Incidental Mutation 'IGL00089:St18'
| ID |
2015 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
St18
|
| Ensembl Gene |
ENSMUSG00000033740 |
| Gene Name |
suppression of tumorigenicity 18 |
| Synonyms |
Nzf3, Myt3 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL00089
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
6557455-6931164 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 6872796 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 177
(D177G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118129
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043578]
[ENSMUST00000131494]
[ENSMUST00000139838]
[ENSMUST00000140079]
[ENSMUST00000150761]
[ENSMUST00000151281]
[ENSMUST00000163727]
|
| AlphaFold |
Q80TY4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043578
AA Change: D177G
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000042056
Gene: ENSMUSG00000033740
AA Change: D177G
| 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 benign
Transcript: ENSMUST00000131494
AA Change: D177G
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000117789
Gene: ENSMUSG00000033740
AA Change: D177G
| 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 benign
Transcript: ENSMUST00000132207
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000139838
AA Change: D177G
PolyPhen 2
Score 0.073 (Sensitivity: 0.93; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000118129
Gene: ENSMUSG00000033740
AA Change: D177G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
188 |
198 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140079
AA Change: D177G
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000118322
Gene: ENSMUSG00000033740
AA Change: D177G
| 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 benign
Transcript: ENSMUST00000150761
AA Change: D177G
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000120298
Gene: ENSMUSG00000033740
AA Change: D177G
| 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 benign
Transcript: ENSMUST00000151281
AA Change: D177G
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000122055
Gene: ENSMUSG00000033740
AA Change: D177G
| 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 benign
Transcript: ENSMUST00000163727
AA Change: D177G
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000131417
Gene: ENSMUSG00000033740
AA Change: D177G
| 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 |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A430033K04Rik |
T |
C |
5: 138,645,854 (GRCm39) |
S580P |
probably damaging |
Het |
| Abca12 |
T |
A |
1: 71,342,700 (GRCm39) |
I927F |
possibly damaging |
Het |
| Abca8a |
A |
G |
11: 109,941,765 (GRCm39) |
V1168A |
possibly damaging |
Het |
| Abcc1 |
T |
A |
16: 14,278,847 (GRCm39) |
N1052K |
probably benign |
Het |
| Adamts13 |
C |
A |
2: 26,895,373 (GRCm39) |
Q1155K |
probably benign |
Het |
| Adgre4 |
A |
T |
17: 56,098,915 (GRCm39) |
|
probably benign |
Het |
| Ahsa2 |
T |
C |
11: 23,446,837 (GRCm39) |
E42G |
probably damaging |
Het |
| Ankk1 |
T |
G |
9: 49,333,200 (GRCm39) |
I95L |
probably benign |
Het |
| Anpep |
A |
T |
7: 79,491,734 (GRCm39) |
L89Q |
probably damaging |
Het |
| Arl5a |
T |
C |
2: 52,306,083 (GRCm39) |
N83S |
probably benign |
Het |
| Atp11b |
A |
G |
3: 35,863,525 (GRCm39) |
|
probably null |
Het |
| Atp6v0a2 |
T |
C |
5: 124,798,841 (GRCm39) |
F849L |
probably benign |
Het |
| BC106179 |
A |
G |
16: 23,043,022 (GRCm39) |
|
probably benign |
Het |
| Bcl2a1c |
T |
C |
9: 114,159,608 (GRCm39) |
*129Q |
probably null |
Het |
| C2cd5 |
T |
C |
6: 142,963,671 (GRCm39) |
I888V |
probably null |
Het |
| Calb2 |
A |
T |
8: 110,872,303 (GRCm39) |
L227Q |
probably damaging |
Het |
| Ccp110 |
G |
T |
7: 118,321,647 (GRCm39) |
C434F |
possibly damaging |
Het |
| Cd209c |
A |
T |
8: 3,990,339 (GRCm39) |
C160S |
probably damaging |
Het |
| Chmp1a |
A |
G |
8: 123,935,758 (GRCm39) |
|
probably null |
Het |
| Col6a6 |
T |
A |
9: 105,635,390 (GRCm39) |
|
probably null |
Het |
| Cyld |
T |
A |
8: 89,432,085 (GRCm39) |
C28S |
probably benign |
Het |
| Dapk1 |
A |
T |
13: 60,908,854 (GRCm39) |
I1156F |
probably benign |
Het |
| Dennd1a |
A |
T |
2: 38,133,454 (GRCm39) |
Y16* |
probably null |
Het |
| Dennd3 |
T |
G |
15: 73,438,982 (GRCm39) |
S1117A |
probably benign |
Het |
| Dgka |
A |
T |
10: 128,568,955 (GRCm39) |
D203E |
probably damaging |
Het |
| Dhx15 |
G |
T |
5: 52,324,117 (GRCm39) |
L392I |
probably damaging |
Het |
| Dnah10 |
A |
G |
5: 124,823,680 (GRCm39) |
D567G |
probably benign |
Het |
| Eaf1 |
T |
A |
14: 31,226,483 (GRCm39) |
|
probably null |
Het |
| Efnb2 |
T |
C |
8: 8,710,589 (GRCm39) |
D9G |
probably benign |
Het |
| Fcrla |
A |
T |
1: 170,755,067 (GRCm39) |
C15S |
probably benign |
Het |
| Flt3 |
T |
C |
5: 147,291,686 (GRCm39) |
N588S |
probably damaging |
Het |
| Garre1 |
A |
T |
7: 33,945,412 (GRCm39) |
|
probably benign |
Het |
| Gm10146 |
A |
T |
10: 78,229,307 (GRCm39) |
|
noncoding transcript |
Het |
| Gnpat |
T |
C |
8: 125,603,653 (GRCm39) |
|
probably benign |
Het |
| Golm2 |
T |
C |
2: 121,741,274 (GRCm39) |
|
probably benign |
Het |
| Gpr39 |
A |
C |
1: 125,800,468 (GRCm39) |
R406S |
probably benign |
Het |
| H2-Aa |
T |
C |
17: 34,503,504 (GRCm39) |
H31R |
probably damaging |
Het |
| Helz2 |
G |
T |
2: 180,871,495 (GRCm39) |
R2706S |
probably damaging |
Het |
| Hip1r |
T |
A |
5: 124,127,798 (GRCm39) |
|
probably null |
Het |
| Hnf4g |
A |
G |
3: 3,713,142 (GRCm39) |
T239A |
probably benign |
Het |
| Hps5 |
A |
T |
7: 46,425,362 (GRCm39) |
I413N |
probably damaging |
Het |
| Hspg2 |
G |
A |
4: 137,256,131 (GRCm39) |
G1413R |
probably damaging |
Het |
| Itgax |
T |
G |
7: 127,734,498 (GRCm39) |
M352R |
probably damaging |
Het |
| Katna1 |
T |
A |
10: 7,638,568 (GRCm39) |
M433K |
probably damaging |
Het |
| Kcna4 |
T |
G |
2: 107,126,207 (GRCm39) |
S314A |
probably damaging |
Het |
| Kif13b |
C |
T |
14: 64,907,142 (GRCm39) |
T42I |
possibly damaging |
Het |
| Krt78 |
G |
A |
15: 101,855,945 (GRCm39) |
T622I |
probably benign |
Het |
| Krt86 |
T |
A |
15: 101,374,396 (GRCm39) |
M263K |
possibly damaging |
Het |
| Lap3 |
A |
G |
5: 45,663,511 (GRCm39) |
|
probably benign |
Het |
| Lepr |
A |
T |
4: 101,672,232 (GRCm39) |
R1085S |
probably benign |
Het |
| Lmcd1 |
A |
G |
6: 112,306,769 (GRCm39) |
I314V |
probably benign |
Het |
| Luc7l2 |
T |
C |
6: 38,585,105 (GRCm39) |
|
probably benign |
Het |
| Mcm2 |
T |
A |
6: 88,870,383 (GRCm39) |
M117L |
probably benign |
Het |
| Mdh2 |
T |
C |
5: 135,815,138 (GRCm39) |
Y133H |
probably damaging |
Het |
| Minar1 |
C |
T |
9: 89,483,853 (GRCm39) |
V515I |
probably benign |
Het |
| Mlkl |
T |
A |
8: 112,046,060 (GRCm39) |
R317* |
probably null |
Het |
| Mrps34 |
T |
C |
17: 25,114,344 (GRCm39) |
L68P |
probably damaging |
Het |
| Muc4 |
G |
A |
16: 32,754,086 (GRCm38) |
G1321R |
probably benign |
Het |
| Myo18a |
A |
G |
11: 77,738,764 (GRCm39) |
E1299G |
probably damaging |
Het |
| Nlrp14 |
T |
C |
7: 106,791,709 (GRCm39) |
L139P |
possibly damaging |
Het |
| Nudcd2 |
A |
G |
11: 40,627,413 (GRCm39) |
D86G |
probably damaging |
Het |
| Or10u4 |
T |
A |
10: 129,801,673 (GRCm39) |
R293W |
probably damaging |
Het |
| Or4c107 |
T |
A |
2: 88,789,110 (GRCm39) |
I100N |
probably damaging |
Het |
| Or4f62 |
A |
T |
2: 111,986,412 (GRCm39) |
M39L |
probably benign |
Het |
| Patj |
T |
C |
4: 98,353,343 (GRCm39) |
F629L |
probably damaging |
Het |
| Rad23a |
A |
G |
8: 85,562,524 (GRCm39) |
F280L |
probably damaging |
Het |
| Ralgapa1 |
C |
A |
12: 55,769,558 (GRCm39) |
G811V |
probably damaging |
Het |
| Sult1c2 |
A |
C |
17: 54,140,147 (GRCm39) |
Y159* |
probably null |
Het |
| Surf6 |
T |
A |
2: 26,783,081 (GRCm39) |
|
probably null |
Het |
| Susd6 |
T |
G |
12: 80,916,841 (GRCm39) |
|
probably benign |
Het |
| Sypl2 |
G |
A |
3: 108,133,742 (GRCm39) |
|
probably benign |
Het |
| Ubr5 |
A |
T |
15: 37,984,280 (GRCm39) |
F2289Y |
probably damaging |
Het |
| Vcl |
T |
C |
14: 21,037,071 (GRCm39) |
I223T |
probably benign |
Het |
| Vmn1r234 |
C |
T |
17: 21,449,860 (GRCm39) |
T258I |
possibly damaging |
Het |
| Vmn2r58 |
T |
A |
7: 41,513,854 (GRCm39) |
K263M |
possibly damaging |
Het |
| Vmo1 |
A |
T |
11: 70,404,424 (GRCm39) |
N192K |
probably damaging |
Het |
| Wrnip1 |
A |
G |
13: 33,000,312 (GRCm39) |
N440D |
probably damaging |
Het |
| Zc3h4 |
T |
C |
7: 16,156,159 (GRCm39) |
Y264H |
unknown |
Het |
| Zfp639 |
T |
G |
3: 32,573,902 (GRCm39) |
|
probably null |
Het |
| Zfp831 |
T |
C |
2: 174,488,078 (GRCm39) |
Y918H |
possibly damaging |
Het |
|
| Other mutations in St18 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
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 |
|
R7098:St18
|
UTSW |
1 |
6,898,066 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
|
| Posted On |
2011-07-12 |
Incidental Mutation