Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49619284C>A | CA364403381 | RHAG | c.236G>T (p.Ser79Ile) n.511G>T | |
6 | g.49619284C= | CA1627477992 | RHAG | c.236G= (p.Ser79=) n.511G= | |
6 | g.49619284C>G | CA3847960 | RHAG | c.236G>C (p.Ser79Thr) n.511G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49619284C>T | CA122827 | RHAG | c.236G>A (p.Ser79Asn) n.511G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49619285T>A | CA364403383 | RHAG | c.235A>T (p.Ser79Cys) n.510A>T | dbSNP |
6 | g.49619285T>C | CA364403384 | RHAG | c.235A>G (p.Ser79Gly) n.510A>G | |
6 | g.49619285T>G | CA364403387 | RHAG | c.235A>C (p.Ser79Arg) n.510A>C | gnomAD v4 |
6 | g.49619286G>A | CA3847961 | RHAG | c.234C>T (p.Ser78=) n.509C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49619286G>C | CA364403394 | RHAG | c.234C>G (p.Ser78Arg) n.509C>G | |
6 | g.49619286G= | CA1627477993 | RHAG | c.234C= (p.Ser78=) n.509C= | |
6 | g.49619286G>T | CA364403396 | RHAG | c.234C>A (p.Ser78Arg) n.509C>A | gnomAD v4 |
6 | g.49619287C>A | CA364403399 | RHAG | c.233G>T (p.Ser78Ile) n.508G>T | |
6 | g.49619287C>G | CA364403397 | RHAG | c.233G>C (p.Ser78Thr) n.508G>C | |
6 | g.49619287C>T | CA364403398 | RHAG | c.233G>A (p.Ser78Asn) n.508G>A | gnomAD v4 |
6 | g.49619288T>A | CA364403400 | RHAG | c.232A>T (p.Ser78Cys) n.507A>T | |
6 | g.49619288T>C | CA364403401 | RHAG | c.232A>G (p.Ser78Gly) n.507A>G | gnomAD v4 |
6 | g.49619288T>G | CA138848220 | RHAG | c.232A>C (p.Ser78Arg) n.507A>C | dbSNP |
6 | g.49619288T= | CA1627477994 | RHAG | c.232A= (p.Ser78=) n.507A= | |
6 | g.49619289G>A | CA3847962 | RHAG | c.231C>T (p.Phe77=) n.506C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49619289G>C | CA364403405 | RHAG | c.231C>G (p.Phe77Leu) n.506C>G | |
6 | g.49619289G= | CA1627477995 | RHAG | c.231C= (p.Phe77=) n.506C= | |
6 | g.49619289G>T | CA364403408 | RHAG | c.231C>A (p.Phe77Leu) n.506C>A | |
6 | g.49619290A= | CA1627477996 | RHAG | c.230T= (p.Phe77=) n.505T= | |
6 | g.49619290A>C | CA364403411 | RHAG | c.230T>G (p.Phe77Cys) n.505T>G | |
6 | g.49619290A>G | CA364403426 | RHAG | c.230T>C (p.Phe77Ser) n.505T>C | |
6 | g.49619290A>T | CA364403429 | RHAG | c.230T>A (p.Phe77Tyr) n.505T>A | |
6 | g.49619290_49619291insT | CA917745010 | RHAG | c.229_230insA (p.Phe77TyrfsTer?) n.504_505insA | dbSNP |
6 | g.49619291A>C | CA364403431 | RHAG | c.229T>G (p.Phe77Val) n.504T>G | |
6 | g.49619291A>G | CA364403432 | RHAG | c.229T>C (p.Phe77Leu) n.504T>C | |
6 | g.49619291A>T | CA364403434 | RHAG | c.229T>A (p.Phe77Ile) n.504T>A | |
6 | g.49619292G>A | CA450402636 | RHAG | c.228C>T (p.Gly76=) n.503C>T | |
6 | g.49619292G>C | CA450402638 | RHAG | c.228C>G (p.Gly76=) n.503C>G | |
6 | g.49619292G>T | CA450402634 | RHAG | c.228C>A (p.Gly76=) n.503C>A | |
6 | g.49619293C>A | CA364403437 | RHAG | c.227G>T (p.Gly76Val) n.502G>T | gnomAD v4 |
6 | g.49619293C>G | CA364403439 | RHAG | c.227G>C (p.Gly76Ala) n.502G>C | |
6 | g.49619293C>T | CA364403438 | RHAG | c.227G>A (p.Gly76Asp) n.502G>A | |
6 | g.49619294C>A | CA364403440 | RHAG | c.226G>T (p.Gly76Cys) n.501G>T | |
6 | g.49619294C>G | CA364403442 | RHAG | c.226G>C (p.Gly76Arg) n.501G>C | |
6 | g.49619294C>T | CA364403441 | RHAG | c.226G>A (p.Gly76Ser) n.501G>A | gnomAD v4 |
6 | g.49619295A= | CA1627477997 | RHAG | c.225T= (p.Tyr75=) n.500T= | |
6 | g.49619295A>C | CA364403445 | RHAG | c.225T>G (p.Tyr75Ter) n.500T>G | gnomAD v4 |
6 | g.49619295A>G | CA450402643 | RHAG | c.225T>C (p.Tyr75=) n.500T>C | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49619295A>T | CA364403447 | RHAG | c.225T>A (p.Tyr75Ter) n.500T>A | |
6 | g.49619296T>A | CA364403453 | RHAG | c.224A>T (p.Tyr75Phe) n.499A>T | |
6 | g.49619296T>C | CA364403455 | RHAG | c.224A>G (p.Tyr75Cys) n.499A>G | gnomAD v4 |
6 | g.49619296T>G | CA364403458 | RHAG | c.224A>C (p.Tyr75Ser) n.499A>C | |
6 | g.49619297A>C | CA364403459 | RHAG | c.223T>G (p.Tyr75Asp) n.498T>G | |
6 | g.49619297A>G | CA364403460 | RHAG | c.223T>C (p.Tyr75His) n.498T>C | gnomAD v4 |
6 | g.49619297A>T | CA364403461 | RHAG | c.223T>A (p.Tyr75Asn) n.498T>A | |
6 | g.49619298T>A | CA364403462 | RHAG | c.222A>T (p.Lys74Asn) n.497A>T |