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PIONEERING CANCER RESEARCH
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Pancreas
BCM-PDAC-28
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: BCM-PDAC-28
Contact Model Developer
Model Contact
Model: BCM-PDAC-28
Model Contact: Qizhi Cathy Yao
Institution: BCM Pancreas PDX Program
Email:
qizhiyao@bcm.edu
Patient Information
Clinical Timeline
Clinical Information at Collection
Clinical Biomarkers/Mutations at Collection
Pathology Information at Collection
Model Information for Model: BCM-PDAC-28
Model Details - Initial Implantation of Patient Tissue
Mutations (Cancer Gene Census List)
Show/Hide Columns
The number of models in this collection with mutations in the listed gene;
may include models that are not publicly available for distribution.
The number of models in this collection with mutations at the listed site;
may include models that are not publicly available for distribution.
Total mutations showing: 85
F
P
1
2
3
4
5
6
N
E
Rows Per Page
10
15
25
50
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Gene
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Chr
Filter by Chr
Start
End
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Alt
cDNA Change
Codon Change
Protein Change
TVAF
Gene Mutation Freq.
Site Mutation Freq.
Most Severe Effect
All Effects
Mutation Impact
Transcript ID
ClinVar Clinical Significance
COSMIC ID
gnomAD Non-Cancer AF
dbSNP ID
Gene Mutation Freq.
Site Mutation Freq.
Transcript ID
ClinVar Clinical Significance
COSMIC ID
dbSNP ID
ABL2
chr1
179108431
179108431
C
T
c.2836G>A
Gtg/Atg
p.V946M
0.918
5
5
Missense Variant
Missense Variant
MODERATE
ENST00000502732.6
COSV61020221
0.000506462000
rs28913889
5
5
ENST00000502732.6
COSV61020221
rs28913889
AFF3
chr2
99593652
99593652
G
C
c.2084C>G
tCg/tGg
p.S695W
0.095
8
4
Missense Variant
Missense Variant
MODERATE
ENST00000409579.5
rs1436457705
8
4
ENST00000409579.5
rs1436457705
APC
chr5
112838202
112838202
C
T
c.2608C>T
Cca/Tca
p.P870S
0.409
6
3
Missense Variant
Missense Variant
MODERATE
ENST00000257430.9
Benign/Likely_benign
COSV57389158
0.002076830000
rs33974176
6
3
ENST00000257430.9
Benign/Likely_benign
COSV57389158
rs33974176
AR
chrX
67546514
67546529
TGGCGGCGGCGGCGGC
T
c.1406_1420del
GGCGGCGGCGGCGGC/-
p.G469_G473del
0.96
17
4
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000374690.9
17
4
ENST00000374690.9
ARID1A
chr1
26775697
26775697
A
G
c.5114A>G
aAc/aGc
p.N1705S
0.894
12
2
Missense Variant
Missense Variant
MODERATE
ENST00000324856.13
Benign
COSV104411707
0.006846420000
rs61756316
12
2
ENST00000324856.13
Benign
COSV104411707
rs61756316
CDK12
chr17
39526140
39526140
C
T
c.3584C>T
aCg/aTg
p.T1195M
0.423
3
3
Missense Variant
Missense Variant
MODERATE
ENST00000447079.6
not_provided
COSV70999311
0.002212950000
rs61741615
3
3
ENST00000447079.6
not_provided
COSV70999311
rs61741615
CHD4
chr12
6578884
6578884
G
A
c.4943C>T
tCa/tTa
p.S1648L
0.519
3
3
Missense Variant
Missense Variant
MODERATE
ENST00000544040.7
Benign
0.005313810000
rs35512811
3
3
ENST00000544040.7
Benign
rs35512811
CIITA
chr16
10909070
10909070
A
G
c.2702A>G
cAg/cGg
p.Q901R
0.981
24
24
Missense Variant
Missense Variant
MODERATE
ENST00000618327.4
Benign
0.983235000000
rs7197779
24
24
ENST00000618327.4
Benign
rs7197779
CNTNAP2
chr7
147132408
147132408
C
T
c.1247C>T
gCg/gTg
p.A416V
0.422
3
3
Missense Variant
Missense Variant
MODERATE
ENST00000361727.8
Benign/Likely_benign
COSV62220340
0.001479540000
rs34456867
3
3
ENST00000361727.8
Benign/Likely_benign
COSV62220340
rs34456867
CREB3L2
chr7
137928167
137928170
CTGG
C
c.299_301del
aCCAgt/agt
p.T100del
0.921
10
10
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000330387.11
COSV57791862
rs3217268
10
10
ENST00000330387.11
COSV57791862
rs3217268
CRTC3
chr15
90604420
90604420
G
A
c.449G>A
gGg/gAg
p.G150E
0.578
4
3
Missense Variant
Missense Variant
MODERATE
ENST00000268184.11
0.000346079000
rs145024567
4
3
ENST00000268184.11
rs145024567
DAXX
chr6
33320508
33320508
C
T
c.1123G>A
Gtc/Atc
p.V375I
0.573
4
3
Missense Variant
Missense Variant
MODERATE
ENST00000374542.10
Benign
COSV105853115
0.001283900000
rs61737694
4
3
ENST00000374542.10
Benign
COSV105853115
rs61737694
ECT2L
chr6
138814569
138814569
G
A
c.145G>A
Gca/Aca
p.A49T
0.13
6
4
Missense Variant
Missense Variant
MODERATE
ENST00000541398.6
not_provided
0.002009010000
rs146769748
6
4
ENST00000541398.6
not_provided
rs146769748
ECT2L
chr6
138876471
138876471
G
C
c.1579-1G>C
0.107
6
3
Splice Acceptor Variant
Splice Acceptor Variant
HIGH
ENST00000541398.6
rs79069095
6
3
ENST00000541398.6
rs79069095
ECT2L
chr6
138844465
138844465
G
A
c.649G>A
Gtg/Atg
p.V217M
0.906
6
3
Missense Variant
Missense Variant
MODERATE
ENST00000541398.6
not_provided
COSV99056751
0.002871950000
rs75478555
6
3
ENST00000541398.6
not_provided
COSV99056751
rs75478555
Total mutations showing: 85
F
P
1
2
3
4
5
6
N
E
Rows Per Page
10
15
25
50
Download
CNV
Histology Information for Model: BCM-PDAC-28
There are no histology images for this model.
Metastasis Information for Model: BCM-PDAC-28
Patient
PDX
Liver
Local recurrence
Lung
Rectum
lymph node
Patient Treatment Information for Model: BCM-PDAC-28
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
Pathologic Response
Reason Stopped
20
Gemcitabine/Abraxane with investigational agent (HALO 301)
Adjuvant
59.34
60.53
434 days
Progressive Disease (PD)
No Response (NR)
Stopped due to disease progression and side effects
Please wait...