Incidental Mutation 'R0432:Clasp2'
| ID |
38841 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Clasp2
|
| Ensembl Gene |
ENSMUSG00000033392 |
| Gene Name |
CLIP associating protein 2 |
| Synonyms |
CLASP2alpha, 1500004F14Rik, CLASP2gamma, CLASP2, CLASP2beta, 8030404L10Rik |
| MMRRC Submission |
038634-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0432 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
113570541-113748750 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 113738487 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 423
(T423A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150145
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000111838]
[ENSMUST00000163895]
[ENSMUST00000166734]
[ENSMUST00000213663]
[ENSMUST00000214522]
[ENSMUST00000215022]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111838
AA Change: T1109A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000107469
Gene: ENSMUSG00000033392
AA Change: T1109A
| Domain | Start | End | E-Value | Type |
|---|
|
TOG
|
90 |
323 |
1.17e-8 |
SMART |
|
low complexity region
|
382 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
472 |
N/A |
INTRINSIC |
|
low complexity region
|
473 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
562 |
572 |
N/A |
INTRINSIC |
|
low complexity region
|
614 |
634 |
N/A |
INTRINSIC |
|
TOG
|
640 |
877 |
2.03e-1 |
SMART |
|
low complexity region
|
995 |
1009 |
N/A |
INTRINSIC |
|
TOG
|
1043 |
1274 |
1.49e-24 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000163895
AA Change: T1130A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000128460
Gene: ENSMUSG00000033392
AA Change: T1130A
| Domain | Start | End | E-Value | Type |
|---|
|
TOG
|
90 |
323 |
1.17e-8 |
SMART |
|
low complexity region
|
382 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
472 |
N/A |
INTRINSIC |
|
low complexity region
|
473 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
583 |
593 |
N/A |
INTRINSIC |
|
low complexity region
|
635 |
655 |
N/A |
INTRINSIC |
|
TOG
|
661 |
898 |
2.03e-1 |
SMART |
|
low complexity region
|
1016 |
1030 |
N/A |
INTRINSIC |
|
TOG
|
1064 |
1295 |
1.49e-24 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000166734
AA Change: T1110A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000130201
Gene: ENSMUSG00000033392
AA Change: T1110A
| Domain | Start | End | E-Value | Type |
|---|
|
TOG
|
90 |
323 |
1.17e-8 |
SMART |
|
low complexity region
|
382 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
472 |
N/A |
INTRINSIC |
|
low complexity region
|
473 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
562 |
572 |
N/A |
INTRINSIC |
|
low complexity region
|
614 |
634 |
N/A |
INTRINSIC |
|
TOG
|
640 |
878 |
7.51e-1 |
SMART |
|
low complexity region
|
996 |
1010 |
N/A |
INTRINSIC |
|
TOG
|
1044 |
1275 |
1.49e-24 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213663
AA Change: T423A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214522
AA Change: T1127A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215022
|
| Meta Mutation Damage Score |
0.0577 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.9%
|
| Validation Efficiency |
99% (91/92) |
| MGI Phenotype |
PHENOTYPE: Targeted deletion of this gene leads to impaired formation of stable microtubules in a wound healing assay, and results in a 2-fold reduction of directionally persistent migration in mutant embryonic fibroblasts. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310061I04Rik |
A |
G |
17: 36,206,708 (GRCm39) |
L110P |
probably damaging |
Het |
| 4930522L14Rik |
A |
T |
5: 109,884,785 (GRCm39) |
C358S |
probably damaging |
Het |
| Abca8b |
C |
A |
11: 109,870,841 (GRCm39) |
V104F |
possibly damaging |
Het |
| Afap1l2 |
T |
C |
19: 56,905,551 (GRCm39) |
|
probably benign |
Het |
| Ahctf1 |
A |
C |
1: 179,611,726 (GRCm39) |
I548R |
probably damaging |
Het |
| Alox12b |
G |
T |
11: 69,060,382 (GRCm39) |
G646V |
probably damaging |
Het |
| Aoah |
C |
T |
13: 21,095,368 (GRCm39) |
|
probably benign |
Het |
| Arhgap39 |
C |
T |
15: 76,619,086 (GRCm39) |
D833N |
probably damaging |
Het |
| Atxn1l |
A |
G |
8: 110,458,325 (GRCm39) |
W646R |
probably damaging |
Het |
| Cabp2 |
T |
C |
19: 4,134,903 (GRCm39) |
I28T |
possibly damaging |
Het |
| Cacna1b |
G |
A |
2: 24,577,716 (GRCm39) |
T719I |
probably damaging |
Het |
| Camk1d |
A |
T |
2: 5,449,946 (GRCm39) |
H70Q |
probably damaging |
Het |
| Car1 |
T |
C |
3: 14,835,236 (GRCm39) |
T170A |
probably benign |
Het |
| Ccdc162 |
T |
C |
10: 41,417,856 (GRCm39) |
T2113A |
probably benign |
Het |
| Cdc5l |
G |
A |
17: 45,726,610 (GRCm39) |
R321W |
probably damaging |
Het |
| Cdh17 |
T |
A |
4: 11,771,273 (GRCm39) |
C18* |
probably null |
Het |
| Cdk17 |
A |
T |
10: 93,073,652 (GRCm39) |
|
probably benign |
Het |
| Chd9 |
T |
A |
8: 91,721,078 (GRCm39) |
|
probably benign |
Het |
| Chrm5 |
T |
A |
2: 112,310,000 (GRCm39) |
K372M |
possibly damaging |
Het |
| Col11a1 |
A |
G |
3: 113,999,550 (GRCm39) |
|
probably benign |
Het |
| Col27a1 |
T |
C |
4: 63,143,848 (GRCm39) |
M512T |
possibly damaging |
Het |
| Dclk3 |
A |
G |
9: 111,314,003 (GRCm39) |
D693G |
probably damaging |
Het |
| Dcun1d3 |
T |
A |
7: 119,457,173 (GRCm39) |
K180* |
probably null |
Het |
| Dmxl2 |
T |
C |
9: 54,324,235 (GRCm39) |
R876G |
probably benign |
Het |
| Dnmbp |
A |
T |
19: 43,843,296 (GRCm39) |
Y432* |
probably null |
Het |
| Elapor2 |
G |
T |
5: 9,490,966 (GRCm39) |
G659* |
probably null |
Het |
| Eml2 |
C |
T |
7: 18,913,456 (GRCm39) |
Q125* |
probably null |
Het |
| Faap100 |
A |
C |
11: 120,264,702 (GRCm39) |
|
probably benign |
Het |
| Foxp2 |
T |
C |
6: 15,254,278 (GRCm39) |
|
probably benign |
Het |
| Gda |
A |
G |
19: 21,394,471 (GRCm39) |
Y129H |
probably damaging |
Het |
| Gga3 |
G |
A |
11: 115,481,350 (GRCm39) |
R207C |
probably damaging |
Het |
| Glg1 |
T |
C |
8: 111,909,201 (GRCm39) |
I496M |
probably damaging |
Het |
| Glt6d1 |
C |
A |
2: 25,684,739 (GRCm39) |
|
probably null |
Het |
| Gm10322 |
A |
T |
10: 59,452,030 (GRCm39) |
H49L |
possibly damaging |
Het |
| Golga5 |
G |
T |
12: 102,442,467 (GRCm39) |
V269F |
possibly damaging |
Het |
| Gramd2b |
G |
A |
18: 56,607,141 (GRCm39) |
C85Y |
probably benign |
Het |
| Grhl1 |
C |
T |
12: 24,632,918 (GRCm39) |
P153L |
probably benign |
Het |
| Hdac9 |
T |
C |
12: 34,487,221 (GRCm39) |
Q60R |
probably damaging |
Het |
| Hdlbp |
T |
C |
1: 93,353,054 (GRCm39) |
I414V |
probably damaging |
Het |
| Itpk1 |
C |
T |
12: 102,572,337 (GRCm39) |
|
probably benign |
Het |
| Itsn1 |
T |
A |
16: 91,612,408 (GRCm39) |
Y266N |
probably damaging |
Het |
| Lipe |
G |
A |
7: 25,097,913 (GRCm39) |
P10L |
probably benign |
Het |
| Lrrc8a |
A |
G |
2: 30,147,079 (GRCm39) |
E631G |
probably damaging |
Het |
| Lvrn |
T |
A |
18: 47,038,366 (GRCm39) |
N973K |
possibly damaging |
Het |
| Man2c1 |
T |
A |
9: 57,042,881 (GRCm39) |
H250Q |
probably damaging |
Het |
| Mup3 |
T |
C |
4: 62,003,519 (GRCm39) |
T117A |
probably benign |
Het |
| Myo6 |
A |
C |
9: 80,181,256 (GRCm39) |
|
probably benign |
Het |
| Nbn |
T |
A |
4: 15,983,951 (GRCm39) |
|
probably benign |
Het |
| Ncapg |
T |
A |
5: 45,829,770 (GRCm39) |
N157K |
probably damaging |
Het |
| Or4p7 |
C |
T |
2: 88,222,377 (GRCm39) |
T262I |
probably damaging |
Het |
| Or5an1 |
T |
A |
19: 12,261,267 (GRCm39) |
M285K |
probably damaging |
Het |
| Or5m12 |
T |
A |
2: 85,734,501 (GRCm39) |
N299I |
probably damaging |
Het |
| Or5w14 |
G |
A |
2: 87,541,774 (GRCm39) |
H159Y |
probably benign |
Het |
| Or9m1 |
T |
C |
2: 87,733,304 (GRCm39) |
T239A |
probably damaging |
Het |
| P4ha1 |
T |
A |
10: 59,184,079 (GRCm39) |
Y180* |
probably null |
Het |
| Pcdhb19 |
T |
A |
18: 37,632,588 (GRCm39) |
F794L |
probably benign |
Het |
| Pdxdc1 |
T |
A |
16: 13,672,264 (GRCm39) |
I379F |
probably damaging |
Het |
| Psme3 |
T |
A |
11: 101,211,268 (GRCm39) |
S185T |
possibly damaging |
Het |
| Ptgr1 |
A |
G |
4: 58,978,045 (GRCm39) |
S116P |
probably damaging |
Het |
| Ptpn23 |
A |
T |
9: 110,218,078 (GRCm39) |
|
probably null |
Het |
| Rabgap1l |
A |
C |
1: 160,549,775 (GRCm39) |
I277R |
probably benign |
Het |
| Rapgef1 |
C |
T |
2: 29,569,828 (GRCm39) |
T93I |
possibly damaging |
Het |
| Rbp3 |
A |
T |
14: 33,676,730 (GRCm39) |
D226V |
probably damaging |
Het |
| Rnf144a |
A |
T |
12: 26,389,328 (GRCm39) |
C38S |
probably damaging |
Het |
| Rptor |
C |
T |
11: 119,671,379 (GRCm39) |
Q281* |
probably null |
Het |
| Rragd |
T |
C |
4: 33,004,332 (GRCm39) |
L208S |
probably damaging |
Het |
| Slc12a4 |
T |
C |
8: 106,686,120 (GRCm39) |
E41G |
probably damaging |
Het |
| Slc16a1 |
G |
T |
3: 104,560,735 (GRCm39) |
V347F |
probably benign |
Het |
| Slit1 |
G |
A |
19: 41,731,732 (GRCm39) |
T39I |
probably damaging |
Het |
| Sra1 |
T |
C |
18: 36,810,556 (GRCm39) |
N98S |
probably benign |
Het |
| Ssx2ip |
T |
C |
3: 146,132,184 (GRCm39) |
L215P |
probably damaging |
Het |
| Syne2 |
A |
T |
12: 75,995,838 (GRCm39) |
H2126L |
probably damaging |
Het |
| Tep1 |
TTTCTTCTTCTT |
TTTCTTCTT |
14: 51,104,280 (GRCm39) |
|
probably benign |
Het |
| Tgfbi |
T |
C |
13: 56,780,004 (GRCm39) |
|
probably benign |
Het |
| Tmem232 |
T |
C |
17: 65,563,498 (GRCm39) |
M632V |
probably damaging |
Het |
| Tmem81 |
C |
G |
1: 132,435,567 (GRCm39) |
I124M |
probably damaging |
Het |
| Tnnt3 |
T |
G |
7: 142,065,823 (GRCm39) |
D153E |
probably benign |
Het |
| Tnrc6b |
T |
A |
15: 80,807,647 (GRCm39) |
|
probably benign |
Het |
| Tpsab1 |
A |
G |
17: 25,562,798 (GRCm39) |
|
probably benign |
Het |
| Usp34 |
T |
A |
11: 23,351,505 (GRCm39) |
V1431D |
probably damaging |
Het |
| Wdr49 |
G |
T |
3: 75,357,329 (GRCm39) |
R285S |
possibly damaging |
Het |
| Wdr7 |
A |
G |
18: 63,929,320 (GRCm39) |
Y1052C |
probably damaging |
Het |
| Zan |
A |
T |
5: 137,380,578 (GRCm39) |
|
probably benign |
Het |
| Zfp652 |
G |
A |
11: 95,654,565 (GRCm39) |
V323I |
possibly damaging |
Het |
| Zfp740 |
A |
G |
15: 102,121,094 (GRCm39) |
T136A |
possibly damaging |
Het |
| Zfp82 |
C |
T |
7: 29,755,754 (GRCm39) |
E443K |
probably damaging |
Het |
| Zfp874b |
A |
G |
13: 67,629,955 (GRCm39) |
S10P |
probably damaging |
Het |
| Zmynd19 |
A |
G |
2: 24,848,134 (GRCm39) |
Y110C |
probably benign |
Het |
|
| Other mutations in Clasp2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00772:Clasp2
|
APN |
9 |
113,735,060 (GRCm39) |
splice site |
probably benign |
|
|
IGL00885:Clasp2
|
APN |
9 |
113,740,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01314:Clasp2
|
APN |
9 |
113,735,195 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL01344:Clasp2
|
APN |
9 |
113,642,360 (GRCm39) |
splice site |
probably null |
|
|
IGL01567:Clasp2
|
APN |
9 |
113,709,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02238:Clasp2
|
APN |
9 |
113,709,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02299:Clasp2
|
APN |
9 |
113,709,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02323:Clasp2
|
APN |
9 |
113,697,794 (GRCm39) |
splice site |
probably benign |
|
|
IGL02635:Clasp2
|
APN |
9 |
113,737,910 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02645:Clasp2
|
APN |
9 |
113,719,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02976:Clasp2
|
APN |
9 |
113,735,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03190:Clasp2
|
APN |
9 |
113,673,208 (GRCm39) |
nonsense |
probably null |
|
|
IGL03219:Clasp2
|
APN |
9 |
113,677,545 (GRCm39) |
splice site |
probably benign |
|
|
PIT4810001:Clasp2
|
UTSW |
9 |
113,735,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0067:Clasp2
|
UTSW |
9 |
113,689,209 (GRCm39) |
splice site |
probably benign |
|
|
R0067:Clasp2
|
UTSW |
9 |
113,689,209 (GRCm39) |
splice site |
probably benign |
|
|
R0421:Clasp2
|
UTSW |
9 |
113,683,370 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0458:Clasp2
|
UTSW |
9 |
113,735,292 (GRCm39) |
splice site |
probably null |
|
|
R0865:Clasp2
|
UTSW |
9 |
113,740,568 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0972:Clasp2
|
UTSW |
9 |
113,676,773 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R1037:Clasp2
|
UTSW |
9 |
113,725,702 (GRCm39) |
splice site |
probably benign |
|
|
R1925:Clasp2
|
UTSW |
9 |
113,735,265 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R2015:Clasp2
|
UTSW |
9 |
113,740,568 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R2066:Clasp2
|
UTSW |
9 |
113,735,225 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2330:Clasp2
|
UTSW |
9 |
113,705,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2568:Clasp2
|
UTSW |
9 |
113,707,832 (GRCm39) |
missense |
probably benign |
|
|
R3011:Clasp2
|
UTSW |
9 |
113,730,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3879:Clasp2
|
UTSW |
9 |
113,719,029 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3915:Clasp2
|
UTSW |
9 |
113,737,805 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3928:Clasp2
|
UTSW |
9 |
113,735,173 (GRCm39) |
missense |
probably benign |
0.28 |
|
R4323:Clasp2
|
UTSW |
9 |
113,719,027 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4571:Clasp2
|
UTSW |
9 |
113,676,789 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4975:Clasp2
|
UTSW |
9 |
113,732,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5445:Clasp2
|
UTSW |
9 |
113,733,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5564:Clasp2
|
UTSW |
9 |
113,641,836 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5697:Clasp2
|
UTSW |
9 |
113,689,190 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5780:Clasp2
|
UTSW |
9 |
113,679,220 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5787:Clasp2
|
UTSW |
9 |
113,691,310 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6011:Clasp2
|
UTSW |
9 |
113,705,315 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6026:Clasp2
|
UTSW |
9 |
113,740,646 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6090:Clasp2
|
UTSW |
9 |
113,681,803 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6262:Clasp2
|
UTSW |
9 |
113,705,420 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6427:Clasp2
|
UTSW |
9 |
113,721,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6464:Clasp2
|
UTSW |
9 |
113,602,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6586:Clasp2
|
UTSW |
9 |
113,642,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6628:Clasp2
|
UTSW |
9 |
113,725,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6745:Clasp2
|
UTSW |
9 |
113,704,338 (GRCm39) |
nonsense |
probably null |
|
|
R7032:Clasp2
|
UTSW |
9 |
113,683,391 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7165:Clasp2
|
UTSW |
9 |
113,615,467 (GRCm39) |
splice site |
probably null |
|
|
R7221:Clasp2
|
UTSW |
9 |
113,681,825 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7336:Clasp2
|
UTSW |
9 |
113,705,421 (GRCm39) |
splice site |
probably null |
|
|
R7583:Clasp2
|
UTSW |
9 |
113,737,755 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7774:Clasp2
|
UTSW |
9 |
113,677,804 (GRCm39) |
splice site |
probably null |
|
|
R7895:Clasp2
|
UTSW |
9 |
113,733,016 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8084:Clasp2
|
UTSW |
9 |
113,676,823 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8109:Clasp2
|
UTSW |
9 |
113,740,588 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8171:Clasp2
|
UTSW |
9 |
113,732,974 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8230:Clasp2
|
UTSW |
9 |
113,721,482 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R8810:Clasp2
|
UTSW |
9 |
113,728,649 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8879:Clasp2
|
UTSW |
9 |
113,602,773 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8888:Clasp2
|
UTSW |
9 |
113,732,936 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R8889:Clasp2
|
UTSW |
9 |
113,709,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8892:Clasp2
|
UTSW |
9 |
113,709,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8922:Clasp2
|
UTSW |
9 |
113,725,728 (GRCm39) |
nonsense |
probably null |
|
|
R9042:Clasp2
|
UTSW |
9 |
113,735,065 (GRCm39) |
missense |
probably benign |
|
|
R9195:Clasp2
|
UTSW |
9 |
113,671,045 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9355:Clasp2
|
UTSW |
9 |
113,664,309 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9481:Clasp2
|
UTSW |
9 |
113,670,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9502:Clasp2
|
UTSW |
9 |
113,737,866 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9523:Clasp2
|
UTSW |
9 |
113,705,372 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9525:Clasp2
|
UTSW |
9 |
113,740,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9653:Clasp2
|
UTSW |
9 |
113,670,993 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9699:Clasp2
|
UTSW |
9 |
113,738,614 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9738:Clasp2
|
UTSW |
9 |
113,590,665 (GRCm39) |
nonsense |
probably null |
|
|
R9775:Clasp2
|
UTSW |
9 |
113,725,740 (GRCm39) |
missense |
probably benign |
|
|
X0022:Clasp2
|
UTSW |
9 |
113,681,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Clasp2
|
UTSW |
9 |
113,599,289 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Clasp2
|
UTSW |
9 |
113,737,863 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGCCTATGCCTCTAGCCTCTGAAG -3'
(R):5'- GGAATATGACAGTGCCTGAACTCGC -3'
Sequencing Primer
(F):5'- ggaggtggaggcagcag -3'
(R):5'- GAATCTTGCTGGTTGATGCC -3'
|
| Posted On |
2013-05-23 |
Incidental Mutation