Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.39724008G>CCA16602465ERBB2c.2305G>C (p.Asp769His)
c.2215G>C (p.Asp739His)
c.1477G>C (p.Asp493His)
c.2260G>C (p.Asp754His)
c.*2095G>C (n.*2095G>C)
c.411G>C
n.3439G>C
n.2629G>C
c.2443G>C (p.Asp815His)
c.2398G>C (p.Asp800His)
c.2353G>C (p.Asp785His)
c.2422G>C (p.Asp808His)
c.2407G>C (p.Asp803His)
c.2386G>C (p.Asp796His)
c.2380G>C (p.Asp794His)
c.2335G>C (p.Asp779His)
c.2326G>C (p.Asp776His)
c.2302G>C (p.Asp768His)
c.2296G>C (p.Asp766His)
c.2269G>C (p.Asp757His)
c.2263G>C (p.Asp755His)
c.2257G>C (p.Asp753His)
c.2208+348G>C (n.2208+348G>C)
c.2125G>C (p.Asp709His)
c.2047G>C (p.Asp683His)
c.1267G>C (p.Asp423His)
n.2543G>C
 ClinVar dbSNP COSMIC COSMIC
17g.39724008G>ACA16602841ERBB2c.2305G>A (p.Asp769Asn)
c.2215G>A (p.Asp739Asn)
c.1477G>A (p.Asp493Asn)
c.2260G>A (p.Asp754Asn)
c.*2095G>A (n.*2095G>A)
c.411G>A
n.3439G>A
n.2629G>A
c.2443G>A (p.Asp815Asn)
c.2398G>A (p.Asp800Asn)
c.2353G>A (p.Asp785Asn)
c.2422G>A (p.Asp808Asn)
c.2407G>A (p.Asp803Asn)
c.2386G>A (p.Asp796Asn)
c.2380G>A (p.Asp794Asn)
c.2335G>A (p.Asp779Asn)
c.2326G>A (p.Asp776Asn)
c.2302G>A (p.Asp768Asn)
c.2296G>A (p.Asp766Asn)
c.2269G>A (p.Asp757Asn)
c.2263G>A (p.Asp755Asn)
c.2257G>A (p.Asp753Asn)
c.2208+348G>A (n.2208+348G>A)
c.2125G>A (p.Asp709Asn)
c.2047G>A (p.Asp683Asn)
c.1267G>A (p.Asp423Asn)
n.2543G>A
 ClinVar dbSNP COSMIC
17g.39724008G>TCA16602466ERBB2c.2305G>T (p.Asp769Tyr)
c.2215G>T (p.Asp739Tyr)
c.1477G>T (p.Asp493Tyr)
c.2260G>T (p.Asp754Tyr)
c.*2095G>T (n.*2095G>T)
c.411G>T
n.3439G>T
n.2629G>T
c.2443G>T (p.Asp815Tyr)
c.2398G>T (p.Asp800Tyr)
c.2353G>T (p.Asp785Tyr)
c.2422G>T (p.Asp808Tyr)
c.2407G>T (p.Asp803Tyr)
c.2386G>T (p.Asp796Tyr)
c.2380G>T (p.Asp794Tyr)
c.2335G>T (p.Asp779Tyr)
c.2326G>T (p.Asp776Tyr)
c.2302G>T (p.Asp768Tyr)
c.2296G>T (p.Asp766Tyr)
c.2269G>T (p.Asp757Tyr)
c.2263G>T (p.Asp755Tyr)
c.2257G>T (p.Asp753Tyr)
c.2208+348G>T (n.2208+348G>T)
c.2125G>T (p.Asp709Tyr)
c.2047G>T (p.Asp683Tyr)
c.1267G>T (p.Asp423Tyr)
n.2543G>T
 ClinVar dbSNP COSMIC COSMIC

Number of alleles fetched