Incidental Mutation 'R1781:Abca17'
ID |
195330 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Abca17
|
Ensembl Gene |
ENSMUSG00000035435 |
Gene Name |
ATP-binding cassette, sub-family A member 17 |
Synonyms |
|
MMRRC Submission |
039812-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1781 (G1)
|
Quality Score |
208 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
24483233-24570042 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 24486531 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 1499
(T1499A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112538
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039324]
[ENSMUST00000121226]
|
AlphaFold |
E9PX95 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000039324
AA Change: T1499A
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000046218 Gene: ENSMUSG00000035435 AA Change: T1499A
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 |
possibly damaging
Transcript: ENSMUST00000121226
AA Change: T1499A
PolyPhen 2
Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000112538 Gene: ENSMUSG00000035435 AA Change: T1499A
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 |
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.7%
- 10x: 94.6%
- 20x: 90.1%
|
Validation Efficiency |
97% (88/91) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2 |
A |
G |
3: 59,932,117 (GRCm39) |
K211E |
probably damaging |
Het |
Abca13 |
T |
A |
11: 9,219,194 (GRCm39) |
L376Q |
probably damaging |
Het |
Anks6 |
A |
C |
4: 47,043,639 (GRCm39) |
N363K |
possibly damaging |
Het |
Apob |
T |
A |
12: 8,059,603 (GRCm39) |
I2695N |
possibly damaging |
Het |
Arhgef18 |
C |
T |
8: 3,430,495 (GRCm39) |
R123W |
probably damaging |
Het |
Atg14 |
T |
A |
14: 47,786,607 (GRCm39) |
|
probably null |
Het |
Atg2a |
A |
T |
19: 6,306,243 (GRCm39) |
I1368F |
probably damaging |
Het |
Btbd9 |
A |
G |
17: 30,732,567 (GRCm39) |
S373P |
probably damaging |
Het |
Ccdc83 |
T |
C |
7: 89,899,749 (GRCm39) |
E41G |
probably damaging |
Het |
Ccnh |
T |
C |
13: 85,354,254 (GRCm39) |
S233P |
possibly damaging |
Het |
Cdh8 |
T |
C |
8: 99,917,094 (GRCm39) |
|
probably null |
Het |
Cdh8 |
A |
T |
8: 100,006,290 (GRCm39) |
I99N |
probably damaging |
Het |
Cdr2 |
G |
A |
7: 120,557,268 (GRCm39) |
P419L |
probably benign |
Het |
Cds1 |
T |
A |
5: 101,960,416 (GRCm39) |
I289K |
possibly damaging |
Het |
Cherp |
G |
A |
8: 73,221,615 (GRCm39) |
T394I |
probably damaging |
Het |
Cyp4f17 |
T |
G |
17: 32,742,993 (GRCm39) |
I222S |
possibly damaging |
Het |
Dcc |
A |
G |
18: 71,511,788 (GRCm39) |
S856P |
probably benign |
Het |
Dcp1a |
C |
T |
14: 30,235,032 (GRCm39) |
T221I |
probably benign |
Het |
Ddx10 |
A |
G |
9: 53,118,845 (GRCm39) |
S475P |
probably damaging |
Het |
Dennd5b |
G |
T |
6: 148,928,896 (GRCm39) |
A759E |
probably damaging |
Het |
Disp2 |
G |
A |
2: 118,623,042 (GRCm39) |
G1258D |
probably damaging |
Het |
Fhdc1 |
A |
T |
3: 84,356,111 (GRCm39) |
D444E |
probably damaging |
Het |
Fhod1 |
T |
C |
8: 106,074,421 (GRCm39) |
|
probably benign |
Het |
Gcnt7 |
T |
C |
2: 172,296,800 (GRCm39) |
K8R |
probably benign |
Het |
Gk5 |
C |
T |
9: 96,015,508 (GRCm39) |
T108I |
possibly damaging |
Het |
Gm8214 |
C |
A |
1: 183,414,129 (GRCm39) |
|
noncoding transcript |
Het |
Gnl1 |
A |
T |
17: 36,298,638 (GRCm39) |
I434F |
probably damaging |
Het |
Golga2 |
T |
C |
2: 32,196,588 (GRCm39) |
Y986H |
probably damaging |
Het |
Gpr21 |
T |
C |
2: 37,407,550 (GRCm39) |
V32A |
probably benign |
Het |
Grb14 |
A |
T |
2: 64,805,899 (GRCm39) |
|
probably null |
Het |
H6pd |
A |
T |
4: 150,080,388 (GRCm39) |
F144L |
probably damaging |
Het |
Hunk |
A |
G |
16: 90,229,448 (GRCm39) |
Y27C |
probably damaging |
Het |
Ints7 |
C |
T |
1: 191,328,396 (GRCm39) |
T223M |
possibly damaging |
Het |
Kcnmb2 |
T |
C |
3: 32,233,152 (GRCm39) |
|
probably null |
Het |
Lilra6 |
A |
T |
7: 3,918,066 (GRCm39) |
L26H |
probably benign |
Het |
Mc4r |
A |
T |
18: 66,992,918 (GRCm39) |
V65E |
probably damaging |
Het |
Mgam |
G |
A |
6: 40,646,797 (GRCm39) |
G708R |
probably damaging |
Het |
Mllt6 |
A |
G |
11: 97,563,395 (GRCm39) |
D326G |
probably benign |
Het |
Myo7a |
A |
T |
7: 97,722,331 (GRCm39) |
V1198D |
probably damaging |
Het |
Nampt |
T |
C |
12: 32,883,037 (GRCm39) |
V74A |
probably damaging |
Het |
Nlrp4b |
G |
C |
7: 10,449,266 (GRCm39) |
V123L |
probably benign |
Het |
Ntpcr |
T |
A |
8: 126,472,141 (GRCm39) |
L150Q |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,997,163 (GRCm39) |
E1513K |
probably damaging |
Het |
Ola1 |
T |
C |
2: 72,987,099 (GRCm39) |
K178E |
possibly damaging |
Het |
Opalin |
T |
C |
19: 41,056,070 (GRCm39) |
|
probably null |
Het |
Or10g6 |
A |
G |
9: 39,934,541 (GRCm39) |
N284S |
probably damaging |
Het |
Or13a20 |
A |
T |
7: 140,232,419 (GRCm39) |
I176F |
probably damaging |
Het |
Or2ad1 |
C |
T |
13: 21,326,934 (GRCm39) |
V98I |
probably benign |
Het |
Or2w2 |
C |
T |
13: 21,757,711 (GRCm39) |
G305D |
probably damaging |
Het |
Or3a10 |
A |
T |
11: 73,935,786 (GRCm39) |
F105I |
probably damaging |
Het |
Or51ah3 |
C |
T |
7: 103,209,773 (GRCm39) |
P30S |
probably benign |
Het |
Or52ae9 |
T |
C |
7: 103,390,028 (GRCm39) |
M140V |
probably benign |
Het |
Or52e15 |
A |
T |
7: 104,645,315 (GRCm39) |
F265L |
possibly damaging |
Het |
Or5p62 |
A |
G |
7: 107,771,090 (GRCm39) |
V287A |
probably benign |
Het |
Or7a35 |
T |
C |
10: 78,853,159 (GRCm39) |
M1T |
probably null |
Het |
P2ry12 |
A |
G |
3: 59,125,199 (GRCm39) |
F159L |
probably benign |
Het |
Paqr7 |
T |
C |
4: 134,234,592 (GRCm39) |
|
probably null |
Het |
Parp1 |
T |
C |
1: 180,415,578 (GRCm39) |
S466P |
probably benign |
Het |
Parp4 |
T |
A |
14: 56,864,838 (GRCm39) |
|
probably null |
Het |
Pcdh1 |
T |
C |
18: 38,322,977 (GRCm39) |
D952G |
probably damaging |
Het |
Pde6c |
T |
C |
19: 38,140,146 (GRCm39) |
S336P |
possibly damaging |
Het |
Pgk2 |
T |
C |
17: 40,519,398 (GRCm39) |
D10G |
probably benign |
Het |
Phf20l1 |
A |
G |
15: 66,504,674 (GRCm39) |
T771A |
probably damaging |
Het |
Pkdrej |
A |
G |
15: 85,705,372 (GRCm39) |
V188A |
possibly damaging |
Het |
Plekhm1 |
A |
G |
11: 103,285,682 (GRCm39) |
L251P |
probably damaging |
Het |
Prex2 |
A |
T |
1: 11,270,179 (GRCm39) |
N1288I |
probably benign |
Het |
Sarnp |
T |
C |
10: 128,669,191 (GRCm39) |
L16P |
probably damaging |
Het |
Scgb3a2 |
T |
C |
18: 43,900,033 (GRCm39) |
|
probably benign |
Het |
Scn11a |
A |
T |
9: 119,584,148 (GRCm39) |
I1489N |
probably damaging |
Het |
Scn3a |
A |
T |
2: 65,302,729 (GRCm39) |
L1239Q |
probably damaging |
Het |
Shisa9 |
T |
C |
16: 12,085,521 (GRCm39) |
S377P |
probably benign |
Het |
Slc22a30 |
T |
A |
19: 8,313,136 (GRCm39) |
T550S |
probably damaging |
Het |
Slc25a11 |
T |
C |
11: 70,535,651 (GRCm39) |
T296A |
probably benign |
Het |
Slc35f1 |
T |
A |
10: 52,938,532 (GRCm39) |
|
probably null |
Het |
Slc6a13 |
A |
G |
6: 121,311,811 (GRCm39) |
E396G |
probably damaging |
Het |
Spata31d1c |
T |
C |
13: 65,183,985 (GRCm39) |
I509T |
probably benign |
Het |
Srsf9 |
C |
A |
5: 115,465,481 (GRCm39) |
Y9* |
probably null |
Het |
Tasor2 |
T |
C |
13: 3,634,759 (GRCm39) |
T683A |
possibly damaging |
Het |
Tbx20 |
T |
C |
9: 24,636,795 (GRCm39) |
I431V |
probably benign |
Het |
Tespa1 |
G |
A |
10: 130,184,119 (GRCm39) |
G67S |
probably benign |
Het |
Trhde |
A |
T |
10: 114,424,405 (GRCm39) |
V460E |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,708,342 (GRCm39) |
F1739I |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Umodl1 |
G |
A |
17: 31,187,524 (GRCm39) |
R196H |
probably damaging |
Het |
Vezf1 |
G |
T |
11: 87,972,447 (GRCm39) |
M269I |
probably benign |
Het |
Vmn1r35 |
A |
T |
6: 66,656,550 (GRCm39) |
M40K |
probably benign |
Het |
Vmn1r9 |
G |
T |
6: 57,048,300 (GRCm39) |
C125F |
probably benign |
Het |
Vmn2r12 |
C |
A |
5: 109,239,594 (GRCm39) |
G323V |
probably benign |
Het |
Vmn2r79 |
A |
T |
7: 86,651,555 (GRCm39) |
H318L |
probably benign |
Het |
Zfhx3 |
T |
A |
8: 109,520,167 (GRCm39) |
S430T |
probably benign |
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 |
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 |
R1997:Abca17
|
UTSW |
17 |
24,504,700 (GRCm39) |
missense |
probably benign |
0.02 |
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'- AGCTGGCACAGCTTAGCTTCCTTC -3'
(R):5'- CATACTGTCATCCCACACATGGCTC -3'
Sequencing Primer
(F):5'- CACCCCCATCTCTGTTGG -3'
(R):5'- CTGCATGAGTGTCCCTATAGTAGAC -3'
|
Posted On |
2014-05-23 |