Incidental Mutation 'R0137:Vps8'
ID |
22067 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vps8
|
Ensembl Gene |
ENSMUSG00000033653 |
Gene Name |
VPS8 CORVET complex subunit |
Synonyms |
|
MMRRC Submission |
038422-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0137 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
21241868-21463430 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to C
at 21323136 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000096191]
[ENSMUST00000096192]
[ENSMUST00000115397]
[ENSMUST00000117598]
[ENSMUST00000118138]
[ENSMUST00000118923]
[ENSMUST00000122235]
|
AlphaFold |
Q0P5W1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000096191
|
SMART Domains |
Protein: ENSMUSP00000093905 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
SCOP:d1g72a_
|
158 |
296 |
1e-8 |
SMART |
Blast:WD40
|
184 |
225 |
7e-22 |
BLAST |
Blast:WD40
|
228 |
268 |
5e-20 |
BLAST |
Pfam:Vps8
|
610 |
794 |
1.7e-61 |
PFAM |
low complexity region
|
992 |
1007 |
N/A |
INTRINSIC |
low complexity region
|
1085 |
1097 |
N/A |
INTRINSIC |
low complexity region
|
1126 |
1137 |
N/A |
INTRINSIC |
Blast:RING
|
1257 |
1277 |
1e-5 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000096192
|
SMART Domains |
Protein: ENSMUSP00000093906 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
SCOP:d1g72a_
|
158 |
298 |
1e-8 |
SMART |
Blast:WD40
|
186 |
227 |
8e-22 |
BLAST |
Blast:WD40
|
230 |
270 |
5e-20 |
BLAST |
Pfam:Vps8
|
612 |
796 |
1.4e-61 |
PFAM |
low complexity region
|
969 |
979 |
N/A |
INTRINSIC |
low complexity region
|
1057 |
1069 |
N/A |
INTRINSIC |
low complexity region
|
1098 |
1109 |
N/A |
INTRINSIC |
RING
|
1229 |
1280 |
1.23e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000115397
|
SMART Domains |
Protein: ENSMUSP00000111055 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
SCOP:d1g72a_
|
158 |
298 |
8e-9 |
SMART |
Blast:WD40
|
186 |
227 |
8e-22 |
BLAST |
Blast:WD40
|
230 |
270 |
5e-20 |
BLAST |
Pfam:Vps8
|
613 |
796 |
1.3e-61 |
PFAM |
low complexity region
|
994 |
1009 |
N/A |
INTRINSIC |
low complexity region
|
1087 |
1099 |
N/A |
INTRINSIC |
low complexity region
|
1128 |
1139 |
N/A |
INTRINSIC |
RING
|
1259 |
1310 |
1.23e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000117598
|
SMART Domains |
Protein: ENSMUSP00000112937 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
SCOP:d1g72a_
|
158 |
296 |
1e-8 |
SMART |
Blast:WD40
|
184 |
225 |
8e-22 |
BLAST |
Blast:WD40
|
228 |
268 |
5e-20 |
BLAST |
Pfam:Vps8
|
610 |
794 |
1.9e-61 |
PFAM |
low complexity region
|
992 |
1007 |
N/A |
INTRINSIC |
low complexity region
|
1085 |
1097 |
N/A |
INTRINSIC |
low complexity region
|
1126 |
1137 |
N/A |
INTRINSIC |
RING
|
1257 |
1308 |
1.23e-4 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000118138
|
SMART Domains |
Protein: ENSMUSP00000113447 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
Pfam:Vps8
|
1 |
76 |
7.7e-21 |
PFAM |
low complexity region
|
274 |
289 |
N/A |
INTRINSIC |
low complexity region
|
367 |
379 |
N/A |
INTRINSIC |
low complexity region
|
408 |
419 |
N/A |
INTRINSIC |
RING
|
539 |
590 |
1.23e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000118923
|
SMART Domains |
Protein: ENSMUSP00000112636 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
SCOP:d1g72a_
|
158 |
298 |
9e-9 |
SMART |
Blast:WD40
|
186 |
227 |
8e-22 |
BLAST |
Blast:WD40
|
230 |
270 |
5e-20 |
BLAST |
Pfam:Vps8
|
612 |
796 |
1.9e-61 |
PFAM |
low complexity region
|
969 |
979 |
N/A |
INTRINSIC |
low complexity region
|
1057 |
1069 |
N/A |
INTRINSIC |
low complexity region
|
1098 |
1109 |
N/A |
INTRINSIC |
RING
|
1229 |
1280 |
1.23e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000125487
|
SMART Domains |
Protein: ENSMUSP00000114719 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
Pfam:Vps8
|
182 |
365 |
8.5e-62 |
PFAM |
low complexity region
|
563 |
578 |
N/A |
INTRINSIC |
low complexity region
|
656 |
668 |
N/A |
INTRINSIC |
low complexity region
|
697 |
708 |
N/A |
INTRINSIC |
RING
|
828 |
879 |
1.23e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000122235
|
SMART Domains |
Protein: ENSMUSP00000112622 Gene: ENSMUSG00000033653
Domain | Start | End | E-Value | Type |
low complexity region
|
96 |
112 |
N/A |
INTRINSIC |
WD40
|
184 |
225 |
2.66e0 |
SMART |
WD40
|
228 |
269 |
5.5e1 |
SMART |
low complexity region
|
371 |
386 |
N/A |
INTRINSIC |
low complexity region
|
480 |
491 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.2%
- 10x: 96.1%
- 20x: 91.8%
|
Validation Efficiency |
95% (94/99) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
A |
T |
8: 120,878,115 (GRCm39) |
H190L |
possibly damaging |
Het |
Adap1 |
A |
G |
5: 139,278,976 (GRCm39) |
|
probably benign |
Het |
Adgra3 |
C |
T |
5: 50,121,182 (GRCm39) |
|
probably benign |
Het |
Adgre5 |
A |
T |
8: 84,451,527 (GRCm39) |
V527E |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,938,695 (GRCm39) |
Y360N |
probably damaging |
Het |
Angptl6 |
C |
A |
9: 20,789,683 (GRCm39) |
A70S |
probably benign |
Het |
Ankdd1a |
C |
A |
9: 65,417,610 (GRCm39) |
K137N |
probably null |
Het |
Ccdc170 |
T |
C |
10: 4,496,950 (GRCm39) |
|
probably benign |
Het |
Ccdc51 |
A |
G |
9: 108,920,698 (GRCm39) |
E195G |
probably damaging |
Het |
Cdc37 |
A |
T |
9: 21,053,426 (GRCm39) |
C204S |
possibly damaging |
Het |
Cfap36 |
T |
C |
11: 29,172,431 (GRCm39) |
|
probably benign |
Het |
Col6a2 |
C |
A |
10: 76,432,259 (GRCm39) |
G965C |
probably damaging |
Het |
Csn1s2a |
G |
A |
5: 87,926,826 (GRCm39) |
S53N |
possibly damaging |
Het |
Dab2ip |
T |
C |
2: 35,582,388 (GRCm39) |
|
probably null |
Het |
Dhx58 |
A |
G |
11: 100,587,823 (GRCm39) |
V578A |
probably damaging |
Het |
Diaph1 |
G |
T |
18: 38,024,902 (GRCm39) |
Q520K |
unknown |
Het |
Eefsec |
C |
A |
6: 88,274,631 (GRCm39) |
K444N |
probably benign |
Het |
Eftud2 |
A |
T |
11: 102,759,443 (GRCm39) |
H153Q |
possibly damaging |
Het |
Eif5b |
T |
G |
1: 38,058,324 (GRCm39) |
S209A |
probably benign |
Het |
Exosc2 |
T |
A |
2: 31,562,497 (GRCm39) |
Y46N |
probably damaging |
Het |
F2 |
C |
T |
2: 91,456,075 (GRCm39) |
G562D |
probably damaging |
Het |
Fgf23 |
G |
A |
6: 127,057,128 (GRCm39) |
G148D |
probably damaging |
Het |
Fmnl3 |
G |
C |
15: 99,220,619 (GRCm39) |
|
probably benign |
Het |
Fstl5 |
G |
A |
3: 76,614,786 (GRCm39) |
G179R |
probably damaging |
Het |
Garre1 |
A |
T |
7: 33,938,644 (GRCm39) |
W246R |
probably damaging |
Het |
Gart |
T |
A |
16: 91,422,282 (GRCm39) |
Q745L |
probably benign |
Het |
Gmeb1 |
T |
A |
4: 131,959,419 (GRCm39) |
M212L |
probably benign |
Het |
Gpaa1 |
T |
C |
15: 76,218,981 (GRCm39) |
Y548H |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 34,986,667 (GRCm39) |
E763G |
probably damaging |
Het |
Grm8 |
T |
A |
6: 27,762,389 (GRCm39) |
I279F |
probably damaging |
Het |
Hcls1 |
T |
A |
16: 36,771,536 (GRCm39) |
H147Q |
probably damaging |
Het |
Hpcal1 |
A |
C |
12: 17,836,389 (GRCm39) |
D73A |
probably damaging |
Het |
Il22ra1 |
T |
C |
4: 135,478,317 (GRCm39) |
S463P |
probably benign |
Het |
Itgbl1 |
G |
A |
14: 124,078,098 (GRCm39) |
|
probably null |
Het |
Izumo3 |
G |
T |
4: 92,035,437 (GRCm39) |
|
probably benign |
Het |
Kcna5 |
A |
T |
6: 126,510,346 (GRCm39) |
L594Q |
probably damaging |
Het |
Kif13a |
A |
T |
13: 46,918,079 (GRCm39) |
D409E |
probably benign |
Het |
Kif9 |
A |
T |
9: 110,314,106 (GRCm39) |
I39F |
probably damaging |
Het |
Klri2 |
C |
T |
6: 129,709,171 (GRCm39) |
R227H |
possibly damaging |
Het |
Lamc3 |
G |
A |
2: 31,798,628 (GRCm39) |
G445S |
probably damaging |
Het |
Lctl |
A |
G |
9: 64,024,980 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
T |
C |
2: 91,325,327 (GRCm39) |
L1384P |
probably damaging |
Het |
Mcm9 |
G |
A |
10: 53,439,526 (GRCm39) |
S549L |
possibly damaging |
Het |
Ms4a15 |
G |
A |
19: 10,956,697 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
C |
4: 148,555,081 (GRCm39) |
V901A |
possibly damaging |
Het |
Nckap1l |
A |
T |
15: 103,390,391 (GRCm39) |
I721F |
probably benign |
Het |
Nemp2 |
T |
C |
1: 52,684,588 (GRCm39) |
V298A |
probably benign |
Het |
Npc1l1 |
T |
A |
11: 6,178,148 (GRCm39) |
K421* |
probably null |
Het |
Npr1 |
C |
T |
3: 90,363,244 (GRCm39) |
V879M |
probably damaging |
Het |
Odad4 |
A |
G |
11: 100,454,394 (GRCm39) |
E393G |
probably damaging |
Het |
Or2ad1 |
A |
G |
13: 21,326,336 (GRCm39) |
V297A |
possibly damaging |
Het |
Or51q1c |
A |
G |
7: 103,652,709 (GRCm39) |
T82A |
probably benign |
Het |
Osgin1 |
A |
T |
8: 120,169,219 (GRCm39) |
I39F |
possibly damaging |
Het |
Phip |
G |
C |
9: 82,809,244 (GRCm39) |
|
probably null |
Het |
Pkdrej |
G |
T |
15: 85,705,768 (GRCm39) |
P56Q |
possibly damaging |
Het |
Plcxd2 |
A |
G |
16: 45,800,889 (GRCm39) |
Y112H |
probably damaging |
Het |
Plekha1 |
C |
T |
7: 130,499,176 (GRCm39) |
T155M |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,558,196 (GRCm39) |
|
probably null |
Het |
Prss1 |
A |
G |
6: 41,439,495 (GRCm39) |
H76R |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,348,558 (GRCm39) |
D83G |
probably benign |
Het |
Ptprd |
T |
A |
4: 76,055,140 (GRCm39) |
Q196L |
probably benign |
Het |
Ranbp3l |
A |
T |
15: 9,063,067 (GRCm39) |
H292L |
probably damaging |
Het |
Ranbp6 |
T |
C |
19: 29,787,097 (GRCm39) |
E1085G |
probably benign |
Het |
Rccd1 |
A |
G |
7: 79,970,326 (GRCm39) |
V97A |
possibly damaging |
Het |
Rchy1 |
T |
C |
5: 92,105,458 (GRCm39) |
S48G |
probably benign |
Het |
Rnmt |
G |
A |
18: 68,446,771 (GRCm39) |
M265I |
probably benign |
Het |
Robo3 |
A |
T |
9: 37,336,640 (GRCm39) |
M376K |
probably benign |
Het |
Rrp12 |
T |
C |
19: 41,862,289 (GRCm39) |
D898G |
probably benign |
Het |
Scg3 |
A |
T |
9: 75,570,462 (GRCm39) |
|
probably benign |
Het |
Sec31b |
A |
T |
19: 44,522,821 (GRCm39) |
M57K |
probably damaging |
Het |
Slc17a6 |
A |
C |
7: 51,315,892 (GRCm39) |
I387L |
probably benign |
Het |
Speer4a1 |
T |
A |
5: 26,240,982 (GRCm39) |
Q170L |
possibly damaging |
Het |
Srsf9 |
A |
G |
5: 115,470,260 (GRCm39) |
D146G |
possibly damaging |
Het |
Ss18 |
A |
G |
18: 14,788,200 (GRCm39) |
M90T |
probably damaging |
Het |
Syna |
A |
T |
5: 134,588,314 (GRCm39) |
F212I |
possibly damaging |
Het |
Tex54 |
A |
G |
19: 8,718,221 (GRCm39) |
|
probably benign |
Het |
Thsd1 |
A |
G |
8: 22,733,055 (GRCm39) |
H34R |
probably damaging |
Het |
Tmem143 |
T |
C |
7: 45,547,086 (GRCm39) |
I84T |
probably benign |
Het |
Trim50 |
T |
C |
5: 135,395,487 (GRCm39) |
V281A |
probably damaging |
Het |
Trp53i11 |
C |
A |
2: 93,029,696 (GRCm39) |
|
probably benign |
Het |
Ttll4 |
C |
T |
1: 74,718,851 (GRCm39) |
T234I |
possibly damaging |
Het |
Ttyh1 |
A |
T |
7: 4,127,719 (GRCm39) |
I136F |
possibly damaging |
Het |
Ube2f |
T |
C |
1: 91,189,976 (GRCm39) |
|
probably benign |
Het |
Vcl |
T |
A |
14: 21,037,083 (GRCm39) |
L227* |
probably null |
Het |
Vmn1r222 |
A |
C |
13: 23,416,974 (GRCm39) |
C80G |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,926,365 (GRCm39) |
A3889S |
probably benign |
Het |
Zbtb44 |
A |
G |
9: 30,978,006 (GRCm39) |
Y422C |
probably damaging |
Het |
Zfp180 |
A |
G |
7: 23,805,158 (GRCm39) |
S526G |
possibly damaging |
Het |
Zfp518a |
A |
C |
19: 40,904,310 (GRCm39) |
E1413A |
probably damaging |
Het |
Zfp629 |
T |
A |
7: 127,210,858 (GRCm39) |
Y317F |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,820,534 (GRCm39) |
E843G |
probably benign |
Het |
|
Other mutations in Vps8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00500:Vps8
|
APN |
16 |
21,261,084 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL00596:Vps8
|
APN |
16 |
21,267,162 (GRCm39) |
splice site |
probably benign |
|
IGL00985:Vps8
|
APN |
16 |
21,296,334 (GRCm39) |
splice site |
probably benign |
|
IGL01356:Vps8
|
APN |
16 |
21,336,107 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01375:Vps8
|
APN |
16 |
21,378,122 (GRCm39) |
nonsense |
probably null |
|
IGL01643:Vps8
|
APN |
16 |
21,336,972 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02159:Vps8
|
APN |
16 |
21,285,234 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02214:Vps8
|
APN |
16 |
21,336,035 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02465:Vps8
|
APN |
16 |
21,340,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02651:Vps8
|
APN |
16 |
21,336,086 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03174:Vps8
|
APN |
16 |
21,285,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03337:Vps8
|
APN |
16 |
21,381,918 (GRCm39) |
missense |
probably benign |
|
IGL03383:Vps8
|
APN |
16 |
21,254,573 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03402:Vps8
|
APN |
16 |
21,267,148 (GRCm39) |
missense |
possibly damaging |
0.68 |
empires
|
UTSW |
16 |
21,400,298 (GRCm39) |
nonsense |
probably null |
|
porky
|
UTSW |
16 |
21,279,988 (GRCm39) |
missense |
probably benign |
0.32 |
realm
|
UTSW |
16 |
21,363,986 (GRCm39) |
intron |
probably benign |
|
realms
|
UTSW |
16 |
21,262,938 (GRCm39) |
splice site |
probably null |
|
Reich
|
UTSW |
16 |
21,297,189 (GRCm39) |
missense |
probably benign |
0.29 |
reichen
|
UTSW |
16 |
21,325,575 (GRCm39) |
splice site |
probably benign |
|
IGL03052:Vps8
|
UTSW |
16 |
21,267,115 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4677001:Vps8
|
UTSW |
16 |
21,319,084 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0066:Vps8
|
UTSW |
16 |
21,296,273 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0066:Vps8
|
UTSW |
16 |
21,296,273 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0125:Vps8
|
UTSW |
16 |
21,288,904 (GRCm39) |
missense |
probably benign |
0.00 |
R0362:Vps8
|
UTSW |
16 |
21,426,977 (GRCm39) |
intron |
probably benign |
|
R0384:Vps8
|
UTSW |
16 |
21,325,575 (GRCm39) |
splice site |
probably benign |
|
R0492:Vps8
|
UTSW |
16 |
21,261,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Vps8
|
UTSW |
16 |
21,358,859 (GRCm39) |
critical splice donor site |
probably null |
|
R0531:Vps8
|
UTSW |
16 |
21,278,561 (GRCm39) |
intron |
probably benign |
|
R0605:Vps8
|
UTSW |
16 |
21,378,087 (GRCm39) |
missense |
probably benign |
0.00 |
R0636:Vps8
|
UTSW |
16 |
21,253,683 (GRCm39) |
missense |
probably benign |
0.32 |
R0707:Vps8
|
UTSW |
16 |
21,261,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0840:Vps8
|
UTSW |
16 |
21,275,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R1170:Vps8
|
UTSW |
16 |
21,278,570 (GRCm39) |
intron |
probably benign |
|
R1203:Vps8
|
UTSW |
16 |
21,330,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Vps8
|
UTSW |
16 |
21,400,348 (GRCm39) |
missense |
probably benign |
0.00 |
R1531:Vps8
|
UTSW |
16 |
21,285,226 (GRCm39) |
nonsense |
probably null |
|
R1642:Vps8
|
UTSW |
16 |
21,400,329 (GRCm39) |
missense |
probably benign |
|
R1956:Vps8
|
UTSW |
16 |
21,279,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Vps8
|
UTSW |
16 |
21,395,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2287:Vps8
|
UTSW |
16 |
21,387,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Vps8
|
UTSW |
16 |
21,378,087 (GRCm39) |
missense |
probably benign |
0.00 |
R3151:Vps8
|
UTSW |
16 |
21,261,123 (GRCm39) |
missense |
probably benign |
0.04 |
R3943:Vps8
|
UTSW |
16 |
21,288,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Vps8
|
UTSW |
16 |
21,288,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Vps8
|
UTSW |
16 |
21,345,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R4302:Vps8
|
UTSW |
16 |
21,314,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R4398:Vps8
|
UTSW |
16 |
21,323,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R4477:Vps8
|
UTSW |
16 |
21,363,986 (GRCm39) |
intron |
probably benign |
|
R4478:Vps8
|
UTSW |
16 |
21,363,986 (GRCm39) |
intron |
probably benign |
|
R4479:Vps8
|
UTSW |
16 |
21,363,986 (GRCm39) |
intron |
probably benign |
|
R4480:Vps8
|
UTSW |
16 |
21,363,986 (GRCm39) |
intron |
probably benign |
|
R4571:Vps8
|
UTSW |
16 |
21,254,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R4653:Vps8
|
UTSW |
16 |
21,318,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Vps8
|
UTSW |
16 |
21,262,938 (GRCm39) |
splice site |
probably null |
|
R4713:Vps8
|
UTSW |
16 |
21,261,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Vps8
|
UTSW |
16 |
21,267,154 (GRCm39) |
splice site |
probably null |
|
R4959:Vps8
|
UTSW |
16 |
21,278,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Vps8
|
UTSW |
16 |
21,278,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Vps8
|
UTSW |
16 |
21,285,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Vps8
|
UTSW |
16 |
21,280,158 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5144:Vps8
|
UTSW |
16 |
21,378,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Vps8
|
UTSW |
16 |
21,351,849 (GRCm39) |
missense |
probably benign |
0.05 |
R5168:Vps8
|
UTSW |
16 |
21,276,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R5222:Vps8
|
UTSW |
16 |
21,400,298 (GRCm39) |
nonsense |
probably null |
|
R5231:Vps8
|
UTSW |
16 |
21,395,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R5876:Vps8
|
UTSW |
16 |
21,280,189 (GRCm39) |
critical splice donor site |
probably null |
|
R5963:Vps8
|
UTSW |
16 |
21,288,871 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6010:Vps8
|
UTSW |
16 |
21,363,955 (GRCm39) |
intron |
probably benign |
|
R6023:Vps8
|
UTSW |
16 |
21,279,988 (GRCm39) |
missense |
probably benign |
0.32 |
R6173:Vps8
|
UTSW |
16 |
21,314,682 (GRCm39) |
splice site |
probably null |
|
R6185:Vps8
|
UTSW |
16 |
21,288,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R6264:Vps8
|
UTSW |
16 |
21,378,099 (GRCm39) |
nonsense |
probably null |
|
R6409:Vps8
|
UTSW |
16 |
21,297,189 (GRCm39) |
missense |
probably benign |
0.29 |
R6522:Vps8
|
UTSW |
16 |
21,261,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R6528:Vps8
|
UTSW |
16 |
21,372,875 (GRCm39) |
nonsense |
probably null |
|
R6784:Vps8
|
UTSW |
16 |
21,381,957 (GRCm39) |
missense |
probably benign |
0.01 |
R7040:Vps8
|
UTSW |
16 |
21,393,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Vps8
|
UTSW |
16 |
21,400,329 (GRCm39) |
missense |
probably benign |
|
R7103:Vps8
|
UTSW |
16 |
21,345,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Vps8
|
UTSW |
16 |
21,278,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Vps8
|
UTSW |
16 |
21,275,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7206:Vps8
|
UTSW |
16 |
21,276,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7403:Vps8
|
UTSW |
16 |
21,253,722 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7782:Vps8
|
UTSW |
16 |
21,330,308 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7806:Vps8
|
UTSW |
16 |
21,278,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Vps8
|
UTSW |
16 |
21,351,070 (GRCm39) |
missense |
probably benign |
0.01 |
R7943:Vps8
|
UTSW |
16 |
21,296,622 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8075:Vps8
|
UTSW |
16 |
21,340,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R8190:Vps8
|
UTSW |
16 |
21,393,780 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8307:Vps8
|
UTSW |
16 |
21,314,652 (GRCm39) |
missense |
probably benign |
0.02 |
R8483:Vps8
|
UTSW |
16 |
21,393,763 (GRCm39) |
missense |
probably damaging |
0.98 |
R8814:Vps8
|
UTSW |
16 |
21,395,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Vps8
|
UTSW |
16 |
21,288,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:Vps8
|
UTSW |
16 |
21,340,668 (GRCm39) |
missense |
possibly damaging |
0.45 |
R9404:Vps8
|
UTSW |
16 |
21,426,927 (GRCm39) |
missense |
probably benign |
0.12 |
R9544:Vps8
|
UTSW |
16 |
21,336,893 (GRCm39) |
missense |
probably benign |
0.00 |
R9570:Vps8
|
UTSW |
16 |
21,462,953 (GRCm39) |
missense |
probably benign |
0.10 |
R9634:Vps8
|
UTSW |
16 |
21,372,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R9702:Vps8
|
UTSW |
16 |
21,462,883 (GRCm39) |
missense |
probably benign |
0.17 |
|
Predicted Primers |
PCR Primer
(F):5'- TGTGCAAGCTGAGCATAAGGTGTAG -3'
(R):5'- TGTTCAACGTAACCAGGGAGCAG -3'
Sequencing Primer
(F):5'- GTAGAACCCCAGGGTCACTTTATTC -3'
(R):5'- GAGACTTCAGACAATGTTAAACGTG -3'
|
Posted On |
2013-04-12 |