Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.39724772T>ACA399302973ERBB2c.2354T>A (p.Leu785His)
c.2264T>A (p.Leu755His)
c.1526T>A (p.Leu509His)
c.2309T>A (p.Leu770His)
c.*2144T>A (n.*2144T>A)
c.460T>A
n.3488T>A
n.2678T>A
c.2492T>A (p.Leu831His)
c.2447T>A (p.Leu816His)
c.2402T>A (p.Leu801His)
c.2471T>A (p.Leu824His)
c.2456T>A (p.Leu819His)
c.2435T>A (p.Leu812His)
c.2429T>A (p.Leu810His)
c.2384T>A (p.Leu795His)
c.2375T>A (p.Leu792His)
c.2351T>A (p.Leu784His)
c.2345T>A (p.Leu782His)
c.2318T>A (p.Leu773His)
c.2312T>A (p.Leu771His)
c.2306T>A (p.Leu769His)
c.2255T>A (p.Leu752His)
c.2174T>A (p.Leu725His)
c.2308-277T>A (n.2308-277T>A)
c.2096T>A (p.Leu699His)
c.2208+1112T>A (n.2208+1112T>A)
c.1316T>A (p.Leu439His)
n.2592T>A
dbSNP
17g.39724772T>GCA399302982ERBB2c.2354T>G (p.Leu785Arg)
c.2264T>G (p.Leu755Arg)
c.1526T>G (p.Leu509Arg)
c.2309T>G (p.Leu770Arg)
c.*2144T>G (n.*2144T>G)
c.460T>G
n.3488T>G
n.2678T>G
c.2492T>G (p.Leu831Arg)
c.2447T>G (p.Leu816Arg)
c.2402T>G (p.Leu801Arg)
c.2471T>G (p.Leu824Arg)
c.2456T>G (p.Leu819Arg)
c.2435T>G (p.Leu812Arg)
c.2429T>G (p.Leu810Arg)
c.2384T>G (p.Leu795Arg)
c.2375T>G (p.Leu792Arg)
c.2351T>G (p.Leu784Arg)
c.2345T>G (p.Leu782Arg)
c.2318T>G (p.Leu773Arg)
c.2312T>G (p.Leu771Arg)
c.2306T>G (p.Leu769Arg)
c.2255T>G (p.Leu752Arg)
c.2174T>G (p.Leu725Arg)
c.2308-277T>G (n.2308-277T>G)
c.2096T>G (p.Leu699Arg)
c.2208+1112T>G (n.2208+1112T>G)
c.1316T>G (p.Leu439Arg)
n.2592T>G
dbSNP
17g.39724772T>CCA16602776ERBB2c.2354T>C (p.Leu785Pro)
c.2264T>C (p.Leu755Pro)
c.1526T>C (p.Leu509Pro)
c.2309T>C (p.Leu770Pro)
c.*2144T>C (n.*2144T>C)
c.460T>C
n.3488T>C
n.2678T>C
c.2492T>C (p.Leu831Pro)
c.2447T>C (p.Leu816Pro)
c.2402T>C (p.Leu801Pro)
c.2471T>C (p.Leu824Pro)
c.2456T>C (p.Leu819Pro)
c.2435T>C (p.Leu812Pro)
c.2429T>C (p.Leu810Pro)
c.2384T>C (p.Leu795Pro)
c.2375T>C (p.Leu792Pro)
c.2351T>C (p.Leu784Pro)
c.2345T>C (p.Leu782Pro)
c.2318T>C (p.Leu773Pro)
c.2312T>C (p.Leu771Pro)
c.2306T>C (p.Leu769Pro)
c.2255T>C (p.Leu752Pro)
c.2174T>C (p.Leu725Pro)
c.2308-277T>C (n.2308-277T>C)
c.2096T>C (p.Leu699Pro)
c.2208+1112T>C (n.2208+1112T>C)
c.1316T>C (p.Leu439Pro)
n.2592T>C
ClinVar dbSNP

Number of alleles fetched