Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.148827330T>A | CA361894733 | ADRB2 | c.499T>A (p.Leu167Met) | |
5 | g.148827330T>C | CA447425613 | ADRB2 | c.499T>C (p.Leu167=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.148827330T>G | CA361894734 | ADRB2 | c.499T>G (p.Leu167Val) | |
5 | g.148827330T= | CA1590223698 | ADRB2 | c.499T= (p.Leu167=) | |
5 | g.148827331T>A | CA361894735 | ADRB2 | c.500T>A (p.Leu167Ter) | |
5 | g.148827331T>C | CA361894736 | ADRB2 | c.500T>C (p.Leu167Ser) | |
5 | g.148827331T>G | CA361894737 | ADRB2 | c.500T>G (p.Leu167Trp) | |
5 | g.148827332G>A | CA447425616 | ADRB2 | c.501G>A (p.Leu167=) | gnomAD v4 |
5 | g.148827332G>C | CA361894738 | ADRB2 | c.501G>C (p.Leu167Phe) | |
5 | g.148827332G>T | CA361894739 | ADRB2 | c.501G>T (p.Leu167Phe) | |
5 | g.148827333C>A | CA361894740 | ADRB2 | c.502C>A (p.Pro168Thr) | |
5 | g.148827333C>G | CA361894742 | ADRB2 | c.502C>G (p.Pro168Ala) | gnomAD v4 |
5 | g.148827333C>T | CA361894741 | ADRB2 | c.502C>T (p.Pro168Ser) | gnomAD v4 COSMIC |
5 | g.148827334C>A | CA361894743 | ADRB2 | c.503C>A (p.Pro168His) | |
5 | g.148827334C>G | CA361894745 | ADRB2 | c.503C>G (p.Pro168Arg) | |
5 | g.148827334C>T | CA361894744 | ADRB2 | c.503C>T (p.Pro168Leu) | |
5 | g.148827335C>A | CA447425621 | ADRB2 | c.504C>A (p.Pro168=) | |
5 | g.148827335C= | CA1590223699 | ADRB2 | c.504C= (p.Pro168=) | |
5 | g.148827335C>G | CA3498419 | ADRB2 | c.504C>G (p.Pro168=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.148827335C>T | CA447425622 | ADRB2 | c.504C>T (p.Pro168=) | |
5 | g.148827336A= | CA1590223700 | ADRB2 | c.505A= (p.Ile169=) | |
5 | g.148827336A>C | CA361894747 | ADRB2 | c.505A>C (p.Ile169Leu) | |
5 | g.148827336A>G | CA361894746 | ADRB2 | c.505A>G (p.Ile169Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
5 | g.148827336A>T | CA361894748 | ADRB2 | c.505A>T (p.Ile169Phe) | |
5 | g.148827337T>A | CA361894749 | ADRB2 | c.506T>A (p.Ile169Asn) | |
5 | g.148827337T>C | CA361894750 | ADRB2 | c.506T>C (p.Ile169Thr) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.148827337T>G | CA361894751 | ADRB2 | c.506T>G (p.Ile169Ser) | |
5 | g.148827337T= | CA1590223701 | ADRB2 | c.506T= (p.Ile169=) | |
5 | g.148827338T>A | CA447425624 | ADRB2 | c.507T>A (p.Ile169=) | |
5 | g.148827338T>C | CA447425625 | ADRB2 | c.507T>C (p.Ile169=) | |
5 | g.148827338T>G | CA361894752 | ADRB2 | c.507T>G (p.Ile169Met) | |
5 | g.148827339C>A | CA361894753 | ADRB2 | c.508C>A (p.Gln170Lys) | COSMIC |
5 | g.148827339C>G | CA361894754 | ADRB2 | c.508C>G (p.Gln170Glu) | |
5 | g.148827339C>T | CA361894755 | ADRB2 | c.508C>T (p.Gln170Ter) | |
5 | g.148827340A>C | CA361894756 | ADRB2 | c.509A>C (p.Gln170Pro) | |
5 | g.148827340A>G | CA361894757 | ADRB2 | c.509A>G (p.Gln170Arg) | |
5 | g.148827340A>T | CA361894758 | ADRB2 | c.509A>T (p.Gln170Leu) | |
5 | g.148827341G>A | CA447425630 | ADRB2 | c.510G>A (p.Gln170=) | |
5 | g.148827341G>C | CA361894759 | ADRB2 | c.510G>C (p.Gln170His) | |
5 | g.148827341G>T | CA361894760 | ADRB2 | c.510G>T (p.Gln170His) | gnomAD v4 |
5 | g.148827342A>C | CA361894763 | ADRB2 | c.511A>C (p.Met171Leu) | |
5 | g.148827342A>G | CA361894761 | ADRB2 | c.511A>G (p.Met171Val) | gnomAD v4 |
5 | g.148827342A>T | CA361894762 | ADRB2 | c.511A>T (p.Met171Leu) | gnomAD v4 |
5 | g.148827343T>A | CA361894764 | ADRB2 | c.512T>A (p.Met171Lys) | |
5 | g.148827343T>C | CA361894765 | ADRB2 | c.512T>C (p.Met171Thr) | |
5 | g.148827343T>G | CA361894766 | ADRB2 | c.512T>G (p.Met171Arg) | |
5 | g.148827344G>A | CA361894767 | ADRB2 | c.513G>A (p.Met171Ile) | |
5 | g.148827344G>C | CA361894768 | ADRB2 | c.513G>C (p.Met171Ile) | |
5 | g.148827344G>T | CA361894769 | ADRB2 | c.513G>T (p.Met171Ile) | |
5 | g.148827344_148827345delinsGC | CA1590223702 | ADRB2 | c.513_514delinsGC (p.Met171=) |