Incidental Mutation 'R1926:Yeats2'
| ID |
213482 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Yeats2
|
| Ensembl Gene |
ENSMUSG00000041215 |
| Gene Name |
YEATS domain containing 2 |
| Synonyms |
|
| MMRRC Submission |
039944-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.960)
|
| Stock # |
R1926 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
19959813-20051323 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 20033176 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 1034
(T1034A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000155892
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090052]
[ENSMUST00000115560]
[ENSMUST00000232019]
[ENSMUST00000232338]
|
| AlphaFold |
Q3TUF7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090052
AA Change: T1019A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000087506
Gene: ENSMUSG00000041215
AA Change: T1019A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:YEATS
|
179 |
262 |
2.6e-27 |
PFAM |
|
low complexity region
|
299 |
309 |
N/A |
INTRINSIC |
|
low complexity region
|
312 |
333 |
N/A |
INTRINSIC |
|
low complexity region
|
409 |
429 |
N/A |
INTRINSIC |
|
low complexity region
|
458 |
467 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
471 |
675 |
3.72e-6 |
PROSPERO |
|
low complexity region
|
683 |
702 |
N/A |
INTRINSIC |
|
low complexity region
|
738 |
775 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
785 |
978 |
3.72e-6 |
PROSPERO |
|
low complexity region
|
1240 |
1249 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115560
AA Change: T1072A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000111222
Gene: ENSMUSG00000041215
AA Change: T1072A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:YEATS
|
232 |
314 |
2.1e-28 |
PFAM |
|
low complexity region
|
352 |
362 |
N/A |
INTRINSIC |
|
low complexity region
|
365 |
386 |
N/A |
INTRINSIC |
|
low complexity region
|
462 |
482 |
N/A |
INTRINSIC |
|
low complexity region
|
511 |
520 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
524 |
728 |
4.68e-6 |
PROSPERO |
|
low complexity region
|
736 |
755 |
N/A |
INTRINSIC |
|
low complexity region
|
791 |
828 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
838 |
1031 |
4.68e-6 |
PROSPERO |
|
low complexity region
|
1293 |
1302 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000232019
AA Change: T1034A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000232094
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000232338
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000232613
AA Change: T56A
|
| Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.7%
- 10x: 95.0%
- 20x: 91.6%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] YEATS2 is a scaffolding subunit of the ADA2A (TADA2A; MIM 602276)-containing (ATAC) histone acetyltransferase complex (Wang et al., 2008 [PubMed 18838386]).[supplied by OMIM, Apr 2010]
|
| Allele List at MGI |
All alleles(34) : Targeted(1) Gene trapped(33)
|
| Other mutations in this stock |
Total: 81 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acsm3 |
C |
T |
7: 119,376,359 (GRCm39) |
T362M |
probably damaging |
Het |
| Ang6 |
A |
G |
14: 44,239,695 (GRCm39) |
V11A |
possibly damaging |
Het |
| Ankrd17 |
A |
G |
5: 90,392,028 (GRCm39) |
Y1880H |
probably damaging |
Het |
| Bmi1 |
A |
G |
2: 18,687,084 (GRCm39) |
I55V |
probably benign |
Het |
| Bnipl |
G |
A |
3: 95,150,354 (GRCm39) |
T297M |
probably damaging |
Het |
| Bpifa2 |
T |
C |
2: 153,855,669 (GRCm39) |
V198A |
probably benign |
Het |
| Brms1l |
G |
T |
12: 55,909,946 (GRCm39) |
V239F |
possibly damaging |
Het |
| Ccdc158 |
A |
G |
5: 92,798,647 (GRCm39) |
V351A |
probably benign |
Het |
| Ces1c |
A |
G |
8: 93,854,232 (GRCm39) |
F101S |
possibly damaging |
Het |
| Cpb2 |
T |
C |
14: 75,479,837 (GRCm39) |
Y15H |
probably benign |
Het |
| Dglucy |
A |
T |
12: 100,833,414 (GRCm39) |
N535I |
possibly damaging |
Het |
| Dop1a |
C |
A |
9: 86,405,072 (GRCm39) |
H1763Q |
probably damaging |
Het |
| Dpy19l1 |
C |
T |
9: 24,385,120 (GRCm39) |
M236I |
probably benign |
Het |
| Efna2 |
T |
C |
10: 80,022,710 (GRCm39) |
Y85H |
probably damaging |
Het |
| Eipr1 |
A |
T |
12: 28,914,836 (GRCm39) |
|
probably null |
Het |
| Eln |
A |
T |
5: 134,735,421 (GRCm39) |
Y787* |
probably null |
Het |
| Erbb2 |
G |
C |
11: 98,315,990 (GRCm39) |
E364D |
probably benign |
Het |
| F5 |
A |
G |
1: 164,007,077 (GRCm39) |
T294A |
probably damaging |
Het |
| Fam47e |
A |
G |
5: 92,733,244 (GRCm39) |
T194A |
possibly damaging |
Het |
| Galk1 |
T |
C |
11: 115,901,073 (GRCm39) |
D202G |
probably damaging |
Het |
| Glb1l2 |
T |
C |
9: 26,682,362 (GRCm39) |
D163G |
probably damaging |
Het |
| Gmip |
A |
G |
8: 70,268,170 (GRCm39) |
E408G |
probably benign |
Het |
| Gp1ba |
A |
T |
11: 70,531,715 (GRCm39) |
|
probably benign |
Het |
| Grm3 |
A |
T |
5: 9,554,881 (GRCm39) |
C804S |
probably damaging |
Het |
| Gzmd |
A |
G |
14: 56,367,737 (GRCm39) |
C179R |
probably damaging |
Het |
| Hadhb |
T |
A |
5: 30,385,935 (GRCm39) |
L415Q |
possibly damaging |
Het |
| Ift80 |
T |
C |
3: 68,823,498 (GRCm39) |
Y588C |
probably damaging |
Het |
| Jazf1 |
T |
C |
6: 53,045,516 (GRCm39) |
T13A |
probably benign |
Het |
| Kat8 |
T |
A |
7: 127,514,467 (GRCm39) |
Y67* |
probably null |
Het |
| Kcnab1 |
G |
A |
3: 65,283,933 (GRCm39) |
E384K |
possibly damaging |
Het |
| Lhx3 |
A |
T |
2: 26,092,200 (GRCm39) |
Y230* |
probably null |
Het |
| Lmx1b |
T |
A |
2: 33,454,674 (GRCm39) |
M365L |
probably damaging |
Het |
| Ly6k |
G |
T |
15: 74,669,051 (GRCm39) |
P76Q |
probably benign |
Het |
| Lypd10 |
G |
A |
7: 24,413,541 (GRCm39) |
G186R |
probably damaging |
Het |
| Map1b |
A |
T |
13: 99,567,200 (GRCm39) |
H1840Q |
unknown |
Het |
| Map3k2 |
A |
G |
18: 32,336,163 (GRCm39) |
I117V |
probably damaging |
Het |
| Med13 |
C |
A |
11: 86,179,899 (GRCm39) |
A1350S |
possibly damaging |
Het |
| Midn |
T |
C |
10: 79,987,495 (GRCm39) |
S109P |
probably damaging |
Het |
| Msh6 |
A |
G |
17: 88,293,653 (GRCm39) |
T803A |
probably benign |
Het |
| Nckap1 |
T |
C |
2: 80,337,182 (GRCm39) |
Y1018C |
probably damaging |
Het |
| Ndufc1 |
A |
T |
3: 51,314,816 (GRCm39) |
N63K |
probably benign |
Het |
| Neb |
A |
T |
2: 52,169,647 (GRCm39) |
S1811R |
probably damaging |
Het |
| Notch1 |
T |
C |
2: 26,371,669 (GRCm39) |
D260G |
probably damaging |
Het |
| Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
| Oas1g |
T |
C |
5: 121,017,205 (GRCm39) |
K283R |
probably benign |
Het |
| Obscn |
T |
C |
11: 58,954,300 (GRCm39) |
T4037A |
|
Het |
| Or6b1 |
T |
G |
6: 42,815,247 (GRCm39) |
L144R |
probably damaging |
Het |
| Or6b3 |
A |
G |
1: 92,439,330 (GRCm39) |
L140P |
probably damaging |
Het |
| Otop2 |
A |
T |
11: 115,217,781 (GRCm39) |
T206S |
probably benign |
Het |
| Pamr1 |
A |
G |
2: 102,471,342 (GRCm39) |
|
probably null |
Het |
| Pkp1 |
G |
A |
1: 135,805,411 (GRCm39) |
T675I |
probably benign |
Het |
| Plxna2 |
G |
A |
1: 194,444,758 (GRCm39) |
V717I |
probably benign |
Het |
| Ptgs2 |
T |
C |
1: 149,975,979 (GRCm39) |
L2P |
possibly damaging |
Het |
| Rarg |
A |
G |
15: 102,147,980 (GRCm39) |
F277S |
probably damaging |
Het |
| Rassf5 |
A |
T |
1: 131,140,076 (GRCm39) |
I161N |
probably damaging |
Het |
| Resf1 |
C |
T |
6: 149,230,902 (GRCm39) |
T1316I |
probably benign |
Het |
| Rxfp4 |
A |
G |
3: 88,559,659 (GRCm39) |
V264A |
probably benign |
Het |
| Secisbp2l |
T |
A |
2: 125,582,597 (GRCm39) |
Q953L |
probably damaging |
Het |
| Serpinb9c |
T |
C |
13: 33,334,218 (GRCm39) |
I275V |
probably benign |
Het |
| Slc2a12 |
T |
C |
10: 22,541,141 (GRCm39) |
V332A |
probably damaging |
Het |
| Slc7a1 |
T |
C |
5: 148,285,113 (GRCm39) |
S127G |
probably damaging |
Het |
| Slc7a4 |
A |
T |
16: 17,393,568 (GRCm39) |
V77E |
probably damaging |
Het |
| Sp8 |
G |
A |
12: 118,812,964 (GRCm39) |
S273N |
possibly damaging |
Het |
| Spag6l |
G |
T |
16: 16,580,921 (GRCm39) |
N475K |
probably benign |
Het |
| St18 |
A |
G |
1: 6,872,913 (GRCm39) |
H216R |
probably benign |
Het |
| Tcirg1 |
C |
T |
19: 3,952,843 (GRCm39) |
|
probably benign |
Het |
| Tmeff1 |
A |
G |
4: 48,658,788 (GRCm39) |
Y87C |
probably damaging |
Het |
| Tmem94 |
T |
C |
11: 115,683,726 (GRCm39) |
V713A |
possibly damaging |
Het |
| Tnrc6b |
G |
T |
15: 80,765,363 (GRCm39) |
R955L |
probably damaging |
Het |
| Trip12 |
A |
G |
1: 84,727,012 (GRCm39) |
V1153A |
probably damaging |
Het |
| Tshz3 |
T |
C |
7: 36,468,800 (GRCm39) |
L263S |
probably damaging |
Het |
| Tubb6 |
G |
A |
18: 67,534,391 (GRCm39) |
|
probably null |
Het |
| Ube3a |
T |
C |
7: 58,926,127 (GRCm39) |
W302R |
probably damaging |
Het |
| Vcpkmt |
A |
T |
12: 69,629,519 (GRCm39) |
V81E |
probably damaging |
Het |
| Vmn1r175 |
T |
A |
7: 23,508,466 (GRCm39) |
I54F |
possibly damaging |
Het |
| Vwa8 |
T |
A |
14: 79,258,075 (GRCm39) |
N741K |
probably benign |
Het |
| Zc3h6 |
G |
A |
2: 128,839,715 (GRCm39) |
R176Q |
probably damaging |
Het |
| Zfp207 |
T |
A |
11: 80,286,253 (GRCm39) |
Y424* |
probably null |
Het |
| Zfp729a |
A |
G |
13: 67,767,676 (GRCm39) |
V851A |
probably benign |
Het |
| Zkscan1 |
G |
T |
5: 138,099,625 (GRCm39) |
A450S |
probably benign |
Het |
| Zkscan3 |
A |
G |
13: 21,580,616 (GRCm39) |
V24A |
possibly damaging |
Het |
|
| Other mutations in Yeats2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01118:Yeats2
|
APN |
16 |
20,005,054 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01128:Yeats2
|
APN |
16 |
19,980,718 (GRCm39) |
splice site |
probably benign |
|
|
IGL01139:Yeats2
|
APN |
16 |
20,033,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01394:Yeats2
|
APN |
16 |
19,980,782 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01482:Yeats2
|
APN |
16 |
20,041,671 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01924:Yeats2
|
APN |
16 |
20,024,917 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01925:Yeats2
|
APN |
16 |
19,998,430 (GRCm39) |
splice site |
probably benign |
|
|
IGL02106:Yeats2
|
APN |
16 |
20,011,970 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL02370:Yeats2
|
APN |
16 |
19,969,221 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02447:Yeats2
|
APN |
16 |
20,012,429 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02669:Yeats2
|
APN |
16 |
20,005,033 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL03155:Yeats2
|
APN |
16 |
20,048,323 (GRCm39) |
critical splice donor site |
probably null |
|
|
tyrion
|
UTSW |
16 |
20,032,151 (GRCm39) |
splice site |
probably benign |
|
|
P0045:Yeats2
|
UTSW |
16 |
19,975,695 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R0051:Yeats2
|
UTSW |
16 |
20,012,474 (GRCm39) |
nonsense |
probably null |
|
|
R0051:Yeats2
|
UTSW |
16 |
20,012,474 (GRCm39) |
nonsense |
probably null |
|
|
R0118:Yeats2
|
UTSW |
16 |
19,975,692 (GRCm39) |
nonsense |
probably null |
|
|
R0157:Yeats2
|
UTSW |
16 |
20,040,427 (GRCm39) |
makesense |
probably null |
|
|
R0184:Yeats2
|
UTSW |
16 |
20,022,435 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0194:Yeats2
|
UTSW |
16 |
19,971,719 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R0612:Yeats2
|
UTSW |
16 |
20,005,175 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0655:Yeats2
|
UTSW |
16 |
20,012,574 (GRCm39) |
nonsense |
probably null |
|
|
R0826:Yeats2
|
UTSW |
16 |
20,011,966 (GRCm39) |
nonsense |
probably null |
|
|
R1526:Yeats2
|
UTSW |
16 |
20,024,836 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1535:Yeats2
|
UTSW |
16 |
20,008,115 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1749:Yeats2
|
UTSW |
16 |
20,005,018 (GRCm39) |
nonsense |
probably null |
|
|
R1842:Yeats2
|
UTSW |
16 |
19,989,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1843:Yeats2
|
UTSW |
16 |
20,048,314 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2000:Yeats2
|
UTSW |
16 |
20,005,141 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2017:Yeats2
|
UTSW |
16 |
19,977,931 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2076:Yeats2
|
UTSW |
16 |
20,005,032 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R2153:Yeats2
|
UTSW |
16 |
19,972,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2167:Yeats2
|
UTSW |
16 |
20,032,151 (GRCm39) |
splice site |
probably benign |
|
|
R2981:Yeats2
|
UTSW |
16 |
20,005,051 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3160:Yeats2
|
UTSW |
16 |
20,012,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3161:Yeats2
|
UTSW |
16 |
20,012,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3162:Yeats2
|
UTSW |
16 |
20,012,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3774:Yeats2
|
UTSW |
16 |
19,969,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4250:Yeats2
|
UTSW |
16 |
19,975,685 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4305:Yeats2
|
UTSW |
16 |
20,027,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4455:Yeats2
|
UTSW |
16 |
19,980,743 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4458:Yeats2
|
UTSW |
16 |
20,032,071 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4811:Yeats2
|
UTSW |
16 |
19,971,645 (GRCm39) |
splice site |
probably null |
|
|
R4902:Yeats2
|
UTSW |
16 |
20,026,418 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5043:Yeats2
|
UTSW |
16 |
20,027,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5047:Yeats2
|
UTSW |
16 |
20,027,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5319:Yeats2
|
UTSW |
16 |
20,005,175 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5328:Yeats2
|
UTSW |
16 |
19,989,955 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5360:Yeats2
|
UTSW |
16 |
19,972,912 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5416:Yeats2
|
UTSW |
16 |
20,030,319 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5672:Yeats2
|
UTSW |
16 |
19,980,779 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5684:Yeats2
|
UTSW |
16 |
20,012,553 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5932:Yeats2
|
UTSW |
16 |
20,011,913 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5946:Yeats2
|
UTSW |
16 |
20,026,513 (GRCm39) |
nonsense |
probably null |
|
|
R6168:Yeats2
|
UTSW |
16 |
19,998,308 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6169:Yeats2
|
UTSW |
16 |
20,038,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6179:Yeats2
|
UTSW |
16 |
20,033,225 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6371:Yeats2
|
UTSW |
16 |
20,040,460 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R6877:Yeats2
|
UTSW |
16 |
19,998,344 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7149:Yeats2
|
UTSW |
16 |
19,972,939 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7405:Yeats2
|
UTSW |
16 |
20,041,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8353:Yeats2
|
UTSW |
16 |
20,041,637 (GRCm39) |
nonsense |
probably null |
|
|
R8367:Yeats2
|
UTSW |
16 |
20,041,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8453:Yeats2
|
UTSW |
16 |
20,041,637 (GRCm39) |
nonsense |
probably null |
|
|
R8506:Yeats2
|
UTSW |
16 |
19,971,684 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8535:Yeats2
|
UTSW |
16 |
19,977,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8828:Yeats2
|
UTSW |
16 |
19,969,260 (GRCm39) |
missense |
probably benign |
0.45 |
|
R8905:Yeats2
|
UTSW |
16 |
20,009,144 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8924:Yeats2
|
UTSW |
16 |
19,969,312 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9087:Yeats2
|
UTSW |
16 |
20,030,500 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9276:Yeats2
|
UTSW |
16 |
19,975,786 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9338:Yeats2
|
UTSW |
16 |
20,041,533 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9338:Yeats2
|
UTSW |
16 |
20,032,078 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9378:Yeats2
|
UTSW |
16 |
20,033,228 (GRCm39) |
missense |
probably benign |
|
|
R9569:Yeats2
|
UTSW |
16 |
19,972,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9664:Yeats2
|
UTSW |
16 |
20,047,491 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGCAGTGCTGGTTAAAAGTC -3'
(R):5'- AGACTATGACACTGTGCGTAG -3'
Sequencing Primer
(F):5'- GCAGCTTTTGGGAGACAGG -3'
(R):5'- ACTATGACACTGTGCGTAGTATGTG -3'
|
| Posted On |
2014-07-14 |
Incidental Mutation