Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.219057619C>A | CA350635600 | IHH | c.391G>T (p.Glu131Ter) | |
2 | g.219057619C= | CA1329041130 | IHH | c.391G= (p.Glu131=) | |
2 | g.219057619C>G | CA350635599 | IHH | c.391G>C (p.Glu131Gln) | COSMIC |
2 | g.219057619C>T | CA119974 | IHH | c.391G>A (p.Glu131Lys) | ClinVar dbSNP |
2 | g.219057620G>A | CA431262272 | IHH | c.390C>T (p.Thr130=) | |
2 | g.219057620G>C | CA431262273 | IHH | c.390C>G (p.Thr130=) | gnomAD v4 |
2 | g.219057620G>T | CA431262276 | IHH | c.390C>A (p.Thr130=) | gnomAD v4 |
2 | g.219057621G>A | CA350635603 | IHH | c.389C>T (p.Thr130Ile) | |
2 | g.219057621G>C | CA350635604 | IHH | c.389C>G (p.Thr130Ser) | |
2 | g.219057621G= | CA1329041131 | IHH | c.389C= (p.Thr130=) | |
2 | g.219057621G>T | CA119985 | IHH | c.389C>A (p.Thr130Asn) | ClinVar dbSNP |
2 | g.219057622T>A | CA350635607 | IHH | c.388A>T (p.Thr130Ser) | gnomAD v4 |
2 | g.219057622T>C | CA350635609 | IHH | c.388A>G (p.Thr130Ala) | |
2 | g.219057622T>G | CA350635610 | IHH | c.388A>C (p.Thr130Pro) | |
2 | g.219057623C>A | CA431262277 | IHH | c.387G>T (p.Val129=) | |
2 | g.219057623C>G | CA431262279 | IHH | c.387G>C (p.Val129=) | |
2 | g.219057623C>T | CA431262278 | IHH | c.387G>A (p.Val129=) | gnomAD v4 |
2 | g.219057627_219057640del | CA2499215674 | IHH | c.374_387del (p.Val125AspfsTer18) | ClinVar dbSNP |
2 | g.219057624A>C | CA350635614 | IHH | c.386T>G (p.Val129Gly) | |
2 | g.219057624A>G | CA350635617 | IHH | c.386T>C (p.Val129Ala) | |
2 | g.219057624A>T | CA350635615 | IHH | c.386T>A (p.Val129Glu) | |
2 | g.219057625C>A | CA350635619 | IHH | c.385G>T (p.Val129Leu) | |
2 | g.219057625C= | CA1329041132 | IHH | c.385G= (p.Val129=) | |
2 | g.219057625C>G | CA350635622 | IHH | c.385G>C (p.Val129Leu) | |
2 | g.219057625C>T | CA350635624 | IHH | c.385G>A (p.Val129Met) | dbSNP |
2 | g.219057626C>A | CA431262281 | IHH | c.384G>T (p.Arg128=) | |
2 | g.219057626C= | CA1329041133 | IHH | c.384G= (p.Arg128=) | |
2 | g.219057626C>G | CA431262282 | IHH | c.384G>C (p.Arg128=) | |
2 | g.219057626C>T | CA431262284 | IHH | c.384G>A (p.Arg128=) | dbSNP |
2 | g.219057627C>A | CA350635625 | IHH | c.383G>T (p.Arg128Leu) | |
2 | g.219057627C= | CA1329041134 | IHH | c.383G= (p.Arg128=) | |
2 | g.219057627C>G | CA350635626 | IHH | c.383G>C (p.Arg128Pro) | |
2 | g.219057627C>T | CA119983 | IHH | c.383G>A (p.Arg128Gln) | ClinVar dbSNP |
2 | g.219057628G>A | CA350635628 | IHH | c.382C>T (p.Arg128Trp) | |
2 | g.219057628G>C | CA350635630 | IHH | c.382C>G (p.Arg128Gly) | |
2 | g.219057628G= | CA1329041136 | IHH | c.382C= (p.Arg128=) | |
2 | g.219057628G>T | CA431262286 | IHH | c.382C>A (p.Arg128=) | dbSNP gnomAD v4 |
2 | g.219057629C>A | CA431262287 | IHH | c.381G>T (p.Leu127=) | |
2 | g.219057629C>G | CA431262288 | IHH | c.381G>C (p.Leu127=) | |
2 | g.219057629C>T | CA431262290 | IHH | c.381G>A (p.Leu127=) | |
2 | g.219057630A>C | CA350635632 | IHH | c.380T>G (p.Leu127Arg) | |
2 | g.219057630A>G | CA350635634 | IHH | c.380T>C (p.Leu127Pro) | |
2 | g.219057630A>T | CA350635637 | IHH | c.380T>A (p.Leu127Gln) | |
2 | g.219057631G>A | CA431262294 | IHH | c.379C>T (p.Leu127=) | |
2 | g.219057631G>C | CA350635641 | IHH | c.379C>G (p.Leu127Val) | |
2 | g.219057631G>T | CA350635643 | IHH | c.379C>A (p.Leu127Met) | |
2 | g.219057632C>A | CA350635645 | IHH | c.378G>T (p.Lys126Asn) | |
2 | g.219057632C= | CA1329041137 | IHH | c.378G= (p.Lys126=) | |
2 | g.219057632C>G | CA350635648 | IHH | c.378G>C (p.Lys126Asn) | |
2 | g.219057632C>T | CA431262295 | IHH | c.378G>A (p.Lys126=) | dbSNP |