Incidental Mutation 'R7252:Wdr64'
| ID |
563963 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Wdr64
|
| Ensembl Gene |
ENSMUSG00000026523 |
| Gene Name |
WD repeat domain 64 |
| Synonyms |
4930415O10Rik, 4930511H01Rik |
| MMRRC Submission |
045385-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
R7252 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
175526159-175643300 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 175603240 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 614
(T614A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000128678
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094288]
[ENSMUST00000171939]
[ENSMUST00000194087]
[ENSMUST00000194783]
|
| AlphaFold |
Q9D565 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000094288
AA Change: T624A
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000091846
Gene: ENSMUSG00000026523
AA Change: T624A
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
118 |
159 |
2.65e1 |
SMART |
|
WD40
|
162 |
200 |
2.13e1 |
SMART |
|
low complexity region
|
259 |
271 |
N/A |
INTRINSIC |
|
Blast:WD40
|
277 |
316 |
5e-19 |
BLAST |
|
WD40
|
323 |
361 |
2.4e-1 |
SMART |
|
WD40
|
365 |
404 |
8.29e-1 |
SMART |
|
WD40
|
407 |
449 |
1.7e2 |
SMART |
|
WD40
|
457 |
493 |
1.19e1 |
SMART |
|
WD40
|
497 |
538 |
4.55e-3 |
SMART |
|
WD40
|
643 |
684 |
3.31e0 |
SMART |
|
WD40
|
742 |
806 |
7.4e0 |
SMART |
|
Blast:WD40
|
811 |
851 |
7e-17 |
BLAST |
|
WD40
|
864 |
903 |
4.62e-4 |
SMART |
|
Blast:XPGN
|
921 |
964 |
9e-19 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000171939
AA Change: T614A
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000128678
Gene: ENSMUSG00000026523
AA Change: T614A
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
151 |
190 |
5.73e0 |
SMART |
|
low complexity region
|
249 |
261 |
N/A |
INTRINSIC |
|
Blast:WD40
|
267 |
306 |
4e-19 |
BLAST |
|
WD40
|
313 |
351 |
2.4e-1 |
SMART |
|
WD40
|
355 |
394 |
8.29e-1 |
SMART |
|
WD40
|
397 |
439 |
1.7e2 |
SMART |
|
WD40
|
447 |
483 |
1.19e1 |
SMART |
|
WD40
|
487 |
528 |
4.55e-3 |
SMART |
|
WD40
|
633 |
674 |
3.31e0 |
SMART |
|
WD40
|
732 |
796 |
7.4e0 |
SMART |
|
Blast:WD40
|
801 |
841 |
5e-17 |
BLAST |
|
WD40
|
854 |
893 |
4.62e-4 |
SMART |
|
Blast:XPGN
|
911 |
954 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000194087
AA Change: T614A
PolyPhen 2
Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000141740
Gene: ENSMUSG00000026523
AA Change: T614A
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
151 |
190 |
3.6e-2 |
SMART |
|
low complexity region
|
249 |
261 |
N/A |
INTRINSIC |
|
Blast:WD40
|
267 |
305 |
5e-19 |
BLAST |
|
WD40
|
313 |
351 |
1.5e-3 |
SMART |
|
WD40
|
355 |
394 |
5.2e-3 |
SMART |
|
WD40
|
397 |
439 |
1.1e0 |
SMART |
|
WD40
|
447 |
483 |
7.6e-2 |
SMART |
|
WD40
|
487 |
528 |
2.9e-5 |
SMART |
|
WD40
|
633 |
674 |
2.1e-2 |
SMART |
|
WD40
|
732 |
796 |
4.7e-2 |
SMART |
|
Blast:WD40
|
801 |
841 |
6e-17 |
BLAST |
|
WD40
|
854 |
893 |
2.9e-6 |
SMART |
|
Blast:XPGN
|
911 |
954 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000194783
AA Change: T173A
PolyPhen 2
Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000141384
Gene: ENSMUSG00000026523
AA Change: T173A
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
6 |
42 |
7.6e-2 |
SMART |
|
WD40
|
46 |
87 |
2.9e-5 |
SMART |
|
WD40
|
192 |
233 |
2.1e-2 |
SMART |
|
WD40
|
291 |
355 |
4.7e-2 |
SMART |
|
Blast:WD40
|
360 |
400 |
4e-17 |
BLAST |
|
WD40
|
413 |
452 |
2.9e-6 |
SMART |
|
Blast:XPGN
|
470 |
519 |
3e-19 |
BLAST |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.5%
|
| Validation Efficiency |
99% (81/82) |
| Allele List at MGI |
All alleles(1) : Gene trapped(1)
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930480E11Rik |
G |
T |
X: 77,414,311 (GRCm39) |
M345I |
probably benign |
Het |
| Abcc2 |
T |
A |
19: 43,816,388 (GRCm39) |
I1226N |
probably damaging |
Het |
| Adarb2 |
A |
G |
13: 8,620,216 (GRCm39) |
E234G |
probably benign |
Het |
| Ankrd52 |
T |
C |
10: 128,217,865 (GRCm39) |
S282P |
probably damaging |
Het |
| Arhgef12 |
A |
T |
9: 42,927,205 (GRCm39) |
S306R |
probably benign |
Het |
| Baiap2 |
G |
T |
11: 119,893,865 (GRCm39) |
A514S |
probably benign |
Het |
| BC030500 |
T |
A |
8: 59,364,838 (GRCm39) |
|
probably null |
Het |
| C1qtnf12 |
T |
A |
4: 156,047,072 (GRCm39) |
W13R |
unknown |
Het |
| Ccdc158 |
A |
G |
5: 92,798,647 (GRCm39) |
V351A |
probably benign |
Het |
| Cct8 |
T |
C |
16: 87,281,807 (GRCm39) |
E485G |
probably benign |
Het |
| Cep85 |
T |
C |
4: 133,875,342 (GRCm39) |
D542G |
probably benign |
Het |
| Clhc1 |
T |
A |
11: 29,513,937 (GRCm39) |
S340R |
probably benign |
Het |
| Cnot4 |
A |
T |
6: 35,046,362 (GRCm39) |
D168E |
probably damaging |
Het |
| Cntn5 |
G |
A |
9: 9,831,640 (GRCm39) |
T375I |
probably benign |
Het |
| Ctc1 |
T |
A |
11: 68,917,000 (GRCm39) |
I298N |
probably damaging |
Het |
| Dchs2 |
T |
A |
3: 83,232,610 (GRCm39) |
N2198K |
probably benign |
Het |
| Ddx6 |
G |
A |
9: 44,535,050 (GRCm39) |
|
probably null |
Het |
| Defb11 |
A |
G |
8: 22,395,473 (GRCm39) |
I68T |
probably benign |
Het |
| Dip2a |
C |
T |
10: 76,109,036 (GRCm39) |
V1212I |
not run |
Het |
| Dop1a |
T |
A |
9: 86,382,874 (GRCm39) |
I269N |
probably damaging |
Het |
| Efna3 |
C |
T |
3: 89,223,971 (GRCm39) |
G73S |
possibly damaging |
Het |
| Fam98b |
C |
G |
2: 117,094,373 (GRCm39) |
R228G |
probably damaging |
Het |
| Fancd2 |
A |
T |
6: 113,533,246 (GRCm39) |
N521I |
probably damaging |
Het |
| Farsa |
A |
G |
8: 85,587,957 (GRCm39) |
D134G |
probably damaging |
Het |
| Fat2 |
A |
T |
11: 55,202,088 (GRCm39) |
F329I |
probably damaging |
Het |
| Gm14399 |
A |
T |
2: 174,974,991 (GRCm39) |
I43K |
probably damaging |
Het |
| Gpr15 |
A |
G |
16: 58,538,760 (GRCm39) |
S110P |
probably damaging |
Het |
| Gpr157 |
T |
C |
4: 150,183,331 (GRCm39) |
V167A |
probably benign |
Het |
| Hacd4 |
A |
G |
4: 88,345,000 (GRCm39) |
I134T |
possibly damaging |
Het |
| Hpgd |
T |
A |
8: 56,751,461 (GRCm39) |
N96K |
probably damaging |
Het |
| Insm2 |
A |
T |
12: 55,647,305 (GRCm39) |
T350S |
probably benign |
Het |
| Iqch |
C |
T |
9: 63,419,518 (GRCm39) |
|
probably null |
Het |
| Kmt2d |
A |
G |
15: 98,742,147 (GRCm39) |
S4338P |
unknown |
Het |
| Krtap9-3 |
A |
G |
11: 99,488,796 (GRCm39) |
S29P |
probably benign |
Het |
| Kyat3 |
T |
A |
3: 142,426,219 (GRCm39) |
S87T |
probably benign |
Het |
| Minar2 |
A |
G |
18: 59,199,980 (GRCm39) |
|
probably null |
Het |
| Mrpl46 |
T |
C |
7: 78,430,336 (GRCm39) |
T145A |
probably benign |
Het |
| Neb |
A |
G |
2: 52,214,973 (GRCm39) |
|
probably null |
Het |
| Or2aj5 |
A |
T |
16: 19,425,249 (GRCm39) |
H55Q |
probably damaging |
Het |
| Or4c124 |
T |
A |
2: 89,156,629 (GRCm39) |
|
probably benign |
Het |
| Or6x1 |
C |
T |
9: 40,098,657 (GRCm39) |
T82I |
probably benign |
Het |
| Or7g17 |
A |
G |
9: 18,768,548 (GRCm39) |
Y200C |
probably damaging |
Het |
| Or9a7 |
A |
G |
6: 40,521,703 (GRCm39) |
I70T |
probably benign |
Het |
| Otogl |
T |
C |
10: 107,657,804 (GRCm39) |
D1042G |
probably benign |
Het |
| Paxip1 |
C |
T |
5: 27,965,084 (GRCm39) |
V659I |
probably damaging |
Het |
| Pfkl |
A |
G |
10: 77,829,263 (GRCm39) |
W382R |
probably damaging |
Het |
| Pfn1 |
A |
G |
11: 70,545,297 (GRCm39) |
W4R |
probably damaging |
Het |
| Pik3c2b |
G |
A |
1: 133,022,472 (GRCm39) |
R1138H |
probably benign |
Het |
| Pkd1l3 |
A |
G |
8: 110,387,330 (GRCm39) |
D1758G |
probably benign |
Het |
| Pmpca |
G |
C |
2: 26,285,046 (GRCm39) |
E424Q |
possibly damaging |
Het |
| Pramel29 |
T |
C |
4: 143,939,510 (GRCm39) |
D9G |
possibly damaging |
Het |
| Prdm12 |
A |
G |
2: 31,532,386 (GRCm39) |
N132S |
possibly damaging |
Het |
| Prokr2 |
T |
A |
2: 132,223,360 (GRCm39) |
M61L |
probably benign |
Het |
| Ralgapa2 |
T |
C |
2: 146,184,671 (GRCm39) |
|
probably null |
Het |
| Ralgps1 |
A |
T |
2: 33,058,200 (GRCm39) |
D301E |
probably benign |
Het |
| Rcbtb2 |
T |
C |
14: 73,404,220 (GRCm39) |
Y231H |
probably damaging |
Het |
| Rcc2 |
G |
A |
4: 140,429,586 (GRCm39) |
C40Y |
probably benign |
Het |
| Relb |
C |
A |
7: 19,346,538 (GRCm39) |
E345* |
probably null |
Het |
| Rhbdl3 |
A |
C |
11: 80,228,411 (GRCm39) |
M294L |
possibly damaging |
Het |
| Rpl24 |
G |
A |
16: 55,790,479 (GRCm39) |
A112T |
possibly damaging |
Het |
| Rsbn1l |
C |
T |
5: 21,113,196 (GRCm39) |
R442Q |
probably damaging |
Het |
| Rxfp3 |
A |
T |
15: 11,036,025 (GRCm39) |
I449N |
probably benign |
Het |
| Sema4c |
A |
C |
1: 36,589,096 (GRCm39) |
C677G |
probably damaging |
Het |
| Sf3b3 |
A |
C |
8: 111,566,562 (GRCm39) |
I256S |
probably damaging |
Het |
| Shank1 |
C |
T |
7: 43,976,585 (GRCm39) |
A561V |
unknown |
Het |
| Slc39a6 |
G |
T |
18: 24,734,442 (GRCm39) |
N82K |
possibly damaging |
Het |
| Slc3a2 |
T |
C |
19: 8,700,521 (GRCm39) |
|
probably benign |
Het |
| Stard13 |
T |
C |
5: 150,986,634 (GRCm39) |
Q292R |
probably benign |
Het |
| Tgm6 |
A |
G |
2: 129,986,884 (GRCm39) |
R451G |
probably damaging |
Het |
| Tspo |
G |
T |
15: 83,456,466 (GRCm39) |
G83V |
probably damaging |
Het |
| Ubxn10 |
T |
C |
4: 138,448,187 (GRCm39) |
Q163R |
probably benign |
Het |
| Ushbp1 |
A |
G |
8: 71,847,246 (GRCm39) |
S129P |
probably benign |
Het |
| Vmn2r23 |
T |
A |
6: 123,718,540 (GRCm39) |
V631D |
probably damaging |
Het |
| Vmn2r24 |
T |
C |
6: 123,764,191 (GRCm39) |
I356T |
possibly damaging |
Het |
| Vmn2r84 |
C |
T |
10: 130,222,279 (GRCm39) |
C647Y |
probably damaging |
Het |
| Vps13a |
T |
C |
19: 16,638,428 (GRCm39) |
E2356G |
probably benign |
Het |
| Zdhhc16 |
G |
T |
19: 41,929,990 (GRCm39) |
W271L |
probably damaging |
Het |
| Zer1 |
A |
C |
2: 29,991,904 (GRCm39) |
S652A |
probably damaging |
Het |
| Zfp287 |
A |
G |
11: 62,615,655 (GRCm39) |
V224A |
probably damaging |
Het |
| Zfp438 |
A |
T |
18: 5,214,874 (GRCm39) |
L28* |
probably null |
Het |
| Zfp830 |
G |
A |
11: 82,655,534 (GRCm39) |
A113T |
probably benign |
Het |
| Zfp865 |
G |
T |
7: 5,037,416 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Wdr64 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00563:Wdr64
|
APN |
1 |
175,526,366 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00902:Wdr64
|
APN |
1 |
175,556,391 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01347:Wdr64
|
APN |
1 |
175,547,899 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL01353:Wdr64
|
APN |
1 |
175,559,151 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01583:Wdr64
|
APN |
1 |
175,594,722 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01643:Wdr64
