Incidental Mutation 'R1997:Abca17'
| ID |
224462 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Abca17
|
| Ensembl Gene |
ENSMUSG00000035435 |
| Gene Name |
ATP-binding cassette, sub-family A member 17 |
| Synonyms |
|
| MMRRC Submission |
040007-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1997 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
24483233-24570042 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 24504700 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 1233
(I1233T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112538
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039324]
[ENSMUST00000121226]
|
| AlphaFold |
E9PX95 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000039324
AA Change: I1233T
PolyPhen 2
Score 0.024 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000046218
Gene: ENSMUSG00000035435
AA Change: I1233T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
18 |
N/A |
INTRINSIC |
|
transmembrane domain
|
22 |
44 |
N/A |
INTRINSIC |
|
Pfam:ABC2_membrane_3
|
252 |
464 |
9.5e-17 |
PFAM |
|
AAA
|
547 |
729 |
5.71e-12 |
SMART |
|
low complexity region
|
846 |
857 |
N/A |
INTRINSIC |
|
Pfam:ABC2_membrane_3
|
905 |
1307 |
6.7e-35 |
PFAM |
|
low complexity region
|
1337 |
1351 |
N/A |
INTRINSIC |
|
AAA
|
1393 |
1577 |
1.15e-1 |
SMART |
|
low complexity region
|
1697 |
1730 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000121226
AA Change: I1233T
PolyPhen 2
Score 0.024 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000112538
Gene: ENSMUSG00000035435
AA Change: I1233T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
18 |
N/A |
INTRINSIC |
|
Pfam:ABC2_membrane_3
|
21 |
464 |
1.2e-15 |
PFAM |
|
AAA
|
547 |
729 |
5.71e-12 |
SMART |
|
low complexity region
|
846 |
857 |
N/A |
INTRINSIC |
|
Pfam:ABC2_membrane_3
|
905 |
1307 |
1.1e-32 |
PFAM |
|
low complexity region
|
1337 |
1351 |
N/A |
INTRINSIC |
|
AAA
|
1393 |
1577 |
1.15e-1 |
SMART |
|
low complexity region
|
1697 |
1730 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.4%
- 20x: 92.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 100 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3425401B19Rik |
A |
G |
14: 32,382,005 (GRCm39) |
F1320S |
possibly damaging |
Het |
| Aaas |
C |
T |
15: 102,248,494 (GRCm39) |
V241I |
probably benign |
Het |
| Acin1 |
T |
C |
14: 54,884,156 (GRCm39) |
|
probably null |
Het |
| Acly |
A |
T |
11: 100,409,977 (GRCm39) |
I185N |
probably damaging |
Het |
| Adamts16 |
T |
C |
13: 70,901,386 (GRCm39) |
D897G |
probably benign |
Het |
| Allc |
A |
C |
12: 28,613,482 (GRCm39) |
D153E |
probably benign |
Het |
| Ankrd12 |
A |
G |
17: 66,291,879 (GRCm39) |
S1185P |
probably damaging |
Het |
| Aoc1l2 |
A |
T |
6: 48,909,363 (GRCm39) |
Q536L |
probably damaging |
Het |
| Ap1g2 |
T |
C |
14: 55,339,835 (GRCm39) |
E448G |
probably benign |
Het |
| Atg9a |
A |
T |
1: 75,166,270 (GRCm39) |
V50D |
probably benign |
Het |
| Bace2 |
A |
T |
16: 97,216,289 (GRCm39) |
D294V |
possibly damaging |
Het |
| Camsap2 |
T |
C |
1: 136,199,283 (GRCm39) |
K708E |
probably damaging |
Het |
| Card10 |
G |
A |
15: 78,678,175 (GRCm39) |
R358C |
probably damaging |
Het |
| Ccdc81 |
A |
T |
7: 89,547,271 (GRCm39) |
V39E |
probably damaging |
Het |
| Cdh20 |
A |
T |
1: 109,976,668 (GRCm39) |
D111V |
probably damaging |
Het |
| Cercam |
C |
A |
2: 29,762,935 (GRCm39) |
T223K |
probably benign |
Het |
| Cimip2a |
T |
G |
2: 25,110,217 (GRCm39) |
L43R |
probably damaging |
Het |
| Cog5 |
A |
G |
12: 31,710,848 (GRCm39) |
H76R |
possibly damaging |
Het |
| Col28a1 |
A |
T |
6: 7,999,644 (GRCm39) |
N1024K |
probably benign |
Het |
| Csrnp3 |
A |
T |
2: 65,779,446 (GRCm39) |
N41Y |
probably damaging |
Het |
| Cyp2t4 |
G |
A |
7: 26,857,038 (GRCm39) |
|
probably null |
Het |
| Dbn1 |
T |
C |
13: 55,630,254 (GRCm39) |
H38R |
probably damaging |
Het |
| Dclre1b |
A |
G |
3: 103,710,672 (GRCm39) |
V287A |
probably benign |
Het |
| Dennd4c |
A |
G |
4: 86,755,634 (GRCm39) |
T1609A |
probably benign |
Het |
| Depdc5 |
T |
A |
5: 33,059,250 (GRCm39) |
|
probably null |
Het |
| Dhcr7 |
T |
G |
7: 143,401,167 (GRCm39) |
D446E |
probably damaging |
Het |
| Dlx5 |
A |
T |
6: 6,879,680 (GRCm39) |
M129K |
possibly damaging |
Het |
| Dnah11 |
C |
G |
12: 118,046,203 (GRCm39) |
G1745A |
possibly damaging |
Het |
| Dnm3 |
T |
C |
1: 162,181,281 (GRCm39) |
T133A |
possibly damaging |
Het |
| Eif3e |
A |
G |
15: 43,129,005 (GRCm39) |
L205P |
probably damaging |
Het |
| Fam91a1 |
A |
G |
15: 58,296,044 (GRCm39) |
|
probably null |
Het |
| Fank1 |
C |
T |
7: 133,463,954 (GRCm39) |
T50I |
probably damaging |
Het |
| Fhod3 |
A |
G |
18: 25,223,473 (GRCm39) |
T940A |
possibly damaging |
Het |
| Fkbp10 |
T |
C |
11: 100,306,841 (GRCm39) |
F78L |
probably damaging |
Het |
| Gabbr2 |
A |
C |
4: 46,787,502 (GRCm39) |
F387C |
probably damaging |
Het |
| Ggnbp2 |
A |
T |
11: 84,751,387 (GRCm39) |
L138I |
probably damaging |
Het |
| Gm2832 |
T |
A |
14: 41,002,943 (GRCm39) |
|
probably null |
Het |
| Gm5084 |
T |
A |
13: 60,360,344 (GRCm39) |
|
noncoding transcript |
Het |
| Gm9979 |
T |
C |
13: 40,859,228 (GRCm39) |
|
noncoding transcript |
Het |
| Hepacam2 |
A |
G |
6: 3,487,241 (GRCm39) |
S39P |
probably damaging |
Het |
| Hesx1 |
A |
T |
14: 26,723,340 (GRCm39) |
N57Y |
probably damaging |
Het |
| Kcnh1 |
G |
A |
1: 191,959,243 (GRCm39) |
V266I |
probably damaging |
Het |
| Kif24 |
T |
C |
4: 41,392,904 (GRCm39) |
T1168A |
possibly damaging |
Het |
| Kng2 |
A |
T |
16: 22,843,626 (GRCm39) |
F118I |
possibly damaging |
Het |
| Lig3 |
C |
T |
11: 82,678,492 (GRCm39) |
P245S |
probably benign |
Het |
| Loxhd1 |
G |
T |
18: 77,383,465 (GRCm39) |
W121C |
probably damaging |
Het |
| Ltn1 |
A |
G |
16: 87,178,525 (GRCm39) |
V1568A |
probably damaging |
Het |
| Map3k4 |
A |
T |
17: 12,473,882 (GRCm39) |
|
probably null |
Het |
| Mcm10 |
C |
T |
2: 4,998,571 (GRCm39) |
V790M |
probably damaging |
Het |
| Mia3 |
A |
T |
1: 183,125,707 (GRCm39) |
F1223I |
possibly damaging |
Het |
| Mlec |
C |
A |
5: 115,288,405 (GRCm39) |
K150N |
probably damaging |
Het |
| Morn4 |
T |
C |
19: 42,064,977 (GRCm39) |
K70R |
possibly damaging |
Het |
| Mphosph10 |
A |
C |
7: 64,037,195 (GRCm39) |
|
probably null |
Het |
| Myocd |
G |
A |
11: 65,095,147 (GRCm39) |
Q47* |
probably null |
Het |
| Nav2 |
T |
A |
7: 49,198,219 (GRCm39) |
S1283T |
probably benign |
Het |
| Nbeal2 |
T |
C |
9: 110,461,266 (GRCm39) |
H1599R |
probably damaging |
Het |
| Nek10 |
G |
T |
14: 14,827,003 (GRCm38) |
G67V |
probably benign |
Het |
| Nlgn2 |
A |
C |
11: 69,718,876 (GRCm39) |
V271G |
probably damaging |
Het |
| Or1o2 |
A |
G |
17: 37,542,523 (GRCm39) |
V246A |
probably damaging |
Het |
| Or2l5 |
A |
C |
16: 19,333,792 (GRCm39) |
V198G |
probably damaging |
Het |
| Pcolce2 |
A |
T |
9: 95,576,793 (GRCm39) |
M355L |
probably benign |
Het |
| Per2 |
T |
C |
1: 91,368,581 (GRCm39) |
E264G |
probably damaging |
Het |
| Phf2 |
A |
G |
13: 48,982,384 (GRCm39) |
L113P |
unknown |
Het |
| Piwil2 |
A |
G |
14: 70,664,107 (GRCm39) |
V14A |
possibly damaging |
Het |
| Plekha6 |
G |
A |
1: 133,191,556 (GRCm39) |
A146T |
probably benign |
Het |
| Plxnb2 |
C |
T |
15: 89,042,971 (GRCm39) |
V1473I |
probably benign |
Het |
| Pms2 |
T |
C |
5: 143,850,518 (GRCm39) |
L111P |
probably damaging |
Het |
| Polg |
A |
G |
7: 79,108,979 (GRCm39) |
L533P |
probably damaging |
Het |
| Ppp1r12b |
A |
G |
1: 134,774,093 (GRCm39) |
|
probably benign |
Het |
| Ppp2r1b |
T |
A |
9: 50,778,671 (GRCm39) |
M208K |
possibly damaging |
Het |
| Prdm5 |
A |
G |
6: 65,913,072 (GRCm39) |
Y207C |
probably damaging |
Het |
| Prkar2b |
A |
G |
12: 32,013,934 (GRCm39) |
V314A |
probably damaging |
Het |
| Proser1 |
T |
A |
3: 53,386,292 (GRCm39) |
S725T |
probably benign |
Het |
| Psg20 |
A |
G |
7: 18,416,535 (GRCm39) |
F194L |
probably benign |
Het |
| Ptprz1 |
A |
G |
6: 23,050,496 (GRCm39) |
I2255V |
probably damaging |
Het |
| Sardh |
T |
G |
2: 27,134,409 (GRCm39) |
T36P |
probably damaging |
Het |
| Sec23a |
T |
A |
12: 59,048,793 (GRCm39) |
I110L |
probably benign |
Het |
| Slc22a29 |
T |
A |
19: 8,195,162 (GRCm39) |
I158L |
probably benign |
Het |
| Slc35c1 |
T |
C |
2: 92,284,984 (GRCm39) |
D210G |
probably benign |
Het |
| Syde2 |
A |
G |
3: 145,704,746 (GRCm39) |
N566S |
probably benign |
Het |
| Tcf20 |
G |
A |
15: 82,741,431 (GRCm39) |
Q7* |
probably null |
Het |
| Terb2 |
T |
A |
2: 122,035,338 (GRCm39) |
H186Q |
possibly damaging |
Het |
| Tet2 |
G |
A |
3: 133,192,350 (GRCm39) |
Q695* |
probably null |
Het |
| Tnfaip1 |
T |
C |
11: 78,420,973 (GRCm39) |
Y29C |
probably damaging |
Het |
| Traf3 |
A |
G |
12: 111,227,095 (GRCm39) |
K328E |
probably benign |
Het |
| Uaca |
A |
G |
9: 60,777,623 (GRCm39) |
E668G |
probably damaging |
Het |
| Ube2o |
T |
A |
11: 116,436,163 (GRCm39) |
E326V |
probably damaging |
Het |
| Ubr1 |
C |
T |
2: 120,776,754 (GRCm39) |
|
probably null |
Het |
| Vmn1r19 |
T |
A |
6: 57,382,033 (GRCm39) |
S195R |
probably damaging |
Het |
| Vmn1r213 |
T |
G |
13: 23,196,473 (GRCm39) |
V352G |
probably benign |
Het |
| Vmn2r19 |
T |
A |
6: 123,292,880 (GRCm39) |
D307E |
probably damaging |
Het |
| Wdfy3 |
T |
C |
5: 102,116,812 (GRCm39) |
D76G |
probably damaging |
Het |
| Zan |
A |
T |
5: 137,401,376 (GRCm39) |
C4114* |
probably null |
Het |
| Zbed6 |
A |
G |
1: 133,584,451 (GRCm39) |
L962P |
probably damaging |
Het |
| Zdhhc23 |
A |
T |
16: 43,799,305 (GRCm39) |
C37S |
probably damaging |
Het |
| Zfp628 |
G |
T |
7: 4,921,831 (GRCm39) |
G18W |
probably damaging |
Het |
| Zfp712 |
T |
A |
13: 67,190,114 (GRCm39) |
K138* |
probably null |
Het |
| Zfp867 |
A |
T |
11: 59,354,417 (GRCm39) |
V304D |
probably damaging |
Het |
| Zfp870 |
T |
C |
17: 33,103,027 (GRCm39) |
T102A |
possibly damaging |
Het |
| Zmym5 |
G |
A |
14: 57,035,210 (GRCm39) |
S286L |
possibly damaging |
Het |
|
| Other mutations in Abca17 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00402:Abca17
|
APN |
17 |
24,514,165 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL00585:Abca17
|
APN |
17 |
24,519,294 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00941:Abca17
|
APN |
17 |
24,536,104 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01987:Abca17
|
APN |
17 |
24,565,202 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01988:Abca17
|
APN |
17 |
24,553,229 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02223:Abca17
|
APN |
17 |
24,506,909 (GRCm39) |
nonsense |
probably null |
|
|
IGL02368:Abca17
|
APN |
17 |
24,506,767 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02405:Abca17
|
APN |
17 |
24,498,036 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02431:Abca17
|
APN |
17 |
24,517,958 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02607:Abca17
|
APN |
17 |
24,546,679 (GRCm39) |
nonsense |
probably null |
|
|
IGL02706:Abca17
|
APN |
17 |
24,517,966 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02729:Abca17
|
APN |
17 |
24,499,455 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02818:Abca17
|
APN |
17 |
24,519,326 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02891:Abca17
|
APN |
17 |
24,500,340 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03236:Abca17
|
APN |
17 |
24,545,450 (GRCm39) |
splice site |
probably benign |
|
|
IGL03299:Abca17
|
APN |
17 |
24,484,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
basin
|
UTSW |
17 |
24,537,159 (GRCm39) |
missense |
probably benign |
0.01 |
|
Bowl
|
UTSW |
17 |
24,536,212 (GRCm39) |
missense |
probably benign |
0.09 |
|
R0018:Abca17
|
UTSW |
17 |
24,532,162 (GRCm39) |
splice site |
probably null |
|
|
R0467:Abca17
|
UTSW |
17 |
24,532,151 (GRCm39) |
splice site |
probably benign |
|
|
R0671:Abca17
|
UTSW |
17 |
24,500,223 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1175:Abca17
|
UTSW |
17 |
24,508,325 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1397:Abca17
|
UTSW |
17 |
24,504,733 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1398:Abca17
|
UTSW |
17 |
24,547,511 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1678:Abca17
|
UTSW |
17 |
24,554,594 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1696:Abca17
|
UTSW |
17 |
24,486,632 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1781:Abca17
|
UTSW |
17 |
24,486,531 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1845:Abca17
|
UTSW |
17 |
24,486,690 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1970:Abca17
|
UTSW |
17 |
24,526,549 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2141:Abca17
|
UTSW |
17 |
24,553,240 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2199:Abca17
|
UTSW |
17 |
24,554,598 (GRCm39) |
missense |
probably benign |
0.19 |
|
R2394:Abca17
|
UTSW |
17 |
24,500,190 (GRCm39) |
splice site |
probably null |
|
|
R2442:Abca17
|
UTSW |
17 |
24,547,606 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2509:Abca17
|
UTSW |
17 |
24,508,587 (GRCm39) |
splice site |
probably benign |
|
|
R2848:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2849:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2859:Abca17
|
UTSW |
17 |
24,500,288 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R2879:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2935:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3153:Abca17
|
UTSW |
17 |
24,547,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3154:Abca17
|
UTSW |
17 |
24,547,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3434:Abca17
|
UTSW |
17 |
24,508,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3695:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3905:Abca17
|
UTSW |
17 |
24,515,257 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4282:Abca17
|
UTSW |
17 |
24,518,034 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R4334:Abca17
|
UTSW |
17 |
24,537,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4350:Abca17
|
UTSW |
17 |
24,498,020 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4548:Abca17
|
UTSW |
17 |
24,553,245 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R4626:Abca17
|
UTSW |
17 |
24,540,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4722:Abca17
|
UTSW |
17 |
24,484,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4745:Abca17
|
UTSW |
17 |
24,526,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4818:Abca17
|
UTSW |
17 |
24,536,135 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5279:Abca17
|
UTSW |
17 |
24,508,388 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5310:Abca17
|
UTSW |
17 |
24,500,204 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5320:Abca17
|
UTSW |
17 |
24,526,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5435:Abca17
|
UTSW |
17 |
24,486,588 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5622:Abca17
|
UTSW |
17 |
24,546,642 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5776:Abca17
|
UTSW |
17 |
24,514,132 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5928:Abca17
|
UTSW |
17 |
24,537,159 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6013:Abca17
|
UTSW |
17 |
24,506,820 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6035:Abca17
|
UTSW |
17 |
24,500,219 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6035:Abca17
|
UTSW |
17 |
24,500,219 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6052:Abca17
|
UTSW |
17 |
24,537,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6063:Abca17
|
UTSW |
17 |
24,483,318 (GRCm39) |
missense |
unknown |
|
|
R6404:Abca17
|
UTSW |
17 |
24,484,892 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6746:Abca17
|
UTSW |
17 |
24,565,195 (GRCm39) |
nonsense |
probably null |
|
|
R6819:Abca17
|
UTSW |
17 |
24,506,767 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6828:Abca17
|
UTSW |
17 |
24,545,389 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7043:Abca17
|
UTSW |
17 |
24,484,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7065:Abca17
|
UTSW |
17 |
24,546,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7123:Abca17
|
UTSW |
17 |
24,484,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7157:Abca17
|
UTSW |
17 |
24,554,564 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7188:Abca17
|
UTSW |
17 |
24,554,600 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7294:Abca17
|
UTSW |
17 |
24,539,983 (GRCm39) |
missense |
not run |
|
|
R7352:Abca17
|
UTSW |
17 |
24,508,028 (GRCm39) |
nonsense |
probably null |
|
|
R7355:Abca17
|
UTSW |
17 |
24,486,621 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7358:Abca17
|
UTSW |
17 |
24,510,529 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7411:Abca17
|
UTSW |
17 |
24,547,543 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R7915:Abca17
|
UTSW |
17 |
24,484,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8039:Abca17
|
UTSW |
17 |
24,547,699 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8095:Abca17
|
UTSW |
17 |
24,536,196 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R8308:Abca17
|
UTSW |
17 |
24,486,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8517:Abca17
|
UTSW |
17 |
24,536,207 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8811:Abca17
|
UTSW |
17 |
24,536,212 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8819:Abca17
|
UTSW |
17 |
24,547,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8820:Abca17
|
UTSW |
17 |
24,547,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8953:Abca17
|
UTSW |
17 |
24,518,015 (GRCm39) |
missense |
probably benign |
|
|
R9095:Abca17
|
UTSW |
17 |
24,500,370 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9313:Abca17
|
UTSW |
17 |
24,565,207 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9314:Abca17
|
UTSW |
17 |
24,547,593 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9347:Abca17
|
UTSW |
17 |
24,483,479 (GRCm39) |
missense |
probably benign |
|
|
R9351:Abca17
|
UTSW |
17 |
24,510,751 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9387:Abca17
|
UTSW |
17 |
24,553,255 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9388:Abca17
|
UTSW |
17 |
24,483,273 (GRCm39) |
missense |
unknown |
|
|
R9440:Abca17
|
UTSW |
17 |
24,499,452 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9498:Abca17
|
UTSW |
17 |
24,484,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9654:Abca17
|
UTSW |
17 |
24,536,099 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9709:Abca17
|
UTSW |
17 |
24,517,934 (GRCm39) |
missense |
probably benign |
|
|
R9770:Abca17
|
UTSW |
17 |
24,514,121 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9773:Abca17
|
UTSW |
17 |
24,508,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF024:Abca17
|
UTSW |
17 |
24,506,706 (GRCm39) |
frame shift |
probably null |
|
|
RF029:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
critical splice donor site |
probably benign |
|
|
RF032:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
frame shift |
probably null |
|
|
RF036:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
critical splice donor site |
probably benign |
|
|
X0017:Abca17
|
UTSW |
17 |
24,536,137 (GRCm39) |
missense |
probably benign |
0.26 |
|
X0065:Abca17
|
UTSW |
17 |
24,553,258 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Abca17
|
UTSW |
17 |
24,498,081 (GRCm39) |
missense |
probably benign |
0.03 |
|
Z1088:Abca17
|
UTSW |
17 |
24,498,053 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Z1088:Abca17
|
UTSW |
17 |
24,565,193 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGCCAAATCGTATTACACAAACC -3'
(R):5'- TGGATAAAGGAAGTGGCAGATCT -3'
Sequencing Primer
(F):5'- CAAGTTCTTAGCACTGCAA -3'
(R):5'- GTCAACACCAGGAGTCAGG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation