chr5:112766273:T>C Detail (hg38) (APC)

Information

Genome

Assembly Position
hg19 chr5:112,101,970-112,101,970 View the variant detail on this assembly version.
hg38 chr5:112,766,273-112,766,273

HGVS

Type Transcript Protein
RefSeq NM_000038.5:c.136-53T>C
NM_001127511.2:c.166-53T>C
NM_001127510.2:c.136-53T>C
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.104
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance Benign
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 tgv22326721 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
other no assertion criteria provided Familial colorectal cancer unknown Detail
Benign no assertion criteria provided not specified unknown Detail
Benign 2015-03-03 criteria provided, single submitter not provided germline Detail
Benign 2023-07-07 criteria provided, single submitter familial adenomatous polyposis 1 germline Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_000038.6(APC):c.136-53T>C AND Familial colorectal cancer ClinVar Detail
NM_000038.6(APC):c.136-53T>C AND not specified ClinVar Detail
NM_000038.6(APC):c.136-53T>C AND not provided ClinVar Detail
NM_000038.6(APC):c.136-53T>C AND Familial adenomatous polyposis 1 ClinVar Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs2304793 dbSNP
Genome
hg38
Position
chr5:112,766,273-112,766,273
Variant Type
snv
Reference Allele
T
Alternative Allele
C
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs2304793
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.1035
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1735
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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