Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.9734502_9734503del | CA16044289 | BRPF1 | c.362_363del (p.Glu121GlyfsTer2) c.354_355del n.782_783del n.776_777del | ClinVar dbSNP |
3 | g.9734502A>C | CA351679999 | BRPF1 | c.362A>C (p.Glu121Ala) c.354A>C n.782A>C n.776A>C | ClinVar dbSNP |
3 | g.9734502A>G | CA351680000 | BRPF1 | c.362A>G (p.Glu121Gly) c.354A>G n.782A>G n.776A>G | |
3 | g.9734502A>T | CA351680002 | BRPF1 | c.362A>T (p.Glu121Val) c.354A>T n.782A>T n.776A>T | |
3 | g.9734503G>A | CA432529218 | BRPF1 | c.363G>A (p.Glu121=) c.355G>A n.783G>A n.777G>A | |
3 | g.9734503G>C | CA351680004 | BRPF1 | c.363G>C (p.Glu121Asp) c.355G>C n.783G>C n.777G>C | ClinVar gnomAD v4 |
3 | g.9734503G>T | CA351680005 | BRPF1 | c.363G>T (p.Glu121Asp) c.355G>T n.783G>T n.777G>T | |
3 | g.9734504G>A | CA351680010 | BRPF1 | c.364G>A (p.Asp122Asn) c.356G>A n.784G>A n.778G>A | dbSNP gnomAD v4 |
3 | g.9734504G>C | CA351680007 | BRPF1 | c.364G>C (p.Asp122His) c.356G>C n.784G>C n.778G>C | |
3 | g.9734504G= | CA1344883227 | BRPF1 | c.364G= (p.Asp122=) c.356G= n.784G= n.778G= | |
3 | g.9734504G>T | CA351680009 | BRPF1 | c.364G>T (p.Asp122Tyr) c.356G>T n.784G>T n.778G>T | |
3 | g.9734505A>C | CA351680012 | BRPF1 | c.365A>C (p.Asp122Ala) c.357A>C n.785A>C n.779A>C | |
3 | g.9734505A>G | CA351680013 | BRPF1 | c.365A>G (p.Asp122Gly) c.357A>G n.785A>G n.779A>G | |
3 | g.9734505A>T | CA351680015 | BRPF1 | c.365A>T (p.Asp122Val) c.357A>T n.785A>T n.779A>T | |
3 | g.9734506T>A | CA351680017 | BRPF1 | c.366T>A (p.Asp122Glu) c.358T>A n.786T>A n.780T>A | |
3 | g.9734506T>C | CA432529222 | BRPF1 | c.366T>C (p.Asp122=) c.358T>C n.786T>C n.780T>C | |
3 | g.9734506T>G | CA351680019 | BRPF1 | c.366T>G (p.Asp122Glu) c.358T>G n.786T>G n.780T>G | |
3 | g.9734507G>A | CA2241688 | BRPF1 | c.367G>A (p.Glu123Lys) c.359G>A n.787G>A n.781G>A | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
3 | g.9734507G>C | CA351680020 | BRPF1 | c.367G>C (p.Glu123Gln) c.359G>C n.787G>C n.781G>C | |
3 | g.9734507G= | CA1344883229 | BRPF1 | c.367G= (p.Glu123=) c.359G= n.787G= n.781G= | |
3 | g.9734507G>T | CA351680021 | BRPF1 | c.367G>T (p.Glu123Ter) c.359G>T n.787G>T n.781G>T | |
3 | g.9734512_9734523del | CA2664327530 | BRPF1 | c.372_383del (p.Ala125_Glu128del) c.364_375del n.792_803del n.786_797del | gnomAD v4 |
3 | g.9734508A>C | CA351680024 | BRPF1 | c.368A>C (p.Glu123Ala) c.360A>C n.788A>C n.782A>C | |
3 | g.9734508A>G | CA351680026 | BRPF1 | c.368A>G (p.Glu123Gly) c.360A>G n.788A>G n.782A>G | |
3 | g.9734508A>T | CA351680027 | BRPF1 | c.368A>T (p.Glu123Val) c.360A>T n.788A>T n.782A>T | |
3 | g.9734509G>A | CA432529226 | BRPF1 | c.369G>A (p.Glu123=) c.361G>A n.789G>A n.783G>A | |
3 | g.9734509G>C | CA69954507 | BRPF1 | c.369G>C (p.Glu123Asp) c.361G>C n.789G>C n.783G>C | dbSNP |
3 | g.9734509G= | CA1344883232 | BRPF1 | c.369G= (p.Glu123=) c.361G= n.789G= n.783G= | |
3 | g.9734509G>T | CA2241689 | BRPF1 | c.369G>T (p.Glu123Asp) c.361G>T n.789G>T n.783G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.9734510G>A | CA351680031 | BRPF1 | c.370G>A (p.Glu124Lys) c.362G>A n.790G>A n.784G>A | gnomAD v4 |
3 | g.9734510G>C | CA69954512 | BRPF1 | c.370G>C (p.Glu124Gln) c.362G>C n.790G>C n.784G>C | dbSNP gnomAD v3 gnomAD v4 |
3 | g.9734510G= | CA1344883234 | BRPF1 | c.370G= (p.Glu124=) c.362G= n.790G= n.784G= | |
3 | g.9734510G>T | CA351680033 | BRPF1 | c.370G>T (p.Glu124Ter) c.362G>T n.790G>T n.784G>T | |
3 | g.9734511A>C | CA351680035 | BRPF1 | c.371A>C (p.Glu124Ala) c.363A>C n.791A>C n.785A>C | |
3 | g.9734511A>G | CA351680036 | BRPF1 | c.371A>G (p.Glu124Gly) c.363A>G n.791A>G n.785A>G | |
3 | g.9734511A>T | CA351680037 | BRPF1 | c.371A>T (p.Glu124Val) c.363A>T n.791A>T n.785A>T | |
3 | g.9734512A= | CA1344883236 | BRPF1 | c.372A= (p.Glu124=) c.364A= n.792A= n.786A= | |
3 | g.9734512A>C | CA351680038 | BRPF1 | c.372A>C (p.Glu124Asp) c.364A>C n.792A>C n.786A>C | |
3 | g.9734512A>G | CA69954517 | BRPF1 | c.372A>G (p.Glu124=) c.364A>G n.792A>G n.786A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.9734512A>T | CA351680040 | BRPF1 | c.372A>T (p.Glu124Asp) c.364A>T n.792A>T n.786A>T | |
3 | g.9734513G>A | CA351680041 | BRPF1 | c.373G>A (p.Ala125Thr) c.365G>A n.793G>A n.787G>A | ClinVar dbSNP |
3 | g.9734513G>C | CA351680044 | BRPF1 | c.373G>C (p.Ala125Pro) c.365G>C n.793G>C n.787G>C | |
3 | g.9734513G= | CA1344883238 | BRPF1 | c.373G= (p.Ala125=) c.365G= n.793G= n.787G= | |
3 | g.9734513G>T | CA351680043 | BRPF1 | c.373G>T (p.Ala125Ser) c.365G>T n.793G>T n.787G>T | |
3 | g.9734514C>A | CA351680046 | BRPF1 | c.374C>A (p.Ala125Asp) c.366C>A n.794C>A n.788C>A | |
3 | g.9734514C>G | CA351680048 | BRPF1 | c.374C>G (p.Ala125Gly) c.366C>G n.794C>G n.788C>G | |
3 | g.9734514C>T | CA351680049 | BRPF1 | c.374C>T (p.Ala125Val) c.366C>T n.794C>T n.788C>T | |
3 | g.9734515C>A | CA432529231 | BRPF1 | c.375C>A (p.Ala125=) c.367C>A n.795C>A n.789C>A | |
3 | g.9734515C= | CA1344883240 | BRPF1 | c.375C= (p.Ala125=) c.367C= n.795C= n.789C= | |
3 | g.9734515C>G | CA432529234 | BRPF1 | c.375C>G (p.Ala125=) c.367C>G n.795C>G n.789C>G |