Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
G |
A |
13: 61,001,057 (GRCm39) |
P160S |
probably benign |
Het |
Adamts12 |
G |
T |
15: 11,311,558 (GRCm39) |
D1272Y |
probably benign |
Het |
Akr1c20 |
A |
T |
13: 4,557,726 (GRCm39) |
V267D |
probably damaging |
Het |
C1s1 |
A |
G |
6: 124,508,010 (GRCm39) |
S660P |
probably damaging |
Het |
Ccdc202 |
A |
G |
14: 96,119,987 (GRCm39) |
N248S |
probably benign |
Het |
Ccdc40 |
A |
G |
11: 119,122,629 (GRCm39) |
T144A |
possibly damaging |
Het |
Cdk20 |
T |
C |
13: 64,585,217 (GRCm39) |
I167T |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,825,023 (GRCm39) |
L1212S |
probably damaging |
Het |
Clock |
G |
C |
5: 76,414,649 (GRCm39) |
D15E |
probably benign |
Het |
Clstn2 |
A |
G |
9: 97,343,446 (GRCm39) |
V667A |
probably benign |
Het |
Cr2 |
A |
T |
1: 194,851,561 (GRCm39) |
|
probably null |
Het |
Cyp2e1 |
A |
G |
7: 140,352,992 (GRCm39) |
D343G |
probably damaging |
Het |
Dync1h1 |
G |
A |
12: 110,602,943 (GRCm39) |
E2195K |
probably benign |
Het |
Etf1 |
G |
A |
18: 35,041,220 (GRCm39) |
T298I |
possibly damaging |
Het |
Gm5431 |
T |
C |
11: 48,786,261 (GRCm39) |
|
probably benign |
Het |
Gss |
G |
A |
2: 155,409,641 (GRCm39) |
T265I |
probably damaging |
Het |
Heatr1 |
C |
T |
13: 12,420,927 (GRCm39) |
S406L |
possibly damaging |
Het |
Hgsnat |
C |
A |
8: 26,447,363 (GRCm39) |
M310I |
possibly damaging |
Het |
Inpp5b |
G |
A |
4: 124,682,873 (GRCm39) |
R598H |
probably damaging |
Het |
Ints2 |
G |
T |
11: 86,140,074 (GRCm39) |
Q253K |
probably damaging |
Het |
Kng1 |
A |
G |
16: 22,897,730 (GRCm39) |
M377V |
probably benign |
Het |
Krt72 |
C |
T |
15: 101,694,440 (GRCm39) |
|
probably null |
Het |
Lemd2 |
G |
C |
17: 27,409,706 (GRCm39) |
R482G |
probably damaging |
Het |
Lrpprc |
C |
T |
17: 85,033,731 (GRCm39) |
D1049N |
possibly damaging |
Het |
Lrrc49 |
A |
T |
9: 60,587,810 (GRCm39) |
H117Q |
probably damaging |
Het |
Mcm6 |
A |
T |
1: 128,279,213 (GRCm39) |
F191Y |
probably damaging |
Het |
Mecom |
T |
C |
3: 30,033,949 (GRCm39) |
T252A |
possibly damaging |
Het |
Mgat4e |
T |
C |
1: 134,469,271 (GRCm39) |
T258A |
probably benign |
Het |
Mpeg1 |
A |
G |
19: 12,440,168 (GRCm39) |
N542S |
probably damaging |
Het |
Nln |
C |
T |
13: 104,198,261 (GRCm39) |
V184I |
probably benign |
Het |
Nova1 |
A |
C |
12: 46,863,676 (GRCm39) |
F91L |
unknown |
Het |
Polk |
T |
C |
13: 96,620,716 (GRCm39) |
I516V |
probably benign |
Het |
Ppig |
C |
T |
2: 69,579,362 (GRCm39) |
P357S |
unknown |
Het |
Rasal2 |
A |
T |
1: 156,992,236 (GRCm39) |
H552Q |
probably damaging |
Het |
Rnf41 |
G |
A |
10: 128,271,440 (GRCm39) |
E117K |
probably benign |
Het |
Sbk3 |
A |
G |
7: 4,970,452 (GRCm39) |
Y306H |
possibly damaging |
Het |
Senp1 |
A |
G |
15: 97,974,435 (GRCm39) |
S126P |
probably benign |
Het |
Sfr1 |
A |
G |
19: 47,722,129 (GRCm39) |
K182E |
probably benign |
Het |
Slc25a4 |
C |
A |
8: 46,662,325 (GRCm39) |
R111L |
probably damaging |
Het |
Slc9c1 |
A |
T |
16: 45,393,710 (GRCm39) |
Y551F |
probably benign |
Het |
Stard4 |
A |
T |
18: 33,339,263 (GRCm39) |
N80K |
probably damaging |
Het |
Tbk1 |
G |
A |
10: 121,407,821 (GRCm39) |
T104M |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tmem102 |
A |
T |
11: 69,695,196 (GRCm39) |
W259R |
probably damaging |
Het |
Tnk1 |
A |
T |
11: 69,743,962 (GRCm39) |
C466S |
probably benign |
Het |
Tspoap1 |
A |
C |
11: 87,656,946 (GRCm39) |
Q307P |
probably damaging |
Het |
Ugt2b35 |
A |
G |
5: 87,159,389 (GRCm39) |
N528D |
possibly damaging |
Het |
Usp6nl |
A |
G |
2: 6,431,809 (GRCm39) |
|
probably null |
Het |
Vmn1r203 |
C |
T |
13: 22,708,678 (GRCm39) |
T153M |
probably benign |
Het |
Vmn1r89 |
T |
A |
7: 12,953,938 (GRCm39) |
S157T |
probably damaging |
Het |
Vmn2r103 |
A |
T |
17: 20,013,230 (GRCm39) |
Y117F |
probably benign |
Het |
Vmn2r116 |
A |
C |
17: 23,605,115 (GRCm39) |
M143L |
probably benign |
Het |
Vmn2r62 |
A |
T |
7: 42,414,261 (GRCm39) |
D727E |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,862,304 (GRCm39) |
I2974V |
probably benign |
Het |
Wrn |
C |
T |
8: 33,758,847 (GRCm39) |
G769D |
probably damaging |
Het |
Zhx3 |
T |
A |
2: 160,622,940 (GRCm39) |
H409L |
possibly damaging |
Het |
|
Other mutations in Ptpro |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Ptpro
|
APN |
6 |
137,371,907 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00844:Ptpro
|
APN |
6 |
137,391,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00983:Ptpro
|
APN |
6 |
137,395,246 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01073:Ptpro
|
APN |
6 |
137,354,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01832:Ptpro
|
APN |
6 |
137,370,666 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02308:Ptpro
|
APN |
6 |
137,431,698 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02387:Ptpro
|
APN |
6 |
137,387,978 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02605:Ptpro
|
APN |
6 |
137,357,316 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02666:Ptpro
|
APN |
6 |
137,355,057 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03275:Ptpro
|
APN |
6 |
137,427,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Brau
|
UTSW |
6 |
137,431,596 (GRCm39) |
missense |
probably damaging |
1.00 |
court
|
UTSW |
6 |
137,370,673 (GRCm39) |
nonsense |
probably null |
|
Hoff
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
Jester
|
UTSW |
6 |
137,426,915 (GRCm39) |
missense |
probably damaging |
1.00 |
mann
|
UTSW |
6 |
137,388,114 (GRCm39) |
splice site |
probably null |
|
R0017:Ptpro
|
UTSW |
6 |
137,393,825 (GRCm39) |
missense |
probably benign |
0.03 |
R0017:Ptpro
|
UTSW |
6 |
137,393,825 (GRCm39) |
missense |
probably benign |
0.03 |
R0020:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ptpro
|
UTSW |
6 |
137,363,350 (GRCm39) |
missense |
probably benign |
0.08 |
R0094:Ptpro
|
UTSW |
6 |
137,363,350 (GRCm39) |
missense |
probably benign |
0.08 |
R0103:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0106:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Ptpro
|
UTSW |
6 |
137,353,987 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0427:Ptpro
|
UTSW |
6 |
137,345,294 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0456:Ptpro
|
UTSW |
6 |
137,391,228 (GRCm39) |
missense |
probably benign |
0.04 |
R0536:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0664:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0708:Ptpro
|
UTSW |
6 |
137,363,251 (GRCm39) |
missense |
probably benign |
0.26 |
R0730:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0735:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0738:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0786:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0811:Ptpro
|
UTSW |
6 |
137,345,077 (GRCm39) |
missense |
probably benign |
0.00 |
R0812:Ptpro
|
UTSW |
6 |
137,345,077 (GRCm39) |
missense |
probably benign |
0.00 |
R0881:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1259:Ptpro
|
UTSW |
6 |
137,369,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R1340:Ptpro
|
UTSW |
6 |
137,418,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1381:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1382:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1385:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1416:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1422:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Ptpro
|
UTSW |
6 |
137,418,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Ptpro
|
UTSW |
6 |
137,438,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R1540:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1571:Ptpro
|
UTSW |
6 |
137,355,128 (GRCm39) |
missense |
probably benign |
|
R1573:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1587:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Ptpro
|
UTSW |
6 |
137,421,015 (GRCm39) |
nonsense |
probably null |
|
R1700:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1701:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Ptpro
|
UTSW |
6 |
137,377,643 (GRCm39) |
missense |
probably benign |
0.03 |
R1772:Ptpro
|
UTSW |
6 |
137,407,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Ptpro
|
UTSW |
6 |
137,377,617 (GRCm39) |
splice site |
probably benign |
|
R1958:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Ptpro
|
UTSW |
6 |
137,393,863 (GRCm39) |
missense |
probably benign |
0.38 |
R2025:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2040:Ptpro
|
UTSW |
6 |
137,363,162 (GRCm39) |
splice site |
probably benign |
|
R2115:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Ptpro
|
UTSW |
6 |
137,388,114 (GRCm39) |
splice site |
probably null |
|
R2161:Ptpro
|
UTSW |
6 |
137,426,885 (GRCm39) |
missense |
probably benign |
0.01 |
R2431:Ptpro
|
UTSW |
6 |
137,420,583 (GRCm39) |
nonsense |
probably null |
|
R2915:Ptpro
|
UTSW |
6 |
137,391,239 (GRCm39) |
start gained |
probably benign |
|
R2988:Ptpro
|
UTSW |
6 |
137,420,597 (GRCm39) |
nonsense |
probably null |
|
R3772:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Ptpro
|
UTSW |
6 |
137,357,307 (GRCm39) |
missense |
probably benign |
|
R3885:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3887:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3893:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4032:Ptpro
|
UTSW |
6 |
137,438,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Ptpro
|
UTSW |
6 |
137,397,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R4377:Ptpro
|
UTSW |
6 |
137,357,264 (GRCm39) |
missense |
probably benign |
0.26 |
R4455:Ptpro
|
UTSW |
6 |
137,370,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Ptpro
|
UTSW |
6 |
137,393,834 (GRCm39) |
nonsense |
probably null |
|
R4827:Ptpro
|
UTSW |
6 |
137,419,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Ptpro
|
UTSW |
6 |
137,354,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R4910:Ptpro
|
UTSW |
6 |
137,345,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R4932:Ptpro
|
UTSW |
6 |
137,388,103 (GRCm39) |
nonsense |
probably null |
|
R4941:Ptpro
|
UTSW |
6 |
137,369,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Ptpro
|
UTSW |
6 |
137,354,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R5032:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Ptpro
|
UTSW |
6 |
137,357,222 (GRCm39) |
missense |
probably benign |
0.04 |
R5423:Ptpro
|
UTSW |
6 |
137,419,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5782:Ptpro
|
UTSW |
6 |
137,376,496 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6103:Ptpro
|
UTSW |
6 |
137,377,704 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6239:Ptpro
|
UTSW |
6 |
137,357,606 (GRCm39) |
missense |
probably benign |
0.28 |
R6488:Ptpro
|
UTSW |
6 |
137,370,673 (GRCm39) |
nonsense |
probably null |
|
R6494:Ptpro
|
UTSW |
6 |
137,359,640 (GRCm39) |
missense |
probably benign |
0.20 |
R6746:Ptpro
|
UTSW |
6 |
137,371,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Ptpro
|
UTSW |
6 |
137,395,279 (GRCm39) |
splice site |
probably null |
|
R6888:Ptpro
|
UTSW |
6 |
137,357,198 (GRCm39) |
missense |
probably benign |
0.30 |
R6983:Ptpro
|
UTSW |
6 |
137,426,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Ptpro
|
UTSW |
6 |
137,357,476 (GRCm39) |
missense |
probably benign |
|
R7218:Ptpro
|
UTSW |
6 |
137,431,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Ptpro
|
UTSW |
6 |
137,345,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Ptpro
|
UTSW |
6 |
137,418,142 (GRCm39) |
critical splice donor site |
probably null |
|
R7381:Ptpro
|
UTSW |
6 |
137,376,559 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7493:Ptpro
|
UTSW |
6 |
137,359,647 (GRCm39) |
missense |
probably benign |
0.01 |
R7733:Ptpro
|
UTSW |
6 |
137,391,284 (GRCm39) |
nonsense |
probably null |
|
R7793:Ptpro
|
UTSW |
6 |
137,393,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R7804:Ptpro
|
UTSW |
6 |
137,376,599 (GRCm39) |
splice site |
probably null |
|
R7833:Ptpro
|
UTSW |
6 |
137,393,861 (GRCm39) |
nonsense |
probably null |
|
R7859:Ptpro
|
UTSW |
6 |
137,369,805 (GRCm39) |
critical splice donor site |
probably null |
|
R7873:Ptpro
|
UTSW |
6 |
137,407,737 (GRCm39) |
missense |
probably benign |
0.44 |
R8042:Ptpro
|
UTSW |
6 |
137,393,881 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8859:Ptpro
|
UTSW |
6 |
137,403,782 (GRCm39) |
nonsense |
probably null |
|
R8979:Ptpro
|
UTSW |
6 |
137,345,140 (GRCm39) |
missense |
probably benign |
|
R9138:Ptpro
|
UTSW |
6 |
137,388,113 (GRCm39) |
critical splice donor site |
probably null |
|
R9309:Ptpro
|
UTSW |
6 |
137,431,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R9420:Ptpro
|
UTSW |
6 |
137,420,933 (GRCm39) |
missense |
probably benign |
0.08 |
R9612:Ptpro
|
UTSW |
6 |
137,391,318 (GRCm39) |
missense |
probably benign |
0.31 |
R9625:Ptpro
|
UTSW |
6 |
137,371,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R9697:Ptpro
|
UTSW |
6 |
137,363,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Ptpro
|
UTSW |
6 |
137,345,108 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Ptpro
|
UTSW |
6 |
137,355,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|