Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.72007888_72007892dup | CA929815578 | CHST3 | c.857_861dup (p.Glu288TrpfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
10 | g.72007888T>A | CA377147343 | CHST3 | c.857T>A (p.Leu286Gln) | ClinVar |
10 | g.72007888T>C | CA253731 | CHST3 | c.857T>C (p.Leu286Pro) | ClinVar dbSNP |
10 | g.72007888T>G | CA377147347 | CHST3 | c.857T>G (p.Leu286Arg) | |
10 | g.72007888T= | CA1918976487 | CHST3 | c.857T= (p.Leu286=) | |
10 | g.72007889G>A | CA470284127 | CHST3 | c.858G>A (p.Leu286=) | gnomAD v4 |
10 | g.72007889G>C | CA470284128 | CHST3 | c.858G>C (p.Leu286=) | |
10 | g.72007889G>T | CA470284129 | CHST3 | c.858G>T (p.Leu286=) | |
10 | g.72007890G>A | CA377147352 | CHST3 | c.859G>A (p.Ala287Thr) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.72007890G>C | CA377147354 | CHST3 | c.859G>C (p.Ala287Pro) | |
10 | g.72007890G= | CA1918976492 | CHST3 | c.859G= (p.Ala287=) | |
10 | g.72007890G>T | CA377147364 | CHST3 | c.859G>T (p.Ala287Ser) | |
10 | g.72007891C>A | CA377147365 | CHST3 | c.860C>A (p.Ala287Asp) | |
10 | g.72007891C>G | CA377147367 | CHST3 | c.860C>G (p.Ala287Gly) | |
10 | g.72007891C>T | CA377147376 | CHST3 | c.860C>T (p.Ala287Val) | |
10 | g.72007892C>A | CA470284131 | CHST3 | c.861C>A (p.Ala287=) | |
10 | g.72007892C= | CA1918976494 | CHST3 | c.861C= (p.Ala287=) | |
10 | g.72007892C>G | CA470284132 | CHST3 | c.861C>G (p.Ala287=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
10 | g.72007892C>T | CA470284137 | CHST3 | c.861C>T (p.Ala287=) | gnomAD v4 |
10 | g.72007893G>A | CA209479283 | CHST3 | c.862G>A (p.Glu288Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
10 | g.72007893G>C | CA377147379 | CHST3 | c.862G>C (p.Glu288Gln) | |
10 | g.72007893G= | CA1918976498 | CHST3 | c.862G= (p.Glu288=) | |
10 | g.72007893G>T | CA377147388 | CHST3 | c.862G>T (p.Glu288Ter) | |
10 | g.72007894A>C | CA377147395 | CHST3 | c.863A>C (p.Glu288Ala) | |
10 | g.72007894A>G | CA377147396 | CHST3 | c.863A>G (p.Glu288Gly) | |
10 | g.72007894A>T | CA377147397 | CHST3 | c.863A>T (p.Glu288Val) | |
10 | g.72007895G>A | CA470284144 | CHST3 | c.864G>A (p.Glu288=) | |
10 | g.72007895G>C | CA377147398 | CHST3 | c.864G>C (p.Glu288Asp) | |
10 | g.72007895G>T | CA377147400 | CHST3 | c.864G>T (p.Glu288Asp) | |
10 | g.72007896G>A | CA377147416 | CHST3 | c.865G>A (p.Asp289Asn) | |
10 | g.72007896G>C | CA377147423 | CHST3 | c.865G>C (p.Asp289His) | |
10 | g.72007896G>T | CA377147427 | CHST3 | c.865G>T (p.Asp289Tyr) | |
10 | g.72007897A>C | CA377147430 | CHST3 | c.866A>C (p.Asp289Ala) | |
10 | g.72007897A>G | CA377147432 | CHST3 | c.866A>G (p.Asp289Gly) | |
10 | g.72007897A>T | CA377147434 | CHST3 | c.866A>T (p.Asp289Val) | |
10 | g.72007898C>A | CA377147437 | CHST3 | c.867C>A (p.Asp289Glu) | gnomAD v4 |
10 | g.72007898C>G | CA377147442 | CHST3 | c.867C>G (p.Asp289Glu) | |
10 | g.72007898C>T | CA470284160 | CHST3 | c.867C>T (p.Asp289=) | |
10 | g.72007899C>A | CA377147444 | CHST3 | c.868C>A (p.Pro290Thr) | |
10 | g.72007899C>G | CA377147445 | CHST3 | c.868C>G (p.Pro290Ala) | |
10 | g.72007899C>T | CA377147446 | CHST3 | c.868C>T (p.Pro290Ser) | |
10 | g.72007900C>A | CA377147448 | CHST3 | c.869C>A (p.Pro290His) | gnomAD v4 |
10 | g.72007900C= | CA1918976501 | CHST3 | c.869C= (p.Pro290=) | |
10 | g.72007900C>G | CA5548186 | CHST3 | c.869C>G (p.Pro290Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.72007900C>T | CA377147459 | CHST3 | c.869C>T (p.Pro290Leu) | |
10 | g.72007901C>A | CA470284169 | CHST3 | c.870C>A (p.Pro290=) | |
10 | g.72007901C= | CA1918976505 | CHST3 | c.870C= (p.Pro290=) | |
10 | g.72007901C>G | CA470284175 | CHST3 | c.870C>G (p.Pro290=) | |
10 | g.72007901C>T | CA209479285 | CHST3 | c.870C>T (p.Pro290=) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.72007902C>A | CA377147461 | CHST3 | c.871C>A (p.Arg291Ser) | gnomAD v4 |