Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017G19Rik |
A |
G |
3: 40,567,240 (GRCm39) |
|
noncoding transcript |
Het |
1700066M21Rik |
T |
C |
1: 57,422,083 (GRCm39) |
F153S |
possibly damaging |
Het |
Acss1 |
A |
G |
2: 150,480,405 (GRCm39) |
V222A |
probably benign |
Het |
Atad2b |
A |
G |
12: 4,993,223 (GRCm39) |
I247M |
probably benign |
Het |
Atxn10 |
A |
G |
15: 85,322,321 (GRCm39) |
I398V |
possibly damaging |
Het |
Cep192 |
T |
A |
18: 68,004,584 (GRCm39) |
C2312S |
probably damaging |
Het |
Cidea |
C |
T |
18: 67,493,298 (GRCm39) |
Q106* |
probably null |
Het |
Cnga4 |
A |
G |
7: 105,054,892 (GRCm39) |
T159A |
probably damaging |
Het |
Cyp2j12 |
G |
T |
4: 96,001,194 (GRCm39) |
S304R |
probably damaging |
Het |
Dennd2b |
A |
G |
7: 109,124,785 (GRCm39) |
F665L |
probably damaging |
Het |
Dsg4 |
T |
A |
18: 20,603,978 (GRCm39) |
V815E |
probably damaging |
Het |
Entrep1 |
G |
A |
19: 24,007,913 (GRCm39) |
S130L |
probably damaging |
Het |
Farp1 |
T |
C |
14: 121,510,213 (GRCm39) |
M737T |
probably damaging |
Het |
Fbn1 |
T |
A |
2: 125,193,634 (GRCm39) |
D1395V |
possibly damaging |
Het |
Fbn2 |
C |
T |
18: 58,209,146 (GRCm39) |
M1076I |
probably benign |
Het |
Fitm2 |
T |
A |
2: 163,314,593 (GRCm39) |
|
probably benign |
Het |
Fras1 |
A |
G |
5: 96,929,148 (GRCm39) |
R3851G |
probably damaging |
Het |
Frem2 |
C |
T |
3: 53,561,742 (GRCm39) |
V922I |
probably benign |
Het |
Gm10719 |
A |
T |
9: 3,018,945 (GRCm39) |
T200S |
probably benign |
Het |
Grin3a |
T |
C |
4: 49,844,555 (GRCm39) |
D176G |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,089,928 (GRCm39) |
|
probably benign |
Het |
Ift140 |
C |
A |
17: 25,309,741 (GRCm39) |
H1090Q |
probably damaging |
Het |
Il20ra |
A |
G |
10: 19,625,032 (GRCm39) |
T104A |
probably damaging |
Het |
Il22ra2 |
A |
G |
10: 19,502,460 (GRCm39) |
D93G |
possibly damaging |
Het |
Ing1 |
A |
G |
8: 11,612,090 (GRCm39) |
K176R |
probably benign |
Het |
Jph1 |
A |
T |
1: 17,074,735 (GRCm39) |
C428S |
probably benign |
Het |
Kif13b |
G |
T |
14: 65,043,581 (GRCm39) |
G1794W |
probably damaging |
Het |
Map10 |
A |
G |
8: 126,398,553 (GRCm39) |
T649A |
probably benign |
Het |
Med12l |
T |
C |
3: 58,914,523 (GRCm39) |
|
probably null |
Het |
Nat8f1 |
A |
G |
6: 85,887,567 (GRCm39) |
I131T |
probably benign |
Het |
Oas1d |
C |
A |
5: 121,054,958 (GRCm39) |
Q177K |
probably benign |
Het |
Or4a74 |
C |
A |
2: 89,440,043 (GRCm39) |
M134I |
probably damaging |
Het |
Or51q1 |
G |
A |
7: 103,628,767 (GRCm39) |
D123N |
probably damaging |
Het |
P2ry2 |
A |
G |
7: 100,647,363 (GRCm39) |
V314A |
possibly damaging |
Het |
Pabir2 |
G |
A |
X: 52,349,554 (GRCm39) |
|
probably benign |
Het |
Pfkl |
G |
T |
10: 77,824,717 (GRCm39) |
R691S |
probably benign |
Het |
Plb1 |
T |
A |
5: 32,490,175 (GRCm39) |
I1005N |
probably damaging |
Het |
Prkacb |
A |
G |
3: 146,451,147 (GRCm39) |
|
probably benign |
Het |
Ptprm |
A |
T |
17: 66,990,403 (GRCm39) |
Y1412N |
possibly damaging |
Het |
Rab22a |
A |
G |
2: 173,503,226 (GRCm39) |
D13G |
probably damaging |
Het |
Rab29 |
G |
A |
1: 131,800,305 (GRCm39) |
W201* |
probably null |
Het |
Rasa3 |
T |
C |
8: 13,648,259 (GRCm39) |
E135G |
probably damaging |
Het |
Rassf10 |
A |
G |
7: 112,554,338 (GRCm39) |
E313G |
probably benign |
Het |
Sf1 |
GGCAGCAGCAGCAGCAGCAGC |
GGCAGCAGCAGCAGCAGC |
19: 6,424,845 (GRCm39) |
|
probably benign |
Het |
Sipa1l3 |
A |
T |
7: 29,031,678 (GRCm39) |
L468Q |
probably damaging |
Het |
Slc6a12 |
G |
A |
6: 121,340,820 (GRCm39) |
|
probably null |
Het |
Slfn8 |
A |
G |
11: 82,895,570 (GRCm39) |
L412P |
probably damaging |
Het |
Taf4b |
T |
C |
18: 14,946,583 (GRCm39) |
S469P |
probably damaging |
Het |
Tgoln1 |
T |
C |
6: 72,592,664 (GRCm39) |
E272G |
probably damaging |
Het |
Tlr12 |
C |
A |
4: 128,509,563 (GRCm39) |
G896W |
probably damaging |
Het |
Tnfrsf1a |
A |
G |
6: 125,337,729 (GRCm39) |
I229V |
probably benign |
Het |
Ttn |
G |
A |
2: 76,749,890 (GRCm39) |
H3720Y |
probably benign |
Het |
|
Other mutations in Slc17a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Slc17a1
|
APN |
13 |
24,062,437 (GRCm39) |
unclassified |
probably benign |
|
IGL01453:Slc17a1
|
APN |
13 |
24,058,714 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01560:Slc17a1
|
APN |
13 |
24,058,612 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01910:Slc17a1
|
APN |
13 |
24,062,440 (GRCm39) |
unclassified |
probably benign |
|
R1077:Slc17a1
|
UTSW |
13 |
24,062,433 (GRCm39) |
unclassified |
probably benign |
|
R1939:Slc17a1
|
UTSW |
13 |
24,059,864 (GRCm39) |
missense |
probably benign |
0.05 |
R2016:Slc17a1
|
UTSW |
13 |
24,062,522 (GRCm39) |
missense |
probably benign |
0.03 |
R2134:Slc17a1
|
UTSW |
13 |
24,059,658 (GRCm39) |
nonsense |
probably null |
|
R3001:Slc17a1
|
UTSW |
13 |
24,062,564 (GRCm39) |
critical splice donor site |
probably null |
|
R3002:Slc17a1
|
UTSW |
13 |
24,062,564 (GRCm39) |
critical splice donor site |
probably null |
|
R4580:Slc17a1
|
UTSW |
13 |
24,071,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Slc17a1
|
UTSW |
13 |
24,062,543 (GRCm39) |
missense |
probably benign |
|
R4696:Slc17a1
|
UTSW |
13 |
24,064,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Slc17a1
|
UTSW |
13 |
24,064,576 (GRCm39) |
missense |
probably benign |
0.05 |
R4845:Slc17a1
|
UTSW |
13 |
24,060,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Slc17a1
|
UTSW |
13 |
24,064,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Slc17a1
|
UTSW |
13 |
24,056,575 (GRCm39) |
utr 5 prime |
probably benign |
|
R6020:Slc17a1
|
UTSW |
13 |
24,059,593 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7403:Slc17a1
|
UTSW |
13 |
24,058,690 (GRCm39) |
missense |
probably benign |
|
R7440:Slc17a1
|
UTSW |
13 |
24,062,466 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7747:Slc17a1
|
UTSW |
13 |
24,072,035 (GRCm39) |
missense |
probably benign |
0.10 |
R8063:Slc17a1
|
UTSW |
13 |
24,059,524 (GRCm39) |
missense |
probably benign |
0.33 |
R8323:Slc17a1
|
UTSW |
13 |
24,071,982 (GRCm39) |
missense |
probably damaging |
0.99 |
R8880:Slc17a1
|
UTSW |
13 |
24,062,732 (GRCm39) |
missense |
probably benign |
0.04 |
R9205:Slc17a1
|
UTSW |
13 |
24,062,794 (GRCm39) |
missense |
probably benign |
0.16 |
R9243:Slc17a1
|
UTSW |
13 |
24,064,432 (GRCm39) |
missense |
probably benign |
0.00 |
|