Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.130880747A>CCA6366590SNX19c.773T>G (p.Leu258Arg)
c.2633T>G (p.Leu878Arg)
c.2574-1036T>G (p.=)
c.2879T>G (p.Leu960Arg)
c.2867T>G (p.Leu956Arg)
c.2759T>G (p.Leu920Arg)
c.1997T>G (p.Leu666Arg)
c.1154T>G (p.Leu385Arg)
c.1019T>G (p.Leu340Arg)
c.899T>G (p.Leu300Arg)
c.2513T>G (p.Leu838Arg)
c.962T>G (p.Leu321Arg)
c.908T>G (p.Leu303Arg)
c.653T>G (p.Leu218Arg)
c.599T>G (p.Leu200Arg)
c.714-1036T>G (p.=)
c.353T>G (p.Leu118Arg)
n.3266T>G
n.3704T>G
n.3050T>G
n.3364T>G
c.*21029T>G (p.=)
n.3258T>G
c.137T>G (p.Leu46Arg)
n.178-1036T>G
n.395T>G
n.369T>G
n.993T>G
dbSNP ExAC gnomAD
11g.130880747A>TCA6366591SNX19c.773T>A (p.Leu258Gln)
c.2633T>A (p.Leu878Gln)
c.2574-1036T>A (p.=)
c.2879T>A (p.Leu960Gln)
c.2867T>A (p.Leu956Gln)
c.2759T>A (p.Leu920Gln)
c.1997T>A (p.Leu666Gln)
c.1154T>A (p.Leu385Gln)
c.1019T>A (p.Leu340Gln)
c.899T>A (p.Leu300Gln)
c.2513T>A (p.Leu838Gln)
c.962T>A (p.Leu321Gln)
c.908T>A (p.Leu303Gln)
c.653T>A (p.Leu218Gln)
c.599T>A (p.Leu200Gln)
c.714-1036T>A (p.=)
c.353T>A (p.Leu118Gln)
n.3266T>A
n.3704T>A
n.3050T>A
n.3364T>A
c.*21029T>A (p.=)
n.3258T>A
c.137T>A (p.Leu46Gln)
n.178-1036T>A
n.395T>A
n.369T>A
n.993T>A
dbSNP ExAC gnomAD COSMIC

Number of alleles fetched