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 |
73960781-73978118 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 73974894 bp (GRCm39)
|
| 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: 114,361,915 (GRCm39) |
T1386S |
probably benign |
Het |
| AI661453 |
T |
G |
17: 47,777,161 (GRCm39) |
S296A |
unknown |
Het |
| Ambp |
G |
T |
4: 63,062,434 (GRCm39) |
N268K |
probably damaging |
Het |
| Ankrd11 |
T |
C |
8: 123,614,332 (GRCm39) |
K2503E |
probably damaging |
Het |
| Ap1g1 |
C |
A |
8: 110,559,367 (GRCm39) |
R221S |
possibly damaging |
Het |
| Ap5z1 |
T |
C |
5: 142,455,904 (GRCm39) |
|
probably null |
Het |
| Aspa |
A |
C |
11: 73,213,032 (GRCm39) |
N103K |
probably benign |
Het |
| Bend7 |
G |
A |
2: 4,757,590 (GRCm39) |
V211I |
probably benign |
Het |
| Bsn |
A |
G |
9: 107,991,603 (GRCm39) |
M1383T |
probably benign |
Het |
| Cad |
G |
T |
5: 31,226,150 (GRCm39) |
V1117F |
probably damaging |
Het |
| Cdh2 |
A |
G |
18: 16,723,358 (GRCm39) |
L856S |
probably damaging |
Het |
| Cdh20 |
T |
A |
1: 109,988,838 (GRCm39) |
S247T |
probably benign |
Het |
| Ces1b |
A |
G |
8: 93,795,943 (GRCm39) |
|
probably null |
Het |
| Chd7 |
T |
A |
4: 8,751,605 (GRCm39) |
V34E |
unknown |
Het |
| Clca3a2 |
A |
T |
3: 144,511,527 (GRCm39) |
F623I |
probably damaging |
Het |
| Cope |
T |
G |
8: 70,765,453 (GRCm39) |
M217R |
probably benign |
Het |
| Crim1 |
T |
A |
17: 78,622,984 (GRCm39) |
I394N |
possibly damaging |
Het |
| Crnkl1 |
A |
T |
2: 145,760,486 (GRCm39) |
I644N |
probably damaging |
Het |
| Cry1 |
G |
A |
10: 84,982,266 (GRCm39) |
A360V |
probably damaging |
Het |
| Ctcfl |
A |
T |
2: 172,960,559 (GRCm39) |
V8D |
probably benign |
Het |
| Cyp2d34 |
G |
A |
15: 82,500,315 (GRCm39) |
Q475* |
probably null |
Het |
| Cyp39a1 |
T |
C |
17: 44,057,468 (GRCm39) |
Y436H |
probably damaging |
Het |
| Cyp3a25 |
T |
A |
5: 145,914,478 (GRCm39) |
Q484L |
probably benign |
Het |
| Dnah1 |
A |
G |
14: 30,986,971 (GRCm39) |
F3607S |
probably damaging |
Het |
| Dnali1 |
T |
A |
4: 124,959,323 (GRCm39) |
K23N |
possibly damaging |
Het |
| Ecel1 |
T |
C |
1: 87,081,052 (GRCm39) |
I313V |
probably benign |
Het |
| Ehhadh |
C |
A |
16: 21,596,570 (GRCm39) |
A53S |
probably benign |
Het |
| Epcam |
T |
C |
17: 87,953,736 (GRCm39) |
S277P |
probably benign |
Het |
| Fbxo10 |
T |
C |
4: 45,062,062 (GRCm39) |
I155V |
possibly damaging |
Het |
| Fgd6 |
A |
T |
10: 93,880,206 (GRCm39) |
K353N |
possibly damaging |
Het |
| Glce |
A |
T |
9: 61,967,873 (GRCm39) |
M426K |
probably benign |
Het |
| Glmp |
A |
T |
3: 88,233,827 (GRCm39) |
N228I |
probably damaging |
Het |
| Gm4787 |
C |
A |
12: 81,424,494 (GRCm39) |
V555F |
possibly damaging |
Het |
| Gm5114 |
T |
A |
7: 39,058,800 (GRCm39) |
H273L |
probably benign |
Het |
| Gzmg |
T |
A |
14: 56,394,903 (GRCm39) |
T122S |
probably benign |
Het |
| Hace1 |
T |
C |
10: 45,577,066 (GRCm39) |
V820A |
probably damaging |
Het |
| Igf2r |
T |
A |
17: 12,937,682 (GRCm39) |
D535V |
probably damaging |
Het |
| Kcnd3 |
A |
G |
3: 105,366,189 (GRCm39) |
M20V |
probably benign |
Het |
| Kcnn3 |
T |
G |
3: 89,517,010 (GRCm39) |
I473S |
possibly damaging |
Het |
| Klhl35 |
T |
A |
7: 99,122,446 (GRCm39) |
F94Y |
unknown |
Het |
| Kmt2c |
C |
T |
5: 25,486,678 (GRCm39) |
V4712I |
possibly damaging |
Het |
| Lepr |
A |
G |
4: 101,639,754 (GRCm39) |
E740G |
probably benign |
Het |
| Lmod3 |
T |
C |
6: 97,225,260 (GRCm39) |
D187G |
probably benign |
Het |
| Lsm3 |
C |
T |
6: 91,496,543 (GRCm39) |
H49Y |
probably benign |
Het |
| Lypd10 |
T |
A |
7: 24,413,599 (GRCm39) |
I205N |
possibly damaging |
Het |
| Magi1 |
T |
C |
6: 93,674,346 (GRCm39) |
S962G |
probably damaging |
Het |
| Man2b1 |
G |
A |
8: 85,822,242 (GRCm39) |
R782Q |
probably damaging |
Het |
| Mical2 |
A |
T |
7: 111,902,974 (GRCm39) |
K148N |
probably damaging |
Het |
| Nbeal1 |
C |
T |
1: 60,299,431 (GRCm39) |
Q1256* |
probably null |
Het |
| Ncam1 |
G |
T |
9: 49,476,192 (GRCm39) |
A299D |
possibly damaging |
Het |
| Ncapg |
A |
G |
5: 45,839,136 (GRCm39) |
D512G |
probably damaging |
Het |
| Nkiras2 |
A |
G |
11: 100,515,113 (GRCm39) |
N28D |
probably benign |
Het |
| Nprl2 |
A |
C |
9: 107,420,260 (GRCm39) |
K53T |
probably damaging |
Het |
| Nr4a3 |
T |
A |
4: 48,051,510 (GRCm39) |
I88N |
probably damaging |
Het |
| Oas3 |
A |
G |
5: 120,895,031 (GRCm39) |
I986T |
possibly damaging |
Het |
| Or6c76 |
A |
T |
10: 129,612,654 (GRCm39) |
L305F |
possibly damaging |
Het |
| Pcsk1 |
A |
T |
13: 75,247,412 (GRCm39) |
Y187F |
possibly damaging |
Het |
| Pgc |
A |
G |
17: 48,039,701 (GRCm39) |
T32A |
probably benign |
Het |
| Ranbp2 |
A |
C |
10: 58,321,683 (GRCm39) |
D2660A |
possibly damaging |
Het |
| Retreg1 |
A |
G |
15: 25,843,565 (GRCm39) |
R46G |
|
Het |
| Rrbp1 |
C |
A |
2: 143,798,712 (GRCm39) |
K1100N |
probably benign |
Het |
| Rsph10b |
A |
T |
5: 143,904,050 (GRCm39) |
T676S |
probably benign |
Het |
| Setdb1 |
A |
T |
3: 95,245,910 (GRCm39) |
F672I |
probably damaging |
Het |
| Setdb1 |
T |
A |
3: 95,254,396 (GRCm39) |
D195V |
probably damaging |
Het |
| Slc12a8 |
A |
G |
16: 33,445,456 (GRCm39) |
E450G |
probably benign |
Het |
| Slc1a7 |
G |
A |
4: 107,869,473 (GRCm39) |
V513M |
probably benign |
Het |
| Slc25a12 |
A |
T |
2: 71,105,533 (GRCm39) |
V667E |
unknown |
Het |
| Slc39a3 |
T |
C |
10: 80,867,111 (GRCm39) |
T212A |
probably benign |
Het |
| Slc45a1 |
C |
T |
4: 150,722,766 (GRCm39) |
G373S |
possibly damaging |
Het |
| Snx11 |
G |
A |
11: 96,663,680 (GRCm39) |
T53M |
probably damaging |
Het |
| Snx33 |
A |
G |
9: 56,832,624 (GRCm39) |
F482L |
possibly damaging |
Het |
| Srebf2 |
C |
T |
15: 82,062,966 (GRCm39) |
R468C |
probably damaging |
Het |
| Stk32a |
C |
T |
18: 43,448,166 (GRCm39) |
Q382* |
probably null |
Het |
| Sun3 |
C |
A |
11: 8,973,376 (GRCm39) |
S167I |
probably damaging |
Het |
| Sycp2 |
A |
G |
2: 177,996,855 (GRCm39) |
L1116P |
probably damaging |
Het |
| Thbs4 |
T |
G |
13: 92,888,955 (GRCm39) |
T913P |
probably damaging |
Het |
| Trav8d-1 |
C |
T |
14: 53,016,284 (GRCm39) |
Q57* |
probably null |
Het |
| Trio |
C |
G |
15: 27,749,952 (GRCm39) |
V2250L |
probably benign |
Het |
| Unc119b |
A |
T |
5: 115,265,102 (GRCm39) |
I204N |
probably damaging |
Het |
| Usp4 |
A |
G |
9: 108,255,670 (GRCm39) |
E576G |
probably damaging |
Het |
| Uvssa |
T |
A |
5: 33,566,848 (GRCm39) |
L515Q |
probably damaging |
Het |
| Xkr8 |
T |
C |
4: 132,459,649 (GRCm39) |
Y43C |
probably damaging |
Het |
| Xpo6 |
G |
A |
7: 125,768,426 (GRCm39) |
L94F |
probably benign |
Het |
| Zbtb11 |
A |
G |
16: 55,826,383 (GRCm39) |
K804R |
probably damaging |
Het |
| Zfp661 |
T |
C |
2: 127,419,844 (GRCm39) |
T99A |
probably benign |
Het |
| Zfp839 |
A |
T |
12: 110,821,532 (GRCm39) |
Q115H |
probably damaging |
Het |
| Zyg11a |
C |
T |
4: 108,046,765 (GRCm39) |
|
probably null |
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 |
|
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 |
|
R9022:Zfp616
|
UTSW |
11 |
73,976,539 (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'- GGATCATACCACATGGAGCC -3'
(R):5'- TTACAGTACAGATCCTGTGAGGG -3'
Sequencing Primer
(F):5'- GCCTTTATAAAAATGACTGGCAGG -3'
(R):5'- ACAGTACAGATCCTGTGAGGGTTTTG -3'
|
| Posted On |
2020-01-23 |
Incidental Mutation