Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
C |
T |
7: 119,960,655 (GRCm39) |
R706C |
probably damaging |
Het |
Adcy3 |
T |
C |
12: 4,258,624 (GRCm39) |
F847S |
probably benign |
Het |
Alyref |
C |
G |
11: 120,486,758 (GRCm39) |
V168L |
probably damaging |
Het |
Arhgap28 |
G |
A |
17: 68,208,336 (GRCm39) |
A44V |
probably benign |
Het |
Asap3 |
C |
T |
4: 135,954,767 (GRCm39) |
R60* |
probably null |
Het |
Baz1b |
T |
A |
5: 135,245,593 (GRCm39) |
N347K |
probably benign |
Het |
Best2 |
T |
A |
8: 85,737,858 (GRCm39) |
N179I |
possibly damaging |
Het |
Bloc1s3 |
A |
G |
7: 19,241,483 (GRCm39) |
V15A |
possibly damaging |
Het |
Borcs5 |
A |
G |
6: 134,687,230 (GRCm39) |
H196R |
unknown |
Het |
Calhm3 |
A |
G |
19: 47,140,256 (GRCm39) |
L279P |
probably benign |
Het |
Cand1 |
A |
T |
10: 119,043,925 (GRCm39) |
|
probably benign |
Het |
Car15 |
T |
C |
16: 17,655,269 (GRCm39) |
D57G |
possibly damaging |
Het |
Casp12 |
G |
A |
9: 5,348,959 (GRCm39) |
|
probably null |
Het |
Cd93 |
T |
C |
2: 148,283,778 (GRCm39) |
T523A |
probably benign |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Ckap5 |
A |
G |
2: 91,386,837 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
G |
A |
9: 105,814,156 (GRCm39) |
R619W |
unknown |
Het |
Colec12 |
G |
A |
18: 9,859,975 (GRCm39) |
|
probably null |
Het |
Crmp1 |
G |
A |
5: 37,430,699 (GRCm39) |
V222I |
possibly damaging |
Het |
Crnkl1 |
G |
A |
2: 145,770,120 (GRCm39) |
A241V |
probably damaging |
Het |
Ctbp2 |
A |
G |
7: 132,616,756 (GRCm39) |
S60P |
probably benign |
Het |
Cyp2c68 |
T |
C |
19: 39,700,972 (GRCm39) |
Y282C |
probably benign |
Het |
Dhx36 |
T |
C |
3: 62,391,694 (GRCm39) |
I551V |
probably damaging |
Het |
Dlg5 |
T |
A |
14: 24,206,537 (GRCm39) |
|
probably benign |
Het |
Dlgap1 |
A |
T |
17: 71,068,306 (GRCm39) |
I300F |
probably damaging |
Het |
Dmd |
T |
A |
X: 82,874,123 (GRCm39) |
I1342N |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,061,704 (GRCm39) |
R2794* |
probably null |
Het |
Fcgr1 |
G |
A |
3: 96,194,386 (GRCm39) |
T167I |
probably damaging |
Het |
Fgl1 |
G |
T |
8: 41,650,387 (GRCm39) |
F187L |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,860,242 (GRCm39) |
V2096E |
probably benign |
Het |
Gm10647 |
A |
G |
9: 66,705,762 (GRCm39) |
|
probably benign |
Het |
Gm14226 |
G |
A |
2: 154,866,255 (GRCm39) |
D71N |
possibly damaging |
Het |
Grip2 |
A |
T |
6: 91,760,829 (GRCm39) |
I284N |
probably damaging |
Het |
Hirip3 |
A |
G |
7: 126,462,038 (GRCm39) |
R19G |
probably damaging |
Het |
Ift70b |
A |
G |
2: 75,767,586 (GRCm39) |
L389P |
probably damaging |
Het |
Irx5 |
A |
G |
8: 93,086,438 (GRCm39) |
N174D |
probably damaging |
Het |
Itgal |
A |
G |
7: 126,929,317 (GRCm39) |
D1078G |
probably damaging |
Het |
Khdc3 |
T |
C |
9: 73,010,519 (GRCm39) |
V123A |
possibly damaging |
Het |
Klhl13 |
A |
G |
X: 23,127,820 (GRCm39) |
|
probably benign |
Het |
Klhl42 |
T |
C |
6: 146,993,321 (GRCm39) |
S98P |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,670,298 (GRCm39) |
N602S |
possibly damaging |
Het |
Lrrd1 |
A |
T |
5: 3,901,488 (GRCm39) |
I598F |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,458,372 (GRCm39) |
T318A |
probably benign |
Het |
Mfsd6 |
A |
G |
1: 52,748,517 (GRCm39) |
F116S |
probably damaging |
Het |
Ncam1 |
T |
C |
9: 49,456,492 (GRCm39) |
I486V |
probably benign |
Het |
Nptx1 |
A |
G |
11: 119,434,006 (GRCm39) |
|
probably null |
Het |
Nrg1 |
T |
C |
8: 32,408,221 (GRCm39) |
Y4C |
probably damaging |
Het |
Nsf |
G |
A |
11: 103,773,702 (GRCm39) |
R271* |
probably null |
Het |
Or5d39 |
A |
G |
2: 87,979,641 (GRCm39) |
S241P |
possibly damaging |
Het |
Or8g24 |
T |
A |
9: 38,989,580 (GRCm39) |
I154F |
probably benign |
Het |
Or8k18 |
G |
C |
2: 86,085,440 (GRCm39) |
T199S |
probably benign |
Het |
Or8k21 |
T |
A |
2: 86,145,504 (GRCm39) |
N42I |
probably damaging |
Het |
Or8k24 |
A |
T |
2: 86,215,855 (GRCm39) |
