Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.156138759T>CCA347066LMNAc.1632+2T>C (p.=)
c.1818+152T>C (p.=)
c.1968+2T>C (p.=)
c.1878+2T>C (p.=)
c.1344+2T>C (p.=)
n.2257+2T>C
n.2255+2T>C
c.1671+2T>C (p.=)
n.2181+2T>C
n.552+2T>C
n.756+2T>C (p.=)
ClinVar dbSNP
1g.156138759T>ACA347065LMNAc.1632+2T>A (p.=)
c.1818+152T>A (p.=)
c.1968+2T>A (p.=)
c.1878+2T>A (p.=)
c.1344+2T>A (p.=)
n.2257+2T>A
n.2255+2T>A
c.1671+2T>A (p.=)
n.2181+2T>A
n.552+2T>A
n.756+2T>A (p.=)
ClinVar dbSNP
1g.156138759T>GCA31015743LMNAc.1632+2T>G (p.=)
c.1818+152T>G (p.=)
c.1968+2T>G (p.=)
c.1878+2T>G (p.=)
c.1344+2T>G (p.=)
n.2257+2T>G
n.2255+2T>G
c.1671+2T>G (p.=)
n.2181+2T>G
n.552+2T>G
n.756+2T>G (p.=)
dbSNP

Number of alleles fetched