Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_004360.5(CDH1):c.2295+1G>C | CDH1 | Likely pathogenic | 16 | 68862208 | 68862208 | G | C | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_004360.5(CDH1):c.2293C>T (p.Gln765Ter) | CDH1 | Pathogenic | 16 | 68862205 | 68862205 | C | T | reviewed by expert panel | ClinGen:CA10580156 |
single nucleotide variant | NM_004360.5(CDH1):c.2287G>T (p.Glu763Ter) | CDH1 | Pathogenic | 16 | 68862199 | 68862199 | G | T | reviewed by expert panel | ClinGen:CA332835 |
Deletion | NM_004360.5(CDH1):c.2276del (p.Gly759fs) | CDH1 | Pathogenic | 16 | 68862187 | 68862187 | AG | A | reviewed by expert panel | - |
single nucleotide variant | NM_004360.5(CDH1):c.2272G>T (p.Glu758Ter) | CDH1 | Pathogenic | 16 | 68862184 | 68862184 | G | T | reviewed by expert panel | ClinGen:CA396470014 |
single nucleotide variant | NM_004360.5(CDH1):c.2272G>A (p.Glu758Lys) | CDH1 | Likely pathogenic | 16 | 68862184 | 68862184 | G | A | criteria provided, single submitter | ClinGen:CA194182 |
single nucleotide variant | NM_004360.5(CDH1):c.2265T>A (p.Tyr755Ter) | CDH1 | Pathogenic | 16 | 68862177 | 68862177 | T | A | reviewed by expert panel | - |
single nucleotide variant | NM_004360.5(CDH1):c.2195G>A (p.Arg732Gln) | CDH1 | Likely pathogenic | 16 | 68862107 | 68862107 | G | A | reviewed by expert panel | ClinGen:CA16615410 |
single nucleotide variant | NM_004360.5(CDH1):c.2165-1G>T | CDH1 | Likely pathogenic | 16 | 68862076 | 68862076 | G | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_004360.5(CDH1):c.2165-1G>C | CDH1 | Likely pathogenic | 16 | 68862076 | 68862076 | G | C | reviewed by expert panel | ClinGen:CA396469209 |