Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
G |
A |
12: 118,875,169 (GRCm39) |
H668Y |
probably benign |
Het |
Adamts10 |
A |
G |
17: 33,762,205 (GRCm39) |
S505G |
probably benign |
Het |
Ahnak |
C |
T |
19: 8,985,243 (GRCm39) |
H2176Y |
possibly damaging |
Het |
Ash1l |
G |
T |
3: 88,973,572 (GRCm39) |
D2544Y |
probably damaging |
Het |
Ccdc88a |
T |
A |
11: 29,350,283 (GRCm39) |
F88L |
probably benign |
Het |
Cdc42bpa |
A |
T |
1: 179,978,723 (GRCm39) |
|
probably null |
Het |
Celsr3 |
T |
C |
9: 108,708,907 (GRCm39) |
V1251A |
probably damaging |
Het |
CN725425 |
T |
A |
15: 91,129,955 (GRCm39) |
F273I |
possibly damaging |
Het |
Eif2b1 |
A |
G |
5: 124,714,965 (GRCm39) |
C104R |
probably damaging |
Het |
Ercc3 |
A |
T |
18: 32,381,372 (GRCm39) |
D396V |
possibly damaging |
Het |
Fga |
A |
T |
3: 82,940,014 (GRCm39) |
D556V |
probably damaging |
Het |
Frg1 |
C |
T |
8: 41,863,362 (GRCm39) |
|
probably benign |
Het |
Fto |
T |
C |
8: 92,136,376 (GRCm39) |
Y217H |
probably damaging |
Het |
Garin4 |
A |
T |
1: 190,896,606 (GRCm39) |
Y12* |
probably null |
Het |
Grin3a |
A |
T |
4: 49,792,533 (GRCm39) |
V400E |
probably damaging |
Het |
Gtse1 |
T |
A |
15: 85,759,855 (GRCm39) |
L682* |
probably null |
Het |
Lama1 |
G |
A |
17: 68,092,065 (GRCm39) |
R1646H |
probably benign |
Het |
Lamp1 |
T |
C |
8: 13,215,905 (GRCm39) |
C35R |
probably damaging |
Het |
Lzts3 |
A |
T |
2: 130,478,126 (GRCm39) |
L324Q |
probably damaging |
Het |
Muc6 |
T |
A |
7: 141,236,069 (GRCm39) |
R453* |
probably null |
Het |
Naa35 |
T |
A |
13: 59,748,777 (GRCm39) |
H132Q |
probably damaging |
Het |
Pgm5 |
C |
A |
19: 24,793,777 (GRCm39) |
G296W |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,805,272 (GRCm39) |
C3275S |
probably damaging |
Het |
Podxl2 |
A |
G |
6: 88,826,331 (GRCm39) |
L325P |
probably benign |
Het |
Prom2 |
A |
G |
2: 127,371,050 (GRCm39) |
|
probably null |
Het |
Rab12 |
T |
C |
17: 66,804,404 (GRCm39) |
S185G |
probably damaging |
Het |
Rnf43 |
T |
G |
11: 87,621,046 (GRCm39) |
M313R |
probably null |
Het |
Rusc2 |
T |
C |
4: 43,415,840 (GRCm39) |
V382A |
probably benign |
Het |
Sbno1 |
A |
T |
5: 124,516,618 (GRCm39) |
|
probably benign |
Het |
Smg6 |
T |
C |
11: 74,816,770 (GRCm39) |
I10T |
probably benign |
Het |
Smpd1 |
T |
C |
7: 105,205,033 (GRCm39) |
F304S |
possibly damaging |
Het |
Spta1 |
G |
A |
1: 174,044,725 (GRCm39) |
V1454I |
probably benign |
Het |
Tdrd7 |
A |
T |
4: 46,018,551 (GRCm39) |
I722F |
possibly damaging |
Het |
Topors |
T |
C |
4: 40,262,364 (GRCm39) |
T307A |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,807,502 (GRCm39) |
R77Q |
probably damaging |
Het |
Vmn1r210 |
C |
T |
13: 23,011,778 (GRCm39) |
M169I |
probably benign |
Het |
Zc3h4 |
A |
G |
7: 16,168,257 (GRCm39) |
S789G |
unknown |
Het |
Zfp629 |
G |
T |
7: 127,211,917 (GRCm39) |
|
probably benign |
Het |
Zfp977 |
C |
A |
7: 42,230,156 (GRCm39) |
R123I |
probably benign |
Het |
|
Other mutations in Igkv6-32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03183:Igkv6-32
|
APN |
6 |
70,051,556 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03196:Igkv6-32
|
APN |
6 |
70,051,042 (GRCm39) |
missense |
probably benign |
0.01 |
R5068:Igkv6-32
|
UTSW |
6 |
70,051,267 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5223:Igkv6-32
|
UTSW |
6 |
70,051,207 (GRCm39) |
missense |
probably benign |
0.00 |
R6425:Igkv6-32
|
UTSW |
6 |
70,051,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R7664:Igkv6-32
|
UTSW |
6 |
70,051,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Igkv6-32
|
UTSW |
6 |
70,051,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R8093:Igkv6-32
|
UTSW |
6 |
70,051,547 (GRCm39) |
missense |
probably benign |
0.30 |
R8679:Igkv6-32
|
UTSW |
6 |
70,051,063 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Igkv6-32
|
UTSW |
6 |
70,051,570 (GRCm39) |
start gained |
probably benign |
|
|