Incidental Mutation 'R8022:Zfp616'
| ID |
617474 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp616
|
| Ensembl Gene |
ENSMUSG00000069476 |
| Gene Name |
zinc finger protein 616 |
| Synonyms |
Gm12330 |
| MMRRC Submission |
067461-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8022 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
74069955-74087292 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 74084068 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glycine
at position 479
(R479G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000104103
(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
AA Change: R479G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000104103
Gene: ENSMUSG00000069476
AA Change: R479G
| 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 |
unknown
Transcript: ENSMUST00000178159
AA Change: R388G
|
| SMART Domains |
Protein: ENSMUSP00000136549
Gene: ENSMUSG00000069476
AA Change: R388G
| 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: 98.6%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acacb |
A |
T |
5: 114,223,854 (GRCm38) |
T1386S |
probably benign |
Het |
| AI661453 |
T |
G |
17: 47,466,236 (GRCm38) |
S296A |
unknown |
Het |
| Ambp |
G |
T |
4: 63,144,197 (GRCm38) |
N268K |
probably damaging |
Het |
| Ankrd11 |
T |
C |
8: 122,887,593 (GRCm38) |
K2503E |
probably damaging |
Het |
| Ap1g1 |
C |
A |
8: 109,832,735 (GRCm38) |
R221S |
possibly damaging |
Het |
| Ap5z1 |
T |
C |
5: 142,470,149 (GRCm38) |
|
probably null |
Het |
| Aspa |
A |
C |
11: 73,322,206 (GRCm38) |
N103K |
probably benign |
Het |
| BC049730 |
T |
A |
7: 24,714,174 (GRCm38) |
I205N |
possibly damaging |
Het |
| Bend7 |
G |
A |
2: 4,752,779 (GRCm38) |
V211I |
probably benign |
Het |
| Bsn |
A |
G |
9: 108,114,404 (GRCm38) |
M1383T |
probably benign |
Het |
| Cad |
G |
T |
5: 31,068,806 (GRCm38) |
V1117F |
probably damaging |
Het |
| Cdh2 |
A |
G |
18: 16,590,301 (GRCm38) |
L856S |
probably damaging |
Het |
| Cdh7 |
T |
A |
1: 110,061,108 (GRCm38) |
S247T |
probably benign |
Het |
| Ces1b |
A |
G |
8: 93,069,315 (GRCm38) |
|
probably null |
Het |
| Chd7 |
T |
A |
4: 8,751,605 (GRCm38) |
V34E |
unknown |
Het |
| Clca3a2 |
A |
T |
3: 144,805,766 (GRCm38) |
F623I |
probably damaging |
Het |
| Cope |
T |
G |
8: 70,312,803 (GRCm38) |
M217R |
probably benign |
Het |
| Crim1 |
T |
A |
17: 78,315,555 (GRCm38) |
I394N |
possibly damaging |
Het |
| Crnkl1 |
A |
T |
2: 145,918,566 (GRCm38) |
I644N |
probably damaging |
Het |
| Cry1 |
G |
A |
10: 85,146,402 (GRCm38) |
A360V |
probably damaging |
Het |
| Ctcfl |
A |
T |
2: 173,118,766 (GRCm38) |
V8D |
probably benign |
Het |
| Cyp2d34 |
G |
A |
15: 82,616,114 (GRCm38) |
Q475* |
probably null |
Het |
| Cyp39a1 |
T |
C |
17: 43,746,577 (GRCm38) |
Y436H |
probably damaging |
Het |
| Cyp3a25 |
T |
A |
5: 145,977,668 (GRCm38) |
Q484L |
probably benign |
Het |
| Dnah1 |
A |
G |
14: 31,265,014 (GRCm38) |
F3607S |
probably damaging |
Het |
| Dnali1 |
T |
A |
4: 125,065,530 (GRCm38) |
K23N |
possibly damaging |
Het |
| Ecel1 |
T |
C |
1: 87,153,330 (GRCm38) |
I313V |
probably benign |
Het |
| Ehhadh |
C |
A |
16: 21,777,820 (GRCm38) |
A53S |
probably benign |
Het |
| Epcam |
T |
C |
17: 87,646,308 (GRCm38) |
S277P |
probably benign |
Het |
| Fbxo10 |
T |
C |
4: 45,062,062 (GRCm38) |
I155V |
possibly damaging |
Het |
| Fgd6 |
A |
T |
10: 94,044,344 (GRCm38) |
K353N |
possibly damaging |
Het |
| Glce |
A |
T |
9: 62,060,591 (GRCm38) |
M426K |
probably benign |
Het |
| Glmp |
A |
T |
3: 88,326,520 (GRCm38) |
N228I |
probably damaging |
Het |
| Gm4787 |
C |
A |
12: 81,377,720 (GRCm38) |
V555F |
possibly damaging |
Het |
| Gm5114 |
T |
A |
7: 39,409,376 (GRCm38) |
H273L |
probably benign |
Het |
| Gzmg |
T |
A |
14: 56,157,446 (GRCm38) |
T122S |
probably benign |
Het |
| Hace1 |
T |
C |
10: 45,700,970 (GRCm38) |
V820A |
probably damaging |
Het |
| Igf2r |
T |
A |
17: 12,718,795 (GRCm38) |
D535V |
probably damaging |
Het |
| Kcnd3 |
A |
G |
3: 105,458,873 (GRCm38) |
M20V |
probably benign |
Het |
| Kcnn3 |
T |
G |
3: 89,609,703 (GRCm38) |
I473S |
possibly damaging |
Het |
| Klhl35 |
T |
A |
7: 99,473,239 (GRCm38) |
F94Y |
unknown |
Het |
| Kmt2c |
C |
T |
5: 25,281,680 (GRCm38) |
V4712I |
possibly damaging |
Het |
| Lepr |
A |
G |
4: 101,782,557 (GRCm38) |
E740G |
probably benign |
Het |
| Lmod3 |
T |
C |
6: 97,248,299 (GRCm38) |
D187G |
probably benign |
Het |
| Lsm3 |
C |
T |
6: 91,519,561 (GRCm38) |
H49Y |
probably benign |
Het |
| Magi1 |
T |
C |
6: 93,697,365 (GRCm38) |
S962G |
probably damaging |
Het |
| Man2b1 |
G |
A |
8: 85,095,613 (GRCm38) |
R782Q |
probably damaging |
Het |
| Mical2 |
A |
T |
7: 112,303,767 (GRCm38) |
K148N |
probably damaging |
Het |
| Nbeal1 |
C |
T |
1: 60,260,272 (GRCm38) |
Q1256* |
probably null |
Het |
| Ncam1 |
G |
T |
9: 49,564,892 (GRCm38) |
A299D |
possibly damaging |
Het |
| Ncapg |
A |
G |
5: 45,681,794 (GRCm38) |
D512G |
probably damaging |
Het |
| Nkiras2 |
A |
G |
11: 100,624,287 (GRCm38) |
N28D |
probably benign |
Het |
| Nprl2 |
A |
C |
9: 107,543,061 (GRCm38) |
K53T |
probably damaging |
Het |
| Nr4a3 |
T |
A |
4: 48,051,510 (GRCm38) |
I88N |
probably damaging |
Het |
| Oas3 |
A |
G |
5: 120,756,966 (GRCm38) |
I986T |
possibly damaging |
Het |
| Olfr809 |
A |
T |
10: 129,776,785 (GRCm38) |
L305F |
possibly damaging |
Het |
| Pcsk1 |
A |
T |
13: 75,099,293 (GRCm38) |
Y187F |
possibly damaging |
Het |
| Pgc |
A |
G |
17: 47,728,776 (GRCm38) |
T32A |
probably benign |
Het |
| Ranbp2 |
A |
C |
10: 58,485,861 (GRCm38) |
D2660A |
possibly damaging |
Het |
| Retreg1 |
A |
G |
15: 25,843,479 (GRCm38) |
R46G |
|
Het |
| Rrbp1 |
C |
A |
2: 143,956,792 (GRCm38) |
K1100N |
probably benign |
Het |
| Rsph10b |
A |
T |
5: 143,967,232 (GRCm38) |
T676S |
probably benign |
Het |
| Setdb1 |
A |
T |
3: 95,338,599 (GRCm38) |
F672I |
probably damaging |
Het |
| Setdb1 |
T |
A |
3: 95,347,085 (GRCm38) |
D195V |
probably damaging |
Het |
| Slc12a8 |
A |
G |
16: 33,625,086 (GRCm38) |
E450G |
probably benign |
Het |
| Slc1a7 |
G |
A |
4: 108,012,276 (GRCm38) |
V513M |
probably benign |
Het |
| Slc25a12 |
A |
T |
2: 71,275,189 (GRCm38) |
V667E |
unknown |
Het |
| Slc39a3 |
T |
C |
10: 81,031,277 (GRCm38) |
T212A |
probably benign |
Het |
| Slc45a1 |
C |
T |
4: 150,638,309 (GRCm38) |
G373S |
possibly damaging |
Het |
| Snx11 |
G |
A |
11: 96,772,854 (GRCm38) |
T53M |
probably damaging |
Het |
| Snx33 |
A |
G |
9: 56,925,340 (GRCm38) |
F482L |
possibly damaging |
Het |
| Srebf2 |
C |
T |
15: 82,178,765 (GRCm38) |
R468C |
probably damaging |
Het |
| Stk32a |
C |
T |
18: 43,315,101 (GRCm38) |
Q382* |
probably null |
Het |
| Sun3 |
C |
A |
11: 9,023,376 (GRCm38) |
S167I |
probably damaging |
Het |
| Sycp2 |
A |
G |
2: 178,355,062 (GRCm38) |
L1116P |
probably damaging |
Het |
| Thbs4 |
T |
G |
13: 92,752,447 (GRCm38) |
T913P |
probably damaging |
Het |
| Trav8d-1 |
C |
T |
14: 52,778,827 (GRCm38) |
Q57* |
probably null |
Het |
| Trio |
C |
G |
15: 27,749,866 (GRCm38) |
V2250L |
probably benign |
Het |
| Unc119b |
A |
T |
5: 115,127,043 (GRCm38) |
I204N |
probably damaging |
Het |
| Usp4 |
A |
G |
9: 108,378,471 (GRCm38) |
E576G |
probably damaging |
Het |
| Uvssa |
T |
A |
5: 33,409,504 (GRCm38) |
L515Q |
probably damaging |
Het |
| Xkr8 |
T |
C |
4: 132,732,338 (GRCm38) |
Y43C |
probably damaging |
Het |
| Xpo6 |
G |
A |
7: 126,169,254 (GRCm38) |
L94F |
probably benign |
Het |
| Zbtb11 |
A |
G |
16: 56,006,020 (GRCm38) |
K804R |
probably damaging |
Het |
| Zfp661 |
T |
C |
2: 127,577,924 (GRCm38) |
T99A |
probably benign |
Het |
| Zfp839 |
A |
T |
12: 110,855,098 (GRCm38) |
Q115H |
probably damaging |
Het |
| Zyg11a |
C |
T |
4: 108,189,568 (GRCm38) |
|
probably null |
Het |
|
| Other mutations in Zfp616 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00530:Zfp616
|
APN |
11 |
74,083,613 (GRCm38) |
missense |
probably damaging |
0.98 |
|
IGL00570:Zfp616
|
APN |
11 |
74,085,805 (GRCm38) |
missense |
probably benign |
0.03 |
|
IGL00594:Zfp616
|
APN |
11 |
74,082,963 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
IGL01861:Zfp616
|
APN |
11 |
74,082,916 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
IGL03022:Zfp616
|
APN |
11 |
74,082,974 (GRCm38) |
missense |
possibly damaging |
0.85 |
|
R0197:Zfp616
|
UTSW |
11 |
74,085,674 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0442:Zfp616
|
UTSW |
11 |
74,084,495 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R0497:Zfp616
|
UTSW |
11 |
74,083,480 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0651:Zfp616
|
UTSW |
11 |
74,083,729 (GRCm38) |
nonsense |
probably null |
|
|
R0730:Zfp616
|
UTSW |
11 |
74,084,822 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0883:Zfp616
|
UTSW |
11 |
74,085,674 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0926:Zfp616
|
UTSW |
11 |
74,085,818 (GRCm38) |
missense |
probably benign |
0.04 |
|
R0940:Zfp616
|
UTSW |
11 |
74,085,024 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1068:Zfp616
|
UTSW |
11 |
74,082,941 (GRCm38) |
makesense |
probably null |
|
|
R1272:Zfp616
|
UTSW |
11 |
74,085,236 (GRCm38) |
missense |
probably benign |
0.08 |
|
R1446:Zfp616
|
UTSW |
11 |
74,083,238 (GRCm38) |
splice site |
probably null |
|
|
R1482:Zfp616
|
UTSW |
11 |
74,083,977 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R1553:Zfp616
|
UTSW |
11 |
74,083,918 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R1564:Zfp616
|
UTSW |
11 |
74,084,722 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1728:Zfp616
|
UTSW |
11 |
74,085,771 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1796:Zfp616
|
UTSW |
11 |
74,085,845 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R1797:Zfp616
|
UTSW |
11 |
74,085,279 (GRCm38) |
nonsense |
probably null |
|
|
R1993:Zfp616
|
UTSW |
11 |
74,084,969 (GRCm38) |
missense |
probably benign |
0.08 |
|
R2026:Zfp616
|
UTSW |
11 |
74,083,587 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R2124:Zfp616
|
UTSW |
11 |
74,083,043 (GRCm38) |
splice site |
probably null |
|
|
R2126:Zfp616
|
UTSW |
11 |
74,085,403 (GRCm38) |
missense |
probably benign |
0.08 |
|
R2199:Zfp616
|
UTSW |
11 |
74,084,630 (GRCm38) |
missense |
possibly damaging |
0.58 |
|
R2265:Zfp616
|
UTSW |
11 |
74,085,463 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R2404:Zfp616
|
UTSW |
11 |
74,084,856 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2508:Zfp616
|
UTSW |
11 |
74,083,295 (GRCm38) |
missense |
probably benign |
0.01 |
|
R2519:Zfp616
|
UTSW |
11 |
74,084,268 (GRCm38) |
nonsense |
probably null |
|
|
R3103:Zfp616
|
UTSW |
11 |
74,071,735 (GRCm38) |
missense |
probably benign |
0.01 |
|
R3611:Zfp616
|
UTSW |
11 |
74,083,442 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R3703:Zfp616
|
UTSW |
11 |
74,083,319 (GRCm38) |
nonsense |
probably null |
|
|
R3744:Zfp616
|
UTSW |
11 |
74,083,987 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4043:Zfp616
|
UTSW |
11 |
74,085,282 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
R4273:Zfp616
|
UTSW |
11 |
74,083,700 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4384:Zfp616
|
UTSW |
11 |
74,083,179 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R4469:Zfp616
|
UTSW |
11 |
74,071,124 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R4560:Zfp616
|
UTSW |
11 |
74,083,034 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4821:Zfp616
|
UTSW |
11 |
74,084,207 (GRCm38) |
missense |
probably benign |
0.41 |
|
R4844:Zfp616
|
UTSW |
11 |
74,084,399 (GRCm38) |
missense |
probably benign |
0.10 |
|
R4948:Zfp616
|
UTSW |
11 |
74,084,004 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R5007:Zfp616
|
UTSW |
11 |
74,083,817 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R5198:Zfp616
|
UTSW |
11 |
74,083,510 (GRCm38) |
missense |
probably benign |
0.33 |
|
R5344:Zfp616
|
UTSW |
11 |
74,084,495 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R5918:Zfp616
|
UTSW |
11 |
74,083,260 (GRCm38) |
missense |
possibly damaging |
0.70 |
|
R5933:Zfp616
|
UTSW |
11 |
74,083,126 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R6084:Zfp616
|
UTSW |
11 |
74,083,846 (GRCm38) |
nonsense |
probably null |
|
|
R6421:Zfp616
|
UTSW |
11 |
74,083,870 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R6494:Zfp616
|
UTSW |
11 |
74,085,192 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6523:Zfp616
|
UTSW |
11 |
74,083,142 (GRCm38) |
missense |
possibly damaging |
0.79 |
|
R6849:Zfp616
|
UTSW |
11 |
74,085,450 (GRCm38) |
missense |
possibly damaging |
0.70 |
|
R6910:Zfp616
|
UTSW |
11 |
74,085,002 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7146:Zfp616
|
UTSW |
11 |
74,085,261 (GRCm38) |
missense |
possibly damaging |
0.61 |
|
R7213:Zfp616
|
UTSW |
11 |
74,085,863 (GRCm38) |
missense |
probably benign |
0.05 |
|
R7302:Zfp616
|
UTSW |
11 |
74,085,379 (GRCm38) |
missense |
probably benign |
0.08 |
|
R7391:Zfp616
|
UTSW |
11 |
74,085,329 (GRCm38) |
missense |
probably benign |
0.08 |
|
R7654:Zfp616
|
UTSW |
11 |
74,083,187 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R7877:Zfp616
|
UTSW |
11 |
74,084,362 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7889:Zfp616
|
UTSW |
11 |
74,085,445 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8061:Zfp616
|
UTSW |
11 |
74,083,514 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R8212:Zfp616
|
UTSW |
11 |
74,085,743 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R8335:Zfp616
|
UTSW |
11 |
74,083,900 (GRCm38) |
nonsense |
probably null |
|
|
R8361:Zfp616
|
UTSW |
11 |
74,084,650 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8486:Zfp616
|
UTSW |
11 |
74,084,083 (GRCm38) |
missense |
probably benign |
0.18 |
|
R8695:Zfp616
|
UTSW |
11 |
74,084,884 (GRCm38) |
missense |
probably benign |
0.45 |
|
R8808:Zfp616
|
UTSW |
11 |
74,085,697 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9022:Zfp616
|
UTSW |
11 |
74,085,713 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9126:Zfp616
|
UTSW |
11 |
74,085,454 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9164:Zfp616
|
UTSW |
11 |
74,084,999 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9293:Zfp616
|
UTSW |
11 |
74,083,918 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R9421:Zfp616
|
UTSW |
11 |
74,083,505 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R9512:Zfp616
|
UTSW |
11 |
74,085,110 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9529:Zfp616
|
UTSW |
11 |
74,085,770 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
R9529:Zfp616
|
UTSW |
11 |
74,084,834 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9606:Zfp616
|
UTSW |
11 |
74,085,394 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9708:Zfp616
|
UTSW |
11 |
74,085,457 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9788:Zfp616
|
UTSW |
11 |
74,084,450 (GRCm38) |
missense |
probably damaging |
0.99 |
|
Z1176:Zfp616
|
UTSW |
11 |
74,085,641 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
Z1176:Zfp616
|
UTSW |
11 |
74,083,219 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
Z1176:Zfp616
|
UTSW |
11 |
74,083,033 (GRCm38) |
missense |
probably benign |
|
|
Z1177:Zfp616
|
UTSW |
11 |
74,085,052 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGATCATACCACATGGAGCC -3'
(R):5'- TTACAGTACAGATCCTGTGAGGG -3'
Sequencing Primer
(F):5'- GCCTTTATAAAAATGACTGGCAGG -3'
(R):5'- ACAGTACAGATCCTGTGAGGGTTTTG -3'
|
| Posted On |
2020-01-23 |
Incidental Mutation