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PIONEERING CANCER RESEARCH
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Breast
HCI-015
Model Details
Patient
PDX Model
Histology
Metastasis
Patient Treatment
Patient Information for Model: HCI-015
Contact Model Developer
Model Contact
Model: HCI-015
Model Contact: Alana Welm
Institution: HCI Breast PDX Program
Email:
Alana.Welm@hci.utah.edu
Patient Information
Clinical Timeline
Color Keys:
Positive
Negative
N/A
Clinical Information at Collection
Clinical Biomarkers/Mutations at Collection
Pathology Information at Collection
Model Information for Model: HCI-015
Model Details - Initial Implantation of Patient Tissue
Biomarkers & Mutations
Model Details - Acceptable Conditions for Passaging
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: 59
F
P
1
2
3
4
N
E
Rows Per Page
10
15
25
50
Download
Gene
Filter by Gene
Chr
Filter by Chr
Start
End
Ref
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
AKAP9
chr7
92022864
92022864
A
AAAC
c.4004_4006dup
aaa/aAACaa
p.K1335_L1336insQ
0.538
50
35
In-frame Insertion
In-frame Insertion
MODERATE
ENST00000356239.8
COSV62337888
rs10644111
50
35
ENST00000356239.8
COSV62337888
rs10644111
AR
chrX
67545316
67545316
T
TGCAGCA
c.234_239dup
ctg/ctGCAGCAg
p.Q79_Q80dup
0.665
48
3
In-frame Insertion
In-frame Insertion
MODERATE
ENST00000374690.9
COSV65953707
48
3
ENST00000374690.9
COSV65953707
ARID1A
chr1
26696664
26696679
AGCCGGCAGCGGCGGC
A
c.263_277del
GCCGGCAGCGGCGGC/-
p.A88_G92del
0.281
19
1
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000324856.13
rs1191458952
19
1
ENST00000324856.13
rs1191458952
BRCA2
chr13
32376714
32376714
C
T
c.8677C>T
Cag/Tag
p.Q2893*
0.968
21
1
Nonsense Mutation
Nonsense Mutation
HIGH
ENST00000380152.7
Pathogenic
rs397507409
21
1
ENST00000380152.7
Pathogenic
rs397507409
BRCA2
chr13
32379413
32379413
G
A
c.8851G>A
Gcc/Acc
p.A2951T
0.989
21
2
Missense Variant
Missense Variant
MODERATE
ENST00000380152.7
Benign
COSV66463542
0.009834290000
rs11571769
21
2
ENST00000380152.7
Benign
COSV66463542
rs11571769
CDH1
chr16
68829687
68829687
G
A
c.2329G>A
Gac/Aac
p.D777N
0.46
7
1
Missense Variant
Missense Variant
MODERATE
ENST00000261769.10
Likely_benign
0.000105520000
rs372989292
7
1
ENST00000261769.10
Likely_benign
rs372989292
CHD2
chr15
93024673
93024673
C
G
c.5455C>G
Cca/Gca
p.P1819A
0.217
5
1
Missense Variant
Missense Variant
MODERATE
ENST00000394196.9
5
1
ENST00000394196.9
CIITA
chr16
10909070
10909070
A
G
c.2702A>G
cAg/cGg
p.Q901R
0.963
85
84
Missense Variant
Missense Variant
MODERATE
ENST00000618327.4
Benign
0.983235000000
rs7197779
85
84
ENST00000618327.4
Benign
rs7197779
CREB3L2
chr7
137928167
137928170
CTGG
C
c.299_301del
aCCAgt/agt
p.T100del
0.982
49
49
In-frame Deletion
In-frame Deletion
MODERATE
ENST00000330387.11
COSV57791862
rs3217268
49
49
ENST00000330387.11
COSV57791862
rs3217268
CSMD3
chr8
112244454
112244454
T
C
c.10342A>G
Aca/Gca
p.T3448A
0.131
24
1
Missense Variant
Missense Variant
MODERATE
ENST00000297405.10
COSV52271112
rs1586513717
24
1
ENST00000297405.10
COSV52271112
rs1586513717
CSMD3
chr8
112265503
112265503
C
A
c.9596G>T
tGc/tTc
p.C3199F
0.032
24
1
Missense Variant
Missense Variant
MODERATE
ENST00000297405.10
COSV99830025
24
1
ENST00000297405.10
COSV99830025
CYP2C8
chr10
95058454
95058454
G
C
c.700C>G
Ctt/Gtt
p.L234V
0.274
3
1
Missense Variant
Missense Variant
MODERATE
ENST00000371270.6
3
1
ENST00000371270.6
DCC
chr18
53322098
53322098
A
G
c.2105A>G
aAt/aGt
p.N702S
0.69
15
3
Missense Variant
Missense Variant
MODERATE
ENST00000442544.7
Uncertain_significance
0.002677680000
rs35691189
15
3
ENST00000442544.7
Uncertain_significance
rs35691189
EP300
chr22
41129899
41129899
G
A
c.1178G>A
tGt/tAt
p.C393Y
0.958
22
1
Missense Variant
Missense Variant
MODERATE
ENST00000263253.9
22
1
ENST00000263253.9
EP300
chr22
41149786
41149786
C
T
c.2405C>T
cCg/cTg
p.P802L
0.951
22
1
Missense Variant
Missense Variant
MODERATE
ENST00000263253.9
Uncertain_significance
COSV54329352
0.000046432300
rs749702423
22
1
ENST00000263253.9
Uncertain_significance
COSV54329352
rs749702423
Total mutations showing: 59
F
P
1
2
3
4
N
E
Rows Per Page
10
15
25
50
Download
CNV
Histology Information for Model: HCI-015
There are no histology images for this model.
Metastasis Information for Model: HCI-015
Patient
PDX
Abdomen
Adrenal gland
Bone
Bones
Brain
CTC
Chest
Chest wall
Contralateral Breast
Dura
Fallopian Tubes
Head
Kidney
Liver
Lung
Lymph node
Lymph nodes
Neck
Ovary
Pancreas
Pericardium
Peritoneal cavity
Peritoneum
Pleura
Pleural effusion
Shoulder
Skin
Spine
Spleen
Thoracic Spine
Thymus
Patient Treatment Information for Model: HCI-015
Event Id
Treatment
Treatment Setting
Age at Start
Age at End
Duration
Clinical Response
10
Doxorubicon, Cyclophosphamide/Paclitaxel
Neoadjuvant
48.33
48.67
124 days
Progressive disease
20
Radiation Therapy Brain
Adjuvant
49.08
49.16
29 days
Progressive disease
25
Radiation Therapy Brain
Adjuvant
49.25
49.33
29 days
Progressive disease
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