single nucleotide variant | NM_000435.3(NOTCH3):c.2953C>T (p.Arg985Cys) | NOTCH3 | Pathogenic/Likely pathogenic | 19 | 15291813 | 15291813 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA404514605 |
single nucleotide variant | NM_000435.3(NOTCH3):c.2956T>G (p.Cys986Gly) | NOTCH3 | Likely pathogenic | 19 | 15291810 | 15291810 | A | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000435.3(NOTCH3):c.2989T>G (p.Cys997Gly) | NOTCH3 | Pathogenic | 19 | 15291777 | 15291777 | A | C | criteria provided, single submitter | ClinGen:CA404514458 |
single nucleotide variant | NM_000435.3(NOTCH3):c.3011G>A (p.Cys1004Tyr) | NOTCH3 | Pathogenic | 19 | 15291623 | 15291623 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA404514396 |
single nucleotide variant | NM_000435.3(NOTCH3):c.3016C>T (p.Arg1006Cys) | NOTCH3 | Pathogenic | 19 | 15291618 | 15291618 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA404514381 |
single nucleotide variant | NM_000435.3(NOTCH3):c.3026G>A (p.Cys1009Tyr) | NOTCH3 | Pathogenic | 19 | 15291608 | 15291608 | C | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000435.3(NOTCH3):c.3040C>T (p.Arg1014Cys) | NOTCH3 | Pathogenic | 19 | 15291594 | 15291594 | G | A | criteria provided, single submitter | ClinGen:CA404514328 |
single nucleotide variant | NM_000435.3(NOTCH3):c.3062A>G (p.Tyr1021Cys) | NOTCH3 | Pathogenic/Likely pathogenic | 19 | 15291572 | 15291572 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA404514283 |
single nucleotide variant | NM_000435.3(NOTCH3):c.3065G>T (p.Cys1022Phe) | NOTCH3 | Pathogenic | 19 | 15291569 | 15291569 | C | A | criteria provided, single submitter | ClinGen:CA404514274 |
single nucleotide variant | NM_000435.3(NOTCH3):c.3091C>T (p.Arg1031Cys) | NOTCH3 | Pathogenic | 19 | 15291543 | 15291543 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA404514218 |