Incidental Mutation 'R1777:Cntln'
| ID |
197087 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cntln
|
| Ensembl Gene |
ENSMUSG00000038070 |
| Gene Name |
centlein, centrosomal protein |
| Synonyms |
D530005L17Rik, B430108F07Rik |
| MMRRC Submission |
039808-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.317)
|
| Stock # |
R1777 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
4 |
| Chromosomal Location |
84802546-85050158 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 85048916 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 1376
(E1376G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000130491
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047023]
[ENSMUST00000107190]
[ENSMUST00000169371]
|
| AlphaFold |
A2AM05 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000047023
AA Change: E1377G
PolyPhen 2
Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000044138
Gene: ENSMUSG00000038070
AA Change: E1377G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
low complexity region
|
58 |
86 |
N/A |
INTRINSIC |
|
coiled coil region
|
96 |
126 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
198 |
219 |
1.25e-5 |
PROSPERO |
|
low complexity region
|
242 |
251 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
321 |
342 |
1.25e-5 |
PROSPERO |
|
low complexity region
|
346 |
358 |
N/A |
INTRINSIC |
|
coiled coil region
|
404 |
433 |
N/A |
INTRINSIC |
|
low complexity region
|
434 |
446 |
N/A |
INTRINSIC |
|
coiled coil region
|
458 |
481 |
N/A |
INTRINSIC |
|
coiled coil region
|
516 |
584 |
N/A |
INTRINSIC |
|
coiled coil region
|
606 |
648 |
N/A |
INTRINSIC |
|
coiled coil region
|
674 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
815 |
829 |
N/A |
INTRINSIC |
|
coiled coil region
|
973 |
1114 |
N/A |
INTRINSIC |
|
low complexity region
|
1206 |
1217 |
N/A |
INTRINSIC |
|
Blast:HisKA
|
1270 |
1326 |
1e-24 |
BLAST |
|
low complexity region
|
1327 |
1348 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000107190
AA Change: E242G
PolyPhen 2
Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000102808
Gene: ENSMUSG00000038070
AA Change: E242G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
71 |
82 |
N/A |
INTRINSIC |
|
Blast:HisKA
|
135 |
191 |
8e-27 |
BLAST |
|
low complexity region
|
192 |
213 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000169371
AA Change: E1376G
PolyPhen 2
Score 0.227 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000130491
Gene: ENSMUSG00000038070
AA Change: E1376G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
low complexity region
|
58 |
86 |
N/A |
INTRINSIC |
|
coiled coil region
|
96 |
126 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
198 |
219 |
1.24e-5 |
PROSPERO |
|
low complexity region
|
242 |
251 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
321 |
342 |
1.24e-5 |
PROSPERO |
|
low complexity region
|
346 |
358 |
N/A |
INTRINSIC |
|
coiled coil region
|
404 |
433 |
N/A |
INTRINSIC |
|
low complexity region
|
434 |
446 |
N/A |
INTRINSIC |
|
coiled coil region
|
458 |
481 |
N/A |
INTRINSIC |
|
coiled coil region
|
516 |
584 |
N/A |
INTRINSIC |
|
coiled coil region
|
606 |
648 |
N/A |
INTRINSIC |
|
coiled coil region
|
674 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
815 |
829 |
N/A |
INTRINSIC |
|
coiled coil region
|
972 |
1113 |
N/A |
INTRINSIC |
|
low complexity region
|
1205 |
1216 |
N/A |
INTRINSIC |
|
Blast:HisKA
|
1269 |
1325 |
1e-24 |
BLAST |
|
low complexity region
|
1326 |
1347 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.1%
- 20x: 92.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930444P10Rik |
T |
A |
1: 16,148,813 (GRCm39) |
D111V |
possibly damaging |
Het |
| Ap2a1 |
G |
A |
7: 44,553,576 (GRCm39) |
T597M |
probably damaging |
Het |
| Arhgap25 |
A |
G |
6: 87,440,289 (GRCm39) |
S364P |
probably benign |
Het |
| Atp6v1a |
G |
T |
16: 43,935,068 (GRCm39) |
Y40* |
probably null |
Het |
| Cdh1 |
T |
A |
8: 107,383,467 (GRCm39) |
H235Q |
probably damaging |
Het |
| Cntnap5b |
T |
A |
1: 100,297,803 (GRCm39) |
S781T |
probably benign |
Het |
| Cpne4 |
A |
G |
9: 104,749,887 (GRCm39) |
T64A |
probably damaging |
Het |
| Ctsg |
T |
C |
14: 56,338,058 (GRCm39) |
Y179C |
probably damaging |
Het |
| Cx3cr1 |
A |
G |
9: 119,880,659 (GRCm39) |
Y248H |
probably damaging |
Het |
| Dhx37 |
T |
C |
5: 125,506,995 (GRCm39) |
E167G |
probably benign |
Het |
| Dnajc21 |
C |
A |
15: 10,449,693 (GRCm39) |
A443S |
probably benign |
Het |
| Drd5 |
T |
C |
5: 38,477,504 (GRCm39) |
S166P |
probably damaging |
Het |
| Dscaml1 |
T |
C |
9: 45,595,054 (GRCm39) |
L719P |
possibly damaging |
Het |
| Eif2ak4 |
T |
C |
2: 118,261,320 (GRCm39) |
I542T |
probably damaging |
Het |
| Ephb3 |
G |
A |
16: 21,035,985 (GRCm39) |
G291E |
probably damaging |
Het |
| Eva1a |
T |
A |
6: 82,069,137 (GRCm39) |
Y155N |
probably damaging |
Het |
| Exog |
C |
T |
9: 119,278,884 (GRCm39) |
P189L |
probably damaging |
Het |
| Fam13b |
A |
G |
18: 34,590,813 (GRCm39) |
V455A |
possibly damaging |
Het |
| Fmn2 |
C |
A |
1: 174,409,488 (GRCm39) |
Q574K |
unknown |
Het |
| Gm6871 |
A |
T |
7: 41,195,143 (GRCm39) |
S531R |
probably benign |
Het |
| Golga2 |
T |
A |
2: 32,195,482 (GRCm39) |
|
probably null |
Het |
| Hydin |
C |
T |
8: 111,316,203 (GRCm39) |
P4365L |
probably benign |
Het |
| Ints8 |
A |
T |
4: 11,225,600 (GRCm39) |
|
probably null |
Het |
| Kbtbd12 |
A |
C |
6: 88,595,042 (GRCm39) |
S263A |
probably benign |
Het |
| Kcng4 |
T |
C |
8: 120,360,226 (GRCm39) |
D50G |
probably benign |
Het |
| Klhl18 |
A |
T |
9: 110,266,469 (GRCm39) |
C217S |
probably benign |
Het |
| Klk1b4 |
A |
G |
7: 43,856,875 (GRCm39) |
|
probably benign |
Het |
| Klk7 |
G |
A |
7: 43,462,753 (GRCm39) |
C186Y |
probably damaging |
Het |
| Krbox5 |
A |
T |
13: 67,981,984 (GRCm39) |
R65S |
probably benign |
Het |
| Krit1 |
T |
C |
5: 3,886,799 (GRCm39) |
Y635H |
probably damaging |
Het |
| Lipo4 |
A |
T |
19: 33,476,721 (GRCm39) |
D342E |
probably damaging |
Het |
| Lsm14b |
T |
G |
2: 179,673,588 (GRCm39) |
D199E |
probably benign |
Het |
| Map3k4 |
A |
T |
17: 12,490,617 (GRCm39) |
N271K |
possibly damaging |
Het |
| Mast1 |
T |
A |
8: 85,638,697 (GRCm39) |
N1544I |
probably benign |
Het |
| Megf6 |
T |
A |
4: 154,355,147 (GRCm39) |
C1487* |
probably null |
Het |
| Mlh3 |
C |
A |
12: 85,315,528 (GRCm39) |
K219N |
possibly damaging |
Het |
| Mtmr4 |
A |
G |
11: 87,493,656 (GRCm39) |
K305E |
probably damaging |
Het |
| Myo15a |
A |
G |
11: 60,405,762 (GRCm39) |
M3105V |
probably benign |
Het |
| Nbas |
A |
T |
12: 13,563,563 (GRCm39) |
I1958F |
probably benign |
Het |
| Nepro |
A |
T |
16: 44,556,216 (GRCm39) |
Q458L |
probably damaging |
Het |
| Opa3 |
T |
C |
7: 18,978,837 (GRCm39) |
Y101H |
probably damaging |
Het |
| Or11g25 |
T |
A |
14: 50,723,757 (GRCm39) |
F281I |
probably benign |
Het |
| Or14c41 |
T |
A |
7: 86,235,272 (GRCm39) |
I263N |
probably benign |
Het |
| Or4f15 |
T |
A |
2: 111,814,042 (GRCm39) |
I126L |
possibly damaging |
Het |
| Or51f1d |
T |
C |
7: 102,700,583 (GRCm39) |
I26T |
probably benign |
Het |
| Or5ac16 |
A |
G |
16: 59,022,379 (GRCm39) |
S137P |
probably benign |
Het |
| Or8b12 |
A |
G |
9: 37,657,607 (GRCm39) |
Y59C |
possibly damaging |
