Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.37966084C>A | CA370695636 | ADRB3 | c.386G>T (p.Cys129Phe) n.514G>T | |
8 | g.37966084C= | CA1777329252 | ADRB3 | c.386G= (p.Cys129=) n.514G= | |
8 | g.37966084C>G | CA370695637 | ADRB3 | c.386G>C (p.Cys129Ser) n.514G>C | |
8 | g.37966084C>T | CA4714407 | ADRB3 | c.386G>A (p.Cys129Tyr) n.514G>A | dbSNP ExAC gnomAD |
8 | g.37966085A= | CA1777329253 | ADRB3 | c.385T= (p.Cys129=) n.513T= | |
8 | g.37966085A>C | CA370695643 | ADRB3 | c.385T>G (p.Cys129Gly) n.513T>G | |
8 | g.37966085A>G | CA370695640 | ADRB3 | c.385T>C (p.Cys129Arg) n.513T>C | |
8 | g.37966085A>T | CA370695641 | ADRB3 | c.385T>A (p.Cys129Ser) n.513T>A | |
8 | g.37966086C>A | CA460494536 | ADRB3 | c.384G>T (p.Leu128=) n.512G>T | |
8 | g.37966086C>G | CA460494537 | ADRB3 | c.384G>C (p.Leu128=) n.512G>C | |
8 | g.37966086C>T | CA460494538 | ADRB3 | c.384G>A (p.Leu128=) n.512G>A | |
8 | g.37966086_37966087delinsCA | CA1777329254 | ADRB3 | c.383_384delinsTG (p.Leu128=) n.511_512delinsTG | |
8 | g.37966087del | CA1777329255 | ADRB3 | c.383del (p.Leu128ArgfsTer12) n.511del | dbSNP |
8 | g.37966087A>C | CA370695646 | ADRB3 | c.383T>G (p.Leu128Arg) n.511T>G | |
8 | g.37966087A>G | CA370695648 | ADRB3 | c.383T>C (p.Leu128Pro) n.511T>C | |
8 | g.37966087A>T | CA370695651 | ADRB3 | c.383T>A (p.Leu128Gln) n.511T>A | |
8 | g.37966087_37966089delinsAGG | CA1777329256 | ADRB3 | c.381_383delinsCCT (p.Thr127=) n.509_511delinsCCT | |
8 | g.37966088G>A | CA460494539 | ADRB3 | c.382C>T (p.Leu128=) n.510C>T | |
8 | g.37966088G>C | CA370695660 | ADRB3 | c.382C>G (p.Leu128Val) n.510C>G | |
8 | g.37966088G= | CA1777329257 | ADRB3 | c.382C= (p.Leu128=) n.510C= | |
8 | g.37966088G>T | CA370695663 | ADRB3 | c.382C>A (p.Leu128Met) n.510C>A | |
8 | g.37966089_37966090del | CA851443405 | ADRB3 | c.381_382del (p.Leu128ValfsTer?) n.509_510del | dbSNP |
8 | g.37966089G>A | CA4714408 | ADRB3 | c.381C>T (p.Thr127=) n.509C>T | dbSNP ExAC gnomAD |
8 | g.37966089G>C | CA460494545 | ADRB3 | c.381C>G (p.Thr127=) n.509C>G | |
8 | g.37966089G= | CA1777329258 | ADRB3 | c.381C= (p.Thr127=) n.509C= | |
8 | g.37966089G>T | CA460494542 | ADRB3 | c.381C>A (p.Thr127=) n.509C>A | |
8 | g.37966090G>A | CA4714409 | ADRB3 | c.380C>T (p.Thr127Ile) n.508C>T | dbSNP ExAC |
8 | g.37966090G>C | CA370695667 | ADRB3 | c.380C>G (p.Thr127Ser) n.508C>G | |
8 | g.37966090G= | CA1777329259 | ADRB3 | c.380C= (p.Thr127=) n.508C= | |
8 | g.37966090G>T | CA370695670 | ADRB3 | c.380C>A (p.Thr127Asn) n.508C>A | |
8 | g.37966091T>A | CA370695672 | ADRB3 | c.379A>T (p.Thr127Ser) n.507A>T | |
8 | g.37966091T>C | CA370695673 | ADRB3 | c.379A>G (p.Thr127Ala) n.507A>G | |
8 | g.37966091T>G | CA370695676 | ADRB3 | c.379A>C (p.Thr127Pro) n.507A>C | |
8 | g.37966092T>A | CA175072192 | ADRB3 | c.378A>T (p.Glu126Asp) n.506A>T | dbSNP |
8 | g.37966092T>C | CA460494546 | ADRB3 | c.378A>G (p.Glu126=) n.506A>G | |
8 | g.37966092T>G | CA370695678 | ADRB3 | c.378A>C (p.Glu126Asp) n.506A>C | |
8 | g.37966092T= | CA1777329260 | ADRB3 | c.378A= (p.Glu126=) n.506A= | |
8 | g.37966093T>A | CA370695681 | ADRB3 | c.377A>T (p.Glu126Val) n.505A>T | |
8 | g.37966093T>C | CA370695683 | ADRB3 | c.377A>G (p.Glu126Gly) n.505A>G | |
8 | g.37966093T>G | CA370695684 | ADRB3 | c.377A>C (p.Glu126Ala) n.505A>C | |
8 | g.37966094C>A | CA370695687 | ADRB3 | c.376G>T (p.Glu126Ter) n.504G>T | |
8 | g.37966094C= | CA1777329261 | ADRB3 | c.376G= (p.Glu126=) n.504G= | |
8 | g.37966094C>G | CA370695689 | ADRB3 | c.376G>C (p.Glu126Gln) n.504G>C | gnomAD |
8 | g.37966094C>T | CA4714410 | ADRB3 | c.376G>A (p.Glu126Lys) n.504G>A | dbSNP ExAC gnomAD COSMIC |
8 | g.37966095G>A | CA460494552 | ADRB3 | c.375C>T (p.Ile125=) n.503C>T | |
8 | g.37966095G>C | CA370695693 | ADRB3 | c.375C>G (p.Ile125Met) n.503C>G | |
8 | g.37966095G= | CA1777329262 | ADRB3 | c.375C= (p.Ile125=) n.503C= | |
8 | g.37966095G>T | CA460494553 | ADRB3 | c.375C>A (p.Ile125=) n.503C>A | |
8 | g.37966096A= | CA1777329263 | ADRB3 | c.374T= (p.Ile125=) n.502T= | |
8 | g.37966096A>C | CA370695694 | ADRB3 | c.374T>G (p.Ile125Ser) n.502T>G |