Incidental Mutation 'R7036:Ahnak2'
| ID |
546709 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ahnak2
|
| Ensembl Gene |
ENSMUSG00000072812 |
| Gene Name |
AHNAK nucleoprotein 2 |
| Synonyms |
LOC382643 |
| MMRRC Submission |
045012-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
R7036 (G1)
|
| Quality Score |
214.009 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
112738631-112766278 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
A to G
at 112745216 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000122404
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000101010]
[ENSMUST00000124526]
[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: ENSMUST00000124526
|
| SMART Domains |
Protein: ENSMUSP00000114522
Gene: ENSMUSG00000072812
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
73 |
94 |
N/A |
INTRINSIC |
|
PDZ
|
118 |
190 |
6e-4 |
SMART |
|
low complexity region
|
268 |
281 |
N/A |
INTRINSIC |
|
low complexity region
|
300 |
319 |
N/A |
INTRINSIC |
|
low complexity region
|
405 |
429 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
465 |
898 |
2.74e-235 |
PROSPERO |
|
low complexity region
|
905 |
923 |
N/A |
INTRINSIC |
|
low complexity region
|
990 |
1013 |
N/A |
INTRINSIC |
|
low complexity region
|
1076 |
1092 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1145 |
1588 |
2.74e-235 |
PROSPERO |
|
low complexity region
|
1590 |
1632 |
N/A |
INTRINSIC |
|
low complexity region
|
1639 |
1700 |
N/A |
INTRINSIC |
|
low complexity region
|
1709 |
1736 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000128258
|
| SMART Domains |
Protein: ENSMUSP00000122404
Gene: ENSMUSG00000072812
| 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 |
|
| SMART Domains |
Protein: ENSMUSP00000116582
Gene: ENSMUSG00000072812
AA Change: S744P
| 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: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700017N19Rik |
T |
A |
10: 100,445,118 (GRCm39) |
|
probably null |
Het |
| Akt2 |
T |
C |
7: 27,336,437 (GRCm39) |
|
probably null |
Het |
| Aldh1a7 |
A |
T |
19: 20,685,542 (GRCm39) |
L336Q |
possibly damaging |
Het |
| Ank2 |
T |
C |
3: 126,740,041 (GRCm39) |
|
probably benign |
Het |
| Ank3 |
C |
T |
10: 69,835,209 (GRCm39) |
T680M |
probably damaging |
Het |
| Apeh |
T |
C |
9: 107,971,470 (GRCm39) |
E59G |
possibly damaging |
Het |
| Arl8a |
G |
C |
1: 135,082,206 (GRCm39) |
E145Q |
probably benign |
Het |
| Armc8 |
C |
T |
9: 99,366,018 (GRCm39) |
|
probably null |
Het |
| Armh3 |
A |
G |
19: 45,953,688 (GRCm39) |
I195T |
probably damaging |
Het |
| Arsj |
T |
C |
3: 126,158,649 (GRCm39) |
L76P |
probably damaging |
Het |
| Atp2b1 |
C |
T |
10: 98,823,172 (GRCm39) |
T244I |
probably damaging |
Het |
| Bcl6 |
A |
T |
16: 23,793,611 (GRCm39) |
L112Q |
probably damaging |
Het |
| Bfsp1 |
T |
A |
2: 143,668,843 (GRCm39) |
T579S |
possibly damaging |
Het |
| Btaf1 |
C |
A |
19: 36,981,869 (GRCm39) |
T1633K |
probably benign |
Het |
| Cacng8 |
A |
G |
7: 3,463,819 (GRCm39) |
S324G |
probably benign |
Het |
| Cd2ap |
A |
T |
17: 43,109,490 (GRCm39) |
L623Q |
