Incidental Mutation 'R4733:Trrap'
ID |
470385 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Trrap
|
Ensembl Gene |
ENSMUSG00000045482 |
Gene Name |
transformation/transcription domain-associated protein |
Synonyms |
transactivation/transformation-domain associated protein |
MMRRC Submission |
042023-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4733 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
144704547-144796588 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 144753380 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Isoleucine
at position 1883
(V1883I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000042544
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038980]
[ENSMUST00000094120]
[ENSMUST00000100467]
[ENSMUST00000213013]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000038980
AA Change: V1883I
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000042544 Gene: ENSMUSG00000045482 AA Change: V1883I
Domain | Start | End | E-Value | Type |
low complexity region
|
482 |
527 |
N/A |
INTRINSIC |
low complexity region
|
529 |
540 |
N/A |
INTRINSIC |
Blast:PI3Kc
|
765 |
864 |
1e-13 |
BLAST |
SCOP:d1gw5a_
|
1184 |
1664 |
2e-6 |
SMART |
low complexity region
|
1832 |
1843 |
N/A |
INTRINSIC |
low complexity region
|
1866 |
1881 |
N/A |
INTRINSIC |
low complexity region
|
2289 |
2303 |
N/A |
INTRINSIC |
Pfam:FAT
|
2830 |
3174 |
4.7e-69 |
PFAM |
low complexity region
|
3363 |
3376 |
N/A |
INTRINSIC |
low complexity region
|
3407 |
3418 |
N/A |
INTRINSIC |
PI3Kc
|
3509 |
3798 |
5.11e-8 |
SMART |
FATC
|
3797 |
3829 |
1.89e-3 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000094120
AA Change: V1901I
PolyPhen 2
Score 0.921 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000091668 Gene: ENSMUSG00000045482 AA Change: V1901I
Domain | Start | End | E-Value | Type |
low complexity region
|
482 |
527 |
N/A |
INTRINSIC |
low complexity region
|
529 |
540 |
N/A |
INTRINSIC |
Blast:PI3Kc
|
765 |
864 |
1e-13 |
BLAST |
SCOP:d1gw5a_
|
1184 |
1682 |
2e-6 |
SMART |
low complexity region
|
1850 |
1861 |
N/A |
INTRINSIC |
low complexity region
|
1884 |
1899 |
N/A |
INTRINSIC |
low complexity region
|
2307 |
2321 |
N/A |
INTRINSIC |
Pfam:FAT
|
2848 |
3203 |
1.1e-68 |
PFAM |
low complexity region
|
3392 |
3405 |
N/A |
INTRINSIC |
low complexity region
|
3436 |
3447 |
N/A |
INTRINSIC |
PI3Kc
|
3538 |
3827 |
5.11e-8 |
SMART |
FATC
|
3826 |
3858 |
1.89e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000100467
AA Change: V1883I
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000098035 Gene: ENSMUSG00000045482 AA Change: V1883I
Domain | Start | End | E-Value | Type |
low complexity region
|
482 |
527 |
N/A |
INTRINSIC |
low complexity region
|
529 |
540 |
N/A |
INTRINSIC |
Blast:PI3Kc
|
765 |
864 |
1e-13 |
BLAST |
SCOP:d1gw5a_
|
1184 |
1664 |
2e-6 |
SMART |
low complexity region
|
1832 |
1843 |
N/A |
INTRINSIC |
low complexity region
|
1866 |
1881 |
N/A |
INTRINSIC |
low complexity region
|
2289 |
2303 |
N/A |
INTRINSIC |
Pfam:FAT
|
2830 |
3174 |
4.7e-69 |
PFAM |
low complexity region
|
3381 |
3394 |
N/A |
INTRINSIC |
low complexity region
|
3425 |
3436 |
N/A |
INTRINSIC |
PI3Kc
|
3527 |
3816 |
5.11e-8 |
SMART |
FATC
|
3815 |
3847 |
1.89e-3 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132347
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000132925
AA Change: V1622I
PolyPhen 2
Score 0.977 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000122021 Gene: ENSMUSG00000045482 AA Change: V1622I
Domain | Start | End | E-Value | Type |
low complexity region
|
197 |
242 |
N/A |
INTRINSIC |
low complexity region
|
244 |
255 |
N/A |
INTRINSIC |
SCOP:d1gw5a_
|
474 |
1003 |
9e-7 |
SMART |
Blast:PI3Kc
|
480 |
579 |
1e-13 |
BLAST |
low complexity region
|
1083 |
1092 |
N/A |
INTRINSIC |
low complexity region
|
1572 |
1583 |
N/A |
INTRINSIC |
low complexity region
|
1606 |
1621 |
N/A |
INTRINSIC |
low complexity region
|
2029 |
2043 |
N/A |
INTRINSIC |
Pfam:FAT
|
2570 |
2914 |
1.5e-69 |
PFAM |
low complexity region
|
3121 |
3134 |
N/A |
INTRINSIC |
low complexity region
|
3165 |
3176 |
N/A |
INTRINSIC |
PI3Kc
|
3267 |
3556 |
5.11e-8 |
SMART |
FATC
|
3555 |
3587 |
1.89e-3 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000143357
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197834
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000213013
AA Change: V1902I
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
Meta Mutation Damage Score |
0.0739 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large multidomain protein of the phosphoinositide 3-kinase-related kinases (PIKK) family. The encoded protein is a common component of many histone acetyltransferase (HAT) complexes and plays a role in transcription and DNA repair by recruiting HAT complexes to chromatin. Deregulation of this gene may play a role in several types of cancer including glioblastoma multiforme. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011] PHENOTYPE: Homozygous embryos die prior to E3.5 and exhibit embryonic and extraembryonic tissue disorganization. Mitotic abnormalities were also noted in homozygous cells. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 180 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
T |
A |
9: 8,222,174 (GRCm39) |
|
noncoding transcript |
Het |
4933409G03Rik |
A |
G |
2: 68,445,065 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
C |
7: 78,748,357 (GRCm39) |
S1043P |
probably damaging |
Het |
Ackr2 |
A |
G |
9: 121,738,249 (GRCm39) |
Y208C |
probably damaging |
Het |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adam1a |
T |
A |
5: 121,657,497 (GRCm39) |
T599S |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Adgrf2 |
A |
C |
17: 43,021,645 (GRCm39) |
I393S |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,984,665 (GRCm39) |
G1983V |
probably damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Ak8 |
A |
G |
2: 28,650,083 (GRCm39) |
Y370C |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,063,901 (GRCm39) |
D1750G |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,718,204 (GRCm39) |
V315E |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Ap3b2 |
C |
T |
7: 81,121,680 (GRCm39) |
A519T |
probably damaging |
Het |
Apool |
C |
T |
X: 111,281,897 (GRCm39) |
T166I |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,539,247 (GRCm39) |
K65* |
probably null |
Het |
Arhgef38 |
G |
T |
3: 132,838,030 (GRCm39) |
Y633* |
probably null |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,059,750 (GRCm39) |
D430G |
possibly damaging |
Het |
Atp8a1 |
G |
A |
5: 67,970,463 (GRCm39) |
S92L |
probably benign |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
C130073F10Rik |
C |
A |
4: 101,747,907 (GRCm39) |
S89I |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,334,041 (GRCm39) |
T867A |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,435,906 (GRCm39) |
N1276K |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,306,268 (GRCm39) |
D2012V |
probably damaging |
Het |
Cenpt |
A |
G |
8: 106,573,768 (GRCm39) |
V254A |
probably benign |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cers5 |
C |
T |
15: 99,639,518 (GRCm39) |
R123Q |
probably benign |
Het |
Ces2h |
A |
G |
8: 105,741,236 (GRCm39) |
E76G |
probably damaging |
Het |
Cfap77 |
T |
A |
2: 28,874,400 (GRCm39) |
E143D |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,969,745 (GRCm39) |
R65L |
probably damaging |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec2g |
C |
A |
6: 128,958,842 (GRCm39) |
Y142* |
probably null |
Het |
Coch |
A |
T |
12: 51,651,802 (GRCm39) |
E549V |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,496,197 (GRCm39) |
H1606R |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,464,779 (GRCm39) |
V348A |
probably benign |
Het |
Cpd |
T |
C |
11: 76,702,620 (GRCm39) |
N583D |
probably damaging |
Het |
Cyp2d11 |
T |
A |
15: 82,273,428 (GRCm39) |
Y481F |
probably benign |
Het |
D130043K22Rik |
T |
C |
13: 25,083,648 (GRCm39) |
S1038P |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,503,741 (GRCm39) |
T1653I |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,352,222 (GRCm39) |
|
probably null |
Het |
Dync1h1 |
C |
T |
12: 110,615,941 (GRCm39) |
Q3030* |
probably null |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Eif2d |
T |
C |
1: 131,092,464 (GRCm39) |
V374A |
probably damaging |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
F5 |
C |
T |
1: 164,009,226 (GRCm39) |
T332M |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,169,439 (GRCm39) |
T156A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,641,671 (GRCm39) |
|
probably null |
Het |
Fnip2 |
A |
T |
3: 79,388,959 (GRCm39) |
S561T |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,909,998 (GRCm39) |
T455S |
probably benign |
Het |
Fry |
G |
A |
5: 150,309,472 (GRCm39) |
E639K |
|
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,032 (GRCm39) |
D844E |
probably benign |
Het |
Gle1 |
T |
C |
2: 29,830,244 (GRCm39) |
S267P |
probably damaging |
Het |
Glg1 |
G |
A |
8: 111,914,387 (GRCm39) |
R466W |
probably damaging |
Het |
Gm10277 |
T |
C |
11: 77,676,923 (GRCm39) |
|
probably benign |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gpr35 |
T |
G |
1: 92,911,107 (GRCm39) |
I57S |
probably damaging |
Het |
Gprin1 |
C |
T |
13: 54,887,770 (GRCm39) |
G168E |
possibly damaging |
Het |
Gtf3c2 |
G |
T |
5: 31,317,401 (GRCm39) |
P586T |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Gucy2c |
A |
G |
6: 136,744,150 (GRCm39) |
S150P |
probably damaging |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Il2ra |
T |
A |
2: 11,681,731 (GRCm39) |
M112K |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Kcnn2 |
T |
A |
18: 45,693,416 (GRCm39) |
S331T |
possibly damaging |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Klra3 |
T |
A |
6: 130,304,095 (GRCm39) |
Y199F |
possibly damaging |
Het |
Lhx2 |
A |
G |
2: 38,250,003 (GRCm39) |
K274R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,363,899 (GRCm39) |
I313V |
probably benign |
Het |
Lrrfip1 |
A |
T |
1: 91,043,369 (GRCm39) |
E591D |
probably benign |
Het |
Lrrk2 |
G |
A |
15: 91,649,950 (GRCm39) |
E1696K |
probably damaging |
Het |
Lrrk2 |
A |
C |
15: 91,573,052 (GRCm39) |
E200A |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,909,080 (GRCm39) |
M465K |
probably damaging |
Het |
Moxd2 |
T |
G |
6: 40,855,793 (GRCm39) |
I599L |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,048,831 (GRCm39) |
S866P |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,231,772 (GRCm39) |
T79A |
possibly damaging |
Het |
Ncoa6 |
C |
A |
2: 155,263,221 (GRCm39) |
Q404H |
probably damaging |
Het |
Neb |
A |
G |
2: 52,169,091 (GRCm39) |
Y1815H |
probably damaging |
Het |
Nell1 |
A |
G |
7: 50,505,965 (GRCm39) |
D724G |
probably damaging |
Het |
Nkx3-2 |
A |
G |
5: 41,919,487 (GRCm39) |
V167A |
probably benign |
Het |
Nsun3 |
C |
A |
16: 62,555,482 (GRCm39) |
C348F |
possibly damaging |
Het |
Obox6 |
A |
T |
7: 15,568,697 (GRCm39) |
S60T |
possibly damaging |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or1e16 |
T |
C |
11: 73,286,521 (GRCm39) |
D109G |
probably benign |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or9s18 |
T |
C |
13: 65,300,467 (GRCm39) |
V143A |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pank4 |
A |
T |
4: 155,055,847 (GRCm39) |
M291L |
probably benign |
Het |
Pcf11 |
T |
C |
7: 92,308,041 (GRCm39) |
D709G |
probably benign |
Het |
Pcgf1 |
T |
A |
6: 83,056,938 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
A |
G |
12: 82,042,525 (GRCm39) |
I2256V |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Piezo2 |
C |
T |
18: 63,163,472 (GRCm39) |
A2149T |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,881,711 (GRCm39) |
E781G |
probably benign |
Het |
Pik3r4 |
G |
A |
9: 105,555,375 (GRCm39) |
V1111I |
possibly damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,722,581 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Polr3c |
A |
T |
3: 96,630,977 (GRCm39) |
F148I |
probably damaging |
Het |
Ppard |
A |
T |
17: 28,505,417 (GRCm39) |
T35S |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Qki |
T |
C |
17: 10,435,217 (GRCm39) |
H269R |
probably damaging |
Het |
Qrsl1 |
T |
C |
10: 43,752,659 (GRCm39) |
Y388C |
probably damaging |
Het |
Rapgef1 |
T |
G |
2: 29,579,172 (GRCm39) |
I182S |
probably damaging |
Het |
Ret |
T |
C |
6: 118,140,154 (GRCm39) |
S1013G |
possibly damaging |
Het |
Rimbp3 |
A |
G |
16: 17,028,465 (GRCm39) |
R630G |
possibly damaging |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Sec31b |
A |
T |
19: 44,521,116 (GRCm39) |
S110T |
probably damaging |
Het |
Serpina3k |
G |
A |
12: 104,307,119 (GRCm39) |
G117D |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,221,902 (GRCm39) |
Y410C |
probably damaging |
Het |
Slc24a1 |
G |
A |
9: 64,856,836 (GRCm39) |
R24C |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slco1a7 |
A |
T |
6: 141,668,905 (GRCm39) |
M509K |
probably benign |
Het |
Slco4a1 |
A |
G |
2: 180,115,408 (GRCm39) |
N662D |
probably damaging |
Het |
Slfn4 |
T |
A |
11: 83,080,108 (GRCm39) |
|
probably benign |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Spib |
A |
G |
7: 44,178,309 (GRCm39) |
S154P |
probably damaging |
Het |
Spty2d1 |
T |
C |
7: 46,645,858 (GRCm39) |
D595G |
probably damaging |
Het |
St7 |
T |
A |
6: 17,906,515 (GRCm39) |
|
probably null |
Het |
Susd1 |
T |
C |
4: 59,428,029 (GRCm39) |
T52A |
possibly damaging |
Het |
Svs5 |
T |
A |
2: 164,079,043 (GRCm39) |
D288V |
possibly damaging |
Het |
Syt7 |
T |
A |
19: 10,420,288 (GRCm39) |
I355N |
probably damaging |
Het |
Tarm1 |
G |
A |
7: 3,545,416 (GRCm39) |
Q145* |
probably null |
Het |
Teddm2 |
T |
A |
1: 153,726,487 (GRCm39) |
E76V |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,540,923 (GRCm39) |
S343P |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,103,317 (GRCm39) |
|
probably null |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Triobp |
G |
A |
15: 78,851,313 (GRCm39) |
R489K |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Ttn |
A |
G |
2: 76,730,171 (GRCm39) |
|
probably benign |
Het |
Tyrp1 |
A |
T |
4: 80,763,172 (GRCm39) |
D353V |
possibly damaging |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Unc13d |
A |
G |
11: 115,964,408 (GRCm39) |
V312A |
possibly damaging |
Het |
Urb2 |
G |
T |
8: 124,755,636 (GRCm39) |
A448S |
probably damaging |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,803 (GRCm39) |
R250S |
probably benign |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,450,195 (GRCm39) |
T147I |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Vxn |
T |
C |
1: 9,677,201 (GRCm39) |
S24P |
probably benign |
Het |
Washc4 |
A |
T |
10: 83,410,343 (GRCm39) |
M644L |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,569,737 (GRCm39) |
V449E |
probably damaging |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp512b |
A |
G |
2: 181,230,532 (GRCm39) |
S453P |
probably benign |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably damaging |
Het |
|
Other mutations in Trrap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Trrap
|
APN |
5 |
144,716,784 (GRCm39) |
splice site |
probably benign |
|
IGL00470:Trrap
|
APN |
5 |
144,754,848 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00490:Trrap
|
APN |
5 |
144,762,035 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01072:Trrap
|
APN |
5 |
144,721,065 (GRCm39) |
splice site |
probably benign |
|
IGL01087:Trrap
|
APN |
5 |
144,783,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01300:Trrap
|
APN |
5 |
144,741,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01350:Trrap
|
APN |
5 |
144,767,779 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01410:Trrap
|
APN |
5 |
144,767,831 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01571:Trrap
|
APN |
5 |
144,770,097 (GRCm39) |
splice site |
probably benign |
|
IGL01748:Trrap
|
APN |
5 |
144,770,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01839:Trrap
|
APN |
5 |
144,758,685 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01976:Trrap
|
APN |
5 |
144,793,799 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02075:Trrap
|
APN |
5 |
144,765,304 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02127:Trrap
|
APN |
5 |
144,753,243 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02131:Trrap
|
APN |
5 |
144,777,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02287:Trrap
|
APN |
5 |
144,769,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02301:Trrap
|
APN |
5 |
144,714,727 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02336:Trrap
|
APN |
5 |
144,735,200 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02526:Trrap
|
APN |
5 |
144,761,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02873:Trrap
|
APN |
5 |
144,777,889 (GRCm39) |
splice site |
probably benign |
|
IGL02953:Trrap
|
APN |
5 |
144,752,774 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03404:Trrap
|
APN |
5 |
144,769,996 (GRCm39) |
missense |
probably benign |
0.00 |
Buffer
|
UTSW |
5 |
144,771,014 (GRCm39) |
missense |
probably benign |
0.06 |
Card-tower
|
UTSW |
5 |
144,741,576 (GRCm39) |
missense |
probably damaging |
1.00 |
Cookie
|
UTSW |
5 |
144,730,859 (GRCm39) |
missense |
probably damaging |
1.00 |
Glass_house
|
UTSW |
5 |
144,782,287 (GRCm39) |
missense |
possibly damaging |
0.67 |
Immovable
|
UTSW |
5 |
144,727,665 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5049_trrap_520
|
UTSW |
5 |
144,763,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167_Trrap_977
|
UTSW |
5 |
144,776,424 (GRCm39) |
missense |
probably benign |
0.39 |
vitreous
|
UTSW |
5 |
144,742,537 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4243001:Trrap
|
UTSW |
5 |
144,733,781 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4466001:Trrap
|
UTSW |
5 |
144,765,410 (GRCm39) |
missense |
probably benign |
0.02 |
R0062:Trrap
|
UTSW |
5 |
144,719,003 (GRCm39) |
splice site |
probably benign |
|
R0062:Trrap
|
UTSW |
5 |
144,719,003 (GRCm39) |
splice site |
probably benign |
|
R0112:Trrap
|
UTSW |
5 |
144,759,571 (GRCm39) |
nonsense |
probably null |
|
R0126:Trrap
|
UTSW |
5 |
144,742,560 (GRCm39) |
nonsense |
probably null |
|
R0257:Trrap
|
UTSW |
5 |
144,741,045 (GRCm39) |
missense |
probably benign |
0.31 |
R0325:Trrap
|
UTSW |
5 |
144,753,205 (GRCm39) |
missense |
probably benign |
0.05 |
R0376:Trrap
|
UTSW |
5 |
144,753,149 (GRCm39) |
missense |
probably benign |
0.03 |
R0396:Trrap
|
UTSW |
5 |
144,751,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R0448:Trrap
|
UTSW |
5 |
144,776,377 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0454:Trrap
|
UTSW |
5 |
144,783,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Trrap
|
UTSW |
5 |
144,790,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R0827:Trrap
|
UTSW |
5 |
144,751,640 (GRCm39) |
missense |
probably benign |
0.00 |
R1005:Trrap
|
UTSW |
5 |
144,742,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Trrap
|
UTSW |
5 |
144,741,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Trrap
|
UTSW |
5 |
144,741,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R1179:Trrap
|
UTSW |
5 |
144,714,749 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1218:Trrap
|
UTSW |
5 |
144,753,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Trrap
|
UTSW |
5 |
144,726,409 (GRCm39) |
splice site |
probably benign |
|
R1374:Trrap
|
UTSW |
5 |
144,783,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Trrap
|
UTSW |
5 |
144,794,232 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1480:Trrap
|
UTSW |
5 |
144,755,123 (GRCm39) |
missense |
probably benign |
|
R1538:Trrap
|
UTSW |
5 |
144,774,012 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1751:Trrap
|
UTSW |
5 |
144,751,385 (GRCm39) |
critical splice donor site |
probably null |
|
R1779:Trrap
|
UTSW |
5 |
144,765,400 (GRCm39) |
missense |
probably benign |
0.01 |
R1782:Trrap
|
UTSW |
5 |
144,759,513 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1792:Trrap
|
UTSW |
5 |
144,790,396 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1859:Trrap
|
UTSW |
5 |
144,767,761 (GRCm39) |
missense |
probably benign |
0.04 |
R1861:Trrap
|
UTSW |
5 |
144,752,727 (GRCm39) |
splice site |
probably null |
|
R1902:Trrap
|
UTSW |
5 |
144,752,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Trrap
|
UTSW |
5 |
144,752,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Trrap
|
UTSW |
5 |
144,790,298 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2026:Trrap
|
UTSW |
5 |
144,739,854 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2036:Trrap
|
UTSW |
5 |
144,765,372 (GRCm39) |
missense |
probably benign |
0.08 |
R2099:Trrap
|
UTSW |
5 |
144,719,049 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2108:Trrap
|
UTSW |
5 |
144,762,684 (GRCm39) |
missense |
probably benign |
0.01 |
R2113:Trrap
|
UTSW |
5 |
144,781,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Trrap
|
UTSW |
5 |
144,758,665 (GRCm39) |
missense |
probably benign |
0.40 |
R2442:Trrap
|
UTSW |
5 |
144,754,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Trrap
|
UTSW |
5 |
144,780,179 (GRCm39) |
critical splice donor site |
probably null |
|
R3442:Trrap
|
UTSW |
5 |
144,729,062 (GRCm39) |
missense |
probably benign |
0.03 |
R3853:Trrap
|
UTSW |
5 |
144,728,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R4401:Trrap
|
UTSW |
5 |
144,780,128 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4493:Trrap
|
UTSW |
5 |
144,767,858 (GRCm39) |
missense |
probably benign |
0.21 |
R4524:Trrap
|
UTSW |
5 |
144,762,131 (GRCm39) |
missense |
probably benign |
0.38 |
R4569:Trrap
|
UTSW |
5 |
144,728,928 (GRCm39) |
missense |
probably benign |
0.13 |
R4672:Trrap
|
UTSW |
5 |
144,722,290 (GRCm39) |
missense |
probably damaging |
0.97 |
R4732:Trrap
|
UTSW |
5 |
144,753,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4791:Trrap
|
UTSW |
5 |
144,740,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Trrap
|
UTSW |
5 |
144,769,298 (GRCm39) |
missense |
probably benign |
0.06 |
R4827:Trrap
|
UTSW |
5 |
144,737,758 (GRCm39) |
missense |
probably benign |
0.02 |
R4839:Trrap
|
UTSW |
5 |
144,782,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Trrap
|
UTSW |
5 |
144,742,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R4951:Trrap
|
UTSW |
5 |
144,742,530 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4959:Trrap
|
UTSW |
5 |
144,793,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Trrap
|
UTSW |
5 |
144,763,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Trrap
|
UTSW |
5 |
144,787,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5236:Trrap
|
UTSW |
5 |
144,754,596 (GRCm39) |
missense |
probably benign |
0.07 |
R5281:Trrap
|
UTSW |
5 |
144,750,313 (GRCm39) |
missense |
probably benign |
0.13 |
R5322:Trrap
|
UTSW |
5 |
144,781,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Trrap
|
UTSW |
5 |
144,786,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5590:Trrap
|
UTSW |
5 |
144,719,075 (GRCm39) |
missense |
probably benign |
0.05 |
R5799:Trrap
|
UTSW |
5 |
144,767,755 (GRCm39) |
missense |
probably benign |
|
R5885:Trrap
|
UTSW |
5 |
144,731,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Trrap
|
UTSW |
5 |
144,786,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5908:Trrap
|
UTSW |
5 |
144,723,518 (GRCm39) |
missense |
probably damaging |
0.96 |
R5956:Trrap
|
UTSW |
5 |
144,744,201 (GRCm39) |
splice site |
silent |
|
R5992:Trrap
|
UTSW |
5 |
144,746,994 (GRCm39) |
missense |
probably benign |
0.00 |
R6017:Trrap
|
UTSW |
5 |
144,781,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Trrap
|
UTSW |
5 |
144,762,724 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6029:Trrap
|
UTSW |
5 |
144,754,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6117:Trrap
|
UTSW |
5 |
144,739,771 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6166:Trrap
|
UTSW |
5 |
144,718,791 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6234:Trrap
|
UTSW |
5 |
144,776,523 (GRCm39) |
splice site |
probably null |
|
R6288:Trrap
|
UTSW |
5 |
144,748,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R6290:Trrap
|
UTSW |
5 |
144,741,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6316:Trrap
|
UTSW |
5 |
144,750,336 (GRCm39) |
missense |
probably benign |
0.02 |
R6398:Trrap
|
UTSW |
5 |
144,727,680 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6413:Trrap
|
UTSW |
5 |
144,720,856 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6499:Trrap
|
UTSW |
5 |
144,793,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R6529:Trrap
|
UTSW |
5 |
144,771,014 (GRCm39) |
missense |
probably benign |
0.06 |
R6574:Trrap
|
UTSW |
5 |
144,752,360 (GRCm39) |
critical splice donor site |
probably null |
|
R6631:Trrap
|
UTSW |
5 |
144,708,460 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6727:Trrap
|
UTSW |
5 |
144,793,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Trrap
|
UTSW |
5 |
144,788,066 (GRCm39) |
nonsense |
probably null |
|
R6914:Trrap
|
UTSW |
5 |
144,720,853 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6942:Trrap
|
UTSW |
5 |
144,720,853 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6945:Trrap
|
UTSW |
5 |
144,727,665 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7023:Trrap
|
UTSW |
5 |
144,728,964 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7107:Trrap
|
UTSW |
5 |
144,733,945 (GRCm39) |
missense |
probably benign |
0.05 |
R7139:Trrap
|
UTSW |
5 |
144,739,988 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7148:Trrap
|
UTSW |
5 |
144,758,613 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7167:Trrap
|
UTSW |
5 |
144,776,424 (GRCm39) |
missense |
probably benign |
0.39 |
R7171:Trrap
|
UTSW |
5 |
144,730,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Trrap
|
UTSW |
5 |
144,779,517 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7215:Trrap
|
UTSW |
5 |
144,733,945 (GRCm39) |
missense |
probably benign |
0.05 |
R7255:Trrap
|
UTSW |
5 |
144,795,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Trrap
|
UTSW |
5 |
144,782,287 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7264:Trrap
|
UTSW |
5 |
144,751,333 (GRCm39) |
missense |
probably benign |
0.05 |
R7372:Trrap
|
UTSW |
5 |
144,726,208 (GRCm39) |
missense |
probably benign |
|
R7447:Trrap
|
UTSW |
5 |
144,776,284 (GRCm39) |
missense |
probably damaging |
0.97 |
R7449:Trrap
|
UTSW |
5 |
144,788,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R7655:Trrap
|
UTSW |
5 |
144,779,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7656:Trrap
|
UTSW |
5 |
144,779,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7662:Trrap
|
UTSW |
5 |
144,769,321 (GRCm39) |
missense |
probably benign |
0.00 |
R7716:Trrap
|
UTSW |
5 |
144,713,956 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8143:Trrap
|
UTSW |
5 |
144,772,707 (GRCm39) |
splice site |
probably null |
|
R8183:Trrap
|
UTSW |
5 |
144,765,343 (GRCm39) |
missense |
probably benign |
0.01 |
R8265:Trrap
|
UTSW |
5 |
144,722,344 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8273:Trrap
|
UTSW |
5 |
144,727,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Trrap
|
UTSW |
5 |
144,762,747 (GRCm39) |
missense |
probably benign |
0.44 |
R8674:Trrap
|
UTSW |
5 |
144,727,842 (GRCm39) |
missense |
probably benign |
0.02 |
R8777:Trrap
|
UTSW |
5 |
144,773,949 (GRCm39) |
missense |
probably benign |
0.10 |
R8777-TAIL:Trrap
|
UTSW |
5 |
144,773,949 (GRCm39) |
missense |
probably benign |
0.10 |
R8817:Trrap
|
UTSW |
5 |
144,782,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Trrap
|
UTSW |
5 |
144,781,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Trrap
|
UTSW |
5 |
144,758,649 (GRCm39) |
missense |
probably benign |
0.30 |
R8937:Trrap
|
UTSW |
5 |
144,757,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Trrap
|
UTSW |
5 |
144,740,162 (GRCm39) |
missense |
probably damaging |
0.96 |
R9010:Trrap
|
UTSW |
5 |
144,783,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9095:Trrap
|
UTSW |
5 |
144,733,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Trrap
|
UTSW |
5 |
144,767,830 (GRCm39) |
missense |
probably benign |
0.16 |
R9132:Trrap
|
UTSW |
5 |
144,726,362 (GRCm39) |
missense |
probably benign |
0.03 |
R9224:Trrap
|
UTSW |
5 |
144,708,049 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9338:Trrap
|
UTSW |
5 |
144,727,925 (GRCm39) |
missense |
probably benign |
|
R9380:Trrap
|
UTSW |
5 |
144,769,981 (GRCm39) |
missense |
probably benign |
|
R9404:Trrap
|
UTSW |
5 |
144,752,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9457:Trrap
|
UTSW |
5 |
144,763,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Trrap
|
UTSW |
5 |
144,763,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R9504:Trrap
|
UTSW |
5 |
144,742,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Trrap
|
UTSW |
5 |
144,777,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9584:Trrap
|
UTSW |
5 |
144,777,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9585:Trrap
|
UTSW |
5 |
144,777,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Trrap
|
UTSW |
5 |
144,780,128 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9728:Trrap
|
UTSW |
5 |
144,726,193 (GRCm39) |
missense |
probably benign |
0.22 |
R9782:Trrap
|
UTSW |
5 |
144,758,716 (GRCm39) |
missense |
probably damaging |
0.99 |
X0060:Trrap
|
UTSW |
5 |
144,780,171 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1088:Trrap
|
UTSW |
5 |
144,771,007 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Trrap
|
UTSW |
5 |
144,756,518 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Trrap
|
UTSW |
5 |
144,747,154 (GRCm39) |
missense |
|
|
Z1177:Trrap
|
UTSW |
5 |
144,793,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
|
Posted On |
2017-03-08 |