Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
A |
T |
15: 57,892,088 (GRCm39) |
M173K |
probably benign |
Het |
Abcb1b |
T |
A |
5: 8,856,009 (GRCm39) |
F39Y |
probably damaging |
Het |
Acbd3 |
A |
G |
1: 180,566,177 (GRCm39) |
Y290C |
probably damaging |
Het |
Alg12 |
A |
C |
15: 88,700,352 (GRCm39) |
I28R |
possibly damaging |
Het |
Amer2 |
A |
T |
14: 60,616,984 (GRCm39) |
D393V |
probably damaging |
Het |
Anxa5 |
A |
T |
3: 36,511,618 (GRCm39) |
V153D |
probably damaging |
Het |
Arl5a |
T |
C |
2: 52,306,141 (GRCm39) |
M64V |
probably benign |
Het |
Astn1 |
T |
C |
1: 158,516,118 (GRCm39) |
L1236P |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,297,713 (GRCm39) |
S424P |
possibly damaging |
Het |
AW551984 |
A |
T |
9: 39,510,617 (GRCm39) |
S239R |
probably benign |
Het |
Baz1b |
T |
C |
5: 135,268,985 (GRCm39) |
V1278A |
probably benign |
Het |
Cbfa2t3 |
G |
T |
8: 123,361,799 (GRCm39) |
L408I |
probably benign |
Het |
Cdc27 |
A |
T |
11: 104,419,250 (GRCm39) |
N227K |
possibly damaging |
Het |
Cdh20 |
A |
T |
1: 110,036,486 (GRCm39) |
Q555H |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,215,094 (GRCm39) |
N1412I |
probably damaging |
Het |
Cdhr2 |
T |
C |
13: 54,866,105 (GRCm39) |
S302P |
probably benign |
Het |
Cep350 |
C |
A |
1: 155,782,317 (GRCm39) |
E1563D |
probably benign |
Het |
Cfap221 |
T |
A |
1: 119,912,753 (GRCm39) |
E107V |
probably benign |
Het |
Col6a3 |
C |
A |
1: 90,715,938 (GRCm39) |
R1641L |
unknown |
Het |
Coro6 |
A |
T |
11: 77,354,916 (GRCm39) |
I60F |
probably benign |
Het |
Dennd2b |
A |
T |
7: 109,138,156 (GRCm39) |
V753E |
probably damaging |
Het |
Dock10 |
G |
T |
1: 80,573,400 (GRCm39) |
N245K |
probably damaging |
Het |
Epb41l2 |
T |
A |
10: 25,345,119 (GRCm39) |
N286K |
probably damaging |
Het |
Fam83g |
G |
T |
11: 61,593,935 (GRCm39) |
E490* |
probably null |
Het |
Gnb1l |
T |
C |
16: 18,371,211 (GRCm39) |
I234T |
possibly damaging |
Het |
Gtf3a |
T |
A |
5: 146,885,747 (GRCm39) |
W53R |
probably damaging |
Het |
Ikzf4 |
T |
C |
10: 128,470,276 (GRCm39) |
I415V |
probably benign |
Het |
Il11ra1 |
T |
C |
4: 41,767,527 (GRCm39) |
V293A |
probably damaging |
Het |
Il17ra |
G |
A |
6: 120,455,410 (GRCm39) |
V340M |
probably benign |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Kif24 |
A |
T |
4: 41,428,731 (GRCm39) |
H76Q |
probably benign |
Het |
Klhl25 |
T |
C |
7: 75,516,264 (GRCm39) |
L390P |
probably damaging |
Het |
Klhl26 |
T |
C |
8: 70,904,479 (GRCm39) |
D443G |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,640,064 (GRCm39) |
R86S |
probably damaging |
Het |
Lrrc24 |
G |
A |
15: 76,599,984 (GRCm39) |
A385V |
probably benign |
Het |
Maea |
C |
T |
5: 33,517,787 (GRCm39) |
A109V |
probably benign |
Het |
Mtor |
A |
T |
4: 148,570,507 (GRCm39) |
Y1188F |
probably benign |
Het |
Nccrp1 |
T |
C |
7: 28,243,977 (GRCm39) |
D202G |
probably damaging |
Het |
Nsun4 |
A |
T |
4: 115,901,935 (GRCm39) |
L177Q |
probably damaging |
Het |
Nup155 |
C |
T |
15: 8,161,027 (GRCm39) |
R571W |
probably damaging |
Het |
Nup160 |
T |
A |
2: 90,539,188 (GRCm39) |
M789K |
probably benign |
Het |
Odad2 |
T |
A |
18: 7,217,800 (GRCm39) |
H638L |
probably benign |
Het |
Or5an1c |
A |
G |
19: 12,218,440 (GRCm39) |
F195S |
probably benign |
Het |
Or5p50 |
A |
T |
7: 107,422,124 (GRCm39) |
L184* |
probably null |
Het |
Or8d2b |
A |
T |
9: 38,788,481 (GRCm39) |
H3L |
probably benign |
Het |
Pgpep1 |
G |
T |
8: 71,105,174 (GRCm39) |
|
probably null |
Het |
Pkd1l2 |
C |
T |
8: 117,748,589 (GRCm39) |
V1861M |
probably benign |
Het |
Plekha5 |
G |
A |
6: 140,537,473 (GRCm39) |
R646K |
possibly damaging |
Het |
Plin4 |
G |
T |
17: 56,411,667 (GRCm39) |
T788K |
possibly damaging |
Het |
Ppp3r2 |
T |
C |
4: 49,681,902 (GRCm39) |
D16G |
possibly damaging |
Het |
Pramel22 |
G |
T |
4: 143,382,071 (GRCm39) |
Y208* |
probably null |
Het |
Prdm16 |
A |
T |
4: 154,426,513 (GRCm39) |
I424N |
probably damaging |
Het |
Psen2 |
T |
A |
1: 180,056,410 (GRCm39) |
I396F |
probably damaging |
Het |
Psip1 |
C |
T |
4: 83,403,949 (GRCm39) |
|
probably null |
Het |
Ptprd |
G |
A |
4: 76,055,083 (GRCm39) |
T215I |
probably damaging |
Het |
Rec114 |
A |
G |
9: 58,648,822 (GRCm39) |
S2P |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,378,410 (GRCm39) |
I1181T |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,527,118 (GRCm39) |
M1436T |
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,316,937 (GRCm39) |
V1020E |
possibly damaging |
Het |
Rorc |
G |
A |
3: 94,296,069 (GRCm39) |
G83S |
probably damaging |
Het |
Ryr2 |
T |
G |
13: 11,683,725 (GRCm39) |
Q3113P |
possibly damaging |
Het |
Shank1 |
T |
C |
7: 44,003,401 (GRCm39) |
S1698P |
possibly damaging |
Het |
Slc2a2 |
T |
C |
3: 28,762,828 (GRCm39) |
|
probably null |
Het |
Slc5a9 |
A |
T |
4: 111,749,033 (GRCm39) |
Y98* |
probably null |
Het |
Smc6 |
T |
C |
12: 11,333,175 (GRCm39) |
|
probably null |
Het |
Sptb |
G |
T |
12: 76,647,157 (GRCm39) |
F1959L |
probably benign |
Het |
Srgap1 |
T |
A |
10: 121,621,610 (GRCm39) |
H984L |
possibly damaging |
Het |
Ssc5d |
T |
A |
7: 4,931,466 (GRCm39) |
C224* |
probably null |
Het |
Ston2 |
A |
T |
12: 91,614,634 (GRCm39) |
H591Q |
probably benign |
Het |
Tbx3 |
C |
T |
5: 119,813,315 (GRCm39) |
A222V |
possibly damaging |
Het |
Usp9y |
T |
C |
Y: 1,364,732 (GRCm39) |
D1027G |
probably damaging |
Het |
Wnt5a |
C |
T |
14: 28,240,461 (GRCm39) |
R184* |
probably null |
Het |
Zfpm2 |
A |
G |
15: 40,637,462 (GRCm39) |
E74G |
possibly damaging |
Het |
Zwint |
C |
A |
10: 72,493,127 (GRCm39) |
S223* |
probably null |
Het |
|
Other mutations in Thsd7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00562:Thsd7a
|
APN |
6 |
12,379,658 (GRCm39) |
splice site |
probably null |
|
IGL00563:Thsd7a
|
APN |
6 |
12,379,658 (GRCm39) |
splice site |
probably null |
|
IGL00753:Thsd7a
|
APN |
6 |
12,327,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00835:Thsd7a
|
APN |
6 |
12,554,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01486:Thsd7a
|
APN |
6 |
12,471,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Thsd7a
|
APN |
6 |
12,554,980 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01931:Thsd7a
|
APN |
6 |
12,504,098 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01935:Thsd7a
|
APN |
6 |
12,317,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01978:Thsd7a
|
APN |
6 |
12,331,005 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02233:Thsd7a
|
APN |
6 |
12,555,257 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02354:Thsd7a
|
APN |
6 |
12,348,192 (GRCm39) |
splice site |
probably benign |
|
IGL02361:Thsd7a
|
APN |
6 |
12,348,192 (GRCm39) |
splice site |
probably benign |
|
IGL02375:Thsd7a
|
APN |
6 |
12,343,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02468:Thsd7a
|
APN |
6 |
12,318,170 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02616:Thsd7a
|
APN |
6 |
12,408,984 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02820:Thsd7a
|
APN |
6 |
12,321,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Thsd7a
|
APN |
6 |
12,500,994 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03074:Thsd7a
|
APN |
6 |
12,324,680 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03234:Thsd7a
|
APN |
6 |
12,343,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03244:Thsd7a
|
APN |
6 |
12,504,167 (GRCm39) |
splice site |
probably benign |
|
IGL03337:Thsd7a
|
APN |
6 |
12,405,173 (GRCm39) |
missense |
probably damaging |
1.00 |
G1patch:Thsd7a
|
UTSW |
6 |
12,555,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
PIT4354001:Thsd7a
|
UTSW |
6 |
12,331,926 (GRCm39) |
critical splice donor site |
probably null |
|
R0095:Thsd7a
|
UTSW |
6 |
12,320,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R0127:Thsd7a
|
UTSW |
6 |
12,554,907 (GRCm39) |
missense |
probably benign |
0.01 |
R0142:Thsd7a
|
UTSW |
6 |
12,418,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Thsd7a
|
UTSW |
6 |
12,321,899 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0242:Thsd7a
|
UTSW |
6 |
12,503,915 (GRCm39) |
missense |
probably benign |
0.32 |
R0242:Thsd7a
|
UTSW |
6 |
12,503,915 (GRCm39) |
missense |
probably benign |
0.32 |
R0359:Thsd7a
|
UTSW |
6 |
12,352,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Thsd7a
|
UTSW |
6 |
12,379,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Thsd7a
|
UTSW |
6 |
12,379,604 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0540:Thsd7a
|
UTSW |
6 |
12,331,541 (GRCm39) |
splice site |
probably null |
|
R0577:Thsd7a
|
UTSW |
6 |
12,321,047 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0607:Thsd7a
|
UTSW |
6 |
12,331,541 (GRCm39) |
splice site |
probably null |
|
R0755:Thsd7a
|
UTSW |
6 |
12,555,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0771:Thsd7a
|
UTSW |
6 |
12,327,576 (GRCm39) |
missense |
probably benign |
0.09 |
R0780:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0870:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0871:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0872:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0873:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Thsd7a
|
UTSW |
6 |
12,555,701 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1144:Thsd7a
|
UTSW |
6 |
12,471,026 (GRCm39) |
splice site |
probably benign |
|
R1265:Thsd7a
|
UTSW |
6 |
12,317,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R1276:Thsd7a
|
UTSW |
6 |
12,418,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Thsd7a
|
UTSW |
6 |
12,555,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Thsd7a
|
UTSW |
6 |
12,338,621 (GRCm39) |
missense |
probably benign |
0.08 |
R1519:Thsd7a
|
UTSW |
6 |
12,471,174 (GRCm39) |
missense |
probably benign |
0.01 |
R1633:Thsd7a
|
UTSW |
6 |
12,471,103 (GRCm39) |
nonsense |
probably null |
|
R1659:Thsd7a
|
UTSW |
6 |
12,504,063 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1769:Thsd7a
|
UTSW |
6 |
12,555,714 (GRCm39) |
nonsense |
probably null |
|
R1824:Thsd7a
|
UTSW |
6 |
12,409,041 (GRCm39) |
splice site |
probably null |
|
R1840:Thsd7a
|
UTSW |
6 |
12,330,973 (GRCm39) |
missense |
probably benign |
0.03 |
R1845:Thsd7a
|
UTSW |
6 |
12,321,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Thsd7a
|
UTSW |
6 |
12,555,434 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2023:Thsd7a
|
UTSW |
6 |
12,327,535 (GRCm39) |
missense |
probably benign |
0.16 |
R2039:Thsd7a
|
UTSW |
6 |
12,408,922 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2058:Thsd7a
|
UTSW |
6 |
12,318,105 (GRCm39) |
splice site |
probably benign |
|
R2138:Thsd7a
|
UTSW |
6 |
12,471,072 (GRCm39) |
nonsense |
probably null |
|
R2155:Thsd7a
|
UTSW |
6 |
12,379,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R2175:Thsd7a
|
UTSW |
6 |
12,331,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2216:Thsd7a
|
UTSW |
6 |
12,337,267 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2318:Thsd7a
|
UTSW |
6 |
12,405,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2375:Thsd7a
|
UTSW |
6 |
12,337,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R3858:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R3890:Thsd7a
|
UTSW |
6 |
12,418,336 (GRCm39) |
missense |
probably benign |
0.09 |
R3910:Thsd7a
|
UTSW |
6 |
12,331,548 (GRCm39) |
missense |
probably damaging |
0.96 |
R3933:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R4369:Thsd7a
|
UTSW |
6 |
12,468,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Thsd7a
|
UTSW |
6 |
12,324,634 (GRCm39) |
missense |
probably damaging |
0.98 |
R4664:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4664:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4665:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4665:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4666:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4666:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4668:Thsd7a
|
UTSW |
6 |
12,408,967 (GRCm39) |
missense |
probably damaging |
0.98 |
R4886:Thsd7a
|
UTSW |
6 |
12,327,659 (GRCm39) |
nonsense |
probably null |
|
R4918:Thsd7a
|
UTSW |
6 |
12,327,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R4938:Thsd7a
|
UTSW |
6 |
12,330,991 (GRCm39) |
missense |
probably benign |
0.09 |
R5064:Thsd7a
|
UTSW |
6 |
12,330,951 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5153:Thsd7a
|
UTSW |
6 |
12,338,654 (GRCm39) |
missense |
probably benign |
0.00 |
R5177:Thsd7a
|
UTSW |
6 |
12,379,582 (GRCm39) |
nonsense |
probably null |
|
R5242:Thsd7a
|
UTSW |
6 |
12,327,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Thsd7a
|
UTSW |
6 |
12,379,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5442:Thsd7a
|
UTSW |
6 |
12,748,799 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Thsd7a
|
UTSW |
6 |
12,332,016 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5525:Thsd7a
|
UTSW |
6 |
12,332,006 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5544:Thsd7a
|
UTSW |
6 |
12,379,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5651:Thsd7a
|
UTSW |
6 |
12,343,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Thsd7a
|
UTSW |
6 |
12,343,147 (GRCm39) |
missense |
probably benign |
0.00 |
R5848:Thsd7a
|
UTSW |
6 |
12,503,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Thsd7a
|
UTSW |
6 |
12,337,261 (GRCm39) |
missense |
probably benign |
0.02 |
R6012:Thsd7a
|
UTSW |
6 |
12,379,388 (GRCm39) |
splice site |
probably null |
|
R6139:Thsd7a
|
UTSW |
6 |
12,379,572 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6243:Thsd7a
|
UTSW |
6 |
12,327,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Thsd7a
|
UTSW |
6 |
12,408,987 (GRCm39) |
nonsense |
probably null |
|
R6273:Thsd7a
|
UTSW |
6 |
12,408,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R6300:Thsd7a
|
UTSW |
6 |
12,471,103 (GRCm39) |
nonsense |
probably null |
|
R6314:Thsd7a
|
UTSW |
6 |
12,554,996 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6392:Thsd7a
|
UTSW |
6 |
12,468,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R6418:Thsd7a
|
UTSW |
6 |
12,555,081 (GRCm39) |
nonsense |
probably null |
|
R6515:Thsd7a
|
UTSW |
6 |
12,501,085 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6725:Thsd7a
|
UTSW |
6 |
12,555,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6742:Thsd7a
|
UTSW |
6 |
12,408,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Thsd7a
|
UTSW |
6 |
12,555,636 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6838:Thsd7a
|
UTSW |
6 |
12,504,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R7104:Thsd7a
|
UTSW |
6 |
12,379,429 (GRCm39) |
missense |
|
|
R7170:Thsd7a
|
UTSW |
6 |
12,352,090 (GRCm39) |
missense |
|
|
R7349:Thsd7a
|
UTSW |
6 |
12,352,067 (GRCm39) |
missense |
|
|
R7460:Thsd7a
|
UTSW |
6 |
12,554,933 (GRCm39) |
missense |
|
|
R7467:Thsd7a
|
UTSW |
6 |
12,331,584 (GRCm39) |
missense |
|
|
R7666:Thsd7a
|
UTSW |
6 |
12,379,437 (GRCm39) |
missense |
|
|
R7869:Thsd7a
|
UTSW |
6 |
12,471,123 (GRCm39) |
nonsense |
probably null |
|
R8032:Thsd7a
|
UTSW |
6 |
12,555,287 (GRCm39) |
missense |
|
|
R8165:Thsd7a
|
UTSW |
6 |
12,468,962 (GRCm39) |
missense |
|
|
R8167:Thsd7a
|
UTSW |
6 |
12,317,400 (GRCm39) |
nonsense |
probably null |
|
R8245:Thsd7a
|
UTSW |
6 |
12,379,592 (GRCm39) |
missense |
|
|
R8310:Thsd7a
|
UTSW |
6 |
12,396,612 (GRCm39) |
missense |
|
|
R8312:Thsd7a
|
UTSW |
6 |
12,471,181 (GRCm39) |
missense |
|
|
R8331:Thsd7a
|
UTSW |
6 |
12,471,157 (GRCm39) |
missense |
|
|
R8755:Thsd7a
|
UTSW |
6 |
12,408,851 (GRCm39) |
nonsense |
probably null |
|
R8843:Thsd7a
|
UTSW |
6 |
12,501,136 (GRCm39) |
missense |
|
|
R8867:Thsd7a
|
UTSW |
6 |
12,338,686 (GRCm39) |
missense |
|
|
R8952:Thsd7a
|
UTSW |
6 |
12,468,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R9036:Thsd7a
|
UTSW |
6 |
12,418,249 (GRCm39) |
missense |
|
|
R9299:Thsd7a
|
UTSW |
6 |
12,504,131 (GRCm39) |
missense |
|
|
R9366:Thsd7a
|
UTSW |
6 |
12,555,480 (GRCm39) |
missense |
|
|
R9489:Thsd7a
|
UTSW |
6 |
12,352,022 (GRCm39) |
missense |
|
|
|