H302Q |
probably benign |
Het |
Pax2 |
A |
G |
19: 44,777,271 (GRCm39) |
T155A |
probably benign |
Het |
Pdia4 |
A |
G |
6: 47,780,813 (GRCm39) |
Y212H |
probably damaging |
Het |
Pgr |
A |
G |
9: 8,946,954 (GRCm39) |
|
probably benign |
Het |
Pitpnm3 |
G |
T |
11: 71,965,450 (GRCm39) |
H112N |
possibly damaging |
Het |
Ppargc1b |
G |
T |
18: 61,431,848 (GRCm39) |
T1000K |
possibly damaging |
Het |
Psd3 |
C |
A |
8: 68,416,139 (GRCm39) |
C586F |
probably benign |
Het |
Ptprm |
A |
T |
17: 67,247,575 (GRCm39) |
S587T |
probably benign |
Het |
Rabep2 |
A |
T |
7: 126,037,736 (GRCm39) |
R169S |
possibly damaging |
Het |
Rad21l |
T |
C |
2: 151,497,179 (GRCm39) |
R309G |
probably benign |
Het |
Rbm12 |
T |
C |
2: 155,939,133 (GRCm39) |
R380G |
probably damaging |
Het |
Selp |
A |
G |
1: 163,954,081 (GRCm39) |
N127S |
probably benign |
Het |
Slc12a2 |
A |
G |
18: 58,012,467 (GRCm39) |
T197A |
possibly damaging |
Het |
Slc22a18 |
C |
T |
7: 143,029,984 (GRCm39) |
T17I |
probably damaging |
Het |
Sptbn4 |
T |
C |
7: 27,065,868 (GRCm39) |
E2026G |
possibly damaging |
Het |
Srf |
A |
T |
17: 46,862,633 (GRCm39) |
M285K |
possibly damaging |
Het |
Tanc1 |
T |
C |
2: 59,622,156 (GRCm39) |
V425A |
possibly damaging |
Het |
Tle4 |
A |
T |
19: 14,493,721 (GRCm39) |
|
probably null |
Het |
Tmem132e |
A |
G |
11: 82,335,908 (GRCm39) |
R905G |
possibly damaging |
Het |
Tmem200c |
A |
T |
17: 69,147,983 (GRCm39) |
I189F |
probably damaging |
Het |
Trappc13 |
T |
C |
13: 104,311,150 (GRCm39) |
Q87R |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,673,219 (GRCm39) |
D511E |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,632,634 (GRCm39) |
I14140N |
possibly damaging |
Het |
Virma |
A |
G |
4: 11,513,907 (GRCm39) |
D587G |
probably benign |
Het |
Vmn1r72 |
A |
G |
7: 11,403,731 (GRCm39) |
L239P |
probably damaging |
Het |
Vmn2r68 |
A |
G |
7: 84,883,102 (GRCm39) |
F217L |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,881,041 (GRCm39) |
|
probably null |
Het |
Vrtn |
T |
C |
12: 84,695,973 (GRCm39) |
V241A |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,214,653 (GRCm39) |
E764G |
probably damaging |
Het |
Zranb3 |
A |
T |
1: 127,927,136 (GRCm39) |
V343D |
probably damaging |
Het |
|
Other mutations in Bfar |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Bfar
|
APN |
16 |
13,516,827 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01067:Bfar
|
APN |
16 |
13,503,105 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Bfar
|
APN |
16 |
13,505,251 (GRCm39) |
splice site |
probably benign |
|
IGL02727:Bfar
|
APN |
16 |
13,506,791 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03189:Bfar
|
APN |
16 |
13,505,365 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1167:Bfar
|
UTSW |
16 |
13,516,758 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1213:Bfar
|
UTSW |
16 |
13,505,308 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1620:Bfar
|
UTSW |
16 |
13,506,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R2193:Bfar
|
UTSW |
16 |
13,515,335 (GRCm39) |
missense |
probably benign |
|
R4578:Bfar
|
UTSW |
16 |
13,505,307 (GRCm39) |
missense |
probably benign |
0.20 |
R4789:Bfar
|
UTSW |
16 |
13,503,001 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R4819:Bfar
|
UTSW |
16 |
13,505,331 (GRCm39) |
nonsense |
probably null |
|
R5271:Bfar
|
UTSW |
16 |
13,510,261 (GRCm39) |
intron |
probably benign |
|
R6346:Bfar
|
UTSW |
16 |
13,519,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R7186:Bfar
|
UTSW |
16 |
13,510,371 (GRCm39) |
missense |
probably benign |
|
R7758:Bfar
|
UTSW |
16 |
13,519,985 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0021:Bfar
|
UTSW |
16 |
13,505,451 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Bfar
|
UTSW |
16 |
13,515,324 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Bfar
|
UTSW |
16 |
13,506,674 (GRCm39) |
missense |
probably benign |
0.03 |
|