chr5:112775742:G>A Detail (hg38) (APC)

Information

Genome

Assembly Position
hg19 chr5:112,111,439-112,111,439 View the variant detail on this assembly version.
hg38 chr5:112,775,742-112,775,742

HGVS

Type Transcript Protein
RefSeq NM_000038.5:c.531+5G>A
NM_001127511.2:c.561+5G>A
NM_001127510.2:c.531+5G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 611731 OMIM
HGNC 583 HGNC
Ensembl ENSG00000134982 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2021-10-26 criteria provided, single submitter not provided germline Detail
Pathogenic 2023-12-29 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
Pathogenic 2023-04-27 criteria provided, single submitter familial adenomatous polyposis 1 unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.121 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000038.6(APC):c.531+5G>A AND not provided ClinVar Detail
NM_000038.6(APC):c.531+5G>A AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_000038.6(APC):c.531+5G>A AND Familial adenomatous polyposis 1 ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs587779798 dbSNP
Genome
hg38
Position
chr5:112,775,742-112,775,742
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser