Incidental Mutation 'R9091:Thada'
ID |
691038 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Thada
|
Ensembl Gene |
ENSMUSG00000024251 |
Gene Name |
thyroid adenoma associated |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R9091 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
84497504-84773633 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 84538589 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Glutamine
at position 1473
(L1473Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000041701
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047524]
|
AlphaFold |
A8C756 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000047524
AA Change: L1473Q
PolyPhen 2
Score 0.965 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000041701 Gene: ENSMUSG00000024251 AA Change: L1473Q
Domain | Start | End | E-Value | Type |
SCOP:d1gw5a_
|
457 |
926 |
3e-6 |
SMART |
Pfam:DUF2428
|
938 |
1239 |
1.6e-93 |
PFAM |
SCOP:d1gw5a_
|
1343 |
1802 |
7e-6 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.4%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is the target of 2p21 choromosomal aberrations in benign thyroid adenomas. Single nucleotide polymorphisms (SNPs) in this gene may be associated with type 2 diabetes and polycystic ovary syndrome. The encoded protein is likely involved in the death receptor pathway and apoptosis. [provided by RefSeq, Sep 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actrt3 |
T |
A |
3: 30,652,781 (GRCm39) |
E104D |
probably damaging |
Het |
Arih2 |
A |
T |
9: 108,493,890 (GRCm39) |
D174E |
probably damaging |
Het |
Asprv1 |
T |
C |
6: 86,606,077 (GRCm39) |
F308L |
probably damaging |
Het |
Baiap2l2 |
A |
G |
15: 79,168,205 (GRCm39) |
|
probably null |
Het |
Btla |
T |
C |
16: 45,064,656 (GRCm39) |
F203L |
possibly damaging |
Het |
C1rb |
A |
T |
6: 124,551,947 (GRCm39) |
D283V |
probably damaging |
Het |
C87436 |
C |
G |
6: 86,442,813 (GRCm39) |
Q462E |
probably benign |
Het |
Ccdc149 |
T |
C |
5: 52,563,352 (GRCm39) |
D147G |
possibly damaging |
Het |
Chd6 |
A |
T |
2: 160,871,793 (GRCm39) |
L214* |
probably null |
Het |
Chrna4 |
C |
A |
2: 180,670,643 (GRCm39) |
R371L |
possibly damaging |
Het |
Cit |
C |
A |
5: 115,984,161 (GRCm39) |
|
probably benign |
Het |
Cpne5 |
A |
G |
17: 29,444,163 (GRCm39) |
|
probably null |
Het |
Cr1l |
T |
C |
1: 194,789,204 (GRCm39) |
E400G |
possibly damaging |
Het |
Creb3l2 |
T |
C |
6: 37,332,583 (GRCm39) |
N304D |
probably damaging |
Het |
Cyp17a1 |
T |
C |
19: 46,656,030 (GRCm39) |
T420A |
probably benign |
Het |
Cyp24a1 |
A |
G |
2: 170,327,853 (GRCm39) |
I463T |
probably damaging |
Het |
Cyp3a41b |
A |
T |
5: 145,514,973 (GRCm39) |
I84N |
probably damaging |
Het |
Dnajc6 |
G |
A |
4: 101,496,559 (GRCm39) |
V909M |
possibly damaging |
Het |
Dtl |
A |
G |
1: 191,288,923 (GRCm39) |
Y264H |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,077,216 (GRCm39) |
R660* |
probably null |
Het |
Egf |
A |
G |
3: 129,529,449 (GRCm39) |
|
probably null |
Het |
Eva1c |
T |
C |
16: 90,701,231 (GRCm39) |
S402P |
probably benign |
Het |
Fcho2 |
A |
T |
13: 98,925,869 (GRCm39) |
|
probably null |
Het |
Fhdc1 |
G |
A |
3: 84,352,290 (GRCm39) |
R197C |
unknown |
Het |
Foxa2 |
T |
A |
2: 147,886,426 (GRCm39) |
M136L |
probably benign |
Het |
Gm10226 |
T |
C |
17: 21,910,866 (GRCm39) |
C34R |
possibly damaging |
Het |
Gm29735 |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
7: 141,710,266 (GRCm39) |
|
probably benign |
Het |
Gm8947 |
T |
C |
1: 151,068,853 (GRCm39) |
S229P |
probably benign |
Het |
Ighv9-2 |
A |
T |
12: 114,072,896 (GRCm39) |
S26T |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kat6a |
T |
G |
8: 23,420,190 (GRCm39) |
I745M |
probably damaging |
Het |
Klhdc1 |
T |
C |
12: 69,309,968 (GRCm39) |
L290P |
probably damaging |
Het |
Lcp2 |
C |
T |
11: 34,039,688 (GRCm39) |
T496I |
|
Het |
Map4k4 |
T |
C |
1: 40,042,923 (GRCm39) |
W593R |
probably benign |
Het |
Mefv |
T |
G |
16: 3,535,841 (GRCm39) |
Q29P |
probably damaging |
Het |
Mgat5b |
T |
C |
11: 116,859,269 (GRCm39) |
Y34H |
|
Het |
Mlip |
C |
T |
9: 77,137,080 (GRCm39) |
R609Q |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,290,816 (GRCm39) |
D34G |
|
Het |
Nbeal1 |
C |
T |
1: 60,307,548 (GRCm39) |
P1687S |
possibly damaging |
Het |
Notch1 |
T |
A |
2: 26,369,895 (GRCm39) |
I477L |
probably damaging |
Het |
Odad2 |
T |
A |
18: 7,217,846 (GRCm39) |
K623* |
probably null |
Het |
Or1l4b |
G |
A |
2: 37,037,047 (GRCm39) |
M274I |
probably benign |
Het |
Or1s2 |
T |
C |
19: 13,758,333 (GRCm39) |
V117A |
probably benign |
Het |
Or4a2 |
A |
T |
2: 89,248,712 (GRCm39) |
L15Q |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,320,124 (GRCm39) |
N38I |
probably damaging |
Het |
Or6c214 |
A |
G |
10: 129,591,148 (GRCm39) |
M57T |
probably damaging |
Het |
Pak5 |
A |
T |
2: 135,958,688 (GRCm39) |
S133R |
probably damaging |
Het |
Pcyt1a |
C |
A |
16: 32,285,332 (GRCm39) |
D187E |
probably benign |
Het |
Pdlim7 |
G |
T |
13: 55,655,354 (GRCm39) |
T161K |
probably damaging |
Het |
Phf8-ps |
A |
C |
17: 33,286,701 (GRCm39) |
C34G |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,547,108 (GRCm39) |
K962R |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,759,433 (GRCm39) |
K1516E |
probably damaging |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Ptchd3 |
A |
T |
11: 121,733,180 (GRCm39) |
Y690F |
probably benign |
Het |
Ptpn13 |
A |
T |
5: 103,649,735 (GRCm39) |
R379S |
possibly damaging |
Het |
Rbm27 |
C |
T |
18: 42,438,829 (GRCm39) |
A410V |
probably benign |
Het |
Rnase4 |
A |
G |
14: 51,342,662 (GRCm39) |
T129A |
probably benign |
Het |
Serpinb11 |
C |
T |
1: 107,304,533 (GRCm39) |
T166I |
probably benign |
Het |
Shank2 |
A |
G |
7: 143,963,705 (GRCm39) |
T438A |
possibly damaging |
Het |
Slc13a2 |
T |
C |
11: 78,295,258 (GRCm39) |
N172D |
probably damaging |
Het |
Slc2a8 |
A |
G |
2: 32,864,864 (GRCm39) |
F428L |
probably damaging |
Het |
Slc38a6 |
T |
C |
12: 73,398,544 (GRCm39) |
M358T |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,213,155 (GRCm39) |
H107R |
probably benign |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Spint3 |
G |
A |
2: 164,415,154 (GRCm39) |
A21V |
probably benign |
Het |
Susd1 |
A |
T |
4: 59,412,226 (GRCm39) |
V162E |
probably benign |
Het |
Syne2 |
T |
G |
12: 75,977,834 (GRCm39) |
N1426K |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,067,875 (GRCm39) |
V638A |
possibly damaging |
Het |
Trim36 |
G |
A |
18: 46,300,580 (GRCm39) |
S697L |
possibly damaging |
Het |
Ttbk1 |
A |
T |
17: 46,781,517 (GRCm39) |
I412N |
possibly damaging |
Het |
Tubb2a |
T |
C |
13: 34,258,578 (GRCm39) |
D404G |
probably damaging |
Het |
Tyk2 |
T |
A |
9: 21,035,841 (GRCm39) |
N114Y |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,185,678 (GRCm39) |
D139G |
probably damaging |
Het |
Vmn2r101 |
T |
A |
17: 19,810,244 (GRCm39) |
N343K |
probably benign |
Het |
Vnn1 |
A |
G |
10: 23,780,464 (GRCm39) |
D484G |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,770,919 (GRCm39) |
T2121A |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,345,216 (GRCm39) |
E17G |
probably benign |
Het |
Wnk2 |
T |
G |
13: 49,224,505 (GRCm39) |
K1117Q |
probably benign |
Het |
Zbtb46 |
C |
T |
2: 181,066,138 (GRCm39) |
R4Q |
probably benign |
Het |
Zfp608 |
T |
A |
18: 55,032,190 (GRCm39) |
K583N |
probably damaging |
Het |
Zfp729b |
A |
T |
13: 67,740,480 (GRCm39) |
L595H |
probably damaging |
Het |
|
Other mutations in Thada |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Thada
|
APN |
17 |
84,751,646 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00902:Thada
|
APN |
17 |
84,755,404 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01634:Thada
|
APN |
17 |
84,700,786 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01689:Thada
|
APN |
17 |
84,754,116 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01693:Thada
|
APN |
17 |
84,754,072 (GRCm39) |
missense |
probably benign |
|
IGL01937:Thada
|
APN |
17 |
84,530,194 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01945:Thada
|
APN |
17 |
84,530,194 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02231:Thada
|
APN |
17 |
84,736,125 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Thada
|
APN |
17 |
84,751,456 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03167:Thada
|
APN |
17 |
84,766,277 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03279:Thada
|
APN |
17 |
84,742,988 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03347:Thada
|
APN |
17 |
84,705,633 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Thada
|
UTSW |
17 |
84,753,972 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03098:Thada
|
UTSW |
17 |
84,641,569 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0006:Thada
|
UTSW |
17 |
84,533,468 (GRCm39) |
missense |
probably benign |
0.00 |
R0052:Thada
|
UTSW |
17 |
84,762,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R0052:Thada
|
UTSW |
17 |
84,762,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R0357:Thada
|
UTSW |
17 |
84,538,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Thada
|
UTSW |
17 |
84,538,524 (GRCm39) |
missense |
probably benign |
0.00 |
R0543:Thada
|
UTSW |
17 |
84,730,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Thada
|
UTSW |
17 |
84,723,731 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0630:Thada
|
UTSW |
17 |
84,536,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0664:Thada
|
UTSW |
17 |
84,644,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R0855:Thada
|
UTSW |
17 |
84,744,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Thada
|
UTSW |
17 |
84,736,490 (GRCm39) |
splice site |
probably benign |
|
R1297:Thada
|
UTSW |
17 |
84,559,863 (GRCm39) |
splice site |
probably benign |
|
R1465:Thada
|
UTSW |
17 |
84,744,104 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1465:Thada
|
UTSW |
17 |
84,744,104 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1490:Thada
|
UTSW |
17 |
84,754,029 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1789:Thada
|
UTSW |
17 |
84,755,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Thada
|
UTSW |
17 |
84,755,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R1802:Thada
|
UTSW |
17 |
84,771,835 (GRCm39) |
missense |
probably benign |
0.34 |
R1831:Thada
|
UTSW |
17 |
84,538,542 (GRCm39) |
missense |
probably damaging |
0.97 |
R1834:Thada
|
UTSW |
17 |
84,533,432 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1881:Thada
|
UTSW |
17 |
84,744,130 (GRCm39) |
missense |
probably benign |
0.19 |
R1925:Thada
|
UTSW |
17 |
84,751,927 (GRCm39) |
missense |
probably benign |
0.05 |
R1969:Thada
|
UTSW |
17 |
84,617,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Thada
|
UTSW |
17 |
84,617,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Thada
|
UTSW |
17 |
84,617,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Thada
|
UTSW |
17 |
84,749,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Thada
|
UTSW |
17 |
84,753,949 (GRCm39) |
missense |
probably benign |
0.00 |
R2571:Thada
|
UTSW |
17 |
84,762,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R3405:Thada
|
UTSW |
17 |
84,538,213 (GRCm39) |
splice site |
probably benign |
|
R3406:Thada
|
UTSW |
17 |
84,538,213 (GRCm39) |
splice site |
probably benign |
|
R3916:Thada
|
UTSW |
17 |
84,749,210 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4044:Thada
|
UTSW |
17 |
84,749,135 (GRCm39) |
missense |
probably benign |
0.41 |
R4461:Thada
|
UTSW |
17 |
84,733,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Thada
|
UTSW |
17 |
84,743,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R4696:Thada
|
UTSW |
17 |
84,733,614 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4786:Thada
|
UTSW |
17 |
84,766,283 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4803:Thada
|
UTSW |
17 |
84,580,245 (GRCm39) |
missense |
probably damaging |
0.96 |
R4835:Thada
|
UTSW |
17 |
84,748,532 (GRCm39) |
splice site |
probably null |
|
R4872:Thada
|
UTSW |
17 |
84,754,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4898:Thada
|
UTSW |
17 |
84,755,470 (GRCm39) |
splice site |
probably null |
|
R4903:Thada
|
UTSW |
17 |
84,559,828 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4929:Thada
|
UTSW |
17 |
84,751,654 (GRCm39) |
missense |
probably benign |
0.01 |
R4959:Thada
|
UTSW |
17 |
84,751,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Thada
|
UTSW |
17 |
84,693,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Thada
|
UTSW |
17 |
84,751,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R5398:Thada
|
UTSW |
17 |
84,733,614 (GRCm39) |
missense |
probably benign |
0.03 |
R5480:Thada
|
UTSW |
17 |
84,739,682 (GRCm39) |
missense |
probably benign |
0.00 |
R5552:Thada
|
UTSW |
17 |
84,736,558 (GRCm39) |
missense |
probably benign |
0.03 |
R5575:Thada
|
UTSW |
17 |
84,723,827 (GRCm39) |
splice site |
probably null |
|
R5623:Thada
|
UTSW |
17 |
84,499,411 (GRCm39) |
missense |
probably benign |
0.00 |
R5688:Thada
|
UTSW |
17 |
84,759,155 (GRCm39) |
missense |
probably benign |
0.00 |
R5704:Thada
|
UTSW |
17 |
84,538,329 (GRCm39) |
missense |
probably benign |
0.01 |
R6008:Thada
|
UTSW |
17 |
84,744,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Thada
|
UTSW |
17 |
84,580,228 (GRCm39) |
missense |
probably benign |
0.00 |
R6072:Thada
|
UTSW |
17 |
84,499,434 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6156:Thada
|
UTSW |
17 |
84,700,795 (GRCm39) |
missense |
probably damaging |
0.98 |
R6243:Thada
|
UTSW |
17 |
84,744,030 (GRCm39) |
missense |
probably benign |
0.01 |
R6449:Thada
|
UTSW |
17 |
84,736,601 (GRCm39) |
missense |
probably benign |
|
R6453:Thada
|
UTSW |
17 |
84,723,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R6474:Thada
|
UTSW |
17 |
84,751,339 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6732:Thada
|
UTSW |
17 |
84,761,842 (GRCm39) |
splice site |
probably null |
|
R6907:Thada
|
UTSW |
17 |
84,700,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Thada
|
UTSW |
17 |
84,538,214 (GRCm39) |
splice site |
probably null |
|
R7167:Thada
|
UTSW |
17 |
84,538,391 (GRCm39) |
missense |
probably benign |
|
R7221:Thada
|
UTSW |
17 |
84,771,794 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7470:Thada
|
UTSW |
17 |
84,533,469 (GRCm39) |
missense |
probably benign |
|
R7753:Thada
|
UTSW |
17 |
84,559,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7809:Thada
|
UTSW |
17 |
84,759,265 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7882:Thada
|
UTSW |
17 |
84,736,624 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7971:Thada
|
UTSW |
17 |
84,580,197 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8004:Thada
|
UTSW |
17 |
84,499,633 (GRCm39) |
missense |
probably benign |
|
R8153:Thada
|
UTSW |
17 |
84,700,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8254:Thada
|
UTSW |
17 |
84,533,468 (GRCm39) |
missense |
probably benign |
0.00 |
R8426:Thada
|
UTSW |
17 |
84,530,131 (GRCm39) |
missense |
probably benign |
0.17 |
R8438:Thada
|
UTSW |
17 |
84,743,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R8670:Thada
|
UTSW |
17 |
84,739,774 (GRCm39) |
missense |
probably benign |
0.16 |
R8679:Thada
|
UTSW |
17 |
84,536,637 (GRCm39) |
missense |
probably benign |
0.28 |
R8952:Thada
|
UTSW |
17 |
84,736,524 (GRCm39) |
missense |
probably benign |
0.01 |
R8983:Thada
|
UTSW |
17 |
84,538,515 (GRCm39) |
missense |
probably benign |
0.00 |
R9009:Thada
|
UTSW |
17 |
84,759,203 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9050:Thada
|
UTSW |
17 |
84,736,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R9225:Thada
|
UTSW |
17 |
84,749,172 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9251:Thada
|
UTSW |
17 |
84,538,564 (GRCm39) |
missense |
probably benign |
0.00 |
R9270:Thada
|
UTSW |
17 |
84,538,589 (GRCm39) |
missense |
probably damaging |
0.96 |
R9299:Thada
|
UTSW |
17 |
84,749,205 (GRCm39) |
missense |
probably benign |
0.01 |
R9337:Thada
|
UTSW |
17 |
84,749,205 (GRCm39) |
missense |
probably benign |
0.01 |
R9360:Thada
|
UTSW |
17 |
84,499,410 (GRCm39) |
missense |
probably benign |
|
R9416:Thada
|
UTSW |
17 |
84,766,292 (GRCm39) |
nonsense |
probably null |
|
R9484:Thada
|
UTSW |
17 |
84,736,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R9584:Thada
|
UTSW |
17 |
84,733,605 (GRCm39) |
missense |
probably benign |
|
R9631:Thada
|
UTSW |
17 |
84,538,584 (GRCm39) |
missense |
probably benign |
0.17 |
Z1176:Thada
|
UTSW |
17 |
84,751,858 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
Predicted Primers |
PCR Primer
(F):5'- CTGCCCTTTAGCTTCAGCAAG -3'
(R):5'- AGAGCCTCTGGTGCATTACAG -3'
Sequencing Primer
(F):5'- TTCAGCAAGCGACGCCC -3'
(R):5'- AGGAGCCCATTTTCTGAG -3'
|
Posted On |
2021-12-30 |