Incidental Mutation 'R7358:Atad5'
| ID |
571127 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Atad5
|
| Ensembl Gene |
ENSMUSG00000017550 |
| Gene Name |
ATPase family, AAA domain containing 5 |
| Synonyms |
LOC237877, C130052G03Rik |
| MMRRC Submission |
045444-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7358 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
79980226-80026620 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 80023862 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Valine
at position 1658
(A1658V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000017694
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000017694]
[ENSMUST00000050207]
[ENSMUST00000108239]
[ENSMUST00000131601]
|
| AlphaFold |
Q4QY64 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000017694
AA Change: A1658V
PolyPhen 2
Score 0.316 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000017694
Gene: ENSMUSG00000017550
AA Change: A1658V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
298 |
311 |
N/A |
INTRINSIC |
|
low complexity region
|
327 |
342 |
N/A |
INTRINSIC |
|
low complexity region
|
467 |
486 |
N/A |
INTRINSIC |
|
coiled coil region
|
665 |
697 |
N/A |
INTRINSIC |
|
low complexity region
|
798 |
807 |
N/A |
INTRINSIC |
|
AAA
|
1111 |
1347 |
5.14e-5 |
SMART |
|
Blast:AAA
|
1409 |
1526 |
1e-31 |
BLAST |
|
low complexity region
|
1573 |
1583 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000050207
|
| SMART Domains |
Protein: ENSMUSP00000059304
Gene: ENSMUSG00000046909
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:HHH_3
|
78 |
136 |
1.7e-11 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000108239
AA Change: A1655V
PolyPhen 2
Score 0.458 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000103874
Gene: ENSMUSG00000017550
AA Change: A1655V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
298 |
311 |
N/A |
INTRINSIC |
|
low complexity region
|
327 |
342 |
N/A |
INTRINSIC |
|
low complexity region
|
467 |
486 |
N/A |
INTRINSIC |
|
coiled coil region
|
665 |
697 |
N/A |
INTRINSIC |
|
low complexity region
|
798 |
807 |
N/A |
INTRINSIC |
|
AAA
|
1108 |
1344 |
5.14e-5 |
SMART |
|
Blast:AAA
|
1406 |
1523 |
1e-31 |
BLAST |
|
low complexity region
|
1570 |
1580 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000131601
|
| SMART Domains |
Protein: ENSMUSP00000114770
Gene: ENSMUSG00000046909
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:HHH_3
|
88 |
147 |
1.3e-10 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136996
|
| SMART Domains |
Protein: ENSMUSP00000122596
Gene: ENSMUSG00000046909
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
27 |
42 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a gene trap allele exhibit prenatal lethality. Mice heterozygous for a gene trap allele exhibit genomic instability, premature death, and a wide spectrum of spontaneous tumors. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca17 |
T |
A |
17: 24,510,529 (GRCm39) |
Q983L |
probably benign |
Het |
| Agtr1a |
A |
T |
13: 30,564,962 (GRCm39) |
D9V |
probably benign |
Het |
| Ahcyl |
T |
C |
16: 45,974,201 (GRCm39) |
E392G |
probably damaging |
Het |
| Ankrd13c |
T |
A |
3: 157,697,374 (GRCm39) |
Y326* |
probably null |
Het |
| Ano2 |
A |
G |
6: 125,687,696 (GRCm39) |
D67G |
probably benign |
Het |
| Arhgef5 |
G |
A |
6: 43,256,507 (GRCm39) |
R1205H |
probably damaging |
Het |
| Ascc3 |
T |
A |
10: 50,590,448 (GRCm39) |
Y1055* |
probably null |
Het |
| Atp6ap1l |
T |
C |
13: 91,031,926 (GRCm39) |
D252G |
probably damaging |
Het |
| Bdkrb2 |
T |
C |
12: 105,558,800 (GRCm39) |
V347A |
possibly damaging |
Het |
| Ccdc187 |
A |
T |
2: 26,146,007 (GRCm39) |
L1194Q |
probably damaging |
Het |
| Chd9 |
A |
C |
8: 91,710,115 (GRCm39) |
D770A |
unknown |
Het |
| Chd9 |
A |
G |
8: 91,760,846 (GRCm39) |
D2197G |
unknown |
Het |
| Clip2 |
C |
A |
5: 134,531,484 (GRCm39) |
E774* |
probably null |
Het |
| Clspn |
A |
G |
4: 126,459,993 (GRCm39) |
T407A |
probably benign |
Het |
| Col24a1 |
T |
A |
3: 144,998,926 (GRCm39) |
|
probably null |
Het |
| Cradd |
T |
A |
10: 95,158,637 (GRCm39) |
T37S |
probably damaging |
Het |
| Cspg4b |
A |
G |
13: 113,456,501 (GRCm39) |
D849G |
|
Het |
| Ctbp2 |
A |
G |
7: 132,600,610 (GRCm39) |
F70S |
probably damaging |
Het |
| D3Ertd751e |
A |
T |
3: 41,701,000 (GRCm39) |
E6D |
probably damaging |
Het |
| Dst |
T |
A |
1: 34,230,754 (GRCm39) |
F2782L |
probably benign |
Het |
| Dync2h1 |
A |
G |
9: 7,159,479 (GRCm39) |
|
probably null |
Het |
| Eif2s1 |
G |
T |
12: 78,927,969 (GRCm39) |
G215V |
probably damaging |
Het |
| Epg5 |
A |
T |
18: 78,002,252 (GRCm39) |
D557V |
possibly damaging |
Het |
| Eya4 |
C |
T |
10: 22,999,749 (GRCm39) |
|
probably null |
Het |
| Fpr1 |
C |
A |
17: 18,097,242 (GRCm39) |
R249L |
probably damaging |
Het |
| Fry |
A |
G |
5: 150,339,788 (GRCm39) |
T1520A |
probably benign |
Het |
| Gapvd1 |
C |
T |
2: 34,580,473 (GRCm39) |
|
probably null |
Het |
| Gemin4 |
A |
C |
11: 76,104,278 (GRCm39) |
L161* |
probably null |
Het |
| Gid8 |
A |
T |
2: 180,359,779 (GRCm39) |
K221I |
probably benign |
Het |
| Gm21028 |
A |
C |
7: 42,227,913 (GRCm39) |
C34G |
probably damaging |
Het |
| Greb1 |
A |
G |
12: 16,774,882 (GRCm39) |
S172P |
probably damaging |
Het |
| Herc2 |
A |
G |
7: 55,832,423 (GRCm39) |
I3040V |
possibly damaging |
Het |
| Hmcn2 |
T |
A |
2: 31,306,824 (GRCm39) |
V3190E |
probably damaging |
Het |
| Hrnr |
G |
T |
3: 93,230,448 (GRCm39) |
G229* |
probably null |
Het |
| Igfn1 |
A |
T |
1: 135,891,738 (GRCm39) |
V2259D |
probably damaging |
Het |
| Ism2 |
A |
G |
12: 87,326,814 (GRCm39) |
F375S |
probably damaging |
Het |
| Kcnk4 |
T |
A |
19: 6,903,478 (GRCm39) |
D357V |
probably damaging |
Het |
| Knl1 |
A |
G |
2: 118,901,040 (GRCm39) |
R914G |
possibly damaging |
Het |
| Mars2 |
T |
C |
1: 55,276,729 (GRCm39) |
S111P |
probably damaging |
Het |
| Mogat2 |
G |
A |
7: 98,881,673 (GRCm39) |
P88S |
possibly damaging |
Het |
| Msh2 |
T |
A |
17: 88,024,957 (GRCm39) |
S612T |
possibly damaging |
Het |
| Nvl |
A |
G |
1: 180,962,601 (GRCm39) |
L123P |
probably damaging |
Het |
| Or1j20 |
T |
C |
2: 36,759,890 (GRCm39) |
V104A |
probably benign |
Het |
| Or2d3c |
A |
T |
7: 106,526,111 (GRCm39) |
L185Q |
probably damaging |
Het |
| Or51v15-ps1 |
A |
G |
7: 103,278,390 (GRCm39) |
L259P |
unknown |
Het |
| Or5m11b |
T |
A |
2: 85,805,780 (GRCm39) |
S64R |
possibly damaging |
Het |
| Or6c202 |
T |
A |
10: 128,995,939 (GRCm39) |
I305F |
probably benign |
Het |
| Or7e174 |
A |
T |
9: 20,012,169 (GRCm39) |
Y38F |
probably damaging |
Het |
| P2rx7 |
A |
T |
5: 122,804,205 (GRCm39) |
|
probably null |
Het |
| Pard3 |
A |
T |
8: 128,319,573 (GRCm39) |
I1149L |
probably damaging |
Het |
| Pcdha8 |
T |
A |
18: 37,125,830 (GRCm39) |
I104N |
probably damaging |
Het |
| Pecr |
G |
A |
1: 72,306,624 (GRCm39) |
T219I |
probably benign |
Het |
| Pgap2 |
A |
T |
7: 101,859,774 (GRCm39) |
|
probably benign |
Het |
| Phf7 |
T |
C |
14: 30,963,745 (GRCm39) |
R76G |
probably benign |
Het |
| Pigu |
T |
C |
2: 155,141,090 (GRCm39) |
T268A |
probably damaging |
Het |
| Piwil4 |
T |
C |
9: 14,641,289 (GRCm39) |
T231A |
possibly damaging |
Het |
| Pkd1l1 |
T |
G |
11: 8,895,202 (GRCm39) |
E636A |
|
Het |
| Plscr3 |
T |
C |
11: 69,738,316 (GRCm39) |
S55P |
unknown |
Het |
| Pnlip |
T |
A |
19: 58,664,976 (GRCm39) |
I268N |
probably damaging |
Het |
| Podxl |
A |
T |
6: 31,501,929 (GRCm39) |
H343Q |
probably benign |
Het |
| Prkcd |
T |
C |
14: 30,327,793 (GRCm39) |
T213A |
probably benign |
Het |
| Prss22 |
T |
A |
17: 24,215,419 (GRCm39) |
Q119L |
probably benign |
Het |
| Psme3ip1 |
T |
C |
8: 95,302,327 (GRCm39) |
N235D |
possibly damaging |
Het |
| Ptprcap |
A |
G |
19: 4,206,238 (GRCm39) |
E107G |
possibly damaging |
Het |
| Ptprg |
A |
G |
14: 12,154,198 (GRCm38) |
T640A |
possibly damaging |
Het |
| Ptprh |
A |
T |
7: 4,554,006 (GRCm39) |
|
probably null |
Het |
| Rasa4 |
A |
G |
5: 136,124,448 (GRCm39) |
T166A |
probably benign |
Het |
| Sbf2 |
T |
C |
7: 109,998,555 (GRCm39) |
E626G |
possibly damaging |
Het |
| Scn2a |
T |
A |
2: 65,512,850 (GRCm39) |
Y203* |
probably null |
Het |
| Serpinb1a |
G |
C |
13: 33,026,981 (GRCm39) |
H320Q |
probably damaging |
Het |
| Shisa7 |
G |
A |
7: 4,832,920 (GRCm39) |
T464I |
probably benign |
Het |
| Slc47a2 |
G |
A |
11: 61,199,699 (GRCm39) |
A399V |
possibly damaging |
Het |
| Snrnp200 |
A |
G |
2: 127,063,746 (GRCm39) |
T642A |
probably benign |
Het |
| Spag16 |
A |
G |
1: 69,883,526 (GRCm39) |
H85R |
probably benign |
Het |
| Spata31h1 |
A |
G |
10: 82,127,847 (GRCm39) |
L1721S |
possibly damaging |
Het |
| Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
| Stag3 |
C |
A |
5: 138,299,770 (GRCm39) |
L894M |
probably damaging |
Het |
| Sun2 |
A |
T |
15: 79,618,313 (GRCm39) |
F284Y |
probably benign |
Het |
| Tpx2 |
T |
A |
2: 152,718,550 (GRCm39) |
N184K |
probably benign |
Het |
| Trpa1 |
A |
T |
1: 14,968,334 (GRCm39) |
N477K |
probably damaging |
Het |
| Ttbk2 |
C |
T |
2: 120,620,791 (GRCm39) |
R157H |
probably damaging |
Het |
| Ttn |
C |
T |
2: 76,537,649 (GRCm39) |
E34760K |
probably benign |
Het |
| Tysnd1 |
T |
C |
10: 61,532,427 (GRCm39) |
S360P |
probably damaging |
Het |
| Uqcc5 |
A |
G |
14: 30,846,560 (GRCm39) |
V53A |
probably damaging |
Het |
| Usp34 |
T |
A |
11: 23,311,683 (GRCm39) |
L511I |
probably damaging |
Het |
| Vmn2r71 |
A |
T |
7: 85,273,468 (GRCm39) |
T761S |
possibly damaging |
Het |
| Zdhhc18 |
G |
T |
4: 133,360,482 (GRCm39) |
C73* |
probably null |
Het |
| Zfp975 |
A |
T |
7: 42,312,215 (GRCm39) |
C133S |
probably damaging |
Het |
| Zfy1 |
T |
C |
Y: 735,141 (GRCm39) |
E214G |
unknown |
Het |
| Zmym5 |
T |
A |
14: 57,031,597 (GRCm39) |
K504* |
probably null |
Het |
|
| Other mutations in Atad5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00753:Atad5
|
APN |
11 |
80,023,684 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL00916:Atad5
|
APN |
11 |
80,009,826 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01348:Atad5
|
APN |
11 |
79,986,390 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01601:Atad5
|
APN |
11 |
79,986,343 (GRCm39) |
missense |
probably benign |
0.45 |
|
IGL01916:Atad5
|
APN |
11 |
80,003,665 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02028:Atad5
|
APN |
11 |
80,024,936 (GRCm39) |
missense |
probably benign |
0.20 |
|
IGL02095:Atad5
|
APN |
11 |
79,985,533 (GRCm39) |
missense |
probably benign |
0.24 |
|
IGL02142:Atad5
|
APN |
11 |
79,985,023 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02206:Atad5
|
APN |
11 |
79,985,009 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02385:Atad5
|
APN |
11 |
79,985,453 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02858:Atad5
|
APN |
11 |
79,980,601 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02962:Atad5
|
APN |
11 |
79,999,405 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
PIT4362001:Atad5
|
UTSW |
11 |
80,002,393 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0040:Atad5
|
UTSW |
11 |
79,988,840 (GRCm39) |
missense |
probably benign |
|
|
R0157:Atad5
|
UTSW |
11 |
79,980,643 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0211:Atad5
|
UTSW |
11 |
79,986,473 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0211:Atad5
|
UTSW |
11 |
79,986,473 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0319:Atad5
|
UTSW |
11 |
80,011,616 (GRCm39) |
splice site |
probably benign |
|
|
R0401:Atad5
|
UTSW |
11 |
80,011,525 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0426:Atad5
|
UTSW |
11 |
80,003,658 (GRCm39) |
missense |
probably benign |
0.14 |
|
R0452:Atad5
|
UTSW |
11 |
79,997,247 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0496:Atad5
|
UTSW |
11 |
79,991,182 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1691:Atad5
|
UTSW |
11 |
79,986,358 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1812:Atad5
|
UTSW |
11 |
80,023,873 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2070:Atad5
|
UTSW |
11 |
79,988,878 (GRCm39) |
splice site |
probably null |
|
|
R2071:Atad5
|
UTSW |
11 |
79,988,878 (GRCm39) |
splice site |
probably null |
|
|
R2153:Atad5
|
UTSW |
11 |
79,997,203 (GRCm39) |
missense |
probably benign |
0.04 |
|
R2415:Atad5
|
UTSW |
11 |
79,985,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3917:Atad5
|
UTSW |
11 |
79,994,120 (GRCm39) |
missense |
probably null |
0.97 |
|
R4025:Atad5
|
UTSW |
11 |
80,011,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4464:Atad5
|
UTSW |
11 |
79,991,137 (GRCm39) |
splice site |
probably null |
|
|
R4561:Atad5
|
UTSW |
11 |
79,986,715 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4579:Atad5
|
UTSW |
11 |
79,986,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4844:Atad5
|
UTSW |
11 |
80,005,137 (GRCm39) |
splice site |
probably null |
|
|
R4853:Atad5
|
UTSW |
11 |
79,986,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4873:Atad5
|
UTSW |
11 |
80,011,515 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4875:Atad5
|
UTSW |
11 |
80,011,515 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5054:Atad5
|
UTSW |
11 |
79,985,502 (GRCm39) |
missense |
probably benign |
0.10 |
|
R5226:Atad5
|
UTSW |
11 |
79,985,888 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5397:Atad5
|
UTSW |
11 |
80,002,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5449:Atad5
|
UTSW |
11 |
80,014,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5571:Atad5
|
UTSW |
11 |
80,002,382 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5575:Atad5
|
UTSW |
11 |
79,991,149 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5857:Atad5
|
UTSW |
11 |
80,022,155 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5927:Atad5
|
UTSW |
11 |
80,018,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5928:Atad5
|
UTSW |
11 |
79,985,003 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5949:Atad5
|
UTSW |
11 |
79,986,835 (GRCm39) |
nonsense |
probably null |
|
|
R6102:Atad5
|
UTSW |
11 |
80,002,398 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6254:Atad5
|
UTSW |
11 |
80,018,215 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6562:Atad5
|
UTSW |
11 |
80,024,032 (GRCm39) |
missense |
probably benign |
0.26 |
|
R6744:Atad5
|
UTSW |
11 |
80,024,858 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7092:Atad5
|
UTSW |
11 |
80,011,546 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R7202:Atad5
|
UTSW |
11 |
79,980,601 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7345:Atad5
|
UTSW |
11 |
79,986,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7352:Atad5
|
UTSW |
11 |
79,994,169 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7420:Atad5
|
UTSW |
11 |
79,986,688 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7453:Atad5
|
UTSW |
11 |
80,009,969 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7990:Atad5
|
UTSW |
11 |
80,024,079 (GRCm39) |
nonsense |
probably null |
|
|
R8012:Atad5
|
UTSW |
11 |
79,985,066 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8152:Atad5
|
UTSW |
11 |
79,985,996 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R8421:Atad5
|
UTSW |
11 |
79,985,384 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8842:Atad5
|
UTSW |
11 |
80,000,910 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R8918:Atad5
|
UTSW |
11 |
79,986,473 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8943:Atad5
|
UTSW |
11 |
79,986,524 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8944:Atad5
|
UTSW |
11 |
79,986,524 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R9134:Atad5
|
UTSW |
11 |
80,023,931 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9137:Atad5
|
UTSW |
11 |
79,986,481 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9301:Atad5
|
UTSW |
11 |
79,986,845 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9372:Atad5
|
UTSW |
11 |
79,985,094 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R9404:Atad5
|
UTSW |
11 |
80,005,064 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9443:Atad5
|
UTSW |
11 |
80,023,388 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9471:Atad5
|
UTSW |
11 |
80,023,524 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R9577:Atad5
|
UTSW |
11 |
80,004,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9656:Atad5
|
UTSW |
11 |
79,980,542 (GRCm39) |
start gained |
probably benign |
|
|
R9659:Atad5
|
UTSW |
11 |
79,980,542 (GRCm39) |
start gained |
probably benign |
|
|
R9661:Atad5
|
UTSW |
11 |
79,980,542 (GRCm39) |
start gained |
probably benign |
|
|
RF003:Atad5
|
UTSW |
11 |
80,002,386 (GRCm39) |
missense |
probably damaging |
0.99 |
|
X0024:Atad5
|
UTSW |
11 |
80,023,609 (GRCm39) |
missense |
probably benign |
0.02 |
|
Z1176:Atad5
|
UTSW |
11 |
79,985,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGGTTTCAAGCCCCACTCTG -3'
(R):5'- CATGGCGCCTTTGTGAAAC -3'
Sequencing Primer
(F):5'- TGTACCTCAGCCCCCTAAG -3'
(R):5'- GCCTTTGTGAAACACAGACTG -3'
|
| Posted On |
2019-09-13 |
Incidental Mutation