Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
A |
G |
5: 113,331,092 (GRCm39) |
S1041P |
probably benign |
Het |
Aatf |
ACACACACACACACACACACACACACACACACACACACACACACACACAC |
ACACACACACACACACACACACACACACACACACACACACACACACACACAC |
11: 84,361,864 (GRCm39) |
|
probably null |
Het |
Asap1 |
A |
G |
15: 63,963,925 (GRCm39) |
V1091A |
probably damaging |
Het |
Asxl3 |
A |
G |
18: 22,657,281 (GRCm39) |
T1764A |
not run |
Het |
Bmp7 |
C |
A |
2: 172,781,784 (GRCm39) |
A27S |
probably benign |
Het |
Ccnh |
T |
A |
13: 85,359,991 (GRCm39) |
Y297* |
probably null |
Het |
Ccno |
C |
A |
13: 113,124,647 (GRCm39) |
D72E |
probably benign |
Het |
Cd70 |
T |
G |
17: 57,455,770 (GRCm39) |
T67P |
probably damaging |
Het |
Chml |
CTGTTTG |
CTG |
1: 175,514,966 (GRCm39) |
|
probably null |
Het |
Chst4 |
A |
G |
8: 110,757,545 (GRCm39) |
F106S |
probably damaging |
Het |
Cntnap3 |
A |
C |
13: 65,051,587 (GRCm39) |
L23R |
probably benign |
Het |
Crybg2 |
T |
A |
4: 133,814,910 (GRCm39) |
L1288H |
probably damaging |
Het |
Cse1l |
T |
A |
2: 166,777,591 (GRCm39) |
|
probably null |
Het |
Cyfip2 |
T |
C |
11: 46,133,177 (GRCm39) |
H841R |
probably damaging |
Het |
Cyp2c39 |
T |
C |
19: 39,549,405 (GRCm39) |
Y308H |
possibly damaging |
Het |
Cyp4f18 |
G |
A |
8: 72,742,487 (GRCm39) |
P498S |
possibly damaging |
Het |
Dennd1b |
G |
A |
1: 138,990,611 (GRCm39) |
E192K |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,566,775 (GRCm39) |
I97F |
|
Het |
Entpd3 |
A |
G |
9: 120,389,652 (GRCm39) |
R313G |
possibly damaging |
Het |
Erg28 |
G |
A |
12: 85,866,253 (GRCm39) |
T75I |
probably damaging |
Het |
Fam171a1 |
A |
G |
2: 3,226,421 (GRCm39) |
H518R |
probably benign |
Het |
Fam50b |
G |
A |
13: 34,931,084 (GRCm39) |
E187K |
possibly damaging |
Het |
Galntl6 |
T |
C |
8: 58,290,222 (GRCm39) |
E457G |
probably damaging |
Het |
Glt8d1 |
A |
T |
14: 30,732,296 (GRCm39) |
H192L |
probably damaging |
Het |
Gm15446 |
T |
A |
5: 110,091,165 (GRCm39) |
C472* |
probably null |
Het |
Gm28363 |
A |
T |
1: 117,625,228 (GRCm39) |
M1L |
unknown |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Gstp3 |
T |
A |
19: 4,108,746 (GRCm39) |
K45* |
probably null |
Het |
Hsd17b13 |
A |
G |
5: 104,113,681 (GRCm39) |
F258L |
possibly damaging |
Het |
Htt |
T |
C |
5: 35,021,993 (GRCm39) |
S1646P |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,028,976 (GRCm39) |
M326V |
probably benign |
Het |
Itpr3 |
T |
A |
17: 27,336,153 (GRCm39) |
I2293N |
probably damaging |
Het |
Klk1b8 |
A |
G |
7: 43,448,750 (GRCm39) |
|
probably null |
Het |
Kntc1 |
T |
A |
5: 123,922,290 (GRCm39) |
L963H |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,810,637 (GRCm39) |
L769* |
probably null |
Het |
Map3k13 |
A |
G |
16: 21,740,346 (GRCm39) |
S558G |
probably benign |
Het |
Mbd1 |
G |
A |
18: 74,407,128 (GRCm39) |
|
probably null |
Het |
Mep1a |
T |
C |
17: 43,790,126 (GRCm39) |
N408D |
probably benign |
Het |
Mtrf1 |
A |
G |
14: 79,644,378 (GRCm39) |
T229A |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,754,935 (GRCm38) |
S1603L |
unknown |
Het |
Myo1b |
A |
C |
1: 51,818,739 (GRCm39) |
I512S |
possibly damaging |
Het |
N4bp2 |
A |
G |
5: 65,964,446 (GRCm39) |
I832V |
probably benign |
Het |
Nadsyn1 |
T |
A |
7: 143,352,233 (GRCm39) |
K618* |
probably null |
Het |
Ncstn |
T |
C |
1: 171,903,023 (GRCm39) |
D87G |
probably benign |
Het |
Neurl4 |
T |
C |
11: 69,794,012 (GRCm39) |
V156A |
probably benign |
Het |
Nfasc |
C |
A |
1: 132,527,751 (GRCm39) |
G885V |
not run |
Het |
Nox4 |
A |
T |
7: 86,963,335 (GRCm39) |
Y180F |
possibly damaging |
Het |
Nuggc |
A |
G |
14: 65,860,700 (GRCm39) |
T449A |
probably benign |
Het |
Or6c209 |
A |
G |
10: 129,483,281 (GRCm39) |
I95V |
probably benign |
Het |
Pik3r4 |
T |
C |
9: 105,540,316 (GRCm39) |
S735P |
probably damaging |
Het |
Ppp1r9b |
T |
C |
11: 94,892,735 (GRCm39) |
I645T |
probably damaging |
Het |
Rras2 |
G |
A |
7: 113,716,783 (GRCm39) |
|
probably benign |
Het |
Rtel1 |
T |
C |
2: 180,962,822 (GRCm39) |
M25T |
probably damaging |
Het |
Serpinb3c |
T |
A |
1: 107,200,883 (GRCm39) |
Y178F |
possibly damaging |
Het |
Sh3bp2 |
A |
G |
5: 34,716,429 (GRCm39) |
H280R |
not run |
Het |
Six4 |
CT |
C |
12: 73,151,013 (GRCm39) |
|
probably benign |
Het |
Skor1 |
T |
C |
9: 63,053,783 (GRCm39) |
E62G |
probably damaging |
Het |
Slc22a22 |
T |
A |
15: 57,126,751 (GRCm39) |
N106I |
possibly damaging |
Het |
Slc44a4 |
T |
A |
17: 35,142,828 (GRCm39) |
|
probably null |
Het |
Sppl2c |
A |
G |
11: 104,079,342 (GRCm39) |
|
probably null |
Het |
Sptbn2 |
C |
G |
19: 4,799,040 (GRCm39) |
R2037G |
probably benign |
Het |
Stx5a |
T |
A |
19: 8,732,482 (GRCm39) |
W384R |
unknown |
Het |
Topaz1 |
A |
G |
9: 122,609,765 (GRCm39) |
Y1111C |
possibly damaging |
Het |
Ttbk1 |
T |
A |
17: 46,757,164 (GRCm39) |
M1157L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,578,489 (GRCm39) |
T24135A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,795,481 (GRCm39) |
E632G |
unknown |
Het |
Ttn |
T |
C |
2: 76,547,559 (GRCm39) |
T32204A |
probably benign |
Het |
Vmn2r109 |
T |
C |
17: 20,760,782 (GRCm39) |
I858M |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,272,869 (GRCm39) |
Q561L |
possibly damaging |
Het |
Yme1l1 |
A |
G |
2: 23,071,077 (GRCm39) |
D271G |
probably damaging |
Het |
Zfp629 |
A |
G |
7: 127,211,167 (GRCm39) |
F214S |
probably damaging |
Het |
Zfp709 |
A |
G |
8: 72,643,308 (GRCm39) |
I246V |
probably benign |
Het |
|
Other mutations in Arpin |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Arpin
|
APN |
7 |
79,577,423 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01393:Arpin
|
APN |
7 |
79,581,588 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02127:Arpin
|
APN |
7 |
79,577,941 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02553:Arpin
|
APN |
7 |
79,577,395 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2350:Arpin
|
UTSW |
7 |
79,581,553 (GRCm39) |
nonsense |
probably null |
|
R3821:Arpin
|
UTSW |
7 |
79,579,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R3924:Arpin
|
UTSW |
7 |
79,579,435 (GRCm39) |
missense |
probably benign |
0.02 |
R5287:Arpin
|
UTSW |
7 |
79,577,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R6353:Arpin
|
UTSW |
7 |
79,585,093 (GRCm39) |
start gained |
probably benign |
|
R8211:Arpin
|
UTSW |
7 |
79,584,992 (GRCm39) |
start codon destroyed |
probably damaging |
1.00 |
R8350:Arpin
|
UTSW |
7 |
79,581,615 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8367:Arpin
|
UTSW |
7 |
79,579,386 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9344:Arpin
|
UTSW |
7 |
79,577,983 (GRCm39) |
missense |
probably benign |
0.10 |
R9488:Arpin
|
UTSW |
7 |
79,584,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R9582:Arpin
|
UTSW |
7 |
79,585,038 (GRCm39) |
start gained |
probably benign |
|
R9700:Arpin
|
UTSW |
7 |
79,578,015 (GRCm39) |
missense |
probably damaging |
0.97 |
|