Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A230072I06Rik |
T |
A |
8: 12,329,824 (GRCm39) |
L93H |
unknown |
Het |
Akap11 |
C |
A |
14: 78,750,413 (GRCm39) |
C658F |
|
Het |
Arid2 |
T |
G |
15: 96,266,592 (GRCm39) |
S547A |
possibly damaging |
Het |
Atf1 |
C |
A |
15: 100,143,170 (GRCm39) |
D46E |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,459,634 (GRCm39) |
F303Y |
possibly damaging |
Het |
Btbd18 |
T |
A |
2: 84,498,260 (GRCm39) |
S633T |
possibly damaging |
Het |
Btg4 |
T |
G |
9: 51,030,445 (GRCm39) |
F182V |
probably benign |
Het |
Cacna1e |
G |
A |
1: 154,437,516 (GRCm39) |
S340F |
probably damaging |
Het |
Camta2 |
A |
G |
11: 70,576,903 (GRCm39) |
W41R |
probably damaging |
Het |
Cbl |
A |
T |
9: 44,074,696 (GRCm39) |
D455E |
probably benign |
Het |
Ccdc162 |
A |
T |
10: 41,488,864 (GRCm39) |
D1208E |
probably benign |
Het |
Cd177 |
A |
T |
7: 24,443,842 (GRCm39) |
M752K |
probably damaging |
Het |
Cep290 |
A |
T |
10: 100,380,793 (GRCm39) |
H100L |
possibly damaging |
Het |
Chrnb2 |
T |
A |
3: 89,668,698 (GRCm39) |
I206F |
probably damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,791,009 (GRCm39) |
L274S |
probably benign |
Het |
Cyp2c40 |
T |
A |
19: 39,791,015 (GRCm39) |
Y272F |
probably benign |
Het |
Cyp2d22 |
C |
A |
15: 82,258,556 (GRCm39) |
A102S |
probably benign |
Het |
Cyp51 |
C |
T |
5: 4,136,490 (GRCm39) |
E435K |
probably benign |
Het |
Dchs2 |
T |
C |
3: 83,262,929 (GRCm39) |
F3066L |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,192 (GRCm39) |
R1076L |
probably damaging |
Het |
Dkk2 |
C |
T |
3: 131,791,801 (GRCm39) |
A3V |
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,165,964 (GRCm39) |
F543S |
probably benign |
Het |
Dpt |
A |
T |
1: 164,624,481 (GRCm39) |
S61C |
probably damaging |
Het |
Drg2 |
A |
T |
11: 60,353,096 (GRCm39) |
Y243F |
probably damaging |
Het |
Dsg2 |
A |
G |
18: 20,716,061 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
G |
1: 34,228,040 (GRCm39) |
L1878V |
possibly damaging |
Het |
F5 |
A |
G |
1: 164,036,509 (GRCm39) |
Y1890C |
probably benign |
Het |
Fat1 |
T |
C |
8: 45,405,739 (GRCm39) |
V830A |
probably damaging |
Het |
Fat2 |
C |
T |
11: 55,186,965 (GRCm39) |
D1294N |
probably benign |
Het |
Fbxo15 |
A |
G |
18: 84,983,618 (GRCm39) |
Y322C |
probably benign |
Het |
Fcsk |
A |
G |
8: 111,622,604 (GRCm39) |
F108S |
probably damaging |
Het |
Fhit |
A |
T |
14: 10,751,666 (GRCm38) |
N7K |
unknown |
Het |
Gabrb2 |
A |
G |
11: 42,488,370 (GRCm39) |
I279V |
probably damaging |
Het |
Galk2 |
T |
C |
2: 125,773,189 (GRCm39) |
F207S |
probably damaging |
Het |
Gtpbp3 |
C |
T |
8: 71,941,480 (GRCm39) |
L17F |
possibly damaging |
Het |
Gucy2c |
T |
A |
6: 136,714,446 (GRCm39) |
D460V |
probably benign |
Het |
Herc1 |
G |
A |
9: 66,400,462 (GRCm39) |
V4329I |
probably damaging |
Het |
Iqcn |
T |
C |
8: 71,162,067 (GRCm39) |
V420A |
probably benign |
Het |
Kirrel3 |
G |
A |
9: 34,946,460 (GRCm39) |
V740M |
probably damaging |
Het |
Macf1 |
C |
A |
4: 123,263,660 (GRCm39) |
V6956L |
probably damaging |
Het |
Mill1 |
C |
T |
7: 17,989,835 (GRCm39) |
A39V |
probably benign |
Het |
Mkln1 |
T |
A |
6: 31,469,588 (GRCm39) |
Y599* |
probably null |
Het |
Mrpl14 |
T |
A |
17: 46,009,039 (GRCm39) |
L46Q |
possibly damaging |
Het |
Myom2 |
G |
T |
8: 15,119,418 (GRCm39) |
R103L |
possibly damaging |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Ndst2 |
A |
T |
14: 20,778,232 (GRCm39) |
V449D |
probably damaging |
Het |
Nell1 |
T |
A |
7: 49,770,335 (GRCm39) |
H131Q |
probably benign |
Het |
Nos3 |
G |
C |
5: 24,572,218 (GRCm39) |
R97P |
probably benign |
Het |
Npc1 |
A |
T |
18: 12,327,297 (GRCm39) |
F1099L |
probably benign |
Het |
Nxpe5 |
T |
A |
5: 138,249,802 (GRCm39) |
W531R |
probably damaging |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or1j1 |
A |
T |
2: 36,702,330 (GRCm39) |
L258H |
probably damaging |
Het |
Or4c110 |
T |
C |
2: 88,832,712 (GRCm39) |
|
probably benign |
Het |
Or5b98 |
A |
T |
19: 12,931,366 (GRCm39) |
T138S |
probably benign |
Het |
Or6c210 |
A |
G |
10: 129,495,933 (GRCm39) |
D86G |
probably damaging |
Het |
Osmr |
T |
C |
15: 6,845,102 (GRCm39) |
N889S |
possibly damaging |
Het |
Oxct2b |
A |
G |
4: 123,010,301 (GRCm39) |
I74V |
possibly damaging |
Het |
Pakap |
A |
G |
4: 57,886,319 (GRCm39) |
T859A |
possibly damaging |
Het |
Phldb3 |
C |
A |
7: 24,326,134 (GRCm39) |
A572D |
probably damaging |
Het |
Pigr |
A |
G |
1: 130,774,247 (GRCm39) |
E409G |
probably damaging |
Het |
Ptprs |
T |
C |
17: 56,735,947 (GRCm39) |
E674G |
probably benign |
Het |
Ptpru |
G |
A |
4: 131,520,903 (GRCm39) |
T801I |
possibly damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,829,631 (GRCm39) |
D200V |
probably damaging |
Het |
Rb1cc1 |
A |
T |
1: 6,333,448 (GRCm39) |
R1429* |
probably null |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rnpep |
A |
T |
1: 135,211,514 (GRCm39) |
L78Q |
probably damaging |
Het |
Rtn2 |
A |
T |
7: 19,027,791 (GRCm39) |
I394F |
probably damaging |
Het |
Satb2 |
A |
T |
1: 56,870,623 (GRCm39) |
V572D |
possibly damaging |
Het |
Sds |
T |
C |
5: 120,617,001 (GRCm39) |
|
probably benign |
Het |
Serpina10 |
TTCCTCCTCCTCCTCCTCCTCCTCC |
TTCCTCCTCCTCCTCCTCCTCC |
12: 103,595,032 (GRCm39) |
|
probably benign |
Het |
Sgo2a |
T |
C |
1: 58,056,300 (GRCm39) |
I828T |
possibly damaging |
Het |
Slc25a33 |
T |
A |
4: 149,840,609 (GRCm39) |
K79N |
probably benign |
Het |
Slc25a51 |
A |
C |
4: 45,399,783 (GRCm39) |
F136V |
probably benign |
Het |
Slfn14 |
T |
A |
11: 83,174,119 (GRCm39) |
K291* |
probably null |
Het |
Sp100 |
A |
G |
1: 85,624,819 (GRCm39) |
K403E |
possibly damaging |
Het |
Spaca1 |
C |
T |
4: 34,049,837 (GRCm39) |
E54K |
possibly damaging |
Het |
Sympk |
T |
G |
7: 18,787,373 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
T |
10: 5,067,031 (GRCm39) |
V7078D |
probably damaging |
Het |
Tas2r121 |
T |
A |
6: 132,677,772 (GRCm39) |
I67L |
probably benign |
Het |
Tha1 |
T |
C |
11: 117,759,323 (GRCm39) |
K389E |
probably benign |
Het |
Thbs2 |
T |
A |
17: 14,900,584 (GRCm39) |
Q541L |
probably benign |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tmem94 |
T |
C |
11: 115,679,218 (GRCm39) |
|
probably null |
Het |
Tnfsf13 |
A |
G |
11: 69,575,983 (GRCm39) |
C35R |
probably damaging |
Het |
Trcg1 |
C |
A |
9: 57,149,564 (GRCm39) |
Q379K |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,168,007 (GRCm39) |
S1507P |
probably damaging |
Het |
Uckl1 |
A |
G |
2: 181,215,049 (GRCm39) |
I268T |
probably damaging |
Het |
Uvrag |
T |
C |
7: 98,641,174 (GRCm39) |
K289E |
possibly damaging |
Het |
Vmn2r104 |
C |
A |
17: 20,250,483 (GRCm39) |
C596F |
possibly damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,201,626 (GRCm39) |
F293I |
probably damaging |
Het |
Vps13b |
T |
A |
15: 35,669,052 (GRCm39) |
|
probably null |
Het |
Wipf1 |
G |
A |
2: 73,267,879 (GRCm39) |
P173L |
possibly damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zscan4f |
T |
A |
7: 11,135,154 (GRCm39) |
C187S |
possibly damaging |
Het |
|
Other mutations in A2ml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00513:A2ml1
|
APN |
6 |
128,555,119 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00596:A2ml1
|
APN |
6 |
128,547,030 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00912:A2ml1
|
APN |
6 |
128,529,270 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01320:A2ml1
|
APN |
6 |
128,552,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01470:A2ml1
|
APN |
6 |
128,557,375 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01576:A2ml1
|
APN |
6 |
128,531,293 (GRCm39) |
splice site |
probably benign |
|
IGL01761:A2ml1
|
APN |
6 |
128,523,300 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01792:A2ml1
|
APN |
6 |
128,537,642 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01843:A2ml1
|
APN |
6 |
128,530,301 (GRCm39) |
splice site |
probably benign |
|
IGL01946:A2ml1
|
APN |
6 |
128,547,442 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02016:A2ml1
|
APN |
6 |
128,535,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:A2ml1
|
APN |
6 |
128,524,173 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02269:A2ml1
|
APN |
6 |
128,530,301 (GRCm39) |
splice site |
probably benign |
|
IGL02589:A2ml1
|
APN |
6 |
128,558,463 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02959:A2ml1
|
APN |
6 |
128,544,023 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02970:A2ml1
|
APN |
6 |
128,546,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:A2ml1
|
APN |
6 |
128,530,239 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03298:A2ml1
|
APN |
6 |
128,520,923 (GRCm39) |
missense |
probably benign |
0.00 |
1mM(1):A2ml1
|
UTSW |
6 |
128,557,923 (GRCm39) |
missense |
probably benign |
0.02 |
R0055:A2ml1
|
UTSW |
6 |
128,547,057 (GRCm39) |
splice site |
probably benign |
|
R0055:A2ml1
|
UTSW |
6 |
128,547,057 (GRCm39) |
splice site |
probably benign |
|
R0069:A2ml1
|
UTSW |
6 |
128,538,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0069:A2ml1
|
UTSW |
6 |
128,538,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:A2ml1
|
UTSW |
6 |
128,552,602 (GRCm39) |
splice site |
probably benign |
|
R0299:A2ml1
|
UTSW |
6 |
128,530,195 (GRCm39) |
splice site |
probably benign |
|
R0523:A2ml1
|
UTSW |
6 |
128,535,289 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0565:A2ml1
|
UTSW |
6 |
128,545,706 (GRCm39) |
nonsense |
probably null |
|
R0599:A2ml1
|
UTSW |
6 |
128,529,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:A2ml1
|
UTSW |
6 |
128,527,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R0732:A2ml1
|
UTSW |
6 |
128,523,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:A2ml1
|
UTSW |
6 |
128,537,609 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1070:A2ml1
|
UTSW |
6 |
128,520,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1166:A2ml1
|
UTSW |
6 |
128,547,880 (GRCm39) |
missense |
probably benign |
0.00 |
R1278:A2ml1
|
UTSW |
6 |
128,535,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:A2ml1
|
UTSW |
6 |
128,520,923 (GRCm39) |
missense |
probably benign |
0.00 |
R1536:A2ml1
|
UTSW |
6 |
128,524,196 (GRCm39) |
nonsense |
probably null |
|
R1786:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:A2ml1
|
UTSW |
6 |
128,520,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:A2ml1
|
UTSW |
6 |
128,543,236 (GRCm39) |
missense |
probably benign |
0.34 |
R1863:A2ml1
|
UTSW |
6 |
128,527,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R2007:A2ml1
|
UTSW |
6 |
128,519,855 (GRCm39) |
missense |
probably benign |
0.13 |
R2062:A2ml1
|
UTSW |
6 |
128,529,271 (GRCm39) |
missense |
probably benign |
0.08 |
R2127:A2ml1
|
UTSW |
6 |
128,535,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:A2ml1
|
UTSW |
6 |
128,524,268 (GRCm39) |
missense |
probably null |
0.34 |
R2319:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2321:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2322:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2369:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2370:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2371:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2372:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2375:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2893:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2894:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R3438:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R3615:A2ml1
|
UTSW |
6 |
128,535,257 (GRCm39) |
missense |
probably benign |
0.07 |
R3616:A2ml1
|
UTSW |
6 |
128,535,257 (GRCm39) |
missense |
probably benign |
0.07 |
R3773:A2ml1
|
UTSW |
6 |
128,532,046 (GRCm39) |
missense |
probably benign |
0.02 |
R3785:A2ml1
|
UTSW |
6 |
128,521,887 (GRCm39) |
critical splice donor site |
probably null |
|
R3803:A2ml1
|
UTSW |
6 |
128,522,033 (GRCm39) |
missense |
probably benign |
0.17 |
R3824:A2ml1
|
UTSW |
6 |
128,545,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R3878:A2ml1
|
UTSW |
6 |
128,531,324 (GRCm39) |
missense |
probably benign |
0.05 |
R4176:A2ml1
|
UTSW |
6 |
128,522,000 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4229:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4230:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4348:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4351:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4352:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4353:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4427:A2ml1
|
UTSW |
6 |
128,522,009 (GRCm39) |
missense |
probably benign |
0.00 |
R4971:A2ml1
|
UTSW |
6 |
128,524,190 (GRCm39) |
missense |
probably damaging |
0.98 |
R5014:A2ml1
|
UTSW |
6 |
128,520,896 (GRCm39) |
missense |
probably benign |
0.00 |
R5369:A2ml1
|
UTSW |
6 |
128,545,796 (GRCm39) |
missense |
probably damaging |
0.97 |
R5532:A2ml1
|
UTSW |
6 |
128,530,293 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5860:A2ml1
|
UTSW |
6 |
128,518,024 (GRCm39) |
missense |
probably benign |
0.15 |
R5872:A2ml1
|
UTSW |
6 |
128,538,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5926:A2ml1
|
UTSW |
6 |
128,537,608 (GRCm39) |
missense |
probably benign |
|
R5977:A2ml1
|
UTSW |
6 |
128,558,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R5980:A2ml1
|
UTSW |
6 |
128,544,018 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6014:A2ml1
|
UTSW |
6 |
128,548,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:A2ml1
|
UTSW |
6 |
128,526,799 (GRCm39) |
nonsense |
probably null |
|
R6032:A2ml1
|
UTSW |
6 |
128,526,799 (GRCm39) |
nonsense |
probably null |
|
R6061:A2ml1
|
UTSW |
6 |
128,545,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:A2ml1
|
UTSW |
6 |
128,535,655 (GRCm39) |
splice site |
probably null |
|
R6331:A2ml1
|
UTSW |
6 |
128,529,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6465:A2ml1
|
UTSW |
6 |
128,518,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R6640:A2ml1
|
UTSW |
6 |
128,530,248 (GRCm39) |
missense |
probably benign |
0.41 |
R6792:A2ml1
|
UTSW |
6 |
128,523,292 (GRCm39) |
nonsense |
probably null |
|
R6793:A2ml1
|
UTSW |
6 |
128,523,292 (GRCm39) |
nonsense |
probably null |
|
R7207:A2ml1
|
UTSW |
6 |
128,527,734 (GRCm39) |
missense |
probably benign |
0.04 |
R7378:A2ml1
|
UTSW |
6 |
128,523,210 (GRCm39) |
critical splice donor site |
probably null |
|
R7556:A2ml1
|
UTSW |
6 |
128,546,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:A2ml1
|
UTSW |
6 |
128,557,303 (GRCm39) |
missense |
probably benign |
0.08 |
R8017:A2ml1
|
UTSW |
6 |
128,558,410 (GRCm39) |
critical splice donor site |
probably null |
|
R8019:A2ml1
|
UTSW |
6 |
128,558,410 (GRCm39) |
critical splice donor site |
probably null |
|
R8035:A2ml1
|
UTSW |
6 |
128,530,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R8144:A2ml1
|
UTSW |
6 |
128,546,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8365:A2ml1
|
UTSW |
6 |
128,557,918 (GRCm39) |
nonsense |
probably null |
|
R8382:A2ml1
|
UTSW |
6 |
128,537,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8388:A2ml1
|
UTSW |
6 |
128,548,937 (GRCm39) |
missense |
probably benign |
0.03 |
R8717:A2ml1
|
UTSW |
6 |
128,543,958 (GRCm39) |
missense |
probably benign |
0.00 |
R8947:A2ml1
|
UTSW |
6 |
128,529,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:A2ml1
|
UTSW |
6 |
128,545,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R9025:A2ml1
|
UTSW |
6 |
128,534,545 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9083:A2ml1
|
UTSW |
6 |
128,534,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9129:A2ml1
|
UTSW |
6 |
128,523,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:A2ml1
|
UTSW |
6 |
128,536,032 (GRCm39) |
missense |
probably benign |
|
R9165:A2ml1
|
UTSW |
6 |
128,537,632 (GRCm39) |
missense |
probably benign |
|
R9285:A2ml1
|
UTSW |
6 |
128,526,756 (GRCm39) |
missense |
probably benign |
|
R9408:A2ml1
|
UTSW |
6 |
128,522,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R9486:A2ml1
|
UTSW |
6 |
128,546,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R9781:A2ml1
|
UTSW |
6 |
128,519,860 (GRCm39) |
missense |
probably benign |
0.01 |
RF014:A2ml1
|
UTSW |
6 |
128,547,031 (GRCm39) |
missense |
probably damaging |
0.96 |
X0063:A2ml1
|
UTSW |
6 |
128,548,975 (GRCm39) |
missense |
probably benign |
|
Z1176:A2ml1
|
UTSW |
6 |
128,548,940 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:A2ml1
|
UTSW |
6 |
128,552,570 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:A2ml1
|
UTSW |
6 |
128,538,579 (GRCm39) |
nonsense |
probably null |
|
Z1177:A2ml1
|
UTSW |
6 |
128,522,039 (GRCm39) |
missense |
probably benign |
|
|