Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
T |
C |
6: 124,333,380 (GRCm39) |
N72S |
possibly damaging |
Het |
A2m |
G |
A |
6: 121,653,862 (GRCm39) |
|
probably null |
Het |
Angptl3 |
A |
T |
4: 98,923,057 (GRCm39) |
|
probably benign |
Het |
Aox4 |
A |
G |
1: 58,301,746 (GRCm39) |
D1106G |
probably benign |
Het |
Capn13 |
G |
A |
17: 73,648,149 (GRCm39) |
|
probably benign |
Het |
Cep250 |
A |
G |
2: 155,832,191 (GRCm39) |
H1371R |
probably benign |
Het |
Chrna1 |
A |
T |
2: 73,400,789 (GRCm39) |
F247Y |
probably benign |
Het |
Col2a1 |
T |
C |
15: 97,879,923 (GRCm39) |
T813A |
unknown |
Het |
Dab2 |
T |
C |
15: 6,464,790 (GRCm39) |
V414A |
possibly damaging |
Het |
Dach2 |
T |
C |
X: 112,465,937 (GRCm39) |
|
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,396 (GRCm39) |
V385D |
probably damaging |
Het |
Fmnl1 |
A |
G |
11: 103,088,008 (GRCm39) |
|
probably null |
Het |
Gorasp2 |
G |
A |
2: 70,513,336 (GRCm39) |
G201D |
probably damaging |
Het |
Gp2 |
T |
A |
7: 119,050,783 (GRCm39) |
Q316L |
probably damaging |
Het |
Gpx8 |
T |
C |
13: 113,179,696 (GRCm39) |
I202V |
probably damaging |
Het |
Gsta3 |
A |
G |
1: 21,335,173 (GRCm39) |
K218R |
probably benign |
Het |
Lama3 |
C |
T |
18: 12,686,340 (GRCm39) |
T1195I |
probably benign |
Het |
Map3k12 |
T |
C |
15: 102,410,514 (GRCm39) |
R488G |
possibly damaging |
Het |
Mapt |
A |
T |
11: 104,173,259 (GRCm39) |
Y18F |
probably damaging |
Het |
Med21 |
T |
C |
6: 146,544,143 (GRCm39) |
V12A |
probably benign |
Het |
Mgat4b |
A |
G |
11: 50,124,936 (GRCm39) |
E457G |
possibly damaging |
Het |
Mybl1 |
T |
A |
1: 9,742,780 (GRCm39) |
K609N |
probably damaging |
Het |
Ncaph2 |
T |
G |
15: 89,247,858 (GRCm39) |
V75G |
probably benign |
Het |
Neb |
A |
G |
2: 52,068,049 (GRCm39) |
Y5795H |
probably benign |
Het |
Nup153 |
A |
G |
13: 46,854,459 (GRCm39) |
|
probably null |
Het |
Or6c215 |
T |
C |
10: 129,638,340 (GRCm39) |
D18G |
probably damaging |
Het |
Or6y1 |
T |
A |
1: 174,276,435 (GRCm39) |
I82N |
probably damaging |
Het |
Plekhf2 |
G |
T |
4: 10,990,703 (GRCm39) |
T213K |
probably benign |
Het |
Plekho2 |
C |
A |
9: 65,466,776 (GRCm39) |
G105W |
probably damaging |
Het |
Polr3b |
G |
A |
10: 84,512,816 (GRCm39) |
G566D |
probably damaging |
Het |
Rasgrf1 |
T |
C |
9: 89,892,504 (GRCm39) |
I1068T |
probably damaging |
Het |
Rnf213 |
A |
T |
11: 119,312,294 (GRCm39) |
E907V |
probably benign |
Het |
Runx1t1 |
C |
T |
4: 13,881,107 (GRCm39) |
S469F |
probably damaging |
Het |
Spata31e4 |
G |
T |
13: 50,857,200 (GRCm39) |
C946F |
possibly damaging |
Het |
Top1 |
A |
T |
2: 160,535,647 (GRCm39) |
D182V |
unknown |
Het |
Uckl1 |
T |
C |
2: 181,211,982 (GRCm39) |
T375A |
probably benign |
Het |
Usp53 |
A |
T |
3: 122,727,370 (GRCm39) |
|
probably benign |
Het |
Vmn2r61 |
T |
A |
7: 41,909,517 (GRCm39) |
I14N |
probably benign |
Het |
Wbp4 |
A |
T |
14: 79,707,558 (GRCm39) |
N184K |
probably damaging |
Het |
|
Other mutations in Fap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01095:Fap
|
APN |
2 |
62,354,545 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01420:Fap
|
APN |
2 |
62,334,846 (GRCm39) |
splice site |
probably benign |
|
IGL01485:Fap
|
APN |
2 |
62,374,655 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01987:Fap
|
APN |
2 |
62,359,020 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02198:Fap
|
APN |
2 |
62,385,142 (GRCm39) |
missense |
probably benign |
|
IGL02355:Fap
|
APN |
2 |
62,403,842 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02362:Fap
|
APN |
2 |
62,403,842 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03227:Fap
|
APN |
2 |
62,361,107 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03266:Fap
|
APN |
2 |
62,367,366 (GRCm39) |
missense |
probably benign |
|
IGL03406:Fap
|
APN |
2 |
62,372,466 (GRCm39) |
splice site |
probably benign |
|
mnemosyne
|
UTSW |
2 |
62,359,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467_Fap_571
|
UTSW |
2 |
62,347,964 (GRCm39) |
missense |
probably benign |
0.18 |
R4812_Fap_496
|
UTSW |
2 |
62,349,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R5661_fap_070
|
UTSW |
2 |
62,367,307 (GRCm39) |
intron |
probably benign |
|
ANU74:Fap
|
UTSW |
2 |
62,378,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Fap
|
UTSW |
2 |
62,333,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R0842:Fap
|
UTSW |
2 |
62,367,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Fap
|
UTSW |
2 |
62,347,964 (GRCm39) |
missense |
probably benign |
0.18 |
R1467:Fap
|
UTSW |
2 |
62,347,964 (GRCm39) |
missense |
probably benign |
0.18 |
R1591:Fap
|
UTSW |
2 |
62,384,201 (GRCm39) |
missense |
probably damaging |
0.99 |
R1671:Fap
|
UTSW |
2 |
62,384,179 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1674:Fap
|
UTSW |
2 |
62,349,349 (GRCm39) |
missense |
probably benign |
|
R1795:Fap
|
UTSW |
2 |
62,378,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Fap
|
UTSW |
2 |
62,359,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2032:Fap
|
UTSW |
2 |
62,372,581 (GRCm39) |
missense |
probably benign |
0.43 |
R2136:Fap
|
UTSW |
2 |
62,354,551 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3546:Fap
|
UTSW |
2 |
62,349,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Fap
|
UTSW |
2 |
62,349,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R3771:Fap
|
UTSW |
2 |
62,363,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Fap
|
UTSW |
2 |
62,376,994 (GRCm39) |
missense |
probably benign |
0.04 |
R3910:Fap
|
UTSW |
2 |
62,386,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R4306:Fap
|
UTSW |
2 |
62,361,051 (GRCm39) |
critical splice donor site |
probably null |
|
R4323:Fap
|
UTSW |
2 |
62,333,716 (GRCm39) |
missense |
probably damaging |
0.97 |
R4517:Fap
|
UTSW |
2 |
62,361,059 (GRCm39) |
missense |
probably benign |
0.01 |
R4793:Fap
|
UTSW |
2 |
62,374,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Fap
|
UTSW |
2 |
62,349,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Fap
|
UTSW |
2 |
62,374,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R5281:Fap
|
UTSW |
2 |
62,363,305 (GRCm39) |
critical splice donor site |
probably null |
|
R5661:Fap
|
UTSW |
2 |
62,367,307 (GRCm39) |
intron |
probably benign |
|
R5696:Fap
|
UTSW |
2 |
62,332,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Fap
|
UTSW |
2 |
62,359,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Fap
|
UTSW |
2 |
62,403,847 (GRCm39) |
missense |
probably benign |
|
R5907:Fap
|
UTSW |
2 |
62,374,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5944:Fap
|
UTSW |
2 |
62,372,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R5991:Fap
|
UTSW |
2 |
62,348,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R6110:Fap
|
UTSW |
2 |
62,385,114 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6270:Fap
|
UTSW |
2 |
62,378,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R6505:Fap
|
UTSW |
2 |
62,376,947 (GRCm39) |
nonsense |
probably null |
|
R6631:Fap
|
UTSW |
2 |
62,333,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Fap
|
UTSW |
2 |
62,334,944 (GRCm39) |
nonsense |
probably null |
|
R7138:Fap
|
UTSW |
2 |
62,372,522 (GRCm39) |
missense |
probably benign |
0.10 |
R7806:Fap
|
UTSW |
2 |
62,333,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R8000:Fap
|
UTSW |
2 |
62,333,142 (GRCm39) |
critical splice donor site |
probably null |
|
R8115:Fap
|
UTSW |
2 |
62,349,385 (GRCm39) |
missense |
probably benign |
0.07 |
R8737:Fap
|
UTSW |
2 |
62,342,777 (GRCm39) |
missense |
probably benign |
0.00 |
R8899:Fap
|
UTSW |
2 |
62,348,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Fap
|
UTSW |
2 |
62,378,165 (GRCm39) |
missense |
probably benign |
|
R8972:Fap
|
UTSW |
2 |
62,378,927 (GRCm39) |
missense |
probably benign |
0.02 |
R8998:Fap
|
UTSW |
2 |
62,367,368 (GRCm39) |
missense |
probably benign |
0.12 |
R8999:Fap
|
UTSW |
2 |
62,367,368 (GRCm39) |
missense |
probably benign |
0.12 |
R9418:Fap
|
UTSW |
2 |
62,385,181 (GRCm39) |
nonsense |
probably null |
|
R9521:Fap
|
UTSW |
2 |
62,372,500 (GRCm39) |
missense |
probably benign |
|
R9686:Fap
|
UTSW |
2 |
62,403,857 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0017:Fap
|
UTSW |
2 |
62,386,524 (GRCm39) |
missense |
probably benign |
0.04 |
X0026:Fap
|
UTSW |
2 |
62,342,734 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fap
|
UTSW |
2 |
62,359,118 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1177:Fap
|
UTSW |
2 |
62,332,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|