Het |
| Pate3 |
T |
C |
9: 35,559,412 (GRCm39) |
N2D |
probably benign |
Het |
| Pcdhb21 |
T |
A |
18: 37,648,771 (GRCm39) |
D633E |
possibly damaging |
Het |
| Pgm2 |
C |
T |
5: 64,285,125 (GRCm39) |
P589L |
probably benign |
Het |
| Pigg |
T |
A |
5: 108,465,257 (GRCm39) |
D163E |
probably damaging |
Het |
| Polq |
A |
G |
16: 36,880,586 (GRCm39) |
T638A |
possibly damaging |
Het |
| Prmt3 |
T |
A |
7: 49,448,094 (GRCm39) |
M268K |
possibly damaging |
Het |
| Prmt9 |
T |
C |
8: 78,291,737 (GRCm39) |
C370R |
probably benign |
Het |
| Prss57 |
A |
T |
10: 79,623,219 (GRCm39) |
V76E |
possibly damaging |
Het |
| Psme3ip1 |
T |
C |
8: 95,315,439 (GRCm39) |
E31G |
probably damaging |
Het |
| Pzp |
T |
C |
6: 128,467,535 (GRCm39) |
E1089G |
possibly damaging |
Het |
| Qars1 |
T |
A |
9: 108,385,400 (GRCm39) |
|
probably null |
Het |
| Ralgapb |
T |
C |
2: 158,304,115 (GRCm39) |
Y625H |
probably damaging |
Het |
| Rgl2 |
G |
A |
17: 34,150,718 (GRCm39) |
D59N |
probably benign |
Het |
| Robo1 |
T |
G |
16: 72,801,555 (GRCm39) |
W1060G |
probably benign |
Het |
| Scaper |
A |
T |
9: 55,771,830 (GRCm39) |
V362E |
probably benign |
Het |
| Schip1 |
T |
C |
3: 68,525,017 (GRCm39) |
F131S |
probably damaging |
Het |
| Sh2b2 |
A |
T |
5: 136,256,276 (GRCm39) |
V252D |
probably damaging |
Het |
| Shld2 |
C |
A |
14: 33,990,130 (GRCm39) |
V259L |
probably benign |
Het |
| Slc17a6 |
A |
T |
7: 51,295,957 (GRCm39) |
H199L |
possibly damaging |
Het |
| Slc29a1 |
A |
G |
17: 45,898,234 (GRCm39) |
Y325H |
probably damaging |
Het |
| Slc29a4 |
G |
T |
5: 142,699,817 (GRCm39) |
W156L |
probably damaging |
Het |
| Slc5a3 |
T |
A |
16: 91,874,644 (GRCm39) |
S234T |
probably benign |
Het |
| Srd5a3 |
T |
G |
5: 76,297,630 (GRCm39) |
V20G |
probably damaging |
Het |
| Stac |
A |
T |
9: 111,433,150 (GRCm39) |
S223T |
possibly damaging |
Het |
| Sytl2 |
A |
T |
7: 90,052,260 (GRCm39) |
T766S |
probably benign |
Het |
| Tas2r102 |
A |
G |
6: 132,739,254 (GRCm39) |
D54G |
probably benign |
Het |
| Tbpl1 |
A |
G |
10: 22,583,742 (GRCm39) |
V105A |
probably damaging |
Het |
| Tenm3 |
G |
T |
8: 48,870,214 (GRCm39) |
P193Q |
probably benign |
Het |
| Tes |
G |
A |
6: 17,104,754 (GRCm39) |
V403M |
probably benign |
Het |
| Tgfbr2 |
A |
C |
9: 115,938,948 (GRCm39) |
I318S |
probably damaging |
Het |
| Tgfbr3 |
C |
A |
5: 107,284,796 (GRCm39) |
V618L |
probably benign |
Het |
| Tmc1 |
C |
T |
19: 20,793,473 (GRCm39) |
|
probably null |
Het |
| Tmem132a |
G |
A |
19: 10,835,870 (GRCm39) |
H887Y |
probably damaging |
Het |
| Tmem43 |
C |
A |
6: 91,454,312 (GRCm39) |
S33* |
probably null |
Het |
| Tob1 |
A |
G |
11: 94,104,580 (GRCm39) |
K39E |
probably damaging |
Het |
| Tut7 |
A |
T |
13: 59,939,635 (GRCm39) |
H705Q |
probably damaging |
Het |
| Unc79 |
T |
A |
12: 103,078,714 (GRCm39) |
D1433E |
probably damaging |
Het |
| Usp25 |
T |
C |
16: 76,878,442 (GRCm39) |
M622T |
probably damaging |
Het |
| Vmn1r158 |
A |
T |
7: 22,489,855 (GRCm39) |
L118Q |
probably damaging |
Het |
| Vmn1r217 |
T |
A |
13: 23,298,495 (GRCm39) |
I136L |
probably benign |
Het |
| Vmn2r15 |
A |
T |
5: 109,442,136 (GRCm39) |
I99K |
possibly damaging |
Het |
| Vwa7 |
T |
A |
17: 35,243,924 (GRCm39) |
V786E |
probably damaging |
Het |
| Xkr5 |
A |
G |
8: 18,989,148 (GRCm39) |
F248S |
probably benign |
Het |
| Zzef1 |
A |
T |
11: 72,801,098 (GRCm39) |
K2444M |
probably damaging |
Het |
|
| Other mutations in Cntln |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00639:Cntln
|
APN |
4 |
84,924,671 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL00743:Cntln
|
APN |
4 |
84,897,652 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL01014:Cntln
|
APN |
4 |
84,968,145 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02217:Cntln
|
APN |
4 |
85,018,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02323:Cntln
|
APN |
4 |
84,968,026 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02353:Cntln
|
APN |
4 |
84,968,087 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02360:Cntln
|
APN |
4 |
84,968,087 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02616:Cntln
|
APN |
4 |
85,033,689 (GRCm39) |
critical splice donor site |
probably null |
|
|
PIT4696001:Cntln
|
UTSW |
4 |
84,892,237 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0110:Cntln
|
UTSW |
4 |
85,014,994 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0324:Cntln
|
UTSW |
4 |
85,010,932 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0349:Cntln
|
UTSW |
4 |
84,914,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0519:Cntln
|
UTSW |
4 |
84,923,290 (GRCm39) |
splice site |
probably benign |
|
|
R0529:Cntln
|
UTSW |
4 |
84,986,062 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0582:Cntln
|
UTSW |
4 |
84,802,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1077:Cntln
|
UTSW |
4 |
84,914,716 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1345:Cntln
|
UTSW |
4 |
84,892,228 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1457:Cntln
|
UTSW |
4 |
85,015,076 (GRCm39) |
missense |
probably benign |
0.33 |
|
R1571:Cntln
|
UTSW |
4 |
84,865,823 (GRCm39) |
nonsense |
probably null |
|
|
R1622:Cntln
|
UTSW |
4 |
84,981,418 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1681:Cntln
|
UTSW |
4 |
84,865,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1808:Cntln
|
UTSW |
4 |
85,015,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1882:Cntln
|
UTSW |
4 |
85,019,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2056:Cntln
|
UTSW |
4 |
84,967,911 (GRCm39) |
missense |
probably benign |
|
|
R2965:Cntln
|
UTSW |
4 |
84,892,264 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2968:Cntln
|
UTSW |
4 |
84,875,504 (GRCm39) |
missense |
probably benign |
0.27 |
|
R3104:Cntln
|
UTSW |
4 |
84,875,406 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3106:Cntln
|
UTSW |
4 |
84,875,406 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3121:Cntln
|
UTSW |
4 |
84,923,289 (GRCm39) |
splice site |
probably benign |
|
|
R3617:Cntln
|
UTSW |
4 |
84,923,214 (GRCm39) |
nonsense |
probably null |
|
|
R4009:Cntln
|
UTSW |
4 |
84,981,452 (GRCm39) |
missense |
probably benign |
0.45 |
|
R4036:Cntln
|
UTSW |
4 |
84,924,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4548:Cntln
|
UTSW |
4 |
85,015,079 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4592:Cntln
|
UTSW |
4 |
84,889,419 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4666:Cntln
|
UTSW |
4 |
84,889,453 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4826:Cntln
|
UTSW |
4 |
84,923,281 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4836:Cntln
|
UTSW |
4 |
84,967,957 (GRCm39) |
nonsense |
probably null |
|
|
R4856:Cntln
|
UTSW |
4 |
84,889,466 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4886:Cntln
|
UTSW |
4 |
84,889,466 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4995:Cntln
|
UTSW |
4 |
84,968,120 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5090:Cntln
|
UTSW |
4 |
84,865,830 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5202:Cntln
|
UTSW |
4 |
84,889,466 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5905:Cntln
|
UTSW |
4 |
84,889,410 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5953:Cntln
|
UTSW |
4 |
84,968,156 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6028:Cntln
|
UTSW |
4 |
84,889,410 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6298:Cntln
|
UTSW |
4 |
85,014,998 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6351:Cntln
|
UTSW |
4 |
85,033,591 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6371:Cntln
|
UTSW |
4 |
84,802,816 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6481:Cntln
|
UTSW |
4 |
84,985,747 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6864:Cntln
|
UTSW |
4 |
85,015,029 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6874:Cntln
|
UTSW |
4 |
84,985,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6919:Cntln
|
UTSW |
4 |
85,033,605 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7071:Cntln
|
UTSW |
4 |
85,018,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7113:Cntln
|
UTSW |
4 |
84,968,064 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7152:Cntln
|
UTSW |
4 |
84,802,937 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7253:Cntln
|
UTSW |
4 |
85,036,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7289:Cntln
|
UTSW |
4 |
84,964,540 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7440:Cntln
|
UTSW |
4 |
84,981,453 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7670:Cntln
|
UTSW |
4 |
84,897,577 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7707:Cntln
|
UTSW |
4 |
84,802,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7895:Cntln
|
UTSW |
4 |
84,981,561 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8176:Cntln
|
UTSW |
4 |
84,806,926 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8247:Cntln
|
UTSW |
4 |
85,019,017 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8264:Cntln
|
UTSW |
4 |
85,016,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8293:Cntln
|
UTSW |
4 |
84,952,075 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8536:Cntln
|
UTSW |
4 |
84,875,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8844:Cntln
|
UTSW |
4 |
84,892,234 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8924:Cntln
|
UTSW |
4 |
84,806,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8955:Cntln
|
UTSW |
4 |
84,986,110 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8960:Cntln
|
UTSW |
4 |
85,018,961 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R8979:Cntln
|
UTSW |
4 |
85,048,910 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9255:Cntln
|
UTSW |
4 |
85,019,103 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9314:Cntln
|
UTSW |
4 |
84,924,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9353:Cntln
|
UTSW |
4 |
84,802,597 (GRCm39) |
unclassified |
probably benign |
|
|
R9361:Cntln
|
UTSW |
4 |
84,968,151 (GRCm39) |
missense |
probably benign |
0.23 |
|
R9376:Cntln
|
UTSW |
4 |
84,875,258 (GRCm39) |
missense |
probably benign |
0.24 |
|
R9382:Cntln
|
UTSW |
4 |
84,968,318 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9471:Cntln
|
UTSW |
4 |
84,968,019 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R9478:Cntln
|
UTSW |
4 |
84,897,630 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9527:Cntln
|
UTSW |
4 |
84,892,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9788:Cntln
|
UTSW |
4 |
84,968,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9793:Cntln
|
UTSW |
4 |
84,985,798 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CGTCTGTTGAAAAGAGATCCAGTAGGG -3'
(R):5'- TTGGGACAACATCCAACATTCAAATGC -3'
Sequencing Primer
(F):5'- ttagtcatccgttctctccttc -3'
(R):5'- GTGGCTATGCACTTAGTCAAC -3'
|
| Posted On |
2014-05-23 |
Incidental Mutation