|
APN |
1 |
175,599,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01673:Wdr64
|
APN |
1 |
175,627,922 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
IGL01992:Wdr64
|
APN |
1 |
175,533,637 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02613:Wdr64
|
APN |
1 |
175,594,613 (GRCm39) |
nonsense |
probably null |
|
|
IGL02834:Wdr64
|
APN |
1 |
175,633,415 (GRCm39) |
splice site |
probably benign |
|
|
IGL03214:Wdr64
|
APN |
1 |
175,571,201 (GRCm39) |
splice site |
probably benign |
|
|
IGL03305:Wdr64
|
APN |
1 |
175,583,152 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL03308:Wdr64
|
APN |
1 |
175,594,562 (GRCm39) |
unclassified |
probably benign |
|
|
PIT4418001:Wdr64
|
UTSW |
1 |
175,571,160 (GRCm39) |
nonsense |
probably null |
|
|
R0036:Wdr64
|
UTSW |
1 |
175,556,496 (GRCm39) |
nonsense |
probably null |
|
|
R0041:Wdr64
|
UTSW |
1 |
175,554,037 (GRCm39) |
nonsense |
probably null |
|
|
R0041:Wdr64
|
UTSW |
1 |
175,554,037 (GRCm39) |
nonsense |
probably null |
|
|
R0079:Wdr64
|
UTSW |
1 |
175,622,668 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0380:Wdr64
|
UTSW |
1 |
175,597,208 (GRCm39) |
splice site |
probably benign |
|
|
R0486:Wdr64
|
UTSW |
1 |
175,622,769 (GRCm39) |
splice site |
probably benign |
|
|
R0520:Wdr64
|
UTSW |
1 |
175,553,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0598:Wdr64
|
UTSW |
1 |
175,633,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0711:Wdr64
|
UTSW |
1 |
175,599,751 (GRCm39) |
missense |
probably benign |
0.39 |
|
R0746:Wdr64
|
UTSW |
1 |
175,620,539 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0927:Wdr64
|
UTSW |
1 |
175,620,647 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0947:Wdr64
|
UTSW |
1 |
175,603,315 (GRCm39) |
missense |
probably benign |
|
|
R1014:Wdr64
|
UTSW |
1 |
175,583,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1332:Wdr64
|
UTSW |
1 |
175,622,706 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R1416:Wdr64
|
UTSW |
1 |
175,633,568 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1421:Wdr64
|
UTSW |
1 |
175,594,716 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1467:Wdr64
|
UTSW |
1 |
175,603,288 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1467:Wdr64
|
UTSW |
1 |
175,603,288 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1796:Wdr64
|
UTSW |
1 |
175,544,897 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1797:Wdr64
|
UTSW |
1 |
175,639,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2145:Wdr64
|
UTSW |
1 |
175,594,661 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2321:Wdr64
|
UTSW |
1 |
175,622,653 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R2449:Wdr64
|
UTSW |
1 |
175,526,479 (GRCm39) |
missense |
probably benign |
|
|
R4049:Wdr64
|
UTSW |
1 |
175,633,422 (GRCm39) |
missense |
probably benign |
0.21 |
|
R4155:Wdr64
|
UTSW |
1 |
175,597,172 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4624:Wdr64
|
UTSW |
1 |
175,599,829 (GRCm39) |
missense |
probably benign |
|
|
R4661:Wdr64
|
UTSW |
1 |
175,554,060 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4711:Wdr64
|
UTSW |
1 |
175,626,795 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4891:Wdr64
|
UTSW |
1 |
175,526,345 (GRCm39) |
unclassified |
probably benign |
|
|
R4925:Wdr64
|
UTSW |
1 |
175,552,268 (GRCm39) |
splice site |
probably null |
|
|
R4943:Wdr64
|
UTSW |
1 |
175,547,882 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5000:Wdr64
|
UTSW |
1 |
175,553,941 (GRCm39) |
splice site |
probably null |
|
|
R5001:Wdr64
|
UTSW |
1 |
175,620,525 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R5143:Wdr64
|
UTSW |
1 |
175,553,979 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5395:Wdr64
|
UTSW |
1 |
175,583,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5813:Wdr64
|
UTSW |
1 |
175,639,623 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6014:Wdr64
|
UTSW |
1 |
175,633,556 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R6417:Wdr64
|
UTSW |
1 |
175,553,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6456:Wdr64
|
UTSW |
1 |
175,613,175 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6555:Wdr64
|
UTSW |
1 |
175,547,856 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6576:Wdr64
|
UTSW |
1 |
175,633,494 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R6797:Wdr64
|
UTSW |
1 |
175,638,176 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6891:Wdr64
|
UTSW |
1 |
175,533,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6959:Wdr64
|
UTSW |
1 |
175,533,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7205:Wdr64
|
UTSW |
1 |
175,617,499 (GRCm39) |
missense |
probably benign |
0.34 |
|
R7552:Wdr64
|
UTSW |
1 |
175,613,147 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7732:Wdr64
|
UTSW |
1 |
175,617,495 (GRCm39) |
missense |
probably benign |
|
|
R7777:Wdr64
|
UTSW |
1 |
175,617,564 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7780:Wdr64
|
UTSW |
1 |
175,556,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7810:Wdr64
|
UTSW |
1 |
175,559,092 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7833:Wdr64
|
UTSW |
1 |
175,591,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7843:Wdr64
|
UTSW |
1 |
175,639,668 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7887:Wdr64
|
UTSW |
1 |
175,613,111 (GRCm39) |
missense |
not run |
|
|
R7991:Wdr64
|
UTSW |
1 |
175,554,051 (GRCm39) |
missense |
probably benign |
0.36 |
|
R8124:Wdr64
|
UTSW |
1 |
175,626,844 (GRCm39) |
splice site |
probably null |
|
|
R8129:Wdr64
|
UTSW |
1 |
175,603,154 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8673:Wdr64
|
UTSW |
1 |
175,633,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8728:Wdr64
|
UTSW |
1 |
175,559,079 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8786:Wdr64
|
UTSW |
1 |
175,636,327 (GRCm39) |
nonsense |
probably null |
|
|
R8822:Wdr64
|
UTSW |
1 |
175,544,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8842:Wdr64
|
UTSW |
1 |
175,599,893 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8887:Wdr64
|
UTSW |
1 |
175,599,850 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9014:Wdr64
|
UTSW |
1 |
175,526,395 (GRCm39) |
missense |
probably benign |
|
|
R9330:Wdr64
|
UTSW |
1 |
175,554,024 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9332:Wdr64
|
UTSW |
1 |
175,599,871 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9465:Wdr64
|
UTSW |
1 |
175,618,823 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9716:Wdr64
|
UTSW |
1 |
175,622,658 (GRCm39) |
missense |
probably benign |
|
|
R9717:Wdr64
|
UTSW |
1 |
175,544,854 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Wdr64
|
UTSW |
1 |
175,533,551 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGTACCTACCAGTCTATGTTTGC -3'
(R):5'- CAGATGGCCCCATACTCAGAAG -3'
Sequencing Primer
(F):5'- ACCTACCAGTCTATGTTTGCTTTAC -3'
(R):5'- GATGGCCCCATACTCAGAAGTATATG -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation