Incidental Mutation 'R6860:Trp53bp1'
ID |
535411 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Trp53bp1
|
Ensembl Gene |
ENSMUSG00000043909 |
Gene Name |
transformation related protein 53 binding protein 1 |
Synonyms |
53BP1, p53BP1 |
MMRRC Submission |
045025-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6860 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
121023762-121101888 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 121029594 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Leucine
at position 1862
(R1862L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000106278
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039541]
[ENSMUST00000110647]
[ENSMUST00000110648]
[ENSMUST00000110657]
[ENSMUST00000110658]
[ENSMUST00000154426]
[ENSMUST00000186659]
|
AlphaFold |
P70399 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000039541
|
SMART Domains |
Protein: ENSMUSP00000044049 Gene: ENSMUSG00000027263
Domain | Start | End | E-Value | Type |
Pfam:Spc97_Spc98
|
4 |
573 |
2.8e-111 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000110647
AA Change: R1812L
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000106277 Gene: ENSMUSG00000043909 AA Change: R1812L
Domain | Start | End | E-Value | Type |
low complexity region
|
136 |
149 |
N/A |
INTRINSIC |
low complexity region
|
158 |
169 |
N/A |
INTRINSIC |
low complexity region
|
647 |
661 |
N/A |
INTRINSIC |
low complexity region
|
1031 |
1042 |
N/A |
INTRINSIC |
low complexity region
|
1099 |
1112 |
N/A |
INTRINSIC |
low complexity region
|
1260 |
1272 |
N/A |
INTRINSIC |
low complexity region
|
1290 |
1332 |
N/A |
INTRINSIC |
Pfam:53-BP1_Tudor
|
1430 |
1551 |
2.5e-80 |
PFAM |
low complexity region
|
1581 |
1601 |
N/A |
INTRINSIC |
BRCT
|
1673 |
1785 |
7.13e-1 |
SMART |
BRCT
|
1813 |
1901 |
1.03e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000110648
AA Change: R1862L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106278 Gene: ENSMUSG00000043909 AA Change: R1862L
Domain | Start | End | E-Value | Type |
low complexity region
|
136 |
149 |
N/A |
INTRINSIC |
low complexity region
|
158 |
169 |
N/A |
INTRINSIC |
low complexity region
|
647 |
661 |
N/A |
INTRINSIC |
low complexity region
|
1031 |
1042 |
N/A |
INTRINSIC |
low complexity region
|
1099 |
1112 |
N/A |
INTRINSIC |
low complexity region
|
1260 |
1272 |
N/A |
INTRINSIC |
low complexity region
|
1290 |
1332 |
N/A |
INTRINSIC |
low complexity region
|
1389 |
1409 |
N/A |
INTRINSIC |
Pfam:53-BP1_Tudor
|
1480 |
1601 |
1.5e-80 |
PFAM |
low complexity region
|
1631 |
1651 |
N/A |
INTRINSIC |
BRCT
|
1723 |
1835 |
7.13e-1 |
SMART |
BRCT
|
1863 |
1951 |
1.03e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110657
|
SMART Domains |
Protein: ENSMUSP00000106285 Gene: ENSMUSG00000027263
Domain | Start | End | E-Value | Type |
Pfam:Spc97_Spc98
|
4 |
572 |
3.1e-115 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110658
|
SMART Domains |
Protein: ENSMUSP00000106286 Gene: ENSMUSG00000027263
Domain | Start | End | E-Value | Type |
Pfam:Spc97_Spc98
|
4 |
572 |
4.1e-115 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000147540
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000154426
|
SMART Domains |
Protein: ENSMUSP00000117548 Gene: ENSMUSG00000043909
Domain | Start | End | E-Value | Type |
Pfam:53-BP1_Tudor
|
1 |
70 |
2.5e-44 |
PFAM |
low complexity region
|
100 |
120 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000186659
|
SMART Domains |
Protein: ENSMUSP00000140417 Gene: ENSMUSG00000027263
Domain | Start | End | E-Value | Type |
Pfam:Spc97_Spc98
|
4 |
572 |
4.1e-115 |
PFAM |
|
Meta Mutation Damage Score |
0.4211 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.3%
|
Validation Efficiency |
100% (86/86) |
MGI Phenotype |
PHENOTYPE: Homozygous mutations in this gene result in growth retardation, immunodeficiency, thymic hypoplasia, and increased incidence of thymic lymphomas. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
T |
C |
11: 72,080,412 (GRCm39) |
E418G |
probably damaging |
Het |
9930012K11Rik |
C |
A |
14: 70,395,071 (GRCm39) |
V28L |
possibly damaging |
Het |
Abtb2 |
C |
T |
2: 103,539,770 (GRCm39) |
R712* |
probably null |
Het |
Acvr1c |
C |
T |
2: 58,177,717 (GRCm39) |
G171S |
probably damaging |
Het |
Ahctf1 |
G |
T |
1: 179,580,853 (GRCm39) |
A1783E |
probably benign |
Het |
Anapc4 |
A |
T |
5: 53,006,170 (GRCm39) |
Q149L |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,327,952 (GRCm39) |
V824A |
possibly damaging |
Het |
Ankrd31 |
G |
C |
13: 96,968,094 (GRCm39) |
C577S |
probably benign |
Het |
Apol7c |
T |
C |
15: 77,410,274 (GRCm39) |
N224S |
probably benign |
Het |
Arl14 |
A |
T |
3: 69,130,029 (GRCm39) |
T59S |
probably benign |
Het |
Astn1 |
T |
A |
1: 158,440,042 (GRCm39) |
I870K |
probably damaging |
Het |
B4galt1 |
A |
T |
4: 40,807,796 (GRCm39) |
V335E |
probably benign |
Het |
C2cd3 |
C |
T |
7: 100,039,448 (GRCm39) |
P216S |
probably benign |
Het |
Cchcr1 |
C |
A |
17: 35,840,015 (GRCm39) |
N711K |
possibly damaging |
Het |
Chd2 |
A |
G |
7: 73,147,558 (GRCm39) |
F467L |
possibly damaging |
Het |
Cntn6 |
A |
T |
6: 104,838,907 (GRCm39) |
E987V |
possibly damaging |
Het |
Col11a2 |
T |
A |
17: 34,272,572 (GRCm39) |
L286H |
probably damaging |
Het |
Cwc22 |
C |
T |
2: 77,759,792 (GRCm39) |
R85Q |
possibly damaging |
Het |
Cyp7a1 |
A |
C |
4: 6,272,587 (GRCm39) |
F209V |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,852,322 (GRCm39) |
T189A |
possibly damaging |
Het |
Dnhd1 |
C |
G |
7: 105,327,473 (GRCm39) |
N777K |
probably benign |
Het |
Dusp16 |
A |
T |
6: 134,702,842 (GRCm39) |
C216* |
probably null |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,170,078 (GRCm39) |
N1993S |
probably damaging |
Het |
Fbxw22 |
A |
G |
9: 109,213,030 (GRCm39) |
S306P |
probably benign |
Het |
Ferd3l |
T |
C |
12: 33,978,651 (GRCm39) |
S55P |
probably benign |
Het |
Fpr-rs3 |
A |
G |
17: 20,844,560 (GRCm39) |
S194P |
possibly damaging |
Het |
Gm19965 |
G |
A |
1: 116,748,609 (GRCm39) |
D97N |
probably benign |
Het |
Gtpbp2 |
A |
G |
17: 46,478,914 (GRCm39) |
|
probably benign |
Het |
H3c7 |
G |
T |
13: 23,728,760 (GRCm39) |
V36L |
probably benign |
Het |
Hcn3 |
A |
C |
3: 89,067,152 (GRCm39) |
I72S |
possibly damaging |
Het |
Hk3 |
T |
A |
13: 55,162,278 (GRCm39) |
N109Y |
probably damaging |
Het |
Iqub |
T |
C |
6: 24,505,737 (GRCm39) |
E57G |
possibly damaging |
Het |
Kcnk3 |
T |
A |
5: 30,779,397 (GRCm39) |
M149K |
possibly damaging |
Het |
Kcp |
C |
T |
6: 29,505,719 (GRCm39) |
G51D |
probably benign |
Het |
Kif26a |
C |
A |
12: 112,113,263 (GRCm39) |
A53D |
probably damaging |
Het |
Lifr |
T |
A |
15: 7,202,418 (GRCm39) |
I353K |
probably benign |
Het |
Llph |
A |
T |
10: 120,067,189 (GRCm39) |
N102I |
probably damaging |
Het |
Lmo3 |
C |
A |
6: 138,393,566 (GRCm39) |
R18L |
possibly damaging |
Het |
Lrrc46 |
T |
C |
11: 96,926,371 (GRCm39) |
E175G |
probably benign |
Het |
Ltk |
A |
T |
2: 119,585,075 (GRCm39) |
C128* |
probably null |
Het |
Map1b |
T |
C |
13: 99,571,275 (GRCm39) |
E482G |
probably damaging |
Het |
Mapk8ip2 |
T |
C |
15: 89,344,655 (GRCm39) |
V740A |
probably damaging |
Het |
Miga2 |
T |
C |
2: 30,261,175 (GRCm39) |
W157R |
probably benign |
Het |
Mlip |
A |
G |
9: 77,009,675 (GRCm39) |
*837Q |
probably null |
Het |
Mroh2a |
G |
T |
1: 88,182,657 (GRCm39) |
R1195L |
possibly damaging |
Het |
Myl1 |
T |
C |
1: 66,984,217 (GRCm39) |
|
probably benign |
Het |
Or1l4 |
T |
C |
2: 37,092,189 (GRCm39) |
L312P |
possibly damaging |
Het |
Or2a5 |
T |
C |
6: 42,873,750 (GRCm39) |
Y122H |
probably benign |
Het |
Or51ab3 |
A |
G |
7: 103,201,075 (GRCm39) |
I28V |
probably benign |
Het |
P3h3 |
A |
T |
6: 124,834,331 (GRCm39) |
V107D |
probably benign |
Het |
Papolb |
A |
T |
5: 142,514,651 (GRCm39) |
S331T |
possibly damaging |
Het |
Pars2 |
T |
G |
4: 106,511,700 (GRCm39) |
V494G |
probably benign |
Het |
Pcdhb3 |
C |
A |
18: 37,434,763 (GRCm39) |
T243K |
probably benign |
Het |
Pde9a |
T |
A |
17: 31,689,698 (GRCm39) |
M415K |
probably damaging |
Het |
Ppp1r9b |
G |
A |
11: 94,882,974 (GRCm39) |
A201T |
probably benign |
Het |
Prl |
A |
G |
13: 27,248,942 (GRCm39) |
N197S |
possibly damaging |
Het |
Prl2c1 |
T |
A |
13: 28,035,724 (GRCm39) |
M32K |
probably benign |
Het |
Prrt4 |
T |
C |
6: 29,170,737 (GRCm39) |
S572G |
possibly damaging |
Het |
Psd |
T |
A |
19: 46,310,858 (GRCm39) |
D397V |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,836,307 (GRCm39) |
Y213* |
probably null |
Het |
Ptcd3 |
T |
A |
6: 71,874,094 (GRCm39) |
|
probably null |
Het |
Ptprk |
T |
G |
10: 28,210,480 (GRCm39) |
F167L |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,524,226 (GRCm39) |
V472A |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,575,100 (GRCm39) |
L58P |
probably damaging |
Het |
Scnn1g |
T |
C |
7: 121,339,576 (GRCm39) |
L125S |
probably damaging |
Het |
Sec16a |
T |
C |
2: 26,320,124 (GRCm39) |
Y1438C |
probably damaging |
Het |
Serinc3 |
C |
T |
2: 163,476,366 (GRCm39) |
S155N |
probably benign |
Het |
Slc3a2 |
A |
T |
19: 8,690,996 (GRCm39) |
V78E |
probably damaging |
Het |
Slc44a4 |
T |
A |
17: 35,140,044 (GRCm39) |
L23Q |
probably damaging |
Het |
Slco5a1 |
C |
T |
1: 12,951,420 (GRCm39) |
|
probably benign |
Het |
Slit1 |
A |
G |
19: 41,605,154 (GRCm39) |
M899T |
probably benign |
Het |
Sorl1 |
A |
G |
9: 41,933,688 (GRCm39) |
I1094T |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,972,196 (GRCm39) |
L258Q |
probably benign |
Het |
Strip1 |
T |
C |
3: 107,526,252 (GRCm39) |
E488G |
possibly damaging |
Het |
Stx18 |
G |
A |
5: 38,262,235 (GRCm39) |
D30N |
possibly damaging |
Het |
Sync |
T |
C |
4: 129,181,583 (GRCm39) |
|
probably null |
Het |
Syncrip |
A |
G |
9: 88,358,849 (GRCm39) |
V220A |
probably damaging |
Het |
Tagln2 |
T |
C |
1: 172,333,476 (GRCm39) |
I110T |
probably benign |
Het |
Taok1 |
T |
C |
11: 77,432,627 (GRCm39) |
T729A |
probably benign |
Het |
Tgfbrap1 |
C |
T |
1: 43,106,759 (GRCm39) |
V75I |
possibly damaging |
Het |
Tnfrsf21 |
A |
G |
17: 43,327,957 (GRCm39) |
T24A |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,932,131 (GRCm39) |
D2221E |
probably damaging |
Het |
Triml1 |
A |
G |
8: 43,583,603 (GRCm39) |
S333P |
probably damaging |
Het |
Tsc22d1 |
T |
G |
14: 76,655,732 (GRCm39) |
I737S |
possibly damaging |
Het |
U2af2 |
A |
T |
7: 5,082,273 (GRCm39) |
K462N |
possibly damaging |
Het |
Ubap2 |
A |
C |
4: 41,233,631 (GRCm39) |
N86K |
probably damaging |
Het |
Uso1 |
A |
G |
5: 92,343,207 (GRCm39) |
K764E |
probably benign |
Het |
Vmn1r192 |
T |
A |
13: 22,372,122 (GRCm39) |
M33L |
probably benign |
Het |
|
Other mutations in Trp53bp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Trp53bp1
|
APN |
2 |
121,087,060 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00690:Trp53bp1
|
APN |
2 |
121,066,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00922:Trp53bp1
|
APN |
2 |
121,038,963 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01475:Trp53bp1
|
APN |
2 |
121,100,800 (GRCm39) |
splice site |
probably null |
|
IGL01639:Trp53bp1
|
APN |
2 |
121,033,173 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01662:Trp53bp1
|
APN |
2 |
121,066,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01757:Trp53bp1
|
APN |
2 |
121,041,785 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01829:Trp53bp1
|
APN |
2 |
121,046,377 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02247:Trp53bp1
|
APN |
2 |
121,067,070 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02349:Trp53bp1
|
APN |
2 |
121,029,555 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02391:Trp53bp1
|
APN |
2 |
121,033,191 (GRCm39) |
missense |
possibly damaging |
0.67 |
chives
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
concur
|
UTSW |
2 |
121,100,800 (GRCm39) |
splice site |
probably null |
|
confirmation
|
UTSW |
2 |
121,035,594 (GRCm39) |
critical splice acceptor site |
probably null |
|
Infra
|
UTSW |
2 |
121,077,980 (GRCm39) |
critical splice donor site |
probably null |
|
Legume
|
UTSW |
2 |
121,029,523 (GRCm39) |
missense |
probably damaging |
0.99 |
lentil
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
lentil2
|
UTSW |
2 |
121,038,368 (GRCm39) |
missense |
probably damaging |
1.00 |
Profundus
|
UTSW |
2 |
121,038,284 (GRCm39) |
missense |
probably damaging |
1.00 |
split_pea
|
UTSW |
2 |
121,059,087 (GRCm39) |
nonsense |
probably null |
|
verily
|
UTSW |
2 |
121,041,794 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Trp53bp1
|
UTSW |
2 |
121,101,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Trp53bp1
|
UTSW |
2 |
121,034,978 (GRCm39) |
missense |
probably benign |
|
R0060:Trp53bp1
|
UTSW |
2 |
121,035,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Trp53bp1
|
UTSW |
2 |
121,035,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Trp53bp1
|
UTSW |
2 |
121,067,240 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0103:Trp53bp1
|
UTSW |
2 |
121,067,240 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0281:Trp53bp1
|
UTSW |
2 |
121,100,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R0386:Trp53bp1
|
UTSW |
2 |
121,035,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Trp53bp1
|
UTSW |
2 |
121,066,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Trp53bp1
|
UTSW |
2 |
121,100,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R0522:Trp53bp1
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
R0523:Trp53bp1
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
R0525:Trp53bp1
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
R0543:Trp53bp1
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
R0559:Trp53bp1
|
UTSW |
2 |
121,058,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Trp53bp1
|
UTSW |
2 |
121,058,653 (GRCm39) |
splice site |
probably benign |
|
R0593:Trp53bp1
|
UTSW |
2 |
121,101,009 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0648:Trp53bp1
|
UTSW |
2 |
121,066,188 (GRCm39) |
missense |
probably benign |
0.20 |
R0680:Trp53bp1
|
UTSW |
2 |
121,082,349 (GRCm39) |
missense |
probably null |
0.13 |
R0732:Trp53bp1
|
UTSW |
2 |
121,078,745 (GRCm39) |
missense |
probably null |
0.96 |
R0905:Trp53bp1
|
UTSW |
2 |
121,034,799 (GRCm39) |
splice site |
probably benign |
|
R1377:Trp53bp1
|
UTSW |
2 |
121,101,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1415:Trp53bp1
|
UTSW |
2 |
121,066,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Trp53bp1
|
UTSW |
2 |
121,082,481 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1971:Trp53bp1
|
UTSW |
2 |
121,035,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Trp53bp1
|
UTSW |
2 |
121,034,964 (GRCm39) |
missense |
probably benign |
|
R2143:Trp53bp1
|
UTSW |
2 |
121,046,545 (GRCm39) |
missense |
probably benign |
0.00 |
R2282:Trp53bp1
|
UTSW |
2 |
121,100,754 (GRCm39) |
nonsense |
probably null |
|
R2296:Trp53bp1
|
UTSW |
2 |
121,039,728 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3106:Trp53bp1
|
UTSW |
2 |
121,067,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Trp53bp1
|
UTSW |
2 |
121,030,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3793:Trp53bp1
|
UTSW |
2 |
121,030,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3946:Trp53bp1
|
UTSW |
2 |
121,059,107 (GRCm39) |
missense |
probably damaging |
0.99 |
R4001:Trp53bp1
|
UTSW |
2 |
121,035,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4327:Trp53bp1
|
UTSW |
2 |
121,087,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Trp53bp1
|
UTSW |
2 |
121,038,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R4630:Trp53bp1
|
UTSW |
2 |
121,038,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R4744:Trp53bp1
|
UTSW |
2 |
121,041,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Trp53bp1
|
UTSW |
2 |
121,058,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R4754:Trp53bp1
|
UTSW |
2 |
121,038,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Trp53bp1
|
UTSW |
2 |
121,059,087 (GRCm39) |
nonsense |
probably null |
|
R4850:Trp53bp1
|
UTSW |
2 |
121,035,594 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4870:Trp53bp1
|
UTSW |
2 |
121,087,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Trp53bp1
|
UTSW |
2 |
121,033,084 (GRCm39) |
missense |
probably damaging |
0.99 |
R4924:Trp53bp1
|
UTSW |
2 |
121,051,701 (GRCm39) |
nonsense |
probably null |
|
R4962:Trp53bp1
|
UTSW |
2 |
121,101,027 (GRCm39) |
missense |
probably benign |
0.12 |
R5019:Trp53bp1
|
UTSW |
2 |
121,100,800 (GRCm39) |
splice site |
probably null |
|
R5111:Trp53bp1
|
UTSW |
2 |
121,041,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R5149:Trp53bp1
|
UTSW |
2 |
121,046,598 (GRCm39) |
missense |
probably benign |
0.00 |
R5252:Trp53bp1
|
UTSW |
2 |
121,074,464 (GRCm39) |
missense |
probably benign |
0.40 |
R5533:Trp53bp1
|
UTSW |
2 |
121,038,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Trp53bp1
|
UTSW |
2 |
121,067,143 (GRCm39) |
missense |
probably benign |
0.00 |
R5773:Trp53bp1
|
UTSW |
2 |
121,074,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5819:Trp53bp1
|
UTSW |
2 |
121,038,873 (GRCm39) |
nonsense |
probably null |
|
R5886:Trp53bp1
|
UTSW |
2 |
121,035,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Trp53bp1
|
UTSW |
2 |
121,067,304 (GRCm39) |
missense |
probably benign |
0.06 |
R6012:Trp53bp1
|
UTSW |
2 |
121,087,083 (GRCm39) |
missense |
probably benign |
0.07 |
R6351:Trp53bp1
|
UTSW |
2 |
121,100,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Trp53bp1
|
UTSW |
2 |
121,101,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R6575:Trp53bp1
|
UTSW |
2 |
121,059,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R6619:Trp53bp1
|
UTSW |
2 |
121,077,980 (GRCm39) |
critical splice donor site |
probably null |
|
R6626:Trp53bp1
|
UTSW |
2 |
121,038,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R6754:Trp53bp1
|
UTSW |
2 |
121,101,057 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6765:Trp53bp1
|
UTSW |
2 |
121,039,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R6806:Trp53bp1
|
UTSW |
2 |
121,059,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R6991:Trp53bp1
|
UTSW |
2 |
121,038,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Trp53bp1
|
UTSW |
2 |
121,029,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7339:Trp53bp1
|
UTSW |
2 |
121,066,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7357:Trp53bp1
|
UTSW |
2 |
121,041,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Trp53bp1
|
UTSW |
2 |
121,066,827 (GRCm39) |
missense |
probably benign |
0.34 |
R7577:Trp53bp1
|
UTSW |
2 |
121,067,119 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7643:Trp53bp1
|
UTSW |
2 |
121,078,295 (GRCm39) |
splice site |
probably null |
|
R7728:Trp53bp1
|
UTSW |
2 |
121,038,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R7806:Trp53bp1
|
UTSW |
2 |
121,035,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R7955:Trp53bp1
|
UTSW |
2 |
121,066,225 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8099:Trp53bp1
|
UTSW |
2 |
121,030,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R8200:Trp53bp1
|
UTSW |
2 |
121,066,657 (GRCm39) |
missense |
probably benign |
0.00 |
R8282:Trp53bp1
|
UTSW |
2 |
121,029,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R9136:Trp53bp1
|
UTSW |
2 |
121,067,092 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9152:Trp53bp1
|
UTSW |
2 |
121,029,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R9292:Trp53bp1
|
UTSW |
2 |
121,046,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R9340:Trp53bp1
|
UTSW |
2 |
121,100,460 (GRCm39) |
missense |
probably benign |
0.40 |
R9475:Trp53bp1
|
UTSW |
2 |
121,039,761 (GRCm39) |
missense |
probably benign |
0.00 |
R9616:Trp53bp1
|
UTSW |
2 |
121,066,657 (GRCm39) |
missense |
probably benign |
0.30 |
R9675:Trp53bp1
|
UTSW |
2 |
121,087,089 (GRCm39) |
missense |
probably benign |
0.03 |
R9779:Trp53bp1
|
UTSW |
2 |
121,066,469 (GRCm39) |
missense |
probably damaging |
1.00 |
RF046:Trp53bp1
|
UTSW |
2 |
121,046,482 (GRCm39) |
frame shift |
probably null |
|
Z1088:Trp53bp1
|
UTSW |
2 |
121,084,126 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Trp53bp1
|
UTSW |
2 |
121,074,541 (GRCm39) |
missense |
probably benign |
0.33 |
|
Predicted Primers |
PCR Primer
(F):5'- CTTGGAATACACATGCTGACAG -3'
(R):5'- TAGCAAAGTCTGGGCTCCTG -3'
Sequencing Primer
(F):5'- TGTGAGTCTAAGGACACCCTG -3'
(R):5'- CAAAGTCTGGGCTCCTGGAATG -3'
|
Posted On |
2018-09-12 |