Incidental Mutation 'R1531:Trappc9'
| ID |
166246 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Trappc9
|
| Ensembl Gene |
ENSMUSG00000047921 |
| Gene Name |
trafficking protein particle complex 9 |
| Synonyms |
TRS130, Nibp, 2900005P22Rik, 4632408O18Rik, 1810044A24Rik |
| MMRRC Submission |
039570-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1531 (G1)
|
| Quality Score |
190 |
|
Status
|
Not validated
|
| Chromosome |
15 |
| Chromosomal Location |
72461469-72933053 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 72565397 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 965
(R965*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000087202
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023276]
[ENSMUST00000089770]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably null
Transcript: ENSMUST00000023276
AA Change: R786*
|
| SMART Domains |
Protein: ENSMUSP00000023276
Gene: ENSMUSG00000047921
AA Change: R786*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TRAPPC9-Trs120
|
2 |
920 |
3.6e-239 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000089770
AA Change: R965*
|
| SMART Domains |
Protein: ENSMUSP00000087202
Gene: ENSMUSG00000047921
AA Change: R965*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TRAPPC9-Trs120
|
182 |
350 |
4.1e-20 |
PFAM |
|
Pfam:TRAPPC9-Trs120
|
434 |
664 |
2.2e-16 |
PFAM |
|
low complexity region
|
993 |
1004 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.1%
- 10x: 95.6%
- 20x: 90.3%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive mental retardation. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Agtpbp1 |
T |
A |
13: 59,648,448 (GRCm39) |
|
probably null |
Het |
| Aldh3b2 |
T |
G |
19: 4,027,543 (GRCm39) |
F28C |
probably damaging |
Het |
| Apaf1 |
T |
C |
10: 90,890,383 (GRCm39) |
N540S |
probably damaging |
Het |
| Apob |
T |
C |
12: 8,047,880 (GRCm39) |
I953T |
possibly damaging |
Het |
| Arhgef1 |
A |
G |
7: 24,624,423 (GRCm39) |
T816A |
probably damaging |
Het |
| Arid4a |
T |
A |
12: 71,122,779 (GRCm39) |
F1053L |
probably benign |
Het |
| Atxn1l |
A |
C |
8: 110,458,691 (GRCm39) |
F524V |
probably damaging |
Het |
| Cad |
T |
A |
5: 31,233,563 (GRCm39) |
M1874K |
probably benign |
Het |
| Ccdc40 |
G |
A |
11: 119,154,015 (GRCm39) |
V1096I |
probably benign |
Het |
| Ccdc93 |
A |
G |
1: 121,408,551 (GRCm39) |
D358G |
probably benign |
Het |
| Cd96 |
T |
C |
16: 45,938,169 (GRCm39) |
T99A |
probably benign |
Het |
| Cdc42ep3 |
A |
T |
17: 79,642,473 (GRCm39) |
M149K |
probably benign |
Het |
| Cgas |
A |
G |
9: 78,349,763 (GRCm39) |
Y200H |
probably damaging |
Het |
| Cog4 |
A |
G |
8: 111,606,353 (GRCm39) |
E613G |
probably benign |
Het |
| Crebbp |
A |
T |
16: 3,902,381 (GRCm39) |
I2286N |
probably benign |
Het |
| Csf1 |
T |
C |
3: 107,655,654 (GRCm39) |
E459G |
possibly damaging |
Het |
| Csrp2 |
A |
T |
10: 110,771,066 (GRCm39) |
Y57F |
probably benign |
Het |
| Ctdspl |
C |
T |
9: 118,869,650 (GRCm39) |
P244L |
probably damaging |
Het |
| Cyp2c29 |
A |
G |
19: 39,313,412 (GRCm39) |
R303G |
probably damaging |
Het |
| Cyp4a10 |
C |
A |
4: 115,375,632 (GRCm39) |
Y38* |
probably null |
Het |
| Dmgdh |
T |
A |
13: 93,880,919 (GRCm39) |
I783N |
probably damaging |
Het |
| Efcc1 |
G |
A |
6: 87,708,148 (GRCm39) |
E92K |
probably benign |
Het |
| Eif2ak4 |
T |
A |
2: 118,273,691 (GRCm39) |
L872H |
probably damaging |
Het |
| Elp2 |
T |
A |
18: 24,764,461 (GRCm39) |
S603T |
probably benign |
Het |
| Eml2 |
T |
A |
7: 18,930,179 (GRCm39) |
L300H |
probably damaging |
Het |
| Esp3 |
A |
G |
17: 40,946,827 (GRCm39) |
K50R |
possibly damaging |
Het |
| Esrp1 |
A |
G |
4: 11,379,375 (GRCm39) |
F136L |
probably damaging |
Het |
| Exoc1 |
T |
A |
5: 76,707,011 (GRCm39) |
D497E |
probably damaging |
Het |
| Fat3 |
A |
G |
9: 15,908,761 (GRCm39) |
S2414P |
probably damaging |
Het |
| Foxj3 |
C |
T |
4: 119,477,398 (GRCm39) |
P369S |
unknown |
Het |
| Gkn2 |
G |
T |
6: 87,352,921 (GRCm39) |
|
probably null |
Het |
| Gm17333 |
AAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAA |
AAGAAGAGAAGAGAAGAGAAGAGAAGAGAA |
16: 77,649,766 (GRCm39) |
|
noncoding transcript |
Het |
| Gm21905 |
A |
T |
5: 68,103,724 (GRCm39) |
|
probably benign |
Het |
| Grhl1 |
T |
A |
12: 24,632,962 (GRCm39) |
|
probably null |
Het |
| Grk6 |
A |
G |
13: 55,599,967 (GRCm39) |
Y221C |
probably damaging |
Het |
| Hcrtr1 |
T |
A |
4: 130,024,720 (GRCm39) |
K389* |
probably null |
Het |
| Hk1 |
G |
A |
10: 62,120,563 (GRCm39) |
R545C |
probably damaging |
Het |
| Hsp90b1 |
A |
T |
10: 86,532,659 (GRCm39) |
I339N |
probably benign |
Het |
| Ikzf3 |
T |
C |
11: 98,381,272 (GRCm39) |
R103G |
probably damaging |
Het |
| Itgad |
A |
C |
7: 127,777,542 (GRCm39) |
I141L |
probably benign |
Het |
| Jmjd6 |
T |
A |
11: 116,733,266 (GRCm39) |
Y137F |
probably benign |
Het |
| Kcna1 |
A |
G |
6: 126,619,030 (GRCm39) |
V430A |
probably benign |
Het |
| Kel |
A |
G |
6: 41,665,560 (GRCm39) |
V520A |
probably damaging |
Het |
| Klhl41 |
G |
A |
2: 69,501,084 (GRCm39) |
V182I |
probably benign |
Het |
| Ldhb |
C |
A |
6: 142,447,121 (GRCm39) |
M64I |
probably benign |
Het |
| Lrrc23 |
A |
G |
6: 124,753,077 (GRCm39) |
S190P |
possibly damaging |
Het |
| Mboat2 |
T |
C |
12: 25,009,029 (GRCm39) |
V445A |
probably benign |
Het |
| Mlycd |
G |
A |
8: 120,128,258 (GRCm39) |
W188* |
probably null |
Het |
| Mpp3 |
C |
T |
11: 101,899,475 (GRCm39) |
E349K |
probably benign |
Het |
| Mtres1 |
A |
G |
10: 43,401,316 (GRCm39) |
V211A |
probably benign |
Het |
| Myh4 |
A |
G |
11: 67,141,366 (GRCm39) |
M780V |
probably benign |
Het |
| Myh6 |
G |
A |
14: 55,193,963 (GRCm39) |
R809C |
probably damaging |
Het |
| Mylip |
G |
A |
13: 45,560,046 (GRCm39) |
V161M |
possibly damaging |
Het |
| Nrp1 |
G |
A |
8: 129,152,450 (GRCm39) |
V220I |
probably null |
Het |
| Nup210 |
A |
T |
6: 91,011,823 (GRCm39) |
N455K |
probably benign |
Het |
| Or14j10 |
A |
T |
17: 37,935,243 (GRCm39) |
Y94* |
probably null |
Het |
| Or51f1d |
C |
A |
7: 102,700,795 (GRCm39) |
Q97K |
probably benign |
Het |
| Pbld2 |
G |
T |
10: 62,889,732 (GRCm39) |
|
probably null |
Het |
| Pclo |
C |
G |
5: 14,571,917 (GRCm39) |
P434R |
probably damaging |
Het |
| Pdlim3 |
A |
G |
8: 46,349,800 (GRCm39) |
K37E |
probably damaging |
Het |
| Prkdc |
T |
A |
16: 15,589,970 (GRCm39) |
I2611N |
probably benign |
Het |
| Prr12 |
T |
C |
7: 44,677,954 (GRCm39) |
D2019G |
unknown |
Het |
| Rab27a |
A |
G |
9: 73,002,685 (GRCm39) |
T205A |
probably benign |
Het |
| Rcan3 |
A |
G |
4: 135,152,595 (GRCm39) |
L42P |
probably damaging |
Het |
| Rchy1 |
T |
C |
5: 92,103,474 (GRCm39) |
|
probably null |
Het |
| Sema6a |
T |
C |
18: 47,382,066 (GRCm39) |
H827R |
probably damaging |
Het |
| Sertad4 |
A |
G |
1: 192,533,258 (GRCm39) |
|
probably null |
Het |
| Smarcd1 |
T |
A |
15: 99,605,264 (GRCm39) |
C282S |
probably damaging |
Het |
| Speg |
A |
G |
1: 75,377,866 (GRCm39) |
T769A |
possibly damaging |
Het |
| Syne1 |
T |
A |
10: 5,297,875 (GRCm39) |
K1141* |
probably null |
Het |
| Synpo2 |
T |
C |
3: 122,911,315 (GRCm39) |
E110G |
probably benign |
Het |
| Tg |
T |
A |
15: 66,722,351 (GRCm39) |
D333E |
probably benign |
Het |
| Tmem132c |
A |
G |
5: 127,436,955 (GRCm39) |
Y148C |
probably damaging |
Het |
| Tmem215 |
T |
A |
4: 40,473,965 (GRCm39) |
V14E |
probably damaging |
Het |
| Tmem229b |
A |
G |
12: 79,011,685 (GRCm39) |
L82P |
probably damaging |
Het |
| Togaram1 |
A |
G |
12: 65,013,039 (GRCm39) |
T97A |
probably benign |
Het |
| Trio |
T |
C |
15: 27,833,071 (GRCm39) |
I104V |
probably benign |
Het |
| Trp73 |
A |
G |
4: 154,148,352 (GRCm39) |
F354S |
probably benign |
Het |
| Ttyh2 |
T |
C |
11: 114,577,278 (GRCm39) |
L63P |
probably damaging |
Het |
| Ulk4 |
G |
C |
9: 120,873,841 (GRCm39) |
P1197A |
probably damaging |
Het |
| Vmn1r176 |
T |
C |
7: 23,534,536 (GRCm39) |
M206V |
possibly damaging |
Het |
| Vps8 |
T |
A |
16: 21,285,226 (GRCm39) |
Y402* |
probably null |
Het |
| Zbtb41 |
A |
G |
1: 139,350,931 (GRCm39) |
I15V |
probably benign |
Het |
| Zc3hav1 |
T |
C |
6: 38,284,170 (GRCm39) |
I982V |
possibly damaging |
Het |
| Zmynd19 |
T |
A |
2: 24,848,123 (GRCm39) |
N106K |
probably benign |
Het |
|
| Other mutations in Trappc9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00092:Trappc9
|
APN |
15 |
72,897,875 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL01348:Trappc9
|
APN |
15 |
72,808,858 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL01367:Trappc9
|
APN |
15 |
72,462,002 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL01521:Trappc9
|
APN |
15 |
72,924,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01726:Trappc9
|
APN |
15 |
72,817,971 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01881:Trappc9
|
APN |
15 |
72,871,841 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02214:Trappc9
|
APN |
15 |
72,884,731 (GRCm39) |
nonsense |
probably null |
|
|
IGL02693:Trappc9
|
APN |
15 |
72,835,542 (GRCm39) |
splice site |
probably benign |
|
|
IGL03229:Trappc9
|
APN |
15 |
72,930,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|
basilio
|
UTSW |
15 |
72,930,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Boomboom
|
UTSW |
15 |
72,608,718 (GRCm39) |
nonsense |
probably null |
|
|
bronto
|
UTSW |
15 |
72,930,087 (GRCm39) |
nonsense |
probably null |
|
|
Earl
|
UTSW |
15 |
72,608,626 (GRCm39) |
nonsense |
probably null |
|
|
Sotto_aceto
|
UTSW |
15 |
72,557,188 (GRCm39) |
missense |
probably damaging |
0.99 |
|
P0026:Trappc9
|
UTSW |
15 |
72,824,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4453001:Trappc9
|
UTSW |
15 |
72,903,447 (GRCm39) |
frame shift |
probably null |
|
|
PIT4519001:Trappc9
|
UTSW |
15 |
72,824,943 (GRCm39) |
missense |
probably benign |
|
|
R0001:Trappc9
|
UTSW |
15 |
72,835,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0094:Trappc9
|
UTSW |
15 |
72,894,929 (GRCm38) |
intron |
probably benign |
|
|
R0745:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0747:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0800:Trappc9
|
UTSW |
15 |
72,824,981 (GRCm39) |
splice site |
