chr16:68812265:T>C Detail (hg38) (CDH1)

Information

Genome

Assembly Position
hg19 chr16:68,846,168-68,846,168 View the variant detail on this assembly version.
hg38 chr16:68,812,265-68,812,265

HGVS

Type Transcript Protein
RefSeq NM_001317184.1:c.1137+2T>C
NM_001317186.1:c.1137+2T>C
NM_004360.4:c.1137+2T>C
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 192090 OMIM
HGNC 1748 HGNC
Ensembl ENSG00000039068 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
Likely pathogenic 2020-05-26 criteria provided, multiple submitters, no conflicts Hereditary cancer-predisposing syndrome germline Detail
Pathogenic 2020-01-31 criteria provided, single submitter Hereditary diffuse gastric adenocarcinoma germline Detail
Likely pathogenic 2023-10-23 reviewed by expert panel CDH1-related diffuse gastric and lobular breast cancer syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.123 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_004360.5(CDH1):c.1137+2T>C AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_004360.5(CDH1):c.1137+2T>C AND Hereditary diffuse gastric adenocarcinoma ClinVar Detail
NM_004360.5(CDH1):c.1137+2T>C AND CDH1-related diffuse gastric and lobular breast cancer syndrome ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs786202817 dbSNP
Genome
hg38
Position
chr16:68,812,265-68,812,265
Variant Type
snv
Reference Allele
T
Alternative Allele
C
Genome browser