Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.18400709G>ACA203566718CACNB2c.49-1215G>A (p.=)
c.130-1215G>A (p.=)
c.-323G>A (p.=)
c.52-1215G>A (p.=)
c.214-1215G>A (p.=)
c.34-1215G>A (p.=)
c.-967G>A (p.=)
n.391-1215G>A
n.214-1215G>A (p.=)
n.130-1215G>A (p.=)
n.262-1215G>A
n.52-1215G>A (p.=)
c.-40-1215G>A (p.=)
dbSNP
10g.18400709G>CCA203566731CACNB2c.49-1215G>C (p.=)
c.130-1215G>C (p.=)
c.-323G>C (p.=)
c.52-1215G>C (p.=)
c.214-1215G>C (p.=)
c.34-1215G>C (p.=)
c.-967G>C (p.=)
n.391-1215G>C
n.214-1215G>C (p.=)
n.130-1215G>C (p.=)
n.262-1215G>C
n.52-1215G>C (p.=)
c.-40-1215G>C (p.=)
dbSNP
10g.18400709G>TCA13260770CACNB2c.49-1215G>T (p.=)
c.130-1215G>T (p.=)
c.-323G>T (p.=)
c.52-1215G>T (p.=)
c.214-1215G>T (p.=)
c.34-1215G>T (p.=)
c.-967G>T (p.=)
n.391-1215G>T
n.214-1215G>T (p.=)
n.130-1215G>T (p.=)
n.262-1215G>T
n.52-1215G>T (p.=)
c.-40-1215G>T (p.=)
dbSNP gnomAD

Number of alleles fetched