Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
C |
17: 48,348,273 (GRCm39) |
T55A |
probably benign |
Het |
3110070M22Rik |
T |
A |
13: 119,624,822 (GRCm39) |
|
probably benign |
Het |
Acot12 |
T |
A |
13: 91,918,221 (GRCm39) |
N171K |
probably benign |
Het |
Adam18 |
G |
A |
8: 25,104,859 (GRCm39) |
Q652* |
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,705,277 (GRCm39) |
E791G |
probably damaging |
Het |
Aff1 |
C |
T |
5: 103,981,685 (GRCm39) |
S608L |
probably damaging |
Het |
Amfr |
A |
T |
8: 94,707,018 (GRCm39) |
F432L |
probably damaging |
Het |
Ankfn1 |
G |
A |
11: 89,332,284 (GRCm39) |
L421F |
possibly damaging |
Het |
Ankrd31 |
T |
C |
13: 97,014,733 (GRCm39) |
V1334A |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,608,858 (GRCm39) |
H1534Y |
possibly damaging |
Het |
Aste1 |
G |
A |
9: 105,273,880 (GRCm39) |
C40Y |
probably benign |
Het |
Atf3 |
T |
C |
1: 190,909,510 (GRCm39) |
H53R |
probably benign |
Het |
Bsn |
C |
A |
9: 107,990,800 (GRCm39) |
V1651F |
probably damaging |
Het |
Bsn |
A |
T |
9: 107,993,361 (GRCm39) |
L797Q |
probably damaging |
Het |
Bzw2 |
T |
C |
12: 36,180,131 (GRCm39) |
D32G |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,361,458 (GRCm39) |
M531K |
possibly damaging |
Het |
Cep120 |
A |
G |
18: 53,851,592 (GRCm39) |
F567L |
possibly damaging |
Het |
Cit |
T |
C |
5: 116,084,914 (GRCm39) |
I815T |
probably benign |
Het |
Cnot6l |
G |
T |
5: 96,276,826 (GRCm39) |
Q121K |
probably benign |
Het |
Col4a2 |
G |
A |
8: 11,483,725 (GRCm39) |
G882R |
probably damaging |
Het |
Copg2 |
T |
A |
6: 30,793,721 (GRCm39) |
H394L |
possibly damaging |
Het |
Cst13 |
A |
G |
2: 148,670,165 (GRCm39) |
M112V |
possibly damaging |
Het |
Cyp2j7 |
G |
T |
4: 96,124,786 (GRCm39) |
N37K |
probably benign |
Het |
Cyp2u1 |
T |
A |
3: 131,091,449 (GRCm39) |
N357I |
possibly damaging |
Het |
Dars1 |
T |
C |
1: 128,344,945 (GRCm39) |
T4A |
probably benign |
Het |
Dclk1 |
G |
T |
3: 55,429,374 (GRCm39) |
C414F |
possibly damaging |
Het |
Dmbt1 |
A |
T |
7: 130,694,832 (GRCm39) |
Y1009F |
unknown |
Het |
Ebf4 |
T |
C |
2: 130,148,775 (GRCm39) |
Y117H |
probably damaging |
Het |
Eif2b4 |
A |
G |
5: 31,348,500 (GRCm39) |
Y196H |
probably benign |
Het |
Enpp2 |
C |
T |
15: 54,739,080 (GRCm39) |
R401H |
probably damaging |
Het |
Epo |
T |
C |
5: 137,484,017 (GRCm39) |
|
probably benign |
Het |
Gli1 |
T |
A |
10: 127,173,359 (GRCm39) |
T100S |
possibly damaging |
Het |
Gml2 |
T |
A |
15: 74,695,957 (GRCm39) |
F117Y |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,335,403 (GRCm39) |
V2314A |
probably benign |
Het |
Hspb8 |
A |
G |
5: 116,547,487 (GRCm39) |
I165T |
probably damaging |
Het |
Itgax |
A |
T |
7: 127,732,849 (GRCm39) |
T243S |
probably benign |
Het |
Itih4 |
G |
T |
14: 30,608,533 (GRCm39) |
L16F |
probably damaging |
Het |
Kmt5a |
C |
T |
5: 124,578,064 (GRCm39) |
|
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,115,009 (GRCm39) |
E1089G |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mcmbp |
A |
T |
7: 128,317,803 (GRCm39) |
N147K |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,981,246 (GRCm39) |
L407F |
probably benign |
Het |
Mybpc2 |
A |
T |
7: 44,158,999 (GRCm39) |
V653D |
probably benign |
Het |
Myo3b |
G |
A |
2: 70,069,242 (GRCm39) |
V522I |
possibly damaging |
Het |
Nbr1 |
A |
G |
11: 101,456,590 (GRCm39) |
T156A |
possibly damaging |
Het |
Neb |
T |
A |
2: 52,039,291 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,116,546 (GRCm39) |
Y964F |
|
Het |
Nr2f2 |
T |
A |
7: 70,007,856 (GRCm39) |
I209F |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,957,740 (GRCm39) |
T357A |
probably damaging |
Het |
Palld |
C |
T |
8: 61,969,691 (GRCm39) |
R1211H |
unknown |
Het |
Pcdhb19 |
T |
A |
18: 37,632,299 (GRCm39) |
V698E |
probably damaging |
Het |
Pcdhga6 |
C |
T |
18: 37,841,570 (GRCm39) |
P430L |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,162,156 (GRCm39) |
L2225S |
possibly damaging |
Het |
Plekhf1 |
A |
T |
7: 37,921,203 (GRCm39) |
W122R |
probably damaging |
Het |
Pold3 |
A |
G |
7: 99,732,993 (GRCm39) |
S418P |
possibly damaging |
Het |
Poldip3 |
T |
C |
15: 83,019,589 (GRCm39) |
N180S |
probably benign |
Het |
Ppp1r21 |
C |
T |
17: 88,852,815 (GRCm39) |
R65* |
probably null |
Het |
Ppp1r3d |
A |
T |
2: 178,055,669 (GRCm39) |
V111E |
probably damaging |
Het |
Prrg4 |
T |
C |
2: 104,669,728 (GRCm39) |
I130V |
probably benign |
Het |
Psma5 |
A |
T |
3: 108,172,448 (GRCm39) |
T55S |
probably benign |
Het |
Rbm5 |
C |
A |
9: 107,627,252 (GRCm39) |
A440S |
probably benign |
Het |
Rdx |
A |
G |
9: 51,980,168 (GRCm39) |
K254E |
possibly damaging |
Het |
Rere |
A |
C |
4: 150,593,342 (GRCm39) |
Q312P |
unknown |
Het |
Rest |
T |
C |
5: 77,416,128 (GRCm39) |
V114A |
possibly damaging |
Het |
Rufy4 |
G |
T |
1: 74,171,879 (GRCm39) |
V201L |
probably benign |
Het |
Scyl1 |
T |
C |
19: 5,809,023 (GRCm39) |
E727G |
probably benign |
Het |
Serpinb6b |
T |
A |
13: 33,152,494 (GRCm39) |
M1K |
probably null |
Het |
Sgsm1 |
C |
A |
5: 113,436,741 (GRCm39) |
V30F |
probably damaging |
Het |
Skap1 |
A |
G |
11: 96,644,921 (GRCm39) |
D344G |
possibly damaging |
Het |
Slc26a7 |
T |
C |
4: 14,516,189 (GRCm39) |
T547A |
probably benign |
Het |
Slc6a3 |
C |
A |
13: 73,692,966 (GRCm39) |
S195R |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,387,048 (GRCm39) |
D6G |
probably damaging |
Het |
Spock3 |
A |
T |
8: 63,798,746 (GRCm39) |
M253L |
probably damaging |
Het |
Ssh2 |
A |
G |
11: 77,298,974 (GRCm39) |
Y107C |
possibly damaging |
Het |
Svil |
T |
C |
18: 5,057,294 (GRCm39) |
S581P |
probably benign |
Het |
Tbc1d14 |
T |
C |
5: 36,662,472 (GRCm39) |
T553A |
probably benign |
Het |
Tet3 |
T |
A |
6: 83,380,596 (GRCm39) |
Q524L |
possibly damaging |
Het |
Uckl1 |
A |
T |
2: 181,211,532 (GRCm39) |
V456E |
probably damaging |
Het |
Ucp2 |
T |
C |
7: 100,146,040 (GRCm39) |
F4S |
probably benign |
Het |
Vmn2r77 |
A |
G |
7: 86,444,442 (GRCm39) |
I32V |
probably benign |
Het |
Vmn2r89 |
T |
A |
14: 51,692,601 (GRCm39) |
Y135N |
probably benign |
Het |
Vtn |
A |
G |
11: 78,390,587 (GRCm39) |
E82G |
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,593,925 (GRCm39) |
N137S |
probably benign |
Het |
Zgpat |
T |
A |
2: 181,021,646 (GRCm39) |
C357* |
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 |
R1448:Col6a3
|
UTSW |
1 |
90,709,577 (GRCm39) |
missense |
unknown |
|
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 |
|
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 |
|