Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.35438105G>ACA635722152GDF5c.-177C>T (p.=)
gnomAD
20g.35438114C>TCA314131797GDF5c.-186G>A (p.=)
dbSNP
20g.35438116G>TCA314131798GDF5c.-188C>A (p.=)
dbSNP gnomAD
20g.35438117T>CCA743890767GDF5c.-189A>G (p.=)
20g.35438123A>GCA743890770GDF5c.-195T>C (p.=)
20g.35438127G>CCA743890775GDF5c.-199C>G (p.=)
20g.35438131T>CCA743890780GDF5c.-203A>G (p.=)
20g.35438134T>GCA635351974GDF5c.-206A>C (p.=)
gnomAD
20g.35438137C>ACA314131799GDF5c.-209G>T (p.=)
dbSNP
20g.35438137C>TCA314131800GDF5c.-209G>A (p.=)
dbSNP
20g.35438138G>ACA657608749GDF5c.-210C>T (p.=)
COSMIC
20g.35438147C>TCA314131801GDF5c.-219G>A (p.=)
dbSNP
20g.35438148G>ACA10643805GDF5c.-220C>T (p.=)
ClinVar dbSNP dbSNP gnomAD
20g.35438154C>TCA314131802GDF5c.-226G>A (p.=)
dbSNP
20g.35438155G>ACA314131803GDF5c.-227C>T (p.=)
dbSNP gnomAD
20g.35438157C>ACA743890789GDF5c.-229G>T (p.=)
20g.35438162G>ACA314131804GDF5c.-234C>T (p.=)
dbSNP
20g.35438164C>TCA635351975GDF5c.-236G>A (p.=)
gnomAD
20g.35438182C>TCA314131805GDF5c.-254G>A (p.=)
c.-241-13G>A (p.=)
dbSNP gnomAD
20g.35438183G>ACA635351976GDF5c.-255C>T (p.=)
c.-241-14C>T (p.=)
gnomAD
20g.35438183G>TCA635351977GDF5c.-255C>A (p.=)
c.-241-14C>A (p.=)
gnomAD
20g.35438189G>TCA314131806GDF5c.-261C>A (p.=)
c.-241-20C>A (p.=)
dbSNP
20g.35438196G>TCA314131807GDF5c.-241-27C>A (p.=)
c.-268C>A (p.=)
dbSNP gnomAD
20g.35438201C>GCA314131808GDF5c.-241-32G>C (p.=)
c.-273G>C (p.=)
dbSNP gnomAD
20g.35438202C>TCA314131809GDF5c.-241-33G>A (p.=)
c.-274G>A (p.=)
dbSNP
20g.35438203G>ACA314131810GDF5c.-241-34C>T (p.=)
c.-275C>T (p.=)
dbSNP
20g.35438203G=CA325631GDF5c.-241-34C= (p.=)
c.-275C= (p.=)
ClinVar

Number of alleles fetched