single nucleotide variant | NM_003242.6(TGFBR2):c.1255G>T (p.Val419Leu) | TGFBR2 | Likely pathogenic | 3 | 30715597 | 30715597 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA322630 |
single nucleotide variant | NM_003242.6(TGFBR2):c.1256T>A (p.Val419Glu) | TGFBR2 | Likely pathogenic | 3 | 30715598 | 30715598 | T | A | criteria provided, single submitter | ClinGen:CA324927 |
single nucleotide variant | NM_003242.6(TGFBR2):c.1279C>T (p.Pro427Ser) | TGFBR2 | Likely pathogenic | 3 | 30715621 | 30715621 | C | T | criteria provided, single submitter | ClinGen:CA319801 |
single nucleotide variant | NM_003242.6(TGFBR2):c.1338T>G (p.Asp446Glu) | TGFBR2 | Likely pathogenic | 3 | 30715680 | 30715680 | T | G | criteria provided, single submitter | ClinGen:CA321430 |
single nucleotide variant | NM_004612.4(TGFBR1):c.696G>C (p.Lys232Asn) | TGFBR1 | Likely pathogenic | 9 | 101900262 | 101900262 | G | C | criteria provided, single submitter | ClinGen:CA325117 |
single nucleotide variant | NM_004612.4(TGFBR1):c.724T>C (p.Trp242Arg) | TGFBR1 | Likely pathogenic | 9 | 101900290 | 101900290 | T | C | criteria provided, single submitter | ClinGen:CA324960 |
single nucleotide variant | NM_004612.4(TGFBR1):c.758T>C (p.Met253Thr) | TGFBR1 | Likely pathogenic | 9 | 101900324 | 101900324 | T | C | criteria provided, single submitter | ClinGen:CA321603 |
single nucleotide variant | NM_004612.4(TGFBR1):c.820A>G (p.Thr274Ala) | TGFBR1 | Likely pathogenic | 9 | 101904832 | 101904832 | A | G | criteria provided, single submitter | ClinGen:CA323920 |
single nucleotide variant | NM_004612.4(TGFBR1):c.824A>G (p.Gln275Arg) | TGFBR1 | Likely pathogenic | 9 | 101904836 | 101904836 | A | G | criteria provided, single submitter | ClinGen:CA319831 |
single nucleotide variant | NM_004612.4(TGFBR1):c.1052A>C (p.Asp351Ala) | TGFBR1 | Likely pathogenic | 9 | 101907092 | 101907092 | A | C | criteria provided, single submitter | ClinGen:CA322591 |