Incidental Mutation 'R5133:Fam186a'
| ID |
395968 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fam186a
|
| Ensembl Gene |
ENSMUSG00000045350 |
| Gene Name |
family with sequence similarity 186, member A |
| Synonyms |
LOC380973, 1700030F18Rik |
| MMRRC Submission |
042721-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.059)
|
| Stock # |
R5133 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
15 |
| Chromosomal Location |
99816229-99864942 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 99853374 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Alanine
at position 122
(D122A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097783
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100209]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
unknown
Transcript: ENSMUST00000100209
AA Change: D122A
|
| SMART Domains |
Protein: ENSMUSP00000097783
Gene: ENSMUSG00000045350
AA Change: D122A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
21 |
N/A |
INTRINSIC |
|
Blast:FBG
|
44 |
222 |
4e-48 |
BLAST |
|
coiled coil region
|
292 |
340 |
N/A |
INTRINSIC |
|
low complexity region
|
423 |
443 |
N/A |
INTRINSIC |
|
low complexity region
|
446 |
458 |
N/A |
INTRINSIC |
|
low complexity region
|
632 |
644 |
N/A |
INTRINSIC |
|
low complexity region
|
702 |
713 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
743 |
1156 |
1.05e-58 |
PROSPERO |
|
internal_repeat_1
|
833 |
1270 |
7.71e-59 |
PROSPERO |
|
low complexity region
|
1271 |
1285 |
N/A |
INTRINSIC |
|
low complexity region
|
1289 |
1300 |
N/A |
INTRINSIC |
|
low complexity region
|
1309 |
1323 |
N/A |
INTRINSIC |
|
low complexity region
|
1327 |
1338 |
N/A |
INTRINSIC |
|
low complexity region
|
1347 |
1361 |
N/A |
INTRINSIC |
|
low complexity region
|
1365 |
1376 |
N/A |
INTRINSIC |
|
low complexity region
|
1384 |
1395 |
N/A |
INTRINSIC |
|
low complexity region
|
1403 |
1414 |
N/A |
INTRINSIC |
|
low complexity region
|
1423 |
1437 |
N/A |
INTRINSIC |
|
low complexity region
|
1441 |
1452 |
N/A |
INTRINSIC |
|
low complexity region
|
1460 |
1471 |
N/A |
INTRINSIC |
|
low complexity region
|
1479 |
1490 |
N/A |
INTRINSIC |
|
low complexity region
|
1498 |
1509 |
N/A |
INTRINSIC |
|
low complexity region
|
1518 |
1532 |
N/A |
INTRINSIC |
|
low complexity region
|
1536 |
1547 |
N/A |
INTRINSIC |
|
low complexity region
|
1555 |
1566 |
N/A |
INTRINSIC |
|
low complexity region
|
1574 |
1585 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1586 |
1981 |
7.71e-59 |
PROSPERO |
|
internal_repeat_2
|
1737 |
2197 |
1.05e-58 |
PROSPERO |
|
low complexity region
|
2367 |
2378 |
N/A |
INTRINSIC |
|
low complexity region
|
2549 |
2564 |
N/A |
INTRINSIC |
|
low complexity region
|
2644 |
2655 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177831
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000180309
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 96.9%
- 20x: 94.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 101 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A3galt2 |
A |
T |
4: 128,655,934 (GRCm39) |
T101S |
probably damaging |
Het |
| Abraxas2 |
C |
T |
7: 132,484,875 (GRCm39) |
A306V |
probably benign |
Het |
| Acvr1c |
T |
A |
2: 58,173,518 (GRCm39) |
N248I |
probably damaging |
Het |
| Adgrv1 |
C |
T |
13: 81,587,560 (GRCm39) |
R4537Q |
probably damaging |
Het |
| Adrb3 |
A |
C |
8: 27,717,798 (GRCm39) |
M217R |
probably damaging |
Het |
| Afg3l1 |
T |
C |
8: 124,216,532 (GRCm39) |
V257A |
probably benign |
Het |
| Agbl1 |
C |
A |
7: 76,071,904 (GRCm39) |
Q334K |
probably benign |
Het |
| Aox4 |
A |
T |
1: 58,275,835 (GRCm39) |
D389V |
probably benign |
Het |
| Apob |
A |
T |
12: 8,058,898 (GRCm39) |
Q2427L |
probably damaging |
Het |
| Asxl3 |
T |
C |
18: 22,649,765 (GRCm39) |
C585R |
probably damaging |
Het |
| Baz2a |
G |
A |
10: 127,951,995 (GRCm39) |
G571D |
probably damaging |
Het |
| Baz2b |
A |
T |
2: 59,792,368 (GRCm39) |
S587T |
probably benign |
Het |
| Bicdl2 |
T |
C |
17: 23,880,795 (GRCm39) |
L14P |
unknown |
Het |
| Cachd1 |
G |
A |
4: 100,851,935 (GRCm39) |
S1177N |
probably damaging |
Het |
| Cacna2d3 |
A |
G |
14: 29,015,135 (GRCm39) |
F86L |
possibly damaging |
Het |
| Ccdc192 |
C |
T |
18: 57,697,041 (GRCm39) |
T65I |
possibly damaging |
Het |
| Cd3d |
A |
T |
9: 44,896,296 (GRCm39) |
E28D |
probably damaging |
Het |
| Cmya5 |
T |
C |
13: 93,229,880 (GRCm39) |
K1736R |
possibly damaging |
Het |
| Col12a1 |
A |
G |
9: 79,512,456 (GRCm39) |
V2913A |
probably damaging |
Het |
| Cops8 |
A |
G |
1: 90,538,724 (GRCm39) |
D51G |
probably damaging |
Het |
| Csgalnact1 |
T |
C |
8: 68,913,623 (GRCm39) |
E194G |
probably benign |
Het |
| Csn1s1 |
A |
G |
5: 87,828,737 (GRCm39) |
D267G |
possibly damaging |
Het |
| Cyp2c40 |
T |
C |
19: 39,795,663 (GRCm39) |
N172S |
probably benign |
Het |
| Dhtkd1 |
T |
A |
2: 5,908,813 (GRCm39) |
K760N |
probably damaging |
Het |
| Dnah17 |
T |
C |
11: 118,007,939 (GRCm39) |
K691E |
probably benign |
Het |
| Dppa4 |
G |
A |
16: 48,113,334 (GRCm39) |
R189Q |
probably benign |
Het |
| Dsp |
G |
A |
13: 38,381,678 (GRCm39) |
D2808N |
possibly damaging |
Het |
| Egr2 |
A |
G |
10: 67,375,605 (GRCm39) |
E17G |
probably damaging |
Het |
| Ehmt1 |
G |
T |
2: 24,767,509 (GRCm39) |
P135T |
probably damaging |
Het |
| Epas1 |
A |
G |
17: 87,116,882 (GRCm39) |
N184S |
probably damaging |
Het |
| Ezh2 |
C |
T |
6: 47,517,684 (GRCm39) |
C584Y |
probably damaging |
Het |
| F10 |
T |
C |
8: 13,105,698 (GRCm39) |
V421A |
probably damaging |
Het |
| Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
| Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
| Fam234b |
T |
C |
6: 135,186,193 (GRCm39) |
V67A |
probably benign |
Het |
| Fbn2 |
T |
C |
18: 58,172,412 (GRCm39) |
D2131G |
probably damaging |
Het |
| Fgfr4 |
T |
C |
13: 55,307,828 (GRCm39) |
Y271H |
probably damaging |
Het |
| Gnmt |
A |
T |
17: 47,036,860 (GRCm39) |
S250T |
probably benign |
Het |
| Golgb1 |
C |
A |
16: 36,711,819 (GRCm39) |
Q208K |
possibly damaging |
Het |
| Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
| Grwd1 |
T |
C |
7: 45,475,298 (GRCm39) |
T415A |
probably benign |
Het |
| Gsk3b |
G |
A |
16: 38,060,882 (GRCm39) |
R418H |
probably damaging |
Het |
| Hap1 |
T |
G |
11: 100,242,357 (GRCm39) |
M382L |
probably benign |
Het |
| Hspa12b |
A |
G |
2: 130,981,428 (GRCm39) |
E221G |
possibly damaging |
Het |
| Hspa4l |
T |
A |
3: 40,741,179 (GRCm39) |
D709E |
possibly damaging |
Het |
| Il17ra |
A |
G |
6: 120,458,514 (GRCm39) |
E555G |
possibly damaging |
Het |
| Il27ra |
T |
C |
8: 84,760,688 (GRCm39) |
T426A |
possibly damaging |
Het |
| Jup |
T |
C |
11: 100,273,941 (GRCm39) |
D200G |
probably benign |
Het |
| Kcnq1 |
T |
C |
7: 142,748,083 (GRCm39) |
|
probably null |
Het |
| Kctd9 |
C |
T |
14: 67,966,805 (GRCm39) |
T106I |
probably damaging |
Het |
| Kmt5b |
T |
A |
19: 3,852,240 (GRCm39) |
H159Q |
probably damaging |
Het |
| Kprp |
C |
T |
3: 92,731,829 (GRCm39) |
R407Q |
unknown |
Het |
| Kras |
T |
C |
6: 145,177,879 (GRCm39) |
Q131R |
probably benign |
Het |
| Krt16 |
T |
A |
11: 100,138,457 (GRCm39) |
R230S |
probably damaging |
Het |
| Lpar6 |
G |
A |
14: 73,476,147 (GRCm39) |
C36Y |
probably damaging |
Het |
| Lrp10 |
T |
C |
14: 54,707,067 (GRCm39) |
S635P |
probably benign |
Het |
| Mapre2 |
C |
A |
18: 23,991,190 (GRCm39) |
H153N |
possibly damaging |
Het |
| Mark3 |
C |
A |
12: 111,621,762 (GRCm39) |
R703S |
probably damaging |
Het |
| Mboat2 |
A |
G |
12: 25,009,065 (GRCm39) |
D457G |
probably benign |
Het |
| Med13 |
T |
C |
11: 86,210,675 (GRCm39) |
D489G |
probably benign |
Het |
| Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
| Mtus1 |
T |
C |
8: 41,536,229 (GRCm39) |
T496A |
probably benign |
Het |
| Nckap5 |
T |
C |
1: 125,961,697 (GRCm39) |
H204R |
probably benign |
Het |
| Nlrc4 |
G |
T |
17: 74,753,712 (GRCm39) |
P224T |
possibly damaging |
Het |
| Oprl1 |
T |
A |
2: 181,360,403 (GRCm39) |
I153N |
probably damaging |
Het |
| Or13a27 |
A |
T |
7: 139,925,236 (GRCm39) |
I222N |
probably damaging |
Het |
| Or4c116 |
A |
T |
2: 88,942,140 (GRCm39) |
|
probably null |
Het |
| Or5an1 |
T |
C |
19: 12,260,670 (GRCm39) |
L86P |
possibly damaging |
Het |
| Or5b121 |
T |
A |
19: 13,507,442 (GRCm39) |
M135K |
probably damaging |
Het |
| Otud4 |
G |
A |
8: 80,382,318 (GRCm39) |
V176I |
probably damaging |
Het |
| Pcdhb5 |
T |
C |
18: 37,453,943 (GRCm39) |
F108L |
probably benign |
Het |
| Pde8b |
T |
C |
13: 95,223,250 (GRCm39) |
I335V |
probably benign |
Het |
| Pdzd7 |
T |
A |
19: 45,016,868 (GRCm39) |
I886L |
possibly damaging |
Het |
| Prune2 |
C |
T |
19: 16,980,995 (GRCm39) |
P51S |
probably damaging |
Het |
| Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
| Pwwp3a |
T |
C |
10: 80,068,702 (GRCm39) |
L282P |
probably benign |
Het |
| Rab27b |
T |
C |
18: 70,122,659 (GRCm39) |
D100G |
probably damaging |
Het |
| Rpf1 |
A |
G |
3: 146,212,293 (GRCm39) |
L349S |
probably damaging |
Het |
| Samd14 |
T |
C |
11: 94,912,409 (GRCm39) |
S233P |
probably damaging |
Het |
| Sema6a |
C |
A |
18: 47,433,195 (GRCm39) |
V79F |
probably damaging |
Het |
| Setbp1 |
A |
G |
18: 78,900,697 (GRCm39) |
I990T |
probably damaging |
Het |
| Setx |
A |
G |
2: 29,070,093 (GRCm39) |
R2633G |
probably benign |
Het |
| Siae |
T |
G |
9: 37,557,816 (GRCm39) |
I541S |
possibly damaging |
Het |
| Slc13a1 |
A |
G |
6: 24,103,428 (GRCm39) |
S372P |
possibly damaging |
Het |
| Smarcc2 |
T |
C |
10: 128,297,342 (GRCm39) |
|
probably null |
Het |
| Snrpf |
T |
C |
10: 93,423,985 (GRCm39) |
S2G |
probably benign |
Het |
| Speer2 |
C |
A |
16: 69,655,708 (GRCm39) |
K39N |
probably null |
Het |
| Spink5 |
T |
G |
18: 44,119,490 (GRCm39) |
F267C |
probably damaging |
Het |
| Tgfbrap1 |
G |
T |
1: 43,114,666 (GRCm39) |
R145S |
probably damaging |
Het |
| Tmem161b |
C |
A |
13: 84,442,887 (GRCm39) |
T269K |
possibly damaging |
Het |
| Tmem64 |
T |
C |
4: 15,281,119 (GRCm39) |
I304T |
probably damaging |
Het |
| Tomm7 |
A |
G |
5: 24,049,004 (GRCm39) |
I23T |
probably benign |
Het |
| Top6bl |
T |
A |
19: 4,708,449 (GRCm39) |
S194C |
probably damaging |
Het |
| Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
| Ttr |
C |
T |
18: 20,803,167 (GRCm39) |
A111V |
possibly damaging |
Het |
| Usp47 |
T |
A |
7: 111,683,089 (GRCm39) |
Y561N |
probably damaging |
Het |
| Vmn1r17 |
A |
G |
6: 57,337,828 (GRCm39) |
V130A |
probably benign |
Het |
| Wdr45b |
A |
G |
11: 121,219,621 (GRCm39) |
I309T |
probably benign |
Het |
| Wnt6 |
T |
C |
1: 74,823,755 (GRCm39) |
L364P |
probably damaging |
Het |
| Zc3h13 |
T |
C |
14: 75,573,449 (GRCm39) |
L1530P |
probably damaging |
Het |
| Zfp933 |
A |
G |
4: 147,911,321 (GRCm39) |
W60R |
probably benign |
Het |
|
| Other mutations in Fam186a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00588:Fam186a
|
APN |
15 |
99,825,572 (GRCm39) |
splice site |
probably benign |
|
|
IGL03047:Fam186a
|
UTSW |
15 |
99,843,589 (GRCm39) |
missense |
unknown |
|
|
R0172:Fam186a
|
UTSW |
15 |
99,852,768 (GRCm39) |
missense |
unknown |
|
|
R0194:Fam186a
|
UTSW |
15 |
99,839,644 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0381:Fam186a
|
UTSW |
15 |
99,840,055 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0799:Fam186a
|
UTSW |
15 |
99,839,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1295:Fam186a
|
UTSW |
15 |
99,837,670 (GRCm39) |
splice site |
probably benign |
|
|
R1366:Fam186a
|
UTSW |
15 |
99,841,270 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1519:Fam186a
|
UTSW |
15 |
99,845,536 (GRCm39) |
missense |
unknown |
|
|
R1592:Fam186a
|
UTSW |
15 |
99,838,199 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1636:Fam186a
|
UTSW |
15 |
99,839,539 (GRCm39) |
missense |
unknown |
|
|
R1719:Fam186a
|
UTSW |
15 |
99,840,227 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R1759:Fam186a
|
UTSW |
15 |
99,864,762 (GRCm39) |
nonsense |
probably null |
|
|
R1856:Fam186a
|
UTSW |
15 |
99,838,183 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R2131:Fam186a
|
UTSW |
15 |
99,831,557 (GRCm39) |
unclassified |
probably benign |
|
|
R2192:Fam186a
|
UTSW |
15 |
99,838,192 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R2239:Fam186a
|
UTSW |
15 |
99,852,745 (GRCm39) |
missense |
unknown |
|
|
R2251:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2902:Fam186a
|
UTSW |
15 |
99,843,049 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R3037:Fam186a
|
UTSW |
15 |
99,841,675 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3744:Fam186a
|
UTSW |
15 |
99,845,416 (GRCm39) |
missense |
unknown |
|
|
R4021:Fam186a
|
UTSW |
15 |
99,839,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4183:Fam186a
|
UTSW |
15 |
99,831,566 (GRCm39) |
unclassified |
probably benign |
|
|
R4238:Fam186a
|
UTSW |
15 |
99,841,523 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4667:Fam186a
|
UTSW |
15 |
99,842,413 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4817:Fam186a
|
UTSW |
15 |
99,831,419 (GRCm39) |
unclassified |
probably benign |
|
|
R4835:Fam186a
|
UTSW |
15 |
99,843,689 (GRCm39) |
missense |
unknown |
|
|
R4837:Fam186a
|
UTSW |
15 |
99,838,678 (GRCm39) |
missense |
unknown |
|
|
R4897:Fam186a
|
UTSW |
15 |
99,843,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4902:Fam186a
|
UTSW |
15 |
99,844,723 (GRCm39) |
missense |
unknown |
|
|
R4950:Fam186a
|
UTSW |
15 |
99,839,534 (GRCm39) |
missense |
unknown |
|
|
R4995:Fam186a
|
UTSW |
15 |
99,842,980 (GRCm39) |
missense |
probably benign |
0.27 |
|
R5062:Fam186a
|
UTSW |
15 |
99,842,527 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5124:Fam186a
|
UTSW |
15 |
99,840,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5424:Fam186a
|
UTSW |
15 |
99,843,644 (GRCm39) |
missense |
unknown |
|
|
R5624:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5628:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5637:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5639:Fam186a
|
UTSW |
15 |
99,844,931 (GRCm39) |
missense |
unknown |
|
|
R5652:Fam186a
|
UTSW |
15 |
99,843,253 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R5673:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5799:Fam186a
|
UTSW |
15 |
99,864,705 (GRCm39) |
nonsense |
probably null |
|
|
R5965:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.37 |
|
R6044:Fam186a
|
UTSW |
15 |
99,839,878 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6077:Fam186a
|
UTSW |
15 |
99,840,584 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R6120:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6185:Fam186a
|
UTSW |
15 |
99,845,530 (GRCm39) |
missense |
unknown |
|
|
R6186:Fam186a
|
UTSW |
15 |
99,845,206 (GRCm39) |
missense |
unknown |
|
|
R6242:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
|
R6351:Fam186a
|
UTSW |
15 |
99,839,623 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6368:Fam186a
|
UTSW |
15 |
99,841,198 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6369:Fam186a
|
UTSW |
15 |
99,845,212 (GRCm39) |
missense |
unknown |
|
|
R6559:Fam186a
|
UTSW |
15 |
99,842,356 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R6855:Fam186a
|
UTSW |
15 |
99,852,756 (GRCm39) |
missense |
unknown |
|
|
R6867:Fam186a
|
UTSW |
15 |
99,843,731 (GRCm39) |
missense |
unknown |
|
|
R6957:Fam186a
|
UTSW |
15 |
99,844,357 (GRCm39) |
missense |
unknown |
|
|
R6961:Fam186a
|
UTSW |
15 |
99,838,082 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6994:Fam186a
|
UTSW |
15 |
99,840,347 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6996:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
|
R7062:Fam186a
|
UTSW |
15 |
99,831,521 (GRCm39) |
unclassified |
probably benign |
|
|
R7064:Fam186a
|
UTSW |
15 |
99,839,557 (GRCm39) |
missense |
unknown |
|
|
R7173:Fam186a
|
UTSW |
15 |
99,843,531 (GRCm39) |
missense |
unknown |
|
|
R7244:Fam186a
|
UTSW |
15 |
99,844,273 (GRCm39) |
missense |
unknown |
|
|
R7270:Fam186a
|
UTSW |
15 |
99,842,033 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7410:Fam186a
|
UTSW |
15 |
99,844,826 (GRCm39) |
nonsense |
probably null |
|
|
R7437:Fam186a
|
UTSW |
15 |
99,840,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7475:Fam186a
|
UTSW |
15 |
99,845,395 (GRCm39) |
missense |
unknown |
|
|
R7487:Fam186a
|
UTSW |
15 |
99,840,017 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7526:Fam186a
|
UTSW |
15 |
99,839,796 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7650:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
|
R7658:Fam186a
|
UTSW |
15 |
99,837,725 (GRCm39) |
missense |
unknown |
|
|
R7663:Fam186a
|
UTSW |
15 |
99,842,950 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7703:Fam186a
|
UTSW |
15 |
99,852,678 (GRCm39) |
missense |
unknown |
|
|
R7814:Fam186a
|
UTSW |
15 |
99,842,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7958:Fam186a
|
UTSW |
15 |
99,841,189 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7970:Fam186a
|
UTSW |
15 |
99,831,467 (GRCm39) |
missense |
unknown |
|
|
R8076:Fam186a
|
UTSW |
15 |
99,841,351 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8087:Fam186a
|
UTSW |
15 |
99,839,725 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8130:Fam186a
|
UTSW |
15 |
99,841,914 (GRCm39) |
frame shift |
probably null |
|
|
R8239:Fam186a
|
UTSW |
15 |
99,839,191 (GRCm39) |
missense |
unknown |
|
|
R8246:Fam186a
|
UTSW |
15 |
99,838,428 (GRCm39) |
missense |
unknown |
|
|
R8446:Fam186a
|
UTSW |
15 |
99,845,335 (GRCm39) |
missense |
unknown |
|
|
R8469:Fam186a
|
UTSW |
15 |
99,845,186 (GRCm39) |
missense |
unknown |
|
|
R8676:Fam186a
|
UTSW |
15 |
99,845,023 (GRCm39) |
missense |
unknown |
|
|
R8790:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R8808:Fam186a
|
UTSW |
15 |
99,842,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8848:Fam186a
|
UTSW |
15 |
99,838,034 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9083:Fam186a
|
UTSW |
15 |
99,843,079 (GRCm39) |
missense |
probably benign |
0.27 |
|
R9106:Fam186a
|
UTSW |
15 |
99,844,107 (GRCm39) |
small deletion |
probably benign |
|
|
R9116:Fam186a
|
UTSW |
15 |
99,840,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9156:Fam186a
|
UTSW |
15 |
99,841,159 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R9227:Fam186a
|
UTSW |
15 |
99,853,384 (GRCm39) |
missense |
unknown |
|
|
R9250:Fam186a
|
UTSW |
15 |
99,845,330 (GRCm39) |
missense |
unknown |
|
|
R9282:Fam186a
|
UTSW |
15 |
99,839,879 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9495:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
|
R9514:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
|
R9521:Fam186a
|
UTSW |
15 |
99,841,471 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9553:Fam186a
|
UTSW |
15 |
99,844,561 (GRCm39) |
missense |
unknown |
|
|
R9641:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9655:Fam186a
|
UTSW |
15 |
99,840,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9661:Fam186a
|
UTSW |
15 |
99,842,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9673:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9762:Fam186a
|
UTSW |
15 |
99,842,393 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
X0021:Fam186a
|
UTSW |
15 |
99,843,316 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1088:Fam186a
|
UTSW |
15 |
99,843,875 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TAAATGCCTCGAGTTTGTTTCC -3'
(R):5'- ACAAGACTTGCCTGGGTCAG -3'
Sequencing Primer
(F):5'- GAGTTTGTTTCCCTCCCACAG -3'
(R):5'- GCCTGGGTCAGCTTTATATTAAC -3'
|
| Posted On |
2016-06-21 |
Incidental Mutation