single nucleotide variant | NM_000238.4(KCNH2):c.164C>A (p.Ser55Ter) | KCNH2 | Pathogenic | 7 | 150671942 | 150671942 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16618417 |
single nucleotide variant | NM_000238.4(KCNH2):c.167G>A (p.Arg56Gln) | KCNH2 | Likely pathogenic | 7 | 150671939 | 150671939 | C | T | criteria provided, single submitter | ClinGen:CA005006,UniProtKB:Q12809#VAR_008910 |
single nucleotide variant | NM_000238.4(KCNH2):c.172G>A (p.Glu58Lys) | KCNH2 | Likely pathogenic | 7 | 150671934 | 150671934 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA005294 |
single nucleotide variant | NM_000238.4(KCNH2):c.173A>G (p.Glu58Gly) | KCNH2 | Likely pathogenic | 7 | 150671933 | 150671933 | T | C | criteria provided, single submitter | ClinGen:CA005331,UniProtKB:Q12809#VAR_074778 |
single nucleotide variant | NM_000238.4(KCNH2):c.202T>C (p.Phe68Leu) | KCNH2 | Likely pathogenic | 7 | 150671904 | 150671904 | A | G | criteria provided, single submitter | ClinGen:CA006163,UniProtKB:Q12809#VAR_074780 |
single nucleotide variant | NM_000238.4(KCNH2):c.206T>C (p.Leu69Pro) | KCNH2 | Pathogenic | 7 | 150671900 | 150671900 | A | G | criteria provided, single submitter | ClinGen:CA006187 |
single nucleotide variant | NM_000238.4(KCNH2):c.209A>G (p.His70Arg) | KCNH2 | Pathogenic/Likely pathogenic | 7 | 150671897 | 150671897 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA006229,UniProtKB:Q12809#VAR_008912 |
single nucleotide variant | NM_000238.4(KCNH2):c.211G>C (p.Gly71Arg) | KCNH2 | Pathogenic | 7 | 150671895 | 150671895 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA006261,UniProtKB:Q12809#VAR_074782 |
single nucleotide variant | NM_000238.4(KCNH2):c.215C>A (p.Pro72Gln) | KCNH2 | Pathogenic/Likely pathogenic | 7 | 150671891 | 150671891 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA006293,UniProtKB:Q12809#VAR_009910 |
Deletion | NM_000238.4(KCNH2):c.221_251del (p.Thr74fs) | KCNH2 | Pathogenic | 7 | 150671855 | 150671885 | CTGCGCGATCTGCGCGGCAGCGCGGCGCTGCG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658761346 |