Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.132334853C>ACA446335133MIR3936HG,SLC22A4c.1182C>A (p.Thr394=)
n.634G>T
c.654C>A (p.Thr218=)
c.906C>A (p.Thr302=)
dbSNP gnomAD v2 gnomAD v4
5g.132334853C>GCA3403605MIR3936HG,SLC22A4c.1182C>G (p.Thr394=)
n.634G>C
c.654C>G (p.Thr218=)
c.906C>G (p.Thr302=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132334853C>TCA446335143MIR3936HG,SLC22A4c.1182C>T (p.Thr394=)
n.634G>A
c.654C>T (p.Thr218=)
c.906C>T (p.Thr302=)
dbSNP

Number of alleles fetched