Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg2 |
G |
A |
X: 159,265,347 (GRCm39) |
M532I |
probably benign |
Het |
Agtpbp1 |
A |
G |
13: 59,598,016 (GRCm39) |
Y1198H |
possibly damaging |
Het |
Ahcyl2 |
G |
A |
6: 29,908,354 (GRCm39) |
V575M |
probably damaging |
Het |
Akp3 |
TCACCACCACCACCACCACCACCACCACCAC |
TCACCACCACCACCACCACCACCACCAC |
1: 87,055,489 (GRCm39) |
|
probably benign |
Het |
Ankrd50 |
A |
T |
3: 38,508,610 (GRCm39) |
N329K |
probably benign |
Het |
Ano4 |
C |
A |
10: 88,807,253 (GRCm39) |
G741V |
probably damaging |
Het |
Anxa1 |
T |
C |
19: 20,357,053 (GRCm39) |
D191G |
probably benign |
Het |
Apc2 |
C |
T |
10: 80,149,482 (GRCm39) |
T1512I |
probably damaging |
Het |
Aph1b |
A |
T |
9: 66,701,395 (GRCm39) |
C81S |
probably benign |
Het |
Arhgap21 |
T |
C |
2: 20,866,015 (GRCm39) |
E893G |
probably damaging |
Het |
Arhgef28 |
A |
T |
13: 98,130,640 (GRCm39) |
H399Q |
probably benign |
Het |
Asic5 |
A |
G |
3: 81,919,294 (GRCm39) |
E304G |
probably benign |
Het |
B4galnt4 |
A |
G |
7: 140,650,446 (GRCm39) |
Y771C |
probably damaging |
Het |
Birc2 |
G |
T |
9: 7,819,518 (GRCm39) |
Q465K |
probably benign |
Het |
Btla |
C |
T |
16: 45,070,737 (GRCm39) |
T232I |
probably damaging |
Het |
Ccl7 |
G |
T |
11: 81,937,378 (GRCm39) |
K37N |
probably benign |
Het |
Cdk17 |
T |
C |
10: 93,061,967 (GRCm39) |
V233A |
probably damaging |
Het |
Cenatac |
A |
G |
9: 44,329,018 (GRCm39) |
C66R |
probably damaging |
Het |
Cilp2 |
C |
A |
8: 70,333,973 (GRCm39) |
Q1008H |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,282,475 (GRCm39) |
D442E |
probably damaging |
Het |
Clcnka |
T |
C |
4: 141,120,113 (GRCm39) |
T269A |
probably damaging |
Het |
Cts6 |
A |
G |
13: 61,349,393 (GRCm39) |
I105T |
probably benign |
Het |
Cyp3a25 |
T |
C |
5: 145,931,739 (GRCm39) |
D123G |
probably damaging |
Het |
D630003M21Rik |
A |
T |
2: 158,045,105 (GRCm39) |
L808Q |
probably damaging |
Het |
Ddrgk1 |
A |
T |
2: 130,496,215 (GRCm39) |
I270N |
probably damaging |
Het |
Dhx15 |
T |
C |
5: 52,342,043 (GRCm39) |
T92A |
possibly damaging |
Het |
Dhx32 |
A |
T |
7: 133,339,025 (GRCm39) |
C197S |
probably benign |
Het |
Diaph2 |
G |
A |
X: 128,860,876 (GRCm39) |
R473Q |
probably damaging |
Het |
Dnd1 |
A |
G |
18: 36,899,057 (GRCm39) |
C11R |
possibly damaging |
Het |
Dock1 |
A |
C |
7: 134,748,236 (GRCm39) |
D1566A |
probably benign |
Het |
Drp2 |
A |
G |
X: 133,327,864 (GRCm39) |
I43V |
probably benign |
Het |
Ecm2 |
T |
C |
13: 49,683,621 (GRCm39) |
V533A |
probably benign |
Het |
Ecpas |
T |
A |
4: 58,849,942 (GRCm39) |
H427L |
possibly damaging |
Het |
Emilin1 |
A |
G |
5: 31,075,934 (GRCm39) |
E725G |
probably damaging |
Het |
Eml2 |
A |
G |
7: 18,935,803 (GRCm39) |
Y487C |
probably damaging |
Het |
Epg5 |
T |
A |
18: 78,018,246 (GRCm39) |
L919H |
probably damaging |
Het |
Fam187a |
T |
A |
11: 102,776,837 (GRCm39) |
S214T |
probably damaging |
Het |
Flna |
T |
C |
X: 73,283,869 (GRCm39) |
T521A |
probably benign |
Het |
Foxi1 |
T |
A |
11: 34,157,531 (GRCm39) |
I165F |
probably damaging |
Het |
Fxr2 |
A |
T |
11: 69,543,103 (GRCm39) |
K633N |
probably benign |
Het |
Gdpd5 |
T |
C |
7: 99,098,206 (GRCm39) |
I209T |
probably benign |
Het |
Gmpr |
G |
T |
13: 45,696,101 (GRCm39) |
V278F |
probably damaging |
Het |
Grm7 |
A |
T |
6: 111,057,384 (GRCm39) |
D328V |
probably benign |
Het |
Heatr6 |
T |
C |
11: 83,660,056 (GRCm39) |
S534P |
probably damaging |
Het |
Heph |
A |
G |
X: 95,573,092 (GRCm39) |
T792A |
probably damaging |
Het |
Hipk2 |
T |
A |
6: 38,695,870 (GRCm39) |
|
probably null |
Het |
Hps3 |
T |
A |
3: 20,074,123 (GRCm39) |
|
probably null |
Het |
Hspa5 |
T |
C |
2: 34,664,553 (GRCm39) |
F336L |
probably damaging |
Het |
Insc |
T |
C |
7: 114,441,413 (GRCm39) |
I409T |
probably benign |
Het |
Kcnj8 |
T |
A |
6: 142,515,966 (GRCm39) |
H47L |
probably damaging |
Het |
Kcnma1 |
T |
A |
14: 23,853,230 (GRCm39) |
Q108L |
probably damaging |
Het |
Klc3 |
A |
G |
7: 19,131,966 (GRCm39) |
V137A |
probably damaging |
Het |
Lcn2 |
T |
C |
2: 32,275,434 (GRCm39) |
T194A |
possibly damaging |
Het |
Lgr4 |
T |
A |
2: 109,841,742 (GRCm39) |
F576I |
possibly damaging |
Het |
Lypd6b |
A |
G |
2: 49,837,459 (GRCm39) |
I144V |
possibly damaging |
Het |
Mctp1 |
G |
A |
13: 76,533,267 (GRCm39) |
C205Y |
possibly damaging |
Het |
Mitf |
A |
T |
6: 97,987,383 (GRCm39) |
N159I |
probably damaging |
Het |
Morc1 |
T |
C |
16: 48,412,893 (GRCm39) |
I678T |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,576,625 (GRCm39) |
|
probably benign |
Het |
Myo7a |
T |
C |
7: 97,701,463 (GRCm39) |
Y2115C |
probably damaging |
Het |
Myof |
T |
C |
19: 37,975,153 (GRCm39) |
I182V |
probably benign |
Het |
Ncor1 |
A |
G |
11: 62,272,245 (GRCm39) |
V635A |
probably damaging |
Het |
Neb |
G |
T |
2: 52,102,772 (GRCm39) |
Y4257* |
probably null |
Het |
Npr2 |
T |
A |
4: 43,641,258 (GRCm39) |
V428E |
probably benign |
Het |
Nufip2 |
A |
G |
11: 77,583,124 (GRCm39) |
D346G |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,469,753 (GRCm39) |
S1088F |
probably benign |
Het |
Or10s1 |
T |
G |
9: 39,986,081 (GRCm39) |
I163M |
possibly damaging |
Het |
Or2ag1 |
T |
C |
7: 106,313,030 (GRCm39) |
N286S |
possibly damaging |
Het |
Or4c127 |
T |
A |
2: 89,832,825 (GRCm39) |
V25E |
probably benign |
Het |
Or4k38 |
C |
T |
2: 111,166,052 (GRCm39) |
V124M |
possibly damaging |
Het |
Or5ac22 |
A |
G |
16: 59,135,378 (GRCm39) |
Y131H |
probably damaging |
Het |
Or8b9 |
T |
A |
9: 37,766,560 (GRCm39) |
Y149N |
probably damaging |
Het |
Pdgfrb |
G |
A |
18: 61,204,789 (GRCm39) |
V550I |
probably benign |
Het |
Pi4ka |
A |
T |
16: 17,185,389 (GRCm39) |
L237* |
probably null |
Het |
Pla2r1 |
G |
A |
2: 60,259,055 (GRCm39) |
T1111M |
probably benign |
Het |
Plxnd1 |
A |
T |
6: 115,946,402 (GRCm39) |
|
probably null |
Het |
Pnp |
G |
C |
14: 51,185,430 (GRCm39) |
A67P |
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,718,404 (GRCm39) |
S837T |
probably damaging |
Het |
Ppp2r5e |
C |
G |
12: 75,516,341 (GRCm39) |
A239P |
probably damaging |
Het |
Prom2 |
T |
C |
2: 127,381,707 (GRCm39) |
D203G |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,478,836 (GRCm39) |
V486A |
possibly damaging |
Het |
Rnf115 |
A |
G |
3: 96,635,153 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Rusc2 |
C |
A |
4: 43,421,719 (GRCm39) |
A713D |
possibly damaging |
Het |
Ryr3 |
A |
T |
2: 112,560,673 (GRCm39) |
H3009Q |
possibly damaging |
Het |
Serpina1d |
C |
A |
12: 103,734,256 (GRCm39) |
C16F |
probably benign |
Het |
Serpinf2 |
G |
T |
11: 75,328,309 (GRCm39) |
R80S |
possibly damaging |
Het |
Sh2d4a |
C |
A |
8: 68,781,967 (GRCm39) |
Q192K |
probably benign |
Het |
Sh3d21 |
T |
A |
4: 126,044,729 (GRCm39) |
|
probably null |
Het |
Sh3rf2 |
T |
A |
18: 42,187,046 (GRCm39) |
L55Q |
probably damaging |
Het |
Shc4 |
T |
C |
2: 125,481,287 (GRCm39) |
D255G |
probably damaging |
Het |
Skint2 |
T |
A |
4: 112,483,106 (GRCm39) |
H170Q |
probably benign |
Het |
Slc29a4 |
A |
G |
5: 142,703,509 (GRCm39) |
Y261C |
probably damaging |
Het |
Slc35a5 |
A |
T |
16: 44,964,071 (GRCm39) |
N102K |
possibly damaging |
Het |
Slc38a3 |
A |
T |
9: 107,533,152 (GRCm39) |
I307K |
probably damaging |
Het |
Sv2b |
A |
T |
7: 74,773,828 (GRCm39) |
S548T |
probably benign |
Het |
Tgfbi |
T |
C |
13: 56,780,694 (GRCm39) |
S524P |
probably benign |
Het |
Tgm5 |
T |
C |
2: 120,905,699 (GRCm39) |
D152G |
probably damaging |
Het |
Tmem213 |
A |
G |
6: 38,086,487 (GRCm39) |
T48A |
possibly damaging |
Het |
Tmem37 |
A |
G |
1: 119,995,952 (GRCm39) |
S42P |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,917,764 (GRCm39) |
K1258R |
probably damaging |
Het |
Ttc22 |
T |
C |
4: 106,494,003 (GRCm39) |
V321A |
probably benign |
Het |
Ube2c |
C |
A |
2: 164,611,943 (GRCm39) |
A15E |
probably benign |
Het |
Ubn2 |
T |
A |
6: 38,417,425 (GRCm39) |
D154E |
possibly damaging |
Het |
Umod |
A |
T |
7: 119,062,478 (GRCm39) |
L631M |
probably damaging |
Het |
Ush1c |
G |
A |
7: 45,868,816 (GRCm39) |
Q373* |
probably null |
Het |
Vmn1r238 |
T |
A |
18: 3,123,040 (GRCm39) |
R125* |
probably null |
Het |
Wnt8b |
T |
C |
19: 44,482,029 (GRCm39) |
L14P |
probably benign |
Het |
Wrn |
G |
A |
8: 33,778,892 (GRCm39) |
A563V |
probably damaging |
Het |
Zfp268 |
A |
T |
4: 145,348,998 (GRCm39) |
Q145L |
possibly damaging |
Het |
Zfp608 |
A |
G |
18: 55,030,983 (GRCm39) |
S986P |
probably benign |
Het |
Znrf3 |
T |
C |
11: 5,233,373 (GRCm39) |
H228R |
possibly damaging |
Het |
|
Other mutations in Col12a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Col12a1
|
APN |
9 |
79,588,819 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL00434:Col12a1
|
APN |
9 |
79,560,614 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00465:Col12a1
|
APN |
9 |
79,604,863 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00568:Col12a1
|
APN |
9 |
79,558,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00576:Col12a1
|
APN |
9 |
79,554,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00580:Col12a1
|
APN |
9 |
79,599,508 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01015:Col12a1
|
APN |
9 |
79,541,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01124:Col12a1
|
APN |
9 |
79,611,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01138:Col12a1
|
APN |
9 |
79,585,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01295:Col12a1
|
APN |
9 |
79,551,208 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01630:Col12a1
|
APN |
9 |
79,564,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01648:Col12a1
|
APN |
9 |
79,508,451 (GRCm39) |
makesense |
probably null |
|
IGL01878:Col12a1
|
APN |
9 |
79,557,257 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01921:Col12a1
|
APN |
9 |
79,557,299 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02064:Col12a1
|
APN |
9 |
79,599,654 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02123:Col12a1
|
APN |
9 |
79,569,740 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02312:Col12a1
|
APN |
9 |
79,588,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02320:Col12a1
|
APN |
9 |
79,523,303 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02328:Col12a1
|
APN |
9 |
79,589,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02342:Col12a1
|
APN |
9 |
79,557,178 (GRCm39) |
splice site |
probably null |
|
IGL02355:Col12a1
|
APN |
9 |
79,537,993 (GRCm39) |
splice site |
probably benign |
|
IGL02362:Col12a1
|
APN |
9 |
79,537,993 (GRCm39) |
splice site |
probably benign |
|
IGL02396:Col12a1
|
APN |
9 |
79,569,865 (GRCm39) |
missense |
probably benign |
|
IGL02449:Col12a1
|
APN |
9 |
79,548,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02682:Col12a1
|
APN |
9 |
79,606,623 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02751:Col12a1
|
APN |
9 |
79,521,141 (GRCm39) |
unclassified |
probably benign |
|
IGL02801:Col12a1
|
APN |
9 |
79,515,696 (GRCm39) |
splice site |
probably null |
|
IGL03001:Col12a1
|
APN |
9 |
79,540,955 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Col12a1
|
APN |
9 |
79,548,833 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03090:Col12a1
|
APN |
9 |
79,585,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Col12a1
|
APN |
9 |
79,588,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03220:Col12a1
|
APN |
9 |
79,606,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03240:Col12a1
|
APN |
9 |
79,585,665 (GRCm39) |
splice site |
probably null |
|
IGL03348:Col12a1
|
APN |
9 |
79,600,712 (GRCm39) |
missense |
possibly damaging |
0.88 |
airship
|
UTSW |
9 |
79,613,619 (GRCm39) |
missense |
possibly damaging |
0.65 |
dirigible
|
UTSW |
9 |
79,611,111 (GRCm39) |
missense |
possibly damaging |
0.73 |
Feast
|
UTSW |
9 |
79,607,544 (GRCm39) |
missense |
probably benign |
0.00 |
hardly
|
UTSW |
9 |
79,607,632 (GRCm39) |
nonsense |
probably null |
|
hearty
|
UTSW |
9 |
79,551,248 (GRCm39) |
missense |
probably damaging |
1.00 |
Hefty
|
UTSW |
9 |
79,569,736 (GRCm39) |
splice site |
probably benign |
|
P0045:Col12a1
|
UTSW |
9 |
79,554,893 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4260001:Col12a1
|
UTSW |
9 |
79,558,662 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4280001:Col12a1
|
UTSW |
9 |
79,585,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Col12a1
|
UTSW |
9 |
79,558,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Col12a1
|
UTSW |
9 |
79,558,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Col12a1
|
UTSW |
9 |
79,559,315 (GRCm39) |
missense |
probably benign |
0.02 |
R0276:Col12a1
|
UTSW |
9 |
79,538,023 (GRCm39) |
nonsense |
probably null |
|
R0309:Col12a1
|
UTSW |
9 |
79,507,293 (GRCm39) |
splice site |
probably null |
|
R0336:Col12a1
|
UTSW |
9 |
79,609,627 (GRCm39) |
missense |
probably damaging |
0.98 |
R0376:Col12a1
|
UTSW |
9 |
79,600,776 (GRCm39) |
missense |
probably benign |
0.10 |
R0413:Col12a1
|
UTSW |
9 |
79,606,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R0504:Col12a1
|
UTSW |
9 |
79,588,750 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0542:Col12a1
|
UTSW |
9 |
79,512,610 (GRCm39) |
critical splice donor site |
probably null |
|
R0610:Col12a1
|
UTSW |
9 |
79,615,130 (GRCm39) |
missense |
probably benign |
|
R0631:Col12a1
|
UTSW |
9 |
79,610,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Col12a1
|
UTSW |
9 |
79,564,017 (GRCm39) |
missense |
probably benign |
0.00 |
R0667:Col12a1
|
UTSW |
9 |
79,535,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Col12a1
|
UTSW |
9 |
79,559,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R0717:Col12a1
|
UTSW |
9 |
79,519,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0762:Col12a1
|
UTSW |
9 |
79,588,656 (GRCm39) |
splice site |
probably benign |
|
R0787:Col12a1
|
UTSW |
9 |
79,545,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R0890:Col12a1
|
UTSW |
9 |
79,607,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R0900:Col12a1
|
UTSW |
9 |
79,591,535 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1109:Col12a1
|
UTSW |
9 |
79,607,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Col12a1
|
UTSW |
9 |
79,527,371 (GRCm39) |
missense |
probably benign |
0.09 |
R1321:Col12a1
|
UTSW |
9 |
79,524,991 (GRCm39) |
nonsense |
probably null |
|
R1344:Col12a1
|
UTSW |
9 |
79,606,837 (GRCm39) |
nonsense |
probably null |
|
R1387:Col12a1
|
UTSW |
9 |
79,588,657 (GRCm39) |
splice site |
probably benign |
|
R1511:Col12a1
|
UTSW |
9 |
79,606,834 (GRCm39) |
missense |
probably benign |
0.02 |
R1523:Col12a1
|
UTSW |
9 |
79,568,278 (GRCm39) |
missense |
probably benign |
0.01 |
R1526:Col12a1
|
UTSW |
9 |
79,564,080 (GRCm39) |
missense |
probably benign |
0.44 |
R1564:Col12a1
|
UTSW |
9 |
79,521,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Col12a1
|
UTSW |
9 |
79,509,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R1603:Col12a1
|
UTSW |
9 |
79,520,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Col12a1
|
UTSW |
9 |
79,600,820 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Col12a1
|
UTSW |
9 |
79,535,660 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1737:Col12a1
|
UTSW |
9 |
79,610,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Col12a1
|
UTSW |
9 |
79,540,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R1748:Col12a1
|
UTSW |
9 |
79,580,279 (GRCm39) |
missense |
probably benign |
0.01 |
R1778:Col12a1
|
UTSW |
9 |
79,511,867 (GRCm39) |
splice site |
probably benign |
|
R1845:Col12a1
|
UTSW |
9 |
79,604,823 (GRCm39) |
missense |
probably benign |
0.09 |
R1876:Col12a1
|
UTSW |
9 |
79,585,563 (GRCm39) |
nonsense |
probably null |
|
R1934:Col12a1
|
UTSW |
9 |
79,511,804 (GRCm39) |
nonsense |
probably null |
|
R1942:Col12a1
|
UTSW |
9 |
79,542,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Col12a1
|
UTSW |
9 |
79,537,831 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2027:Col12a1
|
UTSW |
9 |
79,553,075 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2061:Col12a1
|
UTSW |
9 |
79,524,987 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2064:Col12a1
|
UTSW |
9 |
79,569,736 (GRCm39) |
splice site |
probably benign |
|
R2070:Col12a1
|
UTSW |
9 |
79,554,978 (GRCm39) |
missense |
probably benign |
0.00 |
R2112:Col12a1
|
UTSW |
9 |
79,551,181 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2209:Col12a1
|
UTSW |
9 |
79,599,634 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2275:Col12a1
|
UTSW |
9 |
79,542,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R2330:Col12a1
|
UTSW |
9 |
79,540,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R2373:Col12a1
|
UTSW |
9 |
79,564,095 (GRCm39) |
missense |
probably benign |
0.03 |
R2425:Col12a1
|
UTSW |
9 |
79,585,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R2428:Col12a1
|
UTSW |
9 |
79,509,533 (GRCm39) |
missense |
probably benign |
0.30 |
R2437:Col12a1
|
UTSW |
9 |
79,599,501 (GRCm39) |
missense |
probably damaging |
0.97 |
R2831:Col12a1
|
UTSW |
9 |
79,604,683 (GRCm39) |
missense |
probably null |
0.99 |
R2851:Col12a1
|
UTSW |
9 |
79,585,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Col12a1
|
UTSW |
9 |
79,606,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Col12a1
|
UTSW |
9 |
79,606,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R2874:Col12a1
|
UTSW |
9 |
79,606,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R2904:Col12a1
|
UTSW |
9 |
79,559,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R2905:Col12a1
|
UTSW |
9 |
79,559,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R2991:Col12a1
|
UTSW |
9 |
79,607,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R3402:Col12a1
|
UTSW |
9 |
79,551,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R3429:Col12a1
|
UTSW |
9 |
79,587,593 (GRCm39) |
missense |
probably benign |
|
R3430:Col12a1
|
UTSW |
9 |
79,587,593 (GRCm39) |
missense |
probably benign |
|
R3547:Col12a1
|
UTSW |
9 |
79,540,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R3789:Col12a1
|
UTSW |
9 |
79,547,005 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4091:Col12a1
|
UTSW |
9 |
79,609,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R4328:Col12a1
|
UTSW |
9 |
79,607,671 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4382:Col12a1
|
UTSW |
9 |
79,538,023 (GRCm39) |
nonsense |
probably null |
|
R4392:Col12a1
|
UTSW |
9 |
79,569,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R4405:Col12a1
|
UTSW |
9 |
79,547,247 (GRCm39) |
critical splice donor site |
probably null |
|
R4465:Col12a1
|
UTSW |
9 |
79,580,192 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4521:Col12a1
|
UTSW |
9 |
79,540,639 (GRCm39) |
missense |
probably benign |
0.00 |
R4612:Col12a1
|
UTSW |
9 |
79,523,339 (GRCm39) |
missense |
probably damaging |
0.99 |
R4613:Col12a1
|
UTSW |
9 |
79,554,883 (GRCm39) |
missense |
probably benign |
0.03 |
R4649:Col12a1
|
UTSW |
9 |
79,547,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Col12a1
|
UTSW |
9 |
79,520,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Col12a1
|
UTSW |
9 |
79,520,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Col12a1
|
UTSW |
9 |
79,606,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R4745:Col12a1
|
UTSW |
9 |
79,559,368 (GRCm39) |
splice site |
probably null |
|
R4761:Col12a1
|
UTSW |
9 |
79,564,592 (GRCm39) |
missense |
probably benign |
0.34 |
R4784:Col12a1
|
UTSW |
9 |
79,585,776 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4785:Col12a1
|
UTSW |
9 |
79,585,776 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4809:Col12a1
|
UTSW |
9 |
79,600,849 (GRCm39) |
missense |
probably benign |
0.10 |
R4821:Col12a1
|
UTSW |
9 |
79,622,622 (GRCm39) |
intron |
probably benign |
|
R4925:Col12a1
|
UTSW |
9 |
79,582,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R4938:Col12a1
|
UTSW |
9 |
79,607,632 (GRCm39) |
nonsense |
probably null |
|
R5034:Col12a1
|
UTSW |
9 |
79,564,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Col12a1
|
UTSW |
9 |
79,512,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R5138:Col12a1
|
UTSW |
9 |
79,551,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R5145:Col12a1
|
UTSW |
9 |
79,613,582 (GRCm39) |
missense |
probably benign |
0.00 |
R5152:Col12a1
|
UTSW |
9 |
79,564,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Col12a1
|
UTSW |
9 |
79,607,544 (GRCm39) |
missense |
probably benign |
0.00 |
R5268:Col12a1
|
UTSW |
9 |
79,585,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R5328:Col12a1
|
UTSW |
9 |
79,527,342 (GRCm39) |
missense |
probably damaging |
0.96 |
R5372:Col12a1
|
UTSW |
9 |
79,585,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R5440:Col12a1
|
UTSW |
9 |
79,521,645 (GRCm39) |
missense |
probably benign |
0.07 |
R5496:Col12a1
|
UTSW |
9 |
79,509,467 (GRCm39) |
splice site |
probably benign |
|
R5537:Col12a1
|
UTSW |
9 |
79,606,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R5596:Col12a1
|
UTSW |
9 |
79,611,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Col12a1
|
UTSW |
9 |
79,606,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Col12a1
|
UTSW |
9 |
79,523,347 (GRCm39) |
nonsense |
probably null |
|
R5796:Col12a1
|
UTSW |
9 |
79,611,111 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5829:Col12a1
|
UTSW |
9 |
79,540,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Col12a1
|
UTSW |
9 |
79,511,760 (GRCm39) |
missense |
probably benign |
0.00 |
R5919:Col12a1
|
UTSW |
9 |
79,509,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R5974:Col12a1
|
UTSW |
9 |
79,589,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R5981:Col12a1
|
UTSW |
9 |
79,585,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R5982:Col12a1
|
UTSW |
9 |
79,537,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Col12a1
|
UTSW |
9 |
79,563,860 (GRCm39) |
critical splice donor site |
probably null |
|
R6090:Col12a1
|
UTSW |
9 |
79,599,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Col12a1
|
UTSW |
9 |
79,521,640 (GRCm39) |
missense |
probably benign |
0.00 |
R6393:Col12a1
|
UTSW |
9 |
79,562,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R6457:Col12a1
|
UTSW |
9 |
79,552,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Col12a1
|
UTSW |
9 |
79,554,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R6508:Col12a1
|
UTSW |
9 |
79,557,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R6620:Col12a1
|
UTSW |
9 |
79,527,331 (GRCm39) |
missense |
probably damaging |
0.98 |
R6718:Col12a1
|
UTSW |
9 |
79,606,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Col12a1
|
UTSW |
9 |
79,540,706 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6774:Col12a1
|
UTSW |
9 |
79,613,619 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6872:Col12a1
|
UTSW |
9 |
79,584,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6884:Col12a1
|
UTSW |
9 |
79,547,091 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6935:Col12a1
|
UTSW |
9 |
79,607,782 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7198:Col12a1
|
UTSW |
9 |
79,557,314 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7296:Col12a1
|
UTSW |
9 |
79,589,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Col12a1
|
UTSW |
9 |
79,613,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R7466:Col12a1
|
UTSW |
9 |
79,562,689 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7516:Col12a1
|
UTSW |
9 |
79,520,192 (GRCm39) |
splice site |
probably null |
|
R7584:Col12a1
|
UTSW |
9 |
79,610,578 (GRCm39) |
critical splice donor site |
probably null |
|
R7624:Col12a1
|
UTSW |
9 |
79,553,076 (GRCm39) |
splice site |
probably null |
|
R7670:Col12a1
|
UTSW |
9 |
79,538,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Col12a1
|
UTSW |
9 |
79,558,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R7702:Col12a1
|
UTSW |
9 |
79,588,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7796:Col12a1
|
UTSW |
9 |
79,585,833 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7902:Col12a1
|
UTSW |
9 |
79,548,863 (GRCm39) |
missense |
probably benign |
0.00 |
R7923:Col12a1
|
UTSW |
9 |
79,585,775 (GRCm39) |
missense |
probably benign |
0.00 |
R7986:Col12a1
|
UTSW |
9 |
79,511,674 (GRCm39) |
critical splice donor site |
probably null |
|
R8004:Col12a1
|
UTSW |
9 |
79,591,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Col12a1
|
UTSW |
9 |
79,613,508 (GRCm39) |
critical splice donor site |
probably null |
|
R8056:Col12a1
|
UTSW |
9 |
79,507,220 (GRCm39) |
missense |
|
|
R8151:Col12a1
|
UTSW |
9 |
79,537,831 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8203:Col12a1
|
UTSW |
9 |
79,588,831 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8221:Col12a1
|
UTSW |
9 |
79,551,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R8294:Col12a1
|
UTSW |
9 |
79,606,594 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8309:Col12a1
|
UTSW |
9 |
79,512,465 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8319:Col12a1
|
UTSW |
9 |
79,555,979 (GRCm39) |
missense |
probably damaging |
0.97 |
R8351:Col12a1
|
UTSW |
9 |
79,588,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R8442:Col12a1
|
UTSW |
9 |
79,542,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Col12a1
|
UTSW |
9 |
79,517,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Col12a1
|
UTSW |
9 |
79,568,358 (GRCm39) |
missense |
probably benign |
0.03 |
R8700:Col12a1
|
UTSW |
9 |
79,527,371 (GRCm39) |
missense |
probably benign |
0.09 |
R8859:Col12a1
|
UTSW |
9 |
79,587,681 (GRCm39) |
nonsense |
probably null |
|
R8898:Col12a1
|
UTSW |
9 |
79,599,577 (GRCm39) |
missense |
probably benign |
0.08 |
R8930:Col12a1
|
UTSW |
9 |
79,580,665 (GRCm39) |
missense |
probably benign |
|
R8932:Col12a1
|
UTSW |
9 |
79,580,665 (GRCm39) |
missense |
probably benign |
|
R8949:Col12a1
|
UTSW |
9 |
79,581,970 (GRCm39) |
missense |
probably benign |
0.17 |
R8962:Col12a1
|
UTSW |
9 |
79,538,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R9045:Col12a1
|
UTSW |
9 |
79,582,034 (GRCm39) |
missense |
probably benign |
0.00 |
R9080:Col12a1
|
UTSW |
9 |
79,517,133 (GRCm39) |
missense |
probably benign |
0.06 |
R9145:Col12a1
|
UTSW |
9 |
79,527,344 (GRCm39) |
missense |
probably benign |
0.16 |
R9163:Col12a1
|
UTSW |
9 |
79,548,729 (GRCm39) |
critical splice donor site |
probably null |
|
R9168:Col12a1
|
UTSW |
9 |
79,548,783 (GRCm39) |
nonsense |
probably null |
|
R9188:Col12a1
|
UTSW |
9 |
79,509,614 (GRCm39) |
missense |
probably benign |
0.22 |
R9258:Col12a1
|
UTSW |
9 |
79,613,645 (GRCm39) |
missense |
probably benign |
0.04 |
R9292:Col12a1
|
UTSW |
9 |
79,585,805 (GRCm39) |
missense |
probably benign |
0.33 |
R9345:Col12a1
|
UTSW |
9 |
79,541,017 (GRCm39) |
missense |
probably benign |
0.08 |
R9382:Col12a1
|
UTSW |
9 |
79,589,364 (GRCm39) |
missense |
probably benign |
0.23 |
R9427:Col12a1
|
UTSW |
9 |
79,589,445 (GRCm39) |
missense |
probably benign |
0.15 |
R9601:Col12a1
|
UTSW |
9 |
79,525,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R9653:Col12a1
|
UTSW |
9 |
79,584,556 (GRCm39) |
missense |
probably benign |
|
R9668:Col12a1
|
UTSW |
9 |
79,546,960 (GRCm39) |
nonsense |
probably null |
|
R9762:Col12a1
|
UTSW |
9 |
79,527,266 (GRCm39) |
missense |
possibly damaging |
0.82 |
X0021:Col12a1
|
UTSW |
9 |
79,515,767 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Col12a1
|
UTSW |
9 |
79,509,506 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0061:Col12a1
|
UTSW |
9 |
79,519,674 (GRCm39) |
splice site |
probably null |
|
Z1177:Col12a1
|
UTSW |
9 |
79,507,268 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:Col12a1
|
UTSW |
9 |
79,546,978 (GRCm39) |
frame shift |
probably null |
|
|