Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,021,461 (GRCm39) |
L1083P |
probably damaging |
Het |
Anxa7 |
G |
T |
14: 20,510,460 (GRCm39) |
T356K |
probably damaging |
Het |
Atg16l1 |
T |
C |
1: 87,693,167 (GRCm39) |
|
probably null |
Het |
Bptf |
A |
G |
11: 106,963,842 (GRCm39) |
V1784A |
probably damaging |
Het |
Cabs1 |
T |
C |
5: 88,128,309 (GRCm39) |
V320A |
probably damaging |
Het |
Camta1 |
A |
C |
4: 151,229,159 (GRCm39) |
S558A |
probably benign |
Het |
Ccdc180 |
A |
T |
4: 45,906,922 (GRCm39) |
K466* |
probably null |
Het |
Cdhr1 |
G |
A |
14: 36,810,924 (GRCm39) |
P279L |
possibly damaging |
Het |
Cenpe |
A |
G |
3: 134,976,572 (GRCm39) |
N2393S |
probably benign |
Het |
Cep104 |
T |
C |
4: 154,063,462 (GRCm39) |
V8A |
probably benign |
Het |
Chaf1a |
T |
A |
17: 56,371,110 (GRCm39) |
V665E |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,431,583 (GRCm39) |
D404E |
probably damaging |
Het |
Clnk |
G |
A |
5: 38,907,751 (GRCm39) |
T169I |
possibly damaging |
Het |
Cnst |
G |
A |
1: 179,437,587 (GRCm39) |
A384T |
possibly damaging |
Het |
Ctnnd2 |
T |
A |
15: 30,332,162 (GRCm39) |
M15K |
possibly damaging |
Het |
Dlgap1 |
T |
A |
17: 70,823,855 (GRCm39) |
L280Q |
possibly damaging |
Het |
Dll1 |
T |
C |
17: 15,588,959 (GRCm39) |
K572R |
probably benign |
Het |
Dnai4 |
T |
A |
4: 102,905,499 (GRCm39) |
K761* |
probably null |
Het |
Dolk |
C |
A |
2: 30,174,542 (GRCm39) |
W501L |
probably damaging |
Het |
Ednrb |
G |
A |
14: 104,080,665 (GRCm39) |
P83L |
probably benign |
Het |
Edrf1 |
T |
C |
7: 133,245,431 (GRCm39) |
W190R |
probably damaging |
Het |
Epha5 |
T |
A |
5: 84,255,886 (GRCm39) |
D468V |
probably damaging |
Het |
Fat2 |
G |
T |
11: 55,194,547 (GRCm39) |
P1164Q |
probably damaging |
Het |
Fbln5 |
A |
T |
12: 101,717,041 (GRCm39) |
V436E |
probably damaging |
Het |
Fbxw10 |
G |
T |
11: 62,758,449 (GRCm39) |
R558L |
possibly damaging |
Het |
Fhod3 |
C |
A |
18: 25,161,140 (GRCm39) |
S557R |
probably benign |
Het |
Gmip |
A |
T |
8: 70,273,298 (GRCm39) |
H863L |
probably damaging |
Het |
Grm3 |
A |
T |
5: 9,620,464 (GRCm39) |
I260N |
probably damaging |
Het |
Gtpbp8 |
G |
A |
16: 44,566,511 (GRCm39) |
P64S |
probably benign |
Het |
Hand1 |
A |
C |
11: 57,722,548 (GRCm39) |
M22R |
probably benign |
Het |
Ift70b |
T |
C |
2: 75,767,596 (GRCm39) |
T386A |
probably benign |
Het |
Igsf21 |
A |
G |
4: 139,884,782 (GRCm39) |
V58A |
probably damaging |
Het |
Ikzf2 |
G |
A |
1: 69,578,637 (GRCm39) |
R291* |
probably null |
Het |
Itih4 |
C |
G |
14: 30,618,650 (GRCm39) |
P687R |
probably benign |
Het |
Kifc3 |
C |
T |
8: 95,853,195 (GRCm39) |
D54N |
possibly damaging |
Het |
Krtap4-1 |
G |
T |
11: 99,518,708 (GRCm39) |
R101S |
unknown |
Het |
L3mbtl2 |
T |
A |
15: 81,560,744 (GRCm39) |
|
probably benign |
Het |
Lcor |
A |
T |
19: 41,573,399 (GRCm39) |
H718L |
probably benign |
Het |
Lrrc73 |
T |
C |
17: 46,565,293 (GRCm39) |
I8T |
probably damaging |
Het |
Med19 |
C |
A |
2: 84,516,532 (GRCm39) |
|
probably benign |
Het |
Mgarp |
C |
T |
3: 51,296,264 (GRCm39) |
S246N |
unknown |
Het |
Mkrn2 |
T |
C |
6: 115,594,681 (GRCm39) |
S414P |
possibly damaging |
Het |
Mucl2 |
C |
T |
15: 103,926,279 (GRCm39) |
R137H |
unknown |
Het |
Myo1g |
A |
G |
11: 6,464,916 (GRCm39) |
Y453H |
probably damaging |
Het |
Nacc2 |
C |
A |
2: 25,951,605 (GRCm39) |
R410L |
probably damaging |
Het |
Ndufs3 |
C |
T |
2: 90,725,217 (GRCm39) |
R210H |
probably damaging |
Het |
Nlgn1 |
G |
T |
3: 25,488,595 (GRCm39) |
T580K |
probably damaging |
Het |
Nobox |
A |
T |
6: 43,284,522 (GRCm39) |
D41E |
probably damaging |
Het |
Nsd1 |
A |
G |
13: 55,393,667 (GRCm39) |
R526G |
possibly damaging |
Het |
Nt5e |
A |
G |
9: 88,246,873 (GRCm39) |
M370V |
probably benign |
Het |
Olfm5 |
T |
A |
7: 103,803,099 (GRCm39) |
N455Y |
probably damaging |
Het |
Or2g7 |
T |
C |
17: 38,378,179 (GRCm39) |
V39A |
probably benign |
Het |
Or4c101 |
T |
A |
2: 88,389,863 (GRCm39) |
F6I |
probably damaging |
Het |
Or52e19 |
T |
C |
7: 102,959,186 (GRCm39) |
I86T |
probably damaging |
Het |
Or8g50 |
G |
A |
9: 39,648,886 (GRCm39) |
M258I |
probably benign |
Het |
Or8k33 |
T |
A |
2: 86,384,021 (GRCm39) |
Y149F |
probably damaging |
Het |
Pcdhac2 |
T |
C |
18: 37,277,758 (GRCm39) |
V246A |
probably damaging |
Het |
Pclo |
A |
T |
5: 14,763,192 (GRCm39) |
Q603H |
|
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,573,176 (GRCm39) |
Q1910L |
probably damaging |
Het |
Plg |
C |
A |
17: 12,609,107 (GRCm39) |
Y137* |
probably null |
Het |
Prkra |
T |
C |
2: 76,460,856 (GRCm39) |
I281V |
probably benign |
Het |
Prrc2c |
A |
C |
1: 162,503,295 (GRCm39) |
L2722R |
possibly damaging |
Het |
Prss12 |
A |
G |
3: 123,279,149 (GRCm39) |
T409A |
probably damaging |
Het |
Rnaseh1 |
A |
G |
12: 28,708,290 (GRCm39) |
Q256R |
probably benign |
Het |
Rpp14 |
T |
A |
14: 8,083,772 (GRCm38) |
Y17N |
possibly damaging |
Het |
Ryr1 |
A |
T |
7: 28,790,422 (GRCm39) |
H1468Q |
probably damaging |
Het |
Scp2 |
C |
T |
4: 107,912,717 (GRCm39) |
V463M |
probably damaging |
Het |
Sf3b4 |
C |
A |
3: 96,080,381 (GRCm39) |
H43Q |
probably damaging |
Het |
Sgpp1 |
T |
C |
12: 75,782,238 (GRCm39) |
S34G |
probably benign |
Het |
Shisa9 |
T |
A |
16: 11,802,902 (GRCm39) |
I153N |
probably damaging |
Het |
Sin3b |
C |
A |
8: 73,450,092 (GRCm39) |
P3H |
unknown |
Het |
Slc15a2 |
C |
A |
16: 36,602,719 (GRCm39) |
K47N |
possibly damaging |
Het |
Slc30a6 |
T |
A |
17: 74,726,586 (GRCm39) |
F297L |
probably benign |
Het |
Slc45a3 |
TGGGG |
TGGGGG |
1: 131,909,187 (GRCm39) |
|
probably null |
Het |
Slfn4 |
A |
T |
11: 83,077,476 (GRCm39) |
D88V |
probably benign |
Het |
Tgs1 |
C |
A |
4: 3,593,491 (GRCm39) |
Q460K |
probably benign |
Het |
Tlr11 |
A |
T |
14: 50,598,434 (GRCm39) |
D140V |
probably benign |
Het |
Tmem215 |
T |
A |
4: 40,473,945 (GRCm39) |
N7K |
probably damaging |
Het |
Tmem245 |
T |
C |
4: 56,922,384 (GRCm39) |
|
probably benign |
Het |
Tnfsf10 |
G |
A |
3: 27,389,379 (GRCm39) |
D147N |
probably benign |
Het |
Tpm1 |
A |
G |
9: 66,955,138 (GRCm39) |
L57P |
possibly damaging |
Het |
Trappc10 |
T |
C |
10: 78,043,723 (GRCm39) |
|
probably benign |
Het |
Trmt9b |
C |
T |
8: 36,978,954 (GRCm39) |
R186* |
probably null |
Het |
Ttn |
T |
C |
2: 76,593,061 (GRCm39) |
T20730A |
possibly damaging |
Het |
Uap1 |
A |
T |
1: 169,977,013 (GRCm39) |
Y395* |
probably null |
Het |
Usp2 |
A |
T |
9: 43,987,176 (GRCm39) |
D158V |
probably damaging |
Het |
Usp30 |
A |
G |
5: 114,243,877 (GRCm39) |
M149V |
probably benign |
Het |
Vmn2r2 |
T |
C |
3: 64,024,172 (GRCm39) |
N803S |
probably damaging |
Het |
Vmn2r85 |
A |
G |
10: 130,261,479 (GRCm39) |
V286A |
probably benign |
Het |
Xdh |
T |
C |
17: 74,217,222 (GRCm39) |
H682R |
probably benign |
Het |
Zbed3 |
T |
A |
13: 95,472,999 (GRCm39) |
L141Q |
probably damaging |
Het |
Zfp623 |
T |
C |
15: 75,820,162 (GRCm39) |
C373R |
possibly damaging |
Het |
|
Other mutations in Kmt2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00436:Kmt2c
|
APN |
5 |
25,486,259 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00694:Kmt2c
|
APN |
5 |
25,498,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00780:Kmt2c
|
APN |
5 |
25,516,049 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00811:Kmt2c
|
APN |
5 |
25,579,531 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL00885:Kmt2c
|
APN |
5 |
25,614,169 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL00948:Kmt2c
|
APN |
5 |
25,582,159 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00959:Kmt2c
|
APN |
5 |
25,481,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01022:Kmt2c
|
APN |
5 |
25,507,699 (GRCm39) |
unclassified |
probably benign |
|
IGL01146:Kmt2c
|
APN |
5 |
25,513,510 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01154:Kmt2c
|
APN |
5 |
25,489,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01434:Kmt2c
|
APN |
5 |
25,614,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01464:Kmt2c
|
APN |
5 |
25,557,242 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01525:Kmt2c
|
APN |
5 |
25,534,439 (GRCm39) |
splice site |
probably benign |
|
IGL01530:Kmt2c
|
APN |
5 |
25,518,498 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01550:Kmt2c
|
APN |
5 |
25,486,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01598:Kmt2c
|
APN |
5 |
25,478,664 (GRCm39) |
makesense |
probably null |
|
IGL01598:Kmt2c
|
APN |
5 |
25,559,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Kmt2c
|
APN |
5 |
25,559,809 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01663:Kmt2c
|
APN |
5 |
25,515,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01707:Kmt2c
|
APN |
5 |
25,505,096 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01714:Kmt2c
|
APN |
5 |
25,518,398 (GRCm39) |
missense |
probably benign |
|
IGL01784:Kmt2c
|
APN |
5 |
25,518,524 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Kmt2c
|
APN |
5 |
25,495,802 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01825:Kmt2c
|
APN |
5 |
25,515,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01834:Kmt2c
|
APN |
5 |
25,600,453 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02072:Kmt2c
|
APN |
5 |
25,610,430 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02159:Kmt2c
|
APN |
5 |
25,516,341 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02303:Kmt2c
|
APN |
5 |
25,515,155 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02417:Kmt2c
|
APN |
5 |
25,578,018 (GRCm39) |
missense |
probably benign |
|
IGL02578:Kmt2c
|
APN |
5 |
25,571,198 (GRCm39) |
intron |
probably benign |
|
IGL02811:Kmt2c
|
APN |
5 |
25,520,026 (GRCm39) |
nonsense |
probably null |
|
IGL02943:Kmt2c
|
APN |
5 |
25,495,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Kmt2c
|
APN |
5 |
25,489,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Kmt2c
|
APN |
5 |
25,515,350 (GRCm39) |
missense |
probably benign |
|
IGL03076:Kmt2c
|
APN |
5 |
25,504,149 (GRCm39) |
nonsense |
probably null |
|
IGL03088:Kmt2c
|
APN |
5 |
25,504,802 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03131:Kmt2c
|
APN |
5 |
25,520,359 (GRCm39) |
missense |
probably benign |
0.00 |
FR4304:Kmt2c
|
UTSW |
5 |
25,520,764 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Kmt2c
|
UTSW |
5 |
25,520,761 (GRCm39) |
small insertion |
probably benign |
|
PIT4520001:Kmt2c
|
UTSW |
5 |
25,520,664 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4585001:Kmt2c
|
UTSW |
5 |
25,520,104 (GRCm39) |
missense |
probably benign |
0.21 |
R0313:Kmt2c
|
UTSW |
5 |
25,549,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Kmt2c
|
UTSW |
5 |
25,514,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Kmt2c
|
UTSW |
5 |
25,580,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Kmt2c
|
UTSW |
5 |
25,520,662 (GRCm39) |
missense |
probably benign |
|
R0453:Kmt2c
|
UTSW |
5 |
25,559,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Kmt2c
|
UTSW |
5 |
25,504,250 (GRCm39) |
missense |
probably benign |
|
R0619:Kmt2c
|
UTSW |
5 |
25,503,914 (GRCm39) |
missense |
probably benign |
0.21 |
R0671:Kmt2c
|
UTSW |
5 |
25,609,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0736:Kmt2c
|
UTSW |
5 |
25,500,432 (GRCm39) |
missense |
probably benign |
|
R0745:Kmt2c
|
UTSW |
5 |
25,564,696 (GRCm39) |
splice site |
probably null |
|
R0760:Kmt2c
|
UTSW |
5 |
25,558,315 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0784:Kmt2c
|
UTSW |
5 |
25,515,893 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Kmt2c
|
UTSW |
5 |
25,500,605 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0893:Kmt2c
|
UTSW |
5 |
25,556,268 (GRCm39) |
splice site |
probably benign |
|
R0942:Kmt2c
|
UTSW |
5 |
25,520,301 (GRCm39) |
missense |
probably benign |
0.10 |
R1110:Kmt2c
|
UTSW |
5 |
25,519,360 (GRCm39) |
missense |
probably benign |
0.01 |
R1137:Kmt2c
|
UTSW |
5 |
25,515,981 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1255:Kmt2c
|
UTSW |
5 |
25,556,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Kmt2c
|
UTSW |
5 |
25,610,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R1497:Kmt2c
|
UTSW |
5 |
25,519,513 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1594:Kmt2c
|
UTSW |
5 |
25,519,876 (GRCm39) |
missense |
probably benign |
0.01 |
R1611:Kmt2c
|
UTSW |
5 |
25,564,309 (GRCm39) |
critical splice donor site |
probably null |
|
R1617:Kmt2c
|
UTSW |
5 |
25,580,925 (GRCm39) |
missense |
probably benign |
0.01 |
R1720:Kmt2c
|
UTSW |
5 |
25,504,182 (GRCm39) |
missense |
probably benign |
0.05 |
R1723:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1724:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Kmt2c
|
UTSW |
5 |
25,495,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Kmt2c
|
UTSW |
5 |
25,577,972 (GRCm39) |
missense |
probably benign |
0.02 |
R1809:Kmt2c
|
UTSW |
5 |
25,489,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Kmt2c
|
UTSW |
5 |
25,578,434 (GRCm39) |
missense |
probably benign |
0.45 |
R1895:Kmt2c
|
UTSW |
5 |
25,520,152 (GRCm39) |
missense |
probably benign |
0.34 |
R1946:Kmt2c
|
UTSW |
5 |
25,520,152 (GRCm39) |
missense |
probably benign |
0.34 |
R1989:Kmt2c
|
UTSW |
5 |
25,703,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2039:Kmt2c
|
UTSW |
5 |
25,534,038 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2049:Kmt2c
|
UTSW |
5 |
25,490,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Kmt2c
|
UTSW |
5 |
25,557,278 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2080:Kmt2c
|
UTSW |
5 |
25,559,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Kmt2c
|
UTSW |
5 |
25,514,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2186:Kmt2c
|
UTSW |
5 |
25,492,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R2395:Kmt2c
|
UTSW |
5 |
25,520,150 (GRCm39) |
missense |
probably benign |
|
R2983:Kmt2c
|
UTSW |
5 |
25,520,755 (GRCm39) |
small deletion |
probably benign |
|
R3109:Kmt2c
|
UTSW |
5 |
25,480,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3500:Kmt2c
|
UTSW |
5 |
25,504,477 (GRCm39) |
missense |
probably benign |
0.02 |
R3738:Kmt2c
|
UTSW |
5 |
25,610,381 (GRCm39) |
missense |
probably benign |
0.41 |
R3809:Kmt2c
|
UTSW |
5 |
25,614,136 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4088:Kmt2c
|
UTSW |
5 |
25,492,711 (GRCm39) |
missense |
probably benign |
|
R4107:Kmt2c
|
UTSW |
5 |
25,503,918 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4212:Kmt2c
|
UTSW |
5 |
25,552,357 (GRCm39) |
critical splice donor site |
probably null |
|
R4376:Kmt2c
|
UTSW |
5 |
25,520,324 (GRCm39) |
missense |
probably benign |
0.00 |
R4377:Kmt2c
|
UTSW |
5 |
25,520,324 (GRCm39) |
missense |
probably benign |
0.00 |
R4383:Kmt2c
|
UTSW |
5 |
25,556,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4435:Kmt2c
|
UTSW |
5 |
25,519,875 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4456:Kmt2c
|
UTSW |
5 |
25,515,210 (GRCm39) |
missense |
probably benign |
|
R4461:Kmt2c
|
UTSW |
5 |
25,504,874 (GRCm39) |
missense |
probably benign |
0.00 |
R4519:Kmt2c
|
UTSW |
5 |
25,568,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4550:Kmt2c
|
UTSW |
5 |
25,505,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Kmt2c
|
UTSW |
5 |
25,505,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Kmt2c
|
UTSW |
5 |
25,559,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Kmt2c
|
UTSW |
5 |
25,571,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Kmt2c
|
UTSW |
5 |
25,519,025 (GRCm39) |
nonsense |
probably null |
|
R4781:Kmt2c
|
UTSW |
5 |
25,648,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Kmt2c
|
UTSW |
5 |
25,520,111 (GRCm39) |
missense |
probably benign |
|
R4855:Kmt2c
|
UTSW |
5 |
25,519,555 (GRCm39) |
missense |
probably benign |
0.00 |
R4919:Kmt2c
|
UTSW |
5 |
25,519,393 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4971:Kmt2c
|
UTSW |
5 |
25,515,870 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Kmt2c
|
UTSW |
5 |
25,500,509 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5012:Kmt2c
|
UTSW |
5 |
25,504,710 (GRCm39) |
nonsense |
probably null |
|
R5033:Kmt2c
|
UTSW |
5 |
25,519,706 (GRCm39) |
missense |
probably benign |
0.03 |
R5093:Kmt2c
|
UTSW |
5 |
25,614,205 (GRCm39) |
missense |
probably benign |
0.17 |
R5125:Kmt2c
|
UTSW |
5 |
25,489,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R5231:Kmt2c
|
UTSW |
5 |
25,520,471 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5254:Kmt2c
|
UTSW |
5 |
25,519,592 (GRCm39) |
missense |
probably benign |
0.01 |
R5396:Kmt2c
|
UTSW |
5 |
25,499,732 (GRCm39) |
splice site |
probably null |
|
R5415:Kmt2c
|
UTSW |
5 |
25,519,699 (GRCm39) |
missense |
probably benign |
0.21 |
R5523:Kmt2c
|
UTSW |
5 |
25,504,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5554:Kmt2c
|
UTSW |
5 |
25,499,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R5701:Kmt2c
|
UTSW |
5 |
25,519,015 (GRCm39) |
missense |
probably benign |
0.16 |
R5762:Kmt2c
|
UTSW |
5 |
25,515,455 (GRCm39) |
missense |
probably benign |
0.01 |
R5819:Kmt2c
|
UTSW |
5 |
25,614,130 (GRCm39) |
critical splice donor site |
probably null |
|
R5838:Kmt2c
|
UTSW |
5 |
25,489,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Kmt2c
|
UTSW |
5 |
25,552,467 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5951:Kmt2c
|
UTSW |
5 |
25,535,801 (GRCm39) |
missense |
probably benign |
0.15 |
R5988:Kmt2c
|
UTSW |
5 |
25,516,118 (GRCm39) |
missense |
probably benign |
0.02 |
R5999:Kmt2c
|
UTSW |
5 |
25,489,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Kmt2c
|
UTSW |
5 |
25,504,127 (GRCm39) |
missense |
probably benign |
|
R6254:Kmt2c
|
UTSW |
5 |
25,554,872 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6311:Kmt2c
|
UTSW |
5 |
25,648,816 (GRCm39) |
critical splice donor site |
probably null |
|
R6329:Kmt2c
|
UTSW |
5 |
25,520,600 (GRCm39) |
missense |
probably benign |
0.01 |
R6347:Kmt2c
|
UTSW |
5 |
25,515,833 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6364:Kmt2c
|
UTSW |
5 |
25,514,634 (GRCm39) |
missense |
probably null |
0.99 |
R6379:Kmt2c
|
UTSW |
5 |
25,564,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R6588:Kmt2c
|
UTSW |
5 |
25,528,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R6628:Kmt2c
|
UTSW |
5 |
25,503,926 (GRCm39) |
missense |
probably benign |
|
R6733:Kmt2c
|
UTSW |
5 |
25,614,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R6787:Kmt2c
|
UTSW |
5 |
25,480,737 (GRCm39) |
splice site |
probably null |
|
R6816:Kmt2c
|
UTSW |
5 |
25,610,530 (GRCm39) |
splice site |
probably null |
|
R6862:Kmt2c
|
UTSW |
5 |
25,515,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7150:Kmt2c
|
UTSW |
5 |
25,505,360 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7220:Kmt2c
|
UTSW |
5 |
25,549,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Kmt2c
|
UTSW |
5 |
25,514,805 (GRCm39) |
missense |
probably benign |
0.00 |
R7250:Kmt2c
|
UTSW |
5 |
25,504,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Kmt2c
|
UTSW |
5 |
25,600,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7465:Kmt2c
|
UTSW |
5 |
25,507,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Kmt2c
|
UTSW |
5 |
25,513,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Kmt2c
|
UTSW |
5 |
25,489,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R7549:Kmt2c
|
UTSW |
5 |
25,619,968 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7637:Kmt2c
|
UTSW |
5 |
25,520,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R7652:Kmt2c
|
UTSW |
5 |
25,520,717 (GRCm39) |
missense |
probably benign |
0.01 |
R7714:Kmt2c
|
UTSW |
5 |
25,580,364 (GRCm39) |
missense |
probably benign |
|
R7838:Kmt2c
|
UTSW |
5 |
25,499,697 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7891:Kmt2c
|
UTSW |
5 |
25,505,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Kmt2c
|
UTSW |
5 |
25,504,814 (GRCm39) |
missense |
probably benign |
0.18 |
R7895:Kmt2c
|
UTSW |
5 |
25,578,174 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7960:Kmt2c
|
UTSW |
5 |
25,520,194 (GRCm39) |
missense |
probably benign |
0.01 |
R7974:Kmt2c
|
UTSW |
5 |
25,505,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7978:Kmt2c
|
UTSW |
5 |
25,564,676 (GRCm39) |
missense |
probably benign |
0.00 |
R8011:Kmt2c
|
UTSW |
5 |
25,556,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R8021:Kmt2c
|
UTSW |
5 |
25,492,117 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8022:Kmt2c
|
UTSW |
5 |
25,486,678 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8079:Kmt2c
|
UTSW |
5 |
25,507,730 (GRCm39) |
missense |
probably damaging |
0.98 |
R8087:Kmt2c
|
UTSW |
5 |
25,534,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8109:Kmt2c
|
UTSW |
5 |
25,486,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8161:Kmt2c
|
UTSW |
5 |
25,579,562 (GRCm39) |
missense |
probably benign |
0.00 |
R8169:Kmt2c
|
UTSW |
5 |
25,559,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Kmt2c
|
UTSW |
5 |
25,519,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R8218:Kmt2c
|
UTSW |
5 |
25,488,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Kmt2c
|
UTSW |
5 |
25,529,216 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8260:Kmt2c
|
UTSW |
5 |
25,610,514 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8330:Kmt2c
|
UTSW |
5 |
25,509,692 (GRCm39) |
missense |
probably null |
1.00 |
R8355:Kmt2c
|
UTSW |
5 |
25,559,499 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8455:Kmt2c
|
UTSW |
5 |
25,559,499 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8508:Kmt2c
|
UTSW |
5 |
25,519,120 (GRCm39) |
missense |
probably benign |
0.34 |
R8885:Kmt2c
|
UTSW |
5 |
25,520,077 (GRCm39) |
missense |
probably benign |
0.34 |
R8907:Kmt2c
|
UTSW |
5 |
25,514,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Kmt2c
|
UTSW |
5 |
25,503,885 (GRCm39) |
missense |
probably benign |
|
R8969:Kmt2c
|
UTSW |
5 |
25,519,387 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9019:Kmt2c
|
UTSW |
5 |
25,488,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Kmt2c
|
UTSW |
5 |
25,489,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Kmt2c
|
UTSW |
5 |
25,489,194 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9130:Kmt2c
|
UTSW |
5 |
25,516,102 (GRCm39) |
missense |
probably benign |
0.01 |
R9171:Kmt2c
|
UTSW |
5 |
25,486,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R9235:Kmt2c
|
UTSW |
5 |
25,504,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Kmt2c
|
UTSW |
5 |
25,554,860 (GRCm39) |
missense |
probably benign |
0.34 |
R9288:Kmt2c
|
UTSW |
5 |
25,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Kmt2c
|
UTSW |
5 |
25,614,165 (GRCm39) |
missense |
probably benign |
0.06 |
R9443:Kmt2c
|
UTSW |
5 |
25,515,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Kmt2c
|
UTSW |
5 |
25,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Kmt2c
|
UTSW |
5 |
25,554,860 (GRCm39) |
missense |
probably benign |
0.34 |
R9526:Kmt2c
|
UTSW |
5 |
25,486,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9653:Kmt2c
|
UTSW |
5 |
25,507,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Kmt2c
|
UTSW |
5 |
25,489,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Kmt2c
|
UTSW |
5 |
25,577,956 (GRCm39) |
missense |
probably benign |
0.18 |
R9784:Kmt2c
|
UTSW |
5 |
25,549,959 (GRCm39) |
missense |
probably damaging |
1.00 |
RF001:Kmt2c
|
UTSW |
5 |
25,520,773 (GRCm39) |
small insertion |
probably benign |
|
RF006:Kmt2c
|
UTSW |
5 |
25,520,770 (GRCm39) |
small insertion |
probably benign |
|
RF011:Kmt2c
|
UTSW |
5 |
25,543,457 (GRCm39) |
missense |
probably damaging |
1.00 |
RF041:Kmt2c
|
UTSW |
5 |
25,520,773 (GRCm39) |
small insertion |
probably benign |
|
RF047:Kmt2c
|
UTSW |
5 |
25,520,758 (GRCm39) |
small insertion |
probably benign |
|
RF051:Kmt2c
|
UTSW |
5 |
25,518,477 (GRCm39) |
unclassified |
probably benign |
|
RF055:Kmt2c
|
UTSW |
5 |
25,520,770 (GRCm39) |
small insertion |
probably benign |
|
RF059:Kmt2c
|
UTSW |
5 |
25,518,477 (GRCm39) |
unclassified |
probably benign |
|
RF063:Kmt2c
|
UTSW |
5 |
25,520,762 (GRCm39) |
small insertion |
probably benign |
|
X0024:Kmt2c
|
UTSW |
5 |
25,610,483 (GRCm39) |
missense |
probably benign |
0.26 |
X0027:Kmt2c
|
UTSW |
5 |
25,535,885 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Kmt2c
|
UTSW |
5 |
25,559,411 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kmt2c
|
UTSW |
5 |
25,571,195 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Kmt2c
|
UTSW |
5 |
25,505,001 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Kmt2c
|
UTSW |
5 |
25,500,395 (GRCm39) |
critical splice donor site |
probably null |
|
|