Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
C |
T |
14: 35,817,121 (GRCm39) |
T57I |
probably benign |
Het |
Adcy8 |
T |
C |
15: 64,576,565 (GRCm39) |
N999S |
possibly damaging |
Het |
Adgrv1 |
T |
A |
13: 81,684,483 (GRCm39) |
I1073F |
possibly damaging |
Het |
Akap3 |
A |
G |
6: 126,843,439 (GRCm39) |
D686G |
probably damaging |
Het |
Alg2 |
A |
T |
4: 47,471,881 (GRCm39) |
I309N |
probably benign |
Het |
Ankrd36 |
A |
G |
11: 5,639,168 (GRCm39) |
E1360G |
probably benign |
Het |
Aox1 |
C |
A |
1: 58,370,051 (GRCm39) |
Q788K |
probably damaging |
Het |
Apoc2 |
A |
T |
7: 19,407,282 (GRCm39) |
D26E |
possibly damaging |
Het |
Bbx |
G |
A |
16: 50,022,851 (GRCm39) |
T703I |
possibly damaging |
Het |
C2cd4d |
T |
C |
3: 94,271,378 (GRCm39) |
Y215H |
probably benign |
Het |
C3 |
C |
T |
17: 57,525,809 (GRCm39) |
E858K |
probably benign |
Het |
Ciita |
T |
C |
16: 10,329,171 (GRCm39) |
L482P |
probably damaging |
Het |
Cldn9 |
T |
C |
17: 23,902,052 (GRCm39) |
E191G |
probably benign |
Het |
Col5a2 |
A |
G |
1: 45,417,609 (GRCm39) |
I1322T |
possibly damaging |
Het |
Cp |
G |
A |
3: 20,024,137 (GRCm39) |
V326M |
probably damaging |
Het |
Cyp7b1 |
G |
A |
3: 18,151,782 (GRCm39) |
Q144* |
probably null |
Het |
Dnah10 |
T |
C |
5: 124,864,490 (GRCm39) |
S2232P |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 118,009,697 (GRCm39) |
E625G |
possibly damaging |
Het |
Dnah7c |
T |
A |
1: 46,571,910 (GRCm39) |
D794E |
probably benign |
Het |
Dusp10 |
G |
A |
1: 183,769,414 (GRCm39) |
V127M |
probably benign |
Het |
Dysf |
G |
C |
6: 84,090,962 (GRCm39) |
W1015C |
probably damaging |
Het |
Fbxw17 |
T |
C |
13: 50,577,808 (GRCm39) |
Y104H |
probably damaging |
Het |
Gm6408 |
G |
A |
5: 146,420,647 (GRCm39) |
E176K |
probably damaging |
Het |
Gp1bb |
T |
A |
16: 18,439,689 (GRCm39) |
D135V |
possibly damaging |
Het |
Gprin1 |
C |
T |
13: 54,886,069 (GRCm39) |
C735Y |
probably damaging |
Het |
Heatr9 |
T |
A |
11: 83,411,446 (GRCm39) |
M30L |
possibly damaging |
Het |
Hhat |
G |
A |
1: 192,376,134 (GRCm39) |
T333I |
possibly damaging |
Het |
Htr5b |
A |
G |
1: 121,438,223 (GRCm39) |
F336S |
probably damaging |
Het |
Ippk |
T |
G |
13: 49,590,181 (GRCm39) |
|
probably null |
Het |
Jph1 |
T |
A |
1: 17,074,410 (GRCm39) |
H11L |
possibly damaging |
Het |
Kif12 |
T |
A |
4: 63,084,717 (GRCm39) |
I534L |
probably benign |
Het |
Lemd3 |
A |
T |
10: 120,788,137 (GRCm39) |
F523I |
probably benign |
Het |
Lgsn |
C |
A |
1: 31,229,508 (GRCm39) |
H76Q |
probably benign |
Het |
Lipm |
T |
A |
19: 34,089,497 (GRCm39) |
W152R |
probably damaging |
Het |
Mei1 |
A |
T |
15: 81,978,200 (GRCm39) |
R216W |
probably damaging |
Het |
Mybpc1 |
C |
T |
10: 88,389,274 (GRCm39) |
G379S |
probably damaging |
Het |
Myh8 |
A |
G |
11: 67,179,142 (GRCm39) |
T512A |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,337,849 (GRCm39) |
|
probably null |
Het |
Npc1 |
T |
C |
18: 12,343,605 (GRCm39) |
T463A |
probably benign |
Het |
Or12e10 |
A |
G |
2: 87,640,230 (GRCm39) |
N22S |
probably damaging |
Het |
Or2y13 |
G |
A |
11: 49,415,011 (GRCm39) |
V154M |
probably benign |
Het |
Or6c7 |
A |
T |
10: 129,323,277 (GRCm39) |
I133F |
probably damaging |
Het |
Osbpl11 |
T |
G |
16: 33,047,309 (GRCm39) |
I424R |
possibly damaging |
Het |
Pnma8b |
A |
T |
7: 16,680,181 (GRCm39) |
K388N |
possibly damaging |
Het |
Ppp1r26 |
A |
T |
2: 28,341,171 (GRCm39) |
K267I |
probably damaging |
Het |
Psmb5 |
A |
T |
14: 54,854,166 (GRCm39) |
M104K |
probably damaging |
Het |
Ptges2 |
T |
C |
2: 32,292,318 (GRCm39) |
V378A |
probably benign |
Het |
Rcan2 |
C |
T |
17: 44,147,216 (GRCm39) |
S18F |
probably benign |
Het |
Saxo5 |
A |
T |
8: 3,526,309 (GRCm39) |
D154V |
probably damaging |
Het |
Sf3b2 |
C |
T |
19: 5,324,545 (GRCm39) |
R859Q |
probably benign |
Het |
Slc7a1 |
G |
A |
5: 148,289,256 (GRCm39) |
|
|
Het |
Spata31d1a |
T |
A |
13: 59,851,448 (GRCm39) |
T227S |
probably benign |
Het |
Sptbn2 |
T |
A |
19: 4,794,173 (GRCm39) |
V1459E |
possibly damaging |
Het |
Srgap2 |
T |
C |
1: 131,247,275 (GRCm39) |
I586V |
probably benign |
Het |
St6galnac1 |
G |
A |
11: 116,657,833 (GRCm39) |
R356* |
probably null |
Het |
Taf5 |
T |
A |
19: 47,059,650 (GRCm39) |
F265I |
probably damaging |
Het |
Tkfc |
T |
A |
19: 10,573,727 (GRCm39) |
I229L |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,436,679 (GRCm39) |
L56Q |
probably damaging |
Het |
Togaram2 |
C |
T |
17: 72,016,638 (GRCm39) |
A665V |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,537,390 (GRCm39) |
T34846I |
probably benign |
Het |
Tyr |
G |
A |
7: 87,142,548 (GRCm39) |
A4V |
probably benign |
Het |
Ubap2 |
A |
C |
4: 41,206,221 (GRCm39) |
F549L |
probably damaging |
Het |
Usp2 |
T |
C |
9: 44,001,339 (GRCm39) |
S294P |
probably damaging |
Het |
Vrk3 |
A |
G |
7: 44,407,187 (GRCm39) |
N53D |
probably damaging |
Het |
Zfp324 |
T |
C |
7: 12,705,142 (GRCm39) |
S444P |
probably damaging |
Het |
Zfp597 |
T |
C |
16: 3,683,791 (GRCm39) |
I322V |
probably benign |
Het |
|
Other mutations in Cnst |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00917:Cnst
|
APN |
1 |
179,452,557 (GRCm39) |
splice site |
probably benign |
|
Doldrums
|
UTSW |
1 |
179,432,638 (GRCm39) |
splice site |
probably null |
|
ennui
|
UTSW |
1 |
179,434,100 (GRCm39) |
critical splice donor site |
probably null |
|
R0360:Cnst
|
UTSW |
1 |
179,407,100 (GRCm39) |
missense |
probably benign |
0.00 |
R1391:Cnst
|
UTSW |
1 |
179,407,051 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1743:Cnst
|
UTSW |
1 |
179,437,957 (GRCm39) |
missense |
probably benign |
0.18 |
R1909:Cnst
|
UTSW |
1 |
179,450,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R3856:Cnst
|
UTSW |
1 |
179,407,279 (GRCm39) |
missense |
probably benign |
0.02 |
R4565:Cnst
|
UTSW |
1 |
179,432,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Cnst
|
UTSW |
1 |
179,432,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R5072:Cnst
|
UTSW |
1 |
179,450,451 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5087:Cnst
|
UTSW |
1 |
179,450,378 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5294:Cnst
|
UTSW |
1 |
179,438,005 (GRCm39) |
missense |
probably benign |
0.03 |
R5349:Cnst
|
UTSW |
1 |
179,450,462 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5394:Cnst
|
UTSW |
1 |
179,429,301 (GRCm39) |
splice site |
probably benign |
|
R6020:Cnst
|
UTSW |
1 |
179,437,440 (GRCm39) |
missense |
probably benign |
|
R6198:Cnst
|
UTSW |
1 |
179,420,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6669:Cnst
|
UTSW |
1 |
179,432,638 (GRCm39) |
splice site |
probably null |
|
R6767:Cnst
|
UTSW |
1 |
179,437,519 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7179:Cnst
|
UTSW |
1 |
179,406,947 (GRCm39) |
start gained |
probably benign |
|
R7356:Cnst
|
UTSW |
1 |
179,434,095 (GRCm39) |
missense |
probably benign |
0.01 |
R7730:Cnst
|
UTSW |
1 |
179,452,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Cnst
|
UTSW |
1 |
179,450,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R8073:Cnst
|
UTSW |
1 |
179,434,002 (GRCm39) |
missense |
probably benign |
0.00 |
R8194:Cnst
|
UTSW |
1 |
179,437,759 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Cnst
|
UTSW |
1 |
179,420,274 (GRCm39) |
missense |
probably benign |
0.00 |
R8857:Cnst
|
UTSW |
1 |
179,437,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Cnst
|
UTSW |
1 |
179,437,587 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9062:Cnst
|
UTSW |
1 |
179,434,100 (GRCm39) |
critical splice donor site |
probably null |
|
R9106:Cnst
|
UTSW |
1 |
179,432,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Cnst
|
UTSW |
1 |
179,407,039 (GRCm39) |
small deletion |
probably benign |
|
R9287:Cnst
|
UTSW |
1 |
179,407,108 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9429:Cnst
|
UTSW |
1 |
179,432,566 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Cnst
|
UTSW |
1 |
179,407,130 (GRCm39) |
missense |
probably damaging |
0.99 |
|