Incidental Mutation 'R9621:Crybg3'
| ID |
724828 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Crybg3
|
| Ensembl Gene |
ENSMUSG00000022723 |
| Gene Name |
beta-gamma crystallin domain containing 3 |
| Synonyms |
Gm9581 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.138)
|
| Stock # |
R9621 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
59312451-59421410 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 59326613 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 1039
(D1039G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000037682
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044604]
[ENSMUST00000172910]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044604
AA Change: D1039G
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
| SMART Domains |
Protein: ENSMUSP00000037682
Gene: ENSMUSG00000022723
AA Change: D1039G
| 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 |
probably benign
Transcript: ENSMUST00000172910
AA Change: D2753G
PolyPhen 2
Score 0.360 (Sensitivity: 0.90; Specificity: 0.89)
|
| Predicted Effect |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca1 |
T |
C |
4: 53,092,918 (GRCm39) |
T289A |
probably benign |
Het |
| Adnp |
A |
T |
2: 168,024,663 (GRCm39) |
S877R |
probably benign |
Het |
| Akap13 |
T |
A |
7: 75,386,090 (GRCm39) |
H555Q |
probably benign |
Het |
| Alg6 |
T |
A |
4: 99,615,131 (GRCm39) |
Y38* |
probably null |
Het |
| Amtn |
C |
A |
5: 88,528,205 (GRCm39) |
Q93K |
probably benign |
Het |
| Ap2b1 |
T |
C |
11: 83,293,424 (GRCm39) |
V937A |
probably damaging |
Het |
| Arih1 |
ATCGTCCGGCTCGTCCTCGTCGTCGTCC |
ATCGTCC |
9: 59,393,520 (GRCm39) |
|
probably benign |
Het |
| Atosa |
A |
G |
9: 74,917,512 (GRCm39) |
N711D |
possibly damaging |
Het |
| Bhmt |
A |
G |
13: 93,758,079 (GRCm39) |
S211P |
possibly damaging |
Het |
| Bltp3a |
T |
A |
17: 28,105,753 (GRCm39) |
S760T |
probably benign |
Het |
| Bmp1 |
T |
C |
14: 70,715,306 (GRCm39) |
Y943C |
probably benign |
Het |
| Calcoco2 |
TCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
TCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
11: 95,990,862 (GRCm39) |
|
probably null |
Het |
| Cbfb |
A |
C |
8: 105,905,243 (GRCm39) |
T62P |
probably damaging |
Het |
| Ccdc154 |
T |
C |
17: 25,386,355 (GRCm39) |
F249L |
probably damaging |
Het |
| Cdh26 |
T |
A |
2: 178,111,983 (GRCm39) |
F514L |
probably damaging |
Het |
| Cdhr2 |
A |
G |
13: 54,866,350 (GRCm39) |
E352G |
|
Het |
| Cep295nl |
G |
A |
11: 118,224,766 (GRCm39) |
P26L |
possibly damaging |
Het |
| Cfdp1 |
A |
G |
8: 112,571,807 (GRCm39) |
V34A |
probably damaging |
Het |
| Cntnap2 |
A |
T |
6: 46,965,726 (GRCm39) |
I846F |
probably damaging |
Het |
| Cntrl |
A |
G |
2: 35,050,278 (GRCm39) |
K1464E |
probably damaging |
Het |
| Csmd3 |
A |
T |
15: 47,713,116 (GRCm39) |
S778R |
|
Het |
| Daam2 |
C |
T |
17: 49,780,332 (GRCm39) |
C729Y |
probably damaging |
Het |
| Ddx18 |
T |
C |
1: 121,489,132 (GRCm39) |
H305R |
probably damaging |
Het |
| Dio1 |
C |
T |
4: 107,149,558 (GRCm39) |
C248Y |
probably benign |
Het |
| Dnah1 |
C |
A |
14: 31,016,772 (GRCm39) |
A1582S |
probably damaging |
Het |
| Eef1a1 |
A |
T |
9: 78,386,632 (GRCm39) |
D319E |
probably benign |
Het |
| Fam171b |
G |
A |
2: 83,643,109 (GRCm39) |
R6H |
probably damaging |
Het |
| Flnb |
G |
A |
14: 7,926,421 (GRCm38) |
G1822R |
probably damaging |
Het |
| Gabrb1 |
G |
A |
5: 72,279,363 (GRCm39) |
V303I |
possibly damaging |
Het |
| Gli3 |
T |
G |
13: 15,901,253 (GRCm39) |
S1547A |
probably benign |
Het |
| Gm4884 |
A |
T |
7: 40,693,111 (GRCm39) |
N360I |
possibly damaging |
Het |
| Ift70b |
T |
C |
2: 75,768,144 (GRCm39) |
Y203C |
probably damaging |
Het |
| Il1rl2 |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
1: 40,366,470 (GRCm39) |
|
probably benign |
Het |
| Ino80 |
C |
G |
2: 119,280,496 (GRCm39) |
K289N |
probably damaging |
Het |
| Itpr1 |
G |
A |
6: 108,393,870 (GRCm39) |
E1638K |
probably damaging |
Het |
| Jakmip1 |
A |
T |
5: 37,274,812 (GRCm39) |
I45F |
unknown |
Het |
| Kif1a |
G |
A |
1: 92,983,445 (GRCm39) |
P684L |
probably benign |
Het |
| Kpnb1 |
A |
T |
11: 97,058,460 (GRCm39) |
S610T |
probably benign |
Het |
| Man1a2 |
A |
G |
3: 100,591,961 (GRCm39) |
V73A |
probably benign |
Het |
| Mbtps1 |
A |
G |
8: 120,235,621 (GRCm39) |
V1019A |
possibly damaging |
Het |
| Muc21 |
T |
A |
17: 35,932,720 (GRCm39) |
T489S |
unknown |
Het |
| Nup210 |
G |
C |
6: 90,994,375 (GRCm39) |
N1774K |
probably benign |
Het |
| Or10p21 |
G |
T |
10: 128,847,759 (GRCm39) |
V202F |
probably benign |
Het |
| Pik3c2b |
T |
C |
1: 132,999,345 (GRCm39) |
S398P |
probably damaging |
Het |
| Pmpca |
A |
G |
2: 26,279,988 (GRCm39) |
T37A |
probably benign |
Het |
| Ppfia1 |
A |
G |
7: 144,052,516 (GRCm39) |
S840P |
probably damaging |
Het |
| Prkcq |
A |
T |
2: 11,261,014 (GRCm39) |
K355N |
probably benign |
Het |
| Prorp |
C |
A |
12: 55,429,042 (GRCm39) |
H538N |
probably benign |
Het |
| Ptprg |
A |
G |
14: 12,237,809 (GRCm38) |
K1422R |
probably benign |
Het |
| Ptprq |
T |
C |
10: 107,378,523 (GRCm39) |
E2006G |
probably damaging |
Het |
| Qsox1 |
TG |
T |
1: 155,671,135 (GRCm39) |
|
probably null |
Het |
| Rcor2 |
A |
T |
19: 7,251,591 (GRCm39) |
T412S |
probably benign |
Het |
| Rnf224 |
A |
T |
2: 25,126,200 (GRCm39) |
M51K |
probably benign |
Het |
| Robo4 |
A |
G |
9: 37,317,509 (GRCm39) |
D521G |
probably damaging |
Het |
| Sf3b4 |
T |
A |
3: 96,084,115 (GRCm39) |
S360T |
unknown |
Het |
| Sgo2b |
T |
C |
8: 64,380,651 (GRCm39) |
D727G |
probably damaging |
Het |
| Smpd2 |
C |
A |
10: 41,364,283 (GRCm39) |
V172L |
probably benign |
Het |
| Spring1 |
C |
T |
5: 118,393,880 (GRCm39) |
T86I |
possibly damaging |
Het |
| Syne1 |
C |
T |
10: 5,273,887 (GRCm39) |
A1966T |
probably benign |
Het |
| Syt13 |
G |
A |
2: 92,745,575 (GRCm39) |
G15D |
possibly damaging |
Het |
| Taf3 |
A |
T |
2: 9,923,070 (GRCm39) |
L18Q |
unknown |
Het |
| Tcam1 |
T |
A |
11: 106,176,259 (GRCm39) |
N328K |
probably damaging |
Het |
| Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
| Tet2 |
A |
T |
3: 133,193,767 (GRCm39) |
Y222* |
probably null |
Het |
| Timm29 |
A |
T |
9: 21,504,218 (GRCm39) |
|
probably benign |
Het |
| Tmc6 |
T |
C |
11: 117,669,995 (GRCm39) |
D17G |
probably benign |
Het |
| Tmem30a |
T |
A |
9: 79,687,926 (GRCm39) |
D81V |
probably benign |
Het |
| Tnnt1 |
T |
C |
7: 4,511,501 (GRCm39) |
I195V |
probably benign |
Het |
| Ttll5 |
T |
A |
12: 85,938,896 (GRCm39) |
V398E |
possibly damaging |
Het |
| Ttn |
T |
C |
2: 76,748,441 (GRCm39) |
T4203A |
possibly damaging |
Het |
| Ubc |
A |
G |
5: 125,464,511 (GRCm39) |
I272T |
probably damaging |
Het |
| Unc45a |
A |
G |
7: 79,983,785 (GRCm39) |
L337P |
probably damaging |
Het |
| Vmn1r229 |
T |
C |
17: 21,035,315 (GRCm39) |
F187L |
probably benign |
Het |
| Wrn |
A |
T |
8: 33,814,301 (GRCm39) |
M381K |
probably benign |
Het |
| Zdbf2 |
A |
G |
1: 63,342,635 (GRCm39) |
N338S |
possibly damaging |
Het |
| Zfp541 |
A |
G |
7: 15,805,892 (GRCm39) |
E9G |
possibly damaging |
Het |
| Zrsr2-ps1 |
G |
A |
11: 22,923,418 (GRCm39) |
R64Q |
possibly damaging |
Het |
| Zswim8 |
T |
A |
14: 20,772,231 (GRCm39) |
S1614T |
probably benign |
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 |
|
R1965:Crybg3
|
UTSW |
16 |
59,323,600 (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 |
|
|
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'- CCGTCTTGTCTTAGAACCAACTG -3'
(R):5'- GGCATTTCTTCTGTCTGACATG -3'
Sequencing Primer
(F):5'- CTGTTATATCCAGATAAACAGGAGC -3'
(R):5'- CTTCTGTCTGACATGAATGGATTC -3'
|
| Posted On |
2022-09-12 |
Incidental Mutation