Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn2 |
A |
T |
13: 12,305,563 (GRCm39) |
Y418N |
probably benign |
Het |
Adam15 |
T |
C |
3: 89,248,812 (GRCm39) |
|
probably benign |
Het |
Adam32 |
C |
A |
8: 25,392,812 (GRCm39) |
|
probably benign |
Het |
Adamts12 |
T |
A |
15: 11,345,680 (GRCm39) |
C1574S |
probably damaging |
Het |
Adck1 |
T |
C |
12: 88,397,926 (GRCm39) |
S187P |
possibly damaging |
Het |
Atp13a3 |
A |
G |
16: 30,156,336 (GRCm39) |
V949A |
possibly damaging |
Het |
Atxn3 |
T |
C |
12: 101,908,439 (GRCm39) |
T138A |
probably benign |
Het |
Atxn7l2 |
C |
T |
3: 108,110,859 (GRCm39) |
R559Q |
probably damaging |
Het |
Bicra |
G |
T |
7: 15,706,741 (GRCm39) |
S1233R |
possibly damaging |
Het |
Cacybp |
G |
T |
1: 160,034,206 (GRCm39) |
N101K |
probably damaging |
Het |
Cops7b |
T |
C |
1: 86,528,828 (GRCm39) |
L185P |
probably damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,420,814 (GRCm39) |
D899G |
possibly damaging |
Het |
Cyp4f37 |
C |
T |
17: 32,844,150 (GRCm39) |
R85* |
probably null |
Het |
Dnah3 |
T |
G |
7: 119,550,437 (GRCm39) |
N3294T |
possibly damaging |
Het |
Elmo1 |
T |
A |
13: 20,526,634 (GRCm39) |
Y395N |
probably damaging |
Het |
Fam234b |
T |
A |
6: 135,202,203 (GRCm39) |
Y308* |
probably null |
Het |
Fam43a |
A |
G |
16: 30,419,481 (GRCm39) |
K22E |
probably damaging |
Het |
Fcer2a |
T |
C |
8: 3,738,302 (GRCm39) |
N123D |
possibly damaging |
Het |
Gm11595 |
A |
G |
11: 99,663,027 (GRCm39) |
C218R |
unknown |
Het |
Gria4 |
T |
C |
9: 4,537,726 (GRCm39) |
Y194C |
probably damaging |
Het |
Grin2d |
T |
C |
7: 45,507,396 (GRCm39) |
E435G |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,844,725 (GRCm39) |
E506G |
probably damaging |
Het |
Htt |
G |
A |
5: 34,989,948 (GRCm39) |
S1160N |
possibly damaging |
Het |
Ift140 |
A |
G |
17: 25,267,417 (GRCm39) |
E605G |
probably damaging |
Het |
Il17re |
T |
C |
6: 113,445,411 (GRCm39) |
V374A |
probably benign |
Het |
Ippk |
A |
G |
13: 49,612,093 (GRCm39) |
Q439R |
possibly damaging |
Het |
Itgam |
G |
A |
7: 127,700,899 (GRCm39) |
V530M |
probably damaging |
Het |
Kirrel3 |
A |
G |
9: 34,931,429 (GRCm39) |
H47R |
possibly damaging |
Het |
Klk1b24 |
A |
T |
7: 43,841,057 (GRCm39) |
I162F |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,059,434 (GRCm39) |
T606S |
probably benign |
Het |
Lama2 |
C |
T |
10: 27,343,199 (GRCm39) |
|
probably null |
Het |
Lrp2 |
A |
G |
2: 69,313,945 (GRCm39) |
I2262T |
probably benign |
Het |
Mamdc4 |
A |
T |
2: 25,458,546 (GRCm39) |
I317N |
possibly damaging |
Het |
Mtmr3 |
G |
T |
11: 4,437,938 (GRCm39) |
H839N |
probably benign |
Het |
Ncr1 |
G |
T |
7: 4,344,253 (GRCm39) |
V177F |
probably benign |
Het |
Nop58 |
T |
C |
1: 59,743,242 (GRCm39) |
S219P |
probably damaging |
Het |
Nrg3 |
T |
C |
14: 38,734,043 (GRCm39) |
Y281C |
probably damaging |
Het |
Nsf |
A |
G |
11: 103,819,608 (GRCm39) |
S54P |
probably damaging |
Het |
Or56b6 |
A |
T |
7: 104,925,153 (GRCm39) |
|
noncoding transcript |
Het |
Or6k8-ps1 |
T |
A |
1: 173,979,102 (GRCm39) |
S7T |
probably benign |
Het |
Plxnc1 |
T |
C |
10: 94,685,801 (GRCm39) |
K730R |
probably damaging |
Het |
Polr2g |
A |
T |
19: 8,771,740 (GRCm39) |
|
probably benign |
Het |
Rps13 |
A |
G |
7: 115,932,925 (GRCm39) |
|
probably benign |
Het |
Slc22a27 |
G |
T |
19: 7,887,108 (GRCm39) |
H260Q |
possibly damaging |
Het |
Spata18 |
G |
T |
5: 73,814,944 (GRCm39) |
|
probably null |
Het |
Tns2 |
A |
G |
15: 102,019,814 (GRCm39) |
E560G |
possibly damaging |
Het |
Trbv16 |
T |
C |
6: 41,128,715 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,851,520 (GRCm39) |
I1829N |
probably damaging |
Het |
Vcl |
C |
T |
14: 21,053,311 (GRCm39) |
T442I |
probably damaging |
Het |
Vmn2r102 |
T |
A |
17: 19,880,731 (GRCm39) |
I24N |
probably benign |
Het |
Vmn2r114 |
T |
C |
17: 23,529,451 (GRCm39) |
D217G |
probably damaging |
Het |
Vmn2r58 |
A |
G |
7: 41,486,394 (GRCm39) |
Y834H |
probably damaging |
Het |
Zdhhc8 |
G |
T |
16: 18,045,636 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Scgb2b7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03242:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03252:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03261:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03280:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03302:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03308:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03388:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03411:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Scgb2b7
|
UTSW |
7 |
31,403,437 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7741:Scgb2b7
|
UTSW |
7 |
31,404,454 (GRCm39) |
critical splice donor site |
probably null |
|
R8925:Scgb2b7
|
UTSW |
7 |
31,404,602 (GRCm39) |
missense |
probably benign |
0.00 |
R8927:Scgb2b7
|
UTSW |
7 |
31,404,602 (GRCm39) |
missense |
probably benign |
0.00 |
R9801:Scgb2b7
|
UTSW |
7 |
31,404,580 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Scgb2b7
|
UTSW |
7 |
31,404,547 (GRCm39) |
missense |
probably benign |
0.13 |
Z1186:Scgb2b7
|
UTSW |
7 |
31,404,489 (GRCm39) |
missense |
probably benign |
|
|