Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
T |
A |
8: 120,878,279 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
C |
T |
1: 179,581,171 (GRCm39) |
S1677N |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,728,025 (GRCm39) |
|
probably benign |
Het |
Arid3c |
A |
T |
4: 41,729,925 (GRCm39) |
I90N |
probably benign |
Het |
Asb1 |
C |
A |
1: 91,480,205 (GRCm39) |
D301E |
unknown |
Het |
Asb1 |
T |
G |
1: 91,480,206 (GRCm39) |
*302G |
probably null |
Het |
Birc2 |
A |
T |
9: 7,833,937 (GRCm39) |
F181L |
probably benign |
Het |
Bnip1 |
T |
A |
17: 27,001,590 (GRCm39) |
|
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
T |
C |
17: 43,116,135 (GRCm39) |
D575G |
possibly damaging |
Het |
Cdca7 |
T |
A |
2: 72,314,273 (GRCm39) |
H248Q |
probably damaging |
Het |
Chd2 |
T |
C |
7: 73,140,402 (GRCm39) |
I609V |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,143,192 (GRCm39) |
D567G |
probably benign |
Het |
Cnmd |
T |
A |
14: 79,894,085 (GRCm39) |
T101S |
probably damaging |
Het |
Col6a4 |
T |
C |
9: 105,954,404 (GRCm39) |
T312A |
probably benign |
Het |
Cript |
C |
A |
17: 87,338,475 (GRCm39) |
T41N |
probably damaging |
Het |
Cts6 |
T |
C |
13: 61,344,261 (GRCm39) |
I264V |
probably benign |
Het |
Cyp4a32 |
C |
T |
4: 115,467,802 (GRCm39) |
T262I |
probably null |
Het |
D430041D05Rik |
T |
A |
2: 104,240,521 (GRCm39) |
|
probably benign |
Het |
Dctd |
C |
T |
8: 48,564,712 (GRCm39) |
P5S |
probably benign |
Het |
Det1 |
T |
C |
7: 78,492,984 (GRCm39) |
N340S |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,262,232 (GRCm39) |
N2032D |
probably benign |
Het |
Dscam |
T |
A |
16: 96,840,116 (GRCm39) |
T164S |
probably benign |
Het |
Emcn |
T |
C |
3: 137,124,775 (GRCm39) |
V196A |
possibly damaging |
Het |
Fbxo32 |
A |
G |
15: 58,046,358 (GRCm39) |
I284T |
possibly damaging |
Het |
Gimap3 |
C |
A |
6: 48,742,094 (GRCm39) |
D279Y |
possibly damaging |
Het |
Gm43302 |
C |
T |
5: 105,427,974 (GRCm39) |
D196N |
probably benign |
Het |
Gpc6 |
C |
A |
14: 117,424,217 (GRCm39) |
H102N |
possibly damaging |
Het |
Gpr158 |
A |
T |
2: 21,581,760 (GRCm39) |
D413V |
probably damaging |
Het |
Ifi207 |
T |
C |
1: 173,555,382 (GRCm39) |
R767G |
probably damaging |
Het |
Kcnip2 |
T |
C |
19: 45,800,634 (GRCm39) |
|
probably benign |
Het |
Kifap3 |
A |
C |
1: 163,696,291 (GRCm39) |
D640A |
probably damaging |
Het |
Lmbrd2 |
A |
T |
15: 9,157,311 (GRCm39) |
Q183L |
possibly damaging |
Het |
Malt1 |
A |
G |
18: 65,577,911 (GRCm39) |
I135V |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,057,109 (GRCm39) |
V528A |
probably damaging |
Het |
Mllt10 |
T |
C |
2: 18,167,163 (GRCm39) |
S363P |
probably damaging |
Het |
Mrnip |
A |
G |
11: 50,073,323 (GRCm39) |
Y44C |
probably damaging |
Het |
Mstn |
C |
T |
1: 53,103,131 (GRCm39) |
Q156* |
probably null |
Het |
Mtmr7 |
T |
C |
8: 41,008,904 (GRCm39) |
D469G |
possibly damaging |
Het |
Muc6 |
A |
G |
7: 141,217,018 (GRCm39) |
S2552P |
possibly damaging |
Het |
Myo1f |
C |
A |
17: 33,823,662 (GRCm39) |
N1063K |
probably benign |
Het |
Or52k2 |
T |
A |
7: 102,253,642 (GRCm39) |
I27N |
probably benign |
Het |
Or5af1 |
A |
T |
11: 58,722,280 (GRCm39) |
Y100F |
probably benign |
Het |
Or6z5 |
G |
A |
7: 6,477,399 (GRCm39) |
V97M |
probably benign |
Het |
Orai2 |
A |
G |
5: 136,179,430 (GRCm39) |
V201A |
possibly damaging |
Het |
Pcdhga6 |
A |
T |
18: 37,841,878 (GRCm39) |
T533S |
possibly damaging |
Het |
Pkd1l1 |
T |
A |
11: 8,881,552 (GRCm39) |
K907N |
|
Het |
Plaat5 |
G |
T |
19: 7,614,823 (GRCm39) |
M228I |
probably benign |
Het |
Ppp1r15a |
A |
T |
7: 45,174,049 (GRCm39) |
V253E |
probably benign |
Het |
Ppp1r9b |
A |
G |
11: 94,887,467 (GRCm39) |
E493G |
probably benign |
Het |
Prdm1 |
T |
C |
10: 44,322,997 (GRCm39) |
N151S |
probably benign |
Het |
Prkcd |
C |
T |
14: 30,329,297 (GRCm39) |
A163T |
probably damaging |
Het |
Prl7a2 |
T |
A |
13: 27,849,994 (GRCm39) |
E26V |
probably damaging |
Het |
Ptprm |
A |
T |
17: 66,996,354 (GRCm39) |
N1278K |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,001,653 (GRCm39) |
S1248T |
possibly damaging |
Het |
Scn9a |
T |
C |
2: 66,338,927 (GRCm39) |
I1186M |
probably damaging |
Het |
Sv2a |
T |
C |
3: 96,094,409 (GRCm39) |
F248S |
probably benign |
Het |
Tas2r116 |
T |
A |
6: 132,832,963 (GRCm39) |
I188K |
probably damaging |
Het |
Tcf21 |
T |
C |
10: 22,693,671 (GRCm39) |
T169A |
probably benign |
Het |
Tecrl |
C |
A |
5: 83,432,121 (GRCm39) |
C258F |
probably damaging |
Het |
Tet2 |
T |
A |
3: 133,193,360 (GRCm39) |
E358V |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,759,203 (GRCm39) |
S219T |
possibly damaging |
Het |
Tpgs2 |
T |
A |
18: 25,301,777 (GRCm39) |
|
probably benign |
Het |
Vmn1r160 |
T |
C |
7: 22,571,127 (GRCm39) |
V160A |
possibly damaging |
Het |
Vmn1r44 |
T |
C |
6: 89,870,671 (GRCm39) |
L139P |
probably damaging |
Het |
|
Other mutations in Ttc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03278:Ttc6
|
APN |
12 |
57,668,812 (GRCm39) |
missense |
probably damaging |
0.99 |
polonius
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
tybalt
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02802:Ttc6
|
UTSW |
12 |
57,622,654 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4802001:Ttc6
|
UTSW |
12 |
57,772,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0698:Ttc6
|
UTSW |
12 |
57,720,002 (GRCm39) |
missense |
probably benign |
0.04 |
R0988:Ttc6
|
UTSW |
12 |
57,735,435 (GRCm39) |
splice site |
probably benign |
|
R1290:Ttc6
|
UTSW |
12 |
57,707,199 (GRCm39) |
missense |
probably benign |
0.00 |
R1338:Ttc6
|
UTSW |
12 |
57,663,155 (GRCm39) |
missense |
probably benign |
0.10 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1481:Ttc6
|
UTSW |
12 |
57,783,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Ttc6
|
UTSW |
12 |
57,696,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1558:Ttc6
|
UTSW |
12 |
57,733,132 (GRCm39) |
missense |
probably benign |
0.14 |
R1570:Ttc6
|
UTSW |
12 |
57,721,549 (GRCm39) |
missense |
probably damaging |
0.98 |
R1619:Ttc6
|
UTSW |
12 |
57,784,454 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1819:Ttc6
|
UTSW |
12 |
57,741,286 (GRCm39) |
critical splice donor site |
probably null |
|
R1826:Ttc6
|
UTSW |
12 |
57,707,033 (GRCm39) |
missense |
probably benign |
0.10 |
R1863:Ttc6
|
UTSW |
12 |
57,760,881 (GRCm39) |
missense |
probably benign |
0.04 |
R1872:Ttc6
|
UTSW |
12 |
57,751,338 (GRCm39) |
critical splice donor site |
probably null |
|
R1887:Ttc6
|
UTSW |
12 |
57,720,044 (GRCm39) |
missense |
probably benign |
0.04 |
R1937:Ttc6
|
UTSW |
12 |
57,663,109 (GRCm39) |
missense |
probably benign |
0.02 |
R2014:Ttc6
|
UTSW |
12 |
57,623,003 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2056:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2058:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2059:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2152:Ttc6
|
UTSW |
12 |
57,752,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R2179:Ttc6
|
UTSW |
12 |
57,719,904 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2275:Ttc6
|
UTSW |
12 |
57,749,084 (GRCm39) |
missense |
probably benign |
0.01 |
R2432:Ttc6
|
UTSW |
12 |
57,668,821 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2474:Ttc6
|
UTSW |
12 |
57,622,713 (GRCm39) |
missense |
probably benign |
0.37 |
R2853:Ttc6
|
UTSW |
12 |
57,622,967 (GRCm39) |
missense |
probably damaging |
0.96 |
R3848:Ttc6
|
UTSW |
12 |
57,723,932 (GRCm39) |
missense |
probably damaging |
0.97 |
R3853:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3950:Ttc6
|
UTSW |
12 |
57,696,292 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3954:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3955:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3957:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R4135:Ttc6
|
UTSW |
12 |
57,679,581 (GRCm39) |
intron |
probably benign |
|
R4387:Ttc6
|
UTSW |
12 |
57,689,836 (GRCm39) |
missense |
probably benign |
0.00 |
R4577:Ttc6
|
UTSW |
12 |
57,623,441 (GRCm39) |
missense |
probably benign |
0.22 |
R4747:Ttc6
|
UTSW |
12 |
57,721,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4779:Ttc6
|
UTSW |
12 |
57,776,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Ttc6
|
UTSW |
12 |
57,775,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Ttc6
|
UTSW |
12 |
57,749,142 (GRCm39) |
missense |
probably damaging |
0.96 |
R4898:Ttc6
|
UTSW |
12 |
57,707,026 (GRCm39) |
missense |
probably benign |
0.00 |
R4930:Ttc6
|
UTSW |
12 |
57,720,609 (GRCm39) |
critical splice donor site |
probably null |
|
R4946:Ttc6
|
UTSW |
12 |
57,689,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5257:Ttc6
|
UTSW |
12 |
57,749,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5303:Ttc6
|
UTSW |
12 |
57,622,606 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5385:Ttc6
|
UTSW |
12 |
57,689,821 (GRCm39) |
splice site |
probably null |
|
R5402:Ttc6
|
UTSW |
12 |
57,783,817 (GRCm39) |
nonsense |
probably null |
|
R5428:Ttc6
|
UTSW |
12 |
57,736,620 (GRCm39) |
missense |
probably null |
0.98 |
R5436:Ttc6
|
UTSW |
12 |
57,721,380 (GRCm39) |
splice site |
probably null |
|
R5646:Ttc6
|
UTSW |
12 |
57,622,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R5697:Ttc6
|
UTSW |
12 |
57,724,000 (GRCm39) |
missense |
probably benign |
0.22 |
R5792:Ttc6
|
UTSW |
12 |
57,719,990 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5808:Ttc6
|
UTSW |
12 |
57,664,397 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5842:Ttc6
|
UTSW |
12 |
57,783,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Ttc6
|
UTSW |
12 |
57,720,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R6144:Ttc6
|
UTSW |
12 |
57,719,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6155:Ttc6
|
UTSW |
12 |
57,784,402 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6283:Ttc6
|
UTSW |
12 |
57,749,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6371:Ttc6
|
UTSW |
12 |
57,775,249 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6715:Ttc6
|
UTSW |
12 |
57,721,556 (GRCm39) |
critical splice donor site |
probably null |
|
R6738:Ttc6
|
UTSW |
12 |
57,735,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R6795:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6959:Ttc6
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
R7053:Ttc6
|
UTSW |
12 |
57,707,318 (GRCm39) |
missense |
probably benign |
0.01 |
R7125:Ttc6
|
UTSW |
12 |
57,623,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7259:Ttc6
|
UTSW |
12 |
57,622,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7304:Ttc6
|
UTSW |
12 |
57,622,837 (GRCm39) |
missense |
probably damaging |
0.96 |
R7369:Ttc6
|
UTSW |
12 |
57,719,717 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7409:Ttc6
|
UTSW |
12 |
57,743,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R7429:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7430:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Ttc6
|
UTSW |
12 |
57,719,922 (GRCm39) |
missense |
probably benign |
0.02 |
R7535:Ttc6
|
UTSW |
12 |
57,623,305 (GRCm39) |
missense |
probably benign |
0.00 |
R7866:Ttc6
|
UTSW |
12 |
57,721,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R7901:Ttc6
|
UTSW |
12 |
57,735,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7945:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7965:Ttc6
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8062:Ttc6
|
UTSW |
12 |
57,783,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8119:Ttc6
|
UTSW |
12 |
57,752,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8142:Ttc6
|
UTSW |
12 |
57,744,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8154:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ttc6
|
UTSW |
12 |
57,720,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Ttc6
|
UTSW |
12 |
57,707,077 (GRCm39) |
missense |
probably benign |
0.00 |
R8343:Ttc6
|
UTSW |
12 |
57,707,282 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8696:Ttc6
|
UTSW |
12 |
57,784,492 (GRCm39) |
missense |
probably benign |
0.20 |
R8875:Ttc6
|
UTSW |
12 |
57,776,194 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8875:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R8876:Ttc6
|
UTSW |
12 |
57,784,489 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8924:Ttc6
|
UTSW |
12 |
57,697,790 (GRCm39) |
nonsense |
probably null |
|
R8944:Ttc6
|
UTSW |
12 |
57,689,826 (GRCm39) |
missense |
|
|
R8956:Ttc6
|
UTSW |
12 |
57,775,196 (GRCm39) |
nonsense |
probably null |
|
R9020:Ttc6
|
UTSW |
12 |
57,752,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Ttc6
|
UTSW |
12 |
57,783,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Ttc6
|
UTSW |
12 |
57,622,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R9304:Ttc6
|
UTSW |
12 |
57,776,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Ttc6
|
UTSW |
12 |
57,753,649 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9331:Ttc6
|
UTSW |
12 |
57,720,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Ttc6
|
UTSW |
12 |
57,784,404 (GRCm39) |
nonsense |
probably null |
|
R9430:Ttc6
|
UTSW |
12 |
57,733,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Ttc6
|
UTSW |
12 |
57,664,299 (GRCm39) |
missense |
probably benign |
|
R9688:Ttc6
|
UTSW |
12 |
57,720,602 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9732:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
probably benign |
0.36 |
R9740:Ttc6
|
UTSW |
12 |
57,736,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Ttc6
|
UTSW |
12 |
57,701,559 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Ttc6
|
UTSW |
12 |
57,622,904 (GRCm39) |
missense |
probably damaging |
0.96 |
X0058:Ttc6
|
UTSW |
12 |
57,753,637 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ttc6
|
UTSW |
12 |
57,744,161 (GRCm39) |
missense |
probably benign |
0.08 |
|