
|
R7052:Ccdc18
|
UTSW |
5 |
108,309,554 (GRCm39) |
missense |
probably benign |
0.15 |
R7058:Ccdc18
|
UTSW |
5 |
108,341,664 (GRCm39) |
missense |
probably benign |
|
R7087:Ccdc18
|
UTSW |
5 |
108,343,988 (GRCm39) |
missense |
probably benign |
|
R7117:Ccdc18
|
UTSW |
5 |
108,296,835 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7176:Ccdc18
|
UTSW |
5 |
108,315,972 (GRCm39) |
missense |
probably benign |
|
R7382:Ccdc18
|
UTSW |
5 |
108,286,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Ccdc18
|
UTSW |
5 |
108,368,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R7493:Ccdc18
|
UTSW |
5 |
108,354,483 (GRCm39) |
nonsense |
probably null |
|
R7506:Ccdc18
|
UTSW |
5 |
108,311,605 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7635:Ccdc18
|
UTSW |
5 |
108,376,915 (GRCm39) |
critical splice donor site |
probably null |
|
R7690:Ccdc18
|
UTSW |
5 |
108,376,528 (GRCm39) |
missense |
probably benign |
0.00 |
R7748:Ccdc18
|
UTSW |
5 |
108,296,907 (GRCm39) |
critical splice donor site |
probably null |
|
R7812:Ccdc18
|
UTSW |
5 |
108,328,699 (GRCm39) |
missense |
probably benign |
0.00 |
R8017:Ccdc18
|
UTSW |
5 |
108,376,511 (GRCm39) |
nonsense |
probably null |
|
R8019:Ccdc18
|
UTSW |
5 |
108,376,511 (GRCm39) |
nonsense |
probably null |
|
R8172:Ccdc18
|
UTSW |
5 |
108,311,640 (GRCm39) |
critical splice donor site |
probably null |
|
R8177:Ccdc18
|
UTSW |
5 |
108,345,661 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8344:Ccdc18
|
UTSW |
5 |
108,309,369 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8351:Ccdc18
|
UTSW |
5 |
108,303,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Ccdc18
|
UTSW |
5 |
108,363,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8451:Ccdc18
|
UTSW |
5 |
108,303,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Ccdc18
|
UTSW |
5 |
108,345,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Ccdc18
|
UTSW |
5 |
108,328,283 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9137:Ccdc18
|
UTSW |
5 |
108,296,856 (GRCm39) |
missense |
probably damaging |
0.98 |
R9391:Ccdc18
|
UTSW |
5 |
108,376,770 (GRCm39) |
missense |
probably benign |
0.02 |
R9418:Ccdc18
|
UTSW |
5 |
108,303,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R9536:Ccdc18
|
UTSW |
5 |
108,286,792 (GRCm39) |
missense |
probably benign |
0.01 |
RF013:Ccdc18
|
UTSW |
5 |
108,368,582 (GRCm39) |
missense |
probably benign |
0.05 |
X0024:Ccdc18
|
UTSW |
5 |
108,339,788 (GRCm39) |
missense |
probably benign |
0.01 |
X0063:Ccdc18
|
UTSW |
5 |
108,360,063 (GRCm39) |
missense |
probably benign |
|
|