Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
CGGG |
CGGGGGG |
15: 76,833,863 (GRCm39) |
|
probably benign |
Het |
Abca17 |
A |
T |
17: 24,486,690 (GRCm39) |
C1446S |
probably damaging |
Het |
Asb16 |
C |
A |
11: 102,167,582 (GRCm39) |
A316E |
possibly damaging |
Het |
Axdnd1 |
C |
T |
1: 156,204,114 (GRCm39) |
V384I |
possibly damaging |
Het |
BC024139 |
A |
T |
15: 76,009,461 (GRCm39) |
L207* |
probably null |
Het |
Bcl3 |
T |
G |
7: 19,543,552 (GRCm39) |
S305R |
probably damaging |
Het |
Cachd1 |
T |
C |
4: 100,634,555 (GRCm39) |
V77A |
probably benign |
Het |
Cd101 |
C |
T |
3: 100,936,764 (GRCm39) |
|
probably null |
Het |
Cela1 |
T |
C |
15: 100,583,048 (GRCm39) |
N64S |
probably benign |
Het |
Cep128 |
T |
C |
12: 91,256,372 (GRCm39) |
D366G |
probably benign |
Het |
Copg1 |
A |
G |
6: 87,870,800 (GRCm39) |
Y201C |
probably damaging |
Het |
Cyp24a1 |
T |
C |
2: 170,329,837 (GRCm39) |
R372G |
probably benign |
Het |
Dcaf1 |
A |
C |
9: 106,729,161 (GRCm39) |
I567L |
probably benign |
Het |
Dcn |
A |
G |
10: 97,342,536 (GRCm39) |
D164G |
probably benign |
Het |
Dnase2a |
T |
A |
8: 85,635,951 (GRCm39) |
H113Q |
probably benign |
Het |
Espl1 |
T |
C |
15: 102,207,448 (GRCm39) |
V304A |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,600,716 (GRCm39) |
D315G |
possibly damaging |
Het |
Fkbp8 |
T |
A |
8: 70,983,685 (GRCm39) |
|
probably null |
Het |
Foxp4 |
T |
A |
17: 48,188,884 (GRCm39) |
T321S |
probably null |
Het |
Fut10 |
A |
G |
8: 31,726,328 (GRCm39) |
N361S |
probably damaging |
Het |
Gyg1 |
A |
T |
3: 20,205,286 (GRCm39) |
V94D |
probably damaging |
Het |
Has2 |
T |
C |
15: 56,531,974 (GRCm39) |
K247R |
probably damaging |
Het |
Helz2 |
G |
T |
2: 180,873,878 (GRCm39) |
D2205E |
probably benign |
Het |
Hps6 |
T |
A |
19: 45,993,409 (GRCm39) |
S449T |
probably benign |
Het |
Ints10 |
T |
C |
8: 69,247,323 (GRCm39) |
Y64H |
probably damaging |
Het |
Kalrn |
T |
C |
16: 34,177,331 (GRCm39) |
H278R |
probably damaging |
Het |
Klhdc8a |
T |
C |
1: 132,231,548 (GRCm39) |
V280A |
possibly damaging |
Het |
Klk1b5 |
A |
G |
7: 43,869,549 (GRCm39) |
M210V |
probably benign |
Het |
Kmt2c |
G |
A |
5: 25,578,434 (GRCm39) |
A614V |
probably benign |
Het |
Lck |
T |
A |
4: 129,451,879 (GRCm39) |
I45F |
probably benign |
Het |
Lin7a |
A |
C |
10: 107,247,920 (GRCm39) |
E75A |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,414,542 (GRCm39) |
C1070S |
probably damaging |
Het |
Mapk8ip3 |
G |
T |
17: 25,133,557 (GRCm39) |
N289K |
probably benign |
Het |
Mbtps1 |
T |
C |
8: 120,249,232 (GRCm39) |
D686G |
probably benign |
Het |
Mknk1 |
T |
A |
4: 115,730,428 (GRCm39) |
C178* |
probably null |
Het |
Mtmr6 |
A |
G |
14: 60,534,184 (GRCm39) |
N474S |
probably damaging |
Het |
Mvb12b |
A |
G |
2: 33,730,169 (GRCm39) |
|
probably null |
Het |
Myh6 |
T |
C |
14: 55,182,131 (GRCm39) |
K1759R |
probably damaging |
Het |
Nfatc1 |
T |
C |
18: 80,678,746 (GRCm39) |
K881E |
possibly damaging |
Het |
Nlrp10 |
A |
G |
7: 108,526,248 (GRCm39) |
F30S |
probably damaging |
Het |
Nop14 |
G |
T |
5: 34,807,672 (GRCm39) |
A430E |
possibly damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or1j18 |
A |
T |
2: 36,624,854 (GRCm39) |
I174F |
probably damaging |
Het |
Or4c107 |
A |
G |
2: 88,789,211 (GRCm39) |
I134V |
probably damaging |
Het |
Or4c108 |
A |
G |
2: 88,803,482 (GRCm39) |
V251A |
probably benign |
Het |
Or6c205 |
A |
G |
10: 129,086,463 (GRCm39) |
E20G |
probably benign |
Het |
Or6c88 |
A |
T |
10: 129,407,217 (GRCm39) |
Q231L |
probably damaging |
Het |
Or7g17 |
A |
T |
9: 18,768,782 (GRCm39) |
Y287F |
possibly damaging |
Het |
Osbpl7 |
C |
A |
11: 96,949,954 (GRCm39) |
S378R |
probably damaging |
Het |
Otof |
A |
T |
5: 30,529,067 (GRCm39) |
Y1775* |
probably null |
Het |
Parp16 |
T |
C |
9: 65,122,876 (GRCm39) |
S46P |
possibly damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pi16 |
A |
T |
17: 29,538,361 (GRCm39) |
Q58L |
possibly damaging |
Het |
Pld3 |
C |
A |
7: 27,238,877 (GRCm39) |
M190I |
probably benign |
Het |
Plscr4 |
T |
G |
9: 92,372,099 (GRCm39) |
I290S |
probably damaging |
Het |
Ppip5k2 |
T |
C |
1: 97,651,531 (GRCm39) |
D928G |
possibly damaging |
Het |
Ppp1r13l |
T |
A |
7: 19,102,536 (GRCm39) |
L15Q |
probably damaging |
Het |
Prorp |
T |
A |
12: 55,351,117 (GRCm39) |
I142N |
possibly damaging |
Het |
Ptpn14 |
C |
A |
1: 189,571,699 (GRCm39) |
S263R |
possibly damaging |
Het |
Sema7a |
G |
A |
9: 57,862,182 (GRCm39) |
V178I |
possibly damaging |
Het |
Sesn2 |
A |
T |
4: 132,224,381 (GRCm39) |
Y342* |
probably null |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Sltm |
A |
G |
9: 70,450,314 (GRCm39) |
N38S |
possibly damaging |
Het |
Smg1 |
T |
C |
7: 117,753,845 (GRCm39) |
|
probably benign |
Het |
Spsb1 |
A |
T |
4: 149,991,367 (GRCm39) |
V67E |
probably damaging |
Het |
Suox |
A |
G |
10: 128,506,408 (GRCm39) |
V540A |
possibly damaging |
Het |
Tbc1d12 |
T |
A |
19: 38,899,529 (GRCm39) |
I483N |
probably damaging |
Het |
Tbcb |
A |
T |
7: 29,923,924 (GRCm39) |
D198E |
possibly damaging |
Het |
Tbce |
T |
C |
13: 14,194,294 (GRCm39) |
K122E |
probably benign |
Het |
Tcap |
T |
A |
11: 98,275,205 (GRCm39) |
L113H |
probably damaging |
Het |
Thsd7a |
A |
T |
6: 12,321,040 (GRCm39) |
I1545N |
probably damaging |
Het |
Tmed10 |
T |
C |
12: 85,421,277 (GRCm39) |
T55A |
possibly damaging |
Het |
Tmem268 |
T |
A |
4: 63,498,180 (GRCm39) |
V200D |
probably damaging |
Het |
Tmem45b |
A |
C |
9: 31,342,651 (GRCm39) |
I50M |
probably damaging |
Het |
Trp53bp2 |
T |
C |
1: 182,286,468 (GRCm39) |
W1103R |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,594,377 (GRCm39) |
V20524M |
probably damaging |
Het |
Ulk2 |
A |
T |
11: 61,703,564 (GRCm39) |
N379K |
probably benign |
Het |
Vmn1r59 |
A |
G |
7: 5,457,553 (GRCm39) |
V69A |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,149,861 (GRCm39) |
Y394* |
probably null |
Het |
Zfp212 |
T |
C |
6: 47,908,475 (GRCm39) |
S485P |
probably benign |
Het |
Zfp512b |
A |
T |
2: 181,227,528 (GRCm39) |
C776S |
probably damaging |
Het |
Zfp518b |
A |
G |
5: 38,829,084 (GRCm39) |
Y974H |
probably 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 |
|
R1864:Col12a1
|
UTSW |
9 |
79,534,385 (GRCm39) |
splice site |
probably null |
|
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 |
|
|