Incidental Mutation 'R8968:Resf1'
| ID |
682851 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Resf1
|
| Ensembl Gene |
ENSMUSG00000032712 |
| Gene Name |
retroelement silencing factor 1 |
| Synonyms |
2810474O19Rik, GET |
| MMRRC Submission |
068802-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8968 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
149210912-149237161 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 149228664 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Aspartic acid
at position 570
(V570D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000041180
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046689]
[ENSMUST00000100765]
[ENSMUST00000127680]
[ENSMUST00000130664]
[ENSMUST00000185930]
[ENSMUST00000187881]
[ENSMUST00000189837]
[ENSMUST00000189932]
[ENSMUST00000190785]
|
| AlphaFold |
Q5DTW7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000046689
AA Change: V570D
PolyPhen 2
Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000041180
Gene: ENSMUSG00000032712
AA Change: V570D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1513 |
N/A |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000100765
AA Change: V570D
PolyPhen 2
Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000098328
Gene: ENSMUSG00000032712
AA Change: V570D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1513 |
N/A |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127680
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000130664
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000185930
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187881
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000189837
AA Change: V570D
PolyPhen 2
Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000139660
Gene: ENSMUSG00000032712
AA Change: V570D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1511 |
N/A |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000189932
AA Change: V570D
PolyPhen 2
Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000140026
Gene: ENSMUSG00000032712
AA Change: V570D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1513 |
N/A |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000190785
AA Change: V570D
PolyPhen 2
Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000139624
Gene: ENSMUSG00000032712
AA Change: V570D
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4617
|
451 |
1173 |
9.4e-255 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 97.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
All alleles(126) : Targeted, knock-out(1) Gene trapped(125) |
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
T |
A |
13: 77,480,429 (GRCm39) |
L1153* |
probably null |
Het |
| Adamts2 |
T |
C |
11: 50,683,550 (GRCm39) |
I944T |
possibly damaging |
Het |
| Aqp9 |
A |
T |
9: 71,045,485 (GRCm39) |
C67* |
probably null |
Het |
| Armt1 |
G |
T |
10: 4,404,150 (GRCm39) |
G412W |
probably damaging |
Het |
| B4galt1 |
T |
C |
4: 40,807,243 (GRCm39) |
D381G |
probably benign |
Het |
| Bmp5 |
A |
T |
9: 75,780,579 (GRCm39) |
H292L |
probably benign |
Het |
| Brpf1 |
T |
C |
6: 113,299,510 (GRCm39) |
F1181S |
probably damaging |
Het |
| Btbd7 |
C |
A |
12: 102,779,025 (GRCm39) |
G414C |
probably damaging |
Het |
| Ccdc65 |
A |
T |
15: 98,616,723 (GRCm39) |
K204* |
probably null |
Het |
| Cdk5 |
T |
A |
5: 24,627,379 (GRCm39) |
K88M |
probably damaging |
Het |
| Cdrt4 |
T |
A |
11: 62,883,634 (GRCm39) |
L112Q |
probably damaging |
Het |
| Cenpb |
T |
C |
2: 131,020,547 (GRCm39) |
E417G |
unknown |
Het |
| Cep135 |
T |
C |
5: 76,754,576 (GRCm39) |
I351T |
possibly damaging |
Het |
| Ces1d |
A |
T |
8: 93,914,383 (GRCm39) |
S226R |
probably damaging |
Het |
| Cfap97 |
T |
A |
8: 46,623,114 (GRCm39) |
V168E |
possibly damaging |
Het |
| CN725425 |
T |
C |
15: 91,130,090 (GRCm39) |
C318R |
possibly damaging |
Het |
| Cnga3 |
T |
A |
1: 37,300,460 (GRCm39) |
D393E |
probably benign |
Het |
| Cplane1 |
A |
T |
15: 8,230,765 (GRCm39) |
H1014L |
possibly damaging |
Het |
| Cpsf1 |
G |
A |
15: 76,486,169 (GRCm39) |
