Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.47862456T>A | CA371162367 | PRKDC | c.5836A>T (p.Asn1946Tyr) n.502A>T | |
8 | g.47862456T>C | CA371162368 | PRKDC | c.5836A>G (p.Asn1946Asp) n.502A>G | ClinVar |
8 | g.47862456T>G | CA371162370 | PRKDC | c.5836A>C (p.Asn1946His) n.502A>C | ClinVar |
8 | g.47862457G>A | CA460607562 | PRKDC | c.5835C>T (p.Tyr1945=) n.501C>T | |
8 | g.47862457G>C | CA371162372 | PRKDC | c.5835C>G (p.Tyr1945Ter) n.501C>G | |
8 | g.47862457G>T | CA371162374 | PRKDC | c.5835C>A (p.Tyr1945Ter) n.501C>A | |
8 | g.47862458T>A | CA371162375 | PRKDC | c.5834A>T (p.Tyr1945Phe) n.500A>T | |
8 | g.47862458T>C | CA371162376 | PRKDC | c.5834A>G (p.Tyr1945Cys) n.500A>G | |
8 | g.47862458T>G | CA371162378 | PRKDC | c.5834A>C (p.Tyr1945Ser) n.500A>C | |
8 | g.47862459A>C | CA371162383 | PRKDC | c.5833T>G (p.Tyr1945Asp) n.499T>G | |
8 | g.47862459A>G | CA371162382 | PRKDC | c.5833T>C (p.Tyr1945His) n.499T>C | gnomAD v4 |
8 | g.47862459A>T | CA371162380 | PRKDC | c.5833T>A (p.Tyr1945Asn) n.499T>A | |
8 | g.47862460T>A | CA460607563 | PRKDC | c.5832A>T (p.Ala1944=) n.498A>T | |
8 | g.47862460T>C | CA460607565 | PRKDC | c.5832A>G (p.Ala1944=) n.498A>G | COSMIC |
8 | g.47862460T>G | CA460607564 | PRKDC | c.5832A>C (p.Ala1944=) n.498A>C | |
8 | g.47862461G>A | CA371162385 | PRKDC | c.5831C>T (p.Ala1944Val) n.497C>T | |
8 | g.47862461G>C | CA371162386 | PRKDC | c.5831C>G (p.Ala1944Gly) n.497C>G | |
8 | g.47862461G>T | CA371162388 | PRKDC | c.5831C>A (p.Ala1944Glu) n.497C>A | |
8 | g.47862462C>A | CA371162390 | PRKDC | c.5830G>T (p.Ala1944Ser) n.496G>T | |
8 | g.47862462C>G | CA371162391 | PRKDC | c.5830G>C (p.Ala1944Pro) n.496G>C | |
8 | g.47862462C>T | CA371162393 | PRKDC | c.5830G>A (p.Ala1944Thr) n.496G>A | |
8 | g.47862463T>A | CA460607566 | PRKDC | c.5829A>T (p.Ala1943=) n.495A>T | dbSNP gnomAD v3 gnomAD v4 |
8 | g.47862463T>C | CA460607567 | PRKDC | c.5829A>G (p.Ala1943=) n.495A>G | ClinVar dbSNP |
8 | g.47862463T>G | CA460607568 | PRKDC | c.5829A>C (p.Ala1943=) n.495A>C | |
8 | g.47862463T= | CA1781860498 | PRKDC | c.5829A= (p.Ala1943=) n.495A= | |
8 | g.47862464G>A | CA371162395 | PRKDC | c.5828C>T (p.Ala1943Val) n.494C>T | gnomAD v4 |
8 | g.47862464G>C | CA371162396 | PRKDC | c.5828C>G (p.Ala1943Gly) n.494C>G | |
8 | g.47862464G>T | CA371162397 | PRKDC | c.5828C>A (p.Ala1943Glu) n.494C>A | |
8 | g.47862465C>A | CA4740560 | PRKDC | c.5827G>T (p.Ala1943Ser) n.493G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.47862465C= | CA1781860504 | PRKDC | c.5827G= (p.Ala1943=) n.493G= | |
8 | g.47862465C>G | CA371162400 | PRKDC | c.5827G>C (p.Ala1943Pro) n.493G>C | |
8 | g.47862465C>T | CA371162401 | PRKDC | c.5827G>A (p.Ala1943Thr) n.493G>A | |
8 | g.47862466A>C | CA371162403 | PRKDC | c.5826T>G (p.Cys1942Trp) n.492T>G | |
8 | g.47862466A>G | CA460607569 | PRKDC | c.5826T>C (p.Cys1942=) n.492T>C | |
8 | g.47862466A>T | CA371162404 | PRKDC | c.5826T>A (p.Cys1942Ter) n.492T>A | |
8 | g.47862467C>A | CA371162407 | PRKDC | c.5825G>T (p.Cys1942Phe) n.491G>T | |
8 | g.47862467C>G | CA371162409 | PRKDC | c.5825G>C (p.Cys1942Ser) n.491G>C | |
8 | g.47862467C>T | CA371162406 | PRKDC | c.5825G>A (p.Cys1942Tyr) n.491G>A | |
8 | g.47862468A>C | CA371162410 | PRKDC | c.5824T>G (p.Cys1942Gly) n.490T>G | |
8 | g.47862468A>G | CA371162411 | PRKDC | c.5824T>C (p.Cys1942Arg) n.490T>C | |
8 | g.47862468A>T | CA371162412 | PRKDC | c.5824T>A (p.Cys1942Ser) n.490T>A | |
8 | g.47862469A>C | CA371162414 | PRKDC | c.5823T>G (p.His1941Gln) n.489T>G | |
8 | g.47862469A>G | CA460607570 | PRKDC | c.5823T>C (p.His1941=) n.489T>C | |
8 | g.47862469A>T | CA371162415 | PRKDC | c.5823T>A (p.His1941Gln) n.489T>A | |
8 | g.47862470T>A | CA371162417 | PRKDC | c.5822A>T (p.His1941Leu) n.488A>T | |
8 | g.47862470T>C | CA371162418 | PRKDC | c.5822A>G (p.His1941Arg) n.488A>G | gnomAD v4 |
8 | g.47862470T>G | CA371162420 | PRKDC | c.5822A>C (p.His1941Pro) n.488A>C | |
8 | g.47862471_47862473del | CA2687202210 | PRKDC | c.5820_5822del (p.His1941del) n.486_488del | gnomAD v4 |
8 | g.47862471G>A | CA371162422 | PRKDC | c.5821C>T (p.His1941Tyr) n.487C>T | gnomAD v4 |
8 | g.47862471G>C | CA371162425 | PRKDC | c.5821C>G (p.His1941Asp) n.487C>G |