Incidental Mutation 'R4908:Ahnak2'
| ID |
379233 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ahnak2
|
| Ensembl Gene |
ENSMUSG00000072812 |
| Gene Name |
AHNAK nucleoprotein 2 |
| Synonyms |
LOC382643 |
| MMRRC Submission |
042510-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.075)
|
| Stock # |
R4908 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
112738631-112766278 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 112741706 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 789
(T789A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000122404
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000101010]
[ENSMUST00000128258]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000101010
|
| SMART Domains |
Protein: ENSMUSP00000098572
Gene: ENSMUSG00000072812
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
14 |
N/A |
INTRINSIC |
|
low complexity region
|
364 |
375 |
N/A |
INTRINSIC |
|
low complexity region
|
545 |
564 |
N/A |
INTRINSIC |
|
low complexity region
|
717 |
733 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000128258
AA Change: T789A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000122404
Gene: ENSMUSG00000072812
AA Change: T789A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
66 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
67 |
251 |
2.35e-83 |
PROSPERO |
|
low complexity region
|
285 |
308 |
N/A |
INTRINSIC |
|
low complexity region
|
371 |
389 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
413 |
597 |
2.35e-83 |
PROSPERO |
|
low complexity region
|
734 |
756 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
820 |
N/A |
INTRINSIC |
|
low complexity region
|
1170 |
1181 |
N/A |
INTRINSIC |
|
low complexity region
|
1351 |
1370 |
N/A |
INTRINSIC |
|
low complexity region
|
1523 |
1539 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000137195
|
| SMART Domains |
Protein: ENSMUSP00000116582
Gene: ENSMUSG00000072812
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
2 |
521 |
3.81e-221 |
PROSPERO |
|
low complexity region
|
557 |
569 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
606 |
1126 |
3.81e-221 |
PROSPERO |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 92.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 99 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110059G10Rik |
T |
A |
9: 122,778,008 (GRCm39) |
I79L |
probably benign |
Het |
| Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
| Acaa1a |
G |
A |
9: 119,177,772 (GRCm39) |
S218N |
probably benign |
Het |
| Acsm5 |
A |
T |
7: 119,137,314 (GRCm39) |
I377F |
probably damaging |
Het |
| Ak9 |
A |
T |
10: 41,296,678 (GRCm39) |
T1475S |
unknown |
Het |
| AU040320 |
A |
T |
4: 126,747,081 (GRCm39) |
N1028Y |
probably damaging |
Het |
| Bahcc1 |
T |
A |
11: 120,178,580 (GRCm39) |
S2380T |
probably benign |
Het |
| Cadps |
A |
G |
14: 12,536,386 (GRCm38) |
Y525H |
probably damaging |
Het |
| Casp8ap2 |
A |
G |
4: 32,639,905 (GRCm39) |
T320A |
possibly damaging |
Het |
| Ccdc138 |
A |
G |
10: 58,380,817 (GRCm39) |
N483D |
possibly damaging |
Het |
| Ccdc39 |
G |
A |
3: 33,893,242 (GRCm39) |
|
probably null |
Het |
| Cd300c2 |
T |
C |
11: 114,887,772 (GRCm39) |
N210S |
probably damaging |
Het |
| Cd84 |
A |
G |
1: 171,700,432 (GRCm39) |
D183G |
probably damaging |
Het |
| Cep95 |
C |
T |
11: 106,702,172 (GRCm39) |
P390S |
probably damaging |
Het |
| Chd9 |
A |
T |
8: 91,741,877 (GRCm39) |
H1622L |
possibly damaging |
Het |
| Cilp |
C |
A |
9: 65,185,302 (GRCm39) |
Q466K |
probably benign |
Het |
| Cinp |
T |
A |
12: 110,850,487 (GRCm39) |
T5S |
probably damaging |
Het |
| Clec4a2 |
T |
C |
6: 123,119,462 (GRCm39) |
L238S |
probably damaging |
Het |
| Cntrob |
T |
C |
11: 69,211,732 (GRCm39) |
Y164C |
probably damaging |
Het |
| Col6a3 |
A |
G |
1: 90,735,246 (GRCm39) |
L1408P |
probably damaging |
Het |
| Cul3 |
G |
A |
1: 80,258,632 (GRCm39) |
S468L |
possibly damaging |
Het |
| Dnah11 |
T |
A |
12: 118,090,618 (GRCm39) |
D1081V |
probably benign |
Het |
| Dnah2 |
C |
A |
11: 69,411,973 (GRCm39) |
V263L |
probably benign |
Het |
| Efna3 |
C |
G |
3: 89,222,805 (GRCm39) |
R185P |
probably damaging |
Het |
| F5 |
A |
T |
1: 164,039,389 (GRCm39) |
I2000F |
probably damaging |
Het |
| Fancm |
G |
A |
12: 65,141,645 (GRCm39) |
G422E |
probably benign |
Het |
| Gcnt2 |
A |
T |
13: 41,014,210 (GRCm39) |
D127V |
probably damaging |
Het |
| Gm21798 |
G |
T |
15: 64,689,618 (GRCm39) |
|
probably benign |
Het |
| Gramd1a |
A |
C |
7: 30,838,292 (GRCm39) |
S320R |
probably benign |
Het |
| Grn |
T |
C |
11: 102,327,344 (GRCm39) |
|
probably benign |
Het |
| Helq |
A |
T |
5: 100,910,507 (GRCm39) |
|
probably null |
Het |
| Herc2 |
A |
G |
7: 55,827,660 (GRCm39) |
I2914V |
probably benign |
Het |
| Hnrnph1 |
T |
C |
11: 50,269,237 (GRCm39) |
V27A |
probably damaging |
Het |
| Hs1bp3 |
G |
T |
12: 8,374,007 (GRCm39) |
G182C |
probably damaging |
Het |
| Idnk |
C |
T |
13: 58,311,267 (GRCm39) |
P78L |
probably benign |
Het |
| Il10ra |
T |
C |
9: 45,166,919 (GRCm39) |
D544G |
probably benign |
Het |
| Inpp5e |
T |
C |
2: 26,290,918 (GRCm39) |
D383G |
probably damaging |
Het |
| Jak1 |
A |
T |
4: 101,036,911 (GRCm39) |
V243D |
probably damaging |
Het |
| Kcnma1 |
A |
T |
14: 23,359,220 (GRCm39) |
S1036T |
probably damaging |
Het |
| Kif26a |
G |
A |
12: 112,123,776 (GRCm39) |
C127Y |
probably damaging |
Het |
| Kif2c |
T |
C |
4: 117,023,608 (GRCm39) |
E368G |
probably damaging |
Het |
| Lasp1 |
T |
A |
11: 97,724,530 (GRCm39) |
|
probably null |
Het |
| Lcor |
T |
A |
19: 41,572,601 (GRCm39) |
V452D |
probably benign |
Het |
| Lrrtm1 |
C |
G |
6: 77,221,661 (GRCm39) |
H373D |
probably benign |
Het |
| Matr3 |
T |
A |
18: 35,705,754 (GRCm39) |
D226E |
probably damaging |
Het |
| Mmp17 |
G |
A |
5: 129,682,730 (GRCm39) |
W456* |
probably null |
Het |
| Mpp4 |
T |
C |
1: 59,164,748 (GRCm39) |
E463G |
probably damaging |
Het |
| Myh6 |
A |
C |
14: 55,194,419 (GRCm39) |
F737V |
probably damaging |
Het |
| Nars2 |
T |
A |
7: 96,672,948 (GRCm39) |
D271E |
probably benign |
Het |
| Nav2 |
A |
G |
7: 49,254,258 (GRCm39) |
E2352G |
probably damaging |
Het |
| Nckap1 |
A |
G |
2: 80,353,718 (GRCm39) |
|
probably null |
Het |
| Nckap5 |
A |
T |
1: 125,955,324 (GRCm39) |
S477R |
probably damaging |
Het |
| Nek11 |
T |
G |
9: 105,175,488 (GRCm39) |
I319L |
probably benign |
Het |
| Neto2 |
A |
G |
8: 86,396,393 (GRCm39) |
I84T |
probably damaging |
Het |
| Nlrp9a |
A |
T |
7: 26,250,369 (GRCm39) |
I45F |
probably damaging |
Het |
| Numa1 |
G |
A |
7: 101,662,012 (GRCm39) |
R548H |
probably damaging |
Het |
| Or10a5 |
A |
C |
7: 106,635,364 (GRCm39) |
M1L |
probably benign |
Het |
| Or14c39 |
A |
C |
7: 86,344,395 (GRCm39) |
I244L |
probably benign |
Het |
| Or2ag1b |
A |
T |
7: 106,288,740 (GRCm39) |
L66H |
probably damaging |
Het |
| Or4c10 |
A |
T |
2: 89,760,923 (GRCm39) |
M257L |
probably benign |
Het |
| Or4c100 |
T |
A |
2: 88,356,254 (GRCm39) |
I109N |
probably damaging |
Het |
| Or4k36 |
T |
A |
2: 111,146,574 (GRCm39) |
F250Y |
probably benign |
Het |
| Or7g25 |
A |
G |
9: 19,160,149 (GRCm39) |
V182A |
probably benign |
Het |
| Or9m1 |
A |
T |
2: 87,733,533 (GRCm39) |
N162K |
probably damaging |
Het |
| Pcdhb16 |
T |
A |
18: 37,612,894 (GRCm39) |
|
probably null |
Het |
| Pdcd10 |
T |
C |
3: 75,448,553 (GRCm39) |
T4A |
probably damaging |
Het |
| Pgc |
A |
T |
17: 48,039,819 (GRCm39) |
Y71F |
probably damaging |
Het |
| Phlpp1 |
G |
A |
1: 106,317,481 (GRCm39) |
G1234E |
probably damaging |
Het |
| Prr27 |
T |
C |
5: 87,990,888 (GRCm39) |
F167L |
probably benign |
Het |
| Prrc2b |
T |
A |
2: 32,116,330 (GRCm39) |
S1421T |
possibly damaging |
Het |
| Pxmp2 |
A |
G |
5: 110,431,518 (GRCm39) |
V75A |
probably benign |
Het |
| Pygl |
A |
T |
12: 70,243,807 (GRCm39) |
M545K |
probably null |
Het |
| Ranbp9 |
A |
G |
13: 43,574,733 (GRCm39) |
Y412H |
possibly damaging |
Het |
| Rcc1 |
A |
G |
4: 132,065,064 (GRCm39) |
V140A |
probably damaging |
Het |
| Reln |
A |
G |
5: 22,184,718 (GRCm39) |
V1599A |
probably benign |
Het |
| Rhebl1 |
A |
T |
15: 98,776,903 (GRCm39) |
D122E |
probably damaging |
Het |
| Rock2 |
C |
T |
12: 17,009,492 (GRCm39) |
L676F |
probably benign |
Het |
| Scn9a |
A |
T |
2: 66,357,087 (GRCm39) |
D1062E |
probably benign |
Het |
| Sec63 |
T |
C |
10: 42,681,186 (GRCm39) |
I390T |
probably damaging |
Het |
| Slc10a6 |
T |
C |
5: 103,754,493 (GRCm39) |
E346G |
probably benign |
Het |
| Slc12a3 |
G |
A |
8: 95,075,216 (GRCm39) |
V737M |
possibly damaging |
Het |
| Slc12a8 |
T |
C |
16: 33,426,629 (GRCm39) |
|
probably null |
Het |
| Slc25a38 |
T |
A |
9: 119,949,354 (GRCm39) |
I102N |
probably damaging |
Het |
| Spg7 |
T |
A |
8: 123,807,394 (GRCm39) |
V390E |
probably damaging |
Het |
| Tbc1d20 |
T |
C |
2: 152,144,228 (GRCm39) |
V75A |
probably benign |
Het |
| Tesk1 |
T |
A |
4: 43,445,555 (GRCm39) |
C243* |
probably null |
Het |
| Ttk |
T |
A |
9: 83,725,739 (GRCm39) |
N220K |
possibly damaging |
Het |
| Ttll5 |
A |
G |
12: 85,965,948 (GRCm39) |
E651G |
probably benign |
Het |
| Tubd1 |
T |
C |
11: 86,457,879 (GRCm39) |
Y426H |
probably damaging |
Het |
| Uba6 |
T |
C |
5: 86,288,293 (GRCm39) |
|
silent |
Het |
| Ube2ql1 |
G |
A |
13: 69,852,289 (GRCm39) |
R263W |
probably damaging |
Het |
| Vmn2r117 |
C |
T |
17: 23,678,812 (GRCm39) |
G804D |
probably damaging |
Het |
| Vmn2r25 |
C |
T |
6: 123,805,406 (GRCm39) |
E484K |
probably benign |
Het |
| Vmn2r4 |
T |
A |
3: 64,296,476 (GRCm39) |
I770F |
possibly damaging |
Het |
| Vmn2r82 |
G |
A |
10: 79,214,589 (GRCm39) |
V191M |
probably benign |
Het |
| Zbtb45 |
C |
T |
7: 12,742,037 (GRCm39) |
V74M |
probably damaging |
Het |
| Zfp366 |
T |
C |
13: 99,370,609 (GRCm39) |
V443A |
possibly damaging |
Het |
| Zfyve1 |
A |
T |
12: 83,598,345 (GRCm39) |
C628S |
probably damaging |
Het |
| Zfyve26 |
A |
T |
12: 79,296,469 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Ahnak2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02257:Ahnak2
|
APN |
12 |
112,748,905 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL02994:Ahnak2
|
APN |
12 |
112,749,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|
PIT4480001:Ahnak2
|
UTSW |
12 |
112,740,358 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
PIT4810001:Ahnak2
|
UTSW |
12 |
112,749,214 (GRCm39) |
missense |
|
|
|
R0025:Ahnak2
|
UTSW |
12 |
112,749,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0025:Ahnak2
|
UTSW |
12 |
112,749,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0038:Ahnak2
|
UTSW |
12 |
112,740,896 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0125:Ahnak2
|
UTSW |
12 |
112,748,776 (GRCm39) |
missense |
probably benign |
0.41 |
|
R1173:Ahnak2
|
UTSW |
12 |
112,749,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1494:Ahnak2
|
UTSW |
12 |
112,751,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1712:Ahnak2
|
UTSW |
12 |
112,748,998 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1888:Ahnak2
|
UTSW |
12 |
112,740,325 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1888:Ahnak2
|
UTSW |
12 |
112,740,325 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R2042:Ahnak2
|
UTSW |
12 |
112,749,439 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2056:Ahnak2
|
UTSW |
12 |
112,748,626 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2417:Ahnak2
|
UTSW |
12 |
112,741,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2762:Ahnak2
|
UTSW |
12 |
112,748,984 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3618:Ahnak2
|
UTSW |
12 |
112,749,842 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3706:Ahnak2
|
UTSW |
12 |
112,740,085 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R3739:Ahnak2
|
UTSW |
12 |
112,740,992 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3950:Ahnak2
|
UTSW |
12 |
112,749,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4485:Ahnak2
|
UTSW |
12 |
112,745,944 (GRCm39) |
unclassified |
probably benign |
|
|
R4651:Ahnak2
|
UTSW |
12 |
112,741,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4652:Ahnak2
|
UTSW |
12 |
112,741,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4831:Ahnak2
|
UTSW |
12 |
112,742,183 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4836:Ahnak2
|
UTSW |
12 |
112,740,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4837:Ahnak2
|
UTSW |
12 |
112,749,359 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4864:Ahnak2
|
UTSW |
12 |
112,740,040 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5067:Ahnak2
|
UTSW |
12 |
112,748,936 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5146:Ahnak2
|
UTSW |
12 |
112,742,160 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5228:Ahnak2
|
UTSW |
12 |
112,741,820 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5255:Ahnak2
|
UTSW |
12 |
112,739,812 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5323:Ahnak2
|
UTSW |
12 |
112,745,989 (GRCm39) |
unclassified |
probably benign |
|
|
R5523:Ahnak2
|
UTSW |
12 |
112,741,642 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5733:Ahnak2
|
UTSW |
12 |
112,742,100 (GRCm39) |
nonsense |
probably null |
|
|
R5799:Ahnak2
|
UTSW |
12 |
112,745,365 (GRCm39) |
unclassified |
probably benign |
|
|
R5817:Ahnak2
|
UTSW |
12 |
112,740,437 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5835:Ahnak2
|
UTSW |
12 |
112,742,230 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6083:Ahnak2
|
UTSW |
12 |
112,746,589 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6083:Ahnak2
|
UTSW |
12 |
112,746,715 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6167:Ahnak2
|
UTSW |
12 |
112,747,750 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6168:Ahnak2
|
UTSW |
12 |
112,747,750 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6405:Ahnak2
|
UTSW |
12 |
112,739,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6460:Ahnak2
|
UTSW |
12 |
112,750,610 (GRCm39) |
missense |
probably null |
0.27 |
|
R6495:Ahnak2
|
UTSW |
12 |
112,740,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6544:Ahnak2
|
UTSW |
12 |
112,746,829 (GRCm39) |
unclassified |
probably benign |
|
|
R6656:Ahnak2
|
UTSW |
12 |
112,748,991 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6679:Ahnak2
|
UTSW |
12 |
112,739,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6723:Ahnak2
|
UTSW |
12 |
112,745,228 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6774:Ahnak2
|
UTSW |
12 |
112,740,172 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6884:Ahnak2
|
UTSW |
12 |
112,741,863 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6906:Ahnak2
|
UTSW |
12 |
112,748,933 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6919:Ahnak2
|
UTSW |
12 |
112,741,118 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R7036:Ahnak2
|
UTSW |
12 |
112,745,216 (GRCm39) |
unclassified |
probably benign |
|
|
R7037:Ahnak2
|
UTSW |
12 |
112,740,712 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7064:Ahnak2
|
UTSW |
12 |
112,746,919 (GRCm39) |
unclassified |
probably benign |
|
|
R7072:Ahnak2
|
UTSW |
12 |
112,751,786 (GRCm39) |
missense |
|
|
|
R7112:Ahnak2
|
UTSW |
12 |
112,747,747 (GRCm39) |
missense |
|
|
|
R7268:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7269:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7270:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7271:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7444:Ahnak2
|
UTSW |
12 |
112,745,831 (GRCm39) |
missense |
|
|
|
R7448:Ahnak2
|
UTSW |
12 |
112,746,605 (GRCm39) |
missense |
|
|
|
R7488:Ahnak2
|
UTSW |
12 |
112,748,641 (GRCm39) |
missense |
|
|
|
R7508:Ahnak2
|
UTSW |
12 |
112,740,839 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7560:Ahnak2
|
UTSW |
12 |
112,745,851 (GRCm39) |
missense |
|
|
|
R7611:Ahnak2
|
UTSW |
12 |
112,751,749 (GRCm39) |
missense |
|
|
|
R7743:Ahnak2
|
UTSW |
12 |
112,748,383 (GRCm39) |
missense |
not run |
|
|
R7762:Ahnak2
|
UTSW |
12 |
112,742,114 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7780:Ahnak2
|
UTSW |
12 |
112,746,716 (GRCm39) |
missense |
|
|
|
R7930:Ahnak2
|
UTSW |
12 |
112,745,560 (GRCm39) |
missense |
|
|
|
R7985:Ahnak2
|
UTSW |
12 |
112,745,398 (GRCm39) |
missense |
|
|
|
R8114:Ahnak2
|
UTSW |
12 |
112,741,163 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8122:Ahnak2
|
UTSW |
12 |
112,742,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8240:Ahnak2
|
UTSW |
12 |
112,741,082 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8289:Ahnak2
|
UTSW |
12 |
112,742,242 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8315:Ahnak2
|
UTSW |
12 |
112,745,756 (GRCm39) |
missense |
|
|
|
R8430:Ahnak2
|
UTSW |
12 |
112,741,121 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8476:Ahnak2
|
UTSW |
12 |
112,747,100 (GRCm39) |
unclassified |
probably benign |
|
|
R8712:Ahnak2
|
UTSW |
12 |
112,750,709 (GRCm39) |
missense |
|
|
|
R8712:Ahnak2
|
UTSW |
12 |
112,749,872 (GRCm39) |
missense |
|
|
|
R8778:Ahnak2
|
UTSW |
12 |
112,783,158 (GRCm38) |
missense |
|
|
|
R8830:Ahnak2
|
UTSW |
12 |
112,750,656 (GRCm39) |
missense |
|
|
|
R9014:Ahnak2
|
UTSW |
12 |
112,740,170 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9055:Ahnak2
|
UTSW |
12 |
112,741,019 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9327:Ahnak2
|
UTSW |
12 |
112,748,446 (GRCm39) |
missense |
|
|
|
R9386:Ahnak2
|
UTSW |
12 |
112,745,428 (GRCm39) |
missense |
|
|
|
R9445:Ahnak2
|
UTSW |
12 |
112,745,978 (GRCm39) |
missense |
|
|
|
R9462:Ahnak2
|
UTSW |
12 |
112,750,655 (GRCm39) |
missense |
|
|
|
R9559:Ahnak2
|
UTSW |
12 |
112,749,782 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9571:Ahnak2
|
UTSW |
12 |
112,742,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9589:Ahnak2
|
UTSW |
12 |
112,746,831 (GRCm39) |
missense |
|
|
|
R9664:Ahnak2
|
UTSW |
12 |
112,741,363 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9711:Ahnak2
|
UTSW |
12 |
112,739,468 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
Z1177:Ahnak2
|
UTSW |
12 |
112,745,822 (GRCm39) |
missense |
|
|
|
| Predicted Primers |
PCR Primer
(F):5'- AACCTTTATCTTGGGTAGTGCCAG -3'
(R):5'- TCACACCCTGTCTGGTTCAG -3'
Sequencing Primer
(F):5'- CCAGTCTTGGCATGGAAAAGCTC -3'
(R):5'- GGTTCAGTAGTCCCTCAGGTC -3'
|
| Posted On |
2016-04-15 |
Incidental Mutation