Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
A |
G |
5: 4,010,677 (GRCm39) |
N478S |
probably damaging |
Het |
Als2 |
T |
A |
1: 59,224,760 (GRCm39) |
|
probably null |
Het |
Ankfy1 |
A |
G |
11: 72,651,155 (GRCm39) |
Y1035C |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,616,608 (GRCm39) |
T2394A |
probably damaging |
Het |
Axin1 |
G |
C |
17: 26,412,938 (GRCm39) |
G780R |
possibly damaging |
Het |
Carm1 |
A |
T |
9: 21,485,812 (GRCm39) |
T127S |
probably benign |
Het |
Ccdc73 |
T |
C |
2: 104,757,280 (GRCm39) |
I81T |
probably benign |
Het |
Cdh12 |
T |
C |
15: 21,237,965 (GRCm39) |
Y67H |
probably damaging |
Het |
Cfap65 |
C |
A |
1: 74,946,819 (GRCm39) |
G1297V |
probably damaging |
Het |
Cfap74 |
T |
C |
4: 155,511,887 (GRCm39) |
|
probably null |
Het |
Chit1 |
A |
G |
1: 134,078,968 (GRCm39) |
Y426C |
probably damaging |
Het |
Clpp |
A |
G |
17: 57,303,039 (GRCm39) |
|
probably benign |
Het |
Clrn3 |
T |
G |
7: 135,115,813 (GRCm39) |
Y179S |
possibly damaging |
Het |
Cntn5 |
A |
C |
9: 9,781,774 (GRCm39) |
M635R |
probably damaging |
Het |
Ctla2b |
T |
C |
13: 61,043,863 (GRCm39) |
N102S |
possibly damaging |
Het |
Cwf19l2 |
A |
T |
9: 3,418,674 (GRCm39) |
I154F |
probably benign |
Het |
Dffa |
C |
A |
4: 149,188,839 (GRCm39) |
S44R |
probably benign |
Het |
Ehbp1 |
T |
A |
11: 22,009,228 (GRCm39) |
K930M |
probably damaging |
Het |
Erc2 |
T |
A |
14: 27,634,857 (GRCm39) |
S473T |
probably damaging |
Het |
Fbxw24 |
A |
T |
9: 109,434,481 (GRCm39) |
L373H |
probably benign |
Het |
Fer1l4 |
T |
C |
2: 155,890,194 (GRCm39) |
I244V |
probably damaging |
Het |
Fgfr2 |
G |
A |
7: 129,800,211 (GRCm39) |
T245M |
probably damaging |
Het |
Garin1b |
C |
T |
6: 29,335,815 (GRCm39) |
|
probably null |
Het |
Gbp9 |
T |
A |
5: 105,229,112 (GRCm39) |
M512L |
probably benign |
Het |
Glg1 |
T |
A |
8: 111,892,271 (GRCm39) |
K251I |
possibly damaging |
Het |
Gm10553 |
A |
G |
1: 85,078,141 (GRCm39) |
D86G |
possibly damaging |
Het |
Gm5622 |
T |
C |
14: 51,893,229 (GRCm39) |
V52A |
probably benign |
Het |
Gucy1b1 |
A |
G |
3: 81,952,716 (GRCm39) |
V239A |
probably benign |
Het |
Gzma |
A |
G |
13: 113,230,463 (GRCm39) |
L246P |
probably damaging |
Het |
Hibadh |
C |
A |
6: 52,533,448 (GRCm39) |
A223S |
probably benign |
Het |
Hydin |
C |
A |
8: 111,336,619 (GRCm39) |
T5132N |
possibly damaging |
Het |
Insrr |
A |
G |
3: 87,721,820 (GRCm39) |
N1198S |
probably damaging |
Het |
Ivl |
T |
C |
3: 92,479,420 (GRCm39) |
E215G |
possibly damaging |
Het |
Jmjd1c |
A |
G |
10: 67,075,701 (GRCm39) |
D2037G |
possibly damaging |
Het |
Kcna3 |
G |
A |
3: 106,944,988 (GRCm39) |
C417Y |
probably damaging |
Het |
Klra2 |
T |
C |
6: 131,207,078 (GRCm39) |
N177S |
probably benign |
Het |
Llgl2 |
T |
C |
11: 115,741,892 (GRCm39) |
S645P |
probably damaging |
Het |
Lrrc15 |
T |
C |
16: 30,092,649 (GRCm39) |
E230G |
probably benign |
Het |
Magel2 |
C |
A |
7: 62,028,163 (GRCm39) |
Q356K |
possibly damaging |
Het |
Mcm6 |
A |
G |
1: 128,273,726 (GRCm39) |
V368A |
probably benign |
Het |
Myh8 |
G |
A |
11: 67,169,830 (GRCm39) |
V50M |
possibly damaging |
Het |
Myrf |
A |
T |
19: 10,195,554 (GRCm39) |
F419I |
possibly damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Or10ak16 |
G |
A |
4: 118,750,537 (GRCm39) |
V86M |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,684 (GRCm39) |
M186V |
probably benign |
Het |
Otud4 |
G |
A |
8: 80,372,961 (GRCm39) |
R93H |
probably damaging |
Het |
Pank4 |
T |
A |
4: 155,056,977 (GRCm39) |
M390K |
probably benign |
Het |
Pecam1 |
A |
G |
11: 106,576,029 (GRCm39) |
V401A |
probably damaging |
Het |
Prdm6 |
C |
A |
18: 53,669,796 (GRCm39) |
T138K |
possibly damaging |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,387,337 (GRCm39) |
E1206G |
possibly damaging |
Het |
Prr30 |
A |
T |
14: 101,435,377 (GRCm39) |
I395N |
probably benign |
Het |
Rab27a |
G |
A |
9: 72,982,751 (GRCm39) |
G19R |
probably damaging |
Het |
Ramacl |
A |
G |
13: 67,055,269 (GRCm39) |
|
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,881,029 (GRCm39) |
V134A |
probably damaging |
Het |
Scly |
A |
G |
1: 91,233,116 (GRCm39) |
T76A |
probably benign |
Het |
Scube3 |
T |
C |
17: 28,383,274 (GRCm39) |
S439P |
possibly damaging |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Sipa1l1 |
T |
C |
12: 82,388,233 (GRCm39) |
F153S |
probably damaging |
Het |
Slc25a30 |
T |
G |
14: 76,007,007 (GRCm39) |
K163T |
possibly damaging |
Het |
Slc26a8 |
T |
A |
17: 28,863,614 (GRCm39) |
D715V |
probably benign |
Het |
Smr2 |
AT |
ATT |
5: 88,256,683 (GRCm39) |
|
probably null |
Het |
Smr2 |
C |
CT |
5: 88,256,685 (GRCm39) |
|
probably null |
Het |
Sp6 |
T |
G |
11: 96,912,940 (GRCm39) |
S218A |
probably benign |
Het |
Spata21 |
T |
C |
4: 140,838,716 (GRCm39) |
V589A |
probably damaging |
Het |
Sycp2 |
T |
C |
2: 178,044,593 (GRCm39) |
I71V |
probably benign |
Het |
Syne2 |
G |
T |
12: 75,999,644 (GRCm39) |
G2347C |
probably benign |
Het |
Tenm2 |
C |
T |
11: 35,954,004 (GRCm39) |
G1236R |
possibly damaging |
Het |
Thbs4 |
A |
T |
13: 92,906,079 (GRCm39) |
N387K |
probably damaging |
Het |
Tmem184a |
T |
C |
5: 139,793,381 (GRCm39) |
D216G |
probably damaging |
Het |
Tprg1 |
T |
A |
16: 25,136,098 (GRCm39) |
S30T |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,738,522 (GRCm39) |
W778R |
probably damaging |
Het |
Ttpa |
T |
C |
4: 20,008,633 (GRCm39) |
L65P |
probably damaging |
Het |
Ush2a |
A |
T |
1: 188,487,382 (GRCm39) |
N3050I |
probably damaging |
Het |
Xpot |
T |
C |
10: 121,455,053 (GRCm39) |
I30V |
probably benign |
Het |
Zfp944 |
A |
G |
17: 22,558,681 (GRCm39) |
S189P |
probably benign |
Het |
Zftraf1 |
A |
G |
15: 76,543,417 (GRCm39) |
|
probably null |
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 |
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 |
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 |
|
|