Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
A |
T |
14: 70,393,635 (GRCm39) |
I287N |
probably benign |
Het |
Aco2 |
G |
T |
15: 81,787,820 (GRCm39) |
E223D |
probably damaging |
Het |
Acsf3 |
T |
A |
8: 123,539,770 (GRCm39) |
I466N |
probably damaging |
Het |
Albfm1 |
G |
A |
5: 90,719,625 (GRCm39) |
|
probably null |
Het |
Aox3 |
T |
A |
1: 58,191,761 (GRCm39) |
F438I |
probably benign |
Het |
Arhgap33 |
T |
C |
7: 30,225,794 (GRCm39) |
T591A |
probably benign |
Het |
Ash1l |
C |
T |
3: 88,888,694 (GRCm39) |
A191V |
probably benign |
Het |
Btg2 |
T |
C |
1: 134,006,779 (GRCm39) |
K5E |
probably benign |
Het |
C1galt1 |
T |
A |
6: 7,871,150 (GRCm39) |
Y329N |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,608,435 (GRCm39) |
I824T |
possibly damaging |
Het |
Carmil3 |
A |
G |
14: 55,731,817 (GRCm39) |
I182V |
probably benign |
Het |
Ccdc150 |
T |
A |
1: 54,302,496 (GRCm39) |
|
probably null |
Het |
Chek1 |
T |
A |
9: 36,633,939 (GRCm39) |
R129W |
probably damaging |
Het |
Chrna6 |
A |
G |
8: 27,896,815 (GRCm39) |
M354T |
possibly damaging |
Het |
Cpq |
A |
G |
15: 33,250,185 (GRCm39) |
T181A |
probably benign |
Het |
Csmd2 |
A |
T |
4: 128,287,472 (GRCm39) |
Y1069F |
|
Het |
Defb28 |
T |
A |
2: 152,361,974 (GRCm39) |
C45S |
possibly damaging |
Het |
Dnah1 |
A |
G |
14: 31,018,551 (GRCm39) |
Y1360H |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,823,608 (GRCm39) |
V3749A |
possibly damaging |
Het |
Dnah7c |
T |
A |
1: 46,819,935 (GRCm39) |
D3728E |
probably benign |
Het |
Dym |
G |
A |
18: 75,196,245 (GRCm39) |
|
probably null |
Het |
Dync2i2 |
G |
A |
2: 29,928,341 (GRCm39) |
P95L |
probably benign |
Het |
Dzip3 |
A |
G |
16: 48,747,903 (GRCm39) |
|
probably null |
Het |
Eef1akmt4 |
A |
G |
16: 20,436,666 (GRCm39) |
K163E |
probably benign |
Het |
Fbrs |
A |
G |
7: 127,081,985 (GRCm39) |
T242A |
possibly damaging |
Het |
Fgfr3 |
G |
A |
5: 33,885,146 (GRCm39) |
V87M |
possibly damaging |
Het |
Fst |
A |
T |
13: 114,595,068 (GRCm39) |
C19S |
probably benign |
Het |
Gm7276 |
G |
A |
18: 77,273,216 (GRCm39) |
R173W |
unknown |
Het |
Gm9195 |
G |
A |
14: 72,697,929 (GRCm39) |
H1284Y |
probably benign |
Het |
Herc6 |
C |
A |
6: 57,581,074 (GRCm39) |
T258K |
probably damaging |
Het |
Hip1r |
A |
G |
5: 124,137,174 (GRCm39) |
Y678C |
probably damaging |
Het |
Ifne |
A |
T |
4: 88,798,243 (GRCm39) |
N58K |
probably damaging |
Het |
Ighv1-26 |
A |
T |
12: 114,752,163 (GRCm39) |
H60Q |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,746,520 (GRCm39) |
F1276L |
probably damaging |
Het |
Itprid2 |
A |
T |
2: 79,466,416 (GRCm39) |
D82V |
probably damaging |
Het |
Kcnc4 |
T |
A |
3: 107,366,100 (GRCm39) |
E36V |
probably benign |
Het |
Kcnq2 |
C |
T |
2: 180,750,895 (GRCm39) |
G315S |
probably damaging |
Het |
Kdm4c |
G |
A |
4: 74,255,200 (GRCm39) |
V585M |
probably damaging |
Het |
Klhl26 |
C |
T |
8: 70,905,592 (GRCm39) |
R106H |
probably damaging |
Het |
Kmo |
T |
C |
1: 175,481,221 (GRCm39) |
F313S |
probably damaging |
Het |
Lmtk3 |
T |
A |
7: 45,443,740 (GRCm39) |
S808T |
unknown |
Het |
Lrch3 |
A |
G |
16: 32,815,363 (GRCm39) |
T585A |
probably benign |
Het |
Lrch4 |
T |
A |
5: 137,637,977 (GRCm39) |
H86Q |
|
Het |
Map3k20 |
A |
G |
2: 72,195,062 (GRCm39) |
D113G |
probably damaging |
Het |
Mbd3l1 |
T |
C |
9: 18,396,417 (GRCm39) |
S181P |
probably benign |
Het |
Mccc2 |
T |
C |
13: 100,104,241 (GRCm39) |
T303A |
probably benign |
Het |
Med27 |
A |
G |
2: 29,303,490 (GRCm39) |
R147G |
possibly damaging |
Het |
Mrps5 |
T |
A |
2: 127,437,762 (GRCm39) |
S196R |
possibly damaging |
Het |
Muc21 |
GGGGTGGGCATAGATCCTGAGGCAGAGCTGGATGCAGTGGTGGTCAGGGTGGG |
GGGGTGGG |
17: 35,932,935 (GRCm39) |
|
probably benign |
Het |
Myo16 |
A |
T |
8: 10,526,185 (GRCm39) |
|
probably null |
Het |
Nudt2 |
A |
T |
4: 41,477,575 (GRCm39) |
M19L |
probably benign |
Het |
Pcdha11 |
C |
T |
18: 37,146,245 (GRCm39) |
P779S |
probably benign |
Het |
Phykpl |
A |
G |
11: 51,489,530 (GRCm39) |
T379A |
probably benign |
Het |
Plekha8 |
A |
C |
6: 54,601,206 (GRCm39) |
M270L |
probably benign |
Het |
Plekhg5 |
A |
G |
4: 152,192,885 (GRCm39) |
H593R |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,637,196 (GRCm39) |
N293S |
possibly damaging |
Het |
Pramel32 |
G |
A |
4: 88,548,184 (GRCm39) |
P74S |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,232,532 (GRCm39) |
N866K |
probably benign |
Het |
Psme4 |
A |
T |
11: 30,757,790 (GRCm39) |
I308L |
probably benign |
Het |
Rbbp8 |
T |
A |
18: 11,865,269 (GRCm39) |
D719E |
probably damaging |
Het |
Rnaset2b |
A |
T |
17: 7,259,166 (GRCm39) |
D144V |
probably benign |
Het |
Senp6 |
T |
G |
9: 80,033,481 (GRCm39) |
D662E |
probably damaging |
Het |
Serpinb3c |
T |
C |
1: 107,200,817 (GRCm39) |
N200S |
possibly damaging |
Het |
Serpinb9g |
C |
G |
13: 33,672,543 (GRCm39) |
Y113* |
probably null |
Het |
Sgf29 |
T |
C |
7: 126,270,821 (GRCm39) |
I134T |
probably benign |
Het |
Sh3bp4 |
T |
G |
1: 89,080,824 (GRCm39) |
|
probably null |
Het |
Stab1 |
G |
A |
14: 30,862,783 (GRCm39) |
L2243F |
probably damaging |
Het |
Sympk |
T |
C |
7: 18,769,770 (GRCm39) |
V149A |
probably benign |
Het |
Syt3 |
C |
T |
7: 44,041,953 (GRCm39) |
Q271* |
probably null |
Het |
Tas2r109 |
A |
G |
6: 132,957,663 (GRCm39) |
I89T |
probably benign |
Het |
Tgif1 |
A |
G |
17: 71,151,847 (GRCm39) |
S255P |
probably damaging |
Het |
Tm9sf1 |
G |
A |
14: 55,875,432 (GRCm39) |
|
probably benign |
Het |
Tnf |
A |
G |
17: 35,419,347 (GRCm39) |
F161S |
possibly damaging |
Het |
Topaz1 |
T |
A |
9: 122,579,428 (GRCm39) |
S779R |
possibly damaging |
Het |
Topors |
A |
G |
4: 40,260,540 (GRCm39) |
S915P |
unknown |
Het |
Tpm4 |
C |
T |
8: 72,900,321 (GRCm39) |
L161F |
probably damaging |
Het |
Trim38 |
C |
T |
13: 23,975,384 (GRCm39) |
T441I |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,141,620 (GRCm39) |
M548V |
probably benign |
Het |
Vmn2r68 |
T |
A |
7: 84,883,042 (GRCm39) |
T237S |
probably benign |
Het |
Zc3hav1 |
A |
G |
6: 38,309,209 (GRCm39) |
S538P |
probably benign |
Het |
Zfp541 |
C |
T |
7: 15,813,294 (GRCm39) |
T649I |
probably benign |
Het |
|
Other mutations in Ptprb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Ptprb
|
APN |
10 |
116,198,553 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01354:Ptprb
|
APN |
10 |
116,179,796 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01404:Ptprb
|
APN |
10 |
116,175,341 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01410:Ptprb
|
APN |
10 |
116,138,179 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01412:Ptprb
|
APN |
10 |
116,179,820 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01731:Ptprb
|
APN |
10 |
116,208,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Ptprb
|
APN |
10 |
116,203,410 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Ptprb
|
APN |
10 |
116,167,108 (GRCm39) |
splice site |
probably benign |
|
IGL02178:Ptprb
|
APN |
10 |
116,158,437 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02304:Ptprb
|
APN |
10 |
116,167,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02324:Ptprb
|
APN |
10 |
116,155,238 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02388:Ptprb
|
APN |
10 |
116,203,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Ptprb
|
APN |
10 |
116,174,569 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02698:Ptprb
|
APN |
10 |
116,199,185 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02876:Ptprb
|
APN |
10 |
116,184,116 (GRCm39) |
splice site |
probably benign |
|
IGL02879:Ptprb
|
APN |
10 |
116,163,873 (GRCm39) |
missense |
probably benign |
|
IGL02982:Ptprb
|
APN |
10 |
116,158,533 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03146:Ptprb
|
APN |
10 |
116,164,032 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03351:Ptprb
|
APN |
10 |
116,175,487 (GRCm39) |
missense |
probably benign |
0.03 |
R0306:Ptprb
|
UTSW |
10 |
116,179,893 (GRCm39) |
missense |
probably benign |
0.04 |
R0385:Ptprb
|
UTSW |
10 |
116,186,083 (GRCm39) |
missense |
probably benign |
0.00 |
R0600:Ptprb
|
UTSW |
10 |
116,204,712 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0613:Ptprb
|
UTSW |
10 |
116,138,283 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0613:Ptprb
|
UTSW |
10 |
116,138,230 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0850:Ptprb
|
UTSW |
10 |
116,175,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R0850:Ptprb
|
UTSW |
10 |
116,138,030 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1331:Ptprb
|
UTSW |
10 |
116,203,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1413:Ptprb
|
UTSW |
10 |
116,175,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Ptprb
|
UTSW |
10 |
116,155,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1545:Ptprb
|
UTSW |
10 |
116,216,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Ptprb
|
UTSW |
10 |
116,175,372 (GRCm39) |
missense |
probably benign |
0.00 |
R1752:Ptprb
|
UTSW |
10 |
116,176,895 (GRCm39) |
missense |
probably benign |
0.44 |
R1837:Ptprb
|
UTSW |
10 |
116,177,531 (GRCm39) |
missense |
probably benign |
0.00 |
R1940:Ptprb
|
UTSW |
10 |
116,155,515 (GRCm39) |
splice site |
probably benign |
|
R1958:Ptprb
|
UTSW |
10 |
116,177,441 (GRCm39) |
missense |
probably benign |
0.10 |
R2029:Ptprb
|
UTSW |
10 |
116,182,958 (GRCm39) |
missense |
probably benign |
0.37 |
R2031:Ptprb
|
UTSW |
10 |
116,153,448 (GRCm39) |
missense |
probably benign |
|
R2101:Ptprb
|
UTSW |
10 |
116,150,943 (GRCm39) |
splice site |
probably benign |
|
R2209:Ptprb
|
UTSW |
10 |
116,205,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R3016:Ptprb
|
UTSW |
10 |
116,193,200 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3076:Ptprb
|
UTSW |
10 |
116,179,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R3821:Ptprb
|
UTSW |
10 |
116,185,979 (GRCm39) |
missense |
probably benign |
0.11 |
R3824:Ptprb
|
UTSW |
10 |
116,186,694 (GRCm39) |
missense |
probably benign |
0.05 |
R3825:Ptprb
|
UTSW |
10 |
116,186,694 (GRCm39) |
missense |
probably benign |
0.05 |
R3841:Ptprb
|
UTSW |
10 |
116,182,887 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3953:Ptprb
|
UTSW |
10 |
116,177,399 (GRCm39) |
missense |
probably benign |
0.00 |
R4125:Ptprb
|
UTSW |
10 |
116,189,754 (GRCm39) |
missense |
probably benign |
0.12 |
R4227:Ptprb
|
UTSW |
10 |
116,138,130 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4385:Ptprb
|
UTSW |
10 |
116,182,772 (GRCm39) |
missense |
probably benign |
|
R4731:Ptprb
|
UTSW |
10 |
116,155,238 (GRCm39) |
missense |
probably benign |
0.03 |
R5009:Ptprb
|
UTSW |
10 |
116,184,032 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5104:Ptprb
|
UTSW |
10 |
116,158,364 (GRCm39) |
missense |
probably benign |
0.17 |
R5114:Ptprb
|
UTSW |
10 |
116,184,088 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5145:Ptprb
|
UTSW |
10 |
116,179,820 (GRCm39) |
missense |
probably benign |
0.27 |
R5214:Ptprb
|
UTSW |
10 |
116,205,229 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5382:Ptprb
|
UTSW |
10 |
116,189,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Ptprb
|
UTSW |
10 |
116,186,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Ptprb
|
UTSW |
10 |
116,216,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R5586:Ptprb
|
UTSW |
10 |
116,189,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5808:Ptprb
|
UTSW |
10 |
116,175,392 (GRCm39) |
missense |
probably benign |
0.00 |
R5875:Ptprb
|
UTSW |
10 |
116,184,071 (GRCm39) |
missense |
probably benign |
0.00 |
R6051:Ptprb
|
UTSW |
10 |
116,176,995 (GRCm39) |
nonsense |
probably null |
|
R6383:Ptprb
|
UTSW |
10 |
116,182,912 (GRCm39) |
nonsense |
probably null |
|
R6511:Ptprb
|
UTSW |
10 |
116,182,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6817:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R6826:Ptprb
|
UTSW |
10 |
116,153,277 (GRCm39) |
missense |
probably benign |
0.26 |
R6958:Ptprb
|
UTSW |
10 |
116,113,153 (GRCm39) |
missense |
probably benign |
0.32 |
R7103:Ptprb
|
UTSW |
10 |
116,174,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R7129:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R7181:Ptprb
|
UTSW |
10 |
116,204,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Ptprb
|
UTSW |
10 |
116,174,681 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7289:Ptprb
|
UTSW |
10 |
116,164,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R7315:Ptprb
|
UTSW |
10 |
116,198,284 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7381:Ptprb
|
UTSW |
10 |
116,177,038 (GRCm39) |
missense |
probably benign |
|
R7412:Ptprb
|
UTSW |
10 |
116,177,043 (GRCm39) |
missense |
probably benign |
|
R7483:Ptprb
|
UTSW |
10 |
116,119,334 (GRCm39) |
missense |
probably benign |
0.01 |
R7495:Ptprb
|
UTSW |
10 |
116,177,353 (GRCm39) |
missense |
probably benign |
0.12 |
R7508:Ptprb
|
UTSW |
10 |
116,189,896 (GRCm39) |
nonsense |
probably null |
|
R7571:Ptprb
|
UTSW |
10 |
116,175,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7586:Ptprb
|
UTSW |
10 |
116,179,779 (GRCm39) |
missense |
probably damaging |
0.97 |
R7623:Ptprb
|
UTSW |
10 |
116,205,214 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7694:Ptprb
|
UTSW |
10 |
116,208,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Ptprb
|
UTSW |
10 |
116,113,389 (GRCm39) |
missense |
probably benign |
0.10 |
R7752:Ptprb
|
UTSW |
10 |
116,205,333 (GRCm39) |
missense |
probably benign |
0.37 |
R7826:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R7833:Ptprb
|
UTSW |
10 |
116,151,156 (GRCm39) |
missense |
probably benign |
0.01 |
R7834:Ptprb
|
UTSW |
10 |
116,175,329 (GRCm39) |
missense |
probably benign |
0.00 |
R7846:Ptprb
|
UTSW |
10 |
116,119,453 (GRCm39) |
missense |
probably benign |
0.17 |
R7896:Ptprb
|
UTSW |
10 |
116,205,362 (GRCm39) |
splice site |
probably null |
|
R7901:Ptprb
|
UTSW |
10 |
116,205,333 (GRCm39) |
missense |
probably benign |
0.37 |
R7912:Ptprb
|
UTSW |
10 |
116,158,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R8147:Ptprb
|
UTSW |
10 |
116,153,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8202:Ptprb
|
UTSW |
10 |
116,189,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8339:Ptprb
|
UTSW |
10 |
116,119,356 (GRCm39) |
missense |
probably benign |
0.14 |
R8400:Ptprb
|
UTSW |
10 |
116,119,477 (GRCm39) |
small deletion |
probably benign |
|
R8504:Ptprb
|
UTSW |
10 |
116,176,936 (GRCm39) |
missense |
probably benign |
0.27 |
R8679:Ptprb
|
UTSW |
10 |
116,203,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8786:Ptprb
|
UTSW |
10 |
116,155,306 (GRCm39) |
missense |
probably benign |
0.40 |
R8914:Ptprb
|
UTSW |
10 |
116,158,567 (GRCm39) |
nonsense |
probably null |
|
R8980:Ptprb
|
UTSW |
10 |
116,119,526 (GRCm39) |
missense |
probably benign |
0.07 |
R8982:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R9256:Ptprb
|
UTSW |
10 |
116,219,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Ptprb
|
UTSW |
10 |
116,155,353 (GRCm39) |
missense |
probably benign |
0.03 |
R9369:Ptprb
|
UTSW |
10 |
116,151,057 (GRCm39) |
missense |
probably benign |
0.00 |
R9448:Ptprb
|
UTSW |
10 |
116,149,819 (GRCm39) |
nonsense |
probably null |
|
R9467:Ptprb
|
UTSW |
10 |
116,158,390 (GRCm39) |
missense |
probably benign |
0.00 |
R9468:Ptprb
|
UTSW |
10 |
116,113,274 (GRCm39) |
missense |
probably benign |
0.00 |
R9481:Ptprb
|
UTSW |
10 |
116,155,353 (GRCm39) |
missense |
probably benign |
0.03 |
R9486:Ptprb
|
UTSW |
10 |
116,155,494 (GRCm39) |
nonsense |
probably null |
|
R9513:Ptprb
|
UTSW |
10 |
116,138,142 (GRCm39) |
missense |
probably benign |
0.00 |
R9529:Ptprb
|
UTSW |
10 |
116,174,519 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9535:Ptprb
|
UTSW |
10 |
116,158,431 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9614:Ptprb
|
UTSW |
10 |
116,203,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Ptprb
|
UTSW |
10 |
116,204,694 (GRCm39) |
missense |
probably damaging |
1.00 |
RF041:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
X0020:Ptprb
|
UTSW |
10 |
116,138,085 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Ptprb
|
UTSW |
10 |
116,138,061 (GRCm39) |
frame shift |
probably null |
|
Z1177:Ptprb
|
UTSW |
10 |
116,198,547 (GRCm39) |
critical splice acceptor site |
probably null |
|
|