Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
A |
T |
1: 11,633,211 (GRCm39) |
D168V |
probably damaging |
Het |
Abcb4 |
A |
T |
5: 9,008,441 (GRCm39) |
D1203V |
probably damaging |
Het |
Acat2 |
G |
A |
17: 13,178,979 (GRCm39) |
|
probably benign |
Het |
Adam3 |
C |
T |
8: 25,179,484 (GRCm39) |
C611Y |
probably damaging |
Het |
Adgrb1 |
A |
G |
15: 74,415,189 (GRCm39) |
D638G |
probably damaging |
Het |
Adra1b |
T |
C |
11: 43,667,218 (GRCm39) |
N340D |
probably damaging |
Het |
Ankrd31 |
A |
G |
13: 96,916,879 (GRCm39) |
H131R |
probably damaging |
Het |
Aoc2 |
T |
C |
11: 101,217,164 (GRCm39) |
S416P |
possibly damaging |
Het |
Armc8 |
G |
A |
9: 99,387,362 (GRCm39) |
R419* |
probably null |
Het |
Atp6v1h |
T |
G |
1: 5,163,638 (GRCm39) |
V90G |
probably damaging |
Het |
Avl9 |
T |
C |
6: 56,707,628 (GRCm39) |
V191A |
probably benign |
Het |
Bsn |
G |
A |
9: 107,990,173 (GRCm39) |
P1860S |
possibly damaging |
Het |
Btd |
A |
G |
14: 31,384,233 (GRCm39) |
K73R |
probably benign |
Het |
Cd22 |
T |
C |
7: 30,567,391 (GRCm39) |
K731R |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,956,911 (GRCm39) |
L332F |
probably damaging |
Het |
Cirop |
T |
G |
14: 54,932,686 (GRCm39) |
S393R |
probably damaging |
Het |
Cldn11 |
A |
G |
3: 31,217,276 (GRCm39) |
E148G |
probably damaging |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Cnbd1 |
A |
T |
4: 18,886,061 (GRCm39) |
Y319* |
probably null |
Het |
Cnnm4 |
A |
G |
1: 36,511,170 (GRCm39) |
T133A |
probably benign |
Het |
Cpeb4 |
A |
T |
11: 31,822,679 (GRCm39) |
E131V |
probably benign |
Het |
Ctns |
A |
G |
11: 73,078,561 (GRCm39) |
|
probably null |
Het |
Dhx36 |
C |
A |
3: 62,414,142 (GRCm39) |
Q73H |
probably benign |
Het |
Dhx36 |
C |
A |
3: 62,414,141 (GRCm39) |
E74* |
probably null |
Het |
Dnah5 |
A |
G |
15: 28,420,107 (GRCm39) |
T3802A |
|
Het |
Fbxo31 |
G |
A |
8: 122,281,136 (GRCm39) |
R337C |
probably damaging |
Het |
Flnc |
C |
T |
6: 29,455,518 (GRCm39) |
Q2056* |
probably null |
Het |
Fmo9 |
T |
C |
1: 166,492,199 (GRCm39) |
D408G |
possibly damaging |
Het |
Gipr |
C |
T |
7: 18,897,495 (GRCm39) |
S117N |
unknown |
Het |
Gm14412 |
T |
A |
2: 177,006,356 (GRCm39) |
H513L |
probably damaging |
Het |
Gm21663 |
G |
C |
5: 26,147,167 (GRCm39) |
C46W |
probably benign |
Het |
Gucy1a2 |
A |
T |
9: 3,634,489 (GRCm39) |
I178L |
probably benign |
Het |
Htr1b |
A |
T |
9: 81,514,481 (GRCm39) |
L42Q |
|
Het |
Htr2b |
T |
C |
1: 86,027,481 (GRCm39) |
T342A |
probably damaging |
Het |
Jkampl |
T |
C |
6: 73,446,517 (GRCm39) |
T11A |
probably benign |
Het |
Jph2 |
C |
T |
2: 163,181,473 (GRCm39) |
V564M |
probably damaging |
Het |
Kcnmb1 |
A |
G |
11: 33,914,806 (GRCm39) |
T36A |
probably damaging |
Het |
Krit1 |
A |
C |
5: 3,863,135 (GRCm39) |
K310N |
probably benign |
Het |
Lama1 |
C |
T |
17: 68,111,508 (GRCm39) |
T2253M |
|
Het |
Lpar6 |
C |
T |
14: 73,476,233 (GRCm39) |
L65F |
probably damaging |
Het |
Megf6 |
G |
A |
4: 154,354,160 (GRCm39) |
G1355R |
probably damaging |
Het |
Mmp3 |
T |
A |
9: 7,446,936 (GRCm39) |
Y39N |
probably damaging |
Het |
Mrtfb |
A |
G |
16: 13,221,053 (GRCm39) |
H743R |
probably benign |
Het |
Ms4a18 |
C |
A |
19: 10,990,741 (GRCm39) |
V118F |
|
Het |
Mthfr |
G |
A |
4: 148,126,082 (GRCm39) |
S51N |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,554,975 (GRCm39) |
T3773S |
unknown |
Het |
Mus81 |
T |
A |
19: 5,534,032 (GRCm39) |
K400* |
probably null |
Het |
Naaladl2 |
A |
T |
3: 24,487,344 (GRCm39) |
D192E |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,366,127 (GRCm39) |
D329G |
possibly damaging |
Het |
Nek11 |
T |
A |
9: 105,170,856 (GRCm39) |
H393L |
probably benign |
Het |
Nmt2 |
T |
A |
2: 3,306,315 (GRCm39) |
|
probably benign |
Het |
Nmur2 |
T |
C |
11: 55,920,408 (GRCm39) |
D279G |
possibly damaging |
Het |
Nol4l |
C |
A |
2: 153,312,630 (GRCm39) |
R226L |
probably damaging |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or10d4c |
A |
G |
9: 39,558,379 (GRCm39) |
D119G |
probably damaging |
Het |
Or1o2 |
T |
C |
17: 37,542,961 (GRCm39) |
Y100C |
probably benign |
Het |
Or5ak22 |
T |
C |
2: 85,229,995 (GRCm39) |
N294S |
probably damaging |
Het |
Palm |
A |
G |
10: 79,654,988 (GRCm39) |
T249A |
probably benign |
Het |
Pramel22 |
A |
T |
4: 143,381,097 (GRCm39) |
Y309N |
probably benign |
Het |
Rhobtb3 |
A |
G |
13: 76,087,702 (GRCm39) |
I95T |
probably damaging |
Het |
Rnpep |
A |
T |
1: 135,206,559 (GRCm39) |
F178L |
possibly damaging |
Het |
Rsl1d1 |
A |
G |
16: 11,019,227 (GRCm39) |
S105P |
probably damaging |
Het |
Rxra |
C |
T |
2: 27,638,756 (GRCm39) |
T253I |
possibly damaging |
Het |
Schip1 |
A |
G |
3: 67,972,318 (GRCm39) |
D15G |
|
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Srcap |
T |
C |
7: 127,151,816 (GRCm39) |
V2125A |
probably damaging |
Het |
Stx7 |
C |
T |
10: 24,058,724 (GRCm39) |
Q199* |
probably null |
Het |
Syt6 |
T |
C |
3: 103,492,895 (GRCm39) |
I134T |
probably damaging |
Het |
Tlr12 |
A |
G |
4: 128,510,870 (GRCm39) |
M460T |
probably benign |
Het |
Tnni3k |
T |
C |
3: 154,647,314 (GRCm39) |
T398A |
possibly damaging |
Het |
Tspan4 |
T |
C |
7: 141,071,816 (GRCm39) |
S188P |
probably benign |
Het |
Ubap2l |
A |
G |
3: 89,909,756 (GRCm39) |
S1025P |
unknown |
Het |
Ubl7 |
A |
G |
9: 57,829,035 (GRCm39) |
D219G |
probably benign |
Het |
Vmn2r115 |
C |
A |
17: 23,564,803 (GRCm39) |
T230K |
probably benign |
Het |
Vmn2r95 |
T |
A |
17: 18,660,167 (GRCm39) |
M193K |
possibly damaging |
Het |
Zfp639 |
A |
G |
3: 32,573,885 (GRCm39) |
E170G |
probably damaging |
Het |
Zfy1 |
A |
G |
Y: 725,987 (GRCm39) |
S593P |
possibly damaging |
Het |
Zscan4-ps1 |
T |
A |
7: 10,799,495 (GRCm39) |
T465S |
probably damaging |
Het |
|
Other mutations in Sis |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00582:Sis
|
APN |
3 |
72,853,969 (GRCm39) |
missense |
probably benign |
|
IGL00715:Sis
|
APN |
3 |
72,841,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00721:Sis
|
APN |
3 |
72,850,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Sis
|
APN |
3 |
72,814,570 (GRCm39) |
splice site |
probably benign |
|
IGL00783:Sis
|
APN |
3 |
72,853,965 (GRCm39) |
missense |
probably benign |
|
IGL00805:Sis
|
APN |
3 |
72,841,532 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00932:Sis
|
APN |
3 |
72,848,289 (GRCm39) |
splice site |
probably benign |
|
IGL01020:Sis
|
APN |
3 |
72,874,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Sis
|
APN |
3 |
72,819,209 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01286:Sis
|
APN |
3 |
72,848,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Sis
|
APN |
3 |
72,868,354 (GRCm39) |
missense |
probably benign |
|
IGL01514:Sis
|
APN |
3 |
72,843,253 (GRCm39) |
splice site |
probably benign |
|
IGL01986:Sis
|
APN |
3 |
72,852,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Sis
|
APN |
3 |
72,836,032 (GRCm39) |
nonsense |
probably null |
|
IGL02132:Sis
|
APN |
3 |
72,854,804 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02152:Sis
|
APN |
3 |
72,796,319 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02200:Sis
|
APN |
3 |
72,850,937 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Sis
|
APN |
3 |
72,863,523 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02307:Sis
|
APN |
3 |
72,819,167 (GRCm39) |
splice site |
probably benign |
|
IGL02374:Sis
|
APN |
3 |
72,832,789 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02437:Sis
|
APN |
3 |
72,826,947 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02571:Sis
|
APN |
3 |
72,863,637 (GRCm39) |
splice site |
probably benign |
|
IGL02601:Sis
|
APN |
3 |
72,820,543 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03063:Sis
|
APN |
3 |
72,835,630 (GRCm39) |
missense |
probably benign |
|
IGL03382:Sis
|
APN |
3 |
72,836,052 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03397:Sis
|
APN |
3 |
72,843,212 (GRCm39) |
missense |
probably benign |
0.44 |
PIT1430001:Sis
|
UTSW |
3 |
72,830,162 (GRCm39) |
missense |
probably damaging |
0.97 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0046:Sis
|
UTSW |
3 |
72,839,427 (GRCm39) |
missense |
probably benign |
0.01 |
R0094:Sis
|
UTSW |
3 |
72,828,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sis
|
UTSW |
3 |
72,835,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Sis
|
UTSW |
3 |
72,867,629 (GRCm39) |
missense |
probably benign |
0.29 |
R0544:Sis
|
UTSW |
3 |
72,858,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Sis
|
UTSW |
3 |
72,832,740 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0617:Sis
|
UTSW |
3 |
72,872,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0698:Sis
|
UTSW |
3 |
72,817,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Sis
|
UTSW |
3 |
72,848,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Sis
|
UTSW |
3 |
72,857,155 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0706:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0710:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0752:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0753:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0754:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0767:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0769:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0772:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0774:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0776:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0818:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0885:Sis
|
UTSW |
3 |
72,819,282 (GRCm39) |
nonsense |
probably null |
|
R1076:Sis
|
UTSW |
3 |
72,841,431 (GRCm39) |
missense |
probably damaging |
0.97 |
R1140:Sis
|
UTSW |
3 |
72,858,949 (GRCm39) |
missense |
probably damaging |
0.98 |
R1175:Sis
|
UTSW |
3 |
72,865,437 (GRCm39) |
splice site |
probably benign |
|
R1301:Sis
|
UTSW |
3 |
72,853,915 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1437:Sis
|
UTSW |
3 |
72,841,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1472:Sis
|
UTSW |
3 |
72,796,360 (GRCm39) |
missense |
probably benign |
0.12 |
R1584:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1707:Sis
|
UTSW |
3 |
72,816,420 (GRCm39) |
splice site |
probably benign |
|
R1715:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1719:Sis
|
UTSW |
3 |
72,872,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1784:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1820:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R1973:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Sis
|
UTSW |
3 |
72,820,570 (GRCm39) |
missense |
probably benign |
0.01 |
R2233:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2235:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2276:Sis
|
UTSW |
3 |
72,821,934 (GRCm39) |
nonsense |
probably null |
|
R2435:Sis
|
UTSW |
3 |
72,819,237 (GRCm39) |
missense |
probably benign |
0.01 |
R2885:Sis
|
UTSW |
3 |
72,816,506 (GRCm39) |
missense |
probably benign |
0.01 |
R2966:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
probably benign |
0.30 |
R3708:Sis
|
UTSW |
3 |
72,850,856 (GRCm39) |
missense |
probably benign |
0.02 |
R3790:Sis
|
UTSW |
3 |
72,828,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Sis
|
UTSW |
3 |
72,832,929 (GRCm39) |
missense |
probably benign |
0.01 |
R3858:Sis
|
UTSW |
3 |
72,835,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R3974:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R3975:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R4037:Sis
|
UTSW |
3 |
72,835,935 (GRCm39) |
missense |
probably benign |
|
R4080:Sis
|
UTSW |
3 |
72,828,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Sis
|
UTSW |
3 |
72,868,415 (GRCm39) |
missense |
probably benign |
|
R4394:Sis
|
UTSW |
3 |
72,863,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Sis
|
UTSW |
3 |
72,835,492 (GRCm39) |
splice site |
probably null |
|
R4573:Sis
|
UTSW |
3 |
72,835,570 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4868:Sis
|
UTSW |
3 |
72,850,881 (GRCm39) |
missense |
probably benign |
0.09 |
R5023:Sis
|
UTSW |
3 |
72,841,455 (GRCm39) |
missense |
probably benign |
0.05 |
R5264:Sis
|
UTSW |
3 |
72,857,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R5414:Sis
|
UTSW |
3 |
72,859,826 (GRCm39) |
missense |
probably benign |
|
R5462:Sis
|
UTSW |
3 |
72,857,171 (GRCm39) |
missense |
probably damaging |
0.96 |
R5523:Sis
|
UTSW |
3 |
72,798,754 (GRCm39) |
missense |
probably benign |
0.00 |
R5584:Sis
|
UTSW |
3 |
72,817,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Sis
|
UTSW |
3 |
72,821,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5725:Sis
|
UTSW |
3 |
72,872,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Sis
|
UTSW |
3 |
72,835,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R5790:Sis
|
UTSW |
3 |
72,835,507 (GRCm39) |
missense |
probably benign |
|
R5864:Sis
|
UTSW |
3 |
72,857,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Sis
|
UTSW |
3 |
72,867,589 (GRCm39) |
critical splice donor site |
probably null |
|
R5925:Sis
|
UTSW |
3 |
72,828,713 (GRCm39) |
splice site |
probably null |
|
R6018:Sis
|
UTSW |
3 |
72,820,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6029:Sis
|
UTSW |
3 |
72,835,641 (GRCm39) |
missense |
probably benign |
0.30 |
R6124:Sis
|
UTSW |
3 |
72,860,544 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6171:Sis
|
UTSW |
3 |
72,868,360 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6182:Sis
|
UTSW |
3 |
72,811,626 (GRCm39) |
missense |
probably benign |
0.05 |
R6295:Sis
|
UTSW |
3 |
72,874,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R6416:Sis
|
UTSW |
3 |
72,819,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Sis
|
UTSW |
3 |
72,865,507 (GRCm39) |
missense |
probably benign |
0.00 |
R6472:Sis
|
UTSW |
3 |
72,846,067 (GRCm39) |
nonsense |
probably null |
|
R6517:Sis
|
UTSW |
3 |
72,814,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Sis
|
UTSW |
3 |
72,856,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Sis
|
UTSW |
3 |
72,872,951 (GRCm39) |
missense |
probably benign |
0.06 |
R6853:Sis
|
UTSW |
3 |
72,798,759 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6906:Sis
|
UTSW |
3 |
72,826,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Sis
|
UTSW |
3 |
72,810,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R7357:Sis
|
UTSW |
3 |
72,832,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Sis
|
UTSW |
3 |
72,820,625 (GRCm39) |
splice site |
probably null |
|
R7439:Sis
|
UTSW |
3 |
72,816,374 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7742:Sis
|
UTSW |
3 |
72,832,431 (GRCm39) |
missense |
probably benign |
0.19 |
R7813:Sis
|
UTSW |
3 |
72,832,801 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Sis
|
UTSW |
3 |
72,828,329 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7899:Sis
|
UTSW |
3 |
72,844,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7915:Sis
|
UTSW |
3 |
72,828,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7985:Sis
|
UTSW |
3 |
72,844,294 (GRCm39) |
splice site |
probably null |
|
R8020:Sis
|
UTSW |
3 |
72,816,298 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Sis
|
UTSW |
3 |
72,859,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R8029:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Sis
|
UTSW |
3 |
72,856,901 (GRCm39) |
nonsense |
probably null |
|
R8062:Sis
|
UTSW |
3 |
72,828,321 (GRCm39) |
nonsense |
probably null |
|
R8074:Sis
|
UTSW |
3 |
72,824,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Sis
|
UTSW |
3 |
72,814,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Sis
|
UTSW |
3 |
72,796,378 (GRCm39) |
missense |
probably benign |
0.22 |
R8349:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8366:Sis
|
UTSW |
3 |
72,865,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8449:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8474:Sis
|
UTSW |
3 |
72,836,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8515:Sis
|
UTSW |
3 |
72,836,742 (GRCm39) |
missense |
probably benign |
0.00 |
R8680:Sis
|
UTSW |
3 |
72,867,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Sis
|
UTSW |
3 |
72,867,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:Sis
|
UTSW |
3 |
72,872,910 (GRCm39) |
critical splice donor site |
probably null |
|
R9574:Sis
|
UTSW |
3 |
72,828,490 (GRCm39) |
missense |
probably benign |
0.05 |
R9630:Sis
|
UTSW |
3 |
72,828,722 (GRCm39) |
missense |
probably benign |
0.11 |
R9680:Sis
|
UTSW |
3 |
72,863,621 (GRCm39) |
missense |
probably benign |
0.12 |
R9709:Sis
|
UTSW |
3 |
72,799,074 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9731:Sis
|
UTSW |
3 |
72,835,543 (GRCm39) |
missense |
probably benign |
0.01 |
X0009:Sis
|
UTSW |
3 |
72,796,355 (GRCm39) |
missense |
probably damaging |
0.99 |
X0024:Sis
|
UTSW |
3 |
72,836,003 (GRCm39) |
missense |
probably benign |
|
X0060:Sis
|
UTSW |
3 |
72,828,239 (GRCm39) |
intron |
probably benign |
|
Z1176:Sis
|
UTSW |
3 |
72,850,890 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Sis
|
UTSW |
3 |
72,811,606 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Sis
|
UTSW |
3 |
72,850,902 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,817,807 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,816,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
|