Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149960981T>CCA340160SLC26A2n.207+2T>C
c.-26+2T>C (n.-26+2T>C)
c.-306+2T>C (n.-306+2T>C)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149960981T=CA1590730110SLC26A2n.207+2T=
c.-26+2T= (n.-26+2T=)
c.-306+2T= (n.-306+2T=)
 dbSNP

Number of alleles fetched