Incidental Mutation 'R4997:Rufy4'
| ID |
385305 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rufy4
|
| Ensembl Gene |
ENSMUSG00000061815 |
| Gene Name |
RUN and FYVE domain containing 4 |
| Synonyms |
F930048N03Rik |
| MMRRC Submission |
042591-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.202)
|
| Stock # |
R4997 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
74164700-74187382 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 74186822 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Arginine
at position 537
(C537R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000115873
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080167]
[ENSMUST00000127134]
|
| AlphaFold |
Q3TYX8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000080167
AA Change: C453R
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000079062
Gene: ENSMUSG00000061815
AA Change: C453R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RUN
|
2 |
81 |
1.5e-8 |
PFAM |
|
coiled coil region
|
331 |
404 |
N/A |
INTRINSIC |
|
Blast:FYVE
|
415 |
472 |
2e-6 |
BLAST |
|
SCOP:d1vfya_
|
428 |
473 |
4e-7 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000127134
AA Change: C537R
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000115873
Gene: ENSMUSG00000061815
AA Change: C537R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:RUN
|
41 |
165 |
6.2e-10 |
PFAM |
|
coiled coil region
|
415 |
488 |
N/A |
INTRINSIC |
|
Blast:FYVE
|
499 |
556 |
2e-6 |
BLAST |
|
SCOP:d1vfya_
|
512 |
557 |
3e-7 |
SMART |
|
| Meta Mutation Damage Score |
0.8605 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A630023A22Rik |
A |
T |
14: 33,775,623 (GRCm39) |
M1L |
probably benign |
Het |
| Abca7 |
C |
A |
10: 79,843,154 (GRCm39) |
Q1210K |
possibly damaging |
Het |
| Abcc4 |
C |
T |
14: 118,753,915 (GRCm39) |
W1024* |
probably null |
Het |
| Accs |
A |
T |
2: 93,672,228 (GRCm39) |
Y213* |
probably null |
Het |
| Adam6a |
G |
T |
12: 113,508,991 (GRCm39) |
G455C |
probably damaging |
Het |
| Adcy1 |
A |
C |
11: 7,111,298 (GRCm39) |
Y863S |
probably benign |
Het |
| Adgrg1 |
A |
G |
8: 95,736,148 (GRCm39) |
D434G |
probably damaging |
Het |
| Afap1l1 |
C |
T |
18: 61,884,879 (GRCm39) |
R202Q |
probably benign |
Het |
| Aldh3a1 |
T |
C |
11: 61,103,137 (GRCm39) |
V27A |
probably benign |
Het |
| Antxr2 |
A |
G |
5: 98,125,553 (GRCm39) |
F235L |
probably benign |
Het |
| Arhgap23 |
T |
A |
11: 97,342,846 (GRCm39) |
V376E |
probably damaging |
Het |
| Brca1 |
A |
C |
11: 101,415,159 (GRCm39) |
S992A |
probably damaging |
Het |
| Brcc3dc |
A |
G |
10: 108,535,649 (GRCm39) |
I102T |
probably benign |
Het |
| Calcrl |
A |
T |
2: 84,181,592 (GRCm39) |
C185* |
probably null |
Het |
| Cep152 |
T |
C |
2: 125,428,271 (GRCm39) |
T787A |
probably benign |
Het |
| Coch |
T |
A |
12: 51,649,964 (GRCm39) |
|
probably null |
Het |
| Col5a1 |
T |
A |
2: 27,922,794 (GRCm39) |
Y287* |
probably null |
Het |
| Dis3l |
A |
G |
9: 64,219,224 (GRCm39) |
S569P |
possibly damaging |
Het |
| Dnai1 |
A |
G |
4: 41,597,919 (GRCm39) |
I74V |
possibly damaging |
Het |
| Dpy19l4 |
A |
G |
4: 11,287,493 (GRCm39) |
V394A |
probably benign |
Het |
| Egfem1 |
A |
G |
3: 29,207,739 (GRCm39) |
H122R |
probably benign |
Het |
| Endou |
A |
G |
15: 97,617,458 (GRCm39) |
L164P |
probably damaging |
Het |
| Epgn |
A |
G |
5: 91,180,098 (GRCm39) |
E80G |
possibly damaging |
Het |
| Fcgbpl1 |
T |
G |
7: 27,843,349 (GRCm39) |
S746A |
possibly damaging |
Het |
| Fitm1 |
T |
C |
14: 55,814,364 (GRCm39) |
S287P |
probably benign |
Het |
| Foxm1 |
A |
G |
6: 128,342,731 (GRCm39) |
N22D |
probably benign |
Het |
| Gsdmc |
A |
T |
15: 63,648,629 (GRCm39) |
M426K |
probably damaging |
Het |
| Hmcn2 |
T |
A |
2: 31,291,720 (GRCm39) |
V2418D |
probably damaging |
Het |
| Hs3st2 |
T |
A |
7: 121,099,679 (GRCm39) |
L175Q |
possibly damaging |
Het |
| Il1r2 |
T |
C |
1: 40,160,206 (GRCm39) |
|
probably null |
Het |
| Il27ra |
A |
T |
8: 84,766,156 (GRCm39) |
Y209* |
probably null |
Het |
| Inpp5a |
A |
T |
7: 138,980,654 (GRCm39) |
S31C |
probably benign |
Het |
| Invs |
A |
G |
4: 48,396,332 (GRCm39) |
D335G |
probably damaging |
Het |
| Isg15 |
C |
T |
4: 156,284,154 (GRCm39) |
E125K |
possibly damaging |
Het |
| Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
| Lama4 |
C |
A |
10: 38,968,262 (GRCm39) |
T1468K |
probably damaging |
Het |
| Lce1a2 |
A |
G |
3: 92,576,395 (GRCm39) |
S56P |
unknown |
Het |
| Llgl1 |
C |
T |
11: 60,600,394 (GRCm39) |
P581L |
probably benign |
Het |
| Lmf1 |
G |
A |
17: 25,807,650 (GRCm39) |
W164* |
probably null |
Het |
| Mad2l1bp |
G |
T |
17: 46,463,804 (GRCm39) |
C73* |
probably null |
Het |
| Mpzl1 |
A |
C |
1: 165,429,350 (GRCm39) |
V230G |
probably damaging |
Het |
| Myo3b |
A |
G |
2: 70,088,427 (GRCm39) |
T869A |
possibly damaging |
Het |
| Ncor2 |
T |
C |
5: 125,111,074 (GRCm39) |
H1316R |
probably damaging |
Het |
| Nlrp1b |
T |
A |
11: 71,109,160 (GRCm39) |
I114F |
probably damaging |
Het |
| Nsun7 |
A |
G |
5: 66,453,182 (GRCm39) |
I632M |
probably benign |
Het |
| Nubp1 |
T |
C |
16: 10,239,185 (GRCm39) |
I234T |
probably benign |
Het |
| Olfml1 |
A |
G |
7: 107,170,413 (GRCm39) |
D100G |
probably damaging |
Het |
| Or1e1b-ps1 |
T |
A |
11: 73,845,612 (GRCm39) |
L32Q |
probably damaging |
Het |
| Or5p73 |
C |
A |
7: 108,064,701 (GRCm39) |
Q57K |
probably benign |
Het |
| Or7g23 |
A |
T |
9: 19,086,627 (GRCm39) |
L115Q |
probably damaging |
Het |
| Osmr |
G |
T |
15: 6,845,120 (GRCm39) |
P882Q |
probably benign |
Het |
| Peg10 |
TCAGGATCC |
TCAGGATCCCCAGCAGGATCC |
6: 4,756,457 (GRCm39) |
|
probably benign |
Het |
| Per2 |
T |
A |
1: 91,378,505 (GRCm39) |
T15S |
probably benign |
Het |
| Piezo2 |
A |
G |
18: 63,216,184 (GRCm39) |
Y1184H |
probably damaging |
Het |
| Pik3c2b |
C |
T |
1: 133,032,819 (GRCm39) |
A1560V |
probably damaging |
Het |
| Pik3cd |
A |
C |
4: 149,743,441 (GRCm39) |
L256R |
probably damaging |
Het |
| Ppl |
C |
A |
16: 4,907,235 (GRCm39) |
R1020L |
probably damaging |
Het |
| Ppp1r10 |
A |
G |
17: 36,234,976 (GRCm39) |
N60S |
probably damaging |
Het |
| Prkcg |
T |
C |
7: 3,371,097 (GRCm39) |
|
probably null |
Het |
| Prkci |
T |
C |
3: 31,085,375 (GRCm39) |
|
probably null |
Het |
| Prrc2b |
A |
G |
2: 32,112,323 (GRCm39) |
Y1929C |
probably damaging |
Het |
| Prss12 |
T |
C |
3: 123,240,857 (GRCm39) |
V17A |
probably benign |
Het |
| Qtrt1 |
A |
G |
9: 21,328,654 (GRCm39) |
N206S |
probably benign |
Het |
| Rad54l2 |
A |
C |
9: 106,600,108 (GRCm39) |
S50A |
possibly damaging |
Het |
| Rhov |
C |
T |
2: 119,100,949 (GRCm39) |
R96H |
probably damaging |
Het |
| Rph3a |
A |
T |
5: 121,101,906 (GRCm39) |
V110E |
probably damaging |
Het |
| Ryr2 |
A |
T |
13: 11,610,192 (GRCm39) |
N646K |
probably benign |
Het |
| Scn8a |
A |
G |
15: 100,854,935 (GRCm39) |
T141A |
probably damaging |
Het |
| Serping1 |
T |
C |
2: 84,600,629 (GRCm39) |
R238G |
possibly damaging |
Het |
| Shank3 |
T |
A |
15: 89,433,901 (GRCm39) |
W1474R |
probably damaging |
Het |
| Slc16a12 |
T |
A |
19: 34,652,358 (GRCm39) |
M263L |
probably benign |
Het |
| Spata13 |
T |
C |
14: 60,946,908 (GRCm39) |
V652A |
probably damaging |
Het |
| Spata31 |
G |
A |
13: 65,067,537 (GRCm39) |
M66I |
probably benign |
Het |
| Spem2 |
T |
C |
11: 69,708,558 (GRCm39) |
I136V |
probably benign |
Het |
| Supt5 |
T |
C |
7: 28,015,462 (GRCm39) |
H925R |
probably benign |
Het |
| Syk |
A |
T |
13: 52,766,484 (GRCm39) |
K190* |
probably null |
Het |
| Thsd1 |
T |
A |
8: 22,733,340 (GRCm39) |
V129D |
probably damaging |
Het |
| Tiprl |
A |
G |
1: 165,047,759 (GRCm39) |
V174A |
possibly damaging |
Het |
| Tmed4 |
T |
A |
11: 6,224,500 (GRCm39) |
|
probably null |
Het |
| Tnfrsf19 |
T |
C |
14: 61,208,658 (GRCm39) |
T288A |
probably benign |
Het |
| Tnfrsf25 |
T |
C |
4: 152,202,153 (GRCm39) |
|
probably null |
Het |
| Tpd52 |
A |
G |
3: 9,000,056 (GRCm39) |
L121S |
probably damaging |
Het |
| Trim30a |
T |
A |
7: 104,060,827 (GRCm39) |
K316N |
probably benign |
Het |
| Ttc3 |
T |
G |
16: 94,253,841 (GRCm39) |
D1221E |
probably damaging |
Het |
| Ttn |
C |
T |
2: 76,714,403 (GRCm39) |
|
probably benign |
Het |
| Ttn |
T |
C |
2: 76,776,615 (GRCm39) |
I1514V |
probably benign |
Het |
| Ulk2 |
T |
C |
11: 61,689,982 (GRCm39) |
T671A |
probably benign |
Het |
| Wasf1 |
C |
T |
10: 40,810,600 (GRCm39) |
P281S |
probably damaging |
Het |
| Wnt10b |
C |
A |
15: 98,672,084 (GRCm39) |
R211L |
probably damaging |
Het |
| Xpnpep3 |
T |
A |
15: 81,332,577 (GRCm39) |
C371* |
probably null |
Het |
| Zfp41 |
C |
T |
15: 75,490,617 (GRCm39) |
|
probably benign |
Het |
| Zfp553 |
T |
A |
7: 126,834,683 (GRCm39) |
N79K |
probably benign |
Het |
| Zmynd8 |
G |
T |
2: 165,634,736 (GRCm39) |
D1096E |
probably benign |
Het |
|
| Other mutations in Rufy4 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01617:Rufy4
|
APN |
1 |
74,168,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02075:Rufy4
|
APN |
1 |
74,168,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02604:Rufy4
|
APN |
1 |
74,173,348 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02606:Rufy4
|
APN |
1 |
74,172,509 (GRCm39) |
splice site |
probably benign |
|
|
IGL02928:Rufy4
|
APN |
1 |
74,168,241 (GRCm39) |
unclassified |
probably benign |
|
|
R0091:Rufy4
|
UTSW |
1 |
74,168,095 (GRCm39) |
unclassified |
probably benign |
|
|
R0507:Rufy4
|
UTSW |
1 |
74,185,875 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0589:Rufy4
|
UTSW |
1 |
74,172,042 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0595:Rufy4
|
UTSW |
1 |
74,180,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0742:Rufy4
|
UTSW |
1 |
74,185,875 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1533:Rufy4
|
UTSW |
1 |
74,169,002 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1666:Rufy4
|
UTSW |
1 |
74,186,837 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1668:Rufy4
|
UTSW |
1 |
74,186,837 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1827:Rufy4
|
UTSW |
1 |
74,173,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2018:Rufy4
|
UTSW |
1 |
74,180,106 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R2095:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2306:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2307:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2472:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2475:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3022:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3054:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3055:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3056:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3117:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3118:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3236:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3237:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3545:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3546:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3547:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3548:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3767:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3768:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3770:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3816:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3817:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3818:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3819:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3895:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4050:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4091:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4117:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4124:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4125:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4127:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4231:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4233:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4234:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4236:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4254:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4255:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4319:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4320:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4321:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4321:Rufy4
|
UTSW |
1 |
74,171,943 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4322:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4323:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4324:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4360:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4361:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4406:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4408:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4516:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4517:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4520:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4522:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4524:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4531:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4533:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4617:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4661:Rufy4
|
UTSW |
1 |
74,172,266 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4778:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4779:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4840:Rufy4
|
UTSW |
1 |
74,168,198 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R4897:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4898:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4899:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4915:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4917:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4918:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5092:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5097:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5189:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5191:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5195:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5196:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5197:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5226:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5227:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5228:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5230:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5372:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5373:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5374:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5375:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5376:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5377:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5378:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5699:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5748:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5750:Rufy4
|
UTSW |
1 |
74,172,068 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5767:Rufy4
|
UTSW |
1 |
74,186,822 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5865:Rufy4
|
UTSW |
1 |
74,185,914 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6083:Rufy4
|
UTSW |
1 |
74,168,556 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6149:Rufy4
|
UTSW |
1 |
74,186,892 (GRCm39) |
missense |
probably benign |
0.15 |
|
R6279:Rufy4
|
UTSW |
1 |
74,172,383 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6300:Rufy4
|
UTSW |
1 |
74,172,383 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6629:Rufy4
|
UTSW |
1 |
74,171,526 (GRCm39) |
splice site |
probably null |
|
|
R6809:Rufy4
|
UTSW |
1 |
74,172,206 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7179:Rufy4
|
UTSW |
1 |
74,172,035 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7218:Rufy4
|
UTSW |
1 |
74,172,174 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7453:Rufy4
|
UTSW |
1 |
74,168,493 (GRCm39) |
splice site |
probably null |
|
|
R9377:Rufy4
|
UTSW |
1 |
74,171,879 (GRCm39) |
missense |
probably benign |
0.08 |
|
X0023:Rufy4
|
UTSW |
1 |
74,180,208 (GRCm39) |
missense |
probably benign |
0.04 |
|
X0025:Rufy4
|
UTSW |
1 |
74,172,178 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CAAGCCATCAGGAGAAGCTG -3'
(R):5'- AGAGCTAGGCCTATCTGTGGAC -3'
Sequencing Primer
(F):5'- GGAGAAGCTGCCACCTCAATTAG -3'
(R):5'- TGGACTGCCAGCTGTTCC -3'
|
| Posted On |
2016-05-10 |
Incidental Mutation