Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asap2 |
G |
T |
12: 21,235,188 (GRCm39) |
A97S |
probably damaging |
Het |
Brd10 |
T |
C |
19: 29,712,545 (GRCm39) |
K785E |
probably damaging |
Het |
C1qtnf1 |
A |
T |
11: 118,334,616 (GRCm39) |
E32V |
possibly damaging |
Het |
Ccdc81 |
A |
G |
7: 89,525,081 (GRCm39) |
L500P |
probably damaging |
Het |
Cdo1 |
T |
C |
18: 46,861,130 (GRCm39) |
E27G |
probably benign |
Het |
Ceacam5 |
G |
A |
7: 17,484,620 (GRCm39) |
G454D |
probably damaging |
Het |
Cemip |
T |
C |
7: 83,600,648 (GRCm39) |
D991G |
probably damaging |
Het |
Cep170 |
A |
C |
1: 176,616,071 (GRCm39) |
I79S |
probably damaging |
Het |
Cep19 |
A |
G |
16: 31,926,039 (GRCm39) |
Q149R |
possibly damaging |
Het |
Cideb |
A |
T |
14: 55,992,619 (GRCm39) |
L99* |
probably null |
Het |
Cntnap5a |
A |
G |
1: 116,356,207 (GRCm39) |
N746S |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,564,080 (GRCm39) |
N1715S |
probably benign |
Het |
Csmd3 |
C |
A |
15: 47,449,028 (GRCm39) |
|
probably null |
Het |
Disp3 |
T |
C |
4: 148,344,373 (GRCm39) |
I510V |
probably benign |
Het |
Drosha |
T |
A |
15: 12,914,070 (GRCm39) |
V1115E |
probably damaging |
Het |
Dzip3 |
A |
C |
16: 48,757,369 (GRCm39) |
L888R |
probably damaging |
Het |
Emx2 |
C |
A |
19: 59,452,442 (GRCm39) |
A242E |
probably benign |
Het |
Fto |
G |
A |
8: 92,168,314 (GRCm39) |
E256K |
possibly damaging |
Het |
Gabrb2 |
A |
C |
11: 42,482,715 (GRCm39) |
Y191S |
possibly damaging |
Het |
Gm6526 |
A |
T |
14: 43,987,394 (GRCm39) |
H110L |
probably damaging |
Het |
Grin3b |
T |
A |
10: 79,810,436 (GRCm39) |
N647K |
probably damaging |
Het |
Ifit2 |
T |
G |
19: 34,550,602 (GRCm39) |
S47R |
probably benign |
Het |
Il5ra |
A |
T |
6: 106,712,781 (GRCm39) |
V244E |
possibly damaging |
Het |
Inppl1 |
A |
G |
7: 101,482,153 (GRCm39) |
L141P |
probably benign |
Het |
Iws1 |
A |
G |
18: 32,213,178 (GRCm39) |
D202G |
probably benign |
Het |
Kctd4 |
A |
C |
14: 76,200,523 (GRCm39) |
I165L |
probably benign |
Het |
Lrch3 |
G |
A |
16: 32,770,746 (GRCm39) |
C116Y |
probably damaging |
Het |
Mettl25 |
T |
C |
10: 105,668,844 (GRCm39) |
T93A |
possibly damaging |
Het |
Mgat4d |
A |
G |
8: 84,095,666 (GRCm39) |
I314V |
probably benign |
Het |
Mrgprb4 |
A |
T |
7: 47,848,159 (GRCm39) |
Y256* |
probably null |
Het |
Myo9b |
G |
T |
8: 71,808,408 (GRCm39) |
V1672L |
probably damaging |
Het |
Nek1 |
C |
T |
8: 61,502,975 (GRCm39) |
P449L |
probably benign |
Het |
Nucb2 |
G |
A |
7: 116,123,642 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,919,412 (GRCm39) |
Y6864C |
probably damaging |
Het |
Omt2b |
A |
T |
9: 78,235,420 (GRCm39) |
|
probably benign |
Het |
Or2y3 |
T |
A |
17: 38,393,486 (GRCm39) |
I128F |
probably damaging |
Het |
Or4p18 |
C |
T |
2: 88,232,777 (GRCm39) |
C167Y |
probably damaging |
Het |
Or5ac15 |
G |
A |
16: 58,940,293 (GRCm39) |
L47F |
probably damaging |
Het |
Or6c208 |
A |
G |
10: 129,224,176 (GRCm39) |
K225E |
probably benign |
Het |
Otogl |
G |
T |
10: 107,705,387 (GRCm39) |
P647T |
probably damaging |
Het |
Oxnad1 |
A |
G |
14: 31,824,244 (GRCm39) |
D271G |
probably benign |
Het |
Pbx3 |
T |
C |
2: 34,261,776 (GRCm39) |
I53V |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,639,865 (GRCm39) |
|
probably null |
Het |
Ppp4r3a |
A |
T |
12: 101,007,000 (GRCm39) |
D810E |
probably damaging |
Het |
Ptpro |
A |
T |
6: 137,438,724 (GRCm39) |
D1189V |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,492,002 (GRCm39) |
N3758S |
probably damaging |
Het |
Scarb2 |
G |
A |
5: 92,594,200 (GRCm39) |
T454M |
possibly damaging |
Het |
Sec23a |
A |
C |
12: 59,032,972 (GRCm39) |
|
probably null |
Het |
Spire2 |
C |
T |
8: 124,095,502 (GRCm39) |
A535V |
probably benign |
Het |
Svopl |
A |
T |
6: 38,006,570 (GRCm39) |
F142L |
probably benign |
Het |
Tas2r144 |
T |
C |
6: 42,192,674 (GRCm39) |
I138T |
probably benign |
Het |
Tbc1d15 |
A |
G |
10: 115,039,135 (GRCm39) |
M535T |
probably benign |
Het |
Tnfaip1 |
C |
T |
11: 78,420,971 (GRCm39) |
V30M |
possibly damaging |
Het |
Topaz1 |
T |
A |
9: 122,625,108 (GRCm39) |
W1398R |
probably damaging |
Het |
Tpo |
A |
G |
12: 30,134,694 (GRCm39) |
S755P |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,606,460 (GRCm39) |
S18116R |
probably damaging |
Het |
Vmn2r78 |
A |
G |
7: 86,571,465 (GRCm39) |
|
probably null |
Het |
Wdr49 |
T |
A |
3: 75,304,227 (GRCm39) |
K494M |
probably benign |
Het |
Yeats2 |
A |
G |
16: 20,024,836 (GRCm39) |
M697V |
probably damaging |
Het |
Zfp407 |
G |
A |
18: 84,579,158 (GRCm39) |
P652S |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,009,002 (GRCm39) |
M323V |
probably benign |
Het |
Zfp629 |
G |
T |
7: 127,209,931 (GRCm39) |
P626Q |
possibly damaging |
Het |
Zfp804a |
A |
T |
2: 82,088,532 (GRCm39) |
Y787F |
probably benign |
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 |
|
R0762:Col3a1
|
UTSW |
1 |
45,360,686 (GRCm39) |
missense |
unknown |
|
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 |
|
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 |
|
|