chr5:112170646:A>G Detail (hg19) (APC)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr5:112,170,646-112,170,646 |
hg38 | chr5:112,834,949-112,834,949 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000038.5:c.1744-2A>G | |
NM_001127511.2:c.1690-2A>G | ||
NM_001127510.2:c.1744-2A>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2023-05-03 | criteria provided, multiple submitters, no conflicts | familial adenomatous polyposis 1 |
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Detail |
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no assertion criteria provided | Carcinoma of colon |
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Detail | |
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2019-12-03 | criteria provided, multiple submitters, no conflicts | Hereditary cancer-predisposing syndrome |
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Detail |
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2022-08-23 | criteria provided, single submitter | Familial multiple polyposis syndrome |
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Detail |
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2023-05-26 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2023-05-09 | criteria provided, single submitter | familial adenomatous polyposis 1 |
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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.1744-2A>G AND Familial adenomatous polyposis 1 | ClinVar | Detail |
NM_000038.6(APC):c.1744-2A>G AND Carcinoma of colon | ClinVar | Detail |
NM_000038.6(APC):c.1744-2A>G AND Hereditary cancer-predisposing syndrome | ClinVar | Detail |
NM_000038.6(APC):c.1744-2A>G AND Familial multiple polyposis syndrome | ClinVar | Detail |
NM_000038.6(APC):c.1744-2A>G AND not provided | ClinVar | Detail |
NM_000038.6(APC):c.1744-2A>G AND Familial adenomatous polyposis 1 | ClinVar | Detail |
NA | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs587783035 dbSNP
- Genome
- hg19
- Position
- chr5:112,170,646-112,170,646
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
Genome browser