Other mutations in this stock |
Total: 127 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
GGTATTGCATTTCTTATCT |
G |
5: 4,031,214 (GRCm39) |
|
probably benign |
Homo |
Amfr |
C |
G |
8: 94,731,787 (GRCm39) |
G30R |
probably damaging |
Homo |
Anxa7 |
C |
T |
14: 20,519,479 (GRCm39) |
G113E |
probably damaging |
Homo |
Apc |
AGC |
AGCCAATAACGC |
18: 34,415,058 (GRCm39) |
|
probably benign |
Het |
Apc |
AATAAAGC |
AATAAAGCCGATAAAGC |
18: 34,415,053 (GRCm39) |
|
probably benign |
Het |
Apol6 |
TTT |
TTTGATT |
15: 76,935,643 (GRCm39) |
|
probably null |
Homo |
Arid1b |
CGG |
CGGTGG |
17: 5,045,864 (GRCm39) |
|
probably benign |
Het |
B430218F22Rik |
CGGCG |
CGGCGATGGCG |
13: 118,523,387 (GRCm39) |
|
probably benign |
Homo |
Blm |
CCTCCTCCTCCTCCTCCTCCTCCT |
CCTCCTCCTCCTTCTCCTCCTCCTCCTCCTCCTCCT |
7: 80,162,656 (GRCm39) |
|
probably benign |
Het |
Brd2 |
CTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA |
CAAAAAAAAAAAAAAA |
17: 34,335,310 (GRCm39) |
|
probably benign |
Het |
Btnl10 |
AAG |
AAGGAG |
11: 58,814,754 (GRCm39) |
|
probably benign |
Homo |
Cacna1a |
ACC |
ACCCCC |
8: 85,365,343 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCGCC |
8: 85,365,352 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCCCC |
8: 85,365,349 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
TGGC |
TGGCTGTGGCTGCGGC |
19: 47,129,713 (GRCm39) |
|
probably benign |
Het |
Ccdc15 |
C |
CTTTAT |
9: 37,226,454 (GRCm39) |
|
probably null |
Het |
Ccdc85c |
CCG |
CCGACG |
12: 108,240,875 (GRCm39) |
|
probably benign |
Het |
Ccnk |
TTCCCAC |
T |
12: 108,168,766 (GRCm39) |
|
probably benign |
Het |
Cdhr2 |
AGTC |
AGTCGTC |
13: 54,873,737 (GRCm39) |
|
probably benign |
Homo |
Cdk15 |
A |
ATCTAAAAGG |
1: 59,296,982 (GRCm39) |
|
probably benign |
Homo |
Cdx1 |
GCTG |
GCTGCTCCTG |
18: 61,152,953 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
T |
C |
7: 139,218,711 (GRCm39) |
|
probably benign |
Homo |
Cgref1 |
TTC |
TTCGTC |
5: 31,091,120 (GRCm39) |
|
probably benign |
Het |
Cgref1 |
CTT |
CTTATT |
5: 31,091,122 (GRCm39) |
|
probably null |
Homo |
Cluh |
G |
GACTGAA |
11: 74,560,358 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
AGCCCC |
AGCCCCCGCCCC |
11: 101,080,395 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
AGCC |
AGCCCCCGCC |
11: 101,080,419 (GRCm39) |
|
probably benign |
Het |
Cpne1 |
CCTACT |
CCT |
2: 155,915,422 (GRCm39) |
|
probably benign |
Homo |
Cracdl |
T |
A |
1: 37,664,116 (GRCm39) |
E594V |
probably benign |
Homo |
Cracdl |
C |
A |
1: 37,664,117 (GRCm39) |
E594* |
probably null |
Homo |
Cttnbp2 |
CTGCTG |
CTGCTGTTGCTG |
6: 18,367,461 (GRCm39) |
|
probably benign |
Het |
Cul9 |
TCC |
TCCGCC |
17: 46,811,782 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGGGGAGG |
9: 99,465,727 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,465,739 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
GGAGGA |
GGAGGAAGAGGA |
9: 99,465,749 (GRCm39) |
|
probably benign |
Het |
Dhx8 |
CG |
CGAGACAG |
11: 101,629,020 (GRCm39) |
|
probably benign |
Homo |
Dhx8 |
CG |
CGAGACAG |
11: 101,629,032 (GRCm39) |
|
probably benign |
Het |
Dhx8 |
G |
GAGACCC |
11: 101,629,033 (GRCm39) |
|
probably benign |
Het |
Dhx8 |
AGACCG |
AGACCGTGACCG |
11: 101,629,010 (GRCm39) |
|
probably benign |
Homo |
Dhx8 |
AGACCGGGACCGGGACCGGGACCGGGAC |
AGACCGGGACCGGGAC |
11: 101,629,016 (GRCm39) |
|
probably benign |
Het |
Dspp |
CGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAG |
CGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAG |
5: 104,326,254 (GRCm39) |
|
probably benign |
Het |
Dusp10 |
G |
T |
1: 183,769,253 (GRCm39) |
C73F |
probably damaging |
Homo |
Erich3 |
GA |
GAGAA |
3: 154,469,150 (GRCm39) |
|
probably benign |
Homo |
Ermn |
CTT |
CTTGTT |
2: 57,938,086 (GRCm39) |
|
probably benign |
Het |
Fgd6 |
GGAT |
G |
10: 93,880,182 (GRCm39) |
|
probably benign |
Homo |
G530012D18Rik |
GAGAGAGAGAGAGAGAGACAGAGA |
GAGAGA |
1: 85,504,901 (GRCm39) |
|
probably benign |
Homo |
Gar1 |
GCCGCCTCCGCC |
GCCGCC |
3: 129,624,353 (GRCm39) |
|
probably benign |
Homo |
Gatad2b |
AGAC |
A |
3: 90,249,224 (GRCm39) |
|
probably benign |
Het |
Gigyf2 |
C |
T |
1: 87,356,307 (GRCm39) |
|
probably benign |
Het |
Gm16519 |
A |
AGAT |
17: 71,236,333 (GRCm39) |
|
probably benign |
Homo |
Gm4340 |
AGC |
AGCGGC |
10: 104,031,946 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
GCA |
GCATCA |
10: 104,031,947 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
AGC |
AGCGGC |
10: 104,031,943 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
AGGAAG |
AGGAAGCGGAAG |
17: 79,149,597 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
GAAGAG |
GAAGAGCAAGAG |
17: 79,149,605 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
GG |
GGCAGACG |
17: 79,149,610 (GRCm39) |
|
probably benign |
Het |
Hoxa10 |
T |
A |
6: 52,211,166 (GRCm39) |
Q250L |
possibly damaging |
Homo |
Igkv12-89 |
GCA |
GCAGCAGCAACA |
6: 68,812,264 (GRCm39) |
|
probably benign |
Homo |
Igsf10 |
G |
A |
3: 59,226,531 (GRCm39) |
R2381C |
probably damaging |
Homo |
Il17rd |
GGC |
GGCAGC |
14: 26,804,635 (GRCm39) |
|
probably benign |
Het |
Ints5 |
G |
A |
19: 8,874,594 (GRCm39) |
R851Q |
probably benign |
Het |
Isg20l2 |
AGA |
AGAGGA |
3: 87,839,020 (GRCm39) |
|
probably benign |
Het |
Kcng4 |
G |
T |
8: 120,360,258 (GRCm39) |
Y39* |
probably null |
Homo |
Kifc5b |
A |
C |
17: 27,143,191 (GRCm39) |
E321A |
probably benign |
Het |
Klra2 |
TCCACAG |
TCCACAGAAACCCACAG |
6: 131,198,809 (GRCm39) |
|
probably null |
Homo |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,794 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,285,786 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCACCTCC |
7: 30,285,791 (GRCm39) |
|
probably benign |
Het |
Krt10 |
ACC |
ACCACCTCC |
11: 99,280,093 (GRCm39) |
|
probably benign |
Het |
Las1l |
GA |
GAGAA |
X: 94,984,438 (GRCm39) |
|
probably benign |
Het |
Lce1m |
AC |
ACTGCTGCTGCCGC |
3: 92,925,459 (GRCm39) |
|
probably benign |
Het |
Leo1 |
GTACCATGCA |
G |
9: 75,357,855 (GRCm39) |
|
probably benign |
Het |
Lkaaear1 |
CA |
CATCTCCAGCTCTA |
2: 181,339,364 (GRCm39) |
|
probably benign |
Het |
Maml2 |
ACAGCAGCAGCAACAGCAGCAGCAGCAGCA |
ACAGCAACAGCAGCAGCAGCAGCA |
9: 13,532,752 (GRCm39) |
|
probably benign |
Homo |
Med12l |
CAG |
CAGTAG |
3: 59,183,384 (GRCm39) |
|
probably null |
Het |
Mgat4e |
GTCGTAGTCATCGT |
GTCGT |
1: 134,468,735 (GRCm39) |
|
probably benign |
Homo |
Mn1 |
GCA |
GCAACA |
5: 111,567,576 (GRCm39) |
|
probably benign |
Het |
Morn4 |
AGGCAGTGAG |
AGGCAGTGAGTCTGGCAGTGAG |
19: 42,064,548 (GRCm39) |
|
probably benign |
Het |
Nat8f2 |
T |
A |
6: 85,844,668 (GRCm39) |
L231F |
possibly damaging |
Homo |
Noc2l |
C |
CTGA |
4: 156,324,558 (GRCm39) |
|
probably benign |
Het |
Nrg3 |
T |
TAGACAC |
14: 38,119,228 (GRCm39) |
|
probably benign |
Het |
Or8b41 |
A |
G |
9: 38,054,484 (GRCm39) |
I13V |
probably benign |
Homo |
Piezo1 |
G |
A |
8: 123,222,308 (GRCm39) |
R503W |
probably damaging |
Homo |
Pih1d2 |
CTCTTGCGAGGATC |
CTC |
9: 50,532,927 (GRCm39) |
|
probably null |
Homo |
Pik3ap1 |
G |
GGAA |
19: 41,270,385 (GRCm39) |
|
probably benign |
Het |
Ppp1r3f |
C |
A |
X: 7,426,575 (GRCm39) |
G562V |
probably damaging |
Homo |
Ptms |
TTC |
TTCGTC |
6: 124,891,422 (GRCm39) |
|
probably benign |
Het |
Ptpn23 |
G |
T |
9: 110,216,701 (GRCm39) |
P1052T |
probably benign |
Homo |
Qrich2 |
AACT |
A |
11: 116,347,025 (GRCm39) |
|
probably benign |
Homo |
Raet1d |
A |
ATATCCTCTCTGG |
10: 22,246,814 (GRCm39) |
|
probably benign |
Het |
Rbm33 |
AGCAGCAGCAGCACCAGCCGCAGCAGCAGCA |
AGCAGCAGCAGCA |
5: 28,599,166 (GRCm39) |
|
probably benign |
Homo |
Rrbp1 |
TGCTTCTCAAAGGTGGCTGCCTTGGCTTC |
TGCTTC |
2: 143,809,376 (GRCm39) |
|
probably null |
Het |
Sbp |
CAACAAAGATGCTGA |
CAACAAAGATGCTGAGAACAAAGATGCTGA |
17: 24,164,338 (GRCm39) |
|
probably benign |
Het |
Setd1a |
G |
A |
7: 127,384,498 (GRCm39) |
|
probably benign |
Het |
Sfswap |
CCCACTCAG |
CCCACTCAGTCCACTCAG |
5: 129,646,812 (GRCm39) |
|
probably benign |
Het |
Sfswap |
CCACTCAGC |
CCACTCAGCTCACTCAGC |
5: 129,646,813 (GRCm39) |
|
probably benign |
Het |
Sh3pxd2b |
T |
TGTCTGC |
11: 32,373,065 (GRCm39) |
|
probably benign |
Homo |
Six3 |
CGG |
CGGGGG |
17: 85,928,790 (GRCm39) |
|
probably benign |
Het |
Slc12a1 |
C |
CTTTGGCCACAACACG |
2: 124,996,136 (GRCm39) |
|
probably benign |
Homo |
Slc26a8 |
CTCTCTG |
C |
17: 28,857,290 (GRCm39) |
|
probably benign |
Het |
Spata31h1 |
TTCAGT |
TT |
10: 82,121,303 (GRCm39) |
|
probably null |
Homo |
Srebf2 |
G |
T |
15: 82,069,536 (GRCm39) |
A693S |
probably damaging |
Homo |
Sry |
ACTG |
ACTGCTG |
Y: 2,662,818 (GRCm39) |
|
probably benign |
Het |
Sry |
TGCTG |
TGCTGCTG |
Y: 2,662,832 (GRCm39) |
|
probably benign |
Homo |
Ston1 |
G |
A |
17: 88,942,953 (GRCm39) |
V120M |
probably benign |
Homo |
Supt20 |
CAGCAG |
CAGCAGGAGCAG |
3: 54,635,070 (GRCm39) |
|
probably benign |
Het |
Tbl3 |
TG |
TGTGG |
17: 24,921,518 (GRCm39) |
|
probably benign |
Homo |
Tctn3 |
AG |
AGAAGCCG |
19: 40,595,646 (GRCm39) |
|
probably benign |
Het |
Tesk1 |
CCC |
CCCACC |
4: 43,447,002 (GRCm39) |
|
probably benign |
Homo |
Tmc2 |
T |
G |
2: 130,082,116 (GRCm39) |
V433G |
probably damaging |
Het |
Tmprss13 |
G |
A |
9: 45,239,856 (GRCm39) |
A55T |
unknown |
Het |
Tnfaip8 |
ACACACACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
AC |
18: 50,179,906 (GRCm39) |
|
probably null |
Homo |
Tob1 |
CAG |
CAGAAG |
11: 94,105,294 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,301 (GRCm39) |
|
probably benign |
Het |
Tpsab1 |
TTGCACCTCCT |
TT |
17: 25,562,756 (GRCm39) |
|
probably benign |
Homo |
Triobp |
GTC |
GTCTTC |
15: 78,877,589 (GRCm39) |
|
probably benign |
Het |
Ubtf |
CCT |
CCTACT |
11: 102,197,774 (GRCm39) |
|
probably null |
Het |
Vps13b |
G |
T |
15: 35,847,103 (GRCm39) |
A2629S |
probably damaging |
Homo |
Xpnpep3 |
G |
C |
15: 81,311,623 (GRCm39) |
D110H |
possibly damaging |
Het |
Zc3h13 |
CGAGATGTG |
CGAGATGTGTGAGATGTG |
14: 75,561,041 (GRCm39) |
|
probably null |
Homo |
Zfhx3 |
GCAACAGCA |
GCAACAGCAACAACAGCA |
8: 109,682,726 (GRCm39) |
|
probably benign |
Homo |
Zfp26 |
C |
A |
9: 20,349,842 (GRCm39) |
A241S |
probably benign |
Homo |
Zfp598 |
ACCACC |
ACCACCTCCACC |
17: 24,899,750 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
ACCACC |
ACCACCCCCACC |
17: 24,899,759 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCACC |
2: 174,487,264 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
CTC |
CTCGTC |
2: 174,487,275 (GRCm39) |
|
probably benign |
Het |
Zfp978 |
G |
T |
4: 147,475,401 (GRCm39) |
S316I |
probably benign |
Het |
|
Other mutations in Zfp335 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Zfp335
|
APN |
2 |
164,734,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00921:Zfp335
|
APN |
2 |
164,736,696 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00980:Zfp335
|
APN |
2 |
164,744,594 (GRCm39) |
nonsense |
probably null |
|
IGL01145:Zfp335
|
APN |
2 |
164,749,422 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01568:Zfp335
|
APN |
2 |
164,736,708 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01612:Zfp335
|
APN |
2 |
164,752,540 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02138:Zfp335
|
APN |
2 |
164,735,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02675:Zfp335
|
APN |
2 |
164,752,609 (GRCm39) |
missense |
probably benign |
|
IGL03206:Zfp335
|
APN |
2 |
164,734,601 (GRCm39) |
splice site |
probably benign |
|
IGL03269:Zfp335
|
APN |
2 |
164,742,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03306:Zfp335
|
APN |
2 |
164,737,904 (GRCm39) |
splice site |
probably benign |
|
FR4342:Zfp335
|
UTSW |
2 |
164,749,397 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Zfp335
|
UTSW |
2 |
164,749,385 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Zfp335
|
UTSW |
2 |
164,749,397 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Zfp335
|
UTSW |
2 |
164,749,392 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfp335
|
UTSW |
2 |
164,749,404 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfp335
|
UTSW |
2 |
164,749,395 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfp335
|
UTSW |
2 |
164,749,394 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Zfp335
|
UTSW |
2 |
164,749,398 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Zfp335
|
UTSW |
2 |
164,749,394 (GRCm39) |
small insertion |
probably benign |
|
PIT4403001:Zfp335
|
UTSW |
2 |
164,735,636 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0005:Zfp335
|
UTSW |
2 |
164,751,222 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0101:Zfp335
|
UTSW |
2 |
164,741,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Zfp335
|
UTSW |
2 |
164,738,065 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0211:Zfp335
|
UTSW |
2 |
164,749,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Zfp335
|
UTSW |
2 |
164,749,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0533:Zfp335
|
UTSW |
2 |
164,749,842 (GRCm39) |
nonsense |
probably null |
|
R0865:Zfp335
|
UTSW |
2 |
164,741,415 (GRCm39) |
splice site |
probably null |
|
R1023:Zfp335
|
UTSW |
2 |
164,734,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1029:Zfp335
|
UTSW |
2 |
164,734,598 (GRCm39) |
splice site |
probably benign |
|
R1052:Zfp335
|
UTSW |
2 |
164,749,388 (GRCm39) |
small deletion |
probably benign |
|
R1106:Zfp335
|
UTSW |
2 |
164,749,471 (GRCm39) |
small deletion |
probably benign |
|
R1146:Zfp335
|
UTSW |
2 |
164,738,043 (GRCm39) |
missense |
probably benign |
0.01 |
R1146:Zfp335
|
UTSW |
2 |
164,738,043 (GRCm39) |
missense |
probably benign |
0.01 |
R1274:Zfp335
|
UTSW |
2 |
164,749,388 (GRCm39) |
small deletion |
probably benign |
|
R1386:Zfp335
|
UTSW |
2 |
164,740,161 (GRCm39) |
missense |
probably benign |
0.00 |
R1433:Zfp335
|
UTSW |
2 |
164,741,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R1813:Zfp335
|
UTSW |
2 |
164,734,525 (GRCm39) |
missense |
probably damaging |
0.99 |
R1959:Zfp335
|
UTSW |
2 |
164,736,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R2372:Zfp335
|
UTSW |
2 |
164,736,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Zfp335
|
UTSW |
2 |
164,742,026 (GRCm39) |
splice site |
probably null |
|
R3937:Zfp335
|
UTSW |
2 |
164,752,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R3946:Zfp335
|
UTSW |
2 |
164,734,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Zfp335
|
UTSW |
2 |
164,752,558 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Zfp335
|
UTSW |
2 |
164,743,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4020:Zfp335
|
UTSW |
2 |
164,743,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4668:Zfp335
|
UTSW |
2 |
164,742,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Zfp335
|
UTSW |
2 |
164,736,588 (GRCm39) |
missense |
probably benign |
|
R5038:Zfp335
|
UTSW |
2 |
164,752,564 (GRCm39) |
nonsense |
probably null |
|
R5245:Zfp335
|
UTSW |
2 |
164,736,678 (GRCm39) |
missense |
probably benign |
|
R5411:Zfp335
|
UTSW |
2 |
164,744,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R5422:Zfp335
|
UTSW |
2 |
164,749,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5968:Zfp335
|
UTSW |
2 |
164,734,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Zfp335
|
UTSW |
2 |
164,737,018 (GRCm39) |
splice site |
probably null |
|
R6551:Zfp335
|
UTSW |
2 |
164,751,285 (GRCm39) |
missense |
probably benign |
|
R6927:Zfp335
|
UTSW |
2 |
164,735,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:Zfp335
|
UTSW |
2 |
164,736,795 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6995:Zfp335
|
UTSW |
2 |
164,735,210 (GRCm39) |
nonsense |
probably null |
|
R7174:Zfp335
|
UTSW |
2 |
164,744,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Zfp335
|
UTSW |
2 |
164,735,164 (GRCm39) |
critical splice donor site |
probably null |
|
R7296:Zfp335
|
UTSW |
2 |
164,742,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R7322:Zfp335
|
UTSW |
2 |
164,752,741 (GRCm39) |
start codon destroyed |
probably null |
0.90 |
R7504:Zfp335
|
UTSW |
2 |
164,751,338 (GRCm39) |
missense |
probably benign |
0.27 |
R7560:Zfp335
|
UTSW |
2 |
164,737,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Zfp335
|
UTSW |
2 |
164,734,459 (GRCm39) |
critical splice donor site |
probably null |
|
R8064:Zfp335
|
UTSW |
2 |
164,749,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8208:Zfp335
|
UTSW |
2 |
164,735,536 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8228:Zfp335
|
UTSW |
2 |
164,746,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Zfp335
|
UTSW |
2 |
164,739,973 (GRCm39) |
missense |
probably damaging |
0.98 |
R8688:Zfp335
|
UTSW |
2 |
164,734,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R8803:Zfp335
|
UTSW |
2 |
164,751,290 (GRCm39) |
missense |
probably benign |
0.14 |
R9266:Zfp335
|
UTSW |
2 |
164,738,007 (GRCm39) |
missense |
probably benign |
0.33 |
R9352:Zfp335
|
UTSW |
2 |
164,742,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R9487:Zfp335
|
UTSW |
2 |
164,735,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R9752:Zfp335
|
UTSW |
2 |
164,749,347 (GRCm39) |
critical splice donor site |
probably null |
|
RF031:Zfp335
|
UTSW |
2 |
164,749,383 (GRCm39) |
small insertion |
probably benign |
|
|