Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
G |
6: 121,616,253 (GRCm39) |
L127R |
probably null |
Het |
Ambp |
T |
C |
4: 63,067,721 (GRCm39) |
E163G |
probably benign |
Het |
Amy1 |
G |
A |
3: 113,349,658 (GRCm39) |
A504V |
probably damaging |
Het |
Angptl3 |
A |
T |
4: 98,921,540 (GRCm39) |
K219N |
probably benign |
Het |
Atp6v1g1 |
A |
G |
4: 63,468,255 (GRCm39) |
N86S |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,713,612 (GRCm39) |
V290A |
probably benign |
Het |
Bad |
A |
G |
19: 6,919,799 (GRCm39) |
R37G |
probably benign |
Het |
Bicra |
T |
C |
7: 15,723,223 (GRCm39) |
D98G |
possibly damaging |
Het |
Col4a4 |
G |
A |
1: 82,474,889 (GRCm39) |
T650M |
unknown |
Het |
Cyp11b2 |
T |
C |
15: 74,727,298 (GRCm39) |
R128G |
probably benign |
Het |
Dst |
T |
C |
1: 34,229,303 (GRCm39) |
S1974P |
probably damaging |
Het |
Fabp1 |
T |
C |
6: 71,178,595 (GRCm39) |
L24P |
probably benign |
Het |
Flnb |
T |
C |
14: 7,942,057 (GRCm38) |
V2345A |
probably damaging |
Het |
Gmnc |
G |
T |
16: 26,779,217 (GRCm39) |
H221Q |
probably benign |
Het |
Homer1 |
T |
C |
13: 93,502,929 (GRCm39) |
|
probably benign |
Het |
Kit |
A |
G |
5: 75,806,565 (GRCm39) |
D690G |
probably damaging |
Het |
Lama2 |
C |
T |
10: 26,877,231 (GRCm39) |
E2652K |
probably benign |
Het |
Mc3r |
C |
T |
2: 172,091,588 (GRCm39) |
T270I |
probably benign |
Het |
Mrgpra3 |
A |
C |
7: 47,239,314 (GRCm39) |
L204W |
probably damaging |
Het |
Mroh1 |
C |
T |
15: 76,317,808 (GRCm39) |
T839I |
possibly damaging |
Het |
Naip2 |
T |
A |
13: 100,291,419 (GRCm39) |
H1173L |
probably benign |
Het |
Optc |
T |
C |
1: 133,825,617 (GRCm39) |
D303G |
probably damaging |
Het |
Or2n1d |
A |
G |
17: 38,646,323 (GRCm39) |
I92V |
probably damaging |
Het |
Or5af1 |
A |
T |
11: 58,722,150 (GRCm39) |
M57L |
probably damaging |
Het |
P4ha3 |
C |
T |
7: 99,934,831 (GRCm39) |
A31V |
possibly damaging |
Het |
Plch2 |
A |
G |
4: 155,075,470 (GRCm39) |
|
probably null |
Het |
Plpp2 |
A |
T |
10: 79,363,647 (GRCm39) |
|
probably null |
Het |
Polq |
A |
T |
16: 36,882,699 (GRCm39) |
N1342I |
probably damaging |
Het |
Pter |
T |
A |
2: 13,005,805 (GRCm39) |
L326H |
probably benign |
Het |
Pwwp2a |
C |
T |
11: 43,597,015 (GRCm39) |
Q452* |
probably null |
Het |
Slc8a2 |
T |
G |
7: 15,892,810 (GRCm39) |
V824G |
probably damaging |
Het |
Slfn2 |
A |
T |
11: 82,960,390 (GRCm39) |
H123L |
probably benign |
Het |
Tmem132e |
A |
G |
11: 82,335,156 (GRCm39) |
Y654C |
probably damaging |
Het |
Trim14 |
C |
T |
4: 46,523,739 (GRCm39) |
V100I |
possibly damaging |
Het |
Tro |
G |
A |
X: 149,429,252 (GRCm39) |
|
probably benign |
Het |
Uspl1 |
T |
A |
5: 149,151,507 (GRCm39) |
|
probably benign |
Het |
Uty |
A |
G |
Y: 1,158,336 (GRCm39) |
I522T |
probably benign |
Het |
Vmn1r120 |
A |
C |
7: 20,787,582 (GRCm39) |
L43W |
probably damaging |
Het |
Vmn2r16 |
A |
T |
5: 109,478,362 (GRCm39) |
D39V |
probably damaging |
Het |
Washc4 |
T |
A |
10: 83,405,866 (GRCm39) |
I454N |
probably benign |
Het |
Wnt16 |
T |
C |
6: 22,298,133 (GRCm39) |
V333A |
probably damaging |
Het |
Ylpm1 |
T |
C |
12: 85,096,644 (GRCm39) |
|
probably null |
Het |
Zfy1 |
A |
T |
Y: 726,357 (GRCm39) |
D469E |
possibly damaging |
Het |
|
Other mutations in Cfap251 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00487:Cfap251
|
APN |
5 |
123,412,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01090:Cfap251
|
APN |
5 |
123,418,052 (GRCm39) |
splice site |
probably benign |
|
IGL01387:Cfap251
|
APN |
5 |
123,421,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01432:Cfap251
|
APN |
5 |
123,418,015 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01642:Cfap251
|
APN |
5 |
123,426,761 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01720:Cfap251
|
APN |
5 |
123,460,557 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02104:Cfap251
|
APN |
5 |
123,440,761 (GRCm39) |
nonsense |
probably null |
|
IGL02160:Cfap251
|
APN |
5 |
123,394,081 (GRCm39) |
missense |
unknown |
|
IGL02238:Cfap251
|
APN |
5 |
123,440,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Cfap251
|
APN |
5 |
123,392,699 (GRCm39) |
unclassified |
probably benign |
|
IGL03183:Cfap251
|
APN |
5 |
123,392,682 (GRCm39) |
unclassified |
probably benign |
|
R0078:Cfap251
|
UTSW |
5 |
123,436,633 (GRCm39) |
missense |
probably benign |
0.04 |
R0207:Cfap251
|
UTSW |
5 |
123,421,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R0411:Cfap251
|
UTSW |
5 |
123,428,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Cfap251
|
UTSW |
5 |
123,425,476 (GRCm39) |
splice site |
probably null |
|
R0722:Cfap251
|
UTSW |
5 |
123,394,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Cfap251
|
UTSW |
5 |
123,392,673 (GRCm39) |
small deletion |
probably benign |
|
R1527:Cfap251
|
UTSW |
5 |
123,425,408 (GRCm39) |
missense |
probably benign |
0.19 |
R1924:Cfap251
|
UTSW |
5 |
123,440,802 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2022:Cfap251
|
UTSW |
5 |
123,411,853 (GRCm39) |
missense |
probably benign |
0.29 |
R2110:Cfap251
|
UTSW |
5 |
123,392,438 (GRCm39) |
unclassified |
probably benign |
|
R2112:Cfap251
|
UTSW |
5 |
123,392,438 (GRCm39) |
unclassified |
probably benign |
|
R2147:Cfap251
|
UTSW |
5 |
123,394,254 (GRCm39) |
missense |
probably benign |
0.01 |
R2258:Cfap251
|
UTSW |
5 |
123,421,411 (GRCm39) |
splice site |
probably null |
|
R2407:Cfap251
|
UTSW |
5 |
123,428,032 (GRCm39) |
missense |
probably benign |
0.11 |
R2418:Cfap251
|
UTSW |
5 |
123,392,331 (GRCm39) |
unclassified |
probably benign |
|
R2497:Cfap251
|
UTSW |
5 |
123,421,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Cfap251
|
UTSW |
5 |
123,394,169 (GRCm39) |
missense |
probably benign |
0.00 |
R3730:Cfap251
|
UTSW |
5 |
123,464,631 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3800:Cfap251
|
UTSW |
5 |
123,392,784 (GRCm39) |
unclassified |
probably benign |
|
R4018:Cfap251
|
UTSW |
5 |
123,460,517 (GRCm39) |
missense |
probably benign |
0.04 |
R4181:Cfap251
|
UTSW |
5 |
123,431,873 (GRCm39) |
missense |
probably benign |
0.33 |
R4302:Cfap251
|
UTSW |
5 |
123,431,873 (GRCm39) |
missense |
probably benign |
0.33 |
R4640:Cfap251
|
UTSW |
5 |
123,440,495 (GRCm39) |
missense |
probably benign |
0.00 |
R4701:Cfap251
|
UTSW |
5 |
123,460,676 (GRCm39) |
missense |
probably benign |
0.00 |
R4799:Cfap251
|
UTSW |
5 |
123,440,835 (GRCm39) |
missense |
probably benign |
0.04 |
R4812:Cfap251
|
UTSW |
5 |
123,425,368 (GRCm39) |
missense |
probably benign |
0.01 |
R4922:Cfap251
|
UTSW |
5 |
123,394,116 (GRCm39) |
missense |
probably benign |
0.00 |
R5123:Cfap251
|
UTSW |
5 |
123,411,696 (GRCm39) |
start gained |
probably benign |
|
R5314:Cfap251
|
UTSW |
5 |
123,460,626 (GRCm39) |
missense |
probably benign |
0.01 |
R5445:Cfap251
|
UTSW |
5 |
123,425,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Cfap251
|
UTSW |
5 |
123,392,508 (GRCm39) |
unclassified |
probably benign |
|
R5462:Cfap251
|
UTSW |
5 |
123,436,695 (GRCm39) |
critical splice donor site |
probably null |
|
R5514:Cfap251
|
UTSW |
5 |
123,425,829 (GRCm39) |
critical splice donor site |
probably null |
|
R5600:Cfap251
|
UTSW |
5 |
123,426,761 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5635:Cfap251
|
UTSW |
5 |
123,460,635 (GRCm39) |
missense |
probably benign |
0.25 |
R5767:Cfap251
|
UTSW |
5 |
123,436,584 (GRCm39) |
missense |
probably benign |
0.01 |
R5943:Cfap251
|
UTSW |
5 |
123,424,420 (GRCm39) |
missense |
probably benign |
0.13 |
R6000:Cfap251
|
UTSW |
5 |
123,392,435 (GRCm39) |
unclassified |
probably benign |
|
R6030:Cfap251
|
UTSW |
5 |
123,412,267 (GRCm39) |
missense |
probably damaging |
0.97 |
R6030:Cfap251
|
UTSW |
5 |
123,412,267 (GRCm39) |
missense |
probably damaging |
0.97 |
R6293:Cfap251
|
UTSW |
5 |
123,460,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Cfap251
|
UTSW |
5 |
123,440,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R6356:Cfap251
|
UTSW |
5 |
123,392,729 (GRCm39) |
unclassified |
probably benign |
|
R6427:Cfap251
|
UTSW |
5 |
123,464,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Cfap251
|
UTSW |
5 |
123,416,421 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6909:Cfap251
|
UTSW |
5 |
123,425,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7503:Cfap251
|
UTSW |
5 |
123,435,521 (GRCm39) |
nonsense |
probably null |
|
R7707:Cfap251
|
UTSW |
5 |
123,391,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7715:Cfap251
|
UTSW |
5 |
123,400,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7809:Cfap251
|
UTSW |
5 |
123,402,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Cfap251
|
UTSW |
5 |
123,392,322 (GRCm39) |
unclassified |
probably benign |
|
R7842:Cfap251
|
UTSW |
5 |
123,392,487 (GRCm39) |
missense |
unknown |
|
R7898:Cfap251
|
UTSW |
5 |
123,460,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R7967:Cfap251
|
UTSW |
5 |
123,421,579 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8004:Cfap251
|
UTSW |
5 |
123,392,513 (GRCm39) |
missense |
unknown |
|
R8068:Cfap251
|
UTSW |
5 |
123,394,229 (GRCm39) |
missense |
not run |
|
R8141:Cfap251
|
UTSW |
5 |
123,424,493 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8222:Cfap251
|
UTSW |
5 |
123,440,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R8242:Cfap251
|
UTSW |
5 |
123,411,914 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8303:Cfap251
|
UTSW |
5 |
123,460,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R8323:Cfap251
|
UTSW |
5 |
123,435,588 (GRCm39) |
missense |
probably benign |
0.16 |
R8773:Cfap251
|
UTSW |
5 |
123,411,913 (GRCm39) |
missense |
probably benign |
0.12 |
R8869:Cfap251
|
UTSW |
5 |
123,460,505 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8881:Cfap251
|
UTSW |
5 |
123,462,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8921:Cfap251
|
UTSW |
5 |
123,424,481 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9099:Cfap251
|
UTSW |
5 |
123,418,082 (GRCm39) |
intron |
probably benign |
|
R9236:Cfap251
|
UTSW |
5 |
123,428,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R9385:Cfap251
|
UTSW |
5 |
123,426,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Cfap251
|
UTSW |
5 |
123,460,557 (GRCm39) |
missense |
probably benign |
0.07 |
R9762:Cfap251
|
UTSW |
5 |
123,460,533 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Cfap251
|
UTSW |
5 |
123,392,317 (GRCm39) |
small insertion |
probably benign |
|
RF010:Cfap251
|
UTSW |
5 |
123,412,224 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF015:Cfap251
|
UTSW |
5 |
123,412,224 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF015:Cfap251
|
UTSW |
5 |
123,392,305 (GRCm39) |
small insertion |
probably benign |
|
RF017:Cfap251
|
UTSW |
5 |
123,391,953 (GRCm39) |
small insertion |
probably benign |
|
RF024:Cfap251
|
UTSW |
5 |
123,391,952 (GRCm39) |
small insertion |
probably benign |
|
RF024:Cfap251
|
UTSW |
5 |
123,391,951 (GRCm39) |
small insertion |
probably benign |
|
RF024:Cfap251
|
UTSW |
5 |
123,391,946 (GRCm39) |
small insertion |
probably benign |
|
X0062:Cfap251
|
UTSW |
5 |
123,412,300 (GRCm39) |
missense |
probably benign |
0.29 |
X0066:Cfap251
|
UTSW |
5 |
123,426,710 (GRCm39) |
missense |
probably benign |
0.05 |
|