chr5:112175639:C>T Detail (hg19) (APC)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr5:112,175,639-112,175,639 |
hg38 | chr5:112,839,942-112,839,942 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000038.5:c.4348C>T | NP_000029.2:p.Arg1450Ter |
NM_001127510.2:c.4348C>T | NP_001120982.1:p.Arg1450Ter | |
NM_001127511.2:c.4294C>T | NP_001120983.2:p.Arg1432Ter |
Summary
MGeND
Clinical significance |
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Variant entry | 45 |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
MGeND
Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
---|---|---|---|---|---|---|---|---|---|
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2020/04/20 | fundus of stomach |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | body of stomach |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | pyloric antrum |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | caecum |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | descending colon |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | colon, unspecified |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | malignant neoplasm of rectosigmoid junction |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2020/04/20 | malignant neoplasm of rectum |
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MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2021/07/26 | duodenum |
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MGS000029
(TMGS000133) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2021/07/26 | connective and other soft tissue |
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MGS000029
(TMGS000133) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2021/07/26 | stomach, unspecified |
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MGS000029
(TMGS000133) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2021/07/26 | other |
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MGS000029
(TMGS000133) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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2021/07/26 | colon, unspecified |
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MGS000029
(TMGS000133) |
Hitoshi Nakagama | National Cancer Center Japan | |||
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Adenocarcinoma of sigmoid colon (disorder) |
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MGS000021
(TMGS000080) |
Manabu Muto | Kyoto University | ||||
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Colorectal |
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MGS000038
(TMGS000091) |
Manabu Muto Ichiro Kinoshita |
Kyoto University Department of Medical Oncology Faculty of Medicine and Graduate School of Medicine Hokkaido University |
||||
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Primary adenocarcinoma of colon (disorder) |
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MGS000023
(TMGS000082) |
Manabu Muto | Kyoto University | ||||
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colorectal cancer |
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MGS000018
(TMGS000110) |
Hitoshi Nakagama | National Cancer Center Japan |
30742731
|
|||
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familial adenomatous polyposis |
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MGS000001
(TMGS000174) |
Kenjiro Kosaki | Keio University | ||||
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2020/04/20 | other |
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MGS000039
(TMGS000092) |
Hitoshi Nakagama | National Cancer Center Japan |
29659903
|
||
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2020/04/20 | rectal carcinoma |
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MGS000039
(TMGS000092) |
Hitoshi Nakagama | National Cancer Center Japan |
29659903
|
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2023-07-07 | criteria provided, multiple submitters, no conflicts | familial adenomatous polyposis 1 |
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Detail |
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2015-07-14 | no assertion criteria provided | Neoplasm of the large intestine |
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Detail |
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2024-02-06 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2022-03-29 | criteria provided, single submitter | Hereditary cancer-predisposing syndrome |
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Detail |
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2016-11-01 | criteria provided, single submitter | Familial multiple polyposis syndrome |
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Detail |
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no assertion provided | APC-Associated Polyposis Disorders |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.120 | Polyposis, Adenomatous Intestinal | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter) AND Familial adenomatous polyposis 1 | ClinVar | Detail |
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter) AND Neoplasm of the large intestine | ClinVar | Detail |
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter) AND not provided | ClinVar | Detail |
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter) AND Hereditary cancer-predisposing syndrome | ClinVar | Detail |
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter) AND Familial multiple polyposis syndrome | ClinVar | Detail |
NM_000038.6(APC):c.4348C>T (p.Arg1450Ter) AND APC-Associated Polyposis Disorders | ClinVar | Detail |
NA | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs121913332 dbSNP
- Genome
- hg19
- Position
- chr5:112,175,639-112,175,639
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
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