Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.100539717_100539743del | CA525178010 | GPR88 | c.751_777del (p.Gln251_Ala259del) | dbSNP gnomAD v2 |
1 | g.100539725_100539747dup | CA2646776911 | GPR88 | c.759_781dup (p.His261ArgfsTer?) | gnomAD v4 |
1 | g.100539725_100539756del | CA2646776910 | GPR88 | c.759_790del (p.Pro254GlyfsTer?) | gnomAD v4 |
1 | g.100539739G>A | CA341392459 | GPR88 | c.773G>A (p.Gly258Asp) | gnomAD v4 |
1 | g.100539739G>C | CA341392458 | GPR88 | c.773G>C (p.Gly258Ala) | |
1 | g.100539739G>T | CA341392457 | GPR88 | c.773G>T (p.Gly258Val) | |
1 | g.100539740C>A | CA419317362 | GPR88 | c.774C>A (p.Gly258=) | gnomAD v4 |
1 | g.100539740C>G | CA419317363 | GPR88 | c.774C>G (p.Gly258=) | |
1 | g.100539740C>T | CA419317365 | GPR88 | c.774C>T (p.Gly258=) | gnomAD v4 |
1 | g.100539741G>A | CA28152863 | GPR88 | c.775G>A (p.Ala259Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.100539741G>C | CA341392461 | GPR88 | c.775G>C (p.Ala259Pro) | |
1 | g.100539741G= | CA1184191058 | GPR88 | c.775G= (p.Ala259=) | |
1 | g.100539741G>T | CA341392460 | GPR88 | c.775G>T (p.Ala259Ser) | dbSNP gnomAD v4 |
1 | g.100539742C>A | CA341392462 | GPR88 | c.776C>A (p.Ala259Asp) | gnomAD v4 |
1 | g.100539742C>G | CA341392463 | GPR88 | c.776C>G (p.Ala259Gly) | |
1 | g.100539742C>T | CA341392464 | GPR88 | c.776C>T (p.Ala259Val) | gnomAD v4 |
1 | g.100539743C>A | CA419317371 | GPR88 | c.777C>A (p.Ala259=) | gnomAD v4 |
1 | g.100539743C= | CA1184191062 | GPR88 | c.777C= (p.Ala259=) | |
1 | g.100539743C>G | CA28152864 | GPR88 | c.777C>G (p.Ala259=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.100539743C>T | CA419317373 | GPR88 | c.777C>T (p.Ala259=) | gnomAD v4 |
1 | g.100539746_100539747del | CA2646776914 | GPR88 | c.780_781del (p.His261ProfsTer?) | gnomAD v4 |
1 | g.100539744G>A | CA341392465 | GPR88 | c.778G>A (p.Ala260Thr) | gnomAD v4 |
1 | g.100539744G>C | CA341392466 | GPR88 | c.778G>C (p.Ala260Pro) | gnomAD v4 |
1 | g.100539744G>T | CA341392467 | GPR88 | c.778G>T (p.Ala260Ser) | gnomAD v4 |
1 | g.100539745C>A | CA341392468 | GPR88 | c.779C>A (p.Ala260Glu) | gnomAD v4 |
1 | g.100539745C>G | CA341392469 | GPR88 | c.779C>G (p.Ala260Gly) | |
1 | g.100539745C>T | CA341392470 | GPR88 | c.779C>T (p.Ala260Val) | gnomAD v4 |
1 | g.100539746G>A | CA419317379 | GPR88 | c.780G>A (p.Ala260=) | gnomAD v4 |
1 | g.100539746G>C | CA419317377 | GPR88 | c.780G>C (p.Ala260=) | |
1 | g.100539746G= | CA1184191065 | GPR88 | c.780G= (p.Ala260=) | |
1 | g.100539746G>T | CA419317375 | GPR88 | c.780G>T (p.Ala260=) | dbSNP gnomAD v4 |
1 | g.100539747C>A | CA341392471 | GPR88 | c.781C>A (p.His261Asn) | gnomAD v4 |
1 | g.100539747C>G | CA341392472 | GPR88 | c.781C>G (p.His261Asp) | |
1 | g.100539747C>T | CA341392473 | GPR88 | c.781C>T (p.His261Tyr) | gnomAD v4 |
1 | g.100539748A>C | CA341392476 | GPR88 | c.782A>C (p.His261Pro) | |
1 | g.100539748A>G | CA341392474 | GPR88 | c.782A>G (p.His261Arg) | |
1 | g.100539748A>T | CA341392475 | GPR88 | c.782A>T (p.His261Leu) | |
1 | g.100539749C>A | CA341392477 | GPR88 | c.783C>A (p.His261Gln) | gnomAD v4 |
1 | g.100539749C>G | CA341392478 | GPR88 | c.783C>G (p.His261Gln) | |
1 | g.100539749C>T | CA419317387 | GPR88 | c.783C>T (p.His261=) | gnomAD v4 |
1 | g.100539750C>A | CA341392479 | GPR88 | c.784C>A (p.Pro262Thr) | gnomAD v4 |
1 | g.100539750C>G | CA341392480 | GPR88 | c.784C>G (p.Pro262Ala) | |
1 | g.100539750C>T | CA341392481 | GPR88 | c.784C>T (p.Pro262Ser) | |
1 | g.100539751C>A | CA341392482 | GPR88 | c.785C>A (p.Pro262Gln) | gnomAD v4 |
1 | g.100539751C= | CA1144950661 | GPR88 | c.785C= (p.Pro262=) | |
1 | g.100539751C>G | CA28152865 | GPR88 | c.785C>G (p.Pro262Arg) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.100539751C>T | CA341392483 | GPR88 | c.785C>T (p.Pro262Leu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.100539752G>A | CA419317394 | GPR88 | c.786G>A (p.Pro262=) | gnomAD v4 |
1 | g.100539752G>C | CA419317395 | GPR88 | c.786G>C (p.Pro262=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.100539752G= | CA1184191068 | GPR88 | c.786G= (p.Pro262=) |