Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300002M23Rik |
T |
A |
17: 35,879,212 (GRCm39) |
F183L |
possibly damaging |
Het |
4930590J08Rik |
T |
A |
6: 91,921,245 (GRCm39) |
M775K |
probably damaging |
Het |
Actn1 |
T |
G |
12: 80,219,772 (GRCm39) |
I700L |
probably benign |
Het |
Adam5 |
T |
C |
8: 25,276,287 (GRCm39) |
Y460C |
probably damaging |
Het |
Akna |
C |
T |
4: 63,313,502 (GRCm39) |
G207E |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,748,688 (GRCm39) |
H527L |
possibly damaging |
Het |
Anks1 |
C |
A |
17: 28,207,779 (GRCm39) |
N383K |
probably damaging |
Het |
Apba3 |
C |
T |
10: 81,105,204 (GRCm39) |
|
probably null |
Het |
Atp9b |
C |
A |
18: 80,779,308 (GRCm39) |
V1121F |
possibly damaging |
Het |
Bsn |
T |
C |
9: 107,988,960 (GRCm39) |
Y2264C |
probably damaging |
Het |
Bst1 |
A |
G |
5: 43,997,799 (GRCm39) |
D266G |
probably damaging |
Het |
Cep55 |
A |
G |
19: 38,060,202 (GRCm39) |
|
probably null |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Ckb |
T |
C |
12: 111,637,664 (GRCm39) |
K156E |
probably benign |
Het |
Cln3 |
T |
A |
7: 126,174,393 (GRCm39) |
H315L |
probably damaging |
Het |
Cnot6l |
A |
G |
5: 96,227,796 (GRCm39) |
F479S |
probably damaging |
Het |
Col1a1 |
A |
G |
11: 94,837,958 (GRCm39) |
D826G |
unknown |
Het |
Cyp27a1 |
T |
C |
1: 74,774,564 (GRCm39) |
V194A |
probably benign |
Het |
Dis3l2 |
C |
T |
1: 86,971,890 (GRCm39) |
P643S |
probably benign |
Het |
Dpf3 |
T |
C |
12: 83,378,740 (GRCm39) |
D108G |
probably damaging |
Het |
Eif2b4 |
C |
T |
5: 31,350,241 (GRCm39) |
G27D |
probably benign |
Het |
Eif4a1 |
T |
G |
11: 69,563,251 (GRCm39) |
|
probably benign |
Het |
Espl1 |
A |
T |
15: 102,213,372 (GRCm39) |
D566V |
probably damaging |
Het |
Ext2 |
T |
A |
2: 93,644,024 (GRCm39) |
R86* |
probably null |
Het |
Fasn |
A |
T |
11: 120,706,911 (GRCm39) |
F914I |
probably damaging |
Het |
Fbf1 |
A |
G |
11: 116,043,378 (GRCm39) |
L477P |
probably benign |
Het |
Fsd1 |
A |
T |
17: 56,303,452 (GRCm39) |
K441N |
possibly damaging |
Het |
Fsip2 |
T |
A |
2: 82,815,384 (GRCm39) |
S3706T |
probably benign |
Het |
Gabra5 |
A |
T |
7: 57,058,547 (GRCm39) |
N400K |
probably benign |
Het |
Gimap8 |
G |
T |
6: 48,633,068 (GRCm39) |
G296W |
probably damaging |
Het |
Gli2 |
A |
G |
1: 118,763,870 (GRCm39) |
V1427A |
probably benign |
Het |
Gm7334 |
A |
T |
17: 51,005,855 (GRCm39) |
Y47F |
probably damaging |
Het |
Gm8674 |
T |
G |
13: 50,054,791 (GRCm39) |
|
noncoding transcript |
Het |
Gmeb2 |
G |
T |
2: 180,896,039 (GRCm39) |
T377K |
probably benign |
Het |
Gp9 |
T |
A |
6: 87,756,229 (GRCm39) |
D81E |
probably benign |
Het |
Il5ra |
T |
A |
6: 106,715,123 (GRCm39) |
I212F |
possibly damaging |
Het |
Klhl18 |
G |
T |
9: 110,258,029 (GRCm39) |
N470K |
possibly damaging |
Het |
Lfng |
G |
T |
5: 140,598,150 (GRCm39) |
|
probably null |
Het |
Lpo |
A |
G |
11: 87,701,166 (GRCm39) |
I430T |
probably benign |
Het |
Lrrc31 |
C |
T |
3: 30,743,417 (GRCm39) |
D183N |
probably damaging |
Het |
Meis2 |
T |
C |
2: 115,694,893 (GRCm39) |
T410A |
probably benign |
Het |
Myo6 |
A |
G |
9: 80,214,963 (GRCm39) |
D1232G |
probably damaging |
Het |
Ncapd2 |
C |
T |
6: 125,146,803 (GRCm39) |
R1261H |
probably benign |
Het |
Nfkb1 |
C |
T |
3: 135,319,743 (GRCm39) |
V251M |
probably damaging |
Het |
Nmbr |
C |
A |
10: 14,642,730 (GRCm39) |
H96Q |
probably damaging |
Het |
Nop14 |
C |
T |
5: 34,809,737 (GRCm39) |
R256H |
probably damaging |
Het |
Nqo2 |
T |
A |
13: 34,165,501 (GRCm39) |
Y133N |
probably damaging |
Het |
Or1f12 |
T |
C |
13: 21,721,357 (GRCm39) |
I273V |
probably benign |
Het |
Or5w20 |
A |
G |
2: 87,727,157 (GRCm39) |
I213V |
probably benign |
Het |
Pbld2 |
C |
A |
10: 62,888,017 (GRCm39) |
S168R |
probably damaging |
Het |
Pcdhb7 |
G |
T |
18: 37,475,202 (GRCm39) |
G113* |
probably null |
Het |
Pcdhb7 |
G |
T |
18: 37,475,203 (GRCm39) |
G113V |
probably damaging |
Het |
Pdgfra |
A |
T |
5: 75,355,687 (GRCm39) |
T1066S |
probably damaging |
Het |
Prdm8 |
A |
T |
5: 98,332,881 (GRCm39) |
|
probably null |
Het |
Prdm8 |
G |
T |
5: 98,332,882 (GRCm39) |
|
probably null |
Het |
Prkg1 |
T |
C |
19: 30,563,775 (GRCm39) |
Y479C |
probably benign |
Het |
Pudp |
T |
C |
18: 50,701,539 (GRCm39) |
T65A |
probably benign |
Het |
Rbbp6 |
C |
T |
7: 122,598,926 (GRCm39) |
|
probably benign |
Het |
Rcc1 |
C |
G |
4: 132,063,046 (GRCm39) |
V187L |
probably damaging |
Het |
Rims2 |
T |
A |
15: 39,301,124 (GRCm39) |
M285K |
probably damaging |
Het |
Rtkn2 |
T |
C |
10: 67,877,745 (GRCm39) |
*602Q |
probably null |
Het |
Rxfp3 |
T |
G |
15: 11,036,866 (GRCm39) |
S169R |
probably damaging |
Het |
Sardh |
T |
C |
2: 27,118,253 (GRCm39) |
|
probably null |
Het |
Slc24a2 |
A |
T |
4: 87,145,584 (GRCm39) |
F157I |
probably damaging |
Het |
Slc25a20 |
T |
C |
9: 108,559,191 (GRCm39) |
Y186H |
probably damaging |
Het |
Slc25a24 |
A |
G |
3: 109,070,864 (GRCm39) |
R408G |
probably damaging |
Het |
Slc44a5 |
T |
G |
3: 153,959,353 (GRCm39) |
I348S |
probably damaging |
Het |
Slc8a2 |
A |
T |
7: 15,868,100 (GRCm39) |
K111* |
probably null |
Het |
Smc5 |
A |
G |
19: 23,211,367 (GRCm39) |
V589A |
probably damaging |
Het |
Thbd |
A |
T |
2: 148,249,655 (GRCm39) |
I71N |
probably damaging |
Het |
Tie1 |
T |
A |
4: 118,341,968 (GRCm39) |
|
silent |
Het |
Tln1 |
A |
G |
4: 43,547,522 (GRCm39) |
F813S |
possibly damaging |
Het |
Tnrc18 |
A |
T |
5: 142,751,732 (GRCm39) |
L1191* |
probably null |
Het |
Tubb2a |
A |
C |
13: 34,259,240 (GRCm39) |
Y183* |
probably null |
Het |
Ubr4 |
T |
A |
4: 139,123,877 (GRCm39) |
V343E |
probably damaging |
Het |
Vmn2r93 |
A |
T |
17: 18,524,327 (GRCm39) |
D107V |
possibly damaging |
Het |
Vwa5a |
T |
G |
9: 38,647,494 (GRCm39) |
S624R |
probably benign |
Het |
Wwox |
G |
A |
8: 115,433,098 (GRCm39) |
V255I |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,638,804 (GRCm39) |
K546E |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,340,163 (GRCm39) |
F801L |
possibly damaging |
Het |
Zfp407 |
T |
C |
18: 84,577,589 (GRCm39) |
I1175V |
probably benign |
Het |
Zfp646 |
T |
A |
7: 127,480,933 (GRCm39) |
C1037S |
possibly damaging |
Het |
Zfp786 |
A |
T |
6: 47,798,202 (GRCm39) |
C245* |
probably null |
Het |
Zfp827 |
T |
C |
8: 79,787,812 (GRCm39) |
V326A |
probably benign |
Het |
|
Other mutations in Thsd7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Thsd7b
|
APN |
1 |
129,523,571 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00850:Thsd7b
|
APN |
1 |
130,092,814 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00987:Thsd7b
|
APN |
1 |
129,541,016 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01068:Thsd7b
|
APN |
1 |
129,523,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01091:Thsd7b
|
APN |
1 |
129,704,071 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01535:Thsd7b
|
APN |
1 |
129,605,954 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01560:Thsd7b
|
APN |
1 |
130,145,918 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01701:Thsd7b
|
APN |
1 |
129,358,665 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01775:Thsd7b
|
APN |
1 |
129,556,676 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02077:Thsd7b
|
APN |
1 |
129,744,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02338:Thsd7b
|
APN |
1 |
129,523,508 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Thsd7b
|
APN |
1 |
130,087,369 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02404:Thsd7b
|
APN |
1 |
129,540,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02519:Thsd7b
|
APN |
1 |
129,540,932 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02543:Thsd7b
|
APN |
1 |
130,092,840 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02740:Thsd7b
|
APN |
1 |
129,540,864 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02793:Thsd7b
|
APN |
1 |
129,879,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02875:Thsd7b
|
APN |
1 |
129,879,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02986:Thsd7b
|
APN |
1 |
129,843,352 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03108:Thsd7b
|
APN |
1 |
130,138,013 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Thsd7b
|
APN |
1 |
130,116,288 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03195:Thsd7b
|
APN |
1 |
129,556,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03291:Thsd7b
|
APN |
1 |
129,688,092 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03397:Thsd7b
|
APN |
1 |
129,523,901 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03399:Thsd7b
|
APN |
1 |
129,556,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Thsd7b
|
UTSW |
1 |
129,358,701 (GRCm39) |
missense |
probably benign |
0.00 |
R0277:Thsd7b
|
UTSW |
1 |
130,123,000 (GRCm39) |
missense |
probably benign |
0.00 |
R0526:Thsd7b
|
UTSW |
1 |
129,879,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Thsd7b
|
UTSW |
1 |
130,116,263 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0746:Thsd7b
|
UTSW |
1 |
130,116,268 (GRCm39) |
missense |
probably benign |
0.00 |
R0784:Thsd7b
|
UTSW |
1 |
129,523,096 (GRCm39) |
splice site |
probably benign |
|
R1158:Thsd7b
|
UTSW |
1 |
130,117,672 (GRCm39) |
splice site |
probably null |
|
R1267:Thsd7b
|
UTSW |
1 |
129,556,577 (GRCm39) |
splice site |
probably null |
|
R1375:Thsd7b
|
UTSW |
1 |
130,087,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Thsd7b
|
UTSW |
1 |
129,523,778 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1728:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1728:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1729:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1729:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1730:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1730:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1739:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1739:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1762:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1762:Thsd7b
|
UTSW |
1 |
130,030,813 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1762:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1783:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1783:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1784:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1784:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1785:Thsd7b
|
UTSW |
1 |
129,605,920 (GRCm39) |
missense |
probably benign |
|
R1785:Thsd7b
|
UTSW |
1 |
129,595,674 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Thsd7b
|
UTSW |
1 |
129,556,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Thsd7b
|
UTSW |
1 |
130,044,368 (GRCm39) |
missense |
probably benign |
|
R1812:Thsd7b
|
UTSW |
1 |
129,686,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1846:Thsd7b
|
UTSW |
1 |
129,540,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Thsd7b
|
UTSW |
1 |
129,605,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R1996:Thsd7b
|
UTSW |
1 |
129,686,188 (GRCm39) |
nonsense |
probably null |
|
R2199:Thsd7b
|
UTSW |
1 |
130,145,895 (GRCm39) |
missense |
probably benign |
0.04 |
R2483:Thsd7b
|
UTSW |
1 |
130,030,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Thsd7b
|
UTSW |
1 |
130,117,587 (GRCm39) |
splice site |
probably benign |
|
R2935:Thsd7b
|
UTSW |
1 |
129,605,824 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3113:Thsd7b
|
UTSW |
1 |
129,977,599 (GRCm39) |
missense |
probably benign |
0.23 |
R3236:Thsd7b
|
UTSW |
1 |
130,145,855 (GRCm39) |
nonsense |
probably null |
|
R3745:Thsd7b
|
UTSW |
1 |
129,605,978 (GRCm39) |
missense |
probably benign |
0.04 |
R3877:Thsd7b
|
UTSW |
1 |
130,117,919 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3880:Thsd7b
|
UTSW |
1 |
129,523,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Thsd7b
|
UTSW |
1 |
130,044,356 (GRCm39) |
missense |
probably benign |
0.18 |
R4112:Thsd7b
|
UTSW |
1 |
130,044,356 (GRCm39) |
missense |
probably benign |
0.18 |
R4255:Thsd7b
|
UTSW |
1 |
129,688,024 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4621:Thsd7b
|
UTSW |
1 |
129,358,652 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4703:Thsd7b
|
UTSW |
1 |
129,977,646 (GRCm39) |
intron |
probably benign |
|
R4732:Thsd7b
|
UTSW |
1 |
129,540,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Thsd7b
|
UTSW |
1 |
129,540,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Thsd7b
|
UTSW |
1 |
130,138,001 (GRCm39) |
missense |
probably benign |
0.01 |
R4805:Thsd7b
|
UTSW |
1 |
130,116,276 (GRCm39) |
missense |
probably benign |
0.04 |
R4840:Thsd7b
|
UTSW |
1 |
129,523,581 (GRCm39) |
missense |
probably benign |
0.00 |
R4879:Thsd7b
|
UTSW |
1 |
130,116,236 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4972:Thsd7b
|
UTSW |
1 |
130,116,309 (GRCm39) |
missense |
probably damaging |
0.97 |
R5304:Thsd7b
|
UTSW |
1 |
129,605,980 (GRCm39) |
nonsense |
probably null |
|
R5422:Thsd7b
|
UTSW |
1 |
129,849,071 (GRCm39) |
missense |
probably benign |
0.41 |
R5495:Thsd7b
|
UTSW |
1 |
129,523,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5598:Thsd7b
|
UTSW |
1 |
129,523,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Thsd7b
|
UTSW |
1 |
130,090,673 (GRCm39) |
critical splice donor site |
probably null |
|
R5638:Thsd7b
|
UTSW |
1 |
129,523,270 (GRCm39) |
missense |
probably benign |
0.00 |
R5640:Thsd7b
|
UTSW |
1 |
130,044,408 (GRCm39) |
nonsense |
probably null |
|
R5655:Thsd7b
|
UTSW |
1 |
129,556,671 (GRCm39) |
splice site |
probably null |
|
R5711:Thsd7b
|
UTSW |
1 |
129,688,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R5823:Thsd7b
|
UTSW |
1 |
129,605,821 (GRCm39) |
missense |
probably benign |
0.00 |
R5888:Thsd7b
|
UTSW |
1 |
130,138,057 (GRCm39) |
nonsense |
probably null |
|
R5932:Thsd7b
|
UTSW |
1 |
129,358,575 (GRCm39) |
missense |
probably benign |
|
R6243:Thsd7b
|
UTSW |
1 |
130,090,599 (GRCm39) |
missense |
probably benign |
0.21 |
R6258:Thsd7b
|
UTSW |
1 |
129,595,655 (GRCm39) |
missense |
probably benign |
|
R6260:Thsd7b
|
UTSW |
1 |
129,595,655 (GRCm39) |
missense |
probably benign |
|
R6399:Thsd7b
|
UTSW |
1 |
129,744,385 (GRCm39) |
missense |
probably benign |
0.13 |
R6437:Thsd7b
|
UTSW |
1 |
129,744,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R6719:Thsd7b
|
UTSW |
1 |
130,087,451 (GRCm39) |
splice site |
probably null |
|
R6785:Thsd7b
|
UTSW |
1 |
129,358,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R7304:Thsd7b
|
UTSW |
1 |
130,030,890 (GRCm39) |
missense |
probably benign |
0.01 |
R7334:Thsd7b
|
UTSW |
1 |
130,123,012 (GRCm39) |
missense |
probably benign |
0.00 |
R7414:Thsd7b
|
UTSW |
1 |
129,556,717 (GRCm39) |
missense |
probably damaging |
0.99 |
R7673:Thsd7b
|
UTSW |
1 |
129,843,487 (GRCm39) |
splice site |
probably null |
|
R7683:Thsd7b
|
UTSW |
1 |
129,523,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7861:Thsd7b
|
UTSW |
1 |
130,087,435 (GRCm39) |
missense |
probably benign |
0.00 |
R8145:Thsd7b
|
UTSW |
1 |
129,688,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R8241:Thsd7b
|
UTSW |
1 |
130,117,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Thsd7b
|
UTSW |
1 |
129,523,193 (GRCm39) |
missense |
probably benign |
0.01 |
R8355:Thsd7b
|
UTSW |
1 |
129,523,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Thsd7b
|
UTSW |
1 |
129,605,790 (GRCm39) |
missense |
probably benign |
0.21 |
R8520:Thsd7b
|
UTSW |
1 |
129,849,157 (GRCm39) |
missense |
probably benign |
0.07 |
R8555:Thsd7b
|
UTSW |
1 |
129,523,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Thsd7b
|
UTSW |
1 |
129,688,011 (GRCm39) |
nonsense |
probably null |
|
R8981:Thsd7b
|
UTSW |
1 |
129,523,187 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9029:Thsd7b
|
UTSW |
1 |
130,087,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R9133:Thsd7b
|
UTSW |
1 |
129,843,382 (GRCm39) |
missense |
probably benign |
0.18 |
R9194:Thsd7b
|
UTSW |
1 |
129,843,371 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9229:Thsd7b
|
UTSW |
1 |
129,849,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Thsd7b
|
UTSW |
1 |
130,087,453 (GRCm39) |
critical splice donor site |
probably null |
|
R9460:Thsd7b
|
UTSW |
1 |
130,090,674 (GRCm39) |
critical splice donor site |
probably null |
|
R9466:Thsd7b
|
UTSW |
1 |
130,122,866 (GRCm39) |
missense |
probably benign |
|
R9588:Thsd7b
|
UTSW |
1 |
130,108,223 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Thsd7b
|
UTSW |
1 |
129,523,809 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Thsd7b
|
UTSW |
1 |
129,556,648 (GRCm39) |
missense |
probably benign |
0.17 |
Z1176:Thsd7b
|
UTSW |
1 |
129,523,397 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Thsd7b
|
UTSW |
1 |
129,523,253 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Thsd7b
|
UTSW |
1 |
130,108,161 (GRCm39) |
missense |
possibly damaging |
0.79 |
|