R358* |
probably null |
Het |
| Cyp2b23 |
G |
A |
7: 26,378,963 (GRCm39) |
P167L |
probably damaging |
Het |
| Cyp2c70 |
A |
T |
19: 40,142,059 (GRCm39) |
H477Q |
probably benign |
Het |
| D930020B18Rik |
A |
C |
10: 121,490,721 (GRCm39) |
Y107S |
probably damaging |
Het |
| Dhrs1 |
A |
T |
14: 55,978,192 (GRCm39) |
F216I |
probably benign |
Het |
| Dmgdh |
A |
T |
13: 93,845,767 (GRCm39) |
K474* |
probably null |
Het |
| Dsp |
T |
C |
13: 38,335,596 (GRCm39) |
I11T |
possibly damaging |
Het |
| Erh |
G |
T |
12: 80,684,282 (GRCm39) |
A65E |
probably benign |
Het |
| Fmnl1 |
AGGCTCTGG |
AGG |
11: 103,077,444 (GRCm39) |
|
probably benign |
Het |
| Grid2 |
A |
C |
6: 64,643,139 (GRCm39) |
H967P |
probably benign |
Het |
| Hc |
A |
G |
2: 34,922,317 (GRCm39) |
I503T |
possibly damaging |
Het |
| Herc3 |
T |
C |
6: 58,867,183 (GRCm39) |
L824S |
probably damaging |
Het |
| Hfm1 |
T |
C |
5: 107,065,439 (GRCm39) |
D80G |
probably benign |
Het |
| Hjurp |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT |
C |
1: 88,193,999 (GRCm39) |
|
probably benign |
Het |
| Hspa1l |
A |
G |
17: 35,196,230 (GRCm39) |
K90E |
possibly damaging |
Het |
| Impa2 |
G |
A |
18: 67,451,497 (GRCm39) |
V264I |
probably benign |
Het |
| Ipmk |
C |
T |
10: 71,199,333 (GRCm39) |
R65W |
probably damaging |
Het |
| Klhl38 |
C |
T |
15: 58,185,500 (GRCm39) |
V410I |
probably benign |
Het |
| Lcn4 |
A |
G |
2: 26,558,360 (GRCm39) |
I175T |
possibly damaging |
Het |
| Lipo2 |
C |
A |
19: 33,726,917 (GRCm39) |
W40L |
probably damaging |
Het |
| Mgam |
A |
T |
6: 40,734,745 (GRCm39) |
|
probably null |
Het |
| Myo16 |
T |
A |
8: 10,619,700 (GRCm39) |
I1417N |
unknown |
Het |
| Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
| Or4a66 |
T |
A |
2: 88,531,137 (GRCm39) |
I179F |
probably benign |
Het |
| Or52e19b |
A |
T |
7: 103,032,667 (GRCm39) |
C181S |
probably damaging |
Het |
| Or5j3 |
G |
A |
2: 86,128,526 (GRCm39) |
R122H |
probably benign |
Het |
| Pcdha11 |
A |
G |
18: 37,145,307 (GRCm39) |
N466S |
probably damaging |
Het |
| Pif1 |
C |
T |
9: 65,499,076 (GRCm39) |
T432M |
probably damaging |
Het |
| Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
| Pkd1l3 |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
8: 110,350,420 (GRCm39) |
|
probably benign |
Het |
| Pole |
T |
C |
5: 110,459,949 (GRCm39) |
S1118P |
possibly damaging |
Het |
| Ppp4r4 |
T |
C |
12: 103,566,706 (GRCm39) |
M652T |
probably benign |
Het |
| Prex2 |
A |
T |
1: 11,180,562 (GRCm39) |
K376* |
probably null |
Het |
| Prps1l1 |
A |
T |
12: 35,035,205 (GRCm39) |
I107F |
probably damaging |
Het |
| Rfc1 |
C |
T |
5: 65,432,778 (GRCm39) |
V761I |
probably benign |
Het |
| Ripk4 |
T |
C |
16: 97,547,203 (GRCm39) |
E353G |
probably benign |
Het |
| Robo2 |
C |
A |
16: 73,767,941 (GRCm39) |
|
probably null |
Het |
| Rrm1 |
C |
T |
7: 102,117,545 (GRCm39) |
A745V |
probably benign |
Het |
| Sash1 |
A |
T |
10: 8,606,179 (GRCm39) |
V737D |
probably benign |
Het |
| Sel1l2 |
T |
C |
2: 140,127,209 (GRCm39) |
K101E |
probably benign |
Het |
| Selenbp2 |
A |
T |
3: 94,607,337 (GRCm39) |
I253F |
probably benign |
Het |
| Setd1a |
C |
T |
7: 127,385,279 (GRCm39) |
P662L |
possibly damaging |
Het |
| Slc16a6 |
C |
T |
11: 109,345,776 (GRCm39) |
V496I |
possibly damaging |
Het |
| Slc4a4 |
A |
T |
5: 89,232,512 (GRCm39) |
M239L |
probably benign |
Het |
| Slc7a8 |
G |
C |
14: 55,018,750 (GRCm39) |
A12G |
probably benign |
Het |
| Snx30 |
T |
C |
4: 59,886,517 (GRCm39) |
S309P |
possibly damaging |
Het |
| Spen |
T |
C |
4: 141,197,701 (GRCm39) |
N3389S |
probably benign |
Het |
| Spg11 |
T |
C |
2: 121,922,687 (GRCm39) |
T921A |
probably damaging |
Het |
| Tanc2 |
T |
A |
11: 105,758,400 (GRCm39) |
D720E |
possibly damaging |
Het |
| Tmprss9 |
A |
T |
10: 80,730,163 (GRCm39) |
I688F |
possibly damaging |
Het |
| Trap1 |
A |
G |
16: 3,862,490 (GRCm39) |
V596A |
possibly damaging |
Het |
| Ttc32 |
G |
T |
12: 9,080,187 (GRCm39) |
R44L |
probably benign |
Het |
| Tusc3 |
T |
A |
8: 39,597,898 (GRCm39) |
N288K |
probably benign |
