Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
T |
A |
2: 19,482,667 (GRCm39) |
N475I |
probably damaging |
Het |
Adar |
T |
C |
3: 89,647,290 (GRCm39) |
|
probably benign |
Het |
Aldh3b3 |
A |
T |
19: 4,015,747 (GRCm39) |
|
probably null |
Het |
Amtn |
C |
T |
5: 88,532,859 (GRCm39) |
T158I |
possibly damaging |
Het |
Ap1g2 |
A |
G |
14: 55,337,868 (GRCm39) |
|
probably benign |
Het |
Arhgef3 |
A |
G |
14: 27,119,584 (GRCm39) |
Y318C |
probably damaging |
Het |
Atg2b |
A |
C |
12: 105,641,229 (GRCm39) |
V69G |
possibly damaging |
Het |
Bbx |
G |
A |
16: 50,045,529 (GRCm39) |
T236I |
possibly damaging |
Het |
Bcl11b |
C |
T |
12: 107,931,922 (GRCm39) |
|
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,889,377 (GRCm39) |
I794V |
probably benign |
Het |
Ccdc88a |
C |
T |
11: 29,413,112 (GRCm39) |
|
probably benign |
Het |
Cdhr3 |
C |
A |
12: 33,110,300 (GRCm39) |
R328L |
probably benign |
Het |
Ces2e |
T |
A |
8: 105,656,496 (GRCm39) |
M242K |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,588,656 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,247,900 (GRCm39) |
|
probably benign |
Het |
Cyp2a5 |
T |
A |
7: 26,538,298 (GRCm39) |
Y220* |
probably null |
Het |
Dcc |
T |
A |
18: 71,475,776 (GRCm39) |
|
probably benign |
Het |
Dnajb8 |
A |
G |
6: 88,200,036 (GRCm39) |
T191A |
probably damaging |
Het |
Ephx2 |
A |
T |
14: 66,339,628 (GRCm39) |
F199I |
probably damaging |
Het |
Fancd2 |
A |
G |
6: 113,551,619 (GRCm39) |
K1062E |
probably benign |
Het |
Fbxo33 |
A |
G |
12: 59,251,285 (GRCm39) |
V410A |
probably benign |
Het |
Gars1 |
T |
G |
6: 55,054,565 (GRCm39) |
|
probably null |
Het |
Git1 |
A |
C |
11: 77,390,660 (GRCm39) |
D132A |
possibly damaging |
Het |
Gp1ba |
C |
T |
11: 70,532,253 (GRCm39) |
P673L |
probably damaging |
Het |
Gucy1a1 |
T |
C |
3: 82,002,203 (GRCm39) |
T44A |
unknown |
Het |
Hjurp |
G |
C |
1: 88,204,937 (GRCm39) |
|
probably benign |
Het |
Ifnlr1 |
A |
G |
4: 135,428,640 (GRCm39) |
K156E |
possibly damaging |
Het |
Klf13 |
T |
C |
7: 63,541,371 (GRCm39) |
N15S |
probably benign |
Het |
Krt77 |
T |
C |
15: 101,769,561 (GRCm39) |
|
probably null |
Het |
Ldc1 |
A |
G |
4: 130,115,417 (GRCm39) |
S44P |
probably damaging |
Het |
Map4 |
C |
A |
9: 109,867,546 (GRCm39) |
|
probably benign |
Het |
Mthfr |
T |
C |
4: 148,139,900 (GRCm39) |
I623T |
possibly damaging |
Het |
Myo7b |
T |
A |
18: 32,116,997 (GRCm39) |
T908S |
probably benign |
Het |
Nbeal2 |
T |
G |
9: 110,472,876 (GRCm39) |
|
probably benign |
Het |
Nwd2 |
T |
G |
5: 63,957,757 (GRCm39) |
F362L |
probably benign |
Het |
Pcm1 |
A |
T |
8: 41,714,057 (GRCm39) |
R208W |
probably damaging |
Het |
Pkd2l1 |
T |
C |
19: 44,138,909 (GRCm39) |
D647G |
probably benign |
Het |
Plbd1 |
C |
T |
6: 136,618,145 (GRCm39) |
V24M |
probably damaging |
Het |
Polr2a |
G |
A |
11: 69,625,943 (GRCm39) |
P1698S |
unknown |
Het |
Prss12 |
T |
C |
3: 123,279,153 (GRCm39) |
I410T |
probably damaging |
Het |
Ptpre |
A |
G |
7: 135,280,964 (GRCm39) |
N565S |
probably damaging |
Het |
Rab44 |
T |
C |
17: 29,364,244 (GRCm39) |
L606P |
unknown |
Het |
Rbm10 |
C |
T |
X: 20,503,903 (GRCm39) |
|
probably benign |
Het |
Rhd |
C |
T |
4: 134,603,612 (GRCm39) |
|
probably benign |
Het |
Rspo3 |
T |
A |
10: 29,375,917 (GRCm39) |
|
probably benign |
Het |
Sdccag8 |
T |
A |
1: 176,773,710 (GRCm39) |
N555K |
probably benign |
Het |
Skint6 |
T |
A |
4: 112,722,848 (GRCm39) |
|
probably benign |
Het |
Slc22a20 |
G |
A |
19: 6,036,036 (GRCm39) |
P45S |
probably damaging |
Het |
Slc5a2 |
A |
G |
7: 127,866,654 (GRCm39) |
Y124C |
probably damaging |
Het |
Spats2l |
T |
C |
1: 57,925,043 (GRCm39) |
L127P |
possibly damaging |
Het |
Taar8a |
T |
A |
10: 23,952,975 (GRCm39) |
I193N |
probably benign |
Het |
Ten1 |
C |
T |
11: 116,107,510 (GRCm39) |
|
probably benign |
Het |
Tfb2m |
T |
C |
1: 179,373,398 (GRCm39) |
E100G |
probably damaging |
Het |
Tom1 |
C |
T |
8: 75,778,934 (GRCm39) |
|
probably benign |
Het |
Vps52 |
G |
T |
17: 34,178,985 (GRCm39) |
R171L |
probably damaging |
Het |
Zcwpw2 |
A |
T |
9: 117,843,182 (GRCm39) |
|
noncoding transcript |
Het |
Zfhx4 |
G |
A |
3: 5,468,880 (GRCm39) |
E3013K |
probably damaging |
Het |
Zfp267 |
G |
A |
3: 36,220,016 (GRCm39) |
D680N |
possibly damaging |
Het |
Zfp777 |
C |
T |
6: 48,006,294 (GRCm39) |
V411M |
probably damaging |
Het |
|
Other mutations in Col3a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Col3a1
|
APN |
1 |
45,386,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00928:Col3a1
|
APN |
1 |
45,380,018 (GRCm39) |
intron |
probably benign |
|
IGL00958:Col3a1
|
APN |
1 |
45,366,755 (GRCm39) |
missense |
unknown |
|
IGL01353:Col3a1
|
APN |
1 |
45,372,798 (GRCm39) |
unclassified |
probably benign |
|
IGL01820:Col3a1
|
APN |
1 |
45,360,768 (GRCm39) |
missense |
unknown |
|
IGL01839:Col3a1
|
APN |
1 |
45,350,990 (GRCm39) |
missense |
unknown |
|
IGL02517:Col3a1
|
APN |
1 |
45,364,963 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02879:Col3a1
|
APN |
1 |
45,380,119 (GRCm39) |
intron |
probably benign |
|
IGL02960:Col3a1
|
APN |
1 |
45,367,615 (GRCm39) |
missense |
unknown |
|
IGL03245:Col3a1
|
APN |
1 |
45,370,269 (GRCm39) |
unclassified |
probably benign |
|
IGL03308:Col3a1
|
APN |
1 |
45,369,777 (GRCm39) |
splice site |
probably benign |
|
Creation
|
UTSW |
1 |
45,385,144 (GRCm39) |
missense |
probably damaging |
1.00 |
Kraken
|
UTSW |
1 |
45,367,026 (GRCm39) |
splice site |
probably null |
|
Wealth
|
UTSW |
1 |
45,379,472 (GRCm39) |
splice site |
probably benign |
|
IGL03050:Col3a1
|
UTSW |
1 |
45,368,085 (GRCm39) |
splice site |
probably null |
|
PIT4520001:Col3a1
|
UTSW |
1 |
45,374,943 (GRCm39) |
critical splice donor site |
probably null |
|
R0063:Col3a1
|
UTSW |
1 |
45,369,701 (GRCm39) |
splice site |
probably benign |
|
R0122:Col3a1
|
UTSW |
1 |
45,380,057 (GRCm39) |
intron |
probably benign |
|
R0131:Col3a1
|
UTSW |
1 |
45,368,028 (GRCm39) |
splice site |
probably benign |
|
R0765:Col3a1
|
UTSW |
1 |
45,375,811 (GRCm39) |
unclassified |
probably benign |
|
R0853:Col3a1
|
UTSW |
1 |
45,382,484 (GRCm39) |
intron |
probably benign |
|
R0898:Col3a1
|
UTSW |
1 |
45,373,153 (GRCm39) |
unclassified |
probably benign |
|
R1170:Col3a1
|
UTSW |
1 |
45,386,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Col3a1
|
UTSW |
1 |
45,366,761 (GRCm39) |
missense |
unknown |
|
R1440:Col3a1
|
UTSW |
1 |
45,382,472 (GRCm39) |
splice site |
probably null |
|
R1449:Col3a1
|
UTSW |
1 |
45,360,771 (GRCm39) |
missense |
unknown |
|
R1526:Col3a1
|
UTSW |
1 |
45,360,848 (GRCm39) |
missense |
unknown |
|
R1572:Col3a1
|
UTSW |
1 |
45,385,128 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1585:Col3a1
|
UTSW |
1 |
45,367,026 (GRCm39) |
splice site |
probably null |
|
R1616:Col3a1
|
UTSW |
1 |
45,367,648 (GRCm39) |
critical splice donor site |
probably null |
|
R1691:Col3a1
|
UTSW |
1 |
45,387,776 (GRCm39) |
unclassified |
probably benign |
|
R1876:Col3a1
|
UTSW |
1 |
45,381,395 (GRCm39) |
splice site |
probably null |
|
R1937:Col3a1
|
UTSW |
1 |
45,373,453 (GRCm39) |
unclassified |
probably benign |
|
R2093:Col3a1
|
UTSW |
1 |
45,372,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R2110:Col3a1
|
UTSW |
1 |
45,369,305 (GRCm39) |
missense |
unknown |
|
R2119:Col3a1
|
UTSW |
1 |
45,385,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Col3a1
|
UTSW |
1 |
45,360,792 (GRCm39) |
missense |
unknown |
|
R2327:Col3a1
|
UTSW |
1 |
45,377,771 (GRCm39) |
unclassified |
probably benign |
|
R2518:Col3a1
|
UTSW |
1 |
45,376,672 (GRCm39) |
unclassified |
probably benign |
|
R2991:Col3a1
|
UTSW |
1 |
45,374,939 (GRCm39) |
unclassified |
probably benign |
|
R3405:Col3a1
|
UTSW |
1 |
45,377,913 (GRCm39) |
unclassified |
probably benign |
|
R3784:Col3a1
|
UTSW |
1 |
45,386,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Col3a1
|
UTSW |
1 |
45,361,150 (GRCm39) |
missense |
unknown |
|
R3848:Col3a1
|
UTSW |
1 |
45,361,150 (GRCm39) |
missense |
unknown |
|
R3849:Col3a1
|
UTSW |
1 |
45,361,150 (GRCm39) |
missense |
unknown |
|
R4502:Col3a1
|
UTSW |
1 |
45,387,837 (GRCm39) |
unclassified |
probably benign |
|
R4503:Col3a1
|
UTSW |
1 |
45,387,837 (GRCm39) |
unclassified |
probably benign |
|
R4764:Col3a1
|
UTSW |
1 |
45,385,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Col3a1
|
UTSW |
1 |
45,362,963 (GRCm39) |
splice site |
probably null |
|
R4934:Col3a1
|
UTSW |
1 |
45,379,112 (GRCm39) |
unclassified |
probably benign |
|
R5033:Col3a1
|
UTSW |
1 |
45,385,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R5123:Col3a1
|
UTSW |
1 |
45,372,756 (GRCm39) |
unclassified |
probably benign |
|
R5190:Col3a1
|
UTSW |
1 |
45,383,967 (GRCm39) |
intron |
probably benign |
|
R5190:Col3a1
|
UTSW |
1 |
45,368,244 (GRCm39) |
missense |
unknown |
|
R5375:Col3a1
|
UTSW |
1 |
45,387,059 (GRCm39) |
splice site |
probably null |
|
R5407:Col3a1
|
UTSW |
1 |
45,385,212 (GRCm39) |
missense |
probably benign |
0.03 |
R5627:Col3a1
|
UTSW |
1 |
45,370,720 (GRCm39) |
unclassified |
probably benign |
|
R5642:Col3a1
|
UTSW |
1 |
45,370,872 (GRCm39) |
unclassified |
probably benign |
|
R6014:Col3a1
|
UTSW |
1 |
45,360,739 (GRCm39) |
nonsense |
probably null |
|
R6052:Col3a1
|
UTSW |
1 |
45,384,173 (GRCm39) |
unclassified |
probably benign |
|
R6263:Col3a1
|
UTSW |
1 |
45,360,735 (GRCm39) |
missense |
unknown |
|
R6453:Col3a1
|
UTSW |
1 |
45,378,538 (GRCm39) |
unclassified |
probably benign |
|
R6463:Col3a1
|
UTSW |
1 |
45,381,365 (GRCm39) |
intron |
probably benign |
|
R6488:Col3a1
|
UTSW |
1 |
45,370,694 (GRCm39) |
unclassified |
probably benign |
|
R6525:Col3a1
|
UTSW |
1 |
45,386,339 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6637:Col3a1
|
UTSW |
1 |
45,386,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6704:Col3a1
|
UTSW |
1 |
45,386,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R6744:Col3a1
|
UTSW |
1 |
45,377,782 (GRCm39) |
unclassified |
probably benign |
|
R6745:Col3a1
|
UTSW |
1 |
45,377,782 (GRCm39) |
unclassified |
probably benign |
|
R6747:Col3a1
|
UTSW |
1 |
45,377,782 (GRCm39) |
unclassified |
probably benign |
|
R6858:Col3a1
|
UTSW |
1 |
45,385,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R6903:Col3a1
|
UTSW |
1 |
45,371,148 (GRCm39) |
missense |
probably damaging |
0.96 |
R7189:Col3a1
|
UTSW |
1 |
45,372,817 (GRCm39) |
missense |
unknown |
|
R7194:Col3a1
|
UTSW |
1 |
45,370,860 (GRCm39) |
missense |
unknown |
|
R7199:Col3a1
|
UTSW |
1 |
45,371,301 (GRCm39) |
missense |
probably null |
0.99 |
R7204:Col3a1
|
UTSW |
1 |
45,361,578 (GRCm39) |
missense |
unknown |
|
R7304:Col3a1
|
UTSW |
1 |
45,386,971 (GRCm39) |
missense |
unknown |
|
R7378:Col3a1
|
UTSW |
1 |
45,366,807 (GRCm39) |
splice site |
probably null |
|
R7398:Col3a1
|
UTSW |
1 |
45,366,973 (GRCm39) |
missense |
unknown |
|
R7742:Col3a1
|
UTSW |
1 |
45,384,161 (GRCm39) |
missense |
unknown |
|
R8072:Col3a1
|
UTSW |
1 |
45,360,734 (GRCm39) |
missense |
unknown |
|
R8177:Col3a1
|
UTSW |
1 |
45,374,924 (GRCm39) |
missense |
unknown |
|
R8183:Col3a1
|
UTSW |
1 |
45,373,970 (GRCm39) |
missense |
unknown |
|
R8445:Col3a1
|
UTSW |
1 |
45,380,340 (GRCm39) |
nonsense |
probably null |
|
R8490:Col3a1
|
UTSW |
1 |
45,385,116 (GRCm39) |
missense |
probably benign |
0.01 |
R8546:Col3a1
|
UTSW |
1 |
45,380,099 (GRCm39) |
intron |
probably benign |
|
R8720:Col3a1
|
UTSW |
1 |
45,386,893 (GRCm39) |
missense |
unknown |
|
R8733:Col3a1
|
UTSW |
1 |
45,379,472 (GRCm39) |
splice site |
probably benign |
|
R8888:Col3a1
|
UTSW |
1 |
45,379,139 (GRCm39) |
missense |
unknown |
|
R9227:Col3a1
|
UTSW |
1 |
45,383,138 (GRCm39) |
missense |
unknown |
|
R9230:Col3a1
|
UTSW |
1 |
45,383,138 (GRCm39) |
missense |
unknown |
|
R9302:Col3a1
|
UTSW |
1 |
45,350,980 (GRCm39) |
nonsense |
probably null |
|
R9366:Col3a1
|
UTSW |
1 |
45,380,391 (GRCm39) |
missense |
unknown |
|
R9653:Col3a1
|
UTSW |
1 |
45,360,728 (GRCm39) |
missense |
unknown |
|
R9677:Col3a1
|
UTSW |
1 |
45,369,727 (GRCm39) |
missense |
unknown |
|
Z1177:Col3a1
|
UTSW |
1 |
45,350,960 (GRCm39) |
missense |
unknown |
|
|