probably benign |
|
|
R0816:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0819:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0820:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0893:Trappc9
|
UTSW |
15 |
72,461,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0976:Trappc9
|
UTSW |
15 |
72,871,823 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1119:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1266:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1453:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1454:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1543:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1563:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1565:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1600:Trappc9
|
UTSW |
15 |
72,808,958 (GRCm39) |
nonsense |
probably null |
|
|
R1712:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1756:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1789:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1978:Trappc9
|
UTSW |
15 |
72,871,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2001:Trappc9
|
UTSW |
15 |
72,929,885 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2312:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2334:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2926:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3123:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3124:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3125:Trappc9
|
UTSW |
15 |
72,897,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3813:Trappc9
|
UTSW |
15 |
72,930,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4012:Trappc9
|
UTSW |
15 |
72,903,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4080:Trappc9
|
UTSW |
15 |
72,813,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4282:Trappc9
|
UTSW |
15 |
72,462,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4572:Trappc9
|
UTSW |
15 |
72,808,916 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R4739:Trappc9
|
UTSW |
15 |
72,808,909 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4959:Trappc9
|
UTSW |
15 |
72,808,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4973:Trappc9
|
UTSW |
15 |
72,808,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5123:Trappc9
|
UTSW |
15 |
72,785,215 (GRCm39) |
intron |
probably benign |
|
|
R5128:Trappc9
|
UTSW |
15 |
72,930,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5228:Trappc9
|
UTSW |
15 |
72,929,844 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5362:Trappc9
|
UTSW |
15 |
72,930,066 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R5802:Trappc9
|
UTSW |
15 |
72,557,188 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6032:Trappc9
|
UTSW |
15 |
72,797,379 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6032:Trappc9
|
UTSW |
15 |
72,797,379 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6154:Trappc9
|
UTSW |
15 |
72,929,930 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6372:Trappc9
|
UTSW |
15 |
72,461,923 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6661:Trappc9
|
UTSW |
15 |
72,461,993 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R6864:Trappc9
|
UTSW |
15 |
72,809,011 (GRCm39) |
splice site |
probably null |
|
|
R6893:Trappc9
|
UTSW |
15 |
72,797,499 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7099:Trappc9
|
UTSW |
15 |
72,565,468 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7276:Trappc9
|
UTSW |
15 |
72,924,119 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7349:Trappc9
|
UTSW |
15 |
72,608,718 (GRCm39) |
nonsense |
probably null |
|
|
R8260:Trappc9
|
UTSW |
15 |
72,813,758 (GRCm39) |
nonsense |
probably null |
|
|
R8399:Trappc9
|
UTSW |
15 |
72,924,131 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8683:Trappc9
|
UTSW |
15 |
72,884,664 (GRCm39) |
missense |
probably benign |
0.26 |
|
R8839:Trappc9
|
UTSW |
15 |
72,930,087 (GRCm39) |
nonsense |
probably null |
|
|
R8945:Trappc9
|
UTSW |
15 |
72,929,945 (GRCm39) |
missense |
probably benign |
|
|
R9083:Trappc9
|
UTSW |
15 |
72,608,626 (GRCm39) |
nonsense |
probably null |
|
|
R9323:Trappc9
|
UTSW |
15 |
72,565,431 (GRCm39) |
missense |
probably benign |
0.41 |
|
R9329:Trappc9
|
UTSW |
15 |
72,673,202 (GRCm39) |
missense |
unknown |
|
|
R9366:Trappc9
|
UTSW |
15 |
72,808,937 (GRCm39) |
missense |
probably benign |
|
|
R9723:Trappc9
|
UTSW |
15 |
72,461,963 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
RF008:Trappc9
|
UTSW |
15 |
72,673,138 (GRCm39) |
small insertion |
probably benign |
|
|
RF009:Trappc9
|
UTSW |
15 |
72,673,136 (GRCm39) |
small insertion |
probably benign |
|
|
RF014:Trappc9
|
UTSW |
15 |
72,673,132 (GRCm39) |
small insertion |
probably benign |
|
|
RF016:Trappc9
|
UTSW |
15 |
72,673,138 (GRCm39) |
small insertion |
probably benign |
|
|
RF023:Trappc9
|
UTSW |
15 |
72,673,180 (GRCm39) |
small insertion |
probably benign |
|
|
RF023:Trappc9
|
UTSW |
15 |
72,673,173 (GRCm39) |
small insertion |
probably benign |
|
|
RF028:Trappc9
|
UTSW |
15 |
72,673,139 (GRCm39) |
small insertion |
probably benign |
|
|
RF029:Trappc9
|
UTSW |
15 |
72,673,172 (GRCm39) |
small insertion |
probably benign |
|
|
RF030:Trappc9
|
UTSW |
15 |
72,673,174 (GRCm39) |
small insertion |
probably benign |
|
|
RF034:Trappc9
|
UTSW |
15 |
72,673,147 (GRCm39) |
small insertion |
probably benign |
|
|
RF036:Trappc9
|
UTSW |
15 |
72,673,169 (GRCm39) |
small insertion |
probably benign |
|
|
RF038:Trappc9
|
UTSW |
15 |
72,673,172 (GRCm39) |
small insertion |
probably benign |
|
|
RF040:Trappc9
|
UTSW |
15 |
72,673,141 (GRCm39) |
small insertion |
probably benign |
|
|
RF042:Trappc9
|
UTSW |
15 |
72,673,132 (GRCm39) |
small insertion |
probably benign |
|
|
RF043:Trappc9
|
UTSW |
15 |
72,673,154 (GRCm39) |
small insertion |
probably benign |
|
|
RF049:Trappc9
|
UTSW |
15 |
72,673,155 (GRCm39) |
small insertion |
probably benign |
|
|
RF049:Trappc9
|
UTSW |
15 |
72,673,150 (GRCm39) |
small insertion |
probably benign |
|
|
RF053:Trappc9
|
UTSW |
15 |
72,673,177 (GRCm39) |
small insertion |
probably benign |
|
|
RF057:Trappc9
|
UTSW |
15 |
72,673,144 (GRCm39) |
small insertion |
probably benign |
|
|
RF063:Trappc9
|
UTSW |
15 |
72,673,173 (GRCm39) |
small insertion |
probably benign |
|
|
RF063:Trappc9
|
UTSW |
15 |
72,673,169 (GRCm39) |
small insertion |
probably benign |
|
|
Z1177:Trappc9
|
UTSW |
15 |
72,924,011 (GRCm39) |
missense |
probably null |
0.51 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACGCTAAGAAAATGCCAGCCCTATG -3'
(R):5'- ATGTGCTGACTCTCCAACAGCTCC -3'
Sequencing Primer
(F):5'- GCCATGCCATTTGAAGCTG -3'
(R):5'- CGGGAAGAAATTGCCCTGC -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation