Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5330417H12Rik |
T |
A |
7: 107,223,952 (GRCm39) |
|
probably benign |
Het |
A1cf |
A |
T |
19: 31,886,196 (GRCm39) |
N35I |
possibly damaging |
Het |
Abca2 |
T |
C |
2: 25,330,542 (GRCm39) |
I1106T |
possibly damaging |
Het |
Abca4 |
G |
A |
3: 121,956,577 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,581,632 (GRCm39) |
D4804G |
probably benign |
Het |
Adk |
T |
A |
14: 21,102,708 (GRCm39) |
M1K |
probably null |
Het |
Aff3 |
T |
C |
1: 38,230,364 (GRCm39) |
N1006D |
probably damaging |
Het |
Akap12 |
A |
G |
10: 4,305,475 (GRCm39) |
T762A |
probably benign |
Het |
Atosa |
C |
G |
9: 74,917,456 (GRCm39) |
S685* |
probably null |
Het |
Atp12a |
T |
A |
14: 56,623,296 (GRCm39) |
M843K |
probably damaging |
Het |
Bbx |
T |
A |
16: 50,086,633 (GRCm39) |
K169* |
probably null |
Het |
Bicra |
A |
T |
7: 15,722,284 (GRCm39) |
V411E |
possibly damaging |
Het |
Camk1d |
A |
T |
2: 5,366,836 (GRCm39) |
Y126* |
probably null |
Het |
Cel |
T |
C |
2: 28,446,338 (GRCm39) |
Y511C |
probably damaging |
Het |
Celf4 |
G |
T |
18: 25,636,140 (GRCm39) |
|
probably null |
Het |
Clasp1 |
A |
G |
1: 118,436,646 (GRCm39) |
N310S |
probably benign |
Het |
Cstf1 |
A |
G |
2: 172,217,795 (GRCm39) |
D136G |
probably damaging |
Het |
Cwc22 |
T |
A |
2: 77,741,899 (GRCm39) |
E470D |
probably damaging |
Het |
Cxcr2 |
A |
T |
1: 74,197,527 (GRCm39) |
D7V |
probably benign |
Het |
Cytip |
A |
G |
2: 58,035,192 (GRCm39) |
I168T |
probably damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,760,083 (GRCm39) |
L1359P |
probably benign |
Het |
Ddx25 |
A |
C |
9: 35,469,034 (GRCm39) |
V26G |
probably benign |
Het |
Dennd4a |
T |
A |
9: 64,813,327 (GRCm39) |
S1429T |
possibly damaging |
Het |
Dmd |
A |
G |
X: 83,892,306 (GRCm39) |
D2990G |
probably damaging |
Het |
Dop1a |
C |
A |
9: 86,424,785 (GRCm39) |
|
probably null |
Het |
Eps8 |
T |
C |
6: 137,499,852 (GRCm39) |
Q209R |
possibly damaging |
Het |
Fabp6 |
T |
A |
11: 43,486,992 (GRCm39) |
I112F |
probably benign |
Het |
Fbxw10 |
T |
C |
11: 62,738,418 (GRCm39) |
V104A |
possibly damaging |
Het |
Gp1ba |
C |
T |
11: 70,532,253 (GRCm39) |
P673L |
probably damaging |
Het |
Grin3a |
T |
C |
4: 49,702,804 (GRCm39) |
Y894C |
probably damaging |
Het |
Hydin |
C |
T |
8: 111,173,217 (GRCm39) |
H967Y |
probably benign |
Het |
Ip6k3 |
T |
C |
17: 27,364,242 (GRCm39) |
K269E |
possibly damaging |
Het |
Jup |
T |
C |
11: 100,274,026 (GRCm39) |
K172E |
probably damaging |
Het |
Katnal1 |
T |
C |
5: 148,841,486 (GRCm39) |
D126G |
probably benign |
Het |
Knl1 |
A |
T |
2: 118,898,788 (GRCm39) |
K163M |
probably damaging |
Het |
Krt17 |
C |
T |
11: 100,148,365 (GRCm39) |
E359K |
possibly damaging |
Het |
Lct |
T |
A |
1: 128,235,559 (GRCm39) |
I483F |
probably damaging |
Het |
Loxl2 |
G |
A |
14: 69,930,489 (GRCm39) |
G751D |
probably damaging |
Het |
Ltbp4 |
G |
A |
7: 27,006,002 (GRCm39) |
R1559C |
possibly damaging |
Het |
Man2c1 |
T |
A |
9: 57,042,503 (GRCm39) |
D183E |
probably benign |
Het |
Med17 |
T |
C |
9: 15,187,139 (GRCm39) |
|
probably null |
Het |
Mrgpra9 |
A |
C |
7: 46,885,561 (GRCm39) |
S34R |
probably benign |
Het |
Mrpl44 |
T |
A |
1: 79,755,677 (GRCm39) |
N94K |
probably damaging |
Het |
Nat8f1 |
A |
G |
6: 85,887,924 (GRCm39) |
V12A |
probably benign |
Het |
Nr2e3 |
C |
A |
9: 59,850,797 (GRCm39) |
G354V |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Nup155 |
T |
C |
15: 8,141,890 (GRCm39) |
V94A |
probably benign |
Het |
Or14a256 |
A |
T |
7: 86,265,569 (GRCm39) |
C95S |
probably damaging |
Het |
Or52h2 |
C |
T |
7: 103,839,082 (GRCm39) |
V111I |
possibly damaging |
Het |
Or5p76 |
T |
C |
7: 108,122,525 (GRCm39) |
I211V |
probably benign |
Het |
Or9q2 |
A |
T |
19: 13,772,140 (GRCm39) |
Y278* |
probably null |
Het |
Pcdhb10 |
A |
T |
18: 37,545,556 (GRCm39) |
I211F |
possibly damaging |
Het |
Phip |
A |
C |
9: 82,797,476 (GRCm39) |
I509S |
possibly damaging |
Het |
Pkhd1 |
C |
T |
1: 20,655,381 (GRCm39) |
|
probably null |
Het |
Psme4 |
T |
G |
11: 30,802,744 (GRCm39) |
L1487R |
probably damaging |
Het |
Ptgdr2 |
A |
G |
19: 10,917,857 (GRCm39) |
S125G |
probably damaging |
Het |
Ptpro |
A |
G |
6: 137,418,114 (GRCm39) |
K126E |
probably damaging |
Het |
Rdh16f2 |
T |
A |
10: 127,712,794 (GRCm39) |
V264E |
probably benign |
Het |
Ric8b |
C |
T |
10: 84,783,535 (GRCm39) |
A131V |
possibly damaging |
Het |
Rock1 |
A |
T |
18: 10,070,233 (GRCm39) |
I1280N |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,725,888 (GRCm39) |
V59A |
possibly damaging |
Het |
Ruvbl1 |
T |
A |
6: 88,444,551 (GRCm39) |
C49S |
probably benign |
Het |
Scn2a |
A |
G |
2: 65,514,189 (GRCm39) |
N291S |
probably benign |
Het |
Serbp1 |
T |
A |
6: 67,254,904 (GRCm39) |
H325Q |
probably damaging |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Shisal2b |
T |
C |
13: 104,982,470 (GRCm39) |
I151V |
probably benign |
Het |
Slitrk3 |
G |
A |
3: 72,957,674 (GRCm39) |
T366I |
probably damaging |
Het |
Spryd3 |
A |
T |
15: 102,026,827 (GRCm39) |
H307Q |
possibly damaging |
Het |
Spx |
A |
T |
6: 142,364,239 (GRCm39) |
D100V |
probably benign |
Het |
Surf4 |
A |
G |
2: 26,814,476 (GRCm39) |
F142L |
probably damaging |
Het |
Syne2 |
T |
A |
12: 76,067,099 (GRCm39) |
|
probably null |
Het |
Syne2 |
T |
C |
12: 76,098,952 (GRCm39) |
M5278T |
possibly damaging |
Het |
Thap12 |
T |
C |
7: 98,365,230 (GRCm39) |
V466A |
probably benign |
Het |
Thap3 |
T |
C |
4: 152,067,673 (GRCm39) |
K135R |
possibly damaging |
Het |
Tmem131 |
G |
T |
1: 36,866,439 (GRCm39) |
D448E |
probably benign |
Het |
Tmem63b |
C |
G |
17: 45,989,904 (GRCm39) |
R88P |
possibly damaging |
Het |
Trim43a |
G |
T |
9: 88,464,146 (GRCm39) |
C19F |
probably damaging |
Het |
Trp63 |
C |
T |
16: 25,707,870 (GRCm39) |
P526L |
possibly damaging |
Het |
Ubqln3 |
T |
C |
7: 103,791,997 (GRCm39) |
D31G |
probably damaging |
Het |
Utp14b |
C |
A |
1: 78,643,162 (GRCm39) |
N353K |
probably damaging |
Het |
Vmn1r40 |
A |
G |
6: 89,691,558 (GRCm39) |
K125R |
probably damaging |
Het |
Vmn2r1 |
A |
G |
3: 64,008,734 (GRCm39) |
Y471C |
probably damaging |
Het |
Vmn2r13 |
A |
G |
5: 109,322,001 (GRCm39) |
I232T |
probably damaging |
Het |
Zfp263 |
A |
C |
16: 3,564,323 (GRCm39) |
E204D |
probably benign |
Het |
Zfp865 |
A |
T |
7: 5,032,278 (GRCm39) |
K88* |
probably null |
Het |
|
Other mutations in Col6a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00391:Col6a3
|
APN |
1 |
90,755,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00425:Col6a3
|
APN |
1 |
90,709,748 (GRCm39) |
missense |
unknown |
|
IGL00541:Col6a3
|
APN |
1 |
90,729,864 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01063:Col6a3
|
APN |
1 |
90,730,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01094:Col6a3
|
APN |
1 |
90,731,655 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01138:Col6a3
|
APN |
1 |
90,735,232 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01291:Col6a3
|
APN |
1 |
90,730,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01674:Col6a3
|
APN |
1 |
90,730,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01756:Col6a3
|
APN |
1 |
90,706,884 (GRCm39) |
missense |
unknown |
|
IGL01827:Col6a3
|
APN |
1 |
90,730,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01845:Col6a3
|
APN |
1 |
90,724,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01869:Col6a3
|
APN |
1 |
90,700,770 (GRCm39) |
missense |
unknown |
|
IGL01900:Col6a3
|
APN |
1 |
90,722,732 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01925:Col6a3
|
APN |
1 |
90,729,958 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02002:Col6a3
|
APN |
1 |
90,709,858 (GRCm39) |
splice site |
probably benign |
|
IGL02115:Col6a3
|
APN |
1 |
90,735,373 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02302:Col6a3
|
APN |
1 |
90,709,482 (GRCm39) |
missense |
unknown |
|
IGL02313:Col6a3
|
APN |
1 |
90,739,328 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02458:Col6a3
|
APN |
1 |
90,706,919 (GRCm39) |
missense |
unknown |
|
IGL02821:Col6a3
|
APN |
1 |
90,731,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Col6a3
|
APN |
1 |
90,724,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Col6a3
|
APN |
1 |
90,739,242 (GRCm39) |
nonsense |
probably null |
|
IGL03129:Col6a3
|
APN |
1 |
90,749,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03132:Col6a3
|
APN |
1 |
90,731,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Col6a3
|
APN |
1 |
90,755,588 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03251:Col6a3
|
APN |
1 |
90,737,898 (GRCm39) |
missense |
probably damaging |
1.00 |
bailey
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
barnum
|
UTSW |
1 |
90,706,874 (GRCm39) |
missense |
unknown |
|
Boneless
|
UTSW |
1 |
90,706,781 (GRCm39) |
missense |
unknown |
|
Noodloid
|
UTSW |
1 |
90,707,011 (GRCm39) |
missense |
unknown |
|
randolf
|
UTSW |
1 |
90,715,673 (GRCm39) |
missense |
unknown |
|
stringy
|
UTSW |
1 |
90,731,400 (GRCm39) |
nonsense |
probably null |
|
wonder
|
UTSW |
1 |
90,719,645 (GRCm39) |
critical splice donor site |
probably null |
|
ANU05:Col6a3
|
UTSW |
1 |
90,730,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03048:Col6a3
|
UTSW |
1 |
90,737,970 (GRCm39) |
missense |
possibly damaging |
0.58 |
PIT4810001:Col6a3
|
UTSW |
1 |
90,706,516 (GRCm39) |
missense |
unknown |
|
R0020:Col6a3
|
UTSW |
1 |
90,739,272 (GRCm39) |
missense |
probably damaging |
0.99 |
R0020:Col6a3
|
UTSW |
1 |
90,739,272 (GRCm39) |
missense |
probably damaging |
0.99 |
R0033:Col6a3
|
UTSW |
1 |
90,729,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Col6a3
|
UTSW |
1 |
90,729,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0105:Col6a3
|
UTSW |
1 |
90,725,883 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0116:Col6a3
|
UTSW |
1 |
90,741,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Col6a3
|
UTSW |
1 |
90,725,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R0319:Col6a3
|
UTSW |
1 |
90,735,426 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0348:Col6a3
|
UTSW |
1 |
90,755,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Col6a3
|
UTSW |
1 |
90,715,938 (GRCm39) |
missense |
unknown |
|
R0512:Col6a3
|
UTSW |
1 |
90,749,520 (GRCm39) |
intron |
probably benign |
|
R0564:Col6a3
|
UTSW |
1 |
90,735,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Col6a3
|
UTSW |
1 |
90,735,808 (GRCm39) |
splice site |
probably null |
|
R0667:Col6a3
|
UTSW |
1 |
90,755,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R0680:Col6a3
|
UTSW |
1 |
90,706,703 (GRCm39) |
missense |
unknown |
|
R0736:Col6a3
|
UTSW |
1 |
90,731,811 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0737:Col6a3
|
UTSW |
1 |
90,756,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:Col6a3
|
UTSW |
1 |
90,730,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1155:Col6a3
|
UTSW |
1 |
90,722,047 (GRCm39) |
missense |
probably null |
1.00 |
R1169:Col6a3
|
UTSW |
1 |
90,749,736 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1180:Col6a3
|
UTSW |
1 |
90,709,577 (GRCm39) |
missense |
unknown |
|
R1225:Col6a3
|
UTSW |
1 |
90,739,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1343:Col6a3
|
UTSW |
1 |
90,696,069 (GRCm39) |
missense |
unknown |
|
R1387:Col6a3
|
UTSW |
1 |
90,750,138 (GRCm39) |
intron |
probably benign |
|
R1437:Col6a3
|
UTSW |
1 |
90,729,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1677:Col6a3
|
UTSW |
1 |
90,749,583 (GRCm39) |
missense |
probably benign |
0.14 |
R1681:Col6a3
|
UTSW |
1 |
90,701,224 (GRCm39) |
missense |
unknown |
|
R1711:Col6a3
|
UTSW |
1 |
90,757,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Col6a3
|
UTSW |
1 |
90,724,296 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1736:Col6a3
|
UTSW |
1 |
90,706,781 (GRCm39) |
missense |
unknown |
|
R1738:Col6a3
|
UTSW |
1 |
90,744,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Col6a3
|
UTSW |
1 |
90,741,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Col6a3
|
UTSW |
1 |
90,755,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Col6a3
|
UTSW |
1 |
90,735,256 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1852:Col6a3
|
UTSW |
1 |
90,735,256 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1872:Col6a3
|
UTSW |
1 |
90,757,936 (GRCm39) |
missense |
probably damaging |
0.96 |
R1889:Col6a3
|
UTSW |
1 |
90,731,433 (GRCm39) |
missense |
probably benign |
0.00 |
R1895:Col6a3
|
UTSW |
1 |
90,731,433 (GRCm39) |
missense |
probably benign |
0.00 |
R1908:Col6a3
|
UTSW |
1 |
90,739,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Col6a3
|
UTSW |
1 |
90,750,081 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1973:Col6a3
|
UTSW |
1 |
90,731,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Col6a3
|
UTSW |
1 |
90,709,733 (GRCm39) |
missense |
unknown |
|
R2121:Col6a3
|
UTSW |
1 |
90,738,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R2197:Col6a3
|
UTSW |
1 |
90,731,467 (GRCm39) |
missense |
probably benign |
0.09 |
R2448:Col6a3
|
UTSW |
1 |
90,741,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R2831:Col6a3
|
UTSW |
1 |
90,731,435 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2877:Col6a3
|
UTSW |
1 |
90,703,321 (GRCm39) |
missense |
unknown |
|
R3052:Col6a3
|
UTSW |
1 |
90,729,852 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3104:Col6a3
|
UTSW |
1 |
90,744,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R3105:Col6a3
|
UTSW |
1 |
90,744,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R3106:Col6a3
|
UTSW |
1 |
90,744,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R3418:Col6a3
|
UTSW |
1 |
90,731,813 (GRCm39) |
missense |
probably benign |
0.42 |
R3419:Col6a3
|
UTSW |
1 |
90,731,813 (GRCm39) |
missense |
probably benign |
0.42 |
R3837:Col6a3
|
UTSW |
1 |
90,707,803 (GRCm39) |
missense |
unknown |
|
R4007:Col6a3
|
UTSW |
1 |
90,730,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4082:Col6a3
|
UTSW |
1 |
90,749,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R4181:Col6a3
|
UTSW |
1 |
90,735,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R4200:Col6a3
|
UTSW |
1 |
90,729,105 (GRCm39) |
missense |
probably benign |
0.28 |
R4244:Col6a3
|
UTSW |
1 |
90,714,361 (GRCm39) |
missense |
unknown |
|
R4297:Col6a3
|
UTSW |
1 |
90,739,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R4302:Col6a3
|
UTSW |
1 |
90,735,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Col6a3
|
UTSW |
1 |
90,749,736 (GRCm39) |
missense |
probably benign |
0.23 |
R4600:Col6a3
|
UTSW |
1 |
90,709,626 (GRCm39) |
missense |
unknown |
|
R4683:Col6a3
|
UTSW |
1 |
90,701,179 (GRCm39) |
missense |
unknown |
|
R4788:Col6a3
|
UTSW |
1 |
90,700,672 (GRCm39) |
critical splice donor site |
probably null |
|
R4851:Col6a3
|
UTSW |
1 |
90,707,011 (GRCm39) |
missense |
unknown |
|
R4899:Col6a3
|
UTSW |
1 |
90,730,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R4904:Col6a3
|
UTSW |
1 |
90,729,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Col6a3
|
UTSW |
1 |
90,735,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Col6a3
|
UTSW |
1 |
90,731,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R4981:Col6a3
|
UTSW |
1 |
90,706,565 (GRCm39) |
missense |
unknown |
|
R5057:Col6a3
|
UTSW |
1 |
90,743,852 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5062:Col6a3
|
UTSW |
1 |
90,707,074 (GRCm39) |
missense |
unknown |
|
R5105:Col6a3
|
UTSW |
1 |
90,725,862 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5127:Col6a3
|
UTSW |
1 |
90,696,067 (GRCm39) |
missense |
unknown |
|
R5166:Col6a3
|
UTSW |
1 |
90,738,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Col6a3
|
UTSW |
1 |
90,701,361 (GRCm39) |
nonsense |
probably null |
|
R5196:Col6a3
|
UTSW |
1 |
90,744,260 (GRCm39) |
splice site |
probably null |
|
R5230:Col6a3
|
UTSW |
1 |
90,716,776 (GRCm39) |
missense |
unknown |
|
R5268:Col6a3
|
UTSW |
1 |
90,712,965 (GRCm39) |
missense |
unknown |
|
R5381:Col6a3
|
UTSW |
1 |
90,703,334 (GRCm39) |
missense |
unknown |
|
R5392:Col6a3
|
UTSW |
1 |
90,729,017 (GRCm39) |
missense |
probably benign |
0.41 |
R5445:Col6a3
|
UTSW |
1 |
90,709,761 (GRCm39) |
nonsense |
probably null |
|
R5571:Col6a3
|
UTSW |
1 |
90,715,938 (GRCm39) |
missense |
unknown |
|
R5665:Col6a3
|
UTSW |
1 |
90,755,602 (GRCm39) |
missense |
probably benign |
0.00 |
R5902:Col6a3
|
UTSW |
1 |
90,729,921 (GRCm39) |
splice site |
probably null |
|
R5914:Col6a3
|
UTSW |
1 |
90,703,922 (GRCm39) |
missense |
unknown |
|
R5955:Col6a3
|
UTSW |
1 |
90,739,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Col6a3
|
UTSW |
1 |
90,749,571 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6006:Col6a3
|
UTSW |
1 |
90,696,105 (GRCm39) |
missense |
unknown |
|
R6010:Col6a3
|
UTSW |
1 |
90,701,219 (GRCm39) |
missense |
unknown |
|
R6025:Col6a3
|
UTSW |
1 |
90,755,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Col6a3
|
UTSW |
1 |
90,741,475 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6154:Col6a3
|
UTSW |
1 |
90,701,387 (GRCm39) |
missense |
unknown |
|
R6181:Col6a3
|
UTSW |
1 |
90,744,096 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6197:Col6a3
|
UTSW |
1 |
90,750,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Col6a3
|
UTSW |
1 |
90,749,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Col6a3
|
UTSW |
1 |
90,738,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R6476:Col6a3
|
UTSW |
1 |
90,709,534 (GRCm39) |
missense |
unknown |
|
R6484:Col6a3
|
UTSW |
1 |
90,719,645 (GRCm39) |
critical splice donor site |
probably null |
|
R6701:Col6a3
|
UTSW |
1 |
90,720,184 (GRCm39) |
missense |
probably benign |
0.14 |
R6702:Col6a3
|
UTSW |
1 |
90,707,161 (GRCm39) |
missense |
unknown |
|
R6703:Col6a3
|
UTSW |
1 |
90,720,184 (GRCm39) |
missense |
probably benign |
0.14 |
R6703:Col6a3
|
UTSW |
1 |
90,707,161 (GRCm39) |
missense |
unknown |
|
R6724:Col6a3
|
UTSW |
1 |
90,706,874 (GRCm39) |
missense |
unknown |
|
R6746:Col6a3
|
UTSW |
1 |
90,706,767 (GRCm39) |
missense |
unknown |
|
R6797:Col6a3
|
UTSW |
1 |
90,731,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Col6a3
|
UTSW |
1 |
90,722,731 (GRCm39) |
splice site |
probably null |
|
R6903:Col6a3
|
UTSW |
1 |
90,721,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6925:Col6a3
|
UTSW |
1 |
90,743,724 (GRCm39) |
missense |
probably benign |
0.00 |
R6978:Col6a3
|
UTSW |
1 |
90,735,192 (GRCm39) |
critical splice donor site |
probably null |
|
R7058:Col6a3
|
UTSW |
1 |
90,755,759 (GRCm39) |
nonsense |
probably null |
|
R7182:Col6a3
|
UTSW |
1 |
90,731,400 (GRCm39) |
nonsense |
probably null |
|
R7294:Col6a3
|
UTSW |
1 |
90,756,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Col6a3
|
UTSW |
1 |
90,755,708 (GRCm39) |
missense |
probably benign |
0.00 |
R7311:Col6a3
|
UTSW |
1 |
90,750,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Col6a3
|
UTSW |
1 |
90,755,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R7561:Col6a3
|
UTSW |
1 |
90,703,463 (GRCm39) |
missense |
unknown |
|
R7575:Col6a3
|
UTSW |
1 |
90,738,321 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7659:Col6a3
|
UTSW |
1 |
90,709,467 (GRCm39) |
missense |
unknown |
|
R7679:Col6a3
|
UTSW |
1 |
90,739,473 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7831:Col6a3
|
UTSW |
1 |
90,724,268 (GRCm39) |
nonsense |
probably null |
|
R7855:Col6a3
|
UTSW |
1 |
90,738,343 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7990:Col6a3
|
UTSW |
1 |
90,709,577 (GRCm39) |
missense |
unknown |
|
R8003:Col6a3
|
UTSW |
1 |
90,703,455 (GRCm39) |
missense |
unknown |
|
R8007:Col6a3
|
UTSW |
1 |
90,705,179 (GRCm39) |
missense |
unknown |
|
R8098:Col6a3
|
UTSW |
1 |
90,731,383 (GRCm39) |
missense |
probably benign |
|
R8312:Col6a3
|
UTSW |
1 |
90,741,412 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8419:Col6a3
|
UTSW |
1 |
90,729,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R8723:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8725:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8737:Col6a3
|
UTSW |
1 |
90,727,747 (GRCm39) |
missense |
probably benign |
0.10 |
R8742:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8743:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8744:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8753:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8754:Col6a3
|
UTSW |
1 |
90,695,328 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8773:Col6a3
|
UTSW |
1 |
90,696,171 (GRCm39) |
missense |
unknown |
|
R8857:Col6a3
|
UTSW |
1 |
90,703,485 (GRCm39) |
missense |
unknown |
|
R8867:Col6a3
|
UTSW |
1 |
90,715,673 (GRCm39) |
missense |
unknown |
|
R8887:Col6a3
|
UTSW |
1 |
90,755,948 (GRCm39) |
missense |
probably benign |
|
R9011:Col6a3
|
UTSW |
1 |
90,710,057 (GRCm39) |
splice site |
probably benign |
|
R9049:Col6a3
|
UTSW |
1 |
90,707,066 (GRCm39) |
missense |
unknown |
|
R9142:Col6a3
|
UTSW |
1 |
90,706,566 (GRCm39) |
missense |
unknown |
|
R9155:Col6a3
|
UTSW |
1 |
90,738,301 (GRCm39) |
missense |
probably benign |
0.27 |
R9249:Col6a3
|
UTSW |
1 |
90,707,020 (GRCm39) |
missense |
unknown |
|
R9258:Col6a3
|
UTSW |
1 |
90,700,703 (GRCm39) |
missense |
unknown |
|
R9274:Col6a3
|
UTSW |
1 |
90,707,020 (GRCm39) |
missense |
unknown |
|
R9276:Col6a3
|
UTSW |
1 |
90,735,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9315:Col6a3
|
UTSW |
1 |
90,738,979 (GRCm39) |
critical splice donor site |
probably null |
|
R9376:Col6a3
|
UTSW |
1 |
90,709,523 (GRCm39) |
missense |
unknown |
|
R9377:Col6a3
|
UTSW |
1 |
90,743,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9429:Col6a3
|
UTSW |
1 |
90,731,585 (GRCm39) |
missense |
probably benign |
0.01 |
R9439:Col6a3
|
UTSW |
1 |
90,744,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R9440:Col6a3
|
UTSW |
1 |
90,707,068 (GRCm39) |
missense |
unknown |
|
R9441:Col6a3
|
UTSW |
1 |
90,705,249 (GRCm39) |
nonsense |
probably null |
|
R9477:Col6a3
|
UTSW |
1 |
90,706,621 (GRCm39) |
missense |
unknown |
|
R9498:Col6a3
|
UTSW |
1 |
90,713,650 (GRCm39) |
nonsense |
probably null |
|
R9528:Col6a3
|
UTSW |
1 |
90,731,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Col6a3
|
UTSW |
1 |
90,731,497 (GRCm39) |
missense |
probably benign |
0.07 |
RF005:Col6a3
|
UTSW |
1 |
90,738,984 (GRCm39) |
missense |
probably benign |
0.00 |
RF012:Col6a3
|
UTSW |
1 |
90,738,282 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Col6a3
|
UTSW |
1 |
90,731,359 (GRCm39) |
critical splice donor site |
probably null |
|
X0063:Col6a3
|
UTSW |
1 |
90,731,627 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Col6a3
|
UTSW |
1 |
90,739,251 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Col6a3
|
UTSW |
1 |
90,739,450 (GRCm39) |
missense |
possibly damaging |
0.82 |
|