Incidental Mutation 'IGL02338:Asap1'
| ID |
288974 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Asap1
|
| Ensembl Gene |
ENSMUSG00000022377 |
| Gene Name |
ArfGAP with SH3 domain, ankyrin repeat and PH domain1 |
| Synonyms |
Ddef1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.114)
|
| Stock # |
IGL02338
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
15 |
| Chromosomal Location |
63958706-64254768 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to T
at 63995519 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134825
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023008]
[ENSMUST00000110114]
[ENSMUST00000110115]
[ENSMUST00000175793]
[ENSMUST00000175799]
[ENSMUST00000176014]
[ENSMUST00000176384]
[ENSMUST00000177035]
[ENSMUST00000177371]
[ENSMUST00000177083]
[ENSMUST00000177374]
|
| AlphaFold |
Q9QWY8 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000023008
|
| SMART Domains |
Protein: ENSMUSP00000023008
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
340 |
433 |
4.12e-15 |
SMART |
|
ArfGap
|
454 |
577 |
2.18e-34 |
SMART |
|
ANK
|
615 |
647 |
1.17e-1 |
SMART |
|
ANK
|
651 |
680 |
3.46e-4 |
SMART |
|
low complexity region
|
727 |
738 |
N/A |
INTRINSIC |
|
low complexity region
|
792 |
803 |
N/A |
INTRINSIC |
|
low complexity region
|
814 |
847 |
N/A |
INTRINSIC |
|
low complexity region
|
856 |
865 |
N/A |
INTRINSIC |
|
low complexity region
|
892 |
903 |
N/A |
INTRINSIC |
|
low complexity region
|
971 |
984 |
N/A |
INTRINSIC |
|
low complexity region
|
1065 |
1077 |
N/A |
INTRINSIC |
|
SH3
|
1088 |
1146 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000110114
|
| SMART Domains |
Protein: ENSMUSP00000105741
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
340 |
433 |
4.12e-15 |
SMART |
|
ArfGap
|
454 |
577 |
2.18e-34 |
SMART |
|
ANK
|
615 |
647 |
1.17e-1 |
SMART |
|
ANK
|
651 |
680 |
3.46e-4 |
SMART |
|
low complexity region
|
727 |
738 |
N/A |
INTRINSIC |
|
low complexity region
|
792 |
803 |
N/A |
INTRINSIC |
|
low complexity region
|
835 |
846 |
N/A |
INTRINSIC |
|
low complexity region
|
914 |
927 |
N/A |
INTRINSIC |
|
low complexity region
|
1008 |
1020 |
N/A |
INTRINSIC |
|
SH3
|
1031 |
1089 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000110115
|
| SMART Domains |
Protein: ENSMUSP00000105742
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
325 |
418 |
4.12e-15 |
SMART |
|
ArfGap
|
439 |
562 |
2.18e-34 |
SMART |
|
ANK
|
600 |
632 |
1.17e-1 |
SMART |
|
ANK
|
636 |
665 |
3.46e-4 |
SMART |
|
low complexity region
|
712 |
723 |
N/A |
INTRINSIC |
|
low complexity region
|
777 |
788 |
N/A |
INTRINSIC |
|
low complexity region
|
799 |
832 |
N/A |
INTRINSIC |
|
low complexity region
|
841 |
850 |
N/A |
INTRINSIC |
|
low complexity region
|
877 |
888 |
N/A |
INTRINSIC |
|
low complexity region
|
956 |
969 |
N/A |
INTRINSIC |
|
low complexity region
|
1050 |
1062 |
N/A |
INTRINSIC |
|
SH3
|
1073 |
1131 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000175793
|
| SMART Domains |
Protein: ENSMUSP00000135718
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
328 |
421 |
4.12e-15 |
SMART |
|
ArfGap
|
442 |
565 |
2.18e-34 |
SMART |
|
ANK
|
603 |
635 |
1.17e-1 |
SMART |
|
ANK
|
639 |
668 |
3.46e-4 |
SMART |
|
low complexity region
|
715 |
726 |
N/A |
INTRINSIC |
|
low complexity region
|
780 |
791 |
N/A |
INTRINSIC |
|
low complexity region
|
802 |
835 |
N/A |
INTRINSIC |
|
low complexity region
|
844 |
853 |
N/A |
INTRINSIC |
|
low complexity region
|
880 |
891 |
N/A |
INTRINSIC |
|
low complexity region
|
959 |
972 |
N/A |
INTRINSIC |
|
low complexity region
|
1053 |
1065 |
N/A |
INTRINSIC |
|
SH3
|
1076 |
1134 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000175799
|
| SMART Domains |
Protein: ENSMUSP00000135359
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
337 |
430 |
4.12e-15 |
SMART |
|
ArfGap
|
451 |
574 |
2.18e-34 |
SMART |
|
ANK
|
612 |
644 |
1.17e-1 |
SMART |
|
ANK
|
648 |
677 |
3.46e-4 |
SMART |
|
low complexity region
|
724 |
735 |
N/A |
INTRINSIC |
|
low complexity region
|
789 |
800 |
N/A |
INTRINSIC |
|
low complexity region
|
832 |
843 |
N/A |
INTRINSIC |
|
low complexity region
|
911 |
924 |
N/A |
INTRINSIC |
|
low complexity region
|
1005 |
1017 |
N/A |
INTRINSIC |
|
SH3
|
1028 |
1086 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000176014
|
| SMART Domains |
Protein: ENSMUSP00000135172
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
337 |
430 |
4.12e-15 |
SMART |
|
ArfGap
|
451 |
574 |
2.18e-34 |
SMART |
|
ANK
|
612 |
644 |
1.17e-1 |
SMART |
|
ANK
|
648 |
677 |
3.46e-4 |
SMART |
|
low complexity region
|
724 |
735 |
N/A |
INTRINSIC |
|
low complexity region
|
789 |
800 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
844 |
N/A |
INTRINSIC |
|
low complexity region
|
853 |
862 |
N/A |
INTRINSIC |
|
low complexity region
|
889 |
900 |
N/A |
INTRINSIC |
|
low complexity region
|
968 |
981 |
N/A |
INTRINSIC |
|
low complexity region
|
1062 |
1074 |
N/A |
INTRINSIC |
|
SH3
|
1085 |
1143 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000176384
|
| SMART Domains |
Protein: ENSMUSP00000135190
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
low complexity region
|
310 |
328 |
N/A |
INTRINSIC |
|
PH
|
340 |
433 |
4.12e-15 |
SMART |
|
ArfGap
|
454 |
577 |
2.18e-34 |
SMART |
|
ANK
|
615 |
647 |
1.17e-1 |
SMART |
|
ANK
|
651 |
680 |
3.46e-4 |
SMART |
|
low complexity region
|
727 |
738 |
N/A |
INTRINSIC |
|
low complexity region
|
792 |
803 |
N/A |
INTRINSIC |
|
low complexity region
|
835 |
846 |
N/A |
INTRINSIC |
|
low complexity region
|
914 |
927 |
N/A |
INTRINSIC |
|
low complexity region
|
1008 |
1020 |
N/A |
INTRINSIC |
|
SH3
|
1031 |
1089 |
3.29e-17 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177475
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000177035
|
| SMART Domains |
Protein: ENSMUSP00000135346
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
147 |
164 |
N/A |
INTRINSIC |
|
PH
|
325 |
418 |
4.12e-15 |
SMART |
|
ArfGap
|
439 |
562 |
2.18e-34 |
SMART |
|
ANK
|
600 |
632 |
1.17e-1 |
SMART |
|
ANK
|
636 |
665 |
3.46e-4 |
SMART |
|
low complexity region
|
712 |
723 |
N/A |
INTRINSIC |
|
low complexity region
|
777 |
788 |
N/A |
INTRINSIC |
|
low complexity region
|
820 |
831 |
N/A |
INTRINSIC |
|
low complexity region
|
899 |
912 |
N/A |
INTRINSIC |
|
low complexity region
|
993 |
1005 |
N/A |
INTRINSIC |
|
SH3
|
1016 |
1074 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000177371
|
| SMART Domains |
Protein: ENSMUSP00000135643
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
102 |
116 |
N/A |
INTRINSIC |
|
low complexity region
|
127 |
144 |
N/A |
INTRINSIC |
|
PH
|
317 |
410 |
4.12e-15 |
SMART |
|
ArfGap
|
431 |
554 |
2.18e-34 |
SMART |
|
ANK
|
592 |
624 |
1.17e-1 |
SMART |
|
ANK
|
628 |
657 |
3.46e-4 |
SMART |
|
low complexity region
|
704 |
715 |
N/A |
INTRINSIC |
|
low complexity region
|
769 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
791 |
824 |
N/A |
INTRINSIC |
|
low complexity region
|
833 |
842 |
N/A |
INTRINSIC |
|
low complexity region
|
869 |
880 |
N/A |
INTRINSIC |
|
low complexity region
|
948 |
961 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1054 |
N/A |
INTRINSIC |
|
SH3
|
1065 |
1123 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000177083
|
| SMART Domains |
Protein: ENSMUSP00000134877
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
102 |
116 |
N/A |
INTRINSIC |
|
low complexity region
|
127 |
144 |
N/A |
INTRINSIC |
|
PH
|
305 |
398 |
4.12e-15 |
SMART |
|
ArfGap
|
419 |
542 |
2.18e-34 |
SMART |
|
ANK
|
580 |
612 |
1.17e-1 |
SMART |
|
ANK
|
616 |
645 |
3.46e-4 |
SMART |
|
low complexity region
|
692 |
703 |
N/A |
INTRINSIC |
|
low complexity region
|
757 |
768 |
N/A |
INTRINSIC |
|
low complexity region
|
779 |
812 |
N/A |
INTRINSIC |
|
low complexity region
|
821 |
830 |
N/A |
INTRINSIC |
|
low complexity region
|
857 |
868 |
N/A |
INTRINSIC |
|
low complexity region
|
936 |
949 |
N/A |
INTRINSIC |
|
low complexity region
|
1030 |
1042 |
N/A |
INTRINSIC |
|
SH3
|
1053 |
1111 |
3.29e-17 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000177374
|
| SMART Domains |
Protein: ENSMUSP00000134825
Gene: ENSMUSG00000022377
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
16 |
N/A |
INTRINSIC |
|
Pfam:BAR
|
18 |
267 |
1.8e-11 |
PFAM |
|
Pfam:BAR_3
|
52 |
286 |
1.2e-29 |
PFAM |
|
low complexity region
|
310 |
328 |
N/A |
INTRINSIC |
|
PH
|
340 |
433 |
4.12e-15 |
SMART |
|
ArfGap
|
454 |
577 |
2.18e-34 |
SMART |
|
ANK
|
615 |
647 |
1.17e-1 |
SMART |
|
ANK
|
651 |
680 |
3.46e-4 |
SMART |
|
low complexity region
|
727 |
738 |
N/A |
INTRINSIC |
|
low complexity region
|
792 |
803 |
N/A |
INTRINSIC |
|
low complexity region
|
814 |
847 |
N/A |
INTRINSIC |
|
low complexity region
|
856 |
865 |
N/A |
INTRINSIC |
|
low complexity region
|
892 |
903 |
N/A |
INTRINSIC |
|
low complexity region
|
971 |
984 |
N/A |
INTRINSIC |
|
low complexity region
|
1065 |
1077 |
N/A |
INTRINSIC |
|
SH3
|
1088 |
1146 |
3.29e-17 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000176427
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an ADP-ribosylation factor (ARF) GTPase-activating protein. The GTPase-activating activity is stimulated by phosphatidylinositol 4,5-biphosphate (PIP2), and is greater towards ARF1 and ARF5, and lesser for ARF6. This gene maybe involved in regulation of membrane trafficking and cytoskeleton remodeling. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
|
| Allele List at MGI |
All alleles(13) : Gene trapped(13) |
| Other mutations in this stock |
Total: 63 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ahdc1 |
G |
A |
4: 132,789,860 (GRCm39) |
C367Y |
possibly damaging |
Het |
| AI182371 |
T |
A |
2: 34,975,728 (GRCm39) |
I279L |
probably benign |
Het |
| Ambp |
A |
T |
4: 63,061,934 (GRCm39) |
C332S |
probably damaging |
Het |
| App |
T |
C |
16: 84,970,407 (GRCm39) |
T14A |
probably benign |
Het |
| Aurka |
T |
C |
2: 172,201,778 (GRCm39) |
R242G |
probably benign |
Het |
| BC034090 |
G |
A |
1: 155,093,217 (GRCm39) |
P747L |
probably damaging |
Het |
| Bcl6b |
T |
C |
11: 70,119,918 (GRCm39) |
D23G |
probably damaging |
Het |
| Cabp2 |
A |
C |
19: 4,134,154 (GRCm39) |
E42A |
possibly damaging |
Het |
| Ccdc14 |
G |
A |
16: 34,542,173 (GRCm39) |
S557N |
probably benign |
Het |
| Ccdc146 |
G |
T |
5: 21,524,604 (GRCm39) |
|
probably benign |
Het |
| Cenpf |
T |
A |
1: 189,412,615 (GRCm39) |
Q216L |
probably damaging |
Het |
| Ces1b |
G |
A |
8: 93,783,675 (GRCm39) |
P515L |
possibly damaging |
Het |
| Col6a5 |
A |
T |
9: 105,755,829 (GRCm39) |
N2198K |
probably damaging |
Het |
| Csmd2 |
A |
G |
4: 128,288,859 (GRCm39) |
S1133G |
possibly damaging |
Het |
| Cspg5 |
G |
A |
9: 110,085,335 (GRCm39) |
R502H |
probably benign |
Het |
| Cyp2g1 |
A |
G |
7: 26,514,229 (GRCm39) |
|
probably benign |
Het |
| Dnajc27 |
A |
G |
12: 4,146,229 (GRCm39) |
Y86C |
probably damaging |
Het |
| Dnm1 |
T |
C |
2: 32,202,783 (GRCm39) |
D715G |
probably damaging |
Het |
| Dock1 |
G |
T |
7: 134,734,804 (GRCm39) |
L1317F |
possibly damaging |
Het |
| Fanci |
T |
A |
7: 79,083,279 (GRCm39) |
Y727* |
probably null |
Het |
| Fbxw20 |
T |
A |
9: 109,055,046 (GRCm39) |
T168S |
probably benign |
Het |
| Folh1 |
A |
T |
7: 86,385,723 (GRCm39) |
|
probably benign |
Het |
| Gas7 |
A |
T |
11: 67,573,557 (GRCm39) |
S379C |
probably damaging |
Het |
| Gbp2b |
A |
G |
3: 142,309,987 (GRCm39) |
E259G |
probably benign |
Het |
| Gm8325 |
T |
C |
3: 60,784,805 (GRCm39) |
|
noncoding transcript |
Het |
| Gpr75 |
A |
T |
11: 30,841,730 (GRCm39) |
T212S |
probably benign |
Het |
| Itgb4 |
A |
G |
11: 115,898,795 (GRCm39) |
T1711A |
probably damaging |
Het |
| Ly75 |
T |
C |
2: 60,184,796 (GRCm39) |
S453G |
probably benign |
Het |
| Maneal |
A |
G |
4: 124,754,276 (GRCm39) |
|
probably benign |
Het |
| Marco |
A |
T |
1: 120,422,508 (GRCm39) |
I58N |
possibly damaging |
Het |
| Mtcl1 |
A |
G |
17: 66,686,965 (GRCm39) |
I647T |
probably damaging |
Het |
| Mtfr1l |
A |
T |
4: 134,258,054 (GRCm39) |
V56D |
probably damaging |
Het |
| Npy1r |
G |
A |
8: 67,156,954 (GRCm39) |
V125I |
probably damaging |
Het |
| Or1j19 |
C |
T |
2: 36,676,557 (GRCm39) |
Q7* |
probably null |
Het |
| Or52n20 |
T |
C |
7: 104,320,888 (GRCm39) |
|
probably benign |
Het |
| Or7g25 |
A |
G |
9: 19,159,960 (GRCm39) |
L245P |
probably damaging |
Het |
| Osmr |
A |
T |
15: 6,867,210 (GRCm39) |
L362* |
probably null |
Het |
| Pdlim2 |
T |
C |
14: 70,411,906 (GRCm39) |
D42G |
probably damaging |
Het |
| Plcb4 |
T |
A |
2: 135,842,100 (GRCm39) |
I89N |
possibly damaging |
Het |
| Prrc2b |
T |
A |
2: 32,104,047 (GRCm39) |
M1175K |
probably benign |
Het |
| Pzp |
T |
A |
6: 128,463,133 (GRCm39) |
N1423I |
probably benign |
Het |
| Retnla |
G |
A |
16: 48,664,561 (GRCm39) |
C105Y |
probably damaging |
Het |
| Samd8 |
T |
A |
14: 21,825,544 (GRCm39) |
S167T |
possibly damaging |
Het |
| Scg2 |
A |
G |
1: 79,414,210 (GRCm39) |
M171T |
possibly damaging |
Het |
| Slc30a5 |
A |
G |
13: 100,939,941 (GRCm39) |
V658A |
probably damaging |
Het |
| Slc41a2 |
T |
C |
10: 83,152,455 (GRCm39) |
R7G |
possibly damaging |
Het |
| Slc44a2 |
A |
G |
9: 21,258,338 (GRCm39) |
T500A |
probably damaging |
Het |
| Slc44a4 |
G |
T |
17: 35,142,786 (GRCm39) |
G396V |
possibly damaging |
Het |
| Smarca5 |
A |
G |
8: 81,446,199 (GRCm39) |
|
probably benign |
Het |
| St8sia6 |
T |
A |
2: 13,798,156 (GRCm39) |
R34W |
probably damaging |
Het |
| Stk-ps2 |
T |
A |
1: 46,069,337 (GRCm39) |
|
noncoding transcript |
Het |
| Stn1 |
T |
C |
19: 47,502,329 (GRCm39) |
Y235C |
probably damaging |
Het |
| Tbx15 |
A |
G |
3: 99,259,800 (GRCm39) |
Y557C |
probably damaging |
Het |
| Tgfbr1 |
G |
A |
4: 47,393,490 (GRCm39) |
|
probably null |
Het |
| Thsd7b |
G |
T |
1: 129,523,508 (GRCm39) |
V181L |
probably damaging |
Het |
| Tmpo |
G |
A |
10: 90,999,104 (GRCm39) |
R228C |
probably benign |
Het |
| Trpm4 |
T |
G |
7: 44,976,422 (GRCm39) |
R51S |
probably damaging |
Het |
| Vmn1r91 |
A |
T |
7: 19,835,671 (GRCm39) |
T197S |
probably damaging |
Het |
| Vmn2r-ps158 |
T |
C |
7: 42,697,160 (GRCm39) |
I739T |
probably damaging |
Het |
| Xrn1 |
A |
G |
9: 95,859,880 (GRCm39) |
D424G |
probably benign |
Het |
| Yap1 |
A |
G |
9: 7,962,282 (GRCm39) |
|
probably null |
Het |
| Zer1 |
T |
C |
2: 30,003,405 (GRCm39) |
D4G |
probably damaging |
Het |
| Zfp462 |
A |
T |
4: 55,010,292 (GRCm39) |
I753F |
possibly damaging |
Het |
|
| Other mutations in Asap1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00428:Asap1
|
APN |
15 |
63,991,803 (GRCm39) |
splice site |
probably benign |
|
|
IGL00473:Asap1
|
APN |
15 |
64,045,064 (GRCm39) |
splice site |
probably benign |
|
|
IGL00519:Asap1
|
APN |
15 |
63,982,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01304:Asap1
|
APN |
15 |
64,184,298 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01510:Asap1
|
APN |
15 |
64,030,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02208:Asap1
|
APN |
15 |
63,993,882 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02429:Asap1
|
APN |
15 |
64,039,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02565:Asap1
|
APN |
15 |
64,001,014 (GRCm39) |
splice site |
probably benign |
|
|
IGL02644:Asap1
|
APN |
15 |
63,982,911 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02684:Asap1
|
APN |
15 |
63,966,018 (GRCm39) |
missense |
probably benign |
|
|
IGL02707:Asap1
|
APN |
15 |
64,001,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03052:Asap1
|
APN |
15 |
64,025,683 (GRCm39) |
splice site |
probably benign |
|
|
IGL03153:Asap1
|
APN |
15 |
64,032,123 (GRCm39) |
missense |
probably damaging |
1.00 |
|
A4554:Asap1
|
UTSW |
15 |
63,996,560 (GRCm39) |
splice site |
probably benign |
|
|
PIT4378001:Asap1
|
UTSW |
15 |
64,007,697 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0081:Asap1
|
UTSW |
15 |
63,971,413 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0555:Asap1
|
UTSW |
15 |
63,966,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1414:Asap1
|
UTSW |
15 |
64,030,733 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1437:Asap1
|
UTSW |
15 |
63,991,956 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1474:Asap1
|
UTSW |
15 |
63,991,869 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1489:Asap1
|
UTSW |
15 |
64,044,579 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1553:Asap1
|
UTSW |
15 |
64,024,701 (GRCm39) |
missense |
probably benign |
0.31 |
|
R1603:Asap1
|
UTSW |
15 |
64,001,106 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1636:Asap1
|
UTSW |
15 |
63,995,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1645:Asap1
|
UTSW |
15 |
63,961,324 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1861:Asap1
|
UTSW |
15 |
64,007,647 (GRCm39) |
splice site |
probably benign |
|
|
R2136:Asap1
|
UTSW |
15 |
63,982,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2351:Asap1
|
UTSW |
15 |
64,007,653 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4436:Asap1
|
UTSW |
15 |
64,221,692 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4618:Asap1
|
UTSW |
15 |
64,024,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4868:Asap1
|
UTSW |
15 |
63,966,030 (GRCm39) |
missense |
probably benign |
|
|
R5077:Asap1
|
UTSW |
15 |
63,999,272 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5333:Asap1
|
UTSW |
15 |
63,999,263 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R5391:Asap1
|
UTSW |
15 |
63,965,901 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R5493:Asap1
|
UTSW |
15 |
64,002,000 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5665:Asap1
|
UTSW |
15 |
64,184,302 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5756:Asap1
|
UTSW |
15 |
64,039,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5790:Asap1
|
UTSW |
15 |
63,966,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6139:Asap1
|
UTSW |
15 |
64,038,388 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6194:Asap1
|
UTSW |
15 |
64,001,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6361:Asap1
|
UTSW |
15 |
64,221,672 (GRCm39) |
splice site |
probably null |
|
|
R6751:Asap1
|
UTSW |
15 |
63,966,261 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7143:Asap1
|
UTSW |
15 |
64,063,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7218:Asap1
|
UTSW |
15 |
64,002,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7225:Asap1
|
UTSW |
15 |
64,002,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7305:Asap1
|
UTSW |
15 |
64,002,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7310:Asap1
|
UTSW |
15 |
63,971,379 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7439:Asap1
|
UTSW |
15 |
64,002,105 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7441:Asap1
|
UTSW |
15 |
64,002,105 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7488:Asap1
|
UTSW |
15 |
63,991,974 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7597:Asap1
|
UTSW |
15 |
64,184,304 (GRCm39) |
missense |
probably benign |
0.37 |
|
R7708:Asap1
|
UTSW |
15 |
64,024,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7871:Asap1
|
UTSW |
15 |
63,963,925 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7990:Asap1
|
UTSW |
15 |
64,044,586 (GRCm39) |
splice site |
probably null |
|
|
R8163:Asap1
|
UTSW |
15 |
63,963,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8171:Asap1
|
UTSW |
15 |
63,982,815 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8416:Asap1
|
UTSW |
15 |
64,002,072 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8778:Asap1
|
UTSW |
15 |
63,999,258 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9462:Asap1
|
UTSW |
15 |
64,038,328 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Posted On |
2015-04-16 |
Incidental Mutation