Other mutations in this stock |
Total: 133 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
T |
C |
7: 45,824,795 (GRCm39) |
K134R |
possibly damaging |
Het |
Adamts17 |
T |
C |
7: 66,774,820 (GRCm39) |
S980P |
probably damaging |
Het |
Adap2 |
T |
A |
11: 80,061,508 (GRCm39) |
I221K |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,539,876 (GRCm39) |
R5681Q |
probably damaging |
Het |
Adipor1 |
T |
A |
1: 134,350,841 (GRCm39) |
L30Q |
probably benign |
Het |
Agpat5 |
A |
G |
8: 18,928,181 (GRCm39) |
T249A |
probably benign |
Het |
Agxt2 |
G |
T |
15: 10,392,021 (GRCm39) |
G329V |
probably damaging |
Het |
Ankrd28 |
A |
G |
14: 31,427,233 (GRCm39) |
V801A |
possibly damaging |
Het |
Ap1g2 |
A |
G |
14: 55,337,229 (GRCm39) |
V702A |
possibly damaging |
Het |
Arid3a |
A |
G |
10: 79,786,540 (GRCm39) |
Q429R |
probably damaging |
Het |
Arsb |
T |
A |
13: 93,998,658 (GRCm39) |
L322Q |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,891,729 (GRCm39) |
T1203A |
probably damaging |
Het |
Atad2 |
T |
A |
15: 57,960,101 (GRCm39) |
N1308Y |
possibly damaging |
Het |
Atp10b |
A |
T |
11: 43,121,245 (GRCm39) |
R969S |
probably benign |
Het |
Bmp10 |
T |
C |
6: 87,410,702 (GRCm39) |
I165T |
possibly damaging |
Het |
Ccdc121rt2 |
C |
A |
5: 112,597,667 (GRCm39) |
C71* |
probably null |
Het |
Ccne1 |
A |
G |
7: 37,805,702 (GRCm39) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 134,953,240 (GRCm39) |
N1565D |
probably damaging |
Het |
Chd1 |
A |
T |
17: 15,982,748 (GRCm39) |
E1404D |
probably benign |
Het |
Chodl |
T |
C |
16: 78,738,314 (GRCm39) |
I94T |
possibly damaging |
Het |
Chsy3 |
T |
C |
18: 59,542,584 (GRCm39) |
F574S |
probably damaging |
Het |
Clpb |
A |
T |
7: 101,412,863 (GRCm39) |
I317F |
probably damaging |
Het |
Cnga3 |
T |
A |
1: 37,300,954 (GRCm39) |
V558D |
possibly damaging |
Het |
Col9a1 |
C |
T |
1: 24,261,554 (GRCm39) |
P573S |
probably damaging |
Het |
Crat |
A |
T |
2: 30,303,073 (GRCm39) |
D71E |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,794,385 (GRCm39) |
T707A |
probably benign |
Het |
Ctsr |
T |
A |
13: 61,310,259 (GRCm39) |
R132S |
probably benign |
Het |
Ctu2 |
T |
C |
8: 123,206,024 (GRCm39) |
L255P |
probably damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,837,810 (GRCm39) |
Y424C |
probably damaging |
Het |
Ddx27 |
A |
T |
2: 166,876,029 (GRCm39) |
K726N |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,749,772 (GRCm39) |
Q121R |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,335,026 (GRCm39) |
F192S |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,020,383 (GRCm39) |
S487N |
probably benign |
Het |
Eml1 |
T |
A |
12: 108,487,655 (GRCm39) |
F524L |
possibly damaging |
Het |
Espl1 |
T |
C |
15: 102,213,477 (GRCm39) |
I601T |
probably benign |
Het |
Fbxo40 |
C |
A |
16: 36,789,713 (GRCm39) |
V466L |
probably damaging |
Het |
Frmpd1 |
C |
T |
4: 45,283,711 (GRCm39) |
T844M |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,917,011 (GRCm39) |
|
probably benign |
Het |
Fuom |
G |
T |
7: 139,679,521 (GRCm39) |
T133K |
probably benign |
Het |
Garnl3 |
T |
A |
2: 32,895,212 (GRCm39) |
H619L |
probably damaging |
Het |
Gm4861 |
G |
T |
3: 137,257,876 (GRCm39) |
N36K |
unknown |
Het |
Gps2 |
G |
T |
11: 69,806,195 (GRCm39) |
M153I |
probably benign |
Het |
Gtf2ird1 |
A |
G |
5: 134,444,099 (GRCm39) |
V52A |
probably damaging |
Het |
Gtpbp8 |
A |
T |
16: 44,565,785 (GRCm39) |
D137E |
probably benign |
Het |
Haus4 |
A |
G |
14: 54,781,733 (GRCm39) |
C213R |
probably damaging |
Het |
Hdc |
T |
A |
2: 126,448,317 (GRCm39) |
H142L |
possibly damaging |
Het |
Hephl1 |
T |
C |
9: 14,965,283 (GRCm39) |
D1069G |
possibly damaging |
Het |
Herc6 |
T |
A |
6: 57,602,926 (GRCm39) |
V535D |
probably damaging |
Het |
Hipk3 |
A |
T |
2: 104,260,533 (GRCm39) |
H1082Q |
possibly damaging |
Het |
Hps5 |
A |
T |
7: 46,422,691 (GRCm39) |
V513D |
probably damaging |
Het |
Ifna13 |
T |
A |
4: 88,562,412 (GRCm39) |
I71F |
probably damaging |
Het |
Il1rl2 |
T |
C |
1: 40,402,484 (GRCm39) |
I426T |
probably damaging |
Het |
Irf5 |
A |
T |
6: 29,536,738 (GRCm39) |
D483V |
probably benign |
Het |
Jakmip3 |
A |
G |
7: 138,621,867 (GRCm39) |
R256G |
probably damaging |
Het |
Jazf1 |
T |
C |
6: 52,754,600 (GRCm39) |
I159V |
probably damaging |
Het |
Kmo |
A |
G |
1: 175,479,154 (GRCm39) |
D230G |
possibly damaging |
Het |
Lrrc74b |
A |
G |
16: 17,371,058 (GRCm39) |
V213A |
probably benign |
Het |
LTO1 |
A |
G |
7: 144,470,205 (GRCm39) |
S45G |
probably damaging |
Het |
Ly6g5b |
T |
C |
17: 35,333,704 (GRCm39) |
D36G |
possibly damaging |
Het |
Mab21l4 |
T |
C |
1: 93,079,730 (GRCm39) |
*453W |
probably null |
Het |
Macc1 |
T |
G |
12: 119,409,466 (GRCm39) |
L78R |
probably damaging |
Het |
Mettl4 |
A |
T |
17: 95,055,285 (GRCm39) |
D51E |
possibly damaging |
Het |
Mfap1a |
G |
A |
2: 121,332,835 (GRCm39) |
L199F |
possibly damaging |
Het |
Mmp17 |
G |
T |
5: 129,679,190 (GRCm39) |
R363L |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,324,052 (GRCm39) |
A1130T |
possibly damaging |
Het |
Mrpl15 |
C |
T |
1: 4,847,805 (GRCm39) |
A165T |
probably damaging |
Het |
Mrpl45 |
G |
A |
11: 97,206,770 (GRCm39) |
|
probably null |
Het |
Ms4a3 |
C |
T |
19: 11,613,204 (GRCm39) |
A85T |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,830,882 (GRCm39) |
D77E |
probably benign |
Het |
Muc6 |
A |
G |
7: 141,217,011 (GRCm39) |
L2489P |
probably damaging |
Het |
Myl3 |
G |
A |
9: 110,595,802 (GRCm39) |
E100K |
probably damaging |
Het |
Nbea |
T |
A |
3: 55,992,743 (GRCm39) |
N288Y |
probably damaging |
Het |
Ncoa7 |
A |
G |
10: 30,574,166 (GRCm39) |
V181A |
probably benign |
Het |
Oat |
C |
T |
7: 132,159,934 (GRCm39) |
V429M |
probably benign |
Het |
Or2ak6 |
A |
T |
11: 58,593,449 (GRCm39) |
*307C |
probably null |
Het |
Or4x6 |
T |
G |
2: 89,949,427 (GRCm39) |
I172L |
probably damaging |
Het |
Or5d36 |
A |
T |
2: 87,901,300 (GRCm39) |
L142Q |
probably damaging |
Het |
Or5p80 |
T |
C |
7: 108,230,045 (GRCm39) |
I282T |
probably benign |
Het |
Or5w19 |
G |
A |
2: 87,698,805 (GRCm39) |
V157I |
probably benign |
Het |
Or6b13 |
A |
G |
7: 139,782,144 (GRCm39) |
F180L |
probably benign |
Het |
Or6c69b |
T |
A |
10: 129,626,759 (GRCm39) |
K233M |
probably damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,146 (GRCm39) |
T116A |
probably benign |
Het |
Or8s16 |
T |
A |
15: 98,211,261 (GRCm39) |
M57L |
probably damaging |
Het |
Otof |
A |
G |
5: 30,533,713 (GRCm39) |
S1464P |
probably benign |
Het |
Otogl |
A |
T |
10: 107,613,436 (GRCm39) |
Y2010N |
probably damaging |
Het |
Pgap3 |
C |
T |
11: 98,291,040 (GRCm39) |
|
probably null |
Het |
Pgbd5 |
T |
A |
8: 125,100,988 (GRCm39) |
K332* |
probably null |
Het |
Pgs1 |
C |
T |
11: 117,896,553 (GRCm39) |
P410L |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,363,434 (GRCm39) |
S618N |
probably benign |
Het |
Plcb1 |
A |
T |
2: 135,228,222 (GRCm39) |
D1073V |
probably damaging |
Het |
Pola2 |
T |
A |
19: 6,001,208 (GRCm39) |
T309S |
probably benign |
Het |
Polg2 |
T |
A |
11: 106,669,787 (GRCm39) |
H161L |
probably damaging |
Het |
Postn |
T |
A |
3: 54,285,033 (GRCm39) |
|
probably null |
Het |
Ppt1 |
G |
T |
4: 122,739,784 (GRCm39) |
C128F |
probably damaging |
Het |
Ptpn12 |
G |
A |
5: 21,198,261 (GRCm39) |
P678S |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,139,812 (GRCm39) |
|
probably null |
Het |
Rgs22 |
T |
C |
15: 36,101,950 (GRCm39) |
N216S |
probably benign |
Het |
Rgs7bp |
T |
A |
13: 105,088,090 (GRCm39) |
D228V |
probably damaging |
Het |
Rhobtb2 |
A |
T |
14: 70,034,062 (GRCm39) |
S388T |
probably benign |
Het |
Rnps1 |
C |
T |
17: 24,639,364 (GRCm39) |
R138C |
unknown |
Het |
Rpl38 |
T |
C |
11: 114,562,602 (GRCm39) |
V36A |
probably benign |
Het |
Rps7 |
G |
T |
12: 28,681,752 (GRCm39) |
H126Q |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,785,010 (GRCm39) |
Q999K |
possibly damaging |
Het |
Slc19a3 |
A |
G |
1: 82,997,089 (GRCm39) |
V373A |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,924,941 (GRCm39) |
V113E |
probably benign |
Het |
Ss18l1 |
A |
T |
2: 179,705,138 (GRCm39) |
T377S |
unknown |
Het |
Surf1 |
A |
G |
2: 26,805,982 (GRCm39) |
F38L |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,325,142 (GRCm39) |
R556H |
probably damaging |
Het |
Tmem184b |
A |
G |
15: 79,250,014 (GRCm39) |
S254P |
probably damaging |
Het |
Tnfrsf4 |
G |
T |
4: 156,100,692 (GRCm39) |
R237L |
possibly damaging |
Het |
Tnk2 |
C |
A |
16: 32,482,560 (GRCm39) |
|
probably benign |
Het |
Tnks |
A |
T |
8: 35,305,684 (GRCm39) |
D1191E |
probably damaging |
Het |
Tnr |
C |
A |
1: 159,722,607 (GRCm39) |
Y1017* |
probably null |
Het |
Tomm34 |
A |
G |
2: 163,902,926 (GRCm39) |
I128T |
probably benign |
Het |
Trim2 |
G |
A |
3: 84,085,099 (GRCm39) |
S540F |
possibly damaging |
Het |
Trio |
A |
T |
15: 27,732,977 (GRCm39) |
I2968N |
probably damaging |
Het |
Ttc24 |
T |
C |
3: 87,982,181 (GRCm39) |
E17G |
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,612,078 (GRCm39) |
H1117R |
probably benign |
Het |
Ttn |
A |
T |
2: 76,565,752 (GRCm39) |
V28200D |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,592,730 (GRCm39) |
S20801T |
possibly damaging |
Het |
Ube3d |
C |
T |
9: 86,330,840 (GRCm39) |
C114Y |
probably damaging |
Het |
Ugt2b37 |
A |
C |
5: 87,388,716 (GRCm39) |
L499R |
probably damaging |
Het |
Vmn1r81 |
T |
C |
7: 11,994,589 (GRCm39) |
I6M |
possibly damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,149,593 (GRCm39) |
Y327F |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,709,653 (GRCm39) |
S1867P |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,208,331 (GRCm39) |
V362A |
probably benign |
Het |
Zan |
T |
A |
5: 137,387,201 (GRCm39) |
M4951L |
unknown |
Het |
Zcwpw1 |
T |
A |
5: 137,809,884 (GRCm39) |
L337Q |
probably damaging |
Het |
Zfp2 |
A |
T |
11: 50,790,809 (GRCm39) |
D411E |
possibly damaging |
Het |
Zfp628 |
C |
T |
7: 4,923,767 (GRCm39) |
T663I |
probably benign |
Het |
Zfpm1 |
T |
A |
8: 123,061,663 (GRCm39) |
|
probably null |
Het |
Zfyve19 |
T |
C |
2: 119,041,693 (GRCm39) |
S87P |
probably benign |
Het |
Zswim9 |
T |
A |
7: 12,994,141 (GRCm39) |
K672* |
probably null |
Het |
|
Other mutations in Chd7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Chd7
|
APN |
4 |
8,859,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00510:Chd7
|
APN |
4 |
8,801,404 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00741:Chd7
|
APN |
4 |
8,839,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00796:Chd7
|
APN |
4 |
8,847,271 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00907:Chd7
|
APN |
4 |
8,840,435 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00930:Chd7
|
APN |
4 |
8,805,181 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01542:Chd7
|
APN |
4 |
8,859,285 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01602:Chd7
|
APN |
4 |
8,833,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01605:Chd7
|
APN |
4 |
8,833,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Chd7
|
APN |
4 |
8,827,033 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02434:Chd7
|
APN |
4 |
8,752,145 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02531:Chd7
|
APN |
4 |
8,854,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02626:Chd7
|
APN |
4 |
8,826,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Chd7
|
APN |
4 |
8,751,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02972:Chd7
|
APN |
4 |
8,855,174 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03329:Chd7
|
APN |
4 |
8,841,108 (GRCm39) |
missense |
probably damaging |
1.00 |
Fili
|
UTSW |
4 |
8,839,523 (GRCm39) |
missense |
probably damaging |
1.00 |
D4043:Chd7
|
UTSW |
4 |
8,862,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Chd7
|
UTSW |
4 |
8,828,398 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4466001:Chd7
|
UTSW |
4 |
8,753,101 (GRCm39) |
missense |
unknown |
|
PIT4472001:Chd7
|
UTSW |
4 |
8,753,101 (GRCm39) |
missense |
unknown |
|
R0157:Chd7
|
UTSW |
4 |
8,833,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0179:Chd7
|
UTSW |
4 |
8,862,516 (GRCm39) |
missense |
probably benign |
0.22 |
R0240:Chd7
|
UTSW |
4 |
8,852,670 (GRCm39) |
unclassified |
probably benign |
|
R0388:Chd7
|
UTSW |
4 |
8,854,560 (GRCm39) |
missense |
probably benign |
0.27 |
R0462:Chd7
|
UTSW |
4 |
8,850,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Chd7
|
UTSW |
4 |
8,805,139 (GRCm39) |
intron |
probably benign |
|
R0657:Chd7
|
UTSW |
4 |
8,753,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R0799:Chd7
|
UTSW |
4 |
8,801,310 (GRCm39) |
intron |
probably benign |
|
R0885:Chd7
|
UTSW |
4 |
8,866,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Chd7
|
UTSW |
4 |
8,822,402 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1086:Chd7
|
UTSW |
4 |
8,866,458 (GRCm39) |
missense |
probably benign |
0.04 |
R1353:Chd7
|
UTSW |
4 |
8,839,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Chd7
|
UTSW |
4 |
8,840,561 (GRCm39) |
splice site |
probably null |
|
R1466:Chd7
|
UTSW |
4 |
8,840,561 (GRCm39) |
splice site |
probably null |
|
R1605:Chd7
|
UTSW |
4 |
8,844,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1693:Chd7
|
UTSW |
4 |
8,864,307 (GRCm39) |
critical splice donor site |
probably null |
|
R1695:Chd7
|
UTSW |
4 |
8,833,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1964:Chd7
|
UTSW |
4 |
8,865,978 (GRCm39) |
missense |
probably damaging |
0.96 |
R2020:Chd7
|
UTSW |
4 |
8,855,226 (GRCm39) |
missense |
probably benign |
0.00 |
R2134:Chd7
|
UTSW |
4 |
8,753,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R2171:Chd7
|
UTSW |
4 |
8,752,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Chd7
|
UTSW |
4 |
8,785,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2300:Chd7
|
UTSW |
4 |
8,855,241 (GRCm39) |
missense |
probably benign |
0.02 |
R2355:Chd7
|
UTSW |
4 |
8,801,350 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3153:Chd7
|
UTSW |
4 |
8,855,174 (GRCm39) |
missense |
probably benign |
0.30 |
R3430:Chd7
|
UTSW |
4 |
8,844,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Chd7
|
UTSW |
4 |
8,752,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Chd7
|
UTSW |
4 |
8,865,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Chd7
|
UTSW |
4 |
8,785,658 (GRCm39) |
intron |
probably benign |
|
R4332:Chd7
|
UTSW |
4 |
8,854,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Chd7
|
UTSW |
4 |
8,866,353 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4571:Chd7
|
UTSW |
4 |
8,866,217 (GRCm39) |
missense |
probably benign |
0.09 |
R4722:Chd7
|
UTSW |
4 |
8,822,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4821:Chd7
|
UTSW |
4 |
8,844,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Chd7
|
UTSW |
4 |
8,838,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R5205:Chd7
|
UTSW |
4 |
8,752,509 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5344:Chd7
|
UTSW |
4 |
8,844,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Chd7
|
UTSW |
4 |
8,828,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Chd7
|
UTSW |
4 |
8,847,149 (GRCm39) |
missense |
probably benign |
0.09 |
R5583:Chd7
|
UTSW |
4 |
8,752,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Chd7
|
UTSW |
4 |
8,866,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R5905:Chd7
|
UTSW |
4 |
8,840,553 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6091:Chd7
|
UTSW |
4 |
8,751,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R6126:Chd7
|
UTSW |
4 |
8,826,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6399:Chd7
|
UTSW |
4 |
8,828,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Chd7
|
UTSW |
4 |
8,833,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6810:Chd7
|
UTSW |
4 |
8,839,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Chd7
|
UTSW |
4 |
8,811,501 (GRCm39) |
splice site |
probably null |
|
R6952:Chd7
|
UTSW |
4 |
8,856,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R6986:Chd7
|
UTSW |
4 |
8,859,285 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6990:Chd7
|
UTSW |
4 |
8,844,525 (GRCm39) |
missense |
probably benign |
0.28 |
R7139:Chd7
|
UTSW |
4 |
8,865,865 (GRCm39) |
missense |
probably benign |
0.00 |
R7288:Chd7
|
UTSW |
4 |
8,847,093 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7355:Chd7
|
UTSW |
4 |
8,752,196 (GRCm39) |
missense |
unknown |
|
R7452:Chd7
|
UTSW |
4 |
8,854,731 (GRCm39) |
missense |
probably benign |
0.03 |
R7471:Chd7
|
UTSW |
4 |
8,859,197 (GRCm39) |
missense |
probably damaging |
0.96 |
R7588:Chd7
|
UTSW |
4 |
8,864,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Chd7
|
UTSW |
4 |
8,805,234 (GRCm39) |
missense |
probably benign |
0.00 |
R7744:Chd7
|
UTSW |
4 |
8,862,485 (GRCm39) |
splice site |
probably null |
|
R7842:Chd7
|
UTSW |
4 |
8,854,115 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Chd7
|
UTSW |
4 |
8,826,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7934:Chd7
|
UTSW |
4 |
8,854,121 (GRCm39) |
missense |
probably benign |
0.00 |
R7983:Chd7
|
UTSW |
4 |
8,844,609 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7983:Chd7
|
UTSW |
4 |
8,752,628 (GRCm39) |
missense |
unknown |
|
R8022:Chd7
|
UTSW |
4 |
8,751,605 (GRCm39) |
missense |
unknown |
|
R8161:Chd7
|
UTSW |
4 |
8,855,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Chd7
|
UTSW |
4 |
8,839,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R8278:Chd7
|
UTSW |
4 |
8,862,485 (GRCm39) |
splice site |
probably null |
|
R8358:Chd7
|
UTSW |
4 |
8,839,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Chd7
|
UTSW |
4 |
8,811,465 (GRCm39) |
missense |
probably benign |
0.06 |
R8483:Chd7
|
UTSW |
4 |
8,822,412 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8507:Chd7
|
UTSW |
4 |
8,858,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Chd7
|
UTSW |
4 |
8,859,211 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8695:Chd7
|
UTSW |
4 |
8,850,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8700:Chd7
|
UTSW |
4 |
8,833,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Chd7
|
UTSW |
4 |
8,866,069 (GRCm39) |
missense |
probably benign |
0.31 |
R8774:Chd7
|
UTSW |
4 |
8,854,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Chd7
|
UTSW |
4 |
8,854,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Chd7
|
UTSW |
4 |
8,838,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Chd7
|
UTSW |
4 |
8,839,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R9018:Chd7
|
UTSW |
4 |
8,847,083 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9122:Chd7
|
UTSW |
4 |
8,840,510 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9131:Chd7
|
UTSW |
4 |
8,785,642 (GRCm39) |
missense |
|
|
R9182:Chd7
|
UTSW |
4 |
8,838,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Chd7
|
UTSW |
4 |
8,805,272 (GRCm39) |
missense |
probably benign |
0.03 |
R9254:Chd7
|
UTSW |
4 |
8,752,210 (GRCm39) |
missense |
unknown |
|
R9379:Chd7
|
UTSW |
4 |
8,752,210 (GRCm39) |
missense |
unknown |
|
R9388:Chd7
|
UTSW |
4 |
8,865,756 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9455:Chd7
|
UTSW |
4 |
8,752,061 (GRCm39) |
missense |
unknown |
|
R9531:Chd7
|
UTSW |
4 |
8,858,489 (GRCm39) |
missense |
|
|
R9577:Chd7
|
UTSW |
4 |
8,752,964 (GRCm39) |
missense |
unknown |
|
R9634:Chd7
|
UTSW |
4 |
8,832,499 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Chd7
|
UTSW |
4 |
8,844,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|