Het |
| Ush2a |
G |
A |
1: 188,127,956 (GRCm39) |
G656E |
probably damaging |
Het |
| Vill |
T |
C |
9: 118,892,671 (GRCm39) |
|
probably null |
Het |
| Vmn1r5 |
A |
T |
6: 56,963,182 (GRCm39) |
R286* |
probably null |
Het |
| Vmn2r14 |
T |
C |
5: 109,365,533 (GRCm39) |
T514A |
probably benign |
Het |
| Vmn2r32 |
G |
A |
7: 7,477,204 (GRCm39) |
H396Y |
probably benign |
Het |
| Vmn2r75 |
A |
T |
7: 85,820,765 (GRCm39) |
Y56* |
probably null |
Het |
| Wdfy3 |
C |
T |
5: 102,011,983 (GRCm39) |
S2668N |
probably benign |
Het |
| Wdr72 |
G |
A |
9: 74,059,729 (GRCm39) |
D392N |
probably benign |
Het |
| Zfp518a |
A |
C |
19: 40,901,870 (GRCm39) |
K600Q |
possibly damaging |
Het |
|
| Other mutations in Resf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00767:Resf1
|
APN |
6 |
149,236,248 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL01401:Resf1
|
APN |
6 |
149,228,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01461:Resf1
|
APN |
6 |
149,233,013 (GRCm39) |
unclassified |
probably benign |
|
|
IGL01610:Resf1
|
APN |
6 |
149,230,449 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02873:Resf1
|
APN |
6 |
149,228,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03202:Resf1
|
APN |
6 |
149,227,937 (GRCm39) |
missense |
probably benign |
0.08 |
|
grand_junction
|
UTSW |
6 |
149,229,376 (GRCm39) |
missense |
probably damaging |
0.98 |
|
grand_marais
|
UTSW |
6 |
149,227,958 (GRCm39) |
nonsense |
probably null |
|
|
3-1:Resf1
|
UTSW |
6 |
149,229,227 (GRCm39) |
missense |
probably damaging |
0.98 |
|
B6584:Resf1
|
UTSW |
6 |
149,230,844 (GRCm39) |
missense |
probably damaging |
0.96 |
|
PIT4280001:Resf1
|
UTSW |
6 |
149,227,023 (GRCm39) |
missense |
probably benign |
0.23 |
|
R0053:Resf1
|
UTSW |
6 |
149,229,088 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0053:Resf1
|
UTSW |
6 |
149,229,088 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0243:Resf1
|
UTSW |
6 |
149,227,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0620:Resf1
|
UTSW |
6 |
149,229,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0633:Resf1
|
UTSW |
6 |
149,227,199 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0727:Resf1
|
UTSW |
6 |
149,227,320 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0904:Resf1
|
UTSW |
6 |
149,229,767 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1221:Resf1
|
UTSW |
6 |
149,227,719 (GRCm39) |
missense |
probably benign |
0.24 |
|
R1282:Resf1
|
UTSW |
6 |
149,230,670 (GRCm39) |
nonsense |
probably null |
|
|
R1435:Resf1
|
UTSW |
6 |
149,227,580 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1452:Resf1
|
UTSW |
6 |
149,228,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1587:Resf1
|
UTSW |
6 |
149,228,018 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1912:Resf1
|
UTSW |
6 |
149,230,342 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R1926:Resf1
|
UTSW |
6 |
149,230,902 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1978:Resf1
|
UTSW |
6 |
149,227,930 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2035:Resf1
|
UTSW |
6 |
149,230,724 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2136:Resf1
|
UTSW |
6 |
149,230,320 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2333:Resf1
|
UTSW |
6 |
149,229,009 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2360:Resf1
|
UTSW |
6 |
149,236,145 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3027:Resf1
|
UTSW |
6 |
149,230,533 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3121:Resf1
|
UTSW |
6 |
149,230,741 (GRCm39) |
nonsense |
probably null |
|
|
R3707:Resf1
|
UTSW |
6 |
149,230,611 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4204:Resf1
|
UTSW |
6 |
149,231,042 (GRCm39) |
nonsense |
probably null |
|
|
R4247:Resf1
|
UTSW |
6 |
149,227,041 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R4249:Resf1
|
UTSW |
6 |
149,227,041 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R4304:Resf1
|
UTSW |
6 |
149,227,736 (GRCm39) |
nonsense |
probably null |
|
|
R4385:Resf1
|
UTSW |
6 |
149,227,706 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4702:Resf1
|
UTSW |
6 |
149,230,901 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4747:Resf1
|
UTSW |
6 |
149,228,392 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4912:Resf1
|
UTSW |
6 |
149,230,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4913:Resf1
|
UTSW |
6 |
149,230,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4965:Resf1
|
UTSW |
6 |
149,229,896 (GRCm39) |
nonsense |
probably null |
|
|
R4971:Resf1
|
UTSW |
6 |
149,227,097 (GRCm39) |
unclassified |
probably benign |
|
|
R5077:Resf1
|
UTSW |
6 |
149,227,528 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5213:Resf1
|
UTSW |
6 |
149,227,551 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R5382:Resf1
|
UTSW |
6 |
149,227,958 (GRCm39) |
nonsense |
probably null |
|
|
R5418:Resf1
|
UTSW |
6 |
149,227,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5452:Resf1
|
UTSW |
6 |
149,230,611 (GRCm39) |
nonsense |
probably null |
|
|
R5498:Resf1
|
UTSW |
6 |
149,229,738 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5673:Resf1
|
UTSW |
6 |
149,229,491 (GRCm39) |
nonsense |
probably null |
|
|
R5690:Resf1
|
UTSW |
6 |
149,229,735 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5916:Resf1
|
UTSW |
6 |
149,228,076 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5917:Resf1
|
UTSW |
6 |
149,236,179 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6160:Resf1
|
UTSW |
6 |
149,233,005 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6280:Resf1
|
UTSW |
6 |
149,228,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6326:Resf1
|
UTSW |
6 |
149,230,493 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6396:Resf1
|
UTSW |
6 |
149,229,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6702:Resf1
|
UTSW |
6 |
149,229,376 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6972:Resf1
|
UTSW |
6 |
149,227,607 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7127:Resf1
|
UTSW |
6 |
149,229,443 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7168:Resf1
|
UTSW |
6 |
149,229,341 (GRCm39) |
missense |
probably benign |
|
|
R7316:Resf1
|
UTSW |
6 |
149,228,136 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7586:Resf1
|
UTSW |
6 |
149,228,291 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R7719:Resf1
|
UTSW |
6 |
149,228,853 (GRCm39) |
missense |
probably benign |
|
|
R7751:Resf1
|
UTSW |
6 |
149,226,936 (GRCm39) |
start gained |
probably benign |
|
|
R8013:Resf1
|
UTSW |
6 |
149,230,368 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8358:Resf1
|
UTSW |
6 |
149,228,076 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8393:Resf1
|
UTSW |
6 |
149,229,998 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R8977:Resf1
|
UTSW |
6 |
149,229,906 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8981:Resf1
|
UTSW |
6 |
149,227,997 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9106:Resf1
|
UTSW |
6 |
149,230,368 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R9208:Resf1
|
UTSW |
6 |
149,228,027 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9294:Resf1
|
UTSW |
6 |
149,227,930 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9352:Resf1
|
UTSW |
6 |
149,236,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9361:Resf1
|
UTSW |
6 |
149,228,132 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R9513:Resf1
|
UTSW |
6 |
149,229,793 (GRCm39) |
nonsense |
probably null |
|
|
R9566:Resf1
|
UTSW |
6 |
149,227,352 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9623:Resf1
|
UTSW |
6 |
149,226,965 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9689:Resf1
|
UTSW |
6 |
149,229,766 (GRCm39) |
nonsense |
probably null |
|
|
R9752:Resf1
|
UTSW |
6 |
149,228,068 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9794:Resf1
|
UTSW |
6 |
149,228,239 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TCAGTACAACCGTAGTGGGC -3'
(R):5'- CACCCTGTATTGGTTTGTGC -3'
Sequencing Primer
(F):5'- TACAACCGTAGTGGGCAGTGC -3'
(R):5'- CTGCTTTTCCTTATCAACAGGCAGAG -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation