Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd13 |
A |
G |
8: 10,038,075 (GRCm39) |
H224R |
probably benign |
Het |
Anapc10 |
T |
C |
8: 80,446,374 (GRCm39) |
F68S |
probably damaging |
Het |
Arid2 |
A |
G |
15: 96,268,830 (GRCm39) |
N981S |
probably benign |
Het |
Bmerb1 |
T |
A |
16: 13,804,670 (GRCm39) |
S6T |
possibly damaging |
Het |
Cfap73 |
A |
G |
5: 120,772,276 (GRCm39) |
F9L |
probably damaging |
Het |
Chd3 |
A |
C |
11: 69,245,296 (GRCm39) |
L1141V |
probably damaging |
Het |
Daam1 |
C |
T |
12: 72,036,582 (GRCm39) |
L1052F |
possibly damaging |
Het |
Dmxl1 |
C |
T |
18: 50,027,041 (GRCm39) |
R2050C |
probably damaging |
Het |
Dpp10 |
G |
A |
1: 123,295,385 (GRCm39) |
Q552* |
probably null |
Het |
Dysf |
A |
G |
6: 84,041,876 (GRCm39) |
D160G |
possibly damaging |
Het |
Ecrg4 |
C |
A |
1: 43,781,551 (GRCm39) |
N144K |
probably damaging |
Het |
Firrm |
T |
C |
1: 163,804,318 (GRCm39) |
I338M |
probably damaging |
Het |
Foxp1 |
TTGCTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGCTGCTGCTG |
6: 99,052,926 (GRCm39) |
|
probably benign |
Het |
Ftcd |
T |
C |
10: 76,425,073 (GRCm39) |
I518T |
probably benign |
Het |
Gapdh |
A |
G |
6: 125,139,236 (GRCm39) |
S248P |
probably damaging |
Het |
Gm5592 |
C |
G |
7: 40,939,153 (GRCm39) |
P812A |
probably damaging |
Het |
Grik2 |
G |
A |
10: 49,232,085 (GRCm39) |
L482F |
probably damaging |
Het |
Gzmg |
C |
T |
14: 56,394,288 (GRCm39) |
G202D |
probably damaging |
Het |
Hectd4 |
G |
A |
5: 121,491,574 (GRCm39) |
A3671T |
possibly damaging |
Het |
Hexa |
G |
T |
9: 59,465,355 (GRCm39) |
W203C |
probably damaging |
Het |
Igdcc4 |
A |
T |
9: 65,042,700 (GRCm39) |
T1217S |
probably benign |
Het |
Ipo7 |
A |
G |
7: 109,646,272 (GRCm39) |
D557G |
probably damaging |
Het |
Irx3 |
T |
A |
8: 92,526,463 (GRCm39) |
T414S |
probably benign |
Het |
Jakmip1 |
G |
A |
5: 37,344,498 (GRCm39) |
E1313K |
probably damaging |
Het |
Kbtbd12 |
T |
C |
6: 88,595,248 (GRCm39) |
D194G |
probably damaging |
Het |
Klk6 |
T |
C |
7: 43,476,298 (GRCm39) |
L46P |
probably damaging |
Het |
Krt86 |
T |
C |
15: 101,374,817 (GRCm39) |
I329T |
probably benign |
Het |
Mroh5 |
A |
G |
15: 73,661,817 (GRCm39) |
|
probably null |
Het |
Mtrf1 |
T |
C |
14: 79,650,521 (GRCm39) |
V323A |
probably damaging |
Het |
Oas3 |
A |
T |
5: 120,896,939 (GRCm39) |
I894N |
probably damaging |
Het |
Oplah |
C |
T |
15: 76,185,053 (GRCm39) |
V887I |
possibly damaging |
Het |
Pag1 |
T |
C |
3: 9,764,848 (GRCm39) |
T102A |
probably benign |
Het |
Pcnx1 |
C |
T |
12: 82,009,496 (GRCm39) |
A1181V |
possibly damaging |
Het |
Pkdrej |
G |
T |
15: 85,701,510 (GRCm39) |
Y1475* |
probably null |
Het |
Pla2g5 |
A |
G |
4: 138,527,964 (GRCm39) |
S101P |
probably benign |
Het |
Plekha4 |
C |
A |
7: 45,184,241 (GRCm39) |
A76E |
probably damaging |
Het |
Plk2 |
T |
C |
13: 110,536,325 (GRCm39) |
I592T |
probably benign |
Het |
Ppp2r3c |
T |
A |
12: 55,345,252 (GRCm39) |
R79* |
probably null |
Het |
Ppp2r3d |
A |
T |
9: 101,090,061 (GRCm39) |
H87Q |
probably benign |
Het |
Prpf40b |
C |
T |
15: 99,212,784 (GRCm39) |
R627W |
probably damaging |
Het |
Prrt4 |
G |
T |
6: 29,176,551 (GRCm39) |
T258K |
possibly damaging |
Het |
Rhpn2 |
T |
A |
7: 35,083,194 (GRCm39) |
|
probably null |
Het |
Slc11a1 |
T |
A |
1: 74,423,244 (GRCm39) |
I365N |
probably damaging |
Het |
Slc7a7 |
C |
T |
14: 54,612,108 (GRCm39) |
G265D |
possibly damaging |
Het |
Thsd7a |
T |
A |
6: 12,555,636 (GRCm39) |
T83S |
possibly damaging |
Het |
Tnfaip3 |
T |
G |
10: 18,881,324 (GRCm39) |
T321P |
probably benign |
Het |
Tnrc6b |
C |
T |
15: 80,808,320 (GRCm39) |
P1623L |
possibly damaging |
Het |
Trpa1 |
T |
C |
1: 14,982,601 (GRCm39) |
N85S |
probably benign |
Het |
Trrap |
C |
T |
5: 144,788,066 (GRCm39) |
R3544* |
probably null |
Het |
Ttf2 |
A |
T |
3: 100,859,869 (GRCm39) |
V695E |
probably benign |
Het |
Ttll4 |
A |
G |
1: 74,720,512 (GRCm39) |
E509G |
probably damaging |
Het |
Vdr |
T |
C |
15: 97,767,709 (GRCm39) |
I94V |
probably damaging |
Het |
Wdfy3 |
G |
T |
5: 102,031,911 (GRCm39) |
Q2304K |
possibly damaging |
Het |
Zfp663 |
T |
C |
2: 165,200,935 (GRCm39) |
Y33C |
probably damaging |
Het |
|
Other mutations in Tln2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Tln2
|
APN |
9 |
67,251,469 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01110:Tln2
|
APN |
9 |
67,157,864 (GRCm39) |
nonsense |
probably null |
|
IGL01112:Tln2
|
APN |
9 |
67,219,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01307:Tln2
|
APN |
9 |
67,302,749 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01374:Tln2
|
APN |
9 |
67,169,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01625:Tln2
|
APN |
9 |
67,277,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01865:Tln2
|
APN |
9 |
67,157,896 (GRCm39) |
nonsense |
probably null |
|
IGL01999:Tln2
|
APN |
9 |
67,299,787 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02002:Tln2
|
APN |
9 |
67,263,980 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02005:Tln2
|
APN |
9 |
67,299,787 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02015:Tln2
|
APN |
9 |
67,268,721 (GRCm39) |
splice site |
probably benign |
|
IGL02368:Tln2
|
APN |
9 |
67,148,092 (GRCm39) |
splice site |
probably benign |
|
IGL02444:Tln2
|
APN |
9 |
67,165,874 (GRCm39) |
splice site |
probably benign |
|
IGL02646:Tln2
|
APN |
9 |
67,163,278 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02744:Tln2
|
APN |
9 |
67,136,658 (GRCm39) |
nonsense |
probably null |
|
IGL02869:Tln2
|
APN |
9 |
67,128,807 (GRCm39) |
splice site |
probably benign |
|
IGL02930:Tln2
|
APN |
9 |
67,300,944 (GRCm39) |
nonsense |
probably null |
|
IGL03100:Tln2
|
APN |
9 |
67,203,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03326:Tln2
|
APN |
9 |
67,241,539 (GRCm39) |
missense |
possibly damaging |
0.67 |
Harrier
|
UTSW |
9 |
67,237,834 (GRCm39) |
nonsense |
probably null |
|
Marsh
|
UTSW |
9 |
67,179,936 (GRCm39) |
missense |
probably benign |
0.19 |
BB008:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
BB018:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
R0047:Tln2
|
UTSW |
9 |
67,147,954 (GRCm39) |
splice site |
probably benign |
|
R0047:Tln2
|
UTSW |
9 |
67,147,954 (GRCm39) |
splice site |
probably benign |
|
R0107:Tln2
|
UTSW |
9 |
67,277,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Tln2
|
UTSW |
9 |
67,262,479 (GRCm39) |
missense |
probably benign |
0.22 |
R0884:Tln2
|
UTSW |
9 |
67,278,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0947:Tln2
|
UTSW |
9 |
67,203,095 (GRCm39) |
missense |
probably benign |
0.08 |
R0989:Tln2
|
UTSW |
9 |
67,136,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1486:Tln2
|
UTSW |
9 |
67,219,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1527:Tln2
|
UTSW |
9 |
67,179,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1584:Tln2
|
UTSW |
9 |
67,203,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Tln2
|
UTSW |
9 |
67,213,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1656:Tln2
|
UTSW |
9 |
67,134,389 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1707:Tln2
|
UTSW |
9 |
67,283,089 (GRCm39) |
missense |
probably benign |
0.00 |
R1749:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1751:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1761:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1767:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1815:Tln2
|
UTSW |
9 |
67,136,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Tln2
|
UTSW |
9 |
67,249,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Tln2
|
UTSW |
9 |
67,269,969 (GRCm39) |
nonsense |
probably null |
|
R1964:Tln2
|
UTSW |
9 |
67,249,417 (GRCm39) |
missense |
probably benign |
0.00 |
R1968:Tln2
|
UTSW |
9 |
67,163,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Tln2
|
UTSW |
9 |
67,179,986 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2038:Tln2
|
UTSW |
9 |
67,304,935 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R2152:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Tln2
|
UTSW |
9 |
67,262,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Tln2
|
UTSW |
9 |
67,262,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Tln2
|
UTSW |
9 |
67,283,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Tln2
|
UTSW |
9 |
67,262,421 (GRCm39) |
missense |
probably benign |
0.10 |
R3151:Tln2
|
UTSW |
9 |
67,237,829 (GRCm39) |
critical splice donor site |
probably null |
|
R3795:Tln2
|
UTSW |
9 |
67,163,197 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Tln2
|
UTSW |
9 |
67,277,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Tln2
|
UTSW |
9 |
67,251,347 (GRCm39) |
critical splice donor site |
probably null |
|
R4685:Tln2
|
UTSW |
9 |
67,209,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Tln2
|
UTSW |
9 |
67,304,935 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R4696:Tln2
|
UTSW |
9 |
67,302,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Tln2
|
UTSW |
9 |
67,302,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Tln2
|
UTSW |
9 |
67,253,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4701:Tln2
|
UTSW |
9 |
67,253,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4741:Tln2
|
UTSW |
9 |
67,293,837 (GRCm39) |
critical splice donor site |
probably null |
|
R4806:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4807:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4808:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4967:Tln2
|
UTSW |
9 |
67,262,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R5061:Tln2
|
UTSW |
9 |
67,261,750 (GRCm39) |
missense |
probably benign |
|
R5092:Tln2
|
UTSW |
9 |
67,163,310 (GRCm39) |
missense |
probably benign |
0.13 |
R5093:Tln2
|
UTSW |
9 |
67,241,596 (GRCm39) |
missense |
probably benign |
0.44 |
R5126:Tln2
|
UTSW |
9 |
67,165,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R5204:Tln2
|
UTSW |
9 |
67,261,764 (GRCm39) |
missense |
probably benign |
0.00 |
R5236:Tln2
|
UTSW |
9 |
67,273,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R5287:Tln2
|
UTSW |
9 |
67,149,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Tln2
|
UTSW |
9 |
67,219,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5571:Tln2
|
UTSW |
9 |
67,241,602 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5642:Tln2
|
UTSW |
9 |
67,203,640 (GRCm39) |
missense |
probably benign |
0.01 |
R5711:Tln2
|
UTSW |
9 |
67,299,829 (GRCm39) |
missense |
probably benign |
0.00 |
R5776:Tln2
|
UTSW |
9 |
67,165,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R5791:Tln2
|
UTSW |
9 |
67,293,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R5866:Tln2
|
UTSW |
9 |
67,174,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Tln2
|
UTSW |
9 |
67,136,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Tln2
|
UTSW |
9 |
67,269,999 (GRCm39) |
missense |
probably benign |
0.02 |
R6106:Tln2
|
UTSW |
9 |
67,230,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R6175:Tln2
|
UTSW |
9 |
67,131,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Tln2
|
UTSW |
9 |
67,185,411 (GRCm39) |
missense |
probably benign |
0.45 |
R6430:Tln2
|
UTSW |
9 |
67,179,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6441:Tln2
|
UTSW |
9 |
67,179,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6738:Tln2
|
UTSW |
9 |
67,293,946 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6794:Tln2
|
UTSW |
9 |
67,193,840 (GRCm39) |
missense |
probably benign |
0.07 |
R6850:Tln2
|
UTSW |
9 |
67,165,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Tln2
|
UTSW |
9 |
67,304,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R6909:Tln2
|
UTSW |
9 |
67,299,814 (GRCm39) |
missense |
probably damaging |
0.97 |
R6951:Tln2
|
UTSW |
9 |
67,165,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R7015:Tln2
|
UTSW |
9 |
67,269,929 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7051:Tln2
|
UTSW |
9 |
67,253,699 (GRCm39) |
missense |
probably benign |
0.00 |
R7246:Tln2
|
UTSW |
9 |
67,170,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Tln2
|
UTSW |
9 |
67,253,743 (GRCm39) |
missense |
probably benign |
|
R7753:Tln2
|
UTSW |
9 |
67,302,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Tln2
|
UTSW |
9 |
67,255,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R7931:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Tln2
|
UTSW |
9 |
67,131,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8081:Tln2
|
UTSW |
9 |
67,264,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8164:Tln2
|
UTSW |
9 |
67,226,702 (GRCm39) |
missense |
probably benign |
0.31 |
R8192:Tln2
|
UTSW |
9 |
67,253,811 (GRCm39) |
nonsense |
probably null |
|
R8495:Tln2
|
UTSW |
9 |
67,261,749 (GRCm39) |
missense |
probably benign |
0.01 |
R8734:Tln2
|
UTSW |
9 |
67,179,936 (GRCm39) |
missense |
probably benign |
0.19 |
R8739:Tln2
|
UTSW |
9 |
67,165,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8757:Tln2
|
UTSW |
9 |
67,274,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Tln2
|
UTSW |
9 |
67,274,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Tln2
|
UTSW |
9 |
67,230,304 (GRCm39) |
missense |
probably benign |
|
R8781:Tln2
|
UTSW |
9 |
67,163,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R8812:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8814:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8816:Tln2
|
UTSW |
9 |
67,128,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8833:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8835:Tln2
|
UTSW |
9 |
67,304,975 (GRCm39) |
splice site |
probably benign |
|
R8837:Tln2
|
UTSW |
9 |
67,157,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R8843:Tln2
|
UTSW |
9 |
67,302,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Tln2
|
UTSW |
9 |
67,237,834 (GRCm39) |
nonsense |
probably null |
|
R8867:Tln2
|
UTSW |
9 |
67,237,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R8921:Tln2
|
UTSW |
9 |
67,174,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R9080:Tln2
|
UTSW |
9 |
67,253,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Tln2
|
UTSW |
9 |
67,269,927 (GRCm39) |
missense |
probably damaging |
0.96 |
R9150:Tln2
|
UTSW |
9 |
67,128,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Tln2
|
UTSW |
9 |
67,277,980 (GRCm39) |
missense |
probably benign |
0.20 |
R9330:Tln2
|
UTSW |
9 |
67,229,213 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9343:Tln2
|
UTSW |
9 |
67,230,353 (GRCm39) |
missense |
probably benign |
0.10 |
R9355:Tln2
|
UTSW |
9 |
67,262,529 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9383:Tln2
|
UTSW |
9 |
67,278,043 (GRCm39) |
missense |
probably benign |
0.17 |
R9386:Tln2
|
UTSW |
9 |
67,273,249 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9407:Tln2
|
UTSW |
9 |
67,136,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9483:Tln2
|
UTSW |
9 |
67,299,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Tln2
|
UTSW |
9 |
67,165,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R9642:Tln2
|
UTSW |
9 |
67,157,826 (GRCm39) |
missense |
probably benign |
0.02 |
R9703:Tln2
|
UTSW |
9 |
67,293,938 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Tln2
|
UTSW |
9 |
67,284,135 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Tln2
|
UTSW |
9 |
67,255,420 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tln2
|
UTSW |
9 |
67,277,973 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tln2
|
UTSW |
9 |
67,253,767 (GRCm39) |
missense |
possibly damaging |
0.46 |
|