chr16:68823557:C>G Detail (hg38) (CDH1)

Information

Genome

Assembly Position
hg19 chr16:68,857,460-68,857,460 View the variant detail on this assembly version.
hg38 chr16:68,823,557-68,823,557

HGVS

Type Transcript Protein
RefSeq NM_001317184.1:c.2095C>G NP_001304113.1:p.Gln699Glu
NM_001317186.1:c.2095C>G NP_001304115.1:p.Gln699Glu
NM_004360.4:c.2095C>G NP_004351.1:p.Gln699Glu
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Uncertain significance
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
Uncertain significance 2015-10-16 criteria provided, single submitter Hereditary cancer-predisposing syndrome germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.389 hereditary diffuse gastric cancer NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_004360.5(CDH1):c.2095C>G (p.Gln699Glu) AND Hereditary cancer-predisposing syndrome 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
rs121964874 dbSNP
Genome
hg38
Position
chr16:68,823,557-68,823,557
Variant Type
snv
Reference Allele
C
Alternative Allele
G
Genome browser