Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930524J08Rik |
C |
A |
5: 100,126,945 (GRCm39) |
A9E |
unknown |
Het |
6030452D12Rik |
A |
T |
8: 107,227,411 (GRCm39) |
|
probably null |
Het |
Abcb11 |
C |
A |
2: 69,117,979 (GRCm39) |
Q466H |
probably damaging |
Het |
Adam20 |
A |
G |
8: 41,248,421 (GRCm39) |
D177G |
probably benign |
Het |
Ampd1 |
A |
T |
3: 102,992,696 (GRCm39) |
Q150L |
probably benign |
Het |
Angpt2 |
A |
C |
8: 18,755,840 (GRCm39) |
M209R |
probably benign |
Het |
Aoc2 |
G |
A |
11: 101,219,371 (GRCm39) |
R598Q |
probably damaging |
Het |
Arap1 |
A |
G |
7: 101,049,418 (GRCm39) |
D960G |
probably damaging |
Het |
Bhlhe40 |
G |
C |
6: 108,642,242 (GRCm39) |
L395F |
probably benign |
Het |
Cacna1i |
T |
C |
15: 80,275,854 (GRCm39) |
C1882R |
possibly damaging |
Het |
Ccr6 |
A |
G |
17: 8,475,611 (GRCm39) |
N272S |
possibly damaging |
Het |
Ces1f |
A |
T |
8: 93,998,472 (GRCm39) |
W175R |
probably damaging |
Het |
Ces3a |
A |
C |
8: 105,782,239 (GRCm39) |
H364P |
possibly damaging |
Het |
Cfap54 |
T |
C |
10: 92,637,000 (GRCm39) |
M3130V |
probably benign |
Het |
Clca3b |
G |
A |
3: 144,531,681 (GRCm39) |
P708S |
possibly damaging |
Het |
Cramp1 |
A |
T |
17: 25,201,379 (GRCm39) |
M701K |
possibly damaging |
Het |
Dnah1 |
A |
G |
14: 31,020,664 (GRCm39) |
I1235T |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,920,837 (GRCm39) |
L4676P |
probably benign |
Het |
Ergic1 |
A |
G |
17: 26,860,644 (GRCm39) |
E244G |
probably damaging |
Het |
Fignl2 |
C |
A |
15: 100,951,382 (GRCm39) |
R300L |
unknown |
Het |
Fry |
T |
C |
5: 150,419,814 (GRCm39) |
M628T |
|
Het |
Fscn3 |
A |
G |
6: 28,431,544 (GRCm39) |
T292A |
possibly damaging |
Het |
Fsip2 |
A |
T |
2: 82,819,860 (GRCm39) |
I5198L |
probably benign |
Het |
Gm4181 |
T |
A |
14: 51,869,990 (GRCm39) |
R104W |
probably damaging |
Het |
Gnl1 |
G |
A |
17: 36,294,305 (GRCm39) |
R308H |
probably benign |
Het |
Gtf2h4 |
G |
T |
17: 35,980,857 (GRCm39) |
L271I |
probably damaging |
Het |
Helq |
GTTT |
GTT |
5: 100,931,051 (GRCm39) |
|
probably null |
Het |
Hhatl |
A |
T |
9: 121,618,652 (GRCm39) |
W117R |
probably benign |
Het |
Hlx |
A |
G |
1: 184,462,993 (GRCm39) |
F220L |
probably benign |
Het |
Il31ra |
T |
C |
13: 112,688,497 (GRCm39) |
I27V |
probably damaging |
Het |
Itga8 |
T |
G |
2: 12,266,940 (GRCm39) |
D165A |
probably damaging |
Het |
Krt33a |
A |
C |
11: 99,902,801 (GRCm39) |
V341G |
probably benign |
Het |
Lrrc3c |
A |
G |
11: 98,490,266 (GRCm39) |
M208V |
possibly damaging |
Het |
Mapk8ip3 |
A |
T |
17: 25,120,135 (GRCm39) |
S947T |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,412,444 (GRCm39) |
I1797V |
unknown |
Het |
Myh2 |
A |
T |
11: 67,088,191 (GRCm39) |
T1936S |
probably benign |
Het |
Nr1h2 |
T |
C |
7: 44,199,746 (GRCm39) |
Y391C |
possibly damaging |
Het |
Or1l8 |
T |
A |
2: 36,817,986 (GRCm39) |
I47F |
probably damaging |
Het |
Or4c114 |
A |
T |
2: 88,904,811 (GRCm39) |
I208K |
probably damaging |
Het |
Or4e2 |
A |
G |
14: 52,688,670 (GRCm39) |
I267V |
probably benign |
Het |
Or5d40 |
A |
G |
2: 88,015,952 (GRCm39) |
T244A |
possibly damaging |
Het |
Phf3 |
A |
G |
1: 30,852,211 (GRCm39) |
M1064T |
probably benign |
Het |
Pkd1 |
A |
G |
17: 24,794,025 (GRCm39) |
E1904G |
probably benign |
Het |
Polrmt |
A |
G |
10: 79,576,483 (GRCm39) |
V491A |
probably benign |
Het |
Ppm1j |
C |
A |
3: 104,691,429 (GRCm39) |
R306S |
probably damaging |
Het |
Prkd2 |
T |
C |
7: 16,581,547 (GRCm39) |
F134S |
probably benign |
Het |
Prpf8 |
C |
A |
11: 75,382,610 (GRCm39) |
Q439K |
probably benign |
Het |
Prss50 |
A |
T |
9: 110,692,800 (GRCm39) |
I307F |
possibly damaging |
Het |
Rgs20 |
A |
G |
1: 4,982,535 (GRCm39) |
|
probably null |
Het |
Rnf144b |
A |
G |
13: 47,393,258 (GRCm39) |
E199G |
probably damaging |
Het |
Slc12a4 |
C |
T |
8: 106,682,347 (GRCm39) |
G121S |
probably damaging |
Het |
Slc22a26 |
A |
T |
19: 7,768,259 (GRCm39) |
V233E |
probably damaging |
Het |
Slc27a2 |
T |
G |
2: 126,395,124 (GRCm39) |
L17R |
probably benign |
Het |
Slc6a17 |
A |
G |
3: 107,398,794 (GRCm39) |
V269A |
probably benign |
Het |
Srp54c |
T |
C |
12: 55,304,237 (GRCm39) |
V395A |
probably benign |
Het |
Sspo |
A |
T |
6: 48,438,581 (GRCm39) |
S1550C |
possibly damaging |
Het |
Tet1 |
A |
G |
10: 62,715,818 (GRCm39) |
|
probably benign |
Het |
Themis |
A |
T |
10: 28,609,497 (GRCm39) |
H88L |
probably benign |
Het |
Tmem63b |
G |
A |
17: 45,971,773 (GRCm39) |
T814M |
possibly damaging |
Het |
Tnc |
G |
A |
4: 63,889,469 (GRCm39) |
T1679I |
probably damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,772,456 (GRCm39) |
D581G |
probably damaging |
Het |
Trim30d |
A |
C |
7: 104,132,555 (GRCm39) |
V244G |
probably benign |
Het |
Trpv1 |
T |
C |
11: 73,151,163 (GRCm39) |
S784P |
possibly damaging |
Het |
Tulp1 |
G |
A |
17: 28,575,398 (GRCm39) |
T103M |
probably damaging |
Het |
Ubap2l |
A |
C |
3: 89,922,713 (GRCm39) |
V775G |
unknown |
Het |
Vmn2r69 |
A |
C |
7: 85,060,972 (GRCm39) |
I204R |
possibly damaging |
Het |
Vmn2r72 |
T |
A |
7: 85,399,771 (GRCm39) |
D426V |
probably benign |
Het |
Vmn2r93 |
G |
A |
17: 18,533,497 (GRCm39) |
W467* |
probably null |
Het |
Wbp2nl |
T |
C |
15: 82,198,542 (GRCm39) |
*360Q |
probably null |
Het |
Xylt1 |
G |
A |
7: 117,191,274 (GRCm39) |
|
probably null |
Het |
Zc3h6 |
T |
G |
2: 128,835,331 (GRCm39) |
N123K |
unknown |
Het |
Zfp853 |
T |
C |
5: 143,275,110 (GRCm39) |
Q185R |
unknown |
Het |
|
Other mutations in Cps1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00757:Cps1
|
APN |
1 |
67,191,539 (GRCm39) |
splice site |
probably benign |
|
IGL00897:Cps1
|
APN |
1 |
67,254,723 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00928:Cps1
|
APN |
1 |
67,162,393 (GRCm39) |
missense |
probably benign |
|
IGL01063:Cps1
|
APN |
1 |
67,234,325 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01081:Cps1
|
APN |
1 |
67,245,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01361:Cps1
|
APN |
1 |
67,234,304 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01396:Cps1
|
APN |
1 |
67,196,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Cps1
|
APN |
1 |
67,269,443 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01695:Cps1
|
APN |
1 |
67,236,194 (GRCm39) |
missense |
probably benign |
|
IGL02022:Cps1
|
APN |
1 |
67,212,031 (GRCm39) |
splice site |
probably benign |
|
IGL02032:Cps1
|
APN |
1 |
67,269,474 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02049:Cps1
|
APN |
1 |
67,183,113 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02197:Cps1
|
APN |
1 |
67,196,923 (GRCm39) |
missense |
probably benign |
|
IGL02217:Cps1
|
APN |
1 |
67,213,541 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02555:Cps1
|
APN |
1 |
67,253,180 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02570:Cps1
|
APN |
1 |
67,187,862 (GRCm39) |
splice site |
probably benign |
|
IGL02633:Cps1
|
APN |
1 |
67,162,396 (GRCm39) |
missense |
probably benign |
|
IGL02711:Cps1
|
APN |
1 |
67,251,676 (GRCm39) |
splice site |
probably benign |
|
IGL02737:Cps1
|
APN |
1 |
67,187,933 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03030:Cps1
|
APN |
1 |
67,182,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Cps1
|
APN |
1 |
67,184,960 (GRCm39) |
nonsense |
probably null |
|
Madman
|
UTSW |
1 |
67,200,030 (GRCm39) |
missense |
probably damaging |
0.96 |
maniac
|
UTSW |
1 |
67,197,037 (GRCm39) |
critical splice donor site |
probably null |
|
R0109:Cps1
|
UTSW |
1 |
67,268,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0109:Cps1
|
UTSW |
1 |
67,268,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0140:Cps1
|
UTSW |
1 |
67,219,275 (GRCm39) |
missense |
probably benign |
|
R0318:Cps1
|
UTSW |
1 |
67,216,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R0486:Cps1
|
UTSW |
1 |
67,204,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0488:Cps1
|
UTSW |
1 |
67,187,967 (GRCm39) |
splice site |
probably benign |
|
R0492:Cps1
|
UTSW |
1 |
67,196,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Cps1
|
UTSW |
1 |
67,254,723 (GRCm39) |
missense |
probably benign |
0.02 |
R0534:Cps1
|
UTSW |
1 |
67,183,059 (GRCm39) |
missense |
probably benign |
0.06 |
R0565:Cps1
|
UTSW |
1 |
67,205,608 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0609:Cps1
|
UTSW |
1 |
67,211,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Cps1
|
UTSW |
1 |
67,178,929 (GRCm39) |
missense |
probably benign |
0.01 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Cps1
|
UTSW |
1 |
67,234,358 (GRCm39) |
missense |
probably benign |
0.00 |
R1220:Cps1
|
UTSW |
1 |
67,243,862 (GRCm39) |
critical splice donor site |
probably null |
|
R1321:Cps1
|
UTSW |
1 |
67,182,178 (GRCm39) |
splice site |
probably benign |
|
R1343:Cps1
|
UTSW |
1 |
67,248,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Cps1
|
UTSW |
1 |
67,268,583 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1374:Cps1
|
UTSW |
1 |
67,269,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1481:Cps1
|
UTSW |
1 |
67,183,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R1711:Cps1
|
UTSW |
1 |
67,207,533 (GRCm39) |
splice site |
probably null |
|
R1712:Cps1
|
UTSW |
1 |
67,269,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R1774:Cps1
|
UTSW |
1 |
67,210,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1799:Cps1
|
UTSW |
1 |
67,248,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Cps1
|
UTSW |
1 |
67,234,355 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2074:Cps1
|
UTSW |
1 |
67,243,797 (GRCm39) |
missense |
probably benign |
0.21 |
R2078:Cps1
|
UTSW |
1 |
67,234,424 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2078:Cps1
|
UTSW |
1 |
67,196,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Cps1
|
UTSW |
1 |
67,216,139 (GRCm39) |
missense |
probably benign |
0.01 |
R2112:Cps1
|
UTSW |
1 |
67,216,139 (GRCm39) |
missense |
probably benign |
0.01 |
R2146:Cps1
|
UTSW |
1 |
67,191,538 (GRCm39) |
splice site |
probably benign |
|
R2355:Cps1
|
UTSW |
1 |
67,195,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2375:Cps1
|
UTSW |
1 |
67,257,019 (GRCm39) |
missense |
probably benign |
0.00 |
R2860:Cps1
|
UTSW |
1 |
67,205,534 (GRCm39) |
missense |
probably benign |
0.44 |
R2861:Cps1
|
UTSW |
1 |
67,205,534 (GRCm39) |
missense |
probably benign |
0.44 |
R2979:Cps1
|
UTSW |
1 |
67,243,863 (GRCm39) |
critical splice donor site |
probably null |
|
R3427:Cps1
|
UTSW |
1 |
67,213,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3833:Cps1
|
UTSW |
1 |
67,178,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3858:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3859:Cps1
|
UTSW |
1 |
67,207,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3887:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3888:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3889:Cps1
|
UTSW |
1 |
67,204,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4386:Cps1
|
UTSW |
1 |
67,210,154 (GRCm39) |
critical splice donor site |
probably null |
|
R4497:Cps1
|
UTSW |
1 |
67,244,358 (GRCm39) |
missense |
probably null |
1.00 |
R4671:Cps1
|
UTSW |
1 |
67,235,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Cps1
|
UTSW |
1 |
67,259,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R4799:Cps1
|
UTSW |
1 |
67,182,145 (GRCm39) |
missense |
probably damaging |
0.96 |
R4853:Cps1
|
UTSW |
1 |
67,195,361 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4884:Cps1
|
UTSW |
1 |
67,216,183 (GRCm39) |
missense |
probably benign |
0.11 |
R4900:Cps1
|
UTSW |
1 |
67,200,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Cps1
|
UTSW |
1 |
67,178,922 (GRCm39) |
missense |
probably benign |
0.10 |
R5091:Cps1
|
UTSW |
1 |
67,268,679 (GRCm39) |
critical splice donor site |
probably null |
|
R5102:Cps1
|
UTSW |
1 |
67,245,952 (GRCm39) |
missense |
probably benign |
0.00 |
R5215:Cps1
|
UTSW |
1 |
67,205,539 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5290:Cps1
|
UTSW |
1 |
67,211,868 (GRCm39) |
missense |
probably benign |
0.21 |
R5732:Cps1
|
UTSW |
1 |
67,196,923 (GRCm39) |
missense |
probably benign |
0.22 |
R5818:Cps1
|
UTSW |
1 |
67,205,647 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5878:Cps1
|
UTSW |
1 |
67,197,037 (GRCm39) |
critical splice donor site |
probably null |
|
R6002:Cps1
|
UTSW |
1 |
67,211,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6034:Cps1
|
UTSW |
1 |
67,196,872 (GRCm39) |
splice site |
probably null |
|
R6034:Cps1
|
UTSW |
1 |
67,196,872 (GRCm39) |
splice site |
probably null |
|
R6199:Cps1
|
UTSW |
1 |
67,201,774 (GRCm39) |
frame shift |
probably null |
|
R6310:Cps1
|
UTSW |
1 |
67,182,140 (GRCm39) |
missense |
probably benign |
0.00 |
R6554:Cps1
|
UTSW |
1 |
67,213,628 (GRCm39) |
nonsense |
probably null |
|
R6700:Cps1
|
UTSW |
1 |
67,268,682 (GRCm39) |
splice site |
probably null |
|
R6731:Cps1
|
UTSW |
1 |
67,200,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R7052:Cps1
|
UTSW |
1 |
67,237,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Cps1
|
UTSW |
1 |
67,210,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Cps1
|
UTSW |
1 |
67,237,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R7339:Cps1
|
UTSW |
1 |
67,236,174 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7485:Cps1
|
UTSW |
1 |
67,179,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Cps1
|
UTSW |
1 |
67,219,240 (GRCm39) |
missense |
probably benign |
|
R7748:Cps1
|
UTSW |
1 |
67,178,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Cps1
|
UTSW |
1 |
67,213,640 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8097:Cps1
|
UTSW |
1 |
67,267,429 (GRCm39) |
missense |
probably benign |
0.08 |
R8357:Cps1
|
UTSW |
1 |
67,196,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R8435:Cps1
|
UTSW |
1 |
67,251,589 (GRCm39) |
missense |
probably benign |
0.07 |
R8457:Cps1
|
UTSW |
1 |
67,196,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Cps1
|
UTSW |
1 |
67,243,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8805:Cps1
|
UTSW |
1 |
67,216,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8811:Cps1
|
UTSW |
1 |
67,253,246 (GRCm39) |
missense |
probably benign |
0.03 |
R8819:Cps1
|
UTSW |
1 |
67,267,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8820:Cps1
|
UTSW |
1 |
67,267,439 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8854:Cps1
|
UTSW |
1 |
67,200,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Cps1
|
UTSW |
1 |
67,254,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Cps1
|
UTSW |
1 |
67,248,831 (GRCm39) |
missense |
probably benign |
0.08 |
R9273:Cps1
|
UTSW |
1 |
67,191,445 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9286:Cps1
|
UTSW |
1 |
67,198,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9308:Cps1
|
UTSW |
1 |
67,200,118 (GRCm39) |
critical splice donor site |
probably null |
|
R9326:Cps1
|
UTSW |
1 |
67,248,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Cps1
|
UTSW |
1 |
67,259,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R9454:Cps1
|
UTSW |
1 |
67,219,311 (GRCm39) |
missense |
probably damaging |
0.97 |
R9518:Cps1
|
UTSW |
1 |
67,259,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Cps1
|
UTSW |
1 |
67,198,048 (GRCm39) |
missense |
probably benign |
0.26 |
R9585:Cps1
|
UTSW |
1 |
67,195,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R9618:Cps1
|
UTSW |
1 |
67,196,975 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9641:Cps1
|
UTSW |
1 |
67,234,342 (GRCm39) |
missense |
probably benign |
0.03 |
R9650:Cps1
|
UTSW |
1 |
67,254,636 (GRCm39) |
missense |
|
|
R9668:Cps1
|
UTSW |
1 |
67,213,649 (GRCm39) |
missense |
probably benign |
0.24 |
R9726:Cps1
|
UTSW |
1 |
67,195,395 (GRCm39) |
missense |
probably benign |
0.39 |
X0024:Cps1
|
UTSW |
1 |
67,162,406 (GRCm39) |
missense |
probably benign |
|
Z1176:Cps1
|
UTSW |
1 |
67,187,878 (GRCm39) |
frame shift |
probably null |
|
Z1176:Cps1
|
UTSW |
1 |
67,162,427 (GRCm39) |
missense |
possibly damaging |
0.54 |
|