probably damaging |
Het |
| Cerkl |
T |
C |
2: 79,171,722 (GRCm39) |
I379V |
probably benign |
Het |
| Cndp2 |
T |
A |
18: 84,688,070 (GRCm39) |
H307L |
possibly damaging |
Het |
| Derl1 |
A |
G |
15: 57,742,443 (GRCm39) |
|
probably null |
Het |
| Dixdc1 |
T |
A |
9: 50,593,864 (GRCm39) |
R254S |
probably benign |
Het |
| Dop1b |
T |
A |
16: 93,574,378 (GRCm39) |
D30E |
probably benign |
Het |
| Duox2 |
T |
G |
2: 122,110,934 (GRCm39) |
H1513P |
probably damaging |
Het |
| Dyrk1a |
G |
A |
16: 94,487,427 (GRCm39) |
V546I |
probably benign |
Het |
| E130308A19Rik |
A |
C |
4: 59,719,991 (GRCm39) |
K508Q |
probably damaging |
Het |
| Emc8 |
A |
T |
8: 121,385,790 (GRCm39) |
V108E |
probably benign |
Het |
| Epb41l1 |
A |
G |
2: 156,371,322 (GRCm39) |
T720A |
probably benign |
Het |
| Fcgr4 |
T |
A |
1: 170,847,657 (GRCm39) |
M85K |
probably benign |
Het |
| Fem1b |
T |
A |
9: 62,704,310 (GRCm39) |
I317F |
probably damaging |
Het |
| Focad |
A |
G |
4: 88,042,874 (GRCm39) |
E36G |
probably benign |
Het |
| Fryl |
C |
T |
5: 73,212,951 (GRCm39) |
E2275K |
probably benign |
Het |
| Galnt11 |
T |
C |
5: 25,463,811 (GRCm39) |
I361T |
probably damaging |
Het |
| Garin3 |
G |
A |
11: 46,298,235 (GRCm39) |
S513N |
|
Het |
| Gatad2a |
A |
T |
8: 70,370,644 (GRCm39) |
N114K |
probably damaging |
Het |
| Gcnt2 |
CTAATG |
C |
13: 41,041,032 (GRCm39) |
|
probably null |
Het |
| Gramd1a |
A |
G |
7: 30,832,181 (GRCm39) |
|
probably null |
Het |
| Gsn |
T |
A |
2: 35,182,611 (GRCm39) |
W187R |
probably damaging |
Het |
| Hoxc12 |
G |
A |
15: 102,846,795 (GRCm39) |
G229D |
probably damaging |
Het |
| Hycc2 |
T |
A |
1: 58,574,696 (GRCm39) |
M282L |
probably benign |
Het |
| Ints14 |
T |
C |
9: 64,871,827 (GRCm39) |
V55A |
probably benign |
Het |
| Itga9 |
T |
C |
9: 118,527,433 (GRCm39) |
L528P |
probably benign |
Het |
| Klf1 |
C |
T |
8: 85,629,379 (GRCm39) |
S68F |
possibly damaging |
Het |
| Kmt2e |
A |
G |
5: 23,683,741 (GRCm39) |
E333G |
probably null |
Het |
| Krt39 |
A |
C |
11: 99,412,062 (GRCm39) |
V8G |
probably benign |
Het |
| Krt71 |
A |
G |
15: 101,646,772 (GRCm39) |
I312T |
probably benign |
Het |
| Lrp1b |
T |
C |
2: 41,002,354 (GRCm39) |
D2001G |
possibly damaging |
Het |
| Lrrc37 |
T |
A |
11: 103,506,638 (GRCm39) |
|
probably benign |
Het |
| Lrrc71 |
T |
C |
3: 87,655,693 (GRCm39) |
T27A |
probably benign |
Het |
| Lrrcc1 |
T |
C |
3: 14,628,069 (GRCm39) |
V958A |
possibly damaging |
Het |
| Med15 |
A |
T |
16: 17,516,019 (GRCm39) |
M1K |
probably null |
Het |
| Mrgpra3 |
G |
T |
7: 47,239,838 (GRCm39) |
N29K |
possibly damaging |
Het |
| Myl1 |
T |
C |
1: 66,969,395 (GRCm39) |
N79S |
probably damaging |
Het |
| Naip2 |
A |
T |
13: 100,291,529 (GRCm39) |
D1136E |
probably benign |
Het |
| Nat10 |
T |
C |
2: 103,584,453 (GRCm39) |
N108S |
probably benign |
Het |
| Ncald |
A |
T |
15: 37,369,122 (GRCm39) |
S178T |
probably benign |
Het |
| Ndufs2 |
T |
C |
1: 171,065,877 (GRCm39) |
D256G |
probably benign |
Het |
| Nek5 |
T |
C |
8: 22,597,739 (GRCm39) |
N280S |
probably benign |
Het |
| Or5ak25 |
A |
G |
2: 85,268,774 (GRCm39) |
S243P |
probably damaging |
Het |
| Or5d39 |
T |
A |
2: 87,979,469 (GRCm39) |
D298V |
probably damaging |
Het |
| Parp1 |
G |
T |
1: 180,425,817 (GRCm39) |
K849N |
possibly damaging |
Het |
| Pcdhb4 |
T |
A |
18: 37,441,835 (GRCm39) |
C382S |
possibly damaging |
Het |
| Plce1 |
A |
G |
19: 38,727,801 (GRCm39) |
N1520S |
probably damaging |
Het |
| Plcg2 |
G |
A |
8: 118,323,045 (GRCm39) |
R700H |
probably benign |
Het |
| Popdc2 |
A |
T |
16: 38,183,173 (GRCm39) |
Y52F |
probably damaging |
Het |
| Prrx1 |
T |
A |
1: 163,075,907 (GRCm39) |
M220L |
probably benign |
Het |
| Pspc1 |
A |
C |
14: 56,996,085 (GRCm39) |
|
probably null |
Het |
| Ptchd1 |
T |
A |
X: 154,357,708 (GRCm39) |
Y499F |
probably damaging |
Het |
| Ptpn20 |
A |
G |
14: 33,336,392 (GRCm39) |
*44W |
probably null |
Het |
| Qars1 |
T |
A |
9: 108,391,976 (GRCm39) |
V83E |
probably damaging |
Het |
| Rrh |
T |
C |
3: 129,609,342 (GRCm39) |
E55G |
possibly damaging |
Het |
| Sash1 |
C |
A |
10: 8,605,847 (GRCm39) |
E848* |
probably null |
Het |
| Sds |
A |
T |
5: 120,618,912 (GRCm39) |
K125M |
possibly damaging |
Het |
| Serpinf2 |
A |
T |
11: 75,329,244 (GRCm39) |
|
probably benign |
Het |
| Sh2b2 |
G |
A |
5: 136,247,739 (GRCm39) |
T604I |
probably benign |
Het |
| Smug1 |
A |
G |
15: 103,064,369 (GRCm39) |
L184P |
probably damaging |
Het |
| Spatc1 |
A |
G |
15: 76,168,080 (GRCm39) |
T180A |
probably benign |
Het |
| Ssr1 |
A |
T |
13: 38,178,001 (GRCm39) |
L20Q |
probably null |
Het |
| Supt4a |
A |
G |
11: 87,634,084 (GRCm39) |
E100G |
probably damaging |
Het |
| Tbx1 |
G |
T |
16: 18,405,551 (GRCm39) |
P38T |
unknown |
Het |
| Tcl1 |
T |
C |
12: 105,183,860 (GRCm39) |
|
probably benign |
Het |
| Teddm2 |
T |
C |
1: 153,726,320 (GRCm39) |
I132V |
probably benign |
Het |
| Tmem131 |
C |
T |
1: 36,832,054 (GRCm39) |
G1861E |
possibly damaging |
Het |
| Tpr |
A |
T |
1: 150,299,358 (GRCm39) |
H1186L |
probably benign |
Het |
| Trim34b |
A |
T |
7: 103,978,743 (GRCm39) |
|
probably benign |
Het |
| Trpm2 |
T |
C |
10: 77,748,426 (GRCm39) |
M1415V |
probably benign |
Het |
| Ttll12 |
A |
G |
15: 83,471,086 (GRCm39) |
F264S |
probably benign |
Het |
| Vmn2r59 |
T |
C |
7: 41,695,644 (GRCm39) |
E256G |
probably benign |
Het |
| Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
| Vps35l |
T |
C |
7: 118,372,315 (GRCm39) |
S290P |
probably damaging |
Het |
| Wdr70 |
T |
C |
15: 7,913,855 (GRCm39) |
D598G |
possibly damaging |
Het |
| Ybey |
T |
C |
10: 76,304,197 (GRCm39) |
S2G |
possibly damaging |
Het |
| Zfp346 |
A |
T |
13: 55,280,200 (GRCm39) |
Q308L |
probably benign |
Het |
| Zfp872 |
C |
T |
9: 22,111,856 (GRCm39) |
P445L |
probably benign |
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 |
|
R4908:Ahnak2
|
UTSW |
12 |
112,741,706 (GRCm39) |
missense |
probably benign |
0.00 |
|
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 |
|
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'- TGAACTTGCTGTCTTTGGCC -3'
(R):5'- TCAAGATGCCCAAGGTGGAC -3'
Sequencing Primer
(F):5'- GTCCACCTTGGGCATCTTGAG -3'
(R):5'- ACCTGAAGGGCCCCAAAGTG -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation