Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
T |
C |
7: 45,639,111 (GRCm39) |
Y944C |
probably damaging |
Het |
Acacb |
T |
C |
5: 114,370,999 (GRCm39) |
V1747A |
probably benign |
Het |
Acad8 |
C |
T |
9: 26,889,698 (GRCm39) |
R332H |
probably damaging |
Het |
Acrbp |
A |
C |
6: 125,027,501 (GRCm39) |
T50P |
probably damaging |
Het |
Ahctf1 |
G |
T |
1: 179,583,077 (GRCm39) |
N1500K |
probably benign |
Het |
Aoc1l3 |
A |
G |
6: 48,964,651 (GRCm39) |
T220A |
possibly damaging |
Het |
Arfgef1 |
A |
G |
1: 10,229,798 (GRCm39) |
I1301T |
possibly damaging |
Het |
Arhgef15 |
T |
C |
11: 68,842,171 (GRCm39) |
S478G |
probably benign |
Het |
Armh1 |
T |
C |
4: 117,094,977 (GRCm39) |
D21G |
probably damaging |
Het |
Atp13a4 |
A |
T |
16: 29,227,779 (GRCm39) |
L1045* |
probably null |
Het |
Atp2a3 |
T |
A |
11: 72,873,506 (GRCm39) |
L793H |
probably damaging |
Het |
B4galnt4 |
C |
A |
7: 140,648,173 (GRCm39) |
P563Q |
probably benign |
Het |
Bcl2a1b |
A |
T |
9: 89,081,713 (GRCm39) |
K94* |
probably null |
Het |
Bod1 |
T |
A |
11: 31,616,853 (GRCm39) |
Q136L |
possibly damaging |
Het |
C2cd3 |
A |
G |
7: 100,055,166 (GRCm39) |
K443R |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,411,588 (GRCm38) |
V1250A |
possibly damaging |
Het |
Car12 |
T |
A |
9: 66,671,600 (GRCm39) |
Y332* |
probably null |
Het |
Ccdc186 |
A |
T |
19: 56,790,432 (GRCm39) |
|
probably null |
Het |
Cdh6 |
T |
C |
15: 13,034,774 (GRCm39) |
T629A |
probably damaging |
Het |
Cep112 |
T |
A |
11: 108,397,471 (GRCm39) |
D353E |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,428,301 (GRCm39) |
S777G |
probably benign |
Het |
Clec4b2 |
A |
C |
6: 123,181,163 (GRCm39) |
K183Q |
probably benign |
Het |
Cngb3 |
T |
C |
4: 19,395,926 (GRCm39) |
Y323H |
probably benign |
Het |
Cnp |
G |
T |
11: 100,467,202 (GRCm39) |
E48D |
probably benign |
Het |
Ctrb1 |
T |
A |
8: 112,413,783 (GRCm39) |
I194F |
probably benign |
Het |
Cyp2d11 |
T |
A |
15: 82,275,224 (GRCm39) |
D241V |
probably benign |
Het |
D5Ertd579e |
T |
A |
5: 36,772,285 (GRCm39) |
E703D |
probably damaging |
Het |
Dlg1 |
T |
C |
16: 31,676,764 (GRCm39) |
V731A |
probably damaging |
Het |
Dlgap5 |
T |
C |
14: 47,651,276 (GRCm39) |
S86G |
probably benign |
Het |
Dock3 |
A |
G |
9: 106,807,266 (GRCm39) |
F1354L |
probably damaging |
Het |
Dock3 |
C |
A |
9: 106,870,171 (GRCm39) |
V638F |
possibly damaging |
Het |
Eif3c |
A |
T |
7: 126,156,626 (GRCm39) |
M407K |
probably benign |
Het |
Eif4a3l1 |
A |
T |
6: 136,305,737 (GRCm39) |
Q66L |
possibly damaging |
Het |
Epha4 |
T |
A |
1: 77,366,712 (GRCm39) |
K578* |
probably null |
Het |
Erc2 |
C |
T |
14: 27,375,285 (GRCm39) |
L168F |
probably damaging |
Het |
Esyt2 |
A |
G |
12: 116,305,708 (GRCm39) |
I313V |
probably benign |
Het |
Far1 |
T |
A |
7: 113,167,432 (GRCm39) |
Y506N |
probably damaging |
Het |
Fbxw26 |
T |
A |
9: 109,547,037 (GRCm39) |
N463Y |
possibly damaging |
Het |
Fgg |
A |
G |
3: 82,915,847 (GRCm39) |
D96G |
probably benign |
Het |
Gfer |
A |
G |
17: 24,914,274 (GRCm39) |
S130P |
probably damaging |
Het |
Hdac10 |
A |
T |
15: 89,012,650 (GRCm39) |
M1K |
probably null |
Het |
Hsd3b1 |
A |
T |
3: 98,760,642 (GRCm39) |
S110R |
probably benign |
Het |
Ints15 |
A |
G |
5: 143,287,592 (GRCm39) |
S438P |
probably benign |
Het |
Itga6 |
T |
C |
2: 71,668,717 (GRCm39) |
L552P |
possibly damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Llgl1 |
C |
T |
11: 60,600,394 (GRCm39) |
P581L |
probably benign |
Het |
Lrrc8b |
A |
T |
5: 105,628,080 (GRCm39) |
Y142F |
probably benign |
Het |
Lyz2 |
T |
A |
10: 117,114,614 (GRCm39) |
D105V |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,460,035 (GRCm39) |
D76G |
probably damaging |
Het |
Map7d1 |
T |
C |
4: 126,127,018 (GRCm39) |
K731E |
unknown |
Het |
Mgam |
A |
C |
6: 40,619,988 (GRCm39) |
I26L |
probably benign |
Het |
Mmp13 |
A |
T |
9: 7,272,953 (GRCm39) |
E104D |
probably benign |
Het |
Morc2a |
C |
T |
11: 3,626,664 (GRCm39) |
R241* |
probably null |
Het |
Mtfmt |
C |
A |
9: 65,359,386 (GRCm39) |
H354N |
probably benign |
Het |
Myh3 |
T |
C |
11: 66,990,233 (GRCm39) |
I1626T |
probably benign |
Het |
Ndst1 |
A |
T |
18: 60,825,059 (GRCm39) |
V753D |
probably benign |
Het |
Neurl4 |
A |
G |
11: 69,793,997 (GRCm39) |
D151G |
probably damaging |
Het |
Nlrx1 |
T |
C |
9: 44,168,194 (GRCm39) |
S568G |
probably benign |
Het |
Or10g3b |
G |
C |
14: 52,586,999 (GRCm39) |
P168R |
probably damaging |
Het |
Or2t45 |
T |
C |
11: 58,669,132 (GRCm39) |
Y60H |
possibly damaging |
Het |
Or2t46 |
T |
G |
11: 58,472,546 (GRCm39) |
L292R |
probably damaging |
Het |
Or4c52 |
T |
C |
2: 89,845,762 (GRCm39) |
F163L |
probably damaging |
Het |
Or52s1 |
A |
G |
7: 102,861,747 (GRCm39) |
I216V |
probably damaging |
Het |
Or6c66 |
A |
T |
10: 129,461,468 (GRCm39) |
I154N |
probably benign |
Het |
Or8b42 |
A |
T |
9: 38,342,111 (GRCm39) |
M178L |
probably benign |
Het |
Osbpl7 |
A |
G |
11: 96,950,976 (GRCm39) |
I608V |
probably damaging |
Het |
Pard3b |
T |
C |
1: 61,807,159 (GRCm39) |
I58T |
probably damaging |
Het |
Pcare |
A |
G |
17: 72,058,066 (GRCm39) |
M537T |
probably damaging |
Het |
Pcdhga1 |
A |
C |
18: 37,795,407 (GRCm39) |
E137A |
possibly damaging |
Het |
Pde6c |
G |
A |
19: 38,139,072 (GRCm39) |
V301I |
possibly damaging |
Het |
Pdia5 |
G |
C |
16: 35,230,786 (GRCm39) |
N338K |
possibly damaging |
Het |
Pex11g |
T |
C |
8: 3,514,042 (GRCm39) |
Y40C |
probably damaging |
Het |
Plekhg3 |
A |
G |
12: 76,610,899 (GRCm39) |
Y183C |
probably damaging |
Het |
Pole |
A |
C |
5: 110,438,090 (GRCm39) |
|
probably null |
Het |
Ppfia1 |
A |
G |
7: 144,045,313 (GRCm39) |
L948P |
probably damaging |
Het |
Prdm2 |
A |
T |
4: 142,860,761 (GRCm39) |
V843E |
probably damaging |
Het |
Prss56 |
C |
A |
1: 87,115,708 (GRCm39) |
F527L |
probably damaging |
Het |
Psmd11 |
T |
C |
11: 80,329,146 (GRCm39) |
L88P |
probably damaging |
Het |
Ptx3 |
G |
C |
3: 66,132,412 (GRCm39) |
G311A |
probably damaging |
Het |
Rars1 |
A |
T |
11: 35,699,385 (GRCm39) |
L636H |
probably damaging |
Het |
Rnft2 |
A |
G |
5: 118,375,507 (GRCm39) |
S81P |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Rxra |
T |
A |
2: 27,631,195 (GRCm39) |
I142N |
probably damaging |
Het |
Scin |
T |
C |
12: 40,154,931 (GRCm39) |
M221V |
probably benign |
Het |
Sfmbt2 |
G |
A |
2: 10,584,069 (GRCm39) |
V809I |
possibly damaging |
Het |
Sirt1 |
T |
A |
10: 63,157,783 (GRCm39) |
I505F |
probably benign |
Het |
Six5 |
T |
C |
7: 18,829,096 (GRCm39) |
Y179H |
probably damaging |
Het |
Slc12a4 |
A |
C |
8: 106,671,241 (GRCm39) |
M982R |
probably damaging |
Het |
Slco4c1 |
T |
A |
1: 96,765,237 (GRCm39) |
L404F |
probably damaging |
Het |
Smn1 |
T |
C |
13: 100,268,931 (GRCm39) |
L259P |
probably damaging |
Het |
Sorl1 |
T |
G |
9: 41,952,935 (GRCm39) |
D702A |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,065,400 (GRCm39) |
E1983G |
possibly damaging |
Het |
Srsf1 |
T |
A |
11: 87,940,788 (GRCm39) |
|
probably null |
Het |
Stard9 |
C |
T |
2: 120,536,900 (GRCm39) |
R4224* |
probably null |
Het |
Sybu |
T |
G |
15: 44,538,895 (GRCm39) |
M383L |
probably benign |
Het |
Tbx15 |
A |
C |
3: 99,259,583 (GRCm39) |
N485H |
possibly damaging |
Het |
Tcerg1l |
A |
T |
7: 137,819,786 (GRCm39) |
F485I |
probably damaging |
Het |
Tdrd7 |
C |
A |
4: 46,005,616 (GRCm39) |
T474N |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,755,470 (GRCm39) |
|
probably null |
Het |
Tnik |
A |
T |
3: 28,704,235 (GRCm39) |
I1020F |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,914,566 (GRCm39) |
D1884G |
possibly damaging |
Het |
Tprn |
T |
C |
2: 25,158,845 (GRCm39) |
M623T |
probably damaging |
Het |
Trdn |
T |
A |
10: 33,350,413 (GRCm39) |
Y661N |
probably damaging |
Het |
Ttc41 |
T |
C |
10: 86,612,056 (GRCm39) |
S1110P |
possibly damaging |
Het |
Ttc6 |
A |
C |
12: 57,707,026 (GRCm39) |
R644S |
probably benign |
Het |
Ttyh1 |
A |
T |
7: 4,136,735 (GRCm39) |
M448L |
probably benign |
Het |
Unc79 |
G |
T |
12: 103,128,079 (GRCm39) |
C2250F |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,358,805 (GRCm39) |
I2110M |
probably benign |
Het |
Uvssa |
G |
T |
5: 33,571,257 (GRCm39) |
E634* |
probably null |
Het |
Vac14 |
A |
C |
8: 111,372,440 (GRCm39) |
T384P |
probably benign |
Het |
Wdr11 |
A |
G |
7: 129,235,445 (GRCm39) |
E1169G |
probably benign |
Het |
Zfp36l1 |
T |
A |
12: 80,157,298 (GRCm39) |
T28S |
probably benign |
Het |
Zfp715 |
A |
T |
7: 42,949,106 (GRCm39) |
Y285N |
possibly damaging |
Het |
Zfp91 |
A |
T |
19: 12,747,424 (GRCm39) |
D566E |
probably damaging |
Het |
Zgrf1 |
G |
A |
3: 127,396,085 (GRCm39) |
V544M |
probably damaging |
Het |
|
Other mutations in Lrrc8a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00693:Lrrc8a
|
APN |
2 |
30,145,327 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01161:Lrrc8a
|
APN |
2 |
30,145,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Lrrc8a
|
APN |
2 |
30,147,111 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01757:Lrrc8a
|
APN |
2 |
30,145,537 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02390:Lrrc8a
|
APN |
2 |
30,146,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Lrrc8a
|
APN |
2 |
30,146,311 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02938:Lrrc8a
|
APN |
2 |
30,145,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02960:Lrrc8a
|
APN |
2 |
30,147,025 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03139:Lrrc8a
|
APN |
2 |
30,145,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03166:Lrrc8a
|
APN |
2 |
30,145,377 (GRCm39) |
missense |
probably benign |
|
R0033:Lrrc8a
|
UTSW |
2 |
30,145,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Lrrc8a
|
UTSW |
2 |
30,145,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Lrrc8a
|
UTSW |
2 |
30,146,800 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0432:Lrrc8a
|
UTSW |
2 |
30,147,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R0751:Lrrc8a
|
UTSW |
2 |
30,146,362 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1924:Lrrc8a
|
UTSW |
2 |
30,145,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Lrrc8a
|
UTSW |
2 |
30,146,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R3852:Lrrc8a
|
UTSW |
2 |
30,151,972 (GRCm39) |
missense |
probably benign |
0.30 |
R5175:Lrrc8a
|
UTSW |
2 |
30,145,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R5616:Lrrc8a
|
UTSW |
2 |
30,145,366 (GRCm39) |
missense |
probably benign |
0.09 |
R5874:Lrrc8a
|
UTSW |
2 |
30,147,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6228:Lrrc8a
|
UTSW |
2 |
30,146,565 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6406:Lrrc8a
|
UTSW |
2 |
30,147,103 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6456:Lrrc8a
|
UTSW |
2 |
30,145,486 (GRCm39) |
missense |
probably benign |
0.14 |
R6833:Lrrc8a
|
UTSW |
2 |
30,145,659 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6834:Lrrc8a
|
UTSW |
2 |
30,145,659 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6945:Lrrc8a
|
UTSW |
2 |
30,146,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R7675:Lrrc8a
|
UTSW |
2 |
30,145,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Lrrc8a
|
UTSW |
2 |
30,146,208 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8528:Lrrc8a
|
UTSW |
2 |
30,145,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Lrrc8a
|
UTSW |
2 |
30,146,619 (GRCm39) |
missense |
probably benign |
0.12 |
R8879:Lrrc8a
|
UTSW |
2 |
30,146,310 (GRCm39) |
missense |
probably benign |
0.16 |
R9112:Lrrc8a
|
UTSW |
2 |
30,145,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R9130:Lrrc8a
|
UTSW |
2 |
30,147,042 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9456:Lrrc8a
|
UTSW |
2 |
30,145,663 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lrrc8a
|
UTSW |
2 |
30,146,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|