Incidental Mutation 'R1721:Brd10'
| ID |
191514 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Brd10
|
| Ensembl Gene |
ENSMUSG00000046138 |
| Gene Name |
bromodomain containing 10 |
| Synonyms |
9930021J03Rik, Gm9832 |
| MMRRC Submission |
039753-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.138)
|
| Stock # |
R1721 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
29691802-29783389 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 29720998 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Threonine
at position 743
(S743T)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000177155]
|
| AlphaFold |
H3BKP8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000059484
AA Change: S743T
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000054060
Gene: ENSMUSG00000046138
AA Change: S743T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
66 |
N/A |
INTRINSIC |
|
BROMO
|
75 |
198 |
1.22e-3 |
SMART |
|
low complexity region
|
225 |
235 |
N/A |
INTRINSIC |
|
coiled coil region
|
248 |
289 |
N/A |
INTRINSIC |
|
low complexity region
|
347 |
365 |
N/A |
INTRINSIC |
|
low complexity region
|
495 |
508 |
N/A |
INTRINSIC |
|
coiled coil region
|
673 |
705 |
N/A |
INTRINSIC |
|
low complexity region
|
722 |
756 |
N/A |
INTRINSIC |
|
coiled coil region
|
764 |
796 |
N/A |
INTRINSIC |
|
low complexity region
|
1146 |
1160 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1164 |
1293 |
9.57e-8 |
PROSPERO |
|
low complexity region
|
1295 |
1304 |
N/A |
INTRINSIC |
|
low complexity region
|
1386 |
1415 |
N/A |
INTRINSIC |
|
low complexity region
|
1468 |
1483 |
N/A |
INTRINSIC |
|
low complexity region
|
1602 |
1624 |
N/A |
INTRINSIC |
|
low complexity region
|
1647 |
1663 |
N/A |
INTRINSIC |
|
low complexity region
|
1732 |
1745 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1766 |
1910 |
9.57e-8 |
PROSPERO |
|
low complexity region
|
1987 |
1993 |
N/A |
INTRINSIC |
|
low complexity region
|
2013 |
2027 |
N/A |
INTRINSIC |
|
low complexity region
|
2053 |
2071 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000175726
AA Change: S620T
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000175764
AA Change: S5T
|
| SMART Domains |
Protein: ENSMUSP00000135031
Gene: ENSMUSG00000046138
AA Change: S5T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
379 |
393 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
397 |
526 |
2.65e-5 |
PROSPERO |
|
low complexity region
|
528 |
537 |
N/A |
INTRINSIC |
|
low complexity region
|
619 |
648 |
N/A |
INTRINSIC |
|
low complexity region
|
701 |
716 |
N/A |
INTRINSIC |
|
low complexity region
|
835 |
857 |
N/A |
INTRINSIC |
|
low complexity region
|
880 |
896 |
N/A |
INTRINSIC |
|
low complexity region
|
965 |
978 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
999 |
1143 |
2.65e-5 |
PROSPERO |
|
low complexity region
|
1220 |
1226 |
N/A |
INTRINSIC |
|
low complexity region
|
1246 |
1260 |
N/A |
INTRINSIC |
|
low complexity region
|
1286 |
1304 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000176773
AA Change: S26T
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000177155
AA Change: S676T
PolyPhen 2
Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000135473
Gene: ENSMUSG00000046138
AA Change: S676T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
66 |
N/A |
INTRINSIC |
|
BROMO
|
75 |
198 |
1.22e-3 |
SMART |
|
low complexity region
|
205 |
219 |
N/A |
INTRINSIC |
|
low complexity region
|
280 |
298 |
N/A |
INTRINSIC |
|
low complexity region
|
428 |
441 |
N/A |
INTRINSIC |
|
coiled coil region
|
606 |
638 |
N/A |
INTRINSIC |
|
low complexity region
|
655 |
689 |
N/A |
INTRINSIC |
|
coiled coil region
|
697 |
729 |
N/A |
INTRINSIC |
|
low complexity region
|
1079 |
1093 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1097 |
1226 |
1.32e-7 |
PROSPERO |
|
low complexity region
|
1228 |
1237 |
N/A |
INTRINSIC |
|
low complexity region
|
1319 |
1348 |
N/A |
INTRINSIC |
|
low complexity region
|
1401 |
1416 |
N/A |
INTRINSIC |
|
low complexity region
|
1535 |
1557 |
N/A |
INTRINSIC |
|
low complexity region
|
1580 |
1596 |
N/A |
INTRINSIC |
|
low complexity region
|
1665 |
1678 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1699 |
1843 |
1.32e-7 |
PROSPERO |
|
low complexity region
|
1920 |
1926 |
N/A |
INTRINSIC |
|
low complexity region
|
1946 |
1960 |
N/A |
INTRINSIC |
|
low complexity region
|
1986 |
2004 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1395 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.1%
|
| Validation Efficiency |
99% (87/88) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 83 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acin1 |
A |
T |
14: 54,901,995 (GRCm39) |
V559E |
probably benign |
Het |
| Adamts20 |
A |
G |
15: 94,236,340 (GRCm39) |
F844L |
probably benign |
Het |
| Adcy5 |
C |
A |
16: 35,118,794 (GRCm39) |
D1048E |
probably damaging |
Het |
| Agrn |
A |
T |
4: 156,259,630 (GRCm39) |
C768* |
probably null |
Het |
| Aldh18a1 |
G |
T |
19: 40,553,282 (GRCm39) |
Q487K |
probably damaging |
Het |
| Aldh3b1 |
G |
A |
19: 3,971,271 (GRCm39) |
|
probably benign |
Het |
| Asb18 |
T |
G |
1: 89,896,302 (GRCm39) |
D246A |
probably benign |
Het |
| Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
| Bcl2l15 |
A |
G |
3: 103,745,914 (GRCm39) |
|
probably null |
Het |
| Cage1 |
T |
A |
13: 38,207,309 (GRCm39) |
K285* |
probably null |
Het |
| Ccn2 |
A |
C |
10: 24,472,695 (GRCm39) |
T202P |
probably damaging |
Het |
| Cldn17 |
A |
G |
16: 88,303,444 (GRCm39) |
L95P |
probably damaging |
Het |
| Cldn20 |
A |
T |
17: 3,583,157 (GRCm39) |
D110V |
probably damaging |
Het |
| Cnot10 |
T |
C |
9: 114,444,067 (GRCm39) |
T443A |
probably benign |
Het |
| Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
| Col23a1 |
T |
C |
11: 51,418,716 (GRCm39) |
Y135H |
unknown |
Het |
| Cse1l |
T |
C |
2: 166,768,331 (GRCm39) |
S210P |
probably damaging |
Het |
| Cspg4 |
T |
G |
9: 56,796,027 (GRCm39) |
V1254G |
probably damaging |
Het |
| Dip2c |
A |
G |
13: 9,709,404 (GRCm39) |
T1415A |
probably damaging |
Het |
| Epc2 |
A |
G |
2: 49,422,117 (GRCm39) |
Y337C |
probably damaging |
Het |
| Epha2 |
A |
G |
4: 141,049,963 (GRCm39) |
S799G |
probably damaging |
Het |
| Fndc10 |
A |
G |
4: 155,779,355 (GRCm39) |
Y133C |
probably damaging |
Het |
| Gli3 |
G |
T |
13: 15,900,882 (GRCm39) |
S1423I |
probably benign |
Het |
| Gm6034 |
A |
T |
17: 36,354,045 (GRCm39) |
|
probably benign |
Het |
| Gmip |
A |
G |
8: 70,263,882 (GRCm39) |
S109G |
probably damaging |
Het |
| Grik2 |
C |
A |
10: 49,399,842 (GRCm39) |
W296L |
possibly damaging |
Het |
| Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
| Il6 |
T |
A |
5: 30,218,490 (GRCm39) |
Y46N |
possibly damaging |
Het |
| Ints8 |
C |
A |
4: 11,241,684 (GRCm39) |
C253F |
probably damaging |
Het |
| Itga9 |
A |
G |
9: 118,527,374 (GRCm39) |
|
probably benign |
Het |
| Kcna7 |
T |
C |
7: 45,056,345 (GRCm39) |
V187A |
possibly damaging |
Het |
| Kdm5b |
G |
T |
1: 134,540,919 (GRCm39) |
|
probably benign |
Het |
| Knl1 |
T |
G |
2: 118,906,815 (GRCm39) |
S1635A |
probably damaging |
Het |
| Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
| Lox |
T |
G |
18: 52,653,983 (GRCm39) |
|
probably null |
Het |
| Mdc1 |
A |
G |
17: 36,158,718 (GRCm39) |
D366G |
possibly damaging |
Het |
| Meiob |
T |
C |
17: 25,053,021 (GRCm39) |
C344R |
probably damaging |
Het |
| Mier2 |
A |
G |
10: 79,384,664 (GRCm39) |
V150A |
probably damaging |
Het |
| Mon2 |
A |
T |
10: 122,867,002 (GRCm39) |
M551K |
probably damaging |
Het |
| Mrps15 |
A |
G |
4: 125,945,187 (GRCm39) |
T125A |
probably benign |
Het |
| Mtmr14 |
A |
G |
6: 113,230,693 (GRCm39) |
H99R |
probably damaging |
Het |
| Mup4 |
A |
G |
4: 59,960,598 (GRCm39) |
M1T |
probably null |
Het |
| Mup5 |
G |
A |
4: 61,750,607 (GRCm39) |
R179* |
probably null |
Het |
| Ncoa3 |
T |
G |
2: 165,911,221 (GRCm39) |
V1326G |
possibly damaging |
Het |
| Noa1 |
A |
T |
5: 77,455,428 (GRCm39) |
N429K |
probably benign |
Het |
| Nrxn1 |
C |
T |
17: 90,469,832 (GRCm39) |
A241T |
probably damaging |
Het |
| Or1p1 |
A |
T |
11: 74,180,126 (GRCm39) |
Y218F |
probably damaging |
Het |
| Or2t49 |
C |
T |
11: 58,392,765 (GRCm39) |
V206M |
probably damaging |
Het |
| Pcdh9 |
G |
A |
14: 94,125,471 (GRCm39) |
S233L |
probably damaging |
Het |
| Peg3 |
C |
A |
7: 6,712,900 (GRCm39) |
S774I |
possibly damaging |
Het |
| Phyh |
A |
G |
2: 4,942,620 (GRCm39) |
K321R |
probably null |
Het |
| Plcg1 |
T |
A |
2: 160,573,840 (GRCm39) |
M35K |
probably damaging |
Het |
| Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
| Ppargc1b |
T |
A |
18: 61,440,275 (GRCm39) |
|
probably null |
Het |
| Prcd |
A |
C |
11: 116,548,371 (GRCm39) |
S27R |
probably benign |
Het |
| Prx |
T |
A |
7: 27,216,948 (GRCm39) |
M622K |
probably benign |
Het |
| Psmd1 |
T |
A |
1: 85,999,567 (GRCm39) |
D51E |
probably damaging |
Het |
| Psmd13 |
C |
T |
7: 140,463,430 (GRCm39) |
T38I |
probably damaging |
Het |
| Ptprf |
A |
C |
4: 118,082,096 (GRCm39) |
D1047E |
possibly damaging |
Het |
| Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
| Riiad1 |
G |
A |
3: 94,380,176 (GRCm39) |
P40S |
possibly damaging |
Het |
| Rnft1 |
T |
A |
11: 86,377,096 (GRCm39) |
N53K |
probably benign |
Het |
| Scn4a |
C |
T |
11: 106,211,646 (GRCm39) |
R1457H |
probably benign |
Het |
| Sema6c |
A |
T |
3: 95,078,099 (GRCm39) |
I492F |
probably damaging |
Het |
| Shbg |
T |
C |
11: 69,505,798 (GRCm39) |
H403R |
probably damaging |
Het |
| Slc15a5 |
A |
T |
6: 138,049,845 (GRCm39) |
|
probably benign |
Het |
| Slc38a1 |
G |
A |
15: 96,485,016 (GRCm39) |
T221M |
probably damaging |
Het |
| Slc6a16 |
T |
A |
7: 44,910,600 (GRCm39) |
V375E |
possibly damaging |
Het |
| Slc6a17 |
T |
A |
3: 107,379,492 (GRCm39) |
M559L |
probably damaging |
Het |
| Slmap |
A |
G |
14: 26,181,373 (GRCm39) |
|
probably benign |
Het |
| Sorcs2 |
G |
A |
5: 36,184,092 (GRCm39) |
R965W |
probably damaging |
Het |
| St8sia4 |
C |
A |
1: 95,581,394 (GRCm39) |
R116L |
probably damaging |
Het |
| Tcaf1 |
A |
C |
6: 42,652,272 (GRCm39) |
S737A |
possibly damaging |
Het |
| Thbs2 |
T |
A |
17: 14,899,072 (GRCm39) |
Y676F |
probably benign |
Het |
| Tmod2 |
A |
G |
9: 75,493,324 (GRCm39) |
|
probably benign |
Het |
| Trim75 |
T |
C |
8: 65,435,391 (GRCm39) |
|
probably null |
Het |
| Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
| Usp54 |
A |
T |
14: 20,633,508 (GRCm39) |
Y37* |
probably null |
Het |
| Vill |
T |
C |
9: 118,895,082 (GRCm39) |
F100S |
probably damaging |
Het |
| Vstm5 |
A |
G |
9: 15,168,663 (GRCm39) |
R76G |
probably benign |
Het |
| Zfp608 |
T |
C |
18: 55,032,321 (GRCm39) |
T540A |
probably benign |
Het |
| Zfp947 |
A |
C |
17: 22,365,184 (GRCm39) |
N163K |
probably benign |
Het |
| Zfyve26 |
T |
C |
12: 79,308,573 (GRCm39) |
H228R |
possibly damaging |
Het |
|
| Other mutations in Brd10 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01311:Brd10
|
APN |
19 |
29,731,420 (GRCm39) |
missense |
probably benign |
0.33 |
|
IGL01535:Brd10
|
APN |
19 |
29,731,212 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
IGL02019:Brd10
|
APN |
19 |
29,694,463 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL02034:Brd10
|
APN |
19 |
29,694,259 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL03114:Brd10
|
APN |
19 |
29,694,532 (GRCm39) |
missense |
probably benign |
0.18 |
|
IGL03382:Brd10
|
APN |
19 |
29,694,676 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0020:Brd10
|
UTSW |
19 |
29,693,597 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0020:Brd10
|
UTSW |
19 |
29,693,597 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0142:Brd10
|
UTSW |
19 |
29,695,654 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0178:Brd10
|
UTSW |
19 |
29,732,188 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0453:Brd10
|
UTSW |
19 |
29,731,068 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0730:Brd10
|
UTSW |
19 |
29,695,381 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0735:Brd10
|
UTSW |
19 |
29,695,038 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0891:Brd10
|
UTSW |
19 |
29,695,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0894:Brd10
|
UTSW |
19 |
29,697,974 (GRCm39) |
splice site |
probably benign |
|
|
R1289:Brd10
|
UTSW |
19 |
29,700,852 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1368:Brd10
|
UTSW |
19 |
29,693,796 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1387:Brd10
|
UTSW |
19 |
29,700,853 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1483:Brd10
|
UTSW |
19 |
29,696,745 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1526:Brd10
|
UTSW |
19 |
29,712,545 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1612:Brd10
|
UTSW |
19 |
29,695,245 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1764:Brd10
|
UTSW |
19 |
29,696,560 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1822:Brd10
|
UTSW |
19 |
29,693,814 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1824:Brd10
|
UTSW |
19 |
29,693,814 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1859:Brd10
|
UTSW |
19 |
29,732,323 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1868:Brd10
|
UTSW |
19 |
29,720,998 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1880:Brd10
|
UTSW |
19 |
29,695,523 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1898:Brd10
|
UTSW |
19 |
29,712,532 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1936:Brd10
|
UTSW |
19 |
29,731,077 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R1939:Brd10
|
UTSW |
19 |
29,731,077 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R1969:Brd10
|
UTSW |
19 |
29,694,075 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2153:Brd10
|
UTSW |
19 |
29,694,229 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2366:Brd10
|
UTSW |
19 |
29,731,035 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2379:Brd10
|
UTSW |
19 |
29,696,275 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3107:Brd10
|
UTSW |
19 |
29,700,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4012:Brd10
|
UTSW |
19 |
29,720,990 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4222:Brd10
|
UTSW |
19 |
29,696,149 (GRCm39) |
missense |
probably benign |
0.18 |
|
R4328:Brd10
|
UTSW |
19 |
29,720,961 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4329:Brd10
|
UTSW |
19 |
29,720,961 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4387:Brd10
|
UTSW |
19 |
29,782,715 (GRCm39) |
unclassified |
probably benign |
|
|
R4688:Brd10
|
UTSW |
19 |
29,694,501 (GRCm39) |
missense |
probably benign |
0.33 |
|
R4796:Brd10
|
UTSW |
19 |
29,731,018 (GRCm39) |
missense |
probably benign |
0.33 |
|
R4820:Brd10
|
UTSW |
19 |
29,695,809 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R4832:Brd10
|
UTSW |
19 |
29,694,616 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R5056:Brd10
|
UTSW |
19 |
29,694,759 (GRCm39) |
missense |
probably benign |
|
|
R5150:Brd10
|
UTSW |
19 |
29,782,950 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5224:Brd10
|
UTSW |
19 |
29,696,450 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5306:Brd10
|
UTSW |
19 |
29,707,230 (GRCm39) |
intron |
probably benign |
|
|
R5460:Brd10
|
UTSW |
19 |
29,732,250 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5477:Brd10
|
UTSW |
19 |
29,731,518 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5531:Brd10
|
UTSW |
19 |
29,731,072 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5559:Brd10
|
UTSW |
19 |
29,694,363 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5647:Brd10
|
UTSW |
19 |
29,731,210 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5886:Brd10
|
UTSW |
19 |
29,696,677 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6029:Brd10
|
UTSW |
19 |
29,732,367 (GRCm39) |
unclassified |
probably benign |
|
|
R6240:Brd10
|
UTSW |
19 |
29,694,640 (GRCm39) |
missense |
probably benign |
0.18 |
|
R6331:Brd10
|
UTSW |
19 |
29,695,147 (GRCm39) |
missense |
probably benign |
0.33 |
|
R6456:Brd10
|
UTSW |
19 |
29,693,914 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6584:Brd10
|
UTSW |
19 |
29,696,128 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R6661:Brd10
|
UTSW |
19 |
29,700,864 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R6991:Brd10
|
UTSW |
19 |
29,696,508 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7059:Brd10
|
UTSW |
19 |
29,696,945 (GRCm39) |
missense |
probably benign |
0.33 |
|
R7128:Brd10
|
UTSW |
19 |
29,693,881 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7211:Brd10
|
UTSW |
19 |
29,763,712 (GRCm39) |
missense |
|
|
|
R7471:Brd10
|
UTSW |
19 |
29,707,139 (GRCm39) |
splice site |
probably null |
|
|
R7686:Brd10
|
UTSW |
19 |
29,694,870 (GRCm39) |
missense |
probably benign |
0.34 |
|
R8012:Brd10
|
UTSW |
19 |
29,695,534 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R8203:Brd10
|
UTSW |
19 |
29,693,443 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8353:Brd10
|
UTSW |
19 |
29,731,242 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8672:Brd10
|
UTSW |
19 |
29,731,564 (GRCm39) |
missense |
probably benign |
|
|
R8755:Brd10
|
UTSW |
19 |
29,693,890 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8918:Brd10
|
UTSW |
19 |
29,696,841 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8954:Brd10
|
UTSW |
19 |
29,696,126 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9038:Brd10
|
UTSW |
19 |
29,731,900 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R9195:Brd10
|
UTSW |
19 |
29,763,703 (GRCm39) |
missense |
|
|
|
R9204:Brd10
|
UTSW |
19 |
29,696,938 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9518:Brd10
|
UTSW |
19 |
29,731,541 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9743:Brd10
|
UTSW |
19 |
29,694,261 (GRCm39) |
missense |
probably benign |
|
|
R9747:Brd10
|
UTSW |
19 |
29,731,911 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
RF011:Brd10
|
UTSW |
19 |
29,721,009 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
X0027:Brd10
|
UTSW |
19 |
29,712,599 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTGAAATCCAGCCATTCTCACAAGGAA -3'
(R):5'- TGCATCACCATGAGCACTACAATCATT -3'
Sequencing Primer
(F):5'- CATTCTCACAAGGAATGGAGC -3'
(R):5'- CGGGCAGTTACAGTTTAACATTTG -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation