Incidental Mutation 'R7098:St18'
ID |
550602 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
St18
|
Ensembl Gene |
ENSMUSG00000033740 |
Gene Name |
suppression of tumorigenicity 18 |
Synonyms |
Nzf3, Myt3 |
MMRRC Submission |
045190-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7098 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
6557455-6931164 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 6898066 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Asparagine
at position 623
(D623N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000042056
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043578]
[ENSMUST00000131494]
[ENSMUST00000140079]
[ENSMUST00000150761]
[ENSMUST00000151281]
[ENSMUST00000163727]
|
AlphaFold |
Q80TY4 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000043578
AA Change: D623N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000042056 Gene: ENSMUSG00000033740 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
Pfam:zf-C2HC
|
365 |
392 |
7.8e-15 |
PFAM |
Pfam:zf-C2HC
|
409 |
437 |
4.2e-17 |
PFAM |
Pfam:MYT1
|
476 |
713 |
1.3e-75 |
PFAM |
Pfam:zf-C2HC
|
721 |
749 |
4e-19 |
PFAM |
Pfam:zf-C2HC
|
765 |
793 |
1.7e-19 |
PFAM |
Pfam:zf-C2HC
|
813 |
841 |
1.1e-17 |
PFAM |
Pfam:zf-C2HC
|
866 |
893 |
9.1e-15 |
PFAM |
coiled coil region
|
918 |
987 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000131494
AA Change: D623N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000117789 Gene: ENSMUSG00000033740 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
Pfam:zf-C2HC
|
363 |
393 |
2.6e-17 |
PFAM |
Pfam:zf-C2HC
|
407 |
437 |
1e-18 |
PFAM |
Pfam:MYT1
|
476 |
714 |
1.5e-116 |
PFAM |
Pfam:zf-C2HC
|
719 |
749 |
1e-19 |
PFAM |
Pfam:zf-C2HC
|
763 |
793 |
1.3e-20 |
PFAM |
Pfam:zf-C2HC
|
811 |
841 |
8.9e-19 |
PFAM |
Pfam:zf-C2HC
|
864 |
894 |
1.3e-16 |
PFAM |
coiled coil region
|
918 |
987 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000140079
AA Change: D623N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000118322 Gene: ENSMUSG00000033740 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
Pfam:zf-C2HC
|
363 |
393 |
2.6e-17 |
PFAM |
Pfam:zf-C2HC
|
407 |
437 |
1e-18 |
PFAM |
Pfam:MYT1
|
476 |
714 |
1.5e-116 |
PFAM |
Pfam:zf-C2HC
|
719 |
749 |
1e-19 |
PFAM |
Pfam:zf-C2HC
|
763 |
793 |
1.3e-20 |
PFAM |
Pfam:zf-C2HC
|
811 |
841 |
8.9e-19 |
PFAM |
Pfam:zf-C2HC
|
864 |
894 |
1.3e-16 |
PFAM |
coiled coil region
|
918 |
987 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000150761
AA Change: D623N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000120298 Gene: ENSMUSG00000033740 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
Pfam:zf-C2HC
|
363 |
393 |
2.6e-17 |
PFAM |
Pfam:zf-C2HC
|
407 |
437 |
1e-18 |
PFAM |
Pfam:MYT1
|
476 |
714 |
1.5e-116 |
PFAM |
Pfam:zf-C2HC
|
719 |
749 |
1e-19 |
PFAM |
Pfam:zf-C2HC
|
763 |
793 |
1.3e-20 |
PFAM |
Pfam:zf-C2HC
|
811 |
841 |
8.9e-19 |
PFAM |
Pfam:zf-C2HC
|
864 |
894 |
1.3e-16 |
PFAM |
coiled coil region
|
918 |
987 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000151281
AA Change: D623N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000122055 Gene: ENSMUSG00000033740 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
Pfam:zf-C2HC
|
363 |
393 |
2.6e-17 |
PFAM |
Pfam:zf-C2HC
|
407 |
437 |
1e-18 |
PFAM |
Pfam:MYT1
|
476 |
714 |
1.5e-116 |
PFAM |
Pfam:zf-C2HC
|
719 |
749 |
1e-19 |
PFAM |
Pfam:zf-C2HC
|
763 |
793 |
1.3e-20 |
PFAM |
Pfam:zf-C2HC
|
811 |
841 |
8.9e-19 |
PFAM |
Pfam:zf-C2HC
|
864 |
894 |
1.3e-16 |
PFAM |
coiled coil region
|
918 |
987 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000163727
AA Change: D623N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000131417 Gene: ENSMUSG00000033740 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
Pfam:zf-C2HC
|
365 |
392 |
7.8e-15 |
PFAM |
Pfam:zf-C2HC
|
409 |
437 |
4.2e-17 |
PFAM |
Pfam:MYT1
|
476 |
713 |
1.3e-75 |
PFAM |
Pfam:zf-C2HC
|
721 |
749 |
4e-19 |
PFAM |
Pfam:zf-C2HC
|
765 |
793 |
1.7e-19 |
PFAM |
Pfam:zf-C2HC
|
813 |
841 |
1.1e-17 |
PFAM |
Pfam:zf-C2HC
|
866 |
893 |
9.1e-15 |
PFAM |
coiled coil region
|
918 |
987 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
100% (78/78) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
T |
A |
5: 138,644,784 (GRCm39) |
M223K |
probably benign |
Het |
Abce1 |
T |
C |
8: 80,412,678 (GRCm39) |
T550A |
probably benign |
Het |
Acoxl |
C |
T |
2: 127,696,835 (GRCm39) |
Q28* |
probably null |
Het |
Adam8 |
T |
C |
7: 139,559,412 (GRCm39) |
K820R |
possibly damaging |
Het |
Adamts3 |
G |
T |
5: 90,009,354 (GRCm39) |
A103D |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,386,696 (GRCm39) |
V441D |
probably damaging |
Het |
Arap2 |
A |
G |
5: 62,833,293 (GRCm39) |
|
probably null |
Het |
Arhgef10l |
T |
A |
4: 140,308,222 (GRCm39) |
M44L |
probably benign |
Het |
Asb4 |
T |
C |
6: 5,398,499 (GRCm39) |
C155R |
probably damaging |
Het |
Bpifb6 |
A |
T |
2: 153,748,810 (GRCm39) |
K269* |
probably null |
Het |
Cc2d2a |
A |
T |
5: 43,840,481 (GRCm39) |
T161S |
probably benign |
Het |
Ccdc15 |
T |
A |
9: 37,255,256 (GRCm39) |
Q98L |
probably damaging |
Het |
Col19a1 |
A |
G |
1: 24,565,555 (GRCm39) |
S259P |
unknown |
Het |
Col5a2 |
A |
T |
1: 45,419,227 (GRCm39) |
D1284E |
possibly damaging |
Het |
Cyp2c70 |
T |
C |
19: 40,168,931 (GRCm39) |
T119A |
probably benign |
Het |
Dennd6b |
C |
T |
15: 89,072,890 (GRCm39) |
C188Y |
probably damaging |
Het |
Dhx8 |
T |
A |
11: 101,628,594 (GRCm39) |
|
probably null |
Het |
Dhx9 |
T |
C |
1: 153,340,768 (GRCm39) |
K624R |
probably benign |
Het |
Dpys |
C |
T |
15: 39,656,727 (GRCm39) |
V447M |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,753,004 (GRCm39) |
S706P |
possibly damaging |
Het |
Esrrb |
A |
G |
12: 86,517,189 (GRCm39) |
D107G |
probably benign |
Het |
Frmd4a |
T |
C |
2: 4,577,244 (GRCm39) |
S367P |
probably damaging |
Het |
Garin2 |
G |
A |
12: 78,766,408 (GRCm39) |
|
probably null |
Het |
Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
Gm136 |
T |
C |
4: 34,746,628 (GRCm39) |
I128V |
probably benign |
Het |
Gm6525 |
T |
A |
3: 84,082,309 (GRCm39) |
C77S |
possibly damaging |
Het |
Grid2ip |
T |
C |
5: 143,343,346 (GRCm39) |
F14S |
probably damaging |
Het |
Hdhd3 |
C |
T |
4: 62,418,152 (GRCm39) |
R8H |
probably damaging |
Het |
Kdelr1 |
C |
A |
7: 45,523,480 (GRCm39) |
A69D |
possibly damaging |
Het |
Krtap16-3 |
T |
A |
16: 88,759,560 (GRCm39) |
Y51F |
unknown |
Het |
Lrrc40 |
T |
A |
3: 157,747,276 (GRCm39) |
N129K |
probably benign |
Het |
Man1b1 |
T |
A |
2: 25,228,196 (GRCm39) |
D155E |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,847,529 (GRCm39) |
V442A |
probably damaging |
Het |
Mfsd14a |
C |
T |
3: 116,435,361 (GRCm39) |
A235T |
probably benign |
Het |
Mmp1a |
C |
A |
9: 7,475,938 (GRCm39) |
T401K |
probably benign |
Het |
Mpig6b |
C |
T |
17: 35,283,320 (GRCm39) |
R196Q |
unknown |
Het |
Mroh1 |
C |
T |
15: 76,292,657 (GRCm39) |
Q262* |
probably null |
Het |
Msh3 |
A |
T |
13: 92,410,619 (GRCm39) |
D656E |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,577,465 (GRCm39) |
T252S |
|
Het |
Myh15 |
C |
T |
16: 48,997,420 (GRCm39) |
A1746V |
possibly damaging |
Het |
Myh8 |
C |
A |
11: 67,169,879 (GRCm39) |
T66K |
probably benign |
Het |
Nemf |
A |
T |
12: 69,359,241 (GRCm39) |
Y999N |
probably damaging |
Het |
Neurod1 |
T |
C |
2: 79,285,029 (GRCm39) |
N118S |
probably damaging |
Het |
Nlrp1b |
T |
A |
11: 71,109,100 (GRCm39) |
I134L |
possibly damaging |
Het |
Nsun7 |
A |
T |
5: 66,418,326 (GRCm39) |
I19F |
probably damaging |
Het |
Ofcc1 |
A |
G |
13: 40,157,442 (GRCm39) |
|
probably null |
Het |
P2rx7 |
A |
G |
5: 122,811,856 (GRCm39) |
E389G |
probably damaging |
Het |
Pam |
C |
T |
1: 97,826,072 (GRCm39) |
R194H |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,220,673 (GRCm39) |
S2052P |
probably benign |
Het |
Pfkfb4 |
T |
A |
9: 108,828,222 (GRCm39) |
Y86N |
probably benign |
Het |
Plcd3 |
T |
A |
11: 102,968,689 (GRCm39) |
D334V |
probably damaging |
Het |
Ppard |
T |
C |
17: 28,517,787 (GRCm39) |
V285A |
possibly damaging |
Het |
Prune2 |
A |
G |
19: 17,097,966 (GRCm39) |
S1157G |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,386,470 (GRCm39) |
L172H |
probably damaging |
Het |
Psme4 |
C |
A |
11: 30,800,661 (GRCm39) |
T1417K |
probably damaging |
Het |
Ptprc |
T |
C |
1: 138,027,423 (GRCm39) |
D336G |
probably benign |
Het |
Ralgapa1 |
A |
T |
12: 55,837,095 (GRCm39) |
|
probably null |
Het |
Rap1gap |
C |
A |
4: 137,443,393 (GRCm39) |
|
probably null |
Het |
Scap |
T |
C |
9: 110,201,310 (GRCm39) |
S100P |
possibly damaging |
Het |
Scpep1 |
T |
C |
11: 88,820,011 (GRCm39) |
I426V |
possibly damaging |
Het |
Sdk1 |
T |
C |
5: 142,082,625 (GRCm39) |
I1341T |
probably damaging |
Het |
Sfmbt2 |
T |
A |
2: 10,584,000 (GRCm39) |
Y786N |
probably benign |
Het |
Sh3tc1 |
A |
T |
5: 35,859,358 (GRCm39) |
|
probably null |
Het |
Slc5a5 |
T |
A |
8: 71,341,182 (GRCm39) |
I386F |
probably damaging |
Het |
Smarca4 |
T |
G |
9: 21,546,116 (GRCm39) |
M98R |
probably benign |
Het |
Sult2a1 |
A |
T |
7: 13,549,978 (GRCm39) |
|
probably null |
Het |
Tgfb2 |
C |
T |
1: 186,362,834 (GRCm39) |
R330H |
probably damaging |
Het |
Thoc3 |
A |
G |
13: 54,614,119 (GRCm39) |
I168T |
probably damaging |
Het |
Tmem126a |
C |
T |
7: 90,100,062 (GRCm39) |
M160I |
possibly damaging |
Het |
Tmem200b |
C |
T |
4: 131,649,704 (GRCm39) |
P208L |
probably benign |
Het |
Tnrc6c |
T |
C |
11: 117,604,952 (GRCm39) |
V29A |
probably benign |
Het |
Tsc1 |
C |
T |
2: 28,565,744 (GRCm39) |
S465F |
probably benign |
Het |
Ttll5 |
A |
G |
12: 85,964,447 (GRCm39) |
|
probably null |
Het |
Unc13d |
G |
T |
11: 115,954,552 (GRCm39) |
L1019I |
probably damaging |
Het |
Vmn2r102 |
A |
T |
17: 19,914,670 (GRCm39) |
H745L |
probably damaging |
Het |
Wars2 |
T |
G |
3: 99,123,957 (GRCm39) |
S273A |
probably damaging |
Het |
Xrcc6 |
C |
A |
15: 81,919,955 (GRCm39) |
S498* |
probably null |
Het |
Ybx1 |
A |
T |
4: 119,140,050 (GRCm39) |
N92K |
possibly damaging |
Het |
|
Other mutations in St18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:St18
|
APN |
1 |
6,872,796 (GRCm39) |
missense |
probably benign |
0.07 |
IGL00840:St18
|
APN |
1 |
6,903,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01016:St18
|
APN |
1 |
6,914,547 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01116:St18
|
APN |
1 |
6,872,856 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01719:St18
|
APN |
1 |
6,916,020 (GRCm39) |
splice site |
probably benign |
|
IGL01885:St18
|
APN |
1 |
6,914,596 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02486:St18
|
APN |
1 |
6,890,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02611:St18
|
APN |
1 |
6,839,114 (GRCm39) |
splice site |
probably benign |
|
IGL02742:St18
|
APN |
1 |
6,872,540 (GRCm39) |
splice site |
probably benign |
|
IGL02953:St18
|
APN |
1 |
6,914,337 (GRCm39) |
splice site |
probably benign |
|
IGL02999:St18
|
APN |
1 |
6,887,829 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03092:St18
|
APN |
1 |
6,839,118 (GRCm39) |
splice site |
probably benign |
|
Smallish
|
UTSW |
1 |
6,925,697 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03055:St18
|
UTSW |
1 |
6,872,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0089:St18
|
UTSW |
1 |
6,919,172 (GRCm39) |
missense |
probably benign |
0.02 |
R0257:St18
|
UTSW |
1 |
6,890,186 (GRCm39) |
missense |
probably benign |
0.04 |
R0383:St18
|
UTSW |
1 |
6,873,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R0588:St18
|
UTSW |
1 |
6,887,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R0989:St18
|
UTSW |
1 |
6,898,105 (GRCm39) |
missense |
probably benign |
0.04 |
R1068:St18
|
UTSW |
1 |
6,865,786 (GRCm39) |
missense |
probably benign |
0.01 |
R1311:St18
|
UTSW |
1 |
6,915,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1530:St18
|
UTSW |
1 |
6,915,793 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1723:St18
|
UTSW |
1 |
6,880,909 (GRCm39) |
splice site |
probably benign |
|
R1926:St18
|
UTSW |
1 |
6,872,913 (GRCm39) |
missense |
probably benign |
0.00 |
R1927:St18
|
UTSW |
1 |
6,872,936 (GRCm39) |
missense |
probably benign |
0.00 |
R2035:St18
|
UTSW |
1 |
6,872,552 (GRCm39) |
missense |
probably benign |
0.00 |
R2091:St18
|
UTSW |
1 |
6,898,195 (GRCm39) |
missense |
probably benign |
0.08 |
R2139:St18
|
UTSW |
1 |
6,880,839 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2261:St18
|
UTSW |
1 |
6,915,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R2300:St18
|
UTSW |
1 |
6,925,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R2322:St18
|
UTSW |
1 |
6,914,348 (GRCm39) |
nonsense |
probably null |
|
R2846:St18
|
UTSW |
1 |
6,915,811 (GRCm39) |
missense |
probably damaging |
0.96 |
R3738:St18
|
UTSW |
1 |
6,925,697 (GRCm39) |
critical splice donor site |
probably null |
|
R3739:St18
|
UTSW |
1 |
6,925,697 (GRCm39) |
critical splice donor site |
probably null |
|
R3772:St18
|
UTSW |
1 |
6,914,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R3805:St18
|
UTSW |
1 |
6,872,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:St18
|
UTSW |
1 |
6,873,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R4034:St18
|
UTSW |
1 |
6,925,697 (GRCm39) |
critical splice donor site |
probably null |
|
R4036:St18
|
UTSW |
1 |
6,898,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R4407:St18
|
UTSW |
1 |
6,898,061 (GRCm39) |
missense |
probably benign |
0.29 |
R4527:St18
|
UTSW |
1 |
6,925,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R4740:St18
|
UTSW |
1 |
6,887,828 (GRCm39) |
missense |
probably benign |
|
R4838:St18
|
UTSW |
1 |
6,873,129 (GRCm39) |
missense |
probably benign |
0.01 |
R5182:St18
|
UTSW |
1 |
6,887,877 (GRCm39) |
missense |
probably benign |
0.03 |
R5186:St18
|
UTSW |
1 |
6,872,541 (GRCm39) |
splice site |
probably null |
|
R5354:St18
|
UTSW |
1 |
6,914,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:St18
|
UTSW |
1 |
6,872,840 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5724:St18
|
UTSW |
1 |
6,841,174 (GRCm39) |
missense |
probably benign |
0.13 |
R6182:St18
|
UTSW |
1 |
6,914,342 (GRCm39) |
splice site |
probably null |
|
R6491:St18
|
UTSW |
1 |
6,898,209 (GRCm39) |
nonsense |
probably null |
|
R6503:St18
|
UTSW |
1 |
6,865,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:St18
|
UTSW |
1 |
6,873,260 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7132:St18
|
UTSW |
1 |
6,929,351 (GRCm39) |
missense |
|
|
R7144:St18
|
UTSW |
1 |
6,903,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7150:St18
|
UTSW |
1 |
6,873,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R7334:St18
|
UTSW |
1 |
6,872,783 (GRCm39) |
missense |
probably benign |
0.00 |
R7502:St18
|
UTSW |
1 |
6,898,194 (GRCm39) |
missense |
probably benign |
0.09 |
R7729:St18
|
UTSW |
1 |
6,872,761 (GRCm39) |
missense |
probably benign |
0.00 |
R7848:St18
|
UTSW |
1 |
6,927,669 (GRCm39) |
critical splice donor site |
probably null |
|
R8088:St18
|
UTSW |
1 |
6,898,229 (GRCm39) |
missense |
probably benign |
0.00 |
R8299:St18
|
UTSW |
1 |
6,873,216 (GRCm39) |
missense |
probably benign |
0.01 |
R8338:St18
|
UTSW |
1 |
6,879,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:St18
|
UTSW |
1 |
6,872,788 (GRCm39) |
missense |
probably benign |
|
R8753:St18
|
UTSW |
1 |
6,916,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8808:St18
|
UTSW |
1 |
6,880,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:St18
|
UTSW |
1 |
6,865,619 (GRCm39) |
nonsense |
probably null |
|
R9055:St18
|
UTSW |
1 |
6,873,206 (GRCm39) |
nonsense |
probably null |
|
R9292:St18
|
UTSW |
1 |
6,898,106 (GRCm39) |
missense |
probably benign |
0.32 |
R9322:St18
|
UTSW |
1 |
6,865,747 (GRCm39) |
missense |
probably benign |
0.00 |
R9530:St18
|
UTSW |
1 |
6,872,997 (GRCm39) |
missense |
probably benign |
0.00 |
R9603:St18
|
UTSW |
1 |
6,915,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:St18
|
UTSW |
1 |
6,873,147 (GRCm39) |
missense |
probably benign |
0.00 |
R9639:St18
|
UTSW |
1 |
6,929,246 (GRCm39) |
missense |
|
|
R9644:St18
|
UTSW |
1 |
6,929,276 (GRCm39) |
missense |
|
|
R9740:St18
|
UTSW |
1 |
6,873,287 (GRCm39) |
nonsense |
probably null |
|
R9750:St18
|
UTSW |
1 |
6,873,216 (GRCm39) |
missense |
probably benign |
0.01 |
|
Predicted Primers |
|
Posted On |
2019-05-15 |