Incidental Mutation 'R1965:Crybg3'
| ID |
218320 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Crybg3
|
| Ensembl Gene |
ENSMUSG00000022723 |
| Gene Name |
beta-gamma crystallin domain containing 3 |
| Synonyms |
Gm9581 |
| MMRRC Submission |
039978-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.138)
|
| Stock # |
R1965 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
59312451-59421410 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 59323600 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 1066
(Y1066C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000037682
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044604]
[ENSMUST00000172910]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000044604
AA Change: Y1066C
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000037682
Gene: ENSMUSG00000022723
AA Change: Y1066C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
258 |
273 |
N/A |
INTRINSIC |
|
low complexity region
|
282 |
290 |
N/A |
INTRINSIC |
|
XTALbg
|
430 |
516 |
2.78e-4 |
SMART |
|
Pfam:Crystall
|
536 |
599 |
3.3e-7 |
PFAM |
|
XTALbg
|
614 |
699 |
1.2e-21 |
SMART |
|
XTALbg
|
707 |
790 |
5.73e-19 |
SMART |
|
XTALbg
|
803 |
881 |
6.87e-5 |
SMART |
|
XTALbg
|
889 |
969 |
1.28e-7 |
SMART |
|
RICIN
|
972 |
1104 |
8.16e-14 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000129762
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000172910
AA Change: Y2780C
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000179383
AA Change: Y1066C
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000137452
Gene: ENSMUSG00000022723
AA Change: Y1066C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
390 |
405 |
N/A |
INTRINSIC |
|
low complexity region
|
414 |
422 |
N/A |
INTRINSIC |
|
XTALbg
|
562 |
648 |
2.78e-4 |
SMART |
|
Pfam:Crystall
|
668 |
731 |
1e-6 |
PFAM |
|
XTALbg
|
746 |
831 |
1.2e-21 |
SMART |
|
XTALbg
|
839 |
922 |
5.73e-19 |
SMART |
|
XTALbg
|
935 |
1013 |
6.87e-5 |
SMART |
|
XTALbg
|
1021 |
1101 |
1.28e-7 |
SMART |
|
RICIN
|
1104 |
1236 |
8.16e-14 |
SMART |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000232544
AA Change: Y91C
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.6%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aco1 |
T |
G |
4: 40,175,730 (GRCm39) |
L157R |
probably damaging |
Het |
| Acot11 |
A |
T |
4: 106,606,550 (GRCm39) |
L513Q |
probably damaging |
Het |
| Amd1 |
A |
G |
10: 40,170,755 (GRCm39) |
I52T |
probably benign |
Het |
| Ap2b1 |
T |
C |
11: 83,237,721 (GRCm39) |
I557T |
probably benign |
Het |
| Arel1 |
T |
A |
12: 84,987,173 (GRCm39) |
|
probably null |
Het |
| Arg1 |
T |
A |
10: 24,792,762 (GRCm39) |
|
probably null |
Het |
| Atf1 |
A |
T |
15: 100,152,052 (GRCm39) |
M135L |
probably benign |
Het |
| Atf2 |
T |
C |
2: 73,681,242 (GRCm39) |
E77G |
possibly damaging |
Het |
| Axin1 |
G |
T |
17: 26,403,199 (GRCm39) |
A394S |
probably damaging |
Het |
| Axin1 |
A |
T |
17: 26,409,202 (GRCm39) |
Q734L |
probably damaging |
Het |
| Brd8 |
G |
C |
18: 34,735,819 (GRCm39) |
A886G |
probably damaging |
Het |
| Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
| Celf3 |
T |
C |
3: 94,392,634 (GRCm39) |
V35A |
probably damaging |
Het |
| Cfap299 |
T |
A |
5: 98,494,093 (GRCm39) |
D32E |
probably damaging |
Het |
| Ckap2 |
T |
C |
8: 22,665,803 (GRCm39) |
T415A |
possibly damaging |
Het |
| Csmd3 |
T |
C |
15: 47,713,144 (GRCm39) |
H1506R |
probably benign |
Het |
| Dnah10 |
A |
G |
5: 124,852,267 (GRCm39) |
D1808G |
probably damaging |
Het |
| Dsc3 |
C |
T |
18: 20,113,729 (GRCm39) |
G398R |
probably damaging |
Het |
| Emc2 |
A |
G |
15: 43,390,863 (GRCm39) |
Q293R |
probably damaging |
Het |
| Evc2 |
A |
G |
5: 37,520,876 (GRCm39) |
N251D |
possibly damaging |
Het |
| Fam151a |
A |
T |
4: 106,591,112 (GRCm39) |
|
probably benign |
Het |
| Fbxw16 |
T |
A |
9: 109,270,289 (GRCm39) |
I151F |
probably damaging |
Het |
| Fmnl2 |
A |
G |
2: 53,004,880 (GRCm39) |
D658G |
probably damaging |
Het |
| Fnip2 |
G |
A |
3: 79,400,779 (GRCm39) |
T314I |
probably benign |
Het |
| Foxc2 |
T |
A |
8: 121,843,413 (GRCm39) |
S20R |
probably damaging |
Het |
| Fpr-rs6 |
C |
T |
17: 20,402,918 (GRCm39) |
G148R |
probably damaging |
Het |
| Fsip2 |
T |
C |
2: 82,823,124 (GRCm39) |
S6286P |
possibly damaging |
Het |
| Fyb2 |
A |
T |
4: 104,770,846 (GRCm39) |
I54F |
probably benign |
Het |
| Gbf1 |
T |
C |
19: 46,260,003 (GRCm39) |
F999L |
probably damaging |
Het |
| Gldc |
G |
A |
19: 30,114,513 (GRCm39) |
R466* |
probably null |
Het |
| Gm12695 |
T |
A |
4: 96,651,082 (GRCm39) |
S124C |
probably benign |
Het |
| Gm4846 |
A |
T |
1: 166,314,533 (GRCm39) |
I370N |
possibly damaging |
Het |
| Gsdmc3 |
T |
C |
15: 63,730,296 (GRCm39) |
T423A |
probably damaging |
Het |
| Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
| Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
| Kcnmb3 |
T |
C |
3: 32,526,492 (GRCm39) |
Y233C |
probably damaging |
Het |
| Kidins220 |
A |
G |
12: 25,044,905 (GRCm39) |
D191G |
probably damaging |
Het |
| Kmt2a |
A |
G |
9: 44,732,757 (GRCm39) |
|
probably benign |
Het |
| Krt1 |
T |
C |
15: 101,757,427 (GRCm39) |
D261G |
probably benign |
Het |
| Lrba |
A |
G |
3: 86,513,175 (GRCm39) |
|
probably null |
Het |
| Myo1f |
C |
T |
17: 33,817,146 (GRCm39) |
R730* |
probably null |
Het |
| Ncoa7 |
C |
A |
10: 30,530,426 (GRCm39) |
E30* |
probably null |
Het |
| Neurod4 |
T |
A |
10: 130,106,918 (GRCm39) |
K119* |
probably null |
Het |
| Npy5r |
T |
C |
8: 67,133,929 (GRCm39) |
D288G |
probably benign |
Het |
| Nr3c2 |
A |
T |
8: 77,636,092 (GRCm39) |
I398L |
probably damaging |
Het |
| Or10a5 |
T |
C |
7: 106,635,565 (GRCm39) |
S68P |
probably damaging |
Het |
| Or12j4 |
C |
A |
7: 140,046,574 (GRCm39) |
F153L |
probably benign |
Het |
| Or4b1 |
T |
C |
2: 89,979,748 (GRCm39) |
S201G |
probably damaging |
Het |
| Or4k35 |
T |
C |
2: 111,099,938 (GRCm39) |
Y258C |
probably damaging |
Het |
| Or51v8 |
A |
T |
7: 103,320,103 (GRCm39) |
I45N |
probably damaging |
Het |
| Or5g25 |
T |
C |
2: 85,478,090 (GRCm39) |
T192A |
possibly damaging |
Het |
| Or5w8 |
A |
G |
2: 87,687,759 (GRCm39) |
K80R |
probably benign |
Het |
| Or9m1b |
A |
G |
2: 87,836,648 (GRCm39) |
F149S |
probably damaging |
Het |
| P3r3urf |
G |
A |
4: 116,031,376 (GRCm39) |
C82Y |
probably damaging |
Het |
| Pcf11 |
A |
T |
7: 92,310,809 (GRCm39) |
M393K |
probably benign |
Het |
| Pck2 |
T |
C |
14: 55,779,964 (GRCm39) |
V71A |
probably benign |
Het |
| Pdzd8 |
G |
T |
19: 59,288,554 (GRCm39) |
L949I |
probably benign |
Het |
| Pdzrn4 |
G |
A |
15: 92,644,190 (GRCm39) |
|
probably null |
Het |
| Phospho1 |
A |
G |
11: 95,721,705 (GRCm39) |
N125S |
probably damaging |
Het |
| Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
| Ppid |
A |
T |
3: 79,509,606 (GRCm39) |
K308* |
probably null |
Het |
| Ppp1r1b |
A |
G |
11: 98,246,189 (GRCm39) |
E57G |
probably damaging |
Het |
| Prtg |
T |
G |
9: 72,755,604 (GRCm39) |
S269A |
probably benign |
Het |
| Rbbp5 |
T |
A |
1: 132,422,035 (GRCm39) |
S312T |
probably damaging |
Het |
| Rbm11 |
T |
A |
16: 75,395,656 (GRCm39) |
|
probably null |
Het |
| Retreg1 |
A |
G |
15: 25,970,250 (GRCm39) |
T139A |
probably damaging |
Het |
| Riok3 |
T |
A |
18: 12,270,019 (GRCm39) |
H120Q |
probably damaging |
Het |
| Rln1 |
A |
T |
19: 29,311,995 (GRCm39) |
M1K |
probably null |
Het |
| Rpp30 |
C |
T |
19: 36,066,549 (GRCm39) |
S94L |
probably damaging |
Het |
| Sccpdh |
C |
T |
1: 179,511,879 (GRCm39) |
P117L |
probably damaging |
Het |
| Serac1 |
T |
C |
17: 6,099,274 (GRCm39) |
K506E |
possibly damaging |
Het |
| Serping1 |
G |
T |
2: 84,596,072 (GRCm39) |
T454K |
probably damaging |
Het |
| Slc1a2 |
T |
A |
2: 102,570,245 (GRCm39) |
N174K |
probably damaging |
Het |
| Slc2a2 |
A |
G |
3: 28,773,634 (GRCm39) |
Q313R |
probably damaging |
Het |
| Slc46a2 |
T |
A |
4: 59,914,249 (GRCm39) |
S225C |
probably damaging |
Het |
| Smarcc2 |
G |
A |
10: 128,310,627 (GRCm39) |
E419K |
probably damaging |
Het |
| Stkld1 |
T |
A |
2: 26,836,744 (GRCm39) |
|
probably null |
Het |
| Szt2 |
A |
G |
4: 118,241,162 (GRCm39) |
M1704T |
probably benign |
Het |
| Tasor |
T |
G |
14: 27,164,511 (GRCm39) |
C272W |
probably damaging |
Het |
| Tfcp2l1 |
C |
T |
1: 118,580,653 (GRCm39) |
Q116* |
probably null |
Het |
| Timm44 |
A |
G |
8: 4,310,603 (GRCm39) |
M383T |
possibly damaging |
Het |
| Tnpo2 |
G |
A |
8: 85,771,946 (GRCm39) |
|
probably null |
Het |
| Tnrc6b |
A |
G |
15: 80,764,640 (GRCm39) |
K714R |
probably damaging |
Het |
| Wdfy3 |
A |
G |
5: 102,099,178 (GRCm39) |
L290P |
probably damaging |
Het |
| Wdr59 |
A |
G |
8: 112,177,709 (GRCm39) |
F898L |
probably damaging |
Het |
| Zfp120 |
A |
T |
2: 149,959,318 (GRCm39) |
C335S |
probably damaging |
Het |
| Zfp518a |
T |
C |
19: 40,901,954 (GRCm39) |
S628P |
probably benign |
Het |
| Zfp879 |
A |
T |
11: 50,724,355 (GRCm39) |
C234S |
probably damaging |
Het |
|
| Other mutations in Crybg3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00516:Crybg3
|
APN |
16 |
59,350,803 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL01305:Crybg3
|
APN |
16 |
59,349,590 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01809:Crybg3
|
APN |
16 |
59,345,216 (GRCm39) |
critical splice donor site |
probably benign |
0.00 |
|
IGL02247:Crybg3
|
APN |
16 |
59,323,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02252:Crybg3
|
APN |
16 |
59,372,887 (GRCm39) |
splice site |
probably benign |
|
|
IGL03036:Crybg3
|
APN |
16 |
59,375,542 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
IGL03202:Crybg3
|
APN |
16 |
59,315,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03232:Crybg3
|
APN |
16 |
59,350,731 (GRCm39) |
missense |
probably damaging |
1.00 |
|
ANU22:Crybg3
|
UTSW |
16 |
59,349,590 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0052:Crybg3
|
UTSW |
16 |
59,386,019 (GRCm39) |
splice site |
probably benign |
|
|
R0335:Crybg3
|
UTSW |
16 |
59,364,503 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0691:Crybg3
|
UTSW |
16 |
59,385,574 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1511:Crybg3
|
UTSW |
16 |
59,374,475 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1579:Crybg3
|
UTSW |
16 |
59,350,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1982:Crybg3
|
UTSW |
16 |
59,364,488 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R2225:Crybg3
|
UTSW |
16 |
59,375,041 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4074:Crybg3
|
UTSW |
16 |
59,376,120 (GRCm39) |
unclassified |
probably benign |
|
|
R4210:Crybg3
|
UTSW |
16 |
59,364,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4393:Crybg3
|
UTSW |
16 |
59,380,458 (GRCm39) |
unclassified |
probably benign |
|
|
R4394:Crybg3
|
UTSW |
16 |
59,380,458 (GRCm39) |
unclassified |
probably benign |
|
|
R4397:Crybg3
|
UTSW |
16 |
59,380,458 (GRCm39) |
unclassified |
probably benign |
|
|
R4427:Crybg3
|
UTSW |
16 |
59,363,562 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4578:Crybg3
|
UTSW |
16 |
59,350,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4720:Crybg3
|
UTSW |
16 |
59,360,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4917:Crybg3
|
UTSW |
16 |
59,350,782 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5007:Crybg3
|
UTSW |
16 |
59,378,463 (GRCm39) |
unclassified |
probably benign |
|
|
R5020:Crybg3
|
UTSW |
16 |
59,375,159 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R5155:Crybg3
|
UTSW |
16 |
59,345,264 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5306:Crybg3
|
UTSW |
16 |
59,380,356 (GRCm39) |
unclassified |
probably benign |
|
|
R5342:Crybg3
|
UTSW |
16 |
59,342,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5687:Crybg3
|
UTSW |
16 |
59,379,529 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5763:Crybg3
|
UTSW |
16 |
59,374,973 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R5860:Crybg3
|
UTSW |
16 |
59,385,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5950:Crybg3
|
UTSW |
16 |
59,313,934 (GRCm39) |
unclassified |
probably benign |
|
|
R6007:Crybg3
|
UTSW |
16 |
59,374,837 (GRCm39) |
nonsense |
probably null |
|
|
R6042:Crybg3
|
UTSW |
16 |
59,370,838 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6049:Crybg3
|
UTSW |
16 |
59,364,417 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6242:Crybg3
|
UTSW |
16 |
59,376,053 (GRCm39) |
missense |
probably benign |
|
|
R6301:Crybg3
|
UTSW |
16 |
59,350,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6408:Crybg3
|
UTSW |
16 |
59,316,053 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R6724:Crybg3
|
UTSW |
16 |
59,364,501 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6745:Crybg3
|
UTSW |
16 |
59,372,607 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6777:Crybg3
|
UTSW |
16 |
59,378,678 (GRCm39) |
unclassified |
probably benign |
|
|
R6843:Crybg3
|
UTSW |
16 |
59,380,159 (GRCm39) |
missense |
probably benign |
0.22 |
|
R6914:Crybg3
|
UTSW |
16 |
59,360,183 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R6942:Crybg3
|
UTSW |
16 |
59,360,183 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7033:Crybg3
|
UTSW |
16 |
59,374,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7091:Crybg3
|
UTSW |
16 |
59,377,531 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R7133:Crybg3
|
UTSW |
16 |
59,357,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7193:Crybg3
|
UTSW |
16 |
59,379,956 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7204:Crybg3
|
UTSW |
16 |
59,379,253 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7398:Crybg3
|
UTSW |
16 |
59,377,688 (GRCm39) |
missense |
probably benign |
0.38 |
|
R7666:Crybg3
|
UTSW |
16 |
59,379,700 (GRCm39) |
nonsense |
probably null |
|
|
R7691:Crybg3
|
UTSW |
16 |
59,376,497 (GRCm39) |
missense |
not run |
|
|
R7714:Crybg3
|
UTSW |
16 |
59,379,236 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7860:Crybg3
|
UTSW |
16 |
59,375,605 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7901:Crybg3
|
UTSW |
16 |
59,377,907 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8371:Crybg3
|
UTSW |
16 |
59,377,414 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8394:Crybg3
|
UTSW |
16 |
59,378,651 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8438:Crybg3
|
UTSW |
16 |
59,385,655 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8529:Crybg3
|
UTSW |
16 |
59,376,984 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8699:Crybg3
|
UTSW |
16 |
59,375,291 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8766:Crybg3
|
UTSW |
16 |
59,375,696 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8767:Crybg3
|
UTSW |
16 |
59,376,500 (GRCm39) |
missense |
probably benign |
|
|
R8789:Crybg3
|
UTSW |
16 |
59,375,359 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8871:Crybg3
|
UTSW |
16 |
59,378,519 (GRCm39) |
missense |
probably benign |
|
|
R8878:Crybg3
|
UTSW |
16 |
59,380,547 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8894:Crybg3
|
UTSW |
16 |
59,342,552 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8928:Crybg3
|
UTSW |
16 |
59,376,715 (GRCm39) |
missense |
probably benign |
0.40 |
|
R8928:Crybg3
|
UTSW |
16 |
59,315,123 (GRCm39) |
missense |
probably benign |
0.31 |
|
R8939:Crybg3
|
UTSW |
16 |
59,376,512 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9010:Crybg3
|
UTSW |
16 |
59,374,702 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9266:Crybg3
|
UTSW |
16 |
59,372,544 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9348:Crybg3
|
UTSW |
16 |
59,421,256 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
|
R9353:Crybg3
|
UTSW |
16 |
59,421,107 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9406:Crybg3
|
UTSW |
16 |
59,378,839 (GRCm39) |
missense |
probably benign |
0.42 |
|
R9429:Crybg3
|
UTSW |
16 |
59,375,556 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9464:Crybg3
|
UTSW |
16 |
59,376,120 (GRCm39) |
unclassified |
probably benign |
|
|
R9621:Crybg3
|
UTSW |
16 |
59,326,613 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9703:Crybg3
|
UTSW |
16 |
59,375,939 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9751:Crybg3
|
UTSW |
16 |
59,377,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9766:Crybg3
|
UTSW |
16 |
59,376,207 (GRCm39) |
missense |
probably benign |
0.03 |
|
RF007:Crybg3
|
UTSW |
16 |
59,377,067 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
Z1177:Crybg3
|
UTSW |
16 |
59,376,841 (GRCm39) |
missense |
probably benign |
0.09 |
|
Z1177:Crybg3
|
UTSW |
16 |
59,375,756 (GRCm39) |
nonsense |
probably null |
|
|
Z1187:Crybg3
|
UTSW |
16 |
59,326,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTCCCTGGTTACAGTAGTGAC -3'
(R):5'- CTCCAGATGCAGTGGCTATC -3'
Sequencing Primer
(F):5'- CCAAGTGGTCAATATTTCAGATCCTG -3'
(R):5'- AGATGCAGTGGCTATCTTCTCAAC -3'
|
| Posted On |
2014-08-01 |
Incidental Mutation