Incidental Mutation 'R9022:Zfp616'
| ID |
686301 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp616
|
| Ensembl Gene |
ENSMUSG00000069476 |
| Gene Name |
zinc finger protein 616 |
| Synonyms |
Gm12330 |
| MMRRC Submission |
068852-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R9022 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
73960781-73978118 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 73976539 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Arginine
at position 936
(K936R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000136549
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000074813]
[ENSMUST00000108463]
[ENSMUST00000116546]
[ENSMUST00000178159]
|
| AlphaFold |
J3QN14 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000074813
|
| SMART Domains |
Protein: ENSMUSP00000074365
Gene: ENSMUSG00000069476
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
8 |
68 |
1.79e-34 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108463
|
| SMART Domains |
Protein: ENSMUSP00000104103
Gene: ENSMUSG00000069476
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
8 |
68 |
1.79e-34 |
SMART |
|
low complexity region
|
249 |
258 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000116546
|
| SMART Domains |
Protein: ENSMUSP00000112245
Gene: ENSMUSG00000069476
| Domain | Start | End | E-Value | Type |
|---|
|
KRAB
|
8 |
68 |
1.79e-34 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000178159
AA Change: K936R
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000136549
Gene: ENSMUSG00000069476
AA Change: K936R
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
125 |
447 |
7.61e-6 |
PROSPERO |
|
ZnF_C2H2
|
452 |
474 |
3.11e-2 |
SMART |
|
ZnF_C2H2
|
509 |
531 |
2.61e-4 |
SMART |
|
ZnF_C2H2
|
537 |
559 |
1.47e-3 |
SMART |
|
ZnF_C2H2
|
565 |
587 |
5.21e-4 |
SMART |
|
ZnF_C2H2
|
593 |
615 |
1.22e-4 |
SMART |
|
ZnF_C2H2
|
621 |
643 |
2.57e-3 |
SMART |
|
ZnF_C2H2
|
649 |
671 |
9.22e-5 |
SMART |
|
ZnF_C2H2
|
677 |
699 |
5.9e-3 |
SMART |
|
ZnF_C2H2
|
705 |
727 |
4.94e-5 |
SMART |
|
ZnF_C2H2
|
733 |
755 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
761 |
783 |
1.6e-4 |
SMART |
|
ZnF_C2H2
|
789 |
811 |
6.88e-4 |
SMART |
|
ZnF_C2H2
|
817 |
839 |
1.6e-4 |
SMART |
|
ZnF_C2H2
|
845 |
867 |
1.3e-4 |
SMART |
|
ZnF_C2H2
|
873 |
895 |
7.37e-4 |
SMART |
|
ZnF_C2H2
|
901 |
923 |
1.6e-4 |
SMART |
|
ZnF_C2H2
|
929 |
951 |
1.3e-4 |
SMART |
|
ZnF_C2H2
|
957 |
979 |
3.95e-4 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.5%
|
| Validation Efficiency |
100% (84/84) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Actl6a |
G |
T |
3: 32,769,649 (GRCm39) |
A155S |
probably benign |
Het |
| Adar |
A |
G |
3: 89,643,045 (GRCm39) |
T309A |
probably benign |
Het |
| Adgrv1 |
A |
T |
13: 81,303,312 (GRCm39) |
W6125R |
probably damaging |
Het |
| Adprhl1 |
A |
G |
8: 13,274,352 (GRCm39) |
L802P |
probably benign |
Het |
| Ahcy |
A |
G |
2: 154,910,779 (GRCm39) |
L63P |
probably damaging |
Het |
| Ang5 |
G |
A |
14: 44,200,352 (GRCm39) |
D139N |
probably damaging |
Het |
| Ankrd31 |
A |
G |
13: 96,962,655 (GRCm39) |
D482G |
probably benign |
Het |
| Arhgef7 |
A |
G |
8: 11,850,469 (GRCm39) |
N257D |
probably benign |
Het |
| Art3 |
C |
A |
5: 92,540,393 (GRCm39) |
S45R |
probably benign |
Het |
| Atxn1 |
T |
C |
13: 45,720,891 (GRCm39) |
R335G |
probably damaging |
Het |
| Bag6 |
T |
A |
17: 35,363,641 (GRCm39) |
L775H |
probably damaging |
Het |
| BC004004 |
T |
G |
17: 29,501,130 (GRCm39) |
H26Q |
possibly damaging |
Het |
| Camsap3 |
T |
C |
8: 3,656,575 (GRCm39) |
L986S |
probably benign |
Het |
| Cbx5 |
T |
C |
15: 103,121,586 (GRCm39) |
E17G |
probably damaging |
Het |
| Cc2d1b |
T |
C |
4: 108,484,617 (GRCm39) |
|
probably null |
Het |
| Ccdc59 |
T |
C |
10: 105,683,007 (GRCm39) |
Y231H |
probably damaging |
Het |
| Cemip2 |
T |
C |
19: 21,789,986 (GRCm39) |
|
probably null |
Het |
| Csnk1g1 |
T |
C |
9: 65,917,854 (GRCm39) |
|
probably null |
Het |
| Cybrd1 |
A |
G |
2: 70,967,904 (GRCm39) |
I158M |
possibly damaging |
Het |
| Disp2 |
T |
A |
2: 118,621,179 (GRCm39) |
I637N |
probably benign |
Het |
| Dll4 |
TC |
T |
2: 119,163,054 (GRCm39) |
|
probably null |
Het |
| Dnah7a |
T |
C |
1: 53,512,116 (GRCm39) |
|
probably null |
Het |
| Duox2 |
C |
A |
2: 122,110,919 (GRCm39) |
*1518L |
probably null |
Het |
| Dym |
A |
G |
18: 75,258,507 (GRCm39) |
I422V |
probably benign |
Het |
| Entpd8 |
A |
C |
2: 24,975,144 (GRCm39) |
I492L |
probably benign |
Het |
| Fabp12 |
A |
G |
3: 10,317,333 (GRCm39) |
S13P |
probably damaging |
Het |
| Fam124b |
A |
G |
1: 80,190,705 (GRCm39) |
I226T |
probably damaging |
Het |
| Fer1l6 |
T |
C |
15: 58,455,329 (GRCm39) |
L763P |
probably damaging |
Het |
| Git2 |
A |
G |
5: 114,907,676 (GRCm39) |
|
probably null |
Het |
| Gltpd2 |
A |
T |
11: 70,410,153 (GRCm39) |
Y37F |
probably benign |
Het |
| Gm44511 |
T |
G |
6: 128,797,271 (GRCm39) |
Q72H |
possibly damaging |
Het |
| Grid2ip |
A |
T |
5: 143,366,204 (GRCm39) |
T565S |
probably benign |
Het |
| Grk6 |
T |
C |
13: 55,606,877 (GRCm39) |
S532P |
possibly damaging |
Het |
| Haspin |
A |
T |
11: 73,026,831 (GRCm39) |
F753I |
probably damaging |
Het |
| Herpud1 |
T |
A |
8: 95,116,197 (GRCm39) |
S92T |
possibly damaging |
Het |
| Heyl |
C |
T |
4: 123,139,768 (GRCm39) |
A109V |
probably damaging |
Het |
| Hivep3 |
T |
C |
4: 119,955,304 (GRCm39) |
S1207P |
probably benign |
Het |
| Hk1 |
A |
G |
10: 62,105,768 (GRCm39) |
S893P |
probably damaging |
Het |
| Itih1 |
C |
A |
14: 30,652,327 (GRCm39) |
V789L |
probably benign |
Het |
| Kif12 |
T |
C |
4: 63,090,121 (GRCm39) |
D10G |
possibly damaging |
Het |
| Kif16b |
C |
T |
2: 142,554,537 (GRCm39) |
E754K |
possibly damaging |
Het |
| Kif20a |
A |
G |
18: 34,760,898 (GRCm39) |
Q191R |
probably benign |
Het |
| Lap3 |
A |
G |
5: 45,652,548 (GRCm39) |
D48G |
probably benign |
Het |
| Matn3 |
T |
A |
12: 9,002,355 (GRCm39) |
V189E |
probably damaging |
Het |
| Mbp |
G |
A |
18: 82,597,067 (GRCm39) |
E143K |
possibly damaging |
Het |
| Mrgprd |
A |
G |
7: 144,875,555 (GRCm39) |
H142R |
probably benign |
Het |
| Nbea |
A |
T |
3: 55,551,110 (GRCm39) |
C2685S |
possibly damaging |
Het |
| Nhsl1 |
A |
C |
10: 18,403,409 (GRCm39) |
I1381L |
possibly damaging |
Het |
| Npc1 |
A |
G |
18: 12,346,422 (GRCm39) |
M258T |
probably benign |
Het |
| Or2w3 |
T |
C |
11: 58,556,550 (GRCm39) |
L55P |
probably damaging |
Het |
| Or7e178 |
T |
A |
9: 20,225,268 (GRCm39) |
N316I |
probably damaging |
Het |
| Osbpl10 |
C |
T |
9: 114,807,939 (GRCm39) |
A65V |
unknown |
Het |
| Pdia4 |
C |
G |
6: 47,785,149 (GRCm39) |
A73P |
probably benign |
Het |
| Plxnb2 |
T |
C |
15: 89,048,471 (GRCm39) |
Y646C |
possibly damaging |
Het |
| Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
| Pold2 |
T |
C |
11: 5,824,121 (GRCm39) |
D228G |
probably benign |
Het |
| Popdc2 |
T |
G |
16: 38,194,508 (GRCm39) |
C310G |
probably benign |
Het |
| Prdm10 |
A |
G |
9: 31,268,424 (GRCm39) |
Y791C |
probably benign |
Het |
| Psg19 |
C |
T |
7: 18,530,762 (GRCm39) |
V131I |
probably benign |
Het |
| Psg19 |
T |
A |
7: 18,531,044 (GRCm39) |
T37S |
probably benign |
Het |
| Psme1 |
A |
G |
14: 55,817,271 (GRCm39) |
E39G |
probably damaging |
Het |
| Rabep2 |
A |
G |
7: 126,043,719 (GRCm39) |
E472G |
probably damaging |
Het |
| Rap1gap |
T |
C |
4: 137,445,309 (GRCm39) |
F297S |
probably damaging |
Het |
| Reln |
A |
G |
5: 22,181,613 (GRCm39) |
S1757P |
possibly damaging |
Het |
| Rybp |
G |
T |
6: 100,210,074 (GRCm39) |
D95E |
possibly damaging |
Het |
| Slc12a8 |
T |
A |
16: 33,466,934 (GRCm39) |
D480E |
probably benign |
Het |
| Slc25a1 |
A |
G |
16: 17,745,294 (GRCm39) |
V80A |
probably benign |
Het |
| Slc25a24 |
A |
T |
3: 109,070,757 (GRCm39) |
D372V |
probably benign |
Het |
| Slc49a4 |
T |
C |
16: 35,570,912 (GRCm39) |
T131A |
probably benign |
Het |
| Stab1 |
T |
C |
14: 30,882,226 (GRCm39) |
T490A |
probably benign |
Het |
| Stat5b |
A |
T |
11: 100,681,634 (GRCm39) |
I540N |
probably benign |
Het |
| Tasor2 |
A |
G |
13: 3,626,659 (GRCm39) |
V1097A |
probably benign |
Het |
| Thy1 |
T |
A |
9: 43,957,947 (GRCm39) |
L25Q |
probably damaging |
Het |
| Trim30a |
A |
G |
7: 104,084,956 (GRCm39) |
S85P |
probably benign |
Het |
| Use1 |
G |
A |
8: 71,819,942 (GRCm39) |
V36I |
probably benign |
Het |
| Vmn1r228 |
T |
A |
17: 20,996,778 (GRCm39) |
I247F |
probably damaging |
Het |
| Vmn2r13 |
T |
A |
5: 109,304,242 (GRCm39) |
T730S |
possibly damaging |
Het |
| Vmn2r9 |
T |
C |
5: 108,992,923 (GRCm39) |
D529G |
possibly damaging |
Het |
| Washc5 |
A |
G |
15: 59,217,233 (GRCm39) |
I778T |
possibly damaging |
Het |
| Washc5 |
A |
T |
15: 59,233,069 (GRCm39) |
M294K |
probably damaging |
Het |
| Wnt8a |
A |
T |
18: 34,680,298 (GRCm39) |
D221V |
probably damaging |
Het |
| Zfp618 |
G |
A |
4: 63,012,687 (GRCm39) |
C133Y |
probably damaging |
Het |
| Zfp82 |
A |
G |
7: 29,761,714 (GRCm39) |
S56P |
probably damaging |
Het |
| Zkscan16 |
T |
A |
4: 58,957,021 (GRCm39) |
D434E |
probably benign |
Het |
|
| Other mutations in Zfp616 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00530:Zfp616
|
APN |
11 |
73,974,439 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL00570:Zfp616
|
APN |
11 |
73,976,631 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL00594:Zfp616
|
APN |
11 |
73,973,789 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
IGL01861:Zfp616
|
APN |
11 |
73,973,742 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
IGL03022:Zfp616
|
APN |
11 |
73,973,800 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0197:Zfp616
|
UTSW |
11 |
73,976,500 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0442:Zfp616
|
UTSW |
11 |
73,975,321 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0497:Zfp616
|
UTSW |
11 |
73,974,306 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0651:Zfp616
|
UTSW |
11 |
73,974,555 (GRCm39) |
nonsense |
probably null |
|
|
R0730:Zfp616
|
UTSW |
11 |
73,975,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0883:Zfp616
|
UTSW |
11 |
73,976,500 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0926:Zfp616
|
UTSW |
11 |
73,976,644 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0940:Zfp616
|
UTSW |
11 |
73,975,850 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1068:Zfp616
|
UTSW |
11 |
73,973,767 (GRCm39) |
makesense |
probably null |
|
|
R1272:Zfp616
|
UTSW |
11 |
73,976,062 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1446:Zfp616
|
UTSW |
11 |
73,974,064 (GRCm39) |
splice site |
probably null |
|
|
R1482:Zfp616
|
UTSW |
11 |
73,974,803 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R1553:Zfp616
|
UTSW |
11 |
73,974,744 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1564:Zfp616
|
UTSW |
11 |
73,975,548 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1728:Zfp616
|
UTSW |
11 |
73,976,597 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1796:Zfp616
|
UTSW |
11 |
73,976,671 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1797:Zfp616
|
UTSW |
11 |
73,976,105 (GRCm39) |
nonsense |
probably null |
|
|
R1993:Zfp616
|
UTSW |
11 |
73,975,795 (GRCm39) |
missense |
probably benign |
0.08 |
|
R2026:Zfp616
|
UTSW |
11 |
73,974,413 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2124:Zfp616
|
UTSW |
11 |
73,973,869 (GRCm39) |
splice site |
probably null |
|
|
R2126:Zfp616
|
UTSW |
11 |
73,976,229 (GRCm39) |
missense |
probably benign |
0.08 |
|
R2199:Zfp616
|
UTSW |
11 |
73,975,456 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R2265:Zfp616
|
UTSW |
11 |
73,976,289 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2404:Zfp616
|
UTSW |
11 |
73,975,682 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2508:Zfp616
|
UTSW |
11 |
73,974,121 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2519:Zfp616
|
UTSW |
11 |
73,975,094 (GRCm39) |
nonsense |
probably null |
|
|
R3103:Zfp616
|
UTSW |
11 |
73,962,561 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3611:Zfp616
|
UTSW |
11 |
73,974,268 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R3703:Zfp616
|
UTSW |
11 |
73,974,145 (GRCm39) |
nonsense |
probably null |
|
|
R3744:Zfp616
|
UTSW |
11 |
73,974,813 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4043:Zfp616
|
UTSW |
11 |
73,976,108 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R4273:Zfp616
|
UTSW |
11 |
73,974,526 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4384:Zfp616
|
UTSW |
11 |
73,974,005 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4469:Zfp616
|
UTSW |
11 |
73,961,950 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4560:Zfp616
|
UTSW |
11 |
73,973,860 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4821:Zfp616
|
UTSW |
11 |
73,975,033 (GRCm39) |
missense |
probably benign |
0.41 |
|
R4844:Zfp616
|
UTSW |
11 |
73,975,225 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4948:Zfp616
|
UTSW |
11 |
73,974,830 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R5007:Zfp616
|
UTSW |
11 |
73,974,643 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R5198:Zfp616
|
UTSW |
11 |
73,974,336 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5344:Zfp616
|
UTSW |
11 |
73,975,321 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5918:Zfp616
|
UTSW |
11 |
73,974,086 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R5933:Zfp616
|
UTSW |
11 |
73,973,952 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6084:Zfp616
|
UTSW |
11 |
73,974,672 (GRCm39) |
nonsense |
probably null |
|
|
R6421:Zfp616
|
UTSW |
11 |
73,974,696 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R6494:Zfp616
|
UTSW |
11 |
73,976,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6523:Zfp616
|
UTSW |
11 |
73,973,968 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6849:Zfp616
|
UTSW |
11 |
73,976,276 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6910:Zfp616
|
UTSW |
11 |
73,975,828 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7146:Zfp616
|
UTSW |
11 |
73,976,087 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R7213:Zfp616
|
UTSW |
11 |
73,976,689 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7302:Zfp616
|
UTSW |
11 |
73,976,205 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7391:Zfp616
|
UTSW |
11 |
73,976,155 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7654:Zfp616
|
UTSW |
11 |
73,974,013 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7877:Zfp616
|
UTSW |
11 |
73,975,188 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7889:Zfp616
|
UTSW |
11 |
73,976,271 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8022:Zfp616
|
UTSW |
11 |
73,974,894 (GRCm39) |
missense |
probably benign |
|
|
R8061:Zfp616
|
UTSW |
11 |
73,974,340 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R8212:Zfp616
|
UTSW |
11 |
73,976,569 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8335:Zfp616
|
UTSW |
11 |
73,974,726 (GRCm39) |
nonsense |
probably null |
|
|
R8361:Zfp616
|
UTSW |
11 |
73,975,476 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8486:Zfp616
|
UTSW |
11 |
73,974,909 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8695:Zfp616
|
UTSW |
11 |
73,975,710 (GRCm39) |
missense |
probably benign |
0.45 |
|
R8808:Zfp616
|
UTSW |
11 |
73,976,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9126:Zfp616
|
UTSW |
11 |
73,976,280 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9164:Zfp616
|
UTSW |
11 |
73,975,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9293:Zfp616
|
UTSW |
11 |
73,974,744 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9421:Zfp616
|
UTSW |
11 |
73,974,331 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9512:Zfp616
|
UTSW |
11 |
73,975,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9529:Zfp616
|
UTSW |
11 |
73,976,596 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9529:Zfp616
|
UTSW |
11 |
73,975,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9606:Zfp616
|
UTSW |
11 |
73,976,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9708:Zfp616
|
UTSW |
11 |
73,976,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9788:Zfp616
|
UTSW |
11 |
73,975,276 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1176:Zfp616
|
UTSW |
11 |
73,976,467 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
Z1176:Zfp616
|
UTSW |
11 |
73,974,045 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
Z1176:Zfp616
|
UTSW |
11 |
73,973,859 (GRCm39) |
missense |
probably benign |
|
|
Z1177:Zfp616
|
UTSW |
11 |
73,975,878 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
| Predicted Primers |
PCR Primer
(F):5'- GTGGTAAATATTTTGCCCGTTCCTC -3'
(R):5'- GATTACTGGGTAAATGATTTCCCAC -3'
Sequencing Primer
(F):5'- CGTTCCTCAAGTCTTAAAGATCAC -3'
(R):5'- GAGGACTGTGTAAATGATTTCCCAC -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation