Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
T |
2: 69,069,513 (GRCm39) |
V1294E |
probably damaging |
Het |
Ada |
C |
T |
2: 163,577,308 (GRCm39) |
G60D |
probably benign |
Het |
Aff3 |
G |
T |
1: 38,291,738 (GRCm39) |
R390S |
possibly damaging |
Het |
Aldh3b3 |
T |
A |
19: 4,013,959 (GRCm39) |
N53K |
possibly damaging |
Het |
Ankrd36 |
G |
A |
11: 5,589,132 (GRCm39) |
M410I |
probably benign |
Het |
Ap2b1 |
T |
A |
11: 83,215,395 (GRCm39) |
I113N |
probably damaging |
Het |
Art5 |
G |
T |
7: 101,747,396 (GRCm39) |
H128N |
probably benign |
Het |
Calhm2 |
A |
C |
19: 47,121,599 (GRCm39) |
L190R |
probably benign |
Het |
Catsperg1 |
G |
C |
7: 28,884,152 (GRCm39) |
T987R |
probably damaging |
Het |
Cdh18 |
A |
T |
15: 23,474,064 (GRCm39) |
I645F |
probably damaging |
Het |
Cenpe |
C |
T |
3: 134,945,641 (GRCm39) |
Q1052* |
probably null |
Het |
Cfap221 |
G |
T |
1: 119,863,856 (GRCm39) |
Q563K |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,651,770 (GRCm39) |
E3093D |
probably benign |
Het |
Chd4 |
A |
G |
6: 125,090,974 (GRCm39) |
M1186V |
probably benign |
Het |
Chst15 |
A |
T |
7: 131,870,646 (GRCm39) |
|
probably null |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Cul1 |
T |
A |
6: 47,495,173 (GRCm39) |
N518K |
probably damaging |
Het |
E230025N22Rik |
G |
T |
18: 36,821,952 (GRCm39) |
L247I |
possibly damaging |
Het |
Eno4 |
A |
T |
19: 58,941,600 (GRCm39) |
K174* |
probably null |
Het |
Enpp3 |
G |
A |
10: 24,671,702 (GRCm39) |
P431S |
probably benign |
Het |
Fbh1 |
T |
A |
2: 11,764,801 (GRCm39) |
Q444H |
probably damaging |
Het |
Fbxo31 |
G |
A |
8: 122,281,136 (GRCm39) |
R337C |
probably damaging |
Het |
Fbxw14 |
A |
G |
9: 109,105,250 (GRCm39) |
I305T |
probably benign |
Het |
Fhip1b |
T |
A |
7: 105,034,599 (GRCm39) |
T408S |
probably damaging |
Het |
Gas2 |
T |
A |
7: 51,602,969 (GRCm39) |
C216S |
probably damaging |
Het |
Gjb3 |
GCCAGATGCGCCCA |
GCCAGATGCGCCCAGATGCGCCCA |
4: 127,220,458 (GRCm39) |
|
probably null |
Het |
Glp2r |
T |
A |
11: 67,621,459 (GRCm39) |
R344* |
probably null |
Het |
Gm17430 |
A |
G |
18: 9,726,640 (GRCm39) |
Y11H |
probably damaging |
Het |
Gyg1 |
T |
A |
3: 20,176,901 (GRCm39) |
D363V |
probably damaging |
Het |
H2bc18 |
G |
A |
3: 96,177,290 (GRCm39) |
A75T |
probably benign |
Het |
Hectd4 |
A |
G |
5: 121,411,677 (GRCm39) |
N451S |
probably benign |
Het |
Hif1a |
T |
C |
12: 73,979,111 (GRCm39) |
Y212H |
probably benign |
Het |
Hoxd11 |
A |
T |
2: 74,514,482 (GRCm39) |
*337C |
probably null |
Het |
Kif24 |
A |
G |
4: 41,428,691 (GRCm39) |
F90L |
probably benign |
Het |
Klhl20 |
A |
T |
1: 160,923,231 (GRCm39) |
C497* |
probably null |
Het |
Loxl1 |
C |
A |
9: 58,219,224 (GRCm39) |
A316S |
probably benign |
Het |
Lrig3 |
C |
T |
10: 125,845,950 (GRCm39) |
P793L |
possibly damaging |
Het |
Macc1 |
A |
G |
12: 119,410,561 (GRCm39) |
D443G |
probably benign |
Het |
Maip1 |
A |
T |
1: 57,446,311 (GRCm39) |
Y127F |
possibly damaging |
Het |
Mrm2 |
A |
T |
5: 140,314,427 (GRCm39) |
F136Y |
probably benign |
Het |
Nasp |
G |
T |
4: 116,468,017 (GRCm39) |
L323I |
probably benign |
Het |
Ndufb8 |
A |
T |
19: 44,538,823 (GRCm39) |
L166Q |
probably damaging |
Het |
Nid2 |
C |
T |
14: 19,858,009 (GRCm39) |
T1274I |
|
Het |
Nup210 |
T |
A |
6: 91,066,872 (GRCm39) |
T160S |
probably benign |
Het |
Nutm2 |
A |
G |
13: 50,628,964 (GRCm39) |
K676R |
probably damaging |
Het |
Odad1 |
G |
A |
7: 45,596,965 (GRCm39) |
V431I |
possibly damaging |
Het |
Or10a3n |
T |
C |
7: 108,493,609 (GRCm39) |
R7G |
probably benign |
Het |
Or2a20 |
A |
G |
6: 43,194,500 (GRCm39) |
T218A |
probably benign |
Het |
Or56b1b |
A |
T |
7: 108,164,454 (GRCm39) |
C183S |
probably damaging |
Het |
Or5ak20 |
T |
A |
2: 85,183,852 (GRCm39) |
R139S |
probably benign |
Het |
Or7g33 |
A |
G |
9: 19,448,914 (GRCm39) |
V104A |
probably benign |
Het |
Or8b9 |
A |
T |
9: 37,766,294 (GRCm39) |
Y60F |
probably damaging |
Het |
Or9m1 |
A |
T |
2: 87,733,480 (GRCm39) |
I180N |
probably benign |
Het |
Pcdhga12 |
C |
A |
18: 37,899,931 (GRCm39) |
N254K |
possibly damaging |
Het |
Pm20d1 |
G |
T |
1: 131,743,753 (GRCm39) |
V473F |
probably benign |
Het |
Pou2af2 |
G |
A |
9: 51,201,516 (GRCm39) |
P180L |
possibly damaging |
Het |
Rab11fip1 |
A |
G |
8: 27,633,355 (GRCm39) |
V596A |
probably damaging |
Het |
Rapgef6 |
C |
T |
11: 54,487,912 (GRCm39) |
Q13* |
probably null |
Het |
Rasef |
T |
C |
4: 73,698,583 (GRCm39) |
D26G |
probably benign |
Het |
Rbfox2 |
A |
T |
15: 77,190,658 (GRCm39) |
V29E |
probably benign |
Het |
Recql4 |
G |
A |
15: 76,589,685 (GRCm39) |
P787S |
unknown |
Het |
Rnf19a |
A |
C |
15: 36,253,450 (GRCm39) |
|
probably benign |
Het |
Rnf214 |
A |
G |
9: 45,811,054 (GRCm39) |
I203T |
probably damaging |
Het |
Rnmt |
A |
C |
18: 68,451,146 (GRCm39) |
E396D |
probably benign |
Het |
Scn4a |
G |
A |
11: 106,210,638 (GRCm39) |
S1793L |
probably benign |
Het |
Sdcbp |
G |
T |
4: 6,386,709 (GRCm39) |
|
probably null |
Het |
Slfn3 |
A |
G |
11: 83,103,948 (GRCm39) |
N273S |
probably damaging |
Het |
Slk |
A |
G |
19: 47,603,883 (GRCm39) |
D209G |
|
Het |
Tent5b |
A |
G |
4: 133,214,352 (GRCm39) |
T408A |
probably damaging |
Het |
Tmem135 |
T |
A |
7: 88,797,204 (GRCm39) |
M351L |
probably benign |
Het |
Tmem64 |
A |
G |
4: 15,266,391 (GRCm39) |
H147R |
probably benign |
Het |
Tnfsf4 |
T |
C |
1: 161,244,629 (GRCm39) |
L106P |
probably damaging |
Het |
Tonsl |
A |
T |
15: 76,515,270 (GRCm39) |
C1039S |
probably damaging |
Het |
Ube4a |
A |
T |
9: 44,864,462 (GRCm39) |
F44I |
possibly damaging |
Het |
Vmn2r40 |
A |
G |
7: 8,911,172 (GRCm39) |
L707P |
|
Het |
Vmn2r87 |
G |
A |
10: 130,308,165 (GRCm39) |
T691I |
probably benign |
Het |
Wbp11 |
A |
T |
6: 136,803,044 (GRCm39) |
S7T |
possibly damaging |
Het |
Zfp386 |
C |
A |
12: 116,023,878 (GRCm39) |
S532* |
probably null |
Het |
|
Other mutations in Clca3a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00419:Clca3a2
|
APN |
3 |
144,804,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01019:Clca3a2
|
APN |
3 |
144,519,388 (GRCm39) |
nonsense |
probably null |
|
IGL01337:Clca3a2
|
APN |
3 |
144,800,939 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01389:Clca3a2
|
APN |
3 |
144,783,629 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01595:Clca3a2
|
APN |
3 |
144,793,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01663:Clca3a2
|
APN |
3 |
144,522,916 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01704:Clca3a2
|
APN |
3 |
144,800,979 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01779:Clca3a2
|
APN |
3 |
144,525,139 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02066:Clca3a2
|
APN |
3 |
144,519,216 (GRCm39) |
missense |
probably benign |
|
IGL02301:Clca3a2
|
APN |
3 |
144,512,133 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02416:Clca3a2
|
APN |
3 |
144,790,777 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02455:Clca3a2
|
APN |
3 |
144,787,172 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02481:Clca3a2
|
APN |
3 |
144,790,701 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02526:Clca3a2
|
APN |
3 |
144,793,779 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02619:Clca3a2
|
APN |
3 |
144,512,083 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02797:Clca3a2
|
APN |
3 |
144,787,024 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02852:Clca3a2
|
APN |
3 |
144,512,104 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02901:Clca3a2
|
APN |
3 |
144,522,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03162:Clca3a2
|
APN |
3 |
144,512,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03253:Clca3a2
|
APN |
3 |
144,777,324 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03256:Clca3a2
|
APN |
3 |
144,792,153 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03294:Clca3a2
|
APN |
3 |
144,803,530 (GRCm39) |
missense |
probably damaging |
1.00 |
3370:Clca3a2
|
UTSW |
3 |
144,783,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:Clca3a2
|
UTSW |
3 |
144,522,494 (GRCm39) |
missense |
probably benign |
0.01 |
R0244:Clca3a2
|
UTSW |
3 |
144,519,659 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0479:Clca3a2
|
UTSW |
3 |
144,796,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Clca3a2
|
UTSW |
3 |
144,781,571 (GRCm39) |
splice site |
probably benign |
|
R0629:Clca3a2
|
UTSW |
3 |
144,778,000 (GRCm39) |
missense |
probably benign |
|
R1249:Clca3a2
|
UTSW |
3 |
144,508,765 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1370:Clca3a2
|
UTSW |
3 |
144,519,624 (GRCm39) |
splice site |
probably benign |
|
R1488:Clca3a2
|
UTSW |
3 |
144,789,925 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1523:Clca3a2
|
UTSW |
3 |
144,777,405 (GRCm39) |
nonsense |
probably null |
|
R1568:Clca3a2
|
UTSW |
3 |
144,781,410 (GRCm39) |
nonsense |
probably null |
|
R1586:Clca3a2
|
UTSW |
3 |
144,516,477 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1650:Clca3a2
|
UTSW |
3 |
144,797,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Clca3a2
|
UTSW |
3 |
144,787,171 (GRCm39) |
missense |
probably benign |
0.12 |
R1776:Clca3a2
|
UTSW |
3 |
144,519,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R1797:Clca3a2
|
UTSW |
3 |
144,503,398 (GRCm39) |
missense |
probably benign |
0.01 |
R1869:Clca3a2
|
UTSW |
3 |
144,512,164 (GRCm39) |
missense |
probably benign |
0.44 |
R1871:Clca3a2
|
UTSW |
3 |
144,503,398 (GRCm39) |
missense |
probably benign |
0.01 |
R1919:Clca3a2
|
UTSW |
3 |
144,516,457 (GRCm39) |
missense |
probably benign |
|
R1923:Clca3a2
|
UTSW |
3 |
144,511,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Clca3a2
|
UTSW |
3 |
144,783,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R2200:Clca3a2
|
UTSW |
3 |
144,519,685 (GRCm39) |
missense |
probably benign |
0.10 |
R2242:Clca3a2
|
UTSW |
3 |
144,796,551 (GRCm39) |
missense |
probably damaging |
0.98 |
R2324:Clca3a2
|
UTSW |
3 |
144,512,041 (GRCm39) |
critical splice donor site |
probably null |
|
R2937:Clca3a2
|
UTSW |
3 |
144,519,679 (GRCm39) |
missense |
probably benign |
0.06 |
R3429:Clca3a2
|
UTSW |
3 |
144,512,088 (GRCm39) |
missense |
probably benign |
0.07 |
R3434:Clca3a2
|
UTSW |
3 |
144,514,522 (GRCm39) |
unclassified |
probably benign |
|
R3551:Clca3a2
|
UTSW |
3 |
144,508,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R3751:Clca3a2
|
UTSW |
3 |
144,777,216 (GRCm39) |
missense |
probably benign |
0.04 |
R3952:Clca3a2
|
UTSW |
3 |
144,508,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Clca3a2
|
UTSW |
3 |
144,516,613 (GRCm39) |
missense |
probably benign |
0.25 |
R4383:Clca3a2
|
UTSW |
3 |
144,512,081 (GRCm39) |
missense |
probably benign |
0.02 |
R4496:Clca3a2
|
UTSW |
3 |
144,797,926 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4518:Clca3a2
|
UTSW |
3 |
144,514,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4598:Clca3a2
|
UTSW |
3 |
144,511,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Clca3a2
|
UTSW |
3 |
144,513,112 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4802:Clca3a2
|
UTSW |
3 |
144,513,112 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4816:Clca3a2
|
UTSW |
3 |
144,516,613 (GRCm39) |
missense |
probably benign |
0.25 |
R4934:Clca3a2
|
UTSW |
3 |
144,523,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Clca3a2
|
UTSW |
3 |
144,512,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Clca3a2
|
UTSW |
3 |
144,783,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Clca3a2
|
UTSW |
3 |
144,512,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Clca3a2
|
UTSW |
3 |
144,511,599 (GRCm39) |
missense |
probably benign |
0.26 |
R5275:Clca3a2
|
UTSW |
3 |
144,519,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Clca3a2
|
UTSW |
3 |
144,793,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Clca3a2
|
UTSW |
3 |
144,503,286 (GRCm39) |
missense |
probably benign |
0.00 |
R5424:Clca3a2
|
UTSW |
3 |
144,789,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R5656:Clca3a2
|
UTSW |
3 |
144,503,393 (GRCm39) |
missense |
probably benign |
0.26 |
R5931:Clca3a2
|
UTSW |
3 |
144,797,886 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6059:Clca3a2
|
UTSW |
3 |
144,516,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Clca3a2
|
UTSW |
3 |
144,525,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R6181:Clca3a2
|
UTSW |
3 |
144,796,469 (GRCm39) |
nonsense |
probably null |
|
R6254:Clca3a2
|
UTSW |
3 |
144,507,895 (GRCm39) |
missense |
probably benign |
|
R6336:Clca3a2
|
UTSW |
3 |
144,512,239 (GRCm39) |
missense |
probably benign |
|
R6470:Clca3a2
|
UTSW |
3 |
144,510,024 (GRCm39) |
splice site |
probably null |
|
R6593:Clca3a2
|
UTSW |
3 |
144,514,338 (GRCm39) |
critical splice donor site |
probably null |
|
R6598:Clca3a2
|
UTSW |
3 |
144,792,246 (GRCm39) |
nonsense |
probably null |
|
R6631:Clca3a2
|
UTSW |
3 |
144,519,405 (GRCm39) |
missense |
probably benign |
|
R6826:Clca3a2
|
UTSW |
3 |
144,523,815 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6836:Clca3a2
|
UTSW |
3 |
144,512,144 (GRCm39) |
missense |
probably damaging |
0.97 |
R6896:Clca3a2
|
UTSW |
3 |
144,514,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167:Clca3a2
|
UTSW |
3 |
144,803,545 (GRCm39) |
missense |
probably benign |
0.40 |
R7211:Clca3a2
|
UTSW |
3 |
144,519,775 (GRCm39) |
missense |
probably benign |
0.00 |
R7229:Clca3a2
|
UTSW |
3 |
144,789,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R7256:Clca3a2
|
UTSW |
3 |
144,796,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R7324:Clca3a2
|
UTSW |
3 |
144,514,372 (GRCm39) |
missense |
probably damaging |
0.99 |
R7365:Clca3a2
|
UTSW |
3 |
144,804,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R7411:Clca3a2
|
UTSW |
3 |
144,507,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Clca3a2
|
UTSW |
3 |
144,503,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Clca3a2
|
UTSW |
3 |
144,519,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R7521:Clca3a2
|
UTSW |
3 |
144,507,674 (GRCm39) |
makesense |
probably null |
|
R7813:Clca3a2
|
UTSW |
3 |
144,790,726 (GRCm39) |
missense |
probably benign |
0.26 |
R7889:Clca3a2
|
UTSW |
3 |
144,516,574 (GRCm39) |
nonsense |
probably null |
|
R7946:Clca3a2
|
UTSW |
3 |
144,513,075 (GRCm39) |
critical splice donor site |
probably null |
|
R7991:Clca3a2
|
UTSW |
3 |
144,519,756 (GRCm39) |
missense |
probably benign |
0.00 |
R8022:Clca3a2
|
UTSW |
3 |
144,511,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8077:Clca3a2
|
UTSW |
3 |
144,777,288 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8169:Clca3a2
|
UTSW |
3 |
144,783,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Clca3a2
|
UTSW |
3 |
144,793,719 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8300:Clca3a2
|
UTSW |
3 |
144,804,692 (GRCm39) |
missense |
probably benign |
0.00 |
R8344:Clca3a2
|
UTSW |
3 |
144,511,703 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8350:Clca3a2
|
UTSW |
3 |
144,783,668 (GRCm39) |
missense |
probably benign |
0.19 |
R8367:Clca3a2
|
UTSW |
3 |
144,523,508 (GRCm39) |
splice site |
probably null |
|
R8371:Clca3a2
|
UTSW |
3 |
144,513,114 (GRCm39) |
nonsense |
probably null |
|
R8814:Clca3a2
|
UTSW |
3 |
144,503,525 (GRCm39) |
missense |
probably benign |
0.18 |
R8854:Clca3a2
|
UTSW |
3 |
144,783,852 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8876:Clca3a2
|
UTSW |
3 |
144,777,360 (GRCm39) |
missense |
probably benign |
0.00 |
R8887:Clca3a2
|
UTSW |
3 |
144,790,810 (GRCm39) |
nonsense |
probably null |
|
R9006:Clca3a2
|
UTSW |
3 |
144,783,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R9031:Clca3a2
|
UTSW |
3 |
144,511,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Clca3a2
|
UTSW |
3 |
144,519,447 (GRCm39) |
splice site |
probably benign |
|
R9190:Clca3a2
|
UTSW |
3 |
144,796,599 (GRCm39) |
missense |
probably benign |
0.00 |
R9201:Clca3a2
|
UTSW |
3 |
144,519,684 (GRCm39) |
missense |
probably benign |
0.00 |
R9209:Clca3a2
|
UTSW |
3 |
144,778,005 (GRCm39) |
missense |
probably benign |
0.00 |
R9261:Clca3a2
|
UTSW |
3 |
144,525,158 (GRCm39) |
missense |
probably benign |
|
R9469:Clca3a2
|
UTSW |
3 |
144,507,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Clca3a2
|
UTSW |
3 |
144,777,322 (GRCm39) |
nonsense |
probably null |
|
R9515:Clca3a2
|
UTSW |
3 |
144,508,808 (GRCm39) |
nonsense |
probably null |
|
R9569:Clca3a2
|
UTSW |
3 |
144,513,075 (GRCm39) |
critical splice donor site |
probably null |
|
R9664:Clca3a2
|
UTSW |
3 |
144,503,575 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Clca3a2
|
UTSW |
3 |
144,792,265 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1177:Clca3a2
|
UTSW |
3 |
144,792,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|