Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
G |
T |
14: 118,943,487 (GRCm39) |
P12Q |
probably damaging |
Het |
Acsf3 |
A |
G |
8: 123,507,163 (GRCm39) |
Y152C |
probably damaging |
Het |
Adam22 |
T |
A |
5: 8,145,049 (GRCm39) |
Q803L |
possibly damaging |
Het |
Adamtsl3 |
G |
A |
7: 82,227,825 (GRCm39) |
V1337I |
probably damaging |
Het |
Adra1b |
T |
C |
11: 43,666,845 (GRCm39) |
D464G |
possibly damaging |
Het |
Alpk3 |
T |
A |
7: 80,726,660 (GRCm39) |
I115K |
probably benign |
Het |
Amdhd2 |
A |
G |
17: 24,380,657 (GRCm39) |
S96P |
|
Het |
Ankib1 |
T |
G |
5: 3,819,586 (GRCm39) |
D111A |
probably benign |
Het |
Arhgef2 |
A |
G |
3: 88,540,873 (GRCm39) |
D216G |
probably damaging |
Het |
Astn1 |
A |
T |
1: 158,380,425 (GRCm39) |
|
probably benign |
Het |
Atosa |
C |
A |
9: 74,913,668 (GRCm39) |
Y107* |
probably null |
Het |
Atrn |
T |
A |
2: 130,789,520 (GRCm39) |
W328R |
probably damaging |
Het |
Atxn7 |
A |
T |
14: 14,095,427 (GRCm38) |
H375L |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,980,915 (GRCm39) |
N1579Y |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,497,671 (GRCm39) |
L2079Q |
probably benign |
Het |
Ccdc102a |
T |
C |
8: 95,629,981 (GRCm39) |
K520R |
probably damaging |
Het |
Cd2ap |
T |
C |
17: 43,116,054 (GRCm39) |
H602R |
possibly damaging |
Het |
Cdkn2aip |
A |
G |
8: 48,164,408 (GRCm39) |
V435A |
possibly damaging |
Het |
Cenpf |
A |
T |
1: 189,391,575 (GRCm39) |
Y735* |
probably null |
Het |
Cep350 |
T |
A |
1: 155,803,961 (GRCm39) |
I1041L |
probably benign |
Het |
Ckap4 |
A |
G |
10: 84,363,863 (GRCm39) |
V400A |
probably damaging |
Het |
Comp |
T |
A |
8: 70,829,854 (GRCm39) |
D359E |
probably benign |
Het |
Coq10b |
A |
C |
1: 55,100,500 (GRCm39) |
K61N |
probably benign |
Het |
Csmd2 |
G |
A |
4: 128,215,889 (GRCm39) |
S548N |
|
Het |
Csmd2 |
A |
C |
4: 128,215,888 (GRCm39) |
S548R |
|
Het |
Ctif |
A |
G |
18: 75,744,807 (GRCm39) |
I99T |
probably benign |
Het |
Ctns |
T |
G |
11: 73,083,903 (GRCm39) |
T40P |
possibly damaging |
Het |
Cyp11b1 |
C |
T |
15: 74,712,674 (GRCm39) |
R129H |
probably damaging |
Het |
Cyp2c68 |
A |
T |
19: 39,729,318 (GRCm39) |
N56K |
probably benign |
Het |
D6Wsu163e |
A |
G |
6: 126,938,968 (GRCm39) |
K401R |
probably damaging |
Het |
Dstn |
T |
A |
2: 143,780,368 (GRCm39) |
C23S |
probably benign |
Het |
Fam72a |
A |
T |
1: 131,466,613 (GRCm39) |
E132D |
probably damaging |
Het |
Fam72a |
G |
T |
1: 131,466,614 (GRCm39) |
E133* |
probably null |
Het |
Gbp8 |
T |
A |
5: 105,179,161 (GRCm39) |
I113F |
probably damaging |
Het |
Gm3095 |
A |
T |
14: 15,170,332 (GRCm39) |
R60S |
possibly damaging |
Het |
Gpa33 |
A |
T |
1: 165,980,263 (GRCm39) |
M109L |
probably damaging |
Het |
Grik2 |
A |
G |
10: 49,411,493 (GRCm39) |
L215P |
probably damaging |
Het |
Gucy2g |
A |
C |
19: 55,194,725 (GRCm39) |
F897L |
probably damaging |
Het |
Hinfp |
A |
G |
9: 44,209,314 (GRCm39) |
L295P |
probably damaging |
Het |
Ift122 |
T |
C |
6: 115,871,283 (GRCm39) |
V526A |
probably benign |
Het |
Ighv5-12 |
T |
C |
12: 113,665,853 (GRCm39) |
T82A |
probably benign |
Het |
Il18rap |
T |
A |
1: 40,564,111 (GRCm39) |
S76R |
probably benign |
Het |
Itga6 |
A |
T |
2: 71,683,897 (GRCm39) |
N1045I |
probably benign |
Het |
Kctd21 |
A |
T |
7: 96,996,970 (GRCm39) |
I148F |
possibly damaging |
Het |
Kif28 |
T |
A |
1: 179,567,644 (GRCm39) |
H42L |
probably benign |
Het |
Knl1 |
T |
A |
2: 118,925,707 (GRCm39) |
L1912* |
probably null |
Het |
Lrfn1 |
A |
T |
7: 28,158,947 (GRCm39) |
I289F |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 103,057,185 (GRCm39) |
K205R |
possibly damaging |
Het |
Mbd5 |
A |
T |
2: 49,147,566 (GRCm39) |
N592I |
probably damaging |
Het |
Mbl2 |
A |
G |
19: 30,216,802 (GRCm39) |
N205D |
possibly damaging |
Het |
Mcm4 |
C |
A |
16: 15,455,042 (GRCm39) |
M1I |
probably null |
Het |
Mgat4a |
T |
A |
1: 37,493,865 (GRCm39) |
H327L |
probably damaging |
Het |
Miox |
A |
G |
15: 89,219,206 (GRCm39) |
D16G |
probably benign |
Het |
Mvk |
C |
A |
5: 114,594,039 (GRCm39) |
P298Q |
possibly damaging |
Het |
Nol6 |
A |
G |
4: 41,118,699 (GRCm39) |
L726P |
probably damaging |
Het |
Nos1 |
T |
C |
5: 118,087,880 (GRCm39) |
I1381T |
probably benign |
Het |
Nup98 |
A |
T |
7: 101,784,144 (GRCm39) |
S1063T |
probably benign |
Het |
Obscn |
T |
G |
11: 58,886,275 (GRCm39) |
M7862L |
unknown |
Het |
Obsl1 |
T |
C |
1: 75,464,348 (GRCm39) |
T1653A |
probably benign |
Het |
Odr4 |
A |
G |
1: 150,262,107 (GRCm39) |
|
probably null |
Het |
Or4c105 |
G |
T |
2: 88,647,687 (GRCm39) |
M57I |
probably damaging |
Het |
Or8g53 |
T |
A |
9: 39,683,260 (GRCm39) |
T279S |
probably benign |
Het |
Or8u9 |
A |
G |
2: 86,001,546 (GRCm39) |
I205T |
probably benign |
Het |
Or9q2 |
C |
T |
19: 13,772,358 (GRCm39) |
V206I |
probably damaging |
Het |
Pcdhb20 |
A |
G |
18: 37,638,005 (GRCm39) |
Y177C |
probably benign |
Het |
Pcdhb3 |
A |
C |
18: 37,434,657 (GRCm39) |
I208L |
probably benign |
Het |
Phlpp1 |
G |
T |
1: 106,317,420 (GRCm39) |
G1214W |
probably damaging |
Het |
Ppp4r3a |
A |
T |
12: 101,025,053 (GRCm39) |
S149T |
possibly damaging |
Het |
Pxdn |
T |
C |
12: 30,052,438 (GRCm39) |
C872R |
probably damaging |
Het |
Rarb |
A |
G |
14: 16,548,419 (GRCm38) |
C101R |
probably damaging |
Het |
Rcor3 |
A |
C |
1: 191,812,283 (GRCm39) |
V114G |
probably benign |
Het |
Rnpepl1 |
A |
G |
1: 92,847,372 (GRCm39) |
Q653R |
probably benign |
Het |
Rpap2 |
T |
A |
5: 107,768,324 (GRCm39) |
Y387* |
probably null |
Het |
Rttn |
C |
T |
18: 89,004,035 (GRCm39) |
T343M |
possibly damaging |
Het |
Samd11 |
T |
C |
4: 156,333,230 (GRCm39) |
T333A |
probably benign |
Het |
Six5 |
T |
C |
7: 18,828,968 (GRCm39) |
L136P |
probably damaging |
Het |
Slc12a5 |
T |
A |
2: 164,824,852 (GRCm39) |
M419K |
probably benign |
Het |
Slc22a21 |
T |
C |
11: 53,851,226 (GRCm39) |
M179V |
probably benign |
Het |
Slc35a4 |
A |
G |
18: 36,813,570 (GRCm39) |
D6G |
unknown |
Het |
Spdye4c |
A |
T |
2: 128,434,261 (GRCm39) |
M1L |
probably benign |
Het |
Svep1 |
A |
T |
4: 58,069,699 (GRCm39) |
C2696S |
possibly damaging |
Het |
Tceanc2 |
T |
C |
4: 107,004,893 (GRCm39) |
N85S |
probably benign |
Het |
Teddm2 |
G |
C |
1: 153,726,344 (GRCm39) |
L124V |
probably benign |
Het |
Teddm2 |
A |
T |
1: 153,726,343 (GRCm39) |
L124Q |
probably damaging |
Het |
Tgfbr1 |
T |
A |
4: 47,405,623 (GRCm39) |
W409R |
probably damaging |
Het |
Tkt |
A |
G |
14: 30,280,755 (GRCm39) |
D62G |
probably damaging |
Het |
Tnrc6b |
T |
A |
15: 80,768,501 (GRCm39) |
V1054D |
probably damaging |
Het |
Trpm7 |
C |
A |
2: 126,641,126 (GRCm39) |
L1564F |
probably damaging |
Het |
Vmn1r43 |
A |
T |
6: 89,846,803 (GRCm39) |
C228S |
probably benign |
Het |
Vmn2r106 |
T |
C |
17: 20,487,883 (GRCm39) |
R839G |
probably damaging |
Het |
Vmn2r5 |
G |
A |
3: 64,403,176 (GRCm39) |
T523I |
probably benign |
Het |
Vwa3b |
C |
T |
1: 37,153,678 (GRCm39) |
Q507* |
probably null |
Het |
Wrn |
C |
G |
8: 33,738,994 (GRCm39) |
W1278S |
probably benign |
Het |
Zfp281 |
T |
G |
1: 136,553,190 (GRCm39) |
L56R |
probably damaging |
Het |
Zfp407 |
G |
A |
18: 84,579,661 (GRCm39) |
T484I |
probably benign |
Het |
Zfp451 |
T |
C |
1: 33,852,843 (GRCm39) |
T24A |
probably benign |
Het |
Zfp607b |
T |
A |
7: 27,392,919 (GRCm39) |
F16I |
probably damaging |
Het |
Zfp638 |
T |
A |
6: 83,905,670 (GRCm39) |
V41E |
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 |
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 |
R9035:Kmt2c
|
UTSW |
5 |
25,524,010 (